<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<source>
  <publisher>Regeneron Pharmaceuticals Inc.</publisher>
  <publisherUrl>https://www.regeneron.com/</publisherUrl>
  <lastBuildDate>Mon, 12 Oct 2026 08:44:12 GMT</lastBuildDate>
  <job>
    <title><![CDATA[HVAC Technician (Nights)]]></title>
    <date><![CDATA[Tue, 21 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46924]]></requisitionid>
    <referencenumber><![CDATA[R46924]]></referencenumber>
    <apijobid><![CDATA[r46924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46924/hvac-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an HVAC Technician to join our Facilities Maintenance team. In this role, you will be responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Working hours: Wednesday-Saturday 2:00pm-12:30am</li><li>Training hours: Monday-Friday 8:00am-4:30pm</li><li>Rensselaer, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers.</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work.</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC equipment</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Coordinating with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li></ul><br><h3>This role requires:</h3><ul><li>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level:</li><li>HVAC Technician II: AAS with 2+ years or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years or equivalent combination of education and experience</li><li>HVAC Technician IV: AAS with 8+ years or equivalent combination of education</li><li>Solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>EPA certified for refrigeration gases</li><li>Able to become fully gown qualified to work in production areas</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs (Standard Operating Procedures, cGMPs (current Good Manufacturing Processes), GDPs (Good Documentation Practices) and quality standards</li><li>Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Delivery and Operations Product Lead – Global Patient Safety]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48288]]></requisitionid>
    <referencenumber><![CDATA[R48288]]></referencenumber>
    <apijobid><![CDATA[r48288]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48288/delivery-and-operations-product-lead-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, the Associate Director, Product Lead for Global Patient Safety sits within the Global Development IT organization, and is a key member of the Delivery & Operations function, responsible for coordinating and guiding their team members in delivering, maintaining & enhancing business solutions. This role partners with key business collaborators to intake, design, implement and improve technology products.</p><p><strong>When & where:</strong> </p><p>This role is based at our Armonk, NY or Warren, NJ location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead implementation, operational support and improvements for Global Patient Safety technology products while guiding Product Analysts and other Delivery & Operations team members.</p></li><li><p>Intake, assess, prioritize, and validate domain specific needs/requirements including partnership with BSPs to ensure alignment between technology roadmaps and product priorities.</p></li><li><p>Act tactically and think strategically, switching leadership styles as needed to influence, guide, and mentor individuals and team.</p></li><li><p>Own end-to-end automating reporting solution, including driving quality and compliance by standardizing report templates, ensuring validated linkages to source data, and automating submission-readiness checks.</p></li><li><p>Harmonize narratives, data structures, and formatting rules to improve report consistency across markets, minimizing regional variability and instilling scientific and regulatory compliance in every output</p></li><li><p>Build relationships with key leaders, partners, and stakeholders to clarify and negotiate (when needed) on demands and solutions.</p></li><li><p>Responsible for identifying resourcing needs and for oversight of internal and vendor delivery, and manage service vendor associates, in support of product.</p></li><li><p>Lead steering committee meetings, working groups, system change requests, issue management, and release management for upgrades to existing product.</p></li><li><p>Accountable for the completion of all necessary project deliverables with responsibility for oversight of Product Analysts, Business Analysts, and other team members as applicable. </p></li><li><p>Responsible for end-to-end product management, including oversight of individual project execution and capability-roadmap planning.</p></li><li><p>Partner with Enterprise IT to help customize service offerings to meet Global Development needs where necessary.</p></li><li><p>Responsible for tracking quantifiable value delivered versus plan and preparing consolidated operational reports summarizing savings.</p></li><li><p>Serves as oversight, quality assurance and escalation point for products within team scope.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors Degree in a related field.</p></li><li><p>At least 10+ years relevant experience, including product owner experience of Global Patient Safety technology solutions (e.g., Argus)</p></li><li><p>Experience working on end-to-end GxP implementations from requirements gathering to IQ and PQ execution</p></li><li><p>Knowledge of the Information Technology Service Management Framework and ITIL v3x</p></li><li><p>Knowledge of Software Development Life Cycle, and agile methodologies and tools (e.g., Jira, Confluence)</p></li><li><p>Strong record of accomplishment of technology project management, stakeholder management, budget management and collaboration skills</p></li><li><p>Experience motivating and building skills within a team of direct reports, instilling a process improvement culture in junior level colleagues.</p></li><li><p>Experience participating in an end-to-end product launch or shut down across multiple teams.</p></li><li><p>Experience hiring, supervising, managing, and mentoring a team in service of complex issues.</p></li></ul><ul><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience</p></li><li><p>Ability to analyze business challenges and present technology solutions</p></li><li><p>Knowledge of pharmaceutical Global Development (e.g., Global Patient Safety, Regulatory Affairs, Clinical Quality) business capabilities, processes, systems, and key trends in the industry</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Government Pricing]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46609]]></requisitionid>
    <referencenumber><![CDATA[R46609]]></referencenumber>
    <apijobid><![CDATA[r46609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46609/associate-director-government-pricing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Government Pricing (GP) position is a key member of Regeneron’s government pricing team, which includes supporting the accurate calculation and timely submission of all required government price reporting.</p><p>Included in this role is responsibility for assuring compliance with all pricing and reporting requirements legislated by the Centers for Medicare & Medicaid Services (CMS), the Department of Veterans Affairs and any state legislation required price reporting. This includes a full understanding of all current legislation and staying abreast of pending legislation. Government Pricing Calculations include: Medicaid, Medicare Part B, Public Health Service (PHS)/340B, and Federal Supply Schedule (FSS), which includes: TriCare and the Industrial Funding Fee (IFF). The Associate Director will work collaboratively with Contracting Strategy supporting the overall strategy, contracting and/or payment activities.</p><h3>When & where:</h3><ul><li>Remote with some travel when needed</li></ul><h3>Discover your role:</h3><ul><li>Ability to calculate, validate and report accurate monthly, quarterly, and annual government pricing.</li><li>Submit and monitor State Price Transparency regulations.</li><li>Complete understanding of calculation reasonable assumptions and methodologies and ability to research and communicate cause of variances of results when comparing current period to prior periods.</li><li>Perform all necessary processes needed to ensure compliant submissions including, but not limited to G/L reconciliations, Class of Trade (COT) review, and PHS/340b eligibility review.</li><li>Associate Director will review calculations with Senior Management and obtain approval signoff (and executes any other required Standard Operating Procedures (SOPs)) before communicating prices to the appropriate government agencies (Center for Medicare and Medicare (CMS), Veterans Affairs (VA)/Department of Defense (DOD), etc.) or internally.</li><li>Responsible for maintaining and updating SOP’s and reasonable assumptions, on a quarterly basis, as related to Government Programs/Pricing.</li><li>Monitor policies, procedures and processes supporting Government Pricing submissions and related areas to ensure ongoing compliance with external and internal requirements and guidance.</li><li>Understand and estimate impact of pricing and policy changes regarding government pricing.</li><li>Perform pricing research and analysis on special projects as assigned.</li><li>Ability to review and understand commercial contract language as pertaining to Best Price (BP), Average Sales Price (ASP) and FSS Tracking Customers.</li><li>Investigate Government pricing trends and cross channel impact. Also provide Government price inputs to the Gross to Net (GTN) team.</li><li>Monitor for Tracking customer violations, Bona Fide Service Fee treatments & Customer COT assignment.</li><li>Participate on cross-functional teams as a subject matter expert representing the Government Pricing and Contract Operations as required to evaluate and implement business strategies and initiatives.</li><li>Serve as a liaison with Commercial Leadership, Pricing, Trade, Brand and Accounting/Finance teams regarding a variety of issues impacting government pricing.</li><li>Familiar with Fair Market Value methodology while determining bona fide service fees paid to Wholesaler, Pharmacy Benefit Manager (PBM) and Group Purchasing Organizations (GPOs).</li></ul><h3>This role requires:</h3><ul><li>Bachelors degree and</li><li>7+ years prior experience in Government Pricing OR a related field such as finance, accounting, Medicare/Medicaid</li><li>Strong analytical skills</li><li>10+ years of professional experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Insights & Analytics - Immunology]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49734]]></requisitionid>
    <referencenumber><![CDATA[R49734]]></referencenumber>
    <apijobid><![CDATA[r49734]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49734/executive-director-commercial-insights-analytics-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director to lead our <strong>Commercial Insights and Analytics (I&A), Immunology</strong> team.</p><p>The Executive Director, Commercial Insights and Analytics (I&A), Immunology, will report directly into the Vice President, Commercial Strategy and Insights & Analytics (CSI&A) within the CSI&A department. This role will lead the high-performing I&A team responsible for the Immunology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions across some of Regeneron’s leading brands. The role will partner with and serve as a strategic advisor for the SVP, Commercial Immunology CBU, and will partner with other leaders to grow and develop talent within the I&A organization.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Immunology team in providing business analytics, customer insights and competitive intelligence to deliver rich insights to solve key business problems </p><p>2) Set the strategic I&A direction that aligns with CBU priorities and helps drive commercial excellence </p><p>3) Serve as a member of the Immunology CBU Leadership Team, providing I&A expertise </p><p>4) Serve as a member of the CSI&A leadership team to drive cross-commercial innovation and best-in-class delivery </p><p><em>Develop</em></p><p>5) Translate complex analyses into compelling insights and recommendations that will be used to inform business decision-making for senior Regeneron teams, including the CBU, Chief Commercial Officer, Chief Executive Officer and Board of Directors </p><p>6) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent </p><p>7) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform brand differentiation, market growth and business impact; and <strong>b)</strong> consider business potential for pipeline products </p><p><em>Partnership and Collaboration</em></p><p>8) Collaborate with the Immunology CBU and other members of senior leadership to contribute to ongoing brand strategies and decisions, including long-term data, analytics and insights roadmap</p><p>9) Develop and maintain a mutually beneficial partnership with CBU stakeholders; ensure insight generation and feedback are embraced; strike a balance between project rigor, timelines and ability to influence decisions</p><p>10) Lead efforts to identify and crystalize insights that inform strategic plans for the Immunology CBU </p><p>11) Work with other CSI&A leaders to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analyses, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>12) Proactively communicate with the Immunology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>13) Construct and deliver integrated business reviews, I&A summary overviews with the Immunology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>This role requires:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with buy-and-bill brands in highly competitive markets is required</p></li><li><p>Minimum Bachelor’s degree in data science, public health, statistics, engineering, or a related field</p></li><li><p>Functional expertise in business analytics, customer insights, analog forecast development, market access, and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, customer insights, market access analytics, and competitive intelligence</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution with hands on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li><li><p>Master’s (MBA, MPH, MS) preferred</p></li><li><p>Experience with co-promotes, as well as the immunology disease category, is strongly desired</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist, Oncology Sales - Minneapolis, MN]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49682]]></requisitionid>
    <referencenumber><![CDATA[R49682]]></referencenumber>
    <apijobid><![CDATA[r49682]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49682/medical-account-specialist-oncology-sales-minneapolis-mn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minneapolis]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Minneapolis, MN</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them</p></li></ul><p>​</p><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred)</p></li><li><p>Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions</p></li><li><p>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. </p></li><li><p>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace</p></li><li><p>You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization</p></li><li><p>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Must have ability to travel and cover large geography territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior QA Validation Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48401]]></requisitionid>
    <referencenumber><![CDATA[R48401]]></referencenumber>
    <apijobid><![CDATA[r48401]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48401/senior-qa-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Senior QA Validation Specialist</strong> to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><ul><li>Location: Raheen, Limerick</li><li>Some travel may be required.</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Generating, executing and/or reviewing master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria</li><li>Analysing the results of testing and determines the acceptability of results against pre-determined criteria</li><li>Investigating and troubleshooting problems which occur and determines solutions or recommendations for changes and/or improvements</li><li>Reviewing, editing and approval deviation notifications, deviation investigations, and corrective actions</li><li>Reviewing and approval of change controls, SOPs, reports and other documentation</li><li>Coordinating with other departments or outside contractors/vendors to complete validation tasks</li><li>Managing projects and prepares status reports</li><li>Providing oversight to contingent workers may be a requirement</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Ability to work independently or as part of a team</li><li>Ability to communicate with transparency</li><li>Meets commitments on scope and on time</li><li>Follows directions, performs well-defined tasks</li><li>Effective time management skills</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>To be considered for this opportunity you must have a BS/BA in Engineering, Chemistry or Life Science and requires at least 5 – 8+ years’ proven experience in Commissioning / Qualification experience with Large Scale Process equipment </li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQA </strong><strong>#REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49351]]></requisitionid>
    <referencenumber><![CDATA[R49351]]></referencenumber>
    <apijobid><![CDATA[r49351]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49351/principal-qa-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Principal QA Specialist </strong>to join our <strong>QA Compliance & Quality Systems </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Serving as a Quality Systems Subject Matter Expert (SME) with primary responsibility for Change Control governance, oversight, and continuous improvement activities.</p></li><li><p>Providing quality and compliance oversight of Quality System processes, including but not limited to: Change Control, Deviations, CAPA's, Audits, Customer Complaints and Risk Management.</p></li><li><p>Ensuring Quality System records are managed in compliance with regulatory requirements, company procedures, and data integrity expectations.</p></li><li><p>Reviewing and approving Quality System documentation, including Change Control records, Deviation investigations, CAPA plans and Risk assessments.</p></li><li><p>Leading or supporting governance forums, review boards, and cross-functional meetings associated with Change Control and Quality System management.</p></li><li><p>Monitoring, analysing, and communicating Quality System performance metrics and trends, finding opportunities to improve process effectiveness, efficiency, and compliance.</p></li><li><p>Performing quality review of complex, high-impact, and cross-functional changes to ensure appropriate assessment of product quality, regulatory, validation, and operational impacts.</p></li><li><p>Supporting regulatory inspections and customer audits, including preparation activities, presentation of Quality System processes, and response development for observations or commitments.</p></li><li><p>Identifying compliance risks, process gaps, and systemic issues within Quality Systems and leads or supports development and implementation of sustainable corrective actions.</p></li><li><p>Collaborating with Manufacturing, Quality Control, Engineering, MSAT, Supply Chain, Validation, Regulatory Affairs, and other site functions to ensure quality and compliance requirements are effectively integrated into business processes.</p></li><li><p>Leading and participating in continuous improvement initiatives aimed at enhancing Quality System performance, inspection readiness, and operational excellence.</p></li><li><p>Supporting the development, implementation, and maintenance of Quality System procedures, policies, and training programs.</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>Experience working with Quality Systems, including one or more of the following: Change Controls, Deviations, CAPA's, Audit Management and Risk Management</p></li><li><p>Working knowledge of cGMP requirements and regulatory expectations.</p></li><li><p>Strong organisational, communication, and stakeholder management skills, with the ability to effectively coordinate activities across multiple functional areas.</p></li><li><p>Able to prioritise, re-prioritise as needed and adapt to change.</p></li><li><p>Comfortable working in a fast-paced setting.</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>Requires BSc/BEng in scientific discipline or related field with 7+ years of relevant work experience in pharmaceutical or related industry.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Manufacturing Sciences & Technology Engineer]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49407]]></requisitionid>
    <referencenumber><![CDATA[R49407]]></referencenumber>
    <apijobid><![CDATA[r49407]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49407/principal-manufacturing-sciences-technology-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking a Principal MSAT Engineer to join our Process Sciences Drug Product Engineering department. This role supports and/or leads equipment selection, CMO selection strategy, management of equipment qualification and/or process validation activities and will be hands-on solving issues during technology transfer and cGMP start-up. The MSAT team establishes best practices for technical support of cGMP drug product manufacturing operations. The Engineer also provides floor support during operations of internal or external manufacturing, reviews process data to ensure operational consistency after processes are successfully transferred and provides support for investigations.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm </li><li>Travel percentage: 25-50% domestic & occasionally international</li></ul><p><strong>Discover your role:</strong></p><ul><li>Serves as technical lead and subject matter expert for drug product manufacturing process transfer, providing oversight for new product introduction, technology transfer, and process troubleshooting/issue resolution</li><li>Tracks and reports project milestones (raw material/component procurement, equipment readiness, analytical transfer, documentation) and partners with/leads cross-functional internal and external teams to ensure successful transfer execution</li><li>Reviews and approves cGMP batch documentation (master batch records, specifications, validation protocols) and authors policies, technical reports, protocols, and change controls in support of cGMP activities</li><li>Monitors cGMP compliance at drug product contract manufacturers to protect product integrity and company reputation</li><li>Trends process performance to establish and improve process capability, ensuring operations remain within the intended control strategy</li><li>Investigates deviations, determines root cause, and identifies/implements CAPA; develops sampling plans for GMP batches (lot release, stability, characterization)</li><li>Collaborates with internal/external teams to identify and drive opportunities for improved process performance and cGMP operations</li><li>Leads or assists in equipment selection, qualification, and start-up activities, and works with Manufacturing to ensure robust operating procedures</li><li>Partners with Strategic Sourcing/Procurement to define technical requirements for raw materials, components, equipment, and services, ensuring on-time vendor delivery</li><li>Works with DP MSAT management to define organizational structure, prioritize strategic initiatives, and assess staffing needs to support growth</li><li>Leverages subject matter expertise to resolve emerging issues and escalates to line management as needed to manage impact</li><li>Bring demonstrated technical knowledge in drug product manufacturing, product development, and validation, along with experience interacting with Contract Manufacturing Organizations</li><li>Apply strong knowledge of industry practices and regulations (cGMP, Annex I) across multiple health authorities, including FDA, EMA, and MHRA</li></ul><p><strong>This role requires: </strong></p><ul><li>BS/BA in Engineering, Chemical Engineering, Biomedical Engineering preferred<ul><li>Principal MSAT Engineer: 8+ years of relevant experience</li><li>Staff MSAT Engineer: 10+ years of relevant experience</li></ul></li><li>Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-New Brunswick, NJ]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49951]]></requisitionid>
    <referencenumber><![CDATA[R49951]]></referencenumber>
    <apijobid><![CDATA[r49951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49951/medical-specialist-i-allergyent-new-brunswick-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists, Otorhinolaryngologists (ENT) and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US</p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Allergy and Otorhinolaryngology (ENT) therapeutic areas to generate product utilization. The MS will develop strong working relationships with Allergy/ENT experts and clinicians in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: New Brunswick, NJ (Flemington, Bridgewater, Princeton, East Brunswick)</p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in Allergy/ENT/Dermatology and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41999]]></requisitionid>
    <referencenumber><![CDATA[R41999]]></referencenumber>
    <apijobid><![CDATA[r41999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r41999/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team at our Menands campus with a Monday-Friday 8:00am-4:30pm shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p><strong>When & where:</strong></p><ul><li>Location: Menands, New York, United States</li><li>Work Shift: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover Your Role:</strong></p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p>This Role Requires:</p><p>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level. Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred.</p><ul><li>HVAC Technician II: AAS with 2+ years of relevant experience or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years of relevant experience or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Engineer]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49585]]></requisitionid>
    <referencenumber><![CDATA[R49585]]></referencenumber>
    <apijobid><![CDATA[r49585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49585/project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><strong>Build our future together:</strong></div><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Project Engineer </strong>to join our <strong>Project Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Designing and specifying cGMP process equipment, piping, and/or controls</p></li><li><p>Managing small projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li><li><p>Preparing process and instrument drawings and other related drawings</p></li><li><p>Developing Process Flow Diagrams for manufacturing processes.</p></li><li><p>Supporting the validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Assisting in investigations of process equipment and control system anomalies</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations for and executes modification change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>Problem-solving and continuous improvement skills</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>To be considered for this opportunity you should have a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Digital Lab Orchestration]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45569]]></requisitionid>
    <referencenumber><![CDATA[R45569]]></referencenumber>
    <apijobid><![CDATA[r45569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/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[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director of Digital Lab Orchestration to join our IOPS IT team, leading the design, integration, and deployment of the orchestration layer that connects QC laboratory systems into a cohesive, compliant, and automated ecosystem. In this role, you will bridge QC operations, IT/OT, automation, and data governance to enable end-to-end digital QC workflows — while partnering with Quality, CSV teams, system integrators, and external vendors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li><li></li></ul><p>​<strong>Discover your role:</strong></p><ul><li>Lead the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across laboratory instruments and middleware; define integration patterns including APIs, event-driven architectures, message queues, and file-based approaches</li><li>Translate QC business processes into orchestrated digital workflows, enabling automated sample lifecycle management, test execution, result capture, review, and release</li><li>Ensure scalability, resilience, and performance of lab integrations; incorporate resiliency into architecture as the organization moves toward a connected lab platform</li><li>Support real-time and near-real-time data flow from lab instruments to enterprise systems; make decisions on integration patterns and drive connected lab progression</li><li>Ensure all integrations comply with GxP, ALCOA+, 21 CFR Part 11, and Annex 11 requirements; partner with Quality and CSV teams to support risk-based validation strategies including CSA where applicable</li><li>Act as the primary integration point between QC, IT, automation, and external vendors; evaluate vendor platforms and integration tools for orchestration capabilities and lead technical discussions with system integrators and software suppliers</li><li>Support incident resolution, root cause analysis, and continuous improvement across the lab orchestration ecosystem</li><li>Assist in annual IT budgeting, vendor negotiations, and resource allocation; ensure auditability, traceability, and controlled change management across all integrations</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology or a related field, or equivalent combination of education and experience</li><li>Senior Manager: 8+ years of experience in Information Systems and Technology, including 6+ years managing employees and budgets, with 5+ years in a GMP biotech or pharma environment</li><li>Associate Director: 10+ years of experience in Information Systems and Technology, including 8+ years managing employees and budgets, with 7+ years in a GMP biotech or pharma environment</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li><li>Industry experience implementing lab orchestration solutions including platforms such as Scitara, Tetra Science, or other emerging tools preferred</li><li>Knowledge of IT compliance guidelines including PIC/S, 21 CFR Part 11, Annex 11, and GAMP preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Digital & Technology - Law, Security, Compliance]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50009]]></requisitionid>
    <referencenumber><![CDATA[R50009]]></referencenumber>
    <apijobid><![CDATA[r50009]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50009/executive-director-digital-technology-law-security-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Building Our Future:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director to lead the digital and technology portfolio for Law, Security, and Compliance, while also holding cross-portfolio accountability for critical operating disciplines across the broader G&A and Commercial Digital and Technology portfolio. This leader will partner with senior management to shape technology strategy, strengthen portfolio governance, and ensure disciplined execution across mission-critical capabilities, including audit preparedness. Decisions carry enterprise-wide, measurable long-term impact, requiring a leader who can translate business priorities into scalable, secure, compliant, and outcome-driven digital capabilities.</p><p><strong>When & Where:</strong></p><p>This role is based in our Sleepy Hollow, NY office a minimum of 4 days per week.</p><p><strong>Discover Your Role:</strong></p><ul><li>Define and execute the multi-year technology strategy and transformation roadmap for Legal, Security, Compliance, aligning with corporate objectives and regulatory requirements.</li><li>Lead and optimize technology platforms supporting legal operations, contract lifecycle management, governance, risk, compliance, privacy, investigations, and corporate security.</li><li>Build and lead a high-performing technology organization, developing talent and delivery capabilities across complex enterprise functions.</li><li>Drive business outcomes through improved contract management, compliance monitoring, investigations, security operations, automation, system reliability, and user productivity.</li><li>Modernize and streamline the application landscape through enhanced integrations, workflow simplification, analytics, reporting, and scalable enterprise solutions.</li><li>Advance AI and automation strategies, including responsible AI governance, to improve decision-making, operational efficiency, risk management, and controls effectiveness.</li><li>Standardize global processes and operating models across legal, compliance, privacy, security, and related shared services functions.</li><li>Oversee vendor management, technology investments, audit readiness, cybersecurity, business continuity, communications, and portfolio governance to ensure secure, compliant, and high-value service delivery.</li></ul><p><strong>This Role Requires:</strong></p><ul><li>BS/BA in Computer Science, Information Systems, Business, or a related field required; MS, JD or MBA preferred.</li><li>17+ years of progressive technology leadership, including teams supporting law, security, compliance, risk, governance, or other highly regulated enterprise functions.</li><li>Strong command of legal, security, compliance, GRC, privacy, investigations, contracts, and enterprise workflow platforms, with the judgment to stay platform-agnostic.</li><li>Experience with enterprise platforms supporting Law, Security, Compliance, GRC, privacy, legal operations, contracts, investigations, service management, and analytics is preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Operations (FTC) – Toronto]]></title>
    <date><![CDATA[Sun, 30 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47104]]></requisitionid>
    <referencenumber><![CDATA[R47104]]></referencenumber>
    <apijobid><![CDATA[r47104]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47104/senior-manager-commercial-operations-ftc-toronto/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></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’re looking for our next team member to proactively support our Oncology Canada Field Sales & Marketing Teams and help ensure Commercial Operations programs land efficiently, compliantly, and on time.</p><p>You’ll partner closely with cross-functional colleagues (including Analytics, Marketing Ops, IT, HR, Training, and Meetings & Events) to keep field enablement running with care and precision—from alignments and communications to onboarding and contracting support. If you enjoy connecting people, details, and execution to make a significant difference for teams (and ultimately patients), this role offers real scope and impact.</p><h3><strong>Senior Manager, Commercial Operations (FTC - 12 months) – Toronto</strong></h3><p><strong>A Typical Day:</strong></p><ul><li>Executing field sizing, alignments, targeting, segmentation, and incentive compensation analyses.</li><li>Coordinating localized promotional materials with Marketing Ops and IT.</li><li>Ensuring materials follow Medical, Legal, Regulatory (MLR) review processes.</li><li>Managing field communications (Sales Updates, Competitive Updates) through approvals and distribution.</li><li>Partnering with HR and IT on routine field roster management.</li><li>Supporting HCP contracting requests for advisory boards and consulting engagements.</li><li>Coordinating meetings, exhibits, sponsorships, and funding requests with Events partners.</li><li>Coordinating onboarding/offboarding logistics and communications with HR, IT, and collaborators.</li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li>You enjoy being a trusted partner for field teams and stakeholders.</li><li>You like balancing structure and flexibility across multiple concurrent deliverables.</li><li>You care about getting communications clear, accurate, and appropriately reviewed.</li><li>You’re comfortable coordinating across Analytics, Marketing Ops and Training.</li><li>You are proactive in identifying issues early and help resolve them thoughtfully.</li><li>You value using secondary data sources (including market research) to support insights.</li></ul><p><strong>To be considered</strong>, you’ll bring 5+ years of relevant pharmaceutical/biotech proven experience in Commercial Operations roles with increasing responsibilities and accountability, along with functional field support experience in the Canadian market and an understanding of Canadian biopharmaceutical commercial dynamics, laws, and regulations. English proficiency is required, and you’re confident working in Microsoft PowerPoint, Excel, and Word, as well as platforms such as Veeva and Power BI.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement- Training and Development]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50164]]></requisitionid>
    <referencenumber><![CDATA[R50164]]></referencenumber>
    <apijobid><![CDATA[r50164]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50164/director-global-procurement-training-and-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Global Procurement - Training and Development to join our Global Procurement organization. In this role, you will lead the design, execution, and evolution of our procurement capability agenda, shaping the learning culture and internal talent pipeline that powers our global procurement function, while collaborating with leaders across Global Procurement and HR. You will also ensure delivery of training programs, development of functional competencies, and early career talent initiatives.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Sleepy Hollow</p></li><li><p>Work model/flexibility: On-site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Develops and implements a global procurement learning and development strategy aligned to business needs and future skills</p></li><li><p>Designs, delivers, and scales training programs spanning onboarding, functional skills, systems, and leadership development</p></li><li><p>Leads the Future Leaders Early Talent Development Program, including graduate hiring, rotations, and mentorship</p></li><li><p>Establishes a procurement competency framework and learning roadmap across all regions and categories</p></li><li><p>Partners with HR, procurement leaders, and external providers to ensure consistent global learning standards</p></li><li><p>Measures training impact through feedback, assessments, and performance outcomes, iterating for continuous improvement</p></li><li><p>Leverages digital learning platforms and analytics to enable scalable, personalized learning experiences</p></li><li><p>Coaches and guides direct reports on performance and career development, modeling leadership for the organization</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Director Level: Bachelor's degree with 10-15 years of experience in procurement or supply chain environments (preferably in Pharma/BioPharma)</p></li><li><p>Demonstrated success leading and supporting procurement or supply chain teams through training and change programs</p></li><li><p>Experience building early career talent programs such as graduate schemes, internships, or rotational programs</p></li></ul><p><strong>Preferred qualifications:</strong></p><ul><li><p>Command of adult learning principles, instructional design, and digital learning technologies</p></li><li><p>Experience leading associate-level professionals in a multi-national firm, including performance reviews and coaching</p></li><li><p> Experience in Pharma/BioPharma</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Biostatistics - Hematology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50347]]></requisitionid>
    <referencenumber><![CDATA[R50347]]></referencenumber>
    <apijobid><![CDATA[r50347]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50347/manager-biostatistics-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager</strong> to join our <strong>Biostatistics Hematology </strong>team. This position is for a qualified Statistician/Biostatistician to support Clinical Biostatistics within Global Development. </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>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Interacting 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>Developing individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.</p></li><li><p>Collaborating with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting. </p></li><li><p>Evaluating appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</p></li><li><p>Analyzing data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making. </p></li><li><p>Preparing 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>This role requires:</strong></p><ul><li><p>PhD or equivalent degree in statistics/biostatistics with >2 years’ experience in the pharmaceutical industry, or MS degree in statistics/biostatistics with >7 years’ 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 such as R or SAS is required</p></li></ul><p>#Regnbiostats</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49618]]></requisitionid>
    <referencenumber><![CDATA[R49618]]></referencenumber>
    <apijobid><![CDATA[r49618]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49618/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Engineer to join our Automation Engineering team to keep our groundbreaking process controls and process monitoring systems running at peak efficiency. In this role, you will build, develop, and optimize systems for our sophisticated biopharmaceutical manufacturing processes. You will collaborate closely with multiple teams to include Manufacturing, Quality Control, and Facilities. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Rensselaer, New York, United States </p></li></ul><ul><li><p>Work model: Monday - Friday 8:00AM - 4:30PM </p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Design, develop, and implement software and hardware improvements to automated and new equipment under change control. </p></li></ul><ul><li><p>Provide PLC- and HMI-based technical support to various departments per established SOPs. </p></li></ul><ul><li><p>Identify, investigate, and resolve manufacturing deviations tied to automated control systems. </p></li></ul><ul><li><p>Develop engineering design documents, technical evaluations, and test plans in line with GAMP 5. </p></li></ul><ul><li><p>Support process control and monitoring equipment through software design, commissioning, testing, and corrective action. </p></li></ul><ul><li><p>Support small manufacturing, engineering, and validation projects. </p></li></ul><ul><li><p>Author and execute Factory Acceptance Test and Site Acceptance Test protocols and system specifications. </p></li></ul><ul><li><p>Champion continuous improvement as an everyday outlook, not just a metric. </p></li></ul><p><strong>This role requires: </strong></p><ul><li><p>BS in Engineering or a related field, with 5+ years of relevant experience; equivalent combination of education and experience may be considered. </p></li></ul><ul><li><p>Experience in the design and maintenance of process control and/or data acquisition systems is required. </p></li></ul><ul><li><p>Experience programming and troubleshooting the DeltaV DCS as well as PLCs. Experience with Allen-Bradley and Siemens control system products and video graphic chart recorders is ideal. </p></li></ul><ul><li><p>Experience in a regulated manufacturing environment is ideal </p></li></ul><ul><li><p><strong>Gowning and Physical Requirements:</strong> </p></li></ul><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></ul><ul><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire is required </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Research Specialist – TPK/PD]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50265]]></requisitionid>
    <referencenumber><![CDATA[R50265]]></referencenumber>
    <apijobid><![CDATA[r50265]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50265/senior-research-specialist-tpkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Research Specialist, TPK-PD to join our nonclinical analysis team supporting our Translational PK-PD organization. In this role, you will perform non-compartmental and compartmental PK/PD analyses in support of nonclinical and (potentially) clinical studies using Phoenix WinNonlin and other analysis software and will prepare and quality-control standardized datasets from CRO and internal bioanalytical data for regulatory submission. This person will contribute to PK/TK protocol design/input, support CRO studies, produce Pharmacometrics deliverables and regulatory tables/figures/listings, and follow all SOPs to ensure GxP/GLP compliance. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & Where</strong></p><p>This role is based in our Tarrytown, NY office and will be onsite four days per week.</p><p><strong>Discover Your Role</strong></p><ul><li>Performs non-compartmental PK and compartmental PK/PD analyses in support of nonclinical and (potentially) clinical studies, according to GxP as appropriate.</li><li>Conducts compliance-related activities (SOPs, etc.); ensures regulatory-submission conformance, data integrity, and GxP compliance; adheres to controlled SOPs; and meets mandatory-training and data-confidentiality requirements.</li><li>Prepares and quality-controls standardized CDISC SEND datasets (e.g., PC/PP domains and associated SUPPQUAL) from CRO and internal bioanalytical data, with auditable, source-traceable derivations that conform to controlled terminology and regulatory-submission standards.</li><li>Supports CRO studies; tracks study requirements, project priorities, status, and milestones; and coordinates with functional groups across the study lifecycle.</li><li>Independently executes a broad array of work supporting department priorities in routine Pharmacometrics deliverables on study design, analysis, and reporting.</li><li>Produces and formats tables and listings (TFLs), including PK concentration and parameter summaries, for regulatory documents using validated tools (e.g., Phoenix WinNonlin, R), to a consistent, submission-ready presentation standard.</li><li>Produces figures and graphical outputs (e.g., concentration-time profiles) for study reports and regulatory submissions using validated tools.</li></ul><p><strong>This Role Requires</strong></p><ul><li>Bachelor's degree and 2-4 years of relevant experience, or a Master's degree with 0-2 years of relevant experience</li><li>An understanding of pharmacokinetics concepts and techniques </li><li>Skilled in the use of relevant software, including Phoenix WinNonlin; may include knowledge of NLME</li><li>Experience in animal PK/TK studies, including protocol design & study conduct</li><li>Able to clearly describe and perform advanced pharmacometric techniques and interpret results</li><li>Experience in working in a GLP environment and following SOPs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement- Direct CMO]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50244]]></requisitionid>
    <referencenumber><![CDATA[R50244]]></referencenumber>
    <apijobid><![CDATA[r50244]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50244/senior-manager-global-procurement-direct-cmo/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Global Procurement Direct CMO to join our Global Procurement team. In this role, you will provide strategic leadership within the CMO category of Direct Global Procurement, driving implementation, resolution, and guidance across Regeneron's External Manufacturing network while collaborating with stakeholders and Procurement category owners to advance stakeholder goals, competitive advantage, and supplier relationships.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Troy, NY</p></li><li><p>Work model/flexibility: On-site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Defines and implements CMO manufacturing category strategy to meet business needs</p></li><li><p>Leads discussions with IOPS stakeholders to align Drug Product manufacturing priorities with Procurement category leads and management</p></li><li><p>Negotiates complex contracts and drives supplier management and stakeholder engagement activities</p></li><li><p>Drives cost savings, cash flow improvement, and other efficiency gains through category management</p></li><li><p>Ensures category activities comply with GxP and other applicable regulations</p></li><li><p>Negotiates contract terms and conditions in consultation with Law, aligned with Regeneron's priorities and business requirements</p></li><li><p>Establishes and drives Supplier Relationship Management (SRM) programs and governance models</p></li><li><p>Navigates a dynamic, fast-changing business environment, proactively identifying opportunities and driving results</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Sr Manager Level: Bachelor's degree in a relevant field with 7+ years of progressive procurement experience, preferably in Pharma/BioPharma</p></li><li><p>Experience in the mAb, large molecule manufacturing environment</p></li><li><p>Strong negotiation and contract management skills</p></li></ul><p><strong>Preferred qualifications:</strong></p><ul><li><p>Experience managing category stage gate processes, including strategy development and execution</p></li><li><p>In-depth knowledge of the Drug Product manufacturing process</p></li><li><p>Success building relationships with stakeholders and suppliers to drive results, using market intelligence, risk, compliance, and financial assessment tools to evaluate global supply markets</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Engineer]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49320]]></requisitionid>
    <referencenumber><![CDATA[R49320]]></referencenumber>
    <apijobid><![CDATA[r49320]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49320/automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Engineer to join our Automation Engineering team to keep our groundbreaking process controls and process monitoring systems running at peak efficiency. In this role, you will build, develop, and optimize systems for our sophisticated biopharmaceutical manufacturing processes. You will collaborate closely with multiple teams to include Manufacturing, Quality Control, and Facilities. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: On-site Monday - Friday 8:00AM - 4:30PM</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Design, develop, and implement software and hardware improvements to automated and new equipment under change control.</p></li><li><p>Provide PLC- and HMI-based technical support to various departments per established SOPs.</p></li><li><p>Identify, investigate, and resolve manufacturing deviations tied to automated control systems.</p></li><li><p>Develop engineering design documents, technical evaluations, and test plans in line with GAMP 5.</p></li><li><p>Support process control and monitoring equipment through software design, commissioning, testing, and corrective action.</p></li><li><p>Support small manufacturing, engineering, and validation projects.</p></li><li><p>Author and execute Factory Acceptance Test and Site Acceptance Test protocols and system specifications.</p></li><li><p>Champion continuous improvement as an everyday outlook, not just a metric.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS in Engineering or a related field, with 2+ years of relevant experience; equivalent combination of education and experience may be considered.</p></li><li><p>Experience in the design and maintenance of process control and/or data acquisition systems is required.</p></li><li><p>Experience programming and troubleshooting the DeltaV DCS as well as PLCs. Experience with Allen-Bradley and Siemens control system products and video graphic chart recorders is ideal.</p></li><li><p>Experience in a regulated manufacturing environment is ideal</p></li><li><p><strong>Gowning and Physical Requirements:</strong></p></li><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 is required</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $123,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Device Development Engineer]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49477]]></requisitionid>
    <referencenumber><![CDATA[R49477]]></referencenumber>
    <apijobid><![CDATA[r49477]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49477/senior-device-development-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Device Development Engineer to join our New Technologies, Combination Products Innovation team. This engineer will be responsible for front-end innovation projects and scenario planning to support Regeneron’s growing pipeline, working cross-functionally to define patient, user, and business needs, identify and advocate for novel device solutions and opportunities, and manage early-stage device design and development programs.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Monitor drug delivery device technologies and competitor activity to keep our device strategy ahead of the curve</li><li>Build relationships with molecule development teams and monitor portfolio to identify device requirements well before they become critical-path decisions, ensuring device readiness never bottlenecks program timelines</li><li>Evaluate and develop device strategy proposals across a diverse portfolio of therapeutics, balancing patient needs, drug product constraints, and commercial considerations through strong relationships with stakeholders</li><li>Project management of early device development projects, coordinating cross-functionally</li><li>Lead and influence drug-device combination product scenario planning for new and lifecycle management programs, collaborating cross-functionally to gather stakeholder input, drive strategic decisions, and gain buy-in on long-term device strategies within therapeutic areas</li><li>Research, monitor, and analyze drug delivery system industry and market trends, competitive landscapes, internal pipeline drug delivery needs, and patient/user needs to identify innovation opportunities and advise device strategy</li><li>Perform technical feasibility evaluations and due diligence assessments, working with external strategic partners to drive toward innovative device solutions</li><li>Lead early-stage drug delivery system design efforts with a multi-functional team, translating business needs and stakeholder requirements into comprehensive project plans and innovative product design</li><li>Generate insights through exploratory, user, and foundational research to inform the drug delivery system portfolio, collaborating with technical teams, human factors, commercial, clinical, and other subject matter experts as applicable</li><li>Maintain a culture of continuous improvement that strives to ensure safety and efficacy while accelerating delivery of commitments</li><li>Represent Regeneron and the device teams at appropriate industry meetings and forums</li><li>Demonstrate strong communication, presentation skills and can strategic alignment</li><li>Possess project management skills and can work effectively across multiple functional teams</li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering field; Biomedical Engineering or Mechanical Engineering is preferred<ul><li>Device Development Engineer: 2+ years of experience</li><li>Sr. Device Development Engineer: 5+ years of experience</li><li>Experience with design history file management (21 CFR 820.30)</li><li>Experience with delivery device branding/marketing is preferred </li></ul></li><li>Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Safety Standards & Training]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50483]]></requisitionid>
    <referencenumber><![CDATA[R50483]]></referencenumber>
    <apijobid><![CDATA[r50483]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50483/associate-director-global-patient-safety-standards-training/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Global Patient Safety Standards & Training</strong> team.</p><br><p>Reporting to the Head of Global Patient Safety (GPS) Standards & Training, this position is responsible for establishing and maintaining procedures and policies consistent with Pharmacovigilance regulatory requirements and industry standards. A key part of the role is close collaboration with the Process and Procedures (P&P) team and support of the Process Owner Network (PONs). The responsibilities of this job are foundational in the creation and maintenance of the Pharmacovigilance (PV) System that is essential in enabling the department, and therefore the company, to comply with regulatory PV requirements in all relevant territories worldwide, and to operate efficiently and effectively in alignment with established industry practices. The role supports GPS activities and ensures procedures remain compliant with applicable global regulations as they evolve.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Sleepy Hollow, NY, Warren, NJ or Cambridge, MA</li><li>4 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Ensure that PV Intelligence updates are systematically assessed and reflected in GPS procedures, so that documented processes remain aligned with current regulatory expectations and the procedural framework is maintained in a state of audit and inspection readiness at all times.</li><li>Act as a key liaison to Process & Procedures (P&P) and the Learning Centre of Excellence (LCoE) for procedural updates, so that procedural changes are accurately captured, appropriately sequenced, and correctly reflected in the associated training curriculum.</li><li>As an SME, partner with the Head of GPS Safety Operations to validate that procedures are fit for purpose against safety practices, closing gaps between documented process and operational execution, including the mapping of procedural documents to regulations and to the training curriculum.</li><li>Apply deep PV process design expertise to develop, implement, and maintain GPS procedures in alignment with regulations, Regeneron Standards, and industry best practices — in partnership with Process & Procedures (P&P), Process Owners, and SMEs — and lead the assessment of evolving global PV regulations.</li><li>As a primary liaison to P&P, partner to set risk-based prioritization and sequencing in managing procedural updates across the GPS framework, in partnership with PONs and GPS Functional Leads.</li><li>Assist in ensuring the correct procedural documents are assigned to the relevant training curriculum.</li><li>Maintain oversight of and support for GPS Planned Process Deviations (PPDs), including guiding SMEs on meeting Global Development Quality (GDQ) approval criteria.</li><li>Coordinate with P&P to align PPD expiration dates with queued procedure projects, adjusting prioritization as needed.</li><li>Serve as GPS's escalation point for internal process and quality-event alignment challenges related to procedural updates, working in alignment with senior management and key stakeholders to investigate and resolve non-compliance.</li><li>Manage, alongside the Process Owners, the content of procedures for GPS, escalating material gaps to senior management, including the maintenance and accuracy of PSMF Annex E in relation to GPS procedures.</li><li>Maintain an overview of CAPAs associated with procedures, including those arising from both audits and inspections, and work closely with SMEs, PONs and the P&P team to ensure timely CAPA closure, including allowing appropriate time for associated training.</li><li>Provide regular metrics on CAPAs, process deviations, and training compliance to GPS department leadership.</li><li>Lead initiatives to enhance GPS process effectiveness and efficiency, including the analytical framework for performance metrics, and present findings and recommendations to leadership.</li><li>Liaise regularly with other functional teams e.g. Corporate and Clinical QA on potential impacts to GPS Processes or GXP-related activities.</li><li>Represent Standards & Training in audits and inspections.</li><li>Serve as the back-up GPS Standards & Training liaison to LCoE.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Minimum Bachelor's degree is required. Education in the life sciences is a strong plus.</li><li>7+ years' experience of Pharmacovigilance/Drug Safety, Regulatory Affairs or Quality Assurance in the pharmaceutical/biotech industry.</li><li>Thorough understanding of Pharmacovigilance/Drug Safety regulations and PV Quality Management Systems.</li><li>Extensive experience managing procedural updates.</li><li>Experience in PV process design and optimization.</li><li>Track record of successful project management relevant to document management.</li><li>Strong organizational skills.</li><li>Ability to write procedural documents to accepted standards of quality.</li><li>Experience presenting in audits and inspections.</li><li>Ability to work collaboratively across functions with SMEs, process owners and cross-functional partners.</li><li>Experience with Data Privacy is a plus</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Applications Analyst, Oracle Cloud WMS]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47859]]></requisitionid>
    <referencenumber><![CDATA[R47859]]></referencenumber>
    <apijobid><![CDATA[r47859]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47859/principal-it-applications-analyst-oracle-cloud-wms/]]></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><strong>Build our future together:</strong></p></div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Analyst (Senior or Principal) to join our IOPS IT team, supporting Regeneron's Digital Fusion program — the global transformation from Oracle EBS to Oracle Fusion and Oracle Cloud WMS, OTM/GTM. In this role, you will serve as a techno-functional SME and delivery lead, translating business needs into working solutions and driving process design in Oracle Cloud WMS and warehouse automation technologies - while partnering closely with Business Process Owners, system integrators, and external implementation partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p></div><div><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul></div><div><p><strong>Discover your role:</strong></p><ul><li>Act as techno-functional SME and delivery lead on Digital Fusion workstreams, partnering with Business Process Owners, system integrators, and implementation partners to deliver functional and technical solutions across Oracle Fusion and adjacent applications</li><li>Lead requirements gathering, business analysis, solution design, and configuration for Oracle Cloud WMS for inbound, inventory, outbound (pick/pack/ship) and integrations with various warehouse automation systems like VNAs, VLMs, ASRS and AMRs</li><li>Support integration design and delivery between Oracle Cloud WMS with Oracle Fusion Applications (Inventory, Order Management, Procurement, and OTM/GTM) and planning tools (Kinaxis)</li><li>Support integration deliverables related to enterprise middleware including OIC, Boomi, Kong, and IBM MQ</li><li>Lead business analysis activities including requirements elicitation, current- and future-state process mapping, gap analysis, fit-gap workshops, and translation of business needs into functional specifications</li><li>Conduct UATs, and solution validation activities, overseeing data migration, testing cycles, and cutover planning related to warehouse operations.</li><li>Drive process flow thinking across cross-functional workstreams — identifying upstream dependencies, downstream impacts, integration touchpoints, and opportunities for harmonization across sites</li><li>Own system documentation including Detailed Design Specifications, configuration test plans, traceability matrices, and summary reports; process change control requests with full impact assessment and stakeholder alignment</li><li>Partner with Validation and Quality teams to ensure IT Applications are implemented following Computer Software Assurance (CSA) and development lifecycle approaches in line with GxP and 21 CFR Part 11 expectations</li><li>Provide end-user support during hypercare and post-go-live phases; facilitate solution handover to operations teams and managed service providers; lead security access reviews and periodic audit trail assessments</li><li>Support day-to-day project activities including RAID log maintenance, status reporting, cross-functional coordination, and prioritization of delivery milestones; train and build capability across IT Applications team members</li><li>Hands-on experience with Oracle Cloud WMS is necessary and experience supporting an EBS-to-Fusion transformation is highly desirable</li><li>Experience in a pharmaceutical, biotech, medical device, or regulated GxP environment strongly preferred; familiarity with GMP, 21 CFR Part 11, ALCOA+, and CSA/CSV practices</li><li>Experience working with implementation partners and managing vendor deliverables</li></ul></div><p><strong>This role requires:</strong></p><div><ul><li>BS/BA in Information Technology, Engineering, Business, or a related field</li><li>Senior IT Applications Analyst: 5+ years of relevant experience </li><li>Principal IT Applications Analyst: 8+ years of relevant experience </li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Safety Scientist Lead - General Medicine]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50472]]></requisitionid>
    <referencenumber><![CDATA[R50472]]></referencenumber>
    <apijobid><![CDATA[r50472]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50472/director-safety-scientist-lead-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global Patient Safety Sciences Delivery </strong>team.</p><p>The Director, Global Patient Safety Sciences Delivery, General Medicine, serves as the first point of contact for all General Medicine operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness. This role is responsible for high quality, compliant execution of safety surveillance, signal management, and aggregate reporting activities across the portfolio. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Dublin, IRE</p></li><li><p>3 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>The Director is responsible for the development of their team, which is comprised of Safety Scientists. The Director will also be expected to work closely with other Directors on driving standardization and consistency in execution of signal detection activities in partnership. This role will report to the ED, Global Patient Safety Sciences Delivery. </p></li><li><p>Develop common practices, processes and templates to drive standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs </p></li><li><p>Ensure compliance and quality management of Safety Sciences Delivery activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Lead all aspects of signal detection coordination and signal management process across General Medicine, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies,</p></li><li><p>Analyze aggregate safety data to identify emerging safety issues and patterns, in partnership with Safety Sciences Strategy </p></li><li><p>Support cross-functional coordination to support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Drive development and implementation of relevant training programs for GPS staff, including maintenance of a standardized Safety Sciences training curriculum, proficiency matrix, and knowledge management repository across both Strategy and Delivery </p></li><li><p>Serve as main point of contact to liaise with Safety Sciences Strategy General Medicine GPS Leads </p></li><li><p>Collaborate with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Implement talent strategy and leadership development initiatives that raise capabilities across the organization </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced Degree required in life sciences or healthcare with 12+ years of PV experience, preferably with a focus on Safety Sciences and General Medicine experience</p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Preferred experience leading a matrixed role working across multiple areas of an organization and people management experience </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€119,900.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regional Market Access Lead - Europe]]></title>
    <date><![CDATA[Tue, 15 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50547]]></requisitionid>
    <referencenumber><![CDATA[R50547]]></referencenumber>
    <apijobid><![CDATA[r50547]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50547/director-regional-market-access-lead-europe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regional Access Lead to join our Market Access function, supporting our European region in a hybrid work mode. In this role, you will drive market access, pricing, and reimbursement strategies for our neurology portfolio while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead European market access strategies aligned with global objectives and country needs.</p></li><li><p>Monitor payer trends, healthcare policies, and reimbursement frameworks across Europe.</p></li><li><p>Represent Europe in global access strategy discussions and shape future approaches.</p></li><li><p>Adapt access tools, payer value propositions, and objection handlers for regional use.</p></li><li><p>Support Health Technology Assessment dossiers, mock negotiations, and payer engagements.</p></li><li><p>Build relationships with payers, policymakers, and patient advocacy groups.</p></li><li><p>Align evidence generation and health economics outcomes research with payer requirements.</p></li><li><p>You bring an agile, collaborative mindset when influencing cross-functional teams.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>Regional market access launch experience across competitive therapeutic areas.</p></li><li><p>Proven European pricing, reimbursement, Health Technology Assessment, and negotiation success.</p></li><li><p>Experience developing and adapting economic models for regional and national submissions.</p></li><li><p>In-depth knowledge of European payer systems and reimbursement challenges.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>Fluent English; another European language and neurology experience are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix working, and stakeholder engagement skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€119,900.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 16 Sep 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Analytical & Bioanalytical Sciences]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51073]]></requisitionid>
    <referencenumber><![CDATA[R51073]]></referencenumber>
    <apijobid><![CDATA[r51073]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51073/2027-co-op-analytical-bioanalytical-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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Analytical & Bioanalytical Sciences to join our Analytical and Biological Mass Spectrometry (ABMS), Assay Development, and R&D Chemistry teams, which develop and apply analytical, bioanalytical, and mass spectrometry-based methods to characterize therapeutic proteins, bioconjugates, and other complex biotherapeutics.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY and Hawthorne, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Develop and run liquid chromatography-mass spectrometry (LC-MS) and mass spectrometry imaging (MSI) methods to characterize therapeutic proteins, bioconjugates, and biomarkers</li><li>Apply mass spectrometry fragmentation techniques, including collision-induced dissociation (CID) and electron-based dissociation (ExD), to characterize conjugated payloads</li><li>Use capillary electrophoresis-mass spectrometry (CE-MS) and imaged capillary isoelectric focusing (iCIEF) to characterize protein charge variants</li><li>Build reference databases and spectral libraries, and process and interpret mass spectrometry data to validate molecular structures</li><li>Run high-throughput proteomics workflows using data-independent acquisition (DIA) methods and perform database searching with false discovery rate (FDR) control</li><li>Develop and evaluate platform immunoassays, including enzyme-linked immunosorbent assay (ELISA) and western blot methods, to support preclinical and clinical bioanalytical studies</li><li>Support the development and purification of antibody-drug conjugates (ADCs) using multiple conjugation chemistries, chromatography, and peptide mapping techniques, and compare platform performance across different bioconjugate modalities</li><li>Document experimental procedures and results, and present findings to the broader analytical sciences team</li></ul><br><p><strong>Relevant majors: </strong>Biology, Chemistry, Biomedical/Chemical Engineering, Pharmacy</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Oncology & Immuno-Oncology Research]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51035]]></requisitionid>
    <referencenumber><![CDATA[R51035]]></referencenumber>
    <apijobid><![CDATA[r51035]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51035/2027-co-op-oncology-immuno-oncology-research/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Oncology & Immuno-Oncology Research to join our Research team, focused on cancer biology and immunotherapy research.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Study how cancer cells interact with the immune system to inform new treatment approaches</li><li>Perform molecular biology techniques such as western blotting, real-time polymerase chain reaction (PCR), and clustered regularly interspaced short palindromic repeats (CRISPR) gene editing</li></ul><ul><li>Support virus production activities used in research experiments</li></ul><ul><li>Conduct mammalian cell culture experiments</li></ul><ul><li>Perform histological methods such as immunohistochemistry, immunofluorescence, and flow cytometry</li></ul><ul><li>Support the engineering, expression, and screening of antibody and bispecific antibody candidates for cancer immunotherapy programs</li></ul><ul><li>Document experimental procedures and results</li></ul><ul><li>Collaborate with researchers across the oncology discovery team</li></ul><br><p><strong>Relevant majors: </strong>Biology, Biochemistry, Biomedical Engineering, Chemistry, Pharmacy</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Precision Medicine Operations]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51082]]></requisitionid>
    <referencenumber><![CDATA[R51082]]></referencenumber>
    <apijobid><![CDATA[r51082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51082/2027-co-op-precision-medicine-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a 2027 Co-op in Precision Medicine Operations to join our Samples, Kits, Data, and Logistics (SKDL) team, which supports clinical laboratory operations through automation tools, data pipelines, and web applications.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Armonk, NY</p><p><strong>Timeframe: </strong>This position is full-time and onsite from May/June-December (Summer-Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Survey candidate workflows across Precision Medicine Operations to identify gaps and high-impact automation opportunities</li><li>Build proof-of-concept solutions, such as dashboards, visualizations, and integrations, that reduce manual effort</li><li>Write and test code in Python and/or R to support automation and data-pipeline development</li><li>Apply large language models (LLMs) to automation tasks where appropriate</li><li>Generate insights from clinical trial and biological data to support treatment-response research</li><li>Collaborate with functional experts across Precision Medicine Operations and partners in Data Management and Global Development IT</li><li>Document technical work clearly, including setup steps, limitations, and maintenance needs</li></ul><br><p><strong>Relevant majors: </strong>Bioinformatics/Statistics/Mathematics/Data Science, Computer Science/Information Technology</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50754]]></requisitionid>
    <referencenumber><![CDATA[R50754]]></referencenumber>
    <apijobid><![CDATA[r50754]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50754/associate-director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated Associate Director (AD) to join the Quantitative Pharmacology (QP) group. The Associate Director will lead model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies. This role combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY, Warren, NJ, Cambridge, MA or Remote, USA</li><li>Work model/flexibility: 4 days per week onsite or remote</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Driving model-informed development (MIDD) and pharmacometrics strategies in partnership with Clinical Pharmacology, Biostatistics, Clinical and Translational teams to support regulatory and clinical decision-making.</li><li>Leading the Quantitative Pharmacology evaluation of one or more assets, accountable for timely delivery of population PK/PD, exposure–response, and translational modeling analyses.</li><li>Representing Quantitative Pharmacology at program and governance meetings, communicating quantitative insights clearly to non-modeling audiences.</li><li>Contributing to regulatory interactions and authoring key components of regulatory documents related to Quantitative Pharmacology (e.g., IB, briefing books, etc.).</li><li>Mentoring and developing junior scientists and fostering a culture of scientific rigor and collaboration.</li><li>Identifying and implementing process improvements, new modeling approaches, and innovative quantitative tools to enhance efficiency and impact.</li><li>Ensuring analyses and documentation are of the highest scientific quality and regulatory compliance.</li></ul><br><p><strong>This may be the right role for you if you:</strong></p><ul><li>Want to make a visible impact on the organization by driving data-driven decisions that shape clinical and regulatory strategy.</li><li>Thrive in multi-disciplinary environments, bridging discovery, clinical, and commercial teams.</li><li>Communicate complex modeling concepts clearly and persuasively to diverse stakeholders.</li><li>Have strong collaboration and leadership skills, influencing cross-functional teams without formal authority.</li><li>Can independently design, execute, and oversee multiple modeling workstreams simultaneously.</li></ul><br><p><strong>To be considered for this role, you must have:</strong></p><ul><li>PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 7+ years of industry experience; or MS with 10+ years of relevant experience.</li><li>Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.</li><li>Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA).</li><li>Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.</li><li>Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams.</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Commercial Strategy]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50734]]></requisitionid>
    <referencenumber><![CDATA[R50734]]></referencenumber>
    <apijobid><![CDATA[r50734]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50734/director-commercial-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><br><p>The Director, Commercial Strategy, is part of a high-performing team helping drive current and future Commercial opportunities for Regeneron. Reporting to the VP, Commercial Strategy, the successful candidate will partner with cross-functional teams to identify, prioritize, innovate and refine strategies and best practices across the business, while anticipating future business needs and mitigating complex global environments.</p><br><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY Office for 4 days a week</li></ul><br><h3>Discover your role:</h3><br><p>This position will be primarily responsible for the following activities:</p><ul><li>Spearhead work to evolve Commercial brand planning processes</li><li>Act as central facilitator for key Commercial collaborative groups, including the Commercial Digital and Privacy Working Group</li><li>Support cross-Commercial collaboration on strategic digital/social governance and innovation, including initiaitives that address the changing privacy landscape and vendor efficiencies</li><li>Prepare high-impact presentations for executive leadership and governance bodies</li><li>Understand and leverage trends in the marketplace and competitive benchmarking to inform strategies for relevant programs, and keep abreast of insights and external advances to reach customers across the commercial biopharmaceutical ecosystem</li><li>Ensure cost effective delivery of programs, including tracking and monitoring KPIs based on individual/project goals</li></ul><br><p>In collaboration with the VP, Commercial Strategy, this role will also participate in the following activities:</p><br><ul><li>Identify and develop annual strategic plans for the Commerical organization</li><li>Partner with Commercial Business Units (CBUs) to drive cross-portfolio strategies and operational effectiveness for in-line brands, with the ultimate objective of helping appropriate patients access and continue to benefit from Regeneron’s medicines</li><li>Support cross-functional global product launch efforts to drive best practice learnings, including launch readiness, uptake optimization and post-launch product performance</li><li>Provide support and expertise for CBUs as they prepare for anticipated market events, including gap assessments, scenario plans, war games, analogues/benchmarks and measurement</li><li>Collaborate with cross-functional partners to plan for and implement priority business initiatives to drive longer-term growth (incl. corporate planning, Business Development assessments and ad-hoc projects)</li><li>In collaboration with Human Resources, identify key Commercial talent needs, and champion learning and development opportunities</li></ul><br><h3>This role requires:</h3><br><ul><li>BA/BS required, MBA or advanced degree (PhD, MD) preferred</li><li>Minimum years of experience: 12+ with Bachelors, 10+ with Masters and 8+ with PhD/Doctorate</li><li>At least 7 years of industry experience working with one or more publicly listed biopharmaceutical company, with a successful track record in strategy, management consulting, brand management and/or marketing</li><li>Experience working with pre-launch, launch and/or on-market biopharmaceutical commercial teams</li><li>Deep understanding of commercial, legal and regulatory landscape governing communications for pre-approval and post-approval pharmaceutical products</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Immuno-Oncology]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48101]]></requisitionid>
    <referencenumber><![CDATA[R48101]]></referencenumber>
    <apijobid><![CDATA[r48101]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48101/senior-associate-scientist-immuno-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Associate Scientist to join our Oncology & Immuno-Oncology group, contributing to the development and evaluation of next-generation bispecific antibodies for solid tumor indications. In this role, you will work at the intersection of tumor biology and immune modulation, generating robust, reproducible datasets that inform program progression from preclinical development toward clinical studies, while collaborating closely with cross-functional teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Execute well-designed in vivo studies to evaluate novel bispecific antibodies, including mouse handling, dosing (IP, IV, subcutaneous), and blood/tissue collection</li><li>Perform ex vivo immune profiling (e.g., flow cytometry, ELISA, MSD) to characterize pharmacodynamic response and mechanism of action</li><li>Process tissues and tumors for immune cell isolation and downstream analysis</li><li>Generate high-quality, well-documented datasets suitable for internal reports supporting program advancement</li><li>Collaborate closely with multidisciplinary teams to ensure alignment of experimental design with program needs</li><li>Present findings in group and cross-functional meetings, contributing to ongoing scientific discussions</li><li>Bring strong attention to detail, organization, and commitment to experimental rigor and reproducibility</li><li>Stay adaptable and eager to learn new techniques, contributing across multiple workflows in a fast-paced environment</li></ul><br><p><strong>This role requires:</strong></p><ul><li>B.S./M.S. with 2-3 years of relevant experience in oncology, immunology, or a related field</li><li>Demonstrated ability to generate high-quality data with strong attention to detail</li><li>Ability to work independently while contributing effectively in a team environment</li><li>Strong analytical skills and clear communication of scientific findings</li><li>Preferred: experience with mouse handling and in vivo tumor models</li><li>Preferred: experience with cell culture, flow cytometry, and/or immunoassays (ELISA, MSD)</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Allergy & Immunology]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50643]]></requisitionid>
    <referencenumber><![CDATA[R50643]]></referencenumber>
    <apijobid><![CDATA[r50643]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50643/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[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Clinical Development team, supporting Regeneron-driven studies within our growing therapeutics organization. In this role, you will provide clinical leadership across assigned protocols and study conduct issues while collaborating with the Clinical Program Lead, Clinical Sciences and cross-functional study teams. This position offers the opportunity to shape research and development programs for early and late-stage assets, contributing to a fast-growing, science-driven organization making a meaningful difference for patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Travel: 10% to relevant conferences and congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Provide clinical leadership for all deliverables within your assigned section of a clinical program, including protocols, regulatory documents, and publications</li><li>Facilitate assigned studies and support investigators on Regeneron-driven trials</li><li>Anticipate and resolve clinical and study conduct issues as they arise</li><li>Initiate, propose, design, and execute research and development programs for early and late-stage assets</li><li>Influence team decisions and drive alignment across functions in a matrix environment</li><li>Communicate clear, concise messages through proficient medical writing and advanced presentation skills</li><li>Identify critical risks to studies and programs and propose mitigation strategies</li><li>Engage colleagues at all levels, internally and externally, with professional diplomacy and cultural awareness</li></ul><br><h3>This role requires:</h3><ul><li>M.D. degree or equivalent</li><li>0-4 years of clinical development experience in industry preferred; academic research experience will also be considered</li><li>Specialized clinical fellowship training in Allergy, Immunology, Infectious Disease, Pulmonology, or Dermatology strongly preferred</li><li>Proficient knowledge of the drug development process, Good Clinical Practice, study design, and research methodology</li><li>Understanding of the regulatory and compliance landscape in the pharmaceutical industry</li><li>Advanced analytical, influencing, and communication skills</li></ul><br><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Viral Vector Process Development]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51023]]></requisitionid>
    <referencenumber><![CDATA[R51023]]></referencenumber>
    <apijobid><![CDATA[r51023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51023/2027-co-op-viral-vector-process-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Viral Vector Process Development to join our Viral Production Core within Preclinical Manufacturing and Process Development (PMPD), which develops the processes used to produce and purify adeno-associated virus (AAV) for gene therapy programs.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support the development of upstream and downstream processes used to produce and purify adeno-associated virus (AAV) for gene therapy programs</li></ul><ul><li>Optimize cell culture conditions to improve viral production</li></ul><ul><li>Develop high-throughput purification workflows for viral vectors</li></ul><ul><li>Build models to predict and improve separation performance</li></ul><ul><li>Conduct wet-lab experiments and analyze the resulting data</li></ul><ul><li>Collaborate with scientists across upstream and downstream teams</li></ul><ul><li>Document experimental procedures and results</li></ul><ul><li>Present progress and findings to the broader team</li></ul><br><p><strong>Relevant majors: </strong>Chemical/Biochemical Engineering, Biochemistry, Microbiology, Molecular Biology</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Associate QC Compliance Specialist]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51002]]></requisitionid>
    <referencenumber><![CDATA[R51002]]></referencenumber>
    <apijobid><![CDATA[r51002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51002/temp-associate-qc-compliance-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Temp Assoc QC Compliance Specialist </strong>to join our <strong>Quality Control</strong> team.</p><br><p>This position offers the opportunity to support quality, compliance, and continuous improvement activities across our QC laboratories, ensuring investigations and quality processes are completed to the highest standards in a GMP-regulated environment.</p><br><p><strong>When & Where:</strong></p><ul><li><strong>Location:</strong> Raheen, Limerick, Ireland.</li><li>This role supports QC laboratories including Chemistry, Bioassay, Microbiology, and Virology.</li><li>You will collaborate with cross-functional teams to drive compliance and quality excellence.</li></ul><br><p><strong>What you'll do:</strong></p><ul><li>Lead and support laboratory investigations, deviations, and non-conformance activities.</li><li>Write and review investigation reports and associated quality documentation.</li><li>Perform root cause analysis and partner with teams to identify effective CAPAs.</li><li>Support the timely implementation and monitoring of corrective and preventative actions.</li><li>Identify recurring trends and recommend process improvements to strengthen Quality Control operations.</li></ul><br><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Thrive in a fast-paced GMP-regulated environment with a strong focus on quality and compliance.</li><li>Balance multiple priorities while meeting deadlines and maintaining attention to detail.</li><li>Collaborate effectively with laboratory, quality, and cross-functional teams.</li><li>Use critical thinking and problem-solving skills to resolve complex quality issues.</li><li>Drive a culture of continuous improvement and operational excellence.</li></ul><br><p><strong>Let's find out if we're a fit:</strong></p><ul><li>Requires a BS/BA in Chemistry, Biology, or a related scientific field, or an equivalent combination of education and experience.</li><li><strong>Associate Specialist:</strong> Relevant degree and/or industry experience.</li><li><strong>Specialist:</strong> 2+ years of Quality Control or Analytical Sciences experience, including laboratory investigation experience in a cGMP environment.</li><li><strong>Senior Specialist:</strong> 5+ years of Quality Control or Analytical Sciences experience, including laboratory investigation experience in a cGMP environment.</li><li>Experience with investigations, deviations, CAPAs, and root cause analysis is highly desirable.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 08:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Next-Generation Sequencing (NGS) Data Analysis]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50398]]></requisitionid>
    <referencenumber><![CDATA[R50398]]></referencenumber>
    <apijobid><![CDATA[r50398]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50398/associate-manager-next-generation-sequencing-ngs-data-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 Regeneron Genetic Center's (RGC) Genome Informatics team is looking for an Associate Manager of Sequencing Informatics Research to serve as the lead scientist and developer for the RGC’s Sequencing Informatics research initiatives. This individual will contribute to development and design of sequencing informatics methods and protocols for new and existing multi-omics platforms, including PacBio, Illumina, Olink, and Ultima. These efforts will be driven by the goal to maximize value from RGC samples and data.</p><p>Working closely with the Sequencing & Lab Operations and Production Informatics teams, this role will also assist the methods engagement with RGC’s technology partners to on-board new sequencing and informatics platforms and ensure they can meet the RGC’s unique scaling and analysis needs.</p><p><strong>When & where: </strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: 4 days onsite</li></ul><br><p><strong>Discover your role: </strong></p><ul><li>Lead the integration of state-of-the-art and novel methods to create multi-omics informatics best-practices that increase value from RGC samples by lowering data requirements and leveraging RGC’s unique data resources</li><li>Identify opportunities that combine multiple sequencing modalities (e.g., short-read, long-read, capture, genome, depth-based) to increase the actionability of RGC sequencing deliverables</li><li>Inform development of novel sequencing informatics protocols to support multi-omics applications on existing and new sequencing platforms, including DNA-seq, RNA-seq, long-read sequencing, and proteomics</li><li>Support RGC’s joint development efforts with technology partners (e.g. NVIDIA, Google Brain) to improve base-calling, read mapping, variant calling and harmonization through bioinformatics R&D</li><li>Collaborate with RGC’s Genomics R&D, Engineering and Production teams to deploy novel methods into the RGC’s Enterprise Research environment as industry-quality software</li></ul><p><strong>This role requires:</strong></p><ul><li>Master’s (PhD preferred) in Bioinformatics or equivalent</li><li>0-3 years of experience in sequencing informatics methodology, including base calling, read mapping, and variant calling algorithms and software. </li><li>Experience with large-scale multi-omics data types, including DNA-seq (short and long read), RNA-seq, proteomics, methylation. </li><li>Expert fluency in state-of-the-art bioinformatic tools and standards.</li><li>Demonstrated engagement in the sequencing bioinformatics community.</li><li>Experience creating or adapting novel bioinformatic data structures and file formats to improve actionability.</li></ul><br><p>#RGC</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 08:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Biostatistician - Hematology]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51195]]></requisitionid>
    <referencenumber><![CDATA[R51195]]></referencenumber>
    <apijobid><![CDATA[r51195]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51195/principal-biostatistician-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Principal Biostatistician</strong> to join our <strong>Global Development</strong> team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Sleepy Hollow, NY or Warren, NJ</li><li>4 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</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><ul><li>Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.</li></ul><ul><li>Develop individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.</li><li>Collaborate with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting. </li><li>Evaluate appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</li><li>Analyze data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making. </li><li>Prepare presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management. </li><li>Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians. </li></ul><br><p><strong>This role requires:</strong></p><ul><li>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. </li><li>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </li><li>Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.</li><li>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</li><li>Expertise in statistical software such as R or SAS is required</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 11:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II- Hematology -Portland, OR; Boise, ID; Reno, NV]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51072]]></requisitionid>
    <referencenumber><![CDATA[R51072]]></referencenumber>
    <apijobid><![CDATA[r51072]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51072/medical-account-specialist-ii-hematology-portland-or-boise-id-reno-nv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Portland]]></city>
    <state><![CDATA[Oregon]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li>Field Based</li></ul><ul><li>Location: Portland, OR; Boise, ID; Reno, NV</li></ul><p><strong>Discover your role:</strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical locations. Deliver clinically focused selling messages to support the launch of a bi-specific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven sophisticated clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Security Administrator]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50819]]></requisitionid>
    <referencenumber><![CDATA[R50819]]></referencenumber>
    <apijobid><![CDATA[r50819]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50819/security-administrator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Saratoga Springs]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Security Administrator to join our Technical Operations team. The Security Administrator plays a key role in supporting the safety and security of the Saratoga Springs site. This role is responsible for administering the Security Access Control System and maintaining security documents and information. They also perform security protection duties including site access and patrol, conducting investigations, and responding to emergency situations as needed. </p><p><strong>When & where:</strong></p><ul><li>Location:</li></ul><ul><li><ul><li>Initial: Rensselaer, New York, United States</li><li>Permanent: Saratoga Springs, New York, United States</li></ul></li></ul><ul><li>Work model:<ul><li>Initial: 1st, Mon- Fri, 8am-4:30pm</li><li>Permanent: 12-hour shifts, 7am-7:30pm, alternating 3–4 days per week, including 1 weekend day</li><li>Transition: candidates must be able to work both schedules. The permanent shift start date will be communicated with reasonable advance notice and is subject to business needs.</li></ul></li></ul><p><strong>What you’ll do:</strong></p><ul><li>Greeting and processing all people entering the site, including new employees, contractors, and visitors; verifying credentials and issuing security badges and parking permits </li><li>Patrolling the buildings and grounds on bike, foot, or vehicle to ensure physical security and safety </li><li>Monitoring electronic protection systems including alarms, CCTV, fire, elevator, and intercom; responding to alarms and calls for security assistance </li><li>Administering the Security Access Control System to ensure the correct individuals are provided access to restricted areas and partnering with area owners to create access groups for their respective areas, ensuring appropriate access is maintained </li><li>Responding to emergency situations (e.g. fire, medical, confined space, hazmat and personnel related issues) and contacting the proper authorities when necessary </li><li>Investigating and following up on incidents that compromise the safety and security of the site as advised by Management and/or Human Resources </li><li>Discreetly handling critical and confidential information and preparing associated reports </li><li>Leading special projects such as conducting security audits and developing risk assessments for audit findings, developing and delivering security training programs, planning and organizing traffic control programs and initiatives, monitoring international security incidents and impact on travelers </li><li>Providing guidance and direction to contract security staff as needed </li></ul><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Requires AAS Degree in Criminal Justice, Security Management, Emergency Management, Business Administration and 2+ years of law enforcement, military or security experience; or equivalent combination of education and experience </li></ul><ul><li><ul><li>Security Administrator II: 2+ years or HSD/GED with 4+ years of related experience </li><li>Security Administrator III: 4+ years or HSD/GED with 6+ years of related experience</li></ul></li></ul><ul><li>Level will be determined based on experience</li></ul><ul><li>Requires Valid NYS Security Guard License or equivalent </li></ul><br><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 20:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer - Genetic Medicines]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47658]]></requisitionid>
    <referencenumber><![CDATA[R47658]]></referencenumber>
    <apijobid><![CDATA[r47658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47658/principal-statistical-programmer-genetic-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: onsite</li><li></li></ul><p><strong>Discover your role:</strong></p><ul><li>Support or lead programming and quality control of analysis datasets, tables, listings, and graphs</li><li>Coordinate activities and communicate shifting timelines and milestones to the study team</li><li>Create and maintain programming specifications for analysis datasets across studies</li><li>Support creation and validation of submission requirements, including annotated CRFs and define documents</li><li>Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch</li><li>Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed</li><li>Participate in department working groups, contributing to tool development and process improvement</li><li>Design and test program logic independently, maintaining documentation in a regulated environment</li><li>Enjoy working independently while staying closely connected to a broader study team</li><li>Communicate clearly and proactively, especially around shifting timelines</li><li>Take pride in accuracy and consistency when documenting and maintaining code</li><li>Think analytically and enjoy solving programming and data challenges</li><li>Stay curious about process improvement and enjoy contributing ideas to working groups</li><li>Adapt comfortably to ad hoc requests and evolving priorities from senior leadership</li><li>Bring attention to detail and a quality mindset to regulated work</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 3+ years of relevant experience</li><li>Proven programming experience supporting clinical study data and analysis deliverables</li><li>Strong documentation and quality control skills within a regulated environment</li><li>Experience collaborating within a multidisciplinary study team</li></ul><br><p>#statprogregn</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Genetics Medicine, MASH]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49566]]></requisitionid>
    <referencenumber><![CDATA[R49566]]></referencenumber>
    <apijobid><![CDATA[r49566]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49566/medical-director-clinical-development-genetics-medicine-mash/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our MASH/Metabolism team, supporting genetic medicine programs from First in Human through Phase 3. In this role, you will lead cross-functional study teams to shape clinical development strategy and ensure the scientific integrity of trials, while collaborating closely with discovery scientists, translational researchers, and regulatory colleagues.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location: </strong>Tarrytown, NY</li><li><strong>Work model/flexibility: </strong>On-site four days per week</li><li><strong>Travel percentage: </strong>10% to relevant conferences/congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Lead cross-functional teams to craft novel clinical development strategy for genetic medicines</li><li>Partner with discovery and translational scientists to understand emerging genetic targets across MASH, metabolism, rare diseases, and other therapeutic areas</li><li>Author and finalize protocols, amendments, monitoring plans, SAPs, and regulatory submissions</li><li>Evaluate the benefits and risks of assigned therapeutic candidates to inform program decisions</li><li>Oversee trial execution, including adverse event review and ongoing monitoring of patient health and data quality</li><li>Ensure team compliance with FDA, EMA, ICH, and GCP guidelines</li><li>Conduct literature reviews to identify development opportunities from mechanistic, pharmacological, and clinical perspectives</li><li>Represent clinical science in communications and meetings with regulatory agencies</li></ul><br><h3>This role requires:</h3><ul><li>M.D. degree (M.D./Ph.D. or prior research experience preferred)</li><li>Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred)</li><li>2-3+ years of clinical practice or industry experience preferred</li><li>Track record of success in clinical or scientific research settings</li></ul><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Centro (Ematologia)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49792]]></requisitionid>
    <referencenumber><![CDATA[R49792]]></referencenumber>
    <apijobid><![CDATA[r49792]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49792/key-account-manager-centro-ematologia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Costruiamo insieme il nostro futuro:</strong></p><p>In Regeneron utilizziamo la scienza e l’innovazione per sviluppare farmaci che cambiano la vita delle persone con malattie gravi. Cerchiamo un Senior Sales Specialist, Ematologia Commerciale, Italia da inserire nel nostro team vendite di ematologia. La posizione supporterà il business italiano con un modello di lavoro sul territorio. In questo ruolo, promuoverai la crescita del territorio e relazioni di valore con i professionisti sanitari. Collaborerai con i colleghi dell’area medica e con altre funzioni. Questa posizione offre l’opportunità di contribuire a un’organizzazione in rapida crescita, guidata dalla scienza e orientata ai pazienti.</p><p><strong>Quando e dove:</strong></p><p>Italia Centro<br>Posizione sul territorio, con trasferte frequenti.</p><p><strong>Scopri il tuo ruolo:</strong></p><ul><li><p>Costruire relazioni di qualità con i professionisti sanitari utilizzando conoscenze scientifiche aggiornate e messaggi di vendita approvati.</p></li><li><p>Attuare i piani commerciali e di marketing per raggiungere gli obiettivi di vendita e gli indicatori di performance.</p></li><li><p>Gestire gli account strategici attraverso pianificazione, targeting e segmentazione, in linea con le indicazioni regionali.</p></li><li><p>Sviluppare piani locali per gli account utilizzando dati di mercato e aggiornarli in base alle dinamiche del mercato.</p></li><li><p>Collaborare con i colleghi dell’area medica su programmi regionali a supporto delle esigenze dei professionisti sanitari.</p></li><li><p>Rappresentare Regeneron Ematologia in congressi e incontri regionali, nazionali e internazionali.</p></li><li><p>Utilizzerai canali diretti e digitali per ottimizzare il coinvolgimento e contribuire al miglioramento della pratica clinica.</p></li></ul><p><strong>Questo ruolo richiede:</strong></p><ul><li><p>Laurea o qualifica equivalente riconosciuta per i professionisti delle vendite.</p></li><li><p>Almeno cinque anni di esperienza nelle vendite farmaceutiche, inclusa un’esperienza essenziale in ematologia.</p></li><li><p>Conoscenza del Codice della Federazione Europea delle Industrie e Associazioni Farmaceutiche e delle normative locali applicabili.</p></li><li><p>Ottima conoscenza dell’italiano; la conoscenza dell’inglese costituisce un vantaggio.</p></li><li><p>Attitudine tecnica alla vendita basata sulla patologia e sui concetti scientifici.</p></li><li><p>Capacità di utilizzare dati, sistemi multipli e piattaforme di Customer Relationship Management.</p></li><li><p>Eccellenti capacità di coinvolgimento del cliente, presentazione, pianificazione e definizione delle priorità.</p></li><li><p>Capacità di lavorare autonomamente entro scadenze ristrette, dimostrando integrità e una comunicazione etica.</p></li><li><p>esperienza nel lancio di prodotti costituisce un vantaggio. </p></li></ul><p>Ti riconosci in questa descrizione? Candidati ora per compiere il tuo primo passo verso il Regeneron Way! Ci impegniamo a costruire un ambiente di lavoro con una cultura inclusiva. Regeneron è un datore di lavoro che garantisce pari opportunità e tutti i candidati qualificati saranno presi in considerazione per l’assunzione senza distinzione di razza, colore della pelle, religione o credo (o loro assenza), sesso, orientamento sessuale, identità o espressione di genere, riassegnazione di genere, stato civile o di unione civile, gravidanza o stato genitoriale, età, disabilità, nazionalità, stato di cittadinanza, origine etnica o nazionale, appartenenza alla comunità dei Viaggiatori, stato familiare, informazioni genetiche, stato militare o di veterano, o qualsiasi altra caratteristica protetta dalla legge applicabile. Ove richiesto, forniremo adeguati accomodamenti ai candidati con disabilità o malattie croniche note durante il processo di selezione, salvo che tali accomodamenti comportino un onere eccessivo.</p><p>Dove necessario, divulghiamo le fasce salariali per i ruoli in tutti i Paesi in cui operiamo. L’offerta finale sarà determinata all’interno della fascia pertinente in base al Paese di impiego, allo specifico livello del ruolo e alle competenze ed esperienze del candidato. In alcuni Paesi possono essere applicati contratti collettivi di lavoro (CCNL), che possono influenzare determinati elementi della retribuzione o dei benefit. Regeneron offre un pacchetto di total rewards competitivo e completo che può includere, a seconda del Paese e del ruolo: bonus annuali o altri piani di incentivazione, assegnazioni azionarie, benefici pensionistici o di previdenza, contributo aziendale al piano 401(k), programmi per la salute e il benessere, centri fitness, coperture assicurative (ad es. sanitaria, odontoiatrica, oculistica, vita e invalidità), ferie e permessi retribuiti e benefit per il supporto alla famiglia. Per ulteriori informazioni sui benefit Regeneron negli Stati Uniti, visita <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. Per le altre sedi, ulteriori informazioni verranno fornite durante il processo di selezione. Per qualsiasi domanda, rivolgiti al tuo recruiter.</p><p>Ti informiamo che in Regeneron crediamo di dare il meglio di noi quando lavoriamo insieme. Per questo motivo, molti ruoli richiedono la presenza in sede. Per maggiori informazioni sulle aspettative di lavoro in presenza per il tuo ruolo e la tua sede, parla con il tuo recruiter e con il responsabile delle assunzioni.</p><p>Nell’ambito del processo di selezione, potranno essere effettuati determinati controlli di background in conformità con le leggi del Paese in cui è basata la posizione. Lo scopo di tali controlli è verificare alcune informazioni prima dell’inizio del rapporto di lavoro, come l’identità, il diritto al lavoro e le qualifiche formative.</p><p>Per le posizioni in Canada: questo annuncio si riferisce a una posizione già esistente.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Scientific Marketing Lead (NSCLC)]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49930]]></requisitionid>
    <referencenumber><![CDATA[R49930]]></referencenumber>
    <apijobid><![CDATA[r49930]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49930/director-scientific-marketing-lead-nsclc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, NSCLC Scientific Marketing Lead is a strategic leadership role within Regeneron's US Oncology Commercial organization. This position is responsible for leading the overall NSCLC Scientific Marketing strategy and organization, serving as the critical link between the commercial organization and the scientific community to drive awareness, education, and engagement for the product.</p><p>Reporting to the US NSCLC Brand Lead, the Director provides strategic leadership for scientific marketing initiatives, thought leader engagement, and field-based scientific marketing activities, ensuring alignment with the overall US brand strategy. The role is a 2nd line leader role with Scientific Marketers and field based marketers reporting up through to them.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY office for 4 days a week with travel approximately for Congresses, Ad Boards, POA including occasional weekend travel/meetings as business needs require (~25% of the time)</li></ul><h3>Discover your role:</h3><ul><li>Lead the development and execution of the US NSCLC Scientific Marketing strategy and annual business plan aligned with overall brand objectives</li><li>Own the scientific marketing budget, including resource allocation, investment decisions, forecasting, and delivery of key strategic initiatives</li><li>Establish and oversee NSCLC KOL engagement strategy, advocacy plan, and insight generation priorities</li><li>Build and maintain strategic relationships with leading academic and community oncology experts across NSCLC</li><li>Oversee advisory boards, steering committee engagements, speaker programs, congress activities, and other scientific engagement initiatives to generate actionable insights</li><li>Drive KOL mapping and engagement strategies across national, regional, and local levels to ensure comprehensive customer coverage and insight generation</li><li>Lead and evolve the US TLL strategy and scientific engagement model, ensuring alignment with brand priorities and customer needs</li><li>Serve as a key member of the US NSCLC Brand Team, providing ongoing tumor area expertise and delivering strategic recommendations based on market dynamics and customer insights</li><li>Partner closely with NSCLC Marketing leadership to ensure seamless integration and execution of brand strategy, customer engagement plans, and educational initiatives</li><li>Collaborate with Medical Affairs, Key Account Marketing, and other cross-functional partners to support aligned customer engagement strategies</li><li>Lead congress strategy and scientific presence planning, including sponsorship opportunities, scientific engagement activities, and collaborator interactions</li><li>Monitor and evaluate tactical plan effectiveness through key performance indicators, insight reporting, and business impact assessments</li><li>Ensure all programs, engagements, and materials follow legal, regulatory, corporate, and ethical requirements</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree required; advanced degree (MBA, PhD, PharmD, MD, MS, or equivalent) preferred</li><li>12+ years of pharmaceutical, biotechnology, healthcare, or related industry experience</li><li>8-10 years of experience in oncology marketing, scientific marketing, medical affairs, or commercial leadership roles</li><li>Demonstrated success developing and driving KOL engagement, thought leader advocacy, and scientific exchange strategies</li><li>Proven leadership experience managing and developing high-performing teams</li><li>Strong understanding of oncology clinical practice, scientific data, and treatment landscapes</li><li>Experience leading advisory boards, congress strategy, speaker bureau programs, and scientific engagement initiatives</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Imaging Scientific Director (Oncology)]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48148]]></requisitionid>
    <referencenumber><![CDATA[R48148]]></referencenumber>
    <apijobid><![CDATA[r48148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48148/clinical-imaging-scientific-director-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Clinical Imaging Scientific Director for Oncology</strong> will own the strategy and execution of sophisticated early and late phase oncology imaging in clinical trials where imaging plays a key role. Imaging includes all modalities with a special focus on PET and CT. In this role, you will champion the development of imaging endpoints and biomarkers and drive the scientific imaging aspects as well as tumor response assessment of oncology clinical studies.<br><br>The successful candidate will be an independent imaging scientific leader and a member of cross-functional program teams including Regeneron clinical and preclinical colleagues as well as external academic and industry partners. This position provides excellent opportunities to develop innovative imaging endpoints and biomarkers in support of clinical development and contribute to bringing new treatment options to patients.</p><p><strong>When & Where: </strong>Tarrytown, NY </p><p><strong>Discover your role:</strong></p><ul><li><p>Create fit-for-purpose imaging biomarker strategies and work closely with research, clinical imaging and the oncology therapeutic area for the development of imaging endpoints to inform and advance the Regeneron clinical pipeline.</p></li><li><p>Prepare and present clinical imaging strategies to senior management.</p></li><li><p>Manage a complex network of stakeholders across Regeneron.</p></li><li><p>Lead, design and implement multi-modality imaging measures as endpoints for oncology therapeutic clinical studies.</p></li><li><p>Collaborate closely with Regeneron clinical teams as imaging subject matter expert to ensure optimal design and execution of imaging strategy including development of protocols, imaging endpoints, imaging manuals, imaging charters, statistical analysis plans and clinical study reports.</p></li><li><p>Work closely with Clinical Imaging Operations and imaging contract research organizations to ensure the flawless conduct and data integrity of studies’ imaging components and endpoints.</p></li><li><p>Serve as Study Scientific Director for clinical trials focused on qualification and utilization of novel imaging biomarkers.</p></li><li><p>Lead the interaction with regulatory agencies for communications regarding imaging endpoints and procedures.</p></li><li><p>Lead the interaction with regulatory agencies and site ethics committees for approval of clinical imaging biomarker development studies</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD program with a minimum of 10+ years of clinical imaging experience (minimum of 7 years within oncology drug development).</p></li><li><p>Superior written/verbal communication and organization skills.</p></li><li><p>Experience implementing central efficacy assessments using tumor response criteria such as RECIST 1.1, iRECIST, PCWG3, Lugano and IMWG in oncology clinical trials is needed. </p></li><li><p>We also are looking for you to have had successful engagement experience with regulatory agencies and the ability to champion imaging innovations and lead projects effectively.</p></li><li><p>Experience as study scientific director of PET imaging biomarker clinical trials in Oncology.</p></li><li><p>Experience applying PET imaging as a quantitative endpoint in clinical and preclinical studies in Oncology.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Facilities Engineer]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47148]]></requisitionid>
    <referencenumber><![CDATA[R47148]]></referencenumber>
    <apijobid><![CDATA[r47148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47148/senior-facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><div><div><ul><li><p>Building and specifies cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</p></li></ul></div><ul><li><p>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</p></li></ul><div><ul><li><p>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</p></li></ul></div><div><ul><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li></ul></div><div><ul><li><p>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</p></li></ul></div><div><ul><li><p>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</p></li></ul></div><div><ul><li><p>Implementing corrective/preventative actions for existing equipment and maintenance processes</p></li></ul></div><div><ul><li><p>Preparing engineering evaluations and test plans for and executes modification change control documentation</p></li></ul></div><div><ul><li><p>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs </p></li></ul></div></div><div><div><ul><li><p>Maintains a clean and safe working environment by enforcing procedures, policies, and regulations</p></li></ul></div></div><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have strong analytical and interpersonal skills</p></li><li><p>You are able to prioritise and re-prioritise as needed and adapt to change</p></li><li><p>You are comfortable working in a fast-paced setting</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Sr Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 5 years’ experience </p></li></ul><div><ul><li><p>Engineer - Requires BS/BA in Mechanical engineering or equivalent along with 2 years’ experience </p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47968]]></requisitionid>
    <referencenumber><![CDATA[R47968]]></referencenumber>
    <apijobid><![CDATA[r47968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47968/senior-manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Regulatory Affairs Advertising and Promotion team. This position requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidance to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). They will provide regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with minimal guidance from the Regulatory Affairs, Advertising and Promotion Director. The Senior Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US and Global (if applicable) regulatory activities associated with advertising and promotion of the company’s marketed products, as well as commercial development of pipeline products. Manages commercial activities from a regulatory advertising and promotion perspective with minimal guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with minimal guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with minimal guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Provide input to direct management with respect to process improvement for promotional review activities and establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With minimal guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 3 to 4 years within regulatory affairs, preferably within advertising and promotion</p></li><li><p>At minimum, a Bachelor’s degree (BS) from an accredited College or University in Life Sciences. Advanced degree (Masters, Pharm D, Ph.D., MD or DO) preferred in the field of medicine or science. Regulatory experience can offset education requirements.</p></li><li><p>Advance knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and managing launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Ability to influence cross-functional teams and interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47967]]></requisitionid>
    <referencenumber><![CDATA[R47967]]></referencenumber>
    <apijobid><![CDATA[r47967]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47967/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager </strong>to join our<strong> Regulatory Affairs Advertising and Promotion</strong> team. In this role, you will apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology (CO, MO, KS, OK and NM)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50063]]></requisitionid>
    <referencenumber><![CDATA[R50063]]></referencenumber>
    <apijobid><![CDATA[r50063]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50063/associate-director-field-medical-affairs-hematology-co-mo-ks-ok-and-nm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Territory: CO, MO, KS, OK and NM (ideally to reside in CO or St. Louis) <br><strong>Travel:</strong> Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. <br> </p><p>#medicalscienceliaison #msl #HFM #AD<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Critical Utilities]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47222]]></requisitionid>
    <referencenumber><![CDATA[R47222]]></referencenumber>
    <apijobid><![CDATA[r47222]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47222/director-critical-utilities/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of Critical Utilities and Facility Management to join our Facilities and Engineering team, supporting our campus Central Utility Plant and MEP operations in an on-site work model. In this role, you will safeguard the reliability, safety, and compliance of our electricity, chilled water, steam, and emergency power systems, ensuring uninterrupted service for 24/7 research and operational needs while collaborating with Engineering, EH&S, and Business Resilience teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><h3>Discover your role:</h3><ul><li>Develop and implement long-term operational strategies for Critical Utilities and Facilities Maintenance programs across a complex pharmaceutical/biotech campus.</li><li>Lead organizational development efforts, including team structure design, workforce planning, and operational model optimization across internal staff and outsourced providers.</li><li>Establish and continuously improve maintenance, reliability, and capital planning programs to strengthen system performance, resiliency, and compliance.</li><li>Provide executive oversight of Central Utility Plant and Powerhouse operations, partnering with operational leadership to ensure safe, uninterrupted utility delivery.</li><li>Collaborate cross-functionally with Engineering, R&D Operations, EH&S, Quality, Procurement, and Capital Projects teams to support infrastructure initiatives and campus growth.</li><li>Drive governance, performance management, and strategic vendor oversight, including metrics development, operational reviews, budget planning, and risk mitigation.</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree in Mechanical, Electrical, Power, Marine, or Energy Engineering, or 15 years of equivalent experience (Navy Nuclear Power School plus 10 years accepted).</li><li>10+ years leading central utility or power-plant operations (chilled water, steam, emergency power) within a hybrid facility management model, plus strong contract-management and vendor-governance skills.</li><li>Proficiency with building automation system (BAS) platforms, such as Metasys, EcoStruxure, or Desigo.</li><li>Proven team-leadership abilities across internal staff and outsourced providers.</li><li>A valid NYS driver's license to support up to 25% travel.</li><li>Turning maintenance data into actionable reliability improvements.</li><li>Holding rigorous safety and regulatory standards in high-risk environments.</li><li>Communicating clearly with researchers, engineers, and executives, and being flexible with travel</li><li>Motivating and coordinating a mixed team of internal technicians, union trades, and third-party providers.</li><li>Balancing hands-on problem solving with strategic planning, budgeting, and long-range asset management.</li><li>Keeping utility plants, chillers, boilers, and generators running with zero unplanned downtime.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Triage]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47759]]></requisitionid>
    <referencenumber><![CDATA[R47759]]></referencenumber>
    <apijobid><![CDATA[r47759]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47759/senior-manager-triage/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our safety team, supporting our operations in a hybrid role. In this role, you will lead Individual Case Safety Report triage while collaborating with healthcare professionals and medical reviewers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid - three days a week on site)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead healthcare professionals performing upfront medical triage in Argus Safety.</p></li><li><p>Assess seriousness, expectedness, causality, and reporting timelines for incoming cases.</p></li><li><p>Apply expedited reporting logic, including seven-day and 15-day requirements.</p></li><li><p>Verify source completeness, identify follow-up needs, and assign Argus workflows.</p></li><li><p>Escalate complex cases to the Lead Medical Reviewer.</p></li><li><p>Author structured summaries covering clinical course, causality, and review considerations.</p></li><li><p>Maintain SOP, data privacy, documentation, and inspection readiness standards.</p></li><li><p>You explore artificial intelligence technologies to improve operational efficiency.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>MD, MBBS, PharmD, BDS, MDS, or Nurse Practitioner qualification.</p></li><li><p>8+ years’ industry experience, including 5+ years in pharmacovigilance case processing.</p></li><li><p>Hands-on ICSR intake, Argus Safety, and expedited reporting experience.</p></li><li><p>Knowledge of ICH E2A, E2B, E2D, FDA, EMA, and Health Canada requirements.</p></li><li><p>Ability to interpret Investigator’s Brochures, US Prescribing Information, and Summaries of Product Characteristics.</p></li><li><p>MedDRA coding familiarity and high-volume case processing experience.</p></li><li><p>Strong clinical judgement and concise written communication under pressure.</p></li><li><p>Triage or first-line safety review experience preferred.</p></li><li><p>AI or generative AI experience or interest.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Hematology (f/m/d) - Austria & Switzerland]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50157]]></requisitionid>
    <referencenumber><![CDATA[R50157]]></referencenumber>
    <apijobid><![CDATA[r50157]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50157/key-account-manager-hematology-fmd-austria-switzerland/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hemato-Oncology to join our Commercial Oncology team, supporting Austria and Switzerland. In this role, you will drive sales performance and customer engagement while collaborating with cross-functional stakeholders and healthcare professionals. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Austria, field-based</p><p>Frequent travel across Austria and Switzerland. Occasional evening and weekend work.</p><br><p><strong>Discover your role:</strong></p><br><ul><li>Build scientific relationships with healthcare professionals across hematology-oncology.</li><li>Develop and update account plans using market insights and key data.</li><li>Execute marketing strategies aligned with territory and account priorities.</li><li>Deliver sales objectives through effective territory budget management.</li><li>Collaborate with stakeholders to achieve shared business objectives.</li><li>Peer-coach sales colleagues and share best practices across the team.</li><li>Contribute to special projects, events, and strategic business initiatives.</li><li>You bring a patient-focused mindset and create value in every interaction.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>Bachelor's degree or similar educational background as well as a successfully completed "Pharmareferentenprüfung" or equivalent academic qualification.</li><li>8-10+ years of biotech or pharmaceutical sales experience.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Previous experience in biologics and oncology disease areas.</li><li>Significant oncology and/or hematology experience across multiple disease areas.</li><li>Strong knowledge of Austrian and Swiss healthcare systems and market structures.</li><li>Established network of relevant healthcare professionals.</li><li>Knowledge of healthcare compliance codes and promotional regulations.</li><li>Fluency in written and spoken German and English.</li><li>Strong customer engagement, presentation, planning, and organizational skills.</li><li>Ability to work independently and execute strategic and tactical plans under tight timelines.</li><li>High integrity, ethical conduct, and effective communication skills.</li><li>Willingness to travel frequently across Austria and Switzerland.</li><li>Experience in Multiple Myeloma, Follicular Lymphoma, and/or DLBCL preferred.</li><li>Experience working across Austria and Switzerland preferred.</li></ul><br><br><p>For this position, the Collective Bargaining Agreement for Trade (Kollektivvertrag Handel) applies; depending on qualifications and professional experience, we offer a salary above the collectively agreed minimum.</p><br><p><strong>Salary Range (annually)</strong></p><p>72.075,00 € - 120.125,00 €</p><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Administrative Coordinator, Regulatory Affairs]]></title>
    <date><![CDATA[Fri, 21 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50068]]></requisitionid>
    <referencenumber><![CDATA[R50068]]></referencenumber>
    <apijobid><![CDATA[r50068]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50068/administrative-coordinator-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Administrative Coordinator to join our Regulatory Affairs team, supporting our Japan Regulatory Affairs organization in a hybrid work model. In this role, you will provide administrative and operational support to local and global Regulatory Affairs activities while collaborating with Regulatory Affairs, safety, Human Resources, Talent Acquisition, and global colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Arrange business meetings and provide meeting minutes for Regulatory Affairs and Marketing Authorization Holder activities.</li><li>Deliver administrative support, including office supplies, filing, business cards, postage, and phone coordination.</li><li>Create, process, and track purchase orders and invoices.</li><li>Coordinate domestic and international travel for Japan Regulatory Affairs members and global visitors.</li><li>Manage the Head of Japan Regulatory Affairs calendar, schedules, and expense reports.</li><li>Support internal communications and onboarding, hiring, and interview activities with Human Resources and Talent Acquisition.</li><li>Provide operational support to regulatory and safety teams in Japan.</li><li>You build trusted relationships while handling sensitive information with discretion.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Relevant degree or related discipline.</li><li>Minimum 5 years of experience as a Group Administrator or Administrative Coordinator in a global company.</li><li>5+ years of relevant experience, preferably within the pharmaceutical industry.</li><li>Ability to independently handle difficult inquiries using sound judgment.</li><li>Strong organizational skills with the ability to multitask and reprioritize work.</li><li>Ability to work under pressure while maintaining attention to detail.</li><li>Strong verbal, written, and interpersonal communication skills in Japanese and English.</li><li>Experience with Microsoft Word, Excel, PowerPoint, and Outlook.</li><li>Interest in helping establish and develop new local entities within global companies.</li><li>Team-oriented mindset and flexibility to support colleagues as needed.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manufacturing Support Technician]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48341]]></requisitionid>
    <referencenumber><![CDATA[R48341]]></referencenumber>
    <apijobid><![CDATA[r48341]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48341/manufacturing-support-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Manufacturing Support Technician</strong> to join our <strong>Manufacturing</strong><strong> </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & Where:</strong></p><ul><li><p>Location: Limerick</p></li><li><p>Shift: 24/7</p></li></ul></div><div><p><strong>What you’ll do:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as advised by Team Leads and Supervisors</p></li><li><p>Ensuring all associated documentation such as manufacturing batch records & logbooks are completed, accurate and verified in accordance with SOPs and cGMP Standards</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Maintaining housekeeping in designated area and adhering to the hygiene standards of the facility</p></li><li><p>Ensuring all required training is up to date and completed in a timely manner</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You will be working in a cleanroom where gowning is required</p></li><li><p>You enjoy working in a team that brings out the best in each other</p></li><li><p>You can adhere to the letter and spirit of policies and regulations</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Leaving Certificate qualification to include math's and a science or engineering subject as a minimum or equivalent qualification. Experience working shift in a GMP (Good Manufacturing Practice) environment/industry is preferred</p></li></ul><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IREADV #JOBSIEST #LI-Onsite #REGNIEEC #REGNIELSM</strong></p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€12.87 - €22.73]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Director Rare Disease Commercial EU4+UK Region]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50197]]></requisitionid>
    <referencenumber><![CDATA[R50197]]></referencenumber>
    <apijobid><![CDATA[r50197]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50197/sales-director-rare-disease-commercial-eu4plusuk-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sales Director Rare Disease</strong> to join our International Rare Disease team, supporting our EU4+UK region. In this role, you will lead a high-performing field organization and drive commercial execution across our rare disease portfolio while collaborating with cross-functional teams and regional leadership. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Location: Munich, Germany (multiple locations are being considered for this role) - Office based, Hybrid.</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead a sales team across EU4+UK to deliver company objectives.</p></li><li><p>Drive account targeting, segmentation, and multichannel customer engagement.</p></li><li><p>Set performance objectives and lead coaching, development, and succession planning.</p></li><li><p>Align incentive compensation plans with brand strategies and targets.</p></li><li><p>Partner with Commercial Operations on training, analytics, KPIs, Veeva CRM, and territory alignment.</p></li><li><p>Provide field insights on customer feedback, patient journey barriers, and competitive intelligence.</p></li><li><p>Partner with cross-functional team members to address market trends and dynamics.</p></li><li><p>You champion excellence, accountability, and patient-centricity across the organization.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree required.</p></li><li><p>Advanced degree in life sciences, pharmacy, medicine, or business strongly preferred.</p></li><li><p>Minimum 10 years’ experience in the pharmaceutical or biotechnology industry.</p></li><li><p>Minimum 3 years in a first-line field sales management role.</p></li><li><p>Proven success hiring, mentoring, developing, and retaining high-performing teams.</p></li><li><p>Experience in rare disease, specialized medicines, or gene therapy/ATMP commercialization preferred.</p></li><li><p>Ability to operate within sophisticated multi-stakeholder account environments.</p></li><li><p>Knowledge of market access and reimbursement frameworks across EU4+UK markets.</p></li><li><p>Ability to mentor teams on value-based and access-oriented payer engagement.</p></li><li><p>Experience with Veeva CRM, Salesforce effectiveness tools, data analytics, and digital promotion.</p></li><li><p>Proficiency in English and one additional European language highly desirable (French, German, Italian, or Spanish)</p></li><li><p>Knowledge of EFPIA and applicable national pharmaceutical industry codes.</p></li><li><p>Ability to travel 50% or more across EU4+UK and hold a valid driving licence.</p></li><li><p>Established KOL relationships in rare metabolic, musculoskeletal, or hearing loss areas are desirable.</p></li><li><p>Strong leadership, communication, and interpersonal skills in multicultural environments.</p></li></ul><p>(€110,250 - €183,750) </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Program Head, Immunology]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48718]]></requisitionid>
    <referencenumber><![CDATA[R48718]]></referencenumber>
    <apijobid><![CDATA[r48718]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48718/executive-director-global-program-head-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Global Program Head to join our Immunology team, leading integrated program strategy for our Immunology portfolio from pre-IND nomination through BLA application. In this role, you will build and lead Strategic Program Teams, drive cross-functional program execution, and guide development of novel therapies for serious ophthalmic diseases while collaborating with research, clinical development, regulatory, commercial, and manufacturing partners across Regeneron.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY</li><li><strong>Work model/flexibility:</strong> 4 days a week on-site</li><li><strong>Travel: </strong>10% to relevant conferences/congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Build and lead Strategic Program Teams in developing long-term, end-to-end integrated program strategy</li><li>Drive scientific rigor and innovation into program development strategies</li><li>Orchestrate execution of program deliverables and governance interactions across functions</li><li>Hold sub-teams and their leads accountable for program strategy, plans, and timelines</li><li>Maintain financial oversight of program budgets and development costs</li><li>Identify and align key stakeholders across Regeneron and partner organizations throughout the program lifecycle</li><li>Oversee risk identification, assessment, and mitigation, making decisions informed by cross-functional input</li><li>Coach and support the professional development of Strategic Program Team members</li></ul><br><h3>This role requires:</h3><ul><li>MD, PhD, or PharmD</li><li>10-15 years of experience in broad drug development in Immunology or autoimmunity</li><li>Deep knowledge of the overall development of molecules for relevant disease areas</li><li>Expert knowledge of the competitive landscape and general regulatory requirements for drug approval</li><li>Experience or knowledge of biologics and alternative therapeutic modalities preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Development Program Management]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44512]]></requisitionid>
    <referencenumber><![CDATA[R44512]]></referencenumber>
    <apijobid><![CDATA[r44512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44512/manager-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Development Program Management to join our Development Program Management function, supporting drug development programs from preclinical through commercialization in a hybrid work model based in Warren, NJ or Tarrytown, NY. In this role, you will help drive strategic planning and execution of development program timelines, budgets, and goals while collaborating with cross-functional Strategic Program Team members across the organization. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><strong>Location:</strong> Warren, NJ or Tarrytown, NY</li><li><strong>Work model/flexibility:</strong> Onsite 4 days/week, 1 day remote</li></ul><p><strong>Discover your role:</strong></p><ul><li>Support subteam and functional area meetings, leading select working groups</li><li>Track deliverables, risks, and issues across assigned programs</li><li>Facilitate cross-functional alignment on key strategic documents</li><li>Manage project planning systems to keep programs on track</li><li>Communicate program status clearly to manager and stakeholders</li><li>Escalate risks and complex issues in a timely, appropriate manner</li><li>Build relationships and collaborate effectively across departments</li><li>Support resolution of team conflicts and roadblocks</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree and 5+ years of relevant project management experience</li><li>Experience in drug development/pharmaceutical industry preferred</li><li>Familiarity with cross-functional development team structures (e.g., Strategic Program Teams)</li><li>Demonstrated sound judgment and critical thinking</li><li>Ability to take feedback and setbacks constructively</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Quality Control (Microbiology)]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46658]]></requisitionid>
    <referencenumber><![CDATA[R46658]]></referencenumber>
    <apijobid><![CDATA[r46658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46658/supervisor-quality-control-microbiology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Supervisor, Quality Control</strong> to join our <strong>Quality Control (QC)</strong> team.</p><p>This position offers the opportunity to lead a team of quality control professionals supporting the manufacture and release of biopharmaceutical products for patients worldwide.</p><h3><strong>When & Where:</strong></h3><ul><li><p><strong>Location:</strong> Raheen, Limerick, Ireland</p></li><li><p>This is an onsite leadership role supporting Quality Control laboratory operations</p></li><li><p>The role involves supervising daily laboratory activities and supporting cross-functional business objectives</p></li></ul><h3><strong>What You'll Do:</strong></h3><ul><li><p>Lead and supervise QC personnel, allocating workload and monitoring team performance</p></li><li><p>Ensure laboratory activities comply with cGMP requirements, SOPs, and quality standards</p></li><li><p>Support investigations, troubleshooting activities, audits, and continuous improvement initiatives</p></li><li><p>Oversee documentation including SOPs, methods, protocols, reports, and training records</p></li><li><p>Manage employee development activities including scheduling, performance reviews, coaching, and training compliance</p></li></ul><h3><strong>The Environment and Physical Rhythms of This Role:</strong></h3><ul><li><p>Thrive in a fast-paced, GMP-regulated laboratory environment</p></li><li><p>Balance leadership responsibilities with operational priorities while maintaining a strong focus on quality and safety</p></li><li><p>Collaborate with cross-functional teams to support manufacturing and quality objectives</p></li><li><p>Foster a culture of continuous improvement, accountability, and employee development</p></li></ul><h3><strong>Let's Find Out if We're a Fit:</strong></h3><ul><li><p>Requires a BS/BA in Life Sciences or a related field; an MS degree is preferred</p></li><li><p>Requires 5+ years of relevant experience within the pharmaceutical, biotechnology, or related industry</p></li><li><p>Previous supervisory or people leadership experience is required</p></li><li><p>Experience working in a GMP-regulated environment with strong communication and problem-solving skills</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, CMC Regulatory Affairs]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50069]]></requisitionid>
    <referencenumber><![CDATA[R50069]]></referencenumber>
    <apijobid><![CDATA[r50069]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50069/manager-cmc-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, CMC Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan organization in a hybrid work mode. In this role, you will lead regulatory CMC activities across therapeutic areas while collaborating with Global Regulatory CMC, CMC Regulatory Science, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplement submissions.</li><li>Prepare Japanese application forms and support high-quality regulatory dossiers.</li><li>Drive regulatory decisions based on requirements while working across cross-functional teams.</li><li>Act as a local liaison with PMDA for CMC submissions and information requests.</li><li>Assess CMC change controls against regulatory filings to maintain compliance.</li><li>Review manufacturing processes and specifications against approved filings.</li><li>Participate in agency meetings and communicate regulatory positions and feedback.</li><li>You navigate ambiguity confidently and build effective partnerships across teams.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in a scientific discipline; Master's degree preferred.</li><li>Strong biopharmaceutical and regulatory Chemistry, Manufacturing and Controls (CMC) background.</li><li>15+ years of regulatory CMC experience, including health authority interactions, major submissions, and approvals in Japan.</li><li>Experience leading CTN, J-NDA, eCTD submissions, PCA, MCN, and PMDA responses.</li><li>Deep knowledge of Japanese regulatory requirements, guidance documents, and regulatory resources.</li><li>Experience managing submission timelines and delivering filings on schedule.</li><li>Ability to obtain and maintain Foreign Manufacturing Accreditation or Foreign Manufacture Registration.</li><li>High fluency in Japanese and English.</li><li>Ability to interpret regulations, communicate effectively, and think strategically.</li><li>Strong work ethic with proven collaboration across diverse teams.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Fill Finish Facilities Maintenance]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49114]]></requisitionid>
    <referencenumber><![CDATA[R49114]]></referencenumber>
    <apijobid><![CDATA[r49114]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49114/senior-director-fill-finish-facilities-maintenance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Facilities Maintenance to lead equipment maintenance and calibration for our manufacturing, laboratory, and warehouse operations, ensuring systems supporting drug product filling, visual inspection, device assembly, and packaging remain validated, compliant, and operational. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Onsite, Monday-Friday 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Own the site's preventive and corrective maintenance programs and calibration program for equipment supporting drug product filling, visual inspection, device assembly, packaging, and other manufacturing, laboratory, and warehouse systems.</li><li>Partner with Manufacturing, Quality Assurance, Engineering, EHS, and Supply Chain leadership to align maintenance and calibration strategies with production schedules and business objectives.</li><li>Drive reliability-centered maintenance and continuous improvement initiatives to minimize downtime and maximize equipment availability; own maintenance planning, scheduling, and contractor/vendor oversight.</li><li>Establish and monitor KPIs (equipment uptime, mean time between failures, mean time to repair, maintenance backlog), leveraging OEE and CMMS data to drive condition-based and predictive maintenance.</li><li>Maintain calibration schedules and traceability to national/international standards, ensuring records and systems are always audit-ready; own or support equipment-related deviation investigations, CAPAs, and change controls.</li><li>Ensure all maintenance and calibration activities comply with cGMP, FDA, ISO 13485, and EU GMP Annex 1, and serve as a key stakeholder during regulatory inspections and audits.</li><li>Build, mentor, and develop a high-performing team, establishing clear accountability, succession planning, and career development pathways; champion a culture of safety, quality, and compliance.</li><li>Identify and lead initiatives to improve operational efficiency, reduce costs, and enhance equipment reliability, including support for facility expansion, equipment tech transfer, and new product introductions.</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA and 15+ years of progressive relevant experience in the pharmaceutical industry, or a MS degree and minimum 13 years of relevant experience.</li><li>Experience managing maintenance/calibration programs and CMMS systems (e.g., Blue Mountain, SAP PM, Maximo) required; experience supporting drug filling, visual inspection, device assembly, and/or packaging strongly preferred.</li><li>Strong working knowledge of cGMP, FDA, ISO 13485, and EU GMP Annex 1, with deep understanding of cleanroom systems and equipment supporting sterile/aseptic manufacturing.</li><li>Proven ability to lead cross-functional teams and influence at all levels, with strong financial acumen managing multi-million dollar operating and capital budgets.</li><li>Ability to work in a manufacturing environment, including cleanroom gowning and availability for after-hours facility emergencies, with excellent problem-solving, project management, and organizational skills, including communication during regulatory inspections.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal External Manufacturing Specialist (Advanced Therapies)]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50156]]></requisitionid>
    <referencenumber><![CDATA[R50156]]></referencenumber>
    <apijobid><![CDATA[r50156]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50156/principal-external-manufacturing-specialist-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill a Principal External Manufacturing Specialist position within the Bulk External Manufacturing (Advanced Therapies) team that specializes in synthetic chemistry-based oligonucleotide manufacturing. This role oversees all aspects of contract manufacturing organizations and partners including day-to-day operations, ensuring timely completion of associated operations/documentation, and assisting in the monitoring of cGMP compliance. </p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li><li><p>Travel: up to 25%</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Serve as the operational contact for contract manufacturing and/or partner sites concerning day-to-day activities</p></li><li><p>Coordination of external manufacturing activities at contract and/or business partner sites, including but not limited to scheduling of all batches, supply of materials, providing direction on shipment of material, tracking and monitoring of cycle times, providing supporting documentation for manufacturing activities and enlisting support from others who will provide any required associated reports and technical expertise</p></li><li><p>Functioning as a liaison between Regeneron Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners</p></li><li><p>Leads a sub-team in continuous process improvements, system/equipment implementation and/or strategy development</p></li><li><p>Supporting investigations which concern external manufacturing and associated shipping operations, as required</p></li><li><p>Supporting and informing strategic initiatives and contract negotiations that drive long-term relationship stability and success</p></li><li><p>Ensuring product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers and business partners</p></li><li><p>Support tech transfer and/or development work of programs at a CMO to ensure scalability toward GMP manufacturing</p></li><li><p>Performing reviews of pre-production master batch records and executed batch records</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in a scientific discipline and 8+ year of experience in cGMP manufacturing operations, or equivalent combination of education and experience</p></li><li><p>Experience in any of the following areas (recommended): small molecule synthetic chemistry and/or siRNA therapy</p></li><li><p>Knowledge of bulk manufacturing techniques (recommended) – chemical synthesis, downstream purification, annealing, lyophilization</p></li><li><p>Basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines, and EU regulations</p></li><li><p>Ability to lead continuous improvements, system implementations and/or strategy development to reduce cycle times and improve efficiencies for area</p></li><li><p>Strong interpersonal, written, and oral communication skills</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager GD GCP Auditing (Ireland)]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50344]]></requisitionid>
    <referencenumber><![CDATA[R50344]]></referencenumber>
    <apijobid><![CDATA[r50344]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50344/senior-manager-gd-gcp-auditing-ireland/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager GD GCP Auditing </strong>to join our Global Development Quality Assurance team, supporting our global development organization in a remote work model. In this role, you will lead risk-based quality auditing activities and strengthen GCP compliance while collaborating with Global Development teams, external partners, and quality stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Ireland</p><p>Work model: Remote</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead end-to-end GCP audits across internal and external global activities.</p></li><li><p>Schedule, conduct, report, and follow up on routine and directed audits.</p></li><li><p>Develop and execute risk-based audit programs for assigned clinical studies.</p></li><li><p>Identify compliance issues and drive process improvements and standardization.</p></li><li><p>Representing Quality Assurance on complex compliance projects and initiatives.</p></li><li><p>Interpret policies, standards, and regulations to address critical issues.</p></li><li><p>Support regulatory inspections and inspection room activities.</p></li><li><p>You thrive in a dynamic environment and build trusted stakeholder partnerships.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree with 8+ years of relevant industry experience; Master’s degree preferred.</p></li><li><p>At least 5 years of direct Good Clinical Practice audit experience.</p></li><li><p>Expert knowledge of FDA regulations, European Union regulations, ICH guidance, and GCP requirements.</p></li><li><p>Experience conducting audit types including process, site, vendor, and partner audits.</p></li><li><p>Experience with regulatory inspections involving investigator sites, sponsors, or Contract Research Organizations.</p></li><li><p>Ability to independently manage complex GxP compliance issues and high-value priorities.</p></li><li><p>Strong leadership skills with experience interfacing with senior leaders.</p></li><li><p>Excellent project management, stakeholder management, collaboration, and negotiation skills.</p></li><li><p>Strong problem-solving, written, and verbal communication skills.</p></li><li><p>Ability to work independently, take initiative, and perform effectively in ambiguous environments.</p></li><li><p>High attention to detail, accuracy, and organizational awareness.</p></li><li><p>Willingness to travel 30-40% domestically and internationally.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager GCP Quality]]></title>
    <date><![CDATA[Wed, 26 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50314]]></requisitionid>
    <referencenumber><![CDATA[R50314]]></referencenumber>
    <apijobid><![CDATA[r50314]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50314/senior-manager-gcp-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Quality Management - Global Development to join our Global Development Quality team, supporting our global clinical development organisation in a hybrid work model. In this role, you will lead risk-based quality management across clinical trials while collaborating with study teams, clinical functions, contract research organisations, and quality colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Multiple locations are being considered for this role (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead risk-based quality management across assigned clinical trials</p></li><li><p>Drive protocol-stage Quality Risk Assessment and Control Tracker activities under ICH E6 R3</p></li><li><p>Manage quality issues, audit responses, corrective actions, preventive actions, and trend analysis</p></li><li><p>Partner with study leads, monitoring teams, and contract research organisations on site risks</p></li><li><p>Escalate significant quality events and trends to Executive Quality Leadership</p></li><li><p>Support inspection readiness, responses, and follow-up actions across relevant functions</p></li><li><p>Manage onboarding, development goals, coaching, performance discussions, and team administration</p></li><li><p>You champion quality, integrity, continuous learning, and trusted partnerships</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and eight years’ relevant healthcare or pharmaceutical industry experience</p></li><li><p>Quality, compliance, clinical development, Good Clinical Practice, or Good Pharmacovigilance Practice experience</p></li><li><p>Advanced risk-based quality management, risk assessment, and compliance knowledge</p></li><li><p>Experience managing complex issues, regulatory inspections, and inspection readiness</p></li><li><p>Subject matter expert, process owner, training, presentation, and staff management experience</p></li><li><p>Process improvement, project management, prioritisation, and time management skills</p></li><li><p>Advanced Microsoft Outlook, Word, Excel, and PowerPoint skills</p></li><li><p>Strong communication, collaboration</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences Delivery, Oncology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50273]]></requisitionid>
    <referencenumber><![CDATA[R50273]]></referencenumber>
    <apijobid><![CDATA[r50273]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50273/director-global-patient-safety-sciences-delivery-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director to join our Safety Sciences Delivery team, supporting our oncology portfolio in a hybrid model. In this role, you will lead compliant safety operations and serve as the primary oncology contact while collaborating with Safety Sciences Strategy and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Dublin (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Standardise practices, processes, and templates for signal detection and safety-document authoring.</p></li><li><p>Ensure compliant Safety Sciences Delivery activities through regulations, standard operating procedures, and monitoring tools.</p></li><li><p>Lead oncology signal detection and management, including Safety Monitoring Teams, surveillance plans, and evaluation reports.</p></li><li><p>Integrate innovative technologies into core safety activities.</p></li><li><p>Analyse aggregate data with Safety Sciences Strategy to identify emerging safety issues and patterns.</p></li><li><p>Coordinate benefit-risk assessments and safety contributions across periodic reports and portfolio documents.</p></li><li><p>Develop standardised training curricula, proficiency matrices, and knowledge repositories across Strategy and Operations.</p></li><li><p>You build, coach, and scale teams through succession planning, talent pipelines, and leadership development.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced life sciences or healthcare degree with 12+ years of pharmacovigilance experience.</p></li><li><p>Safety Sciences experience, preferably within oncology.</p></li><li><p>Strong leadership, communication, organisation, workload planning, and detail orientation.</p></li><li><p>Ability to optimise safety operations and manage multiple projects.</p></li><li><p>Global patient safety operations oversight experience preferred.</p></li><li><p>Matrix leadership, people management, and artificial intelligence technology experience preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€119,900.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Finance]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50327]]></requisitionid>
    <referencenumber><![CDATA[R50327]]></referencenumber>
    <apijobid><![CDATA[r50327]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50327/senior-manager-commercial-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Building Our Future Together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Commercial Finance to join our Commercial Finance Team, supporting our therapeutic area program teams. In this role, you will responsible for the generation, analysis, tracking and dissemination of the commercial revenue forecasts, analyzing actual sales performance and providing related insights for the company’s new Neurology product(s), including providing oversight for the brand P&L. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & Where</strong></p><p>This role will sit on-site in our Sleepy Hollow, NY office four days per week.</p><p><strong>Discover Your Role</strong></p><div><ul><li>Develop and maintain patient-based revenue forecast models using epidemiology, market research, and commercial data.</li><li>Translate forecast assumptions into demand, sales units, and gross-to-net revenue projections.</li><li>Analyze actual performance, conduct variance analyses, and identify key business drivers.</li><li>Partner with Commercial leaders and stakeholders to align forecasts, scenarios, and assumptions across products and indications.</li><li>Provide financial insights on sales performance, including pricing, volume, market share, and net/gross sales dynamics.</li><li>Monitor market, competitive, regulatory, and R&D developments impacting product performance and forecasts.</li><li>Create financial reports, presentations, ad hoc analyses, and modeling to support senior leadership decision-making.</li><li>Manage brand P&L activities, including budgeting, reforecasting, monthly close, financial systems oversight, expense reporting, and compliance with corporate and industry regulations.</li></ul></div><p><strong>This Role Requires</strong></p><ul><li>Bachelors Degree in Finance required; Masters degree or MBA preferred.</li><li>10+ years of experience in finance, with a minimum of 2 years in sales forecasting in pharma for commercial program finance</li><li>Basic understanding of Commercialization of products in Biotech/Pharma industry</li><li>Biotech/Pharma Sales/Revenue forecasting experience required</li><li>Experience with Oracle platform (Hyperion) in an administrative capacity</li><li>Extensive technical expertise in finance, budgeting, and forecasting. Knowledge of automated systems for estimating, budgeting, forecasting, monitoring, planning, and allocating resources for Commercial operations. Develops concepts, techniques, and standards. Considered to be an expert in the field within the organization.</li><li>Ability to analyze Commercial financial data and prepare management reports. Strong modeling skills required.</li><li>Required to produce accurate and timely financial budgets, forecasts, actuals, and variance analyses under tight deadlines. Must possess the ability to manage multiple competing priorities.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Program Operations Leader]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49342]]></requisitionid>
    <referencenumber><![CDATA[R49342]]></referencenumber>
    <apijobid><![CDATA[r49342]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49342/director-program-operations-leader/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></p><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director Clinical Trial Management Program Operations Leader to join our Clinical Trial Management team, supporting our clinical development organization in a hybrid work mode. In this role, you will lead operational strategy and delivery for complex clinical programs while collaborating with senior leaders, vendors, collaboration partners, and clinical study teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p></div><p><strong>When</strong> <strong>&</strong> <strong>where:</strong></p><div><p>US - Armonk, Warren or Cambridge - Hybrid (3 days in the office)</p></div><p><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></p><ul><li><p>Lead operational strategy and overall delivery for complex clinical programs.</p></li><li><p>Oversee program quality, timelines, budgets, and study team success.</p></li><li><p>Provide operational input to Clinical Study Concepts, feasibility, timelines, and cost estimates.</p></li><li><p>Review plans during protocol design, study startup, and study conduct.</p></li><li><p>Drive decisions, monitor KPIs, and implement risk mitigation strategies.</p></li><li><p>Lead vendor selection, CRO oversight, governance activities, and partner meetings.</p></li><li><p>Ensure inspection readiness and lead cross-functional support for Regulatory Authority inspections.</p></li><li><p>You bring an innovative approach to solving operational challenges and advancing guidelines.</p></li></ul><div><strong>This</strong> <strong>role</strong> <strong>requires:</strong></div><ul><li><p>Bachelor’s degree.</p></li><li><p>Advanced degree may be considered in lieu of proven experience.</p></li><li><p>Minimum 12 years of relevant proven experience.</p></li><li><p>Minimum 8 years of experience within clinical operations.</p></li><li><p>Knowledge of applicable regulations, International Council for Harmonisation/Good Clinical Practice (ICH/GCP), and SOPs.</p></li><li><p>Experience leading complex clinical programs and handling operational strategy, budgets, timelines, and resources.</p></li><li><p>Experience forecasting and allocating Clinical Trial Management resources across programs.</p></li><li><p>Experience managing Clinical Research Organizations (CROs), vendors, and external partners.</p></li><li><p>Experience representing Clinical Trial Management at review committees and governance meetings.</p></li><li><p>Experience leading staff recruitment, performance management, development, coaching, mentoring, training, and compliance activities.</p></li><li><p>Ability to communicate effectively with senior management, partners, and cross-functional teams.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff External Manufacturing Specialist (Drug Product)]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47766]]></requisitionid>
    <referencenumber><![CDATA[R47766]]></referencenumber>
    <apijobid><![CDATA[r47766]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47766/staff-external-manufacturing-specialist-drug-product/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are currently looking to fill a Staff External Manufacturing Specialist as the technical and operational authority for clinical contract drug product (DP) filling operations at CMO and business partner sites. Owns the tech transfer process end-to-end, drives active batch management from pre-production through lot disposition, and is a key GMP decision-maker. Provides technical mentorship and leadership to mid-level specialists, and collaborates with management on compliance strategy and CMO performance in the clinical operations space.</p><p><strong>When & where:</strong></p><ul><li><p>Rensselaer, NY</p></li><li><p>Monday-Friday</p></li></ul><p><strong>Discover your role:</strong></p><p>Drug Product Filling – Technical Expertise</p><ul><li><p>Apply deep technical knowledge of aseptic filling unit operations: sterile filtration (bioburden reduction and sterilizing-grade filters), filling (time-pressure, peristaltic, rotary piston), stoppering, capping, and lyophilization cycle development and scale-up.</p></li><li><p>Interpret environmental monitoring (EM) data, airborne particulate results, and media fill (APS) outcomes; assess implications for batch disposition and process adequacy.</p></li><li><p>Partner with DP MSAT to evaluate and apply lessons learned across the network as it relates to CCI, APS, filling operations, CMO assessments, etc.</p></li><li><p>Assess cleanroom design and equipment suitability (ISO 5/Grade A filling zones, Grade B/C support areas) relative to product contamination control requirements.</p></li><li><p>Support extractables and leachables (E&L) risk assessments for product-contact materials and container closure system selection.</p></li></ul><p>Technical Transfer:</p><ul><li><p>Own and lead end-to-end operations of tech transfer to CMO filling sites, gap assessments, risk evaluations and assessments, facility/equipment readiness, engineering run execution.</p></li><li><p>Approve Technical requirements document (TRD), Master Batch Records (MBR), validation reports, summary reports, etc</p></li><li><p>Oversee tech transfer, qualification, and validation of filling lines and critical equipment: isolator/RABS, vial/syringe filling systems, lyophilizers, and component prep (depyrogenation tunnels, washers, autoclave).</p></li><li><p>Coordinates/oversees DP manufacturing at CMO as dictated by project tech transfer and clinical operations.</p></li><li><p>Liaises between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments, Legal, Regulatory, Strategic Sourcing and contract manufacturers or business partners.</p></li></ul><p>Technical Mentorship & Leadership</p><ul><li><p>Serve as the primary technical resource for mid-level EM Specialists; provide hands-on guidance on aseptic filling operations, batch record review, deviation management, and CMO oversight.</p></li><li><p>Coach Specialists on interpreting in-process data, applying GMP regulations to real-world filling scenarios, and escalating issues appropriately.</p></li><li><p>Lead sub-teams on continuous improvement initiatives, filling technology upgrades, and CMO performance management.</p></li><li><p>Collaborate with management to communicate CMO operational status, proactively, surface risks, and shape external manufacturing strategy.</p></li></ul><p>Active Batch Management:</p><ul><li><p>Serve as Regeneron’s primary technical contact for all active clinical batches at CMO sites — track filling status, in-process results, and lot disposition milestones in real time.</p></li><li><p>Monitor in-process data: fill weight/volume checks, filter integrity test results, visual/automated inspection outcomes, and lyophilization cycle data.</p></li><li><p>Lead deviation investigations and drive CAPA closure for events occurring during or after filling operations; assess impact on batch and filing.</p></li><li><p>Track cycle times, yield trends, and reject rates across batches; analyze data for process drift and drive continuous improvement actions with the CMO.</p></li><li><p>Lead sub-teams in continuous process improvements, system/equipment implementation and/or strategy development.</p></li></ul><ul><li><p>Ensures product integrity and company reputation monitoring of cGMP compliance at external manufacturing contract manufacturers and business partners.</p></li></ul><p>Regulatory & GMP Compliance</p><ul><li><p>Key GMP decision-maker for external DP filling operations; apply FDA 21 CFR, EU GMP Annex 1, and USP/EP/JP compendia requirements.</p></li><li><p>Ensure CMO change controls are appropriately evaluated for regulatory impact; coordinate post-approval change strategies with Regulatory Affairs.</p></li><li><p>Review CMC sections of regulatory submissions (IND, BLA/NDA, MAA) related to DP manufacturing and filling as required.</p></li><li><p>Support GMP audits of CMO sites; identify compliance gaps, assess risk</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree or advanced degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, Biochemistry, or related discipline and 10+ years in pharmaceutical/biopharmaceutical DP manufacturing, with significant direct experience in sterile filling and CMO oversight.</p></li><li><p>Hands-on technical experience with sterile drug product filling operations (aseptic filling, lyophilization, CCI, inspection) in a GMP environment.</p></li><li><p>Demonstrated experience leading or executing tech transfer of DP filling processes to CMO sites, including MBR/TRD approval, PPQ, and process validation.</p></li><li><p>Experience leading deviation investigations and CAPA development for sterile filling operations.</p></li><li><p>Demonstrated ability to mentor and develop technical staff; experience providing guidance in a team or lead capacity.</p></li><li><p>Strong analytical, communication, and cross-functional collaboration skills; ability to influence and make decisions in ambiguous situations.</p></li><li><p>Willingness to travel domestically and internationally up to 25%+ as required.</p></li></ul><p>May substitute proven experience for education requirement.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 13:26:17 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Allergy-ENT - Birmingham S, AL]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50555]]></requisitionid>
    <referencenumber><![CDATA[R50555]]></referencenumber>
    <apijobid><![CDATA[r50555]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50555/medical-specialist-i-allergy-ent-birmingham-s-al/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Alabama]]></city>
    <state><![CDATA[Alabama]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><strong>Build our future together: </strong></div><div><div><div><div><div><div><div><div><div><p><strong> </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists, Otolaryngologists (ENT) and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently deliver product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Allergy and Otolaryngology (ENT) therapeutic areas to generate product utilization. The MS will develop strong working relationships with Allergy/ENT experts and clinicians in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate in and help lead initiatives to support sales success as assigned (e.g. participate in industry-related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Birmingham, AL region</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven history of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Allergy/ENT/Dermatology market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 11 Sep 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Field Medical Affairs Oncology - Paris Est & Région Est]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49888]]></requisitionid>
    <referencenumber><![CDATA[R49888]]></referencenumber>
    <apijobid><![CDATA[r49888]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49888/associate-director-field-medical-affairs-oncology-paris-est-region-est/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Associate Director Field Medical Affairs (MSL) Oncology - Paris Est & Région Est</h3><p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director Field Medical Affairs (MSL) Oncology France to join our Medical Affairs team, supporting our Oncology medical affairs organization in a field-based role. In this role, you will drive scientific exchange, share medical insights, and support research initiatives while collaborating with healthcare professionals, Clinical Development, Market Access, Commercial, and Medical Affairs colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Field-based, Paris Est & Région Est</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li><p>Build and manage relationships with Oncology Key Opinion Leaders and investigators.</p></li><li><p>Identify medical insights and advise internal stakeholders.</p></li><li><p>Serve as a scientific resource on disease state and portfolio-related data.</p></li><li><p>Support company-sponsored studies through investigator and site identification.</p></li><li><p>Advance investigator-initiated study concepts with researchers and site personnel.</p></li><li><p>Respond to scientific inquiries and present clinical data compliantly.</p></li><li><p>Attend conferences and report scientific, clinical, and competitive intelligence.</p></li><li><p>You thrive in a matrix environment and build trusted scientific partnerships.</p></li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li><p>PhD, PharmD, MD or DVM.</p></li><li><p>8+ years of proven experience, including 5+ years in Field Medical Affairs or Medical Management within Oncology.</p></li><li><p>Oncology expertise required with Skin cancers and/or Lung cancer experience preferred.</p></li><li><p>Knowledge of treatment guidelines, clinical research processes, European Union regulations, and compliant pharmaceutical practices.</p></li><li><p>Experience supporting company-sponsored studies, investigator-initiated studies, or clinical research activities.</p></li><li><p>Established Oncology Key Opinion Leaders relationships and institutional knowledge preferred.</p></li><li><p>Drug launch experience strongly preferred.</p></li><li><p>Ability to communicate complex scientific data and engage as a peer with Healthcare Professionals.</p></li><li><p>Strong planning, prioritization, problem-solving, and project participation skills.</p></li><li><p>Ability to work autonomously while maintaining compliance standards.</p></li><li><p>Proficiency with word processing, presentation, and spreadsheet applications.</p></li><li><p>Valid driver's license and ability to travel up to 70%, including overnight and occasional weekend travel.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€84,675.00 - €141,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regional Market Access Lead - Europe]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50653]]></requisitionid>
    <referencenumber><![CDATA[R50653]]></referencenumber>
    <apijobid><![CDATA[r50653]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50653/director-regional-market-access-lead-europe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regional Access Lead to join our Market Access function, supporting our European region in a hybrid work mode. In this role, you will drive market access, pricing, and reimbursement strategies for our neurology portfolio while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead European market access strategies aligned with global objectives and country needs.</p></li><li><p>Monitor payer trends, healthcare policies, and reimbursement frameworks across Europe.</p></li><li><p>Represent Europe in global access strategy discussions and shape future approaches.</p></li><li><p>Adapt access tools, payer value propositions, and objection handlers for regional use.</p></li><li><p>Support Health Technology Assessment dossiers, mock negotiations, and payer engagements.</p></li><li><p>Build relationships with payers, policymakers, and patient advocacy groups.</p></li><li><p>Align evidence generation and health economics outcomes research with payer requirements.</p></li><li><p>You bring an agile, collaborative mindset when influencing cross-functional teams.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>Regional market access launch experience across competitive therapeutic areas.</p></li><li><p>Proven European pricing, reimbursement, Health Technology Assessment, and negotiation success.</p></li><li><p>Experience developing and adapting economic models for regional and national submissions.</p></li><li><p>In-depth knowledge of European payer systems and reimbursement challenges.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>Fluent English; another European language and neurology experience are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix working, and stakeholder engagement skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€125,250.00 - €208,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Market Access DACH (f/m/d)]]></title>
    <date><![CDATA[Mon, 21 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45066]]></requisitionid>
    <referencenumber><![CDATA[R45066]]></referencenumber>
    <apijobid><![CDATA[r45066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/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[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager Market Access - DACH Region</strong> to join our Market Access team, supporting Germany, Austria and Switzerland in a hybrid work model. In this role, you will secure market access and reimbursement across our product portfolio while collaborating with Medical, Commercial, Global Market Access and Pricing teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Munich, Germany - Office-based role, hybrid</p><br><p><strong>Discover your role:</strong></p><br><ul><li>Develop market access and pricing strategies across Germany, Austria and Switzerland.</li><li>Lead dossier development under §35a SGB V, including consultations and G-BA hearings.</li><li>Support reimbursement price negotiations under §130b SGB V, including GKV SV engagement.</li><li>Develop contracting strategies and manage rebate contract tender processes.</li><li>Monitor healthcare policy developments and assess portfolio implications.</li><li>Identify market access barriers and build tailored action plans.</li><li>Provide market access input to clinical development programs and evidence generation.</li><li>You build trusted stakeholder partnerships to advance access objectives.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>University degree in health economics, natural sciences, pharmacy, medicine, business administration, or a comparable field.</li><li>Experience in Market Access & Pricing, including market access strategy development and benefit assessment dossiers.</li><li>Good knowledge of the German healthcare system, healthcare policy, and medicines legislation.</li><li>Experience handling contracts with statutory health insurance funds.</li><li>Ability to evaluate clinical, health economic, and market data and develop strategic recommendations.</li><li>Experience with reimbursement price negotiations under §130b SGB V.</li><li>Experience in oncology, hematology, neurology, rare disease, or related therapeutic areas.</li><li>Experience working in an international environment.</li><li>Excellent written and spoken German and English.</li><li>Strong analytical, communication, influencing, engagement, problem-solving, ownership, and strategic planning skills.</li></ul><p><br><br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€92,250.00 - €153,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Oncology]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50601]]></requisitionid>
    <referencenumber><![CDATA[R50601]]></referencenumber>
    <apijobid><![CDATA[r50601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50601/key-account-manager-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<br><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Oncology Netherlands to join our Commercial Oncology team, supporting the Netherlands in a field-based role. In this role, you will achieve sales objectives by building strong relationships with healthcare professionals, tailoring account strategies to local healthcare environments, and driving customer engagement through multiple channels while collaborating with medical colleagues and the Netherlands leadership team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Netherlands North </p><p>Work model: Field-based</p><br><p><strong>Discover your role:</strong></p><ul><li>Identify key stakeholders within oncology accounts and tailor engagement strategies to local healthcare needs and priorities.</li><li>Establish and lead high-quality interactions with healthcare professionals by maintaining current scientific knowledge and delivering aligned brand messaging.</li><li>Communicate the value proposition effectively through clear and consistent key message delivery to healthcare professionals.</li><li>Develop and execute local account plans aligned to the Dutch Brand Plan using market insights and relevant data sources.</li><li>Partner closely with medical colleagues to implement regional programs and activities that support healthcare professional needs.</li><li>Proactively communicate account results, market developments, and business updates to the Netherlands leadership team.</li><li>You balance face-to-face and digital engagement channels to optimize customer interactions and impact.</li><li>You work independently to execute strategic and tactical plans while adapting to changing priorities and timelines.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree or equivalent experience and minimum of 10 years of pharmaceutical sales experience, including experience within the biologics market.</li><li>Essential experience in oncology.</li><li>Previous experience in lung cancer and/or skin cancer is preferred.</li><li>Fluency in Dutch and English.</li><li>Ability to develop and implement account plans using market insights and data-driven decision making.</li><li>Experience working cross-functionally with medical and commercial stakeholders.</li><li>Ability to manage multiple customer engagement channels, including face-to-face interactions, remote calls, approved email communications, and digital platforms.</li></ul><br><br><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director: Data Management, Analytics, AI & Architecture]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50609]]></requisitionid>
    <referencenumber><![CDATA[R50609]]></referencenumber>
    <apijobid><![CDATA[r50609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50609/executive-director-data-management-analytics-ai-architecture/]]></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 Executive Director, Data Management & Architecture will lead a unified Data Management and Architecture function within Global Development IT, bringing together data enablement and architecture capabilities into a single end-to-end organization. This role will define the strategy for data platforms, AI architecture, and data governance while ensuring Global Development's technology landscape supports secure, scalable, and compliant data capabilities. The Executive Director will partner across Enterprise Data & AI, Enterprise Architecture, Information Security, and Global Development leadership to advance enterprise data priorities and enable business outcomes.</p><p>This role reports to the Executive Director, Global Development IT and will collaborate closely with enterprise and business leaders to shape data strategy, architecture standards, and long-term technology investments.</p><p><strong>Where and When</strong></p><p>This is an on-site position 4 days/week, primarily based at our Sleepy Hollow, NY or Warren, NJ office. If eligible, we can offer relocation benefits; we cannot offer a fully remote option.</p><p><strong>Key Responsibilities</strong></p><p>In this role, you will own data management and architecture for Global Development IT, working closely with Enterprise Data & AI, Enterprise Architecture, Information Security, and Global Development business and technology leadership. Your day-to-day responsibilities will include:</p><p><strong>Data Management & Enablement Leadership</strong></p><ul><li>Own and lead the unified Data Management & Enablement function, integrating the current Data Enablement organization and its data engineering, analytics, and data repository capabilities into a single team.</li></ul><ul><li>Absorb and lead the Services & Architecture function, consolidating data delivery and architecture and creating one point of accountability for data across the vertical.</li></ul><ul><li>Drive Data platforms and standards, including advancing toward a validated, centralized data repository.</li></ul><ul><li>Build and scale a data engineering and analytics team, including growing capability in the Global Capability Center (India-based team) in partnership with GCC leadership.</li></ul><p><strong>Data & Solutions Architecture (Domain Authority)</strong></p><ul><li>Serve as Global Development's data and AI architecture authority, owning the end-to-end architecture strategy for data platforms, pipelines, and solutions within the vertical.</li></ul><ul><li>Provide domain-specific solution architecture, ensuring designs are scalable, compliant, and aligned to business strategy in adherence to Enterprise Architecture standards.</li></ul><ul><li>Define integration, API, and data exchange patterns between vertical systems and enterprise platforms, reducing point-to-point integrations and promoting reusable architecture components.</li></ul><ul><li>Represent Global Development at the Architecture Review Board (ARB), presenting proposed investments for approval and ensuring alignment with enterprise-wide standards.</li></ul><p><strong>Data Governance & Regulatory Compliance</strong></p><ul><li>Partner with Enterprise Data Governance and Data Quality Management teams to enforce data quality, lineage, and regulatory compliance standards (e.g., GxP) within Global Development.</li></ul><ul><li>Own data classification, access, and quality standards for clinical trial, safety, and regulatory data, ensuring audit-readiness across the data estate.</li></ul><ul><li>Establish clear data stewardship accountability across Global Development's data domains, in partnership with business and functional leaders.</li></ul><ul><li>Ensure master data management (MDM) and data catalog practices are adopted consistently across the vertical.</li></ul><p><strong>Partnership with Enterprise Data & AI and Enterprise Architecture</strong></p><ul><li>Partner with Enterprise Data & AI as the primary governance and standards partner, aligning on data platform usage, AI architecture patterns, AI governance, and MDM/data catalog adoption.</li></ul><ul><li>Coordinate with the enterprise Architect community on cross-vertical architecture and ARB participation, ensuring vertical architecture conforms to enterprise-wide standards.</li></ul><ul><li>Partner with Vertical Solution Architect on end-to-end solution design, ensuring domain architecture decisions reflect broader vertical delivery needs.</li></ul><ul><li>Maintain a clear, non-duplicative division of accountability between core enterprise AI and data capability delivery, owned by Enterprise Data & AI, and domain-specific architecture and delivery, owned by this role.</li></ul><ul><li>Partner with Information Security on data security architecture, AI risk controls, and compliance with data protection standards.</li></ul><p><strong>Organizational Leadership & Talent</strong></p><ul><li>Build and lead a combined team spanning data enablement, data engineering, analytics, and architecture, defining a clear organizational structure and career paths for the function.</li></ul><ul><li>Recruit and develop senior technical talent, including growing architecture and engineering capability in the Global Capability Center (India-based team).</li></ul><ul><li>Serve as a mentor and technical authority for direct reports and the broader data community across Global Development.</li></ul><ul><li>Model and reinforce a culture of data governance discipline and architectural rigor across the organization.</li></ul><p><strong>Stakeholder Engagement & Executive Communication</strong></p><ul><li>Communicate data and AI architecture tradeoffs, platform investment needs, and long-term technology implications to business unit leadership.</li></ul><ul><li>Serve as a trusted advisor to senior Global Development IT and business leadership on data strategy, platform investments, and risk.</li></ul><ul><li>Prepare and deliver executive-level materials for governance forums, steering committees, and senior leadership on the health and roadmap of the data and architecture portfolio.</li></ul><ul><li>Build relationships with the Office of the CIO to ensure enterprise compliance considerations and enterprise-wide data investment decisions reflect Global Development's needs, surfacing technical debt and platform gaps as needed.</li></ul><p><strong>Qualifications and Requirements</strong></p><p><strong>Education & Experience</strong></p><ul><li>Bachelor’s degree in Computer Science, Information Systems, Business Administration, or a related field (Master’s degree preferred).</li></ul><ul><li>17+ years of experience in product ownership or management roles, with a focus on enterprise platforms, PPM tools, TBM frameworks, and financial-based systems.</li></ul><ul><li>Experience in the biotech, pharma, or life sciences industry strongly preferred.</li></ul><ul><li>Track record leading organizational integration or restructuring of technical functions.</li></ul><p><strong>Technical Expertise</strong></p><ul><li>Deep expertise in enterprise data architecture, data modelling, reference architecture design, and system integration strategies.</li></ul><ul><li>Hands-on experience with cloud data platforms (e.g., AWS, Azure) and modern data platforms (e.g., Snowflake, Databricks).</li></ul><ul><li>Strong grounding in data governance frameworks, master data management (MDM), and data catalog practices.</li></ul><ul><li>Familiarity with GenAI and agentic AI/LLM architectural patterns, and how they apply to enterprise data platforms.</li></ul><ul><li>Experience integrating or consolidating data engineering, analytics, and architecture functions across teams.</li></ul><p><strong>Skills & Competencies</strong></p><ul><li>Proven ability to lead complex, cross-functional data and architecture initiatives, delivering results across matrixed enterprise and business stakeholders in a fast-paced environment.</li></ul><ul><li>Exceptional ability to translate complex data and architecture tradeoffs into clear, executive-ready narratives for governance forums and senior leadership.</li></ul><ul><li>Experience establishing data governance frameworks and ensuring regulatory compliance (e.g., GxP) across clinical, safety, and regulatory data domains.</li></ul><ul><li>Experience in data governance, financial reporting, and compliance.</li></ul><ul><li>Strong stakeholder management across technical, business, and executive audiences; comfortable serving as a principal spokesperson for the function on highly significant matters.</li></ul><ul><li>Comfortable operating through cross-functional influence rather than direct authority, given shared accountability with Enterprise Data & AI, Information Security, and Enterprise Architecture</li></ul><p><strong>Certifications (Preferred)</strong></p><ul><li>TOGAF (The Open Group Architecture Framework)</li></ul><ul><li>DAMA CDMP (Certified Data Management Professional)</li></ul><ul><li>PMP or equivalent project/program management certification</li></ul><ul><li>Cloud platform certification (AWS/Azure/GCP data or architecture track)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Local Lab Delivery]]></title>
    <date><![CDATA[Mon, 21 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50673]]></requisitionid>
    <referencenumber><![CDATA[R50673]]></referencenumber>
    <apijobid><![CDATA[r50673]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50673/manager-local-lab-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Local Lab Delivery to lead the operational delivery, oversight, and continuous improvement of local laboratory reference range data management supporting our clinical development portfolio. In this role, you will oversee the end-to-end local laboratory data process, ensuring reference ranges, units, conversion factors, analyse mappings, and associated metadata are accurately interpreted, quality controlled, maintained, and configured within laboratory management systems. You will also lead and develop a team of Local Lab Delivery Specialists and collaborate across Clinical Data Management, Clinical Operations, study teams, technology teams, and external partners.</p><br><p><strong>When & where:</strong></p><p><strong>Hyderabad (hybrid)</strong></p><p><br><br></p><p><strong>Discover your role:</strong></p><ul><li>Lead the operational delivery of local laboratory data activities across clinical studies, ensuring timely execution, quality oversight, issue resolution, and effective study support.</li><li>Oversee the intake, interpretation, quality control, maintenance, and delivery of local laboratory reference ranges and metadata, including units, conversion factors, analyse mappings, and study-specific configurations.</li><li>Ensure accurate and timely configuration, maintenance, and quality oversight of local laboratory information within the EDC Lab Administration system.</li><li>Provide consultation and guidance on study-specific local laboratory setup requirements, metadata, and complex local laboratory data issues.</li><li>Oversee the maintenance, harmonization, and reuse of local laboratory metadata assets, including analyte libraries, laboratory templates, analyte mappings, units of measure, and reference range information.</li><li>Serve as the escalation point for complex local laboratory data issues and lead root cause analysis, CAPA development, issue resolution, and process remediation activities.</li><li>Partner with Clinical Data Management, Clinical Operations, study teams, system owners, technology teams, laboratory vendors, and external partners to drive successful local laboratory delivery.</li><li>Establish and monitor turnaround times, operational targets, and quality metrics supporting study startup, ongoing data management activities, and database lock achievements.</li><li>Ensure local laboratory data processes, systems, and documentation comply with SOPs, work instructions, quality standards, GxP requirements, and inspection-readiness expectations.</li><li>Drive continuous improvement and technology enablement, including opportunities involving automation, AI-enabled solutions, document extraction, unit harmonization, metadata classification, test synonym mapping, and quality review.</li><li>Lead, coach, mentor, and develop a team of Local Lab Delivery Specialists while managing performance objectives, development plans, workload allocation, resource planning, and operational priorities.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>Bachelor’s degree in Science, Health, Data Management, Mathematics, Computing, or a related field.</li><li>7+ years of Clinical Data Management experience within biotechnology, pharmaceutical, CRO, or healthcare environments.</li><li>5+ years of direct Local Laboratory Delivery experience and 2+ years of people management experience.</li><li>Advanced knowledge of local laboratory reference range management, including analyte interpretation, unit conversions, conversion algorithms, test synonym mapping, reference range evaluation, and metadata management.</li><li>Strong understanding of local laboratory data collection, validation, maintenance, quality control, and delivery processes supporting Clinical Data Management.</li><li>Strong knowledge of clinical trial processes, Clinical Data Management principles, EDC systems, laboratory administration systems, and related clinical data technologies.</li><li>Experience managing complex laboratory data issues through root cause analysis, CAPA development, issue resolution, and process remediation.</li><li>Knowledge of applicable regulations, GxP requirements, clinical data quality principles, SOPs, and inspection-readiness expectations.</li><li>Demonstrated experience with operational metrics, targets, turnaround times, quality indicators, process improvement, and operational excellence.</li><li>Strong leadership and people-management capabilities, including coaching, mentoring, performance management, resource planning, and staff development.</li><li>Strong analytical, problem-solving, decision-making, stakeholder management, and cross-functional collaboration skills.</li><li>Exposure to automation, AI-enabled solutions, workflow optimization, metadata management, or digital transformation within laboratory data management is preferred.</li><li>Excellent verbal, written, and interpersonal communication skills, with the ability to manage multiple priorities in a fast-paced environment.</li><li>May require up to 25% travel</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quantitative Pharmacologist]]></title>
    <date><![CDATA[Thu, 24 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50756]]></requisitionid>
    <referencenumber><![CDATA[R50756]]></referencenumber>
    <apijobid><![CDATA[r50756]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50756/senior-quantitative-pharmacologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><br><p>As a Senior Quantitative Pharmacologist this individual is expected to provide significant contributions to Pharmacometrics deliverables in support of multiple programs while also developing an ability to understand the strategic positioning for these programs in Pharmacometrics as well as across the organization. Through the application of state-of-the-art knowledge in pharmacokinetics and pharmacodynamics; is responsible for the execution of PK, PD, and other types of quantitative analyses that significantly contribute to the development of multiple programs. </p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY, Warren, NJ, Cambridge, MA </li><li>Work model/flexibility: 4 days per week onsite or remote</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Collaborate across functions to plan, design, implement, and analyze pharmacometrics (PMx) studies supporting drug development programs.</li><li>Apply standardized scientific approaches to evaluate and interpret in vitro and in vivo pharmacokinetic (PK), pharmacodynamic (PD), and PK/PD data.</li><li>Conduct a broad range of quantitative analyses including NCA, compartmental modeling, population PK, exposure-response, translational, and disease modeling.</li><li>Interpret study results and develop scientifically sound conclusions and recommendations to support development decisions.</li><li>Prepare accurate, timely, and well-articulated study reports, technical summaries, and regulatory submission documents.</li><li>Partner with PMx Research Specialists, programmers, statisticians, and scientific writers to develop tables, figures, listings (TFLs), and supporting analyses for internal and regulatory deliverables.</li><li>Contribute PMx expertise to Research and Global Clinical Study Team (GCST) meetings, including input on study design, analysis strategy, and interpretation of results.</li><li>Support regulatory interactions by preparing analyses and background materials for agency meetings, including pre-IND, End-of-Phase 2, and pre-BLA submissions.</li><li>Monitor project timelines, deliverables, and completion of assigned tasks; may serve as the PMx representative on cross-functional development teams with appropriate guidance.</li><li>Maintain compliance with PMx operating procedures, quality standards, and the company's code of ethical conduct.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 3+ years of experience</li><li>Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.</li><li>Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.</li><li>Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams.<br><br></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 25 Sep 2026 19:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Analyst, Strategic Finance]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50733]]></requisitionid>
    <referencenumber><![CDATA[R50733]]></referencenumber>
    <apijobid><![CDATA[r50733]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50733/senior-analyst-strategic-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Analyst Strategic Finance Partnerships Hyderabad to join our Strategic Finance team, supporting our strategic partnership and licensing finance activities in a hybrid work model. In this role, you will support the financial management of collaboration partnerships through budgeting, forecasting, partner reconciliations, financial modeling, and reporting while collaborating with Strategic Alliances, Commercial Finance, R&D Finance, Accounting, and global finance colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Support annual budget and forecast cycles for strategic collaborations by consolidating inputs from Commercial, R&D, and Manufacturing partners.</li><li>Prepare monthly and quarterly management reporting packages, including variance analysis against budget, forecast, and prior-period results.</li><li>Perform financial reconciliations for partner cost-sharing and profit-sharing arrangements, ensuring data accuracy and completeness.</li><li>Build and maintain financial models covering cost-sharing true-ups, royalty and profit-share calculations, and foreign exchange impacts.</li><li>Prepare supporting schedules and documentation for partner invoicing activities and audit requests.</li><li>Investigate reporting anomalies, maintain process documentation, templates, and controls, and proactively raise issues when needed.</li><li>Collaborate with global finance colleagues and partner-company counterparts across time zones to deliver high-quality financial insights and reporting.</li><li>You bring a proactive, solution-oriented approach and thrive managing multiple priorities while maintaining accuracy and meeting deadlines.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in finance, Accounting, Economics, or a related field.</li><li>Minimum 5 years of relevant finance experience, ideally including financial planning and analysis (FP&A), financial reporting, reconciliations, or alliance/partnership finance.</li><li>Strong Excel modeling skills, including advanced formulas, sensitivity and scenario analysis, and management of large datasets.</li><li>Demonstrated experience with budgeting, forecasting, variance analysis, and month-end or quarter-end close and reconciliation processes.</li><li>Experience working with collaboration and licensing finance concepts such as cost-sharing, profit-sharing, and royalties preferred.</li><li>Experience with Hyperion is a plus.</li><li>Master's degree in finance, Accounting, or Business Administration preferred.</li><li>Prior exposure to the biopharmaceutical, life sciences, or healthcare industry preferred.</li><li>Experience supporting multinational or cross-border finance teams, including work across multiple currencies and time zones preferred.</li><li>Strong attention to detail, communication, forecasting accuracy, ownership, adaptability, teamwork, and the ability to manage multiple concurrent deliverables in a global environment.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Laboratory Automation & Robotics Engineering]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51030]]></requisitionid>
    <referencenumber><![CDATA[R51030]]></referencenumber>
    <apijobid><![CDATA[r51030]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51030/2027-co-op-laboratory-automation-robotics-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Laboratory Automation & Robotics Engineering to join our Preclinical Manufacturing and Process Development (PMPD) team, which supports the automation infrastructure that keeps its labs running efficiently.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support the development and maintenance of liquid-handling robotics used across Preclinical Manufacturing and Process Development (PMPD) labs</li></ul><ul><li>Build and test 3-D printed lab tooling and fixtures</li></ul><ul><li>Contribute to automation projects spanning upstream, downstream, and analytics teams</li></ul><ul><li>Write and test basic programming scripts to support automation workflows</li></ul><ul><li>Provide hands-on lab support alongside automation development work</li></ul><ul><li>Troubleshoot equipment and workflow issues as they arise</li></ul><ul><li>Collaborate with engineers and scientists across multiple teams</li></ul><ul><li>Document automation processes and improvements</li></ul><br><p><strong>Relevant majors: </strong>Chemical Engineering, Biomedical Engineering, Mechanical Engineering, Computer Science</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Data Analytics & Digital Tools (IOPS)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50983]]></requisitionid>
    <referencenumber><![CDATA[R50983]]></referencenumber>
    <apijobid><![CDATA[r50983]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50983/2027-co-op-data-analytics-digital-tools-iops/]]></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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Data Analytics & Digital Tools (IOPS) to join our Process Sciences team within Regeneron Industrial Operations and Product Supply (IOPS) <strong>Process Sciences</strong> department. This team builds data-driven tools that support process teams across Regeneron.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Rensselaer, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$25.50 per hour.</p><p><strong>What you’ll do:</strong></p><ul><li>Contribute to the development of a conversational analytics platform supporting bioprocess data analysis</li></ul><ul><li>Expand data analysis dashboards to ingest additional data types from analytical tools</li></ul><ul><li>Support process monitoring, manufacturing investigations, and process characterization efforts</li></ul><ul><li>Build automated pipelines that unify multiple data streams and reduce manual data-processing effort</li></ul><ul><li>Apply generative artificial intelligence and machine learning techniques to bioprocess data</li></ul><ul><li>Support algorithm design and multi-agent system development</li></ul><ul><li>Work with databases and application programming interfaces (APIs) to build data solutions</li></ul><ul><li>Collaborate cross-functionally with teams across Regeneron</li></ul><p><strong> </strong></p><p><strong>Relevant majors: </strong>Computer Science, Data Science, Statistics, or a related quantitative field (a biology or bioprocess background is a plus)</p><p><strong> </strong></p><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li></ul><ul><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li></ul><ul><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li></ul><ul><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><em><strong>Please note our intern pay ranges are determined by level of education (year in school) and degree program.</strong></em></p><ul><li><em><strong>The hourly rate range for these locations is $17.90 - $25.50 per hour.</strong></em></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Dir Preclinical & Translational PK/PD]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50644]]></requisitionid>
    <referencenumber><![CDATA[R50644]]></referencenumber>
    <apijobid><![CDATA[r50644]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50644/sr-dir-preclinical-translational-pkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director to support PK and PK/PD requirements for early-stage drug discovery through IND/CTA projects. You'll utilize a mastery level of PK/PD knowledge and strategic leadership skills to effectively develop and implement strategic analyses supporting research and development projects. You'll exert influence across the organization at multiple levels, including individual contributors (in and out of the function), development program teams, and other functional managers, and will be accountable for the PK/PD evaluation of a portfolio of projects and/or highly complex programs/platforms that can be wide in scope.</p><br><p>This role is suited for individuals who thrive in a fast-paced, collaborative environment, are passionate about science and motivated to contribute to bringing new drugs to patients, and desire exposure to multiple therapeutic areas and emerging modalities. We're looking for seasoned and tenured scientists with a demonstrated ability to provide significant impact on the organization and external groups, readily able to influence and effect change.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><br><ul><li>Location: Tarrytown, NY</li></ul><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Serves as a subject matter expert regarding Preclinical and Translational PK/PD on Discovery-stage project teams, guiding the design of preclinical pharmacology, PK, and PK/PD studies</li><li>Collaborates with various internal groups such as Therapeutic Proteins, Therapeutic Function Areas, Assay Development, Precision Medicine, Preclinical Operations, and TPK/PD management to develop and execute PK/PD strategies for projects</li><li>Provides input and oversight for preclinical in vivo studies, coordinating with scientific teams conducting these studies</li><li>Manages nonclinical PK and PK/PD studies, and conducts and reports PK/PD analyses based on data from preclinical studies</li><li>Analyzes and presents PK and PK/PD data to project teams, TPK/PD, and senior management</li><li>Derives first in human (FIH) dose predictions in collaboration with Clinical Pharmacology</li><li>Works closely with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams within the Drug Safety and Pharmacometrics department to deliver data and regulatory documents supporting project progression</li><li>Prepares summary reports for regulatory submissions</li><li>Effectively communicates project team queries, expectations, and timelines to management</li><li>Maintains current knowledge of scientific literature, regulatory guidance, and best practices related to PK/PD of protein therapeutics, siRNA, CAR-T, and gene therapy modalities</li></ul><br><h3><strong>This role requires:</strong></h3><br><ul><li>A PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry, with more than 12–14 years of relevant experience in biotech or pharma</li><li>Deep theoretical and applied understanding of PK and PD to interpret the pharmacology and biology of therapeutic proteins; experience with other modalities such as siRNA, peptide-conjugates, CRISPR-based therapeutics, and cell therapies is highly beneficial</li><li>Proven ability to plan, coordinate, and lead PK and/or PK/PD studies, and analyze related data</li><li>Excellent written and verbal communication, presentation, influencing, and leadership skills</li><li>Familiarity with PK/PD software (e.g., WinNonLin), data visualization and AI software, and extensive experience writing scientific reports and regulatory summaries</li></ul><p> <br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Technician (Overnights)]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49539]]></requisitionid>
    <referencenumber><![CDATA[R49539]]></referencenumber>
    <apijobid><![CDATA[r49539]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49539/automation-technician-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science, technology, and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Automation Technician to join our Industrial Operations and Product Supply organization in Rensselaer, NY. In this role, you will help ensure the reliable operation of automated manufacturing systems that support biologics production and fill/finish operations. Working closely with Manufacturing, Maintenance, Facilities, and Engineering teams, you will troubleshoot complex process control systems, support continuous improvement efforts, and contribute to the production of high-quality medicines. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Working shift: Sunday-Thursday 12:00am-8:30am</li><li>Training shift: Monday-Friday 8:00am-4:30pm for approximately 6 months</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Troubleshoot automation, computerized process control, and process monitoring systems supporting GMP manufacturing operations</li><li>Coordinate automation response activities to resolve equipment and system issues while minimizing operational disruption.</li><li>Partner with multiple teams during equipment setup, changeovers, and maintenance activities</li><li>Implement automation testing and verification activities to confirm systems perform as intended</li><li>Support deviation investigations, corrective actions, and system improvements to enhance reliability and compliance</li><li>Interpret user documentation and communicate findings, recommendations, and status updates to multi-functional partners</li><li>Help maintain reliable manufacturing operations during overnight production hours on a dedicated third-shift schedule</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Associate degree in Engineering or a related technical field and the following years of experience supporting process control and/or data acquisition systems; equivalent experience may be considered in lieu of a degree:<ul><li>Automation Technician II: 3+ years </li><li>Automation Technician III: 5+ years</li></ul></li><li>Experience troubleshooting PLCs, HMIs, and computerized automation systems in a cGMP or industrial manufacturing environment</li><li>Knowledge of Allen-Bradley and Siemens control systems</li><li>Understanding of ladder logic, electrical systems, instrumentation, and process controls</li><li>Ability to interpret software lifecycle documentation, engineering drawings, technical evaluations, and test protocols for regulated manufacturing equipment</li><li><strong>Preferred:</strong></li><li>Experience supporting pharmaceutical, biotechnology, or biopharmaceutical manufacturing operations</li><li>Experience with servers, networking fundamentals, and industrial data systems</li><li>Knowledge of process control and machine automation within regulated manufacturing environments</li><li>Understanding of bioprocess equipment, sanitary design principles, and data integrity requirements.</li><li>Strong communication skills and proficiency with standard business software applications</li><li><strong>Gowning & Physical Requirements:</strong></li><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><br><p>Level will be determined based on qualifications relevant to the role </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Biostatistician - Oncology]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51221]]></requisitionid>
    <referencenumber><![CDATA[R51221]]></referencenumber>
    <apijobid><![CDATA[r51221]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51221/principal-biostatistician-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Principal Biostatistician</strong> to join our <strong>Global Development</strong> team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Sleepy Hollow, NY or Warren, NJ</li><li>4 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</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><ul><li>Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.</li></ul><ul><li>Develop individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.</li><li>Collaborate with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting. </li><li>Evaluate appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</li><li>Analyze data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making. </li><li>Prepare presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management. </li><li>Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians. </li></ul><br><p><strong>This role requires:</strong></p><ul><li>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. </li><li>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </li><li>Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.</li><li>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</li><li>Expertise in statistical software such as R or SAS is required</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 11:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Technician (Nights)]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51059]]></requisitionid>
    <referencenumber><![CDATA[R51059]]></referencenumber>
    <apijobid><![CDATA[r51059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51059/automation-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking for an experienced Automation Technician to join our growing team. Our Automation Technicians are responsible for supporting and troubleshooting biopharmaceutical manufacturing/filling/packaging equipment that utilize Human Machine Interfaces (HMIs) and Programmable Logic Controllers (PLCs) at Regeneron's Industrial Operation and Product Supply organization. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: East Greenbush, New York, United States</li><li>Working shift: Tuesday-Saturday, 4:00pm-12:30am</li><li>Training shift: Monday-Friday, 8:00am-4:30pm for approximately 6 months</li></ul><h3>Discover your role:</h3><ul><li>Provide automation technical support, troubleshooting, and assistance during routine operations, maintenance activities, equipment setups, and changeovers for manufacturing operations of GMP Bulk Biologics, Fill/Finish, and Clean Utilities systems</li><li>Identify and implement corrective or preventive maintenance, component replacements, or corrections on automated systems as needed</li><li>Communicate and coordinate Automation issue resolution for manufacturing and facilities groups</li><li>Full gowning when entering and working on production floor</li><li>Utilize specialized personal protective equipment as required, including arc flash, when working near energized equipment or when working in construction environments</li><li>Work independently and safely around all industrial equipment</li></ul><br><h3>This role requires:</h3><ul><li>Associate degree in Engineering or a related technical field and the following years of experience supporting process control and/or data acquisition systems; equivalent combination of education and experience may be considered:<ul><li>Automation Technician II: 2+ years of related experience</li><li>Automation Technician III: 5+ years of related experience</li><li>Automation Technician IV: 8+ years of related experience</li></ul></li><li>Experience troubleshooting PLCs, HMIs, and computerized systems, preferably in a regulated environment</li><li>Knowledge of ladder logic, PID control, electrical control systems, instrumentation, and current and voltage characteristics in DC and 120/240/480 VAC circuits</li><li>Ability to diagnose or troubleshoot electrical control circuits utilizing a digital multimeter and electrical schematics</li><li>Basic understanding of data integrity regulations</li><li>Special emphasis on machine controls preferred, with specific knowledge of Allen-Bradley and Siemens control system products strongly preferred; basic knowledge of B&R control system products is helpful</li><li>Experience with servers, virtualization, distributed control, and basic networking is preferred</li><li>Strong written and verbal communication skills</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Corporate Counsel, R&D Regulatory]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50845]]></requisitionid>
    <referencenumber><![CDATA[R50845]]></referencenumber>
    <apijobid><![CDATA[r50845]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50845/associate-director-corporate-counsel-rd-regulatory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><br><p>Regeneron’s R&D Legal team is seeking an attorney to provide strategic legal advice to the Global Clinical Development teams that support Regeneron’s robust and growing pipeline. The attorney will provide advice on a wide range of legal, regulatory, contractual, privacy, and compliance issues related to drug discovery and development. The attorney will work closely with scientists, clinicians, regulatory, and clinical operations colleagues in a global, matrixed environment. The attorney will be an integral part of a proactive and solutions-oriented legal team that provides advice to advance Regeneron’s pipeline</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Sleepy Hollow, NY</li><li>Work model/flexibility: 4 days per week on site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Provide proactive and strategic legal advice and counsel on global drug discovery and development activities in one or more therapeutic areas</li><li>Advise Global Clinical Development teams on laws impacting drug discovery, research, and clinical development, including FDA regulations, human subject protection, data use and sharing, use of AI in research, GxP compliance, and other laws impacting research and development of innovative medicines</li><li>Interact with internal business stakeholders, R&D management, and third-party partners including CROs</li><li>Draft and negotiate a wide range of R&D documents including clinical trial agreements, consent forms, research collaboration agreements, and other contracts in support of our global clinical trial operations and medical affairs</li><li>Counsel on patient privacy and patient rights on matters related to clinical research</li><li>Serve as a subject matter expert on R&D matters within the Law Department and collaborate with other legal functions (e.g., Business Development and Contracting, Compliance, Data Protection/Privacy, Litigation and Products/Regulatory Law group)</li><li>Legal support on Regeneron policies, governance, operating procedures, and training to ensure compliance with regulatory requirements and promote effective risk management. </li><li>Provide legal support on other matters as needed for the R&D, Regulatory and Commercialization Law team</li><li>Maintain an independent and objective perspective while developing and maintaining a strong partnership with clients</li></ul><p><strong>This role requires:</strong></p><ul><li>Juris Doctor (J.D) degree with excellent law school credentials</li><li>Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel</li><li>4+ years experience working at a top-tier law firm or in-house healthcare company</li><li>In-house biotech/pharmaceutical experience a significant plus</li><li> Demonstrated ability to learn new subject matters quickly and translate complex legal concepts into practical business advic</li><li> Interest in emerging technologies, AI, evolving regulatory frameworks that are shaping the future of biotechnology research and development</li><li>Excellent interpersonal and conflict resolution skills and the ability to work in a highly collaborative, team-oriented environment.</li></ul><br><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Physician Scientist, Therapeutic Area Genetics (Immunology)]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46254]]></requisitionid>
    <referencenumber><![CDATA[R46254]]></referencenumber>
    <apijobid><![CDATA[r46254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46254/physician-scientist-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[<h3><strong>Build our future together: </strong></h3><p>We are looking for an extremely talented Physician Scientist to join our Immunology Therapeutic Area Genetics (TAG) team. Within the Regeneron Genetics Center, the Immunology TAG team is using large-scale human exome sequencing for discovery and validation of new therapeutic targets in autoimmune and other immune-mediated disease. You will be responsible for designing and executing studies integrating large scale human genetics and multidimensional omics datasets derived from RGC and public resources in the immunology space to identify new targets for inflammatory and auto-immune diseases and accelerate target transition to novel therapeutics. You will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to catalyze therapeutic development for genetically-validated targets in immunologic diseases.</p><div><h3><strong>When & where: </strong></h3><ul><li><p>Location: Tarrytown, NY</p></li></ul></div><div><h3><strong>Discover your role: </strong></h3></div><ul><li><p>Understand and leverage RGC and Regeneron datasets, external resources, and the scientific/medical literature to generate research questions and then generate relevant phenotypes from longitudinal clinical data, design and execute genetic association studies, and perform integrative omics analyses to address these research questions</p></li><li><p>Deploy computational methods to integrate genetic data with multiple omics data to more effectively identify/prioritize drug targets illuminated by genetic association data.</p></li><li><p>Work closely with other members of the Immunology and other TAG teams, Analytic Genetics, Sequencing, and GIDE in cross-functional initiatives within the RGC and Regeneron.</p></li><li><p>Collaboratively summarize insights of investigations into a variety of formats (e.g. documents, presentations, patent applications, publications, etc.) for audiences with broad backgrounds.</p></li><li><p>Partner with Clinical Development to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations.</p></li></ul><h3><strong>This role requires: </strong></h3><ul><li><p>MD or MD/PhD with a strong background in human genetics or genetic epidemiology</p></li><li><p>Experience in the use of WES/GWAS datasets, RNA-Seq, proteomics and other large-scale platforms for genomic/proteomics.</p></li><li><p>Demonstrated expertise in immunobiology, genetics, and mechanisms; familiarity with large genetic studies that deliver novel genetic findings and medically relevant gene discoveries;</p></li><li><p>Demonstrated ability to manage and collaborate in a multi-disciplinary team, to discover and evolve immunology-related drug discovery pipelines.</p></li><li><p>Individuals with proficiency in computational immunology research are particularly encouraged to apply.</p></li></ul><p>#MDJobs, #MDJobsRGC</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$243,600.00 - $329,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 12:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist (External CRO Management)]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50964]]></requisitionid>
    <referencenumber><![CDATA[R50964]]></referencenumber>
    <apijobid><![CDATA[r50964]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50964/scientist-external-cro-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>A Scientist within the Bioanalytical Outsourcing will be responsible for overseeing all bioanalysis (nonclinical and clinical) at external CROs. They will be responsible for coordination of assay development/qualification/validation efforts on various analytical platforms as well as the subsequent sample analysis and reporting efforts for each drug program. They will be responsible for communicating progress on these deliverables to the appropriate nonclinical and clinical colleagues and project teams. The successful candidate will have demonstrated technical proficiency, solid understanding of the GLPs, exhibit scientific rigor and independent thought as well as the ability to thrive in a team-oriented environment.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY United State – Onsite</p><br><p><strong>Discover your role:</strong></p><ul><li>Provide scientific and operational oversight on all aspects of bioanalytical activities conducted at Contract Research Organizations (CROs), independently and in collaboration with representatives of the Bioanalytical Outsourcing Team.</li></ul><ul><li>Provide scientific support to CRO efforts in design, development, and implementation of a variety of analytical methods in a regulated (GLP, GCLP) environment and ensure that these activities are in line with current regulatory guidelines.</li></ul><ul><li>Work with internal and external SMEs (Subject Matter Experts) to address any/all issues that may occur during assay development and/or sample analysis.</li></ul><ul><li>Interface with CROs to ensure on time delivery of required milestones and proactively communicate with the CRO to ensure transparency and adherence to the timelines, availability of required contracts, quotes, purchase orders etc.</li></ul><ul><li>Provide CRO with critical material, obtain and archive needed documentation, work with CRO to reconcile any scientific or operational concerns, manage standing review meetings, arrange vendor visits as appropriate.</li></ul><ul><li>Facilitate with the review of GLP and GCLP compliance status at CROs.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>A BS/MS with 10+ years experience in an industry setting.</li></ul><ul><li>Hands-on experience with regulated bioanalysis.</li></ul><ul><li>Hands-on experience with assay validation/qualification relevant under multiple platforms: LBA, LC/MS, PCR-based methods.</li></ul><ul><li>Excellent documentation skills with attention to detail and overall data quality.</li></ul><ul><li>Ability to clearly and concisely communicate project goals, deliverables internally and externally.</li></ul><ul><li>Ability to multi-task and work under tight timelines.</li></ul><ul><li>Preferred: Previous experience managing external CROs, coordinating bioanalysis, assay validation etc.</li></ul><ul><li>Preferred: Experience with novel drug candidates (gene therapies, CAR-T, mAbs, ADCs etc).</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49636]]></requisitionid>
    <referencenumber><![CDATA[R49636]]></referencenumber>
    <apijobid><![CDATA[r49636]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49636/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Engineer to join our Automation Engineering team to keep our groundbreaking process controls and process monitoring systems running at peak efficiency.</p><p>Make an impact from day one - lead improvements that enhance reliability, quality, and performance as you build, develop, and optimize systems for our highly-regulated biopharmaceutical manufacturing processes. In this role, you'll provide technical leadership and partner with Manufacturing, Quality Control, Facilities, Engineering, and Validation teams to maintain system reliability, drive continuous improvement, and deliver automation projects that support operational excellence.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: On-site Monday - Friday, 8:00AM - 4:30PM</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Design, develop, and implement software and hardware improvements to automated and new equipment under change control</li><li>Provide PLC- and HMI-based technical support to various departments per established SOPs</li><li>Identify, investigate, and resolve manufacturing deviations tied to automated control systems</li><li>Develop engineering design documents, technical evaluations, and test plans in line with GAMP 5</li><li>Support process control and monitoring equipment through software design, commissioning, testing, corrective action, and continuous improvement initiatives</li><li>Support manufacturing, engineering, and validation projects, including authoring and implementing Factory Acceptance Test (FAT), Site Acceptance Test (SAT), protocols, and system specifications</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Engineering or a related field, with 5+ years of aligned experience; equivalent combination of education and experience may be considered</li><li>Experience in the design and maintenance of process control and/or data acquisition systems is required</li><li>Experience programming, diagnosing, and resolving issues with the DeltaV DCS as well as PLCs</li><li>Proficiency with Allen-Bradley and Siemens control system products and video graphic chart recorders</li><li>Experience in a regulated manufacturing environment is ideal</li><li><strong>Gowning and Physical Requirements:</strong></li><li>Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) Ability to remove jewelry, makeup and nail adornments when wearing cleanroom attire</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Systems Administrator, Infrastructure]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48763]]></requisitionid>
    <referencenumber><![CDATA[R48763]]></referencenumber>
    <apijobid><![CDATA[r48763]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48763/senior-automation-systems-administrator-infrastructure/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Automation System Administrator to join our IOPS team, a tight-knit group responsible for administering the operational technology (OT) systems that run our biopharmaceutical manufacturing environment. This is a manufacturing floor and laboratory systems role, not an enterprise IT role. You will specify and maintain software and firmware configurations for process control, monitoring, and testing systems, evaluate new software for functional equivalence, and carry out the validation activities that demonstrate its suitability. You will keep these systems in a qualified, cGMP-compliant state throughout their lifecycle through change control, working closely with Manufacturing, Quality Control, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Menands, New York, United States</li><li>Work model/flexibility: Monday - Friday, 8am - 4:30pm</li></ul><br><p><strong>Discover your role:</strong></p><p>In this role, a typical day might include:</p><ul><li>Administering process control, monitoring, and testing system applications, including user access control (adding, modifying, and removing users), user types and groups, and security settings</li><li>Monitoring data backup and archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective) targets</li><li>Using configuration management and recipe/method management to maintain system configurations</li><li>Integrating manufacturing and laboratory systems with platforms such as LIMS and Historian</li><li>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and design specifications, test plans, technical evaluations, and quality risk assessments</li><li>Authoring impact statements, Configuration Specifications, risk assessments, SOPs, Work Instructions, policies, and corrective and preventive action plans</li><li>Supporting and leading system SAT (Site Acceptance Testing), FAT (Factory Acceptance Testing), validation, and qualification efforts</li><li>Evaluating new software for functional equivalence and supporting validation activities across the system lifecycle</li><li>Participating in, leading, or authoring investigations and root cause analyses for non-compliance issues</li><li>Providing end-user support on the manufacturing floor and in the lab, including system functionality training, application-level problem solving, and hardware troubleshooting in coordination with vendors</li><li>Leading aspects of work for contractors and providing guidance as applicable</li><li>Driving continuous process improvement, designing and implementing sustainable technical and procedural solutions in a complex environment</li></ul><br><p>Experience and skills we are looking for:</p><ul><li>Hands-on experience with process control systems and product release testing systems in a regulated manufacturing or laboratory environment</li><li>Experience supporting OT or industrial automation systems (for example, SCADA, DCS, PLC/HMI, or manufacturing execution platforms), as opposed to enterprise IT or help desk environments</li><li>Experience with a combination of Ignition, MQTT brokers, HiveMQ, HighByte, or similar industrial data platforms</li><li>Solid understanding of System Design Lifecycle and Quality Risk Management</li><li>Familiarity with regulatory and quality policies, procedures, and documentation methods in a cGMP environment</li><li>Interest in the manufacturing process within a regulated technical environment</li><li>Ability to work independently as part of a broader team, with a proven focus on customer service and maintaining compliance</li><li>Project management experience and strong organizational skills</li></ul><br><p><strong>This role requires:</strong></p><ul><li>BS/BA in Science, Engineering, or a related field</li><li>Automation Systems Administrator: 2+ years of relevant experience</li><li>Senior Automation Systems Administrator: 5+ years of relevant experience</li><li>May consider equivalent comb ination of education and experience. Level is determined based on qualifications relevant to the role</li><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Site Start Up Lead]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51074]]></requisitionid>
    <referencenumber><![CDATA[R51074]]></referencenumber>
    <apijobid><![CDATA[r51074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51074/senior-manager-global-site-start-up-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build Our Future Together</strong></h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager, Global Site Start-Up Lead</strong> to join our <strong>Global Development team</strong>, supporting complex, high-profile clinical trials across our global portfolio. In this role, you will lead the strategic execution of site and country start-up activities, driving efficient study activation and operational excellence while ensuring compliance with regulatory requirements and industry standards. Working closely with cross-functional partners, clinical operations teams, and CROs, you will play a critical role in accelerating study timelines, mitigating risks, and enabling the successful delivery of clinical development programs that bring innovative therapies to patients worldwide.</p><br><h3><strong>When & Where</strong></h3><br><ul><li><strong>Location:</strong> United States (Remote) or Regeneron office location</li><li><strong>Work Model/Flexibility:</strong> Remote </li><li><strong>Shift Requirements:</strong> Standard business hours with flexibility to support global teams across time zones</li><li><strong>Travel Percentage:</strong> Up to 25%</li></ul><br><h3><strong>Discover Your Role</strong></h3><br><ul><li>Develop and execute global site and country start-up strategies for complex clinical trials, identifying risks, dependencies, and mitigation plans.</li><li>Lead site activation planning and forecasting activities to ensure study milestones and timelines are achieved.</li><li>Partner with Clinical Operations, Regulatory Affairs, CROs, and other stakeholders to drive efficient study start-up execution.</li><li>Monitor and evaluate start-up metrics, leveraging data and trends to improve performance and inform strategic decision-making.</li><li>Oversee site activation activities including regulatory document collection, submissions, site initiation readiness, and milestone tracking.</li><li>Provide leadership and direction to CRO partners and internal teams to ensure high-quality and compliant start-up delivery.</li><li>Serve as the primary escalation point for site start-up challenges, proactively resolving issues and driving cross-functional alignment.</li><li>Manage and develop a team of Site Start-Up professionals through coaching, performance management, mentoring, and career development initiatives.</li></ul><br><h3><strong>This Role Requires</strong></h3><h3><br></h3><h3><strong>Must-Haves</strong></h3><ul><li>Bachelor's degree and <strong>8+ years of pharmaceutical, biotechnology, or clinical research industry experience</strong>.</li><li>Extensive experience leading global clinical trial start-up activities, including country and site activation strategies.</li><li>Strong knowledge of <strong>ICH-GCP guidelines</strong>, clinical trial regulations, and global study start-up processes.</li><li>Demonstrated ability to lead cross-functional teams and influence stakeholders across a global organization.</li><li>Proven experience managing vendors and CROs, including performance oversight and issue resolution.</li><li>Excellent project management, communication, negotiation, and risk management skills.</li></ul><h3><br></h3><h3><strong>Preferred Qualifications</strong></h3><ul><li>Previous direct line management experience with responsibility for staff development and performance management.</li><li>Experience supporting complex, high-profile, and global clinical development programs.</li><li>Strong analytical mindset with a data-driven approach to forecasting, metrics review, and operational decision-making.</li><li>Experience driving process improvements and operational excellence initiatives within Clinical Development.</li><li>Advanced understanding of country-specific regulatory and site activation requirements across multiple regions.</li></ul><h3><br></h3><h3><strong>Physical Requirements</strong></h3><ul><li>Ability to work primarily in a computer-based environment.</li><li>Ability to travel domestically and internationally up to 25% as required.</li><li>Ability to participate in meetings across multiple global time zones.</li></ul><p><br><br></p><p> <br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 19:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Site Start-Up Lead]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51079]]></requisitionid>
    <referencenumber><![CDATA[R51079]]></referencenumber>
    <apijobid><![CDATA[r51079]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51079/senior-manager-global-site-start-up-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build Our Future Together</strong></h3><p><br><br></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager, Global Site Start-Up Lead</strong> to join our <strong>Global Development team</strong>, supporting complex, high-profile clinical trials across our global portfolio. In this role, you will lead the strategic execution of site and country start-up activities, driving efficient study activation and operational excellence while ensuring compliance with regulatory requirements and industry standards. Working closely with cross-functional partners, clinical operations teams, and CROs, you will play a critical role in accelerating study timelines, mitigating risks, and enabling the successful delivery of clinical development programs that bring innovative therapies to patients worldwide.</p><h3><br></h3><h3><strong>When & Where</strong></h3><br><ul><li><strong>Location:</strong> United States (Remote) or Regeneron office location</li><li><strong>Work Model/Flexibility:</strong> Remote or Hybrid, based on business needs</li><li><strong>Shift Requirements:</strong> Standard business hours with flexibility to support global teams across time zones</li><li><strong>Travel Percentage:</strong> Up to 25%</li></ul><br><h3><strong>Discover Your Role</strong></h3><br><ul><li>Develop and execute global site and country start-up strategies for complex clinical trials, identifying risks, dependencies, and mitigation plans.</li><li>Lead site activation planning and forecasting activities to ensure study milestones and timelines are achieved.</li><li>Partner with Clinical Operations, Regulatory Affairs, CROs, and other stakeholders to drive efficient study start-up execution.</li><li>Monitor and evaluate start-up metrics, leveraging data and trends to improve performance and inform strategic decision-making.</li><li>Oversee site activation activities including regulatory document collection, submissions, site initiation readiness, and milestone tracking.</li><li>Provide leadership and direction to CRO partners and internal teams to ensure high-quality and compliant start-up delivery.</li><li>Serve as the primary escalation point for site start-up challenges, proactively resolving issues and driving cross-functional alignment.</li><li>Manage and develop a team of Site Start-Up professionals through coaching, performance management, mentoring, and career development initiatives.</li></ul><h3><br></h3><h3><strong>This Role Requires</strong></h3><h3><strong>Must-Haves</strong></h3><ul><li>Bachelor's degree and <strong>8+ years of pharmaceutical, biotechnology, or clinical research industry experience</strong>.</li><li>Extensive experience leading global clinical trial start-up activities, including country and site activation strategies.</li><li>Strong knowledge of <strong>ICH-GCP guidelines</strong>, clinical trial regulations, and global study start-up processes.</li><li>Demonstrated ability to lead cross-functional teams and influence stakeholders across a global organization.</li><li>Proven experience managing vendors and CROs, including performance oversight and issue resolution.</li><li>Excellent project management, communication, negotiation, and risk management skills.</li></ul><br><h3><strong>Preferred Qualifications</strong></h3><ul><li>Previous direct line management experience with responsibility for staff development and performance management.</li><li>Experience supporting complex, high-profile, and global clinical development programs.</li><li>Strong analytical mindset with a data-driven approach to forecasting, metrics review, and operational decision-making.</li><li>Experience driving process improvements and operational excellence initiatives within Clinical Development.</li><li>Advanced understanding of country-specific regulatory and site activation requirements across multiple regions.</li></ul><br><h3><strong>Physical Requirements</strong></h3><ul><li>Ability to work primarily in a computer-based environment.</li><li>Ability to travel domestically and internationally up to 25% as required.</li><li>Ability to participate in meetings across multiple global time zones.</li></ul><br><br><p> <br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Market Reporting & Analytics]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51057]]></requisitionid>
    <referencenumber><![CDATA[R51057]]></referencenumber>
    <apijobid><![CDATA[r51057]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51057/manager-market-reporting-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><br><p>At Regeneron, we are seeking a Manager, Market Reporting & Analytics to join our growing Global Capability Center (GCC) in Hyderabad. As a founding member of Regeneron's first GCC, you will play a key role in establishing reporting processes, analytics frameworks, and operating standards that will support international commercial reporting capabilities across key markets including Europe, Canada, and Japan. Working closely with global Commercial Insights & Analytics, Commercial Operations, Data Management, and IT partners, you will lead teams responsible for incentive compensation, reporting, dashboarding, and analytics while driving operational excellence, data quality, and process standardization.</p><br><p><strong>When & where:</strong></p><p>Hyderabad (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead the in-country Incentive Compensation and Market Reporting & Analytics teams supporting international markets, including Europe, Canada, and Japan.</li><li>Handle day-to-day team activities, prioritize deliverables, review outputs for quality and accuracy, and support team development in a matrixed environment.</li><li>Establish reporting documentation standards, analytics workflows, and operating norms as part of the GCC build-out.</li><li>Partner with International Commercial Strategy & Operations leadership to align reporting priorities, requirements, and delivery timelines.</li><li>Collaborate with country Commercial Operations teams to understand business needs and drive timely execution of reporting and analytics results.</li><li>Lead governance meetings with international and country stakeholders, monitoring KPIs, SLAs, backlogs, and overall team performance.</li><li>Work closely with Commercial IT teams to handle reporting enhancements, analytics requests, and data structure changes.</li><li>Partner with Data Management teams to drive data harmonization, taxonomy management, and reporting consistency across markets.</li><li>Support knowledge transfer initiatives with U.S. and international teams to transition and expand reporting capabilities within the Hyderabad GCC.</li><li>Supervise incentive compensation reporting, dashboarding, field analytics support, and reporting results across international markets.</li><li>Monitor reporting quality, resolve raised data issues, and implement process improvements to enhance efficiency and accuracy.</li><li>Ensure consistent application of reporting standards, business rules, and documentation practices across all supported markets.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Business, Analytics, Statistics, Economics, Life Sciences, Data Science, Information Systems, or a related field.</li><li>7+ years of experience in Commercial Analytics, Market Reporting, Incentive Compensation, Sales Operations, Business Intelligence, or related commercial functions within the pharmaceutical, biotechnology, healthcare, or consulting industry.</li><li>Prior people leadership experience, including managing reporting and analytics teams in a matrixed environment.</li><li>Experience supporting international markets and working with global stakeholders across multiple geographies and time zones.</li><li>Strong understanding of incentive compensation processes, sales performance reporting, dashboarding, and commercial analytics.</li><li>Experience working with reporting and visualization tools such as Power BI, Tableau, Qlik, or similar platforms.</li><li>Knowledge of pharmaceutical commercial data sources, reporting frameworks, and business performance metrics.</li><li>Experience partnering with data management and IT teams on data governance, harmonization, and reporting enhancements.</li><li>Strong project management, stakeholder management, and communication skills.</li><li>Ability to identify process improvement opportunities and drive operational excellence.</li><li>Proven ability to work effectively in a fast-paced, collaborative, and matrixed global environment.</li><li>Strategic thinking, problem-solving, and leadership capabilities with a continuous improvement attitude.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 02:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[International Payroll Associate Manager]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51404]]></requisitionid>
    <referencenumber><![CDATA[R51404]]></referencenumber>
    <apijobid><![CDATA[r51404]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51404/international-payroll-associate-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an International Payroll Associate Manager to join our payroll team, supporting our international payroll operations in a hybrid arrangement. In this role, you will help lead accurate, compliant and timely multi-country payroll delivery while collaborating with HR, Finance and Tax. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Dublin (Hybrid)</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Supervise analysts through allocation, review, coaching, onboarding, development plans and performance feedback.</li><li>Oversee international payroll from submission, register and variance review through delegated approval and funding.</li><li>Manage provider service-level agreements, issues and escalations, including complex team cases and employee or partner queries.</li><li>Maintain statutory compliance, legislative monitoring, documented controls, segregation of duties and audit evidence.</li><li>Review bi-weekly/monthly payroll-to-general-ledger reconciliations with Finance, supporting audits, year-end filings and management metrics.</li><li>Coordinate tax equalisation and shadow payroll with external advisers, plus equity processing and Irish reporting with Stock Administration.</li><li>Document and standardise processes, identifying automation opportunities and contributing to system/vendor implementations or migrations.</li><li>You bring a careful, collaborative approach to confidential payroll work.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Payroll experience, including 2+ years in multi-country or international payroll.</li><li>Bachelor’s degree or equivalent experience.</li><li>Supervisory, mentoring or team-lead experience; formal line management preferred.</li><li>Irish payroll legislation: Pay As You Earn, Pay Related Social Insurance, Universal Social Charge and Revenue reporting/PAYE Modernisation.</li><li>Payroll vendor/bureau and human resources information system experience, such as Workday, ADP or SAP SuccessFactors.</li><li>Controls-environment and audit-support experience.</li><li>Advanced Excel: XLOOKUP, pivot tables and reconciliations.</li><li>Clear cross-functional, cross-time-zone communication and stakeholder management; integrity and sound judgement with confidential data.</li><li>Preferred payroll qualification, such as CIPP Payroll Ireland Certificate or Diploma in Payroll.</li><li>Preferred shadow payroll, expatriate tax or share-plan experience: restricted stock units, employee stock purchase plans, options and Irish reporting.</li><li>Preferred exposure to Sarbanes-Oxley controls and payroll system implementations or vendor transitions.</li><li>Additional European language skills preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 04:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HCP Engagement Risk Governance Analyst]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51051]]></requisitionid>
    <referencenumber><![CDATA[R51051]]></referencenumber>
    <apijobid><![CDATA[r51051]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51051/hcp-engagement-risk-governance-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>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><br><p>At Regeneron, we are seeking an HCP Engagement Risk Governance Analyst to join our growing Global Capability Center (GCC) in Hyderabad. As one of the founding members of the GCC, you will play a critical role in supporting Healthcare Professional (HCP) transparency, compliance monitoring, and risk governance activities. You will help establish operational processes, documentation standards, and reporting frameworks while partnering with US-based teams to ensure HCP engagements are conducted in compliance with internal policies and external regulatory requirements. This role offers a unique opportunity to contribute to a high-impact function that supports ethical business practices and regulatory excellence across the organization.</p><br><p><strong>When & Where:</strong></p><p>Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Monitor HCP engagement activities and support compliance with regulatory requirements and company policies.</li><li>Conduct transactional monitoring reviews of HCP engagements and associated payments to ensure adherence to federal, state, and company compliance standards.</li><li>Perform data tracking, validation, and analysis of HCP interactions, transfers of value, engagement records, and invoicing information.</li><li>Develop subject matter expertise in Regeneron compliance policies, HCP engagement procedures, and applicable healthcare regulations.</li><li>Prepare transparency reports, disclosure submissions, state reporting documentation, and compliance-related reporting results.</li><li>Identify and raise potential compliance risks, data anomalies, or engagement exceptions for further review.</li><li>Compile data, supporting documentation, and analyses for compliance audits and monitoring activities.</li><li>Maintain records, documentation repositories, dashboards, and compliance monitoring reports.</li><li>Partner with Compliance, Transparency, Legal, and business stakeholders to investigate and resolve operational issues.</li><li>Collaborate with third-party vendors supporting transparency and regulatory reporting requirements.</li><li>Support knowledge transfer initiatives and process localization activities from US-based teams into the Hyderabad GCC.</li><li>Assist in establishing governance procedures, documentation standards, and guidelines as part of the GCC build-out phase.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Life Sciences, Analytics, Business Administration, or a related field.</li><li>2-3 years of experience in compliance monitoring, transparency reporting, HCP engagement operations, risk management, or related pharmaceutical industry functions.</li><li>Proficiency in Microsoft Excel and SQL for data analysis, data validation, reporting, and compliance monitoring activities.</li><li>Experience working with compliance monitoring systems, reporting platforms, and audit support processes.</li><li>Understanding of HCP engagement processes, transparency reporting requirements, and healthcare compliance principles.</li><li>Knowledge of pharmaceutical compliance regulations, including the Physician Open Payments Act, PhRMA Code, Federal Anti-Kickback Statute, False Claims Act, and related reporting obligations preferred.</li><li>Experience performing data validation, auditing, reconciliation, and exception reporting activities.</li><li>Familiarity with tools and systems used to capture, monitor, and report HCP engagement data.</li><li>Strong analytical and problem-solving skills with the ability to identify risks, discrepancies, and emerging trends.</li><li>Excellent attention to detail with a focus on accuracy, compliance, and documentation quality.</li><li>Strong verbal and written communication skills with the ability to collaborate across global and cross-functional teams.</li><li>Ability to work effectively in a matrixed environment and support multiple stakeholders across different time zones.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Category Management]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48239]]></requisitionid>
    <referencenumber><![CDATA[R48239]]></referencenumber>
    <apijobid><![CDATA[r48239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48239/associate-director-category-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking an Associate Director, Global Procurement Category Management to join our Global Procurement team, supporting our global categories in a hybrid work model. In this role, you will lead category management across global procurement categories while collaborating with team members, suppliers, Law, procurement colleagues and direct reports. This position offers the opportunity to help shape a procurement capability that acts as a competitive advantage to Regeneron.</p><p><strong>When & where:</strong></p><p>Hyderabad - (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead category management across a range of global categories.</p></li><li><p>Align category priorities with leaders, team members and suppliers.</p></li><li><p>Manage negotiations, supplier relationships and stakeholder engagement.</p></li><li><p>Drive cost savings, cash flow and efficiency improvements.</p></li><li><p>Negotiate contract terms with Law and business partners.</p></li><li><p>Use data and market insight to guide category decisions.</p></li><li><p>Coach procurement skills and career development across the team.</p></li><li><p>You bring clarity and integrity when driving change.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree in a relevant field of study.</p></li><li><p>Progressive procurement experience, including Pharma or BioPharma experience.</p></li><li><p>Experience managing global category processes and suppliers.</p></li><li><p>S-u+ccess leading cross-functional teams across sourcing, negotiations and contracting.</p></li><li><p>Experience managing supply market evaluation using market intelligence, risk, compliance and financial assessment tools.</p></li><li><p>Working knowledge of sourcing, contracting, ERP and eRFx systems preferred, including Oracle, Zycus or Ariba.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Direct and FC&L Procurement]]></title>
    <date><![CDATA[Thu, 25 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48234]]></requisitionid>
    <referencenumber><![CDATA[R48234]]></referencenumber>
    <apijobid><![CDATA[r48234]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48234/manager-direct-and-fcl-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Direct Materials Procurement to join our Global Procurement team, supporting our India operations in a hybrid work model. In this role, you will drive category strategy, sourcing, and supplier performance for direct materials while collaborating with cross-functional partners and global procurement colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Drive the definition and implementation of global direct material category strategies aligned to regional and global business needs</p></li><li><p>Partner with collaborators to manage category priorities, sourcing decisions, and procurement activities across direct materials</p></li><li><p>Lead negotiations, contracting, and supplier management to deliver cost savings, cash flow improvements, and operational efficiencies</p></li><li><p>Ensure category activities align with GxP and applicable regulatory standards</p></li><li><p>Collaborate with Legal to negotiate contract terms and conditions aligned to business requirements</p></li><li><p>Use market intelligence, supplier insights, and data analytics to inform decision-making and improve category performance</p></li><li><p>Contribute to organizational decisions and initiatives that shape global procurement capabilities and category outcomes</p></li><li><p>You operate effectively in a matrixed, global environment and build strong, trusted relationships with internal and external partners.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in a relevant field with progressive experience in procurement, including Pharma/Biopharma.</p></li><li><p>Proven experience managing category strategies, sourcing, contracting, and supplier relationships across direct materials or related categories.</p></li><li><p>Strong negotiation capability with understanding of cost structures, rates, and supply market dynamics.</p></li><li><p>Demonstrated success working with cross-functional teams to deliver results across procurement activities.</p></li><li><p>Experience supporting supplier evaluation processes using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Knowledge of global procurement processes and operating models within the biopharmaceutical industry.</p></li><li><p>Ability to demonstrate data and analytics to drive category decisions and project outcomes</p></li><li><p>Experience managing or coaching professional-level employees preferred.</p></li><li><p>Working knowledge of sourcing and contracting tools, ERP systems, and eRFx platforms (e.g., Oracle, Zycus, Ariba) preferred.</p></li><li><p>Proficiency in standard business applications (Word, Excel, PowerPoint)</p></li><li><p>Strong communication, collaboration, and collaborator management skills with the ability to work effectively in ambiguous environments.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48306]]></requisitionid>
    <referencenumber><![CDATA[R48306]]></referencenumber>
    <apijobid><![CDATA[r48306]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48306/specialist-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Specialist, External Data Acquisition and Delivery to join our Clinical Data Management team. In this role, you will manage non-Case Report Form data across assigned studies or Clinical Development Units while collaborating with external data vendors, CRO partners, Clinical Data Management and cross-functional stakeholders. This position offers the opportunity to support data integrity, improve external data delivery and strengthen compliant study execution.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Manage end-to-end non-Case Report Form data delivery.</li><li>Develop low-complexity Data Transfer Specifications for assigned studies.</li><li>Reconcile external vendor data with clinical database outputs.</li><li>Track specification status across data types and programmes.</li><li>Support data structure issue resolution and change requests.</li><li>Maintain documentation, audit trails and inspection readiness standards.</li><li>You collaborate across teams to resolve data discrepancies.</li><li>You support continuous improvement in external data processes.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in Science, Health, Mathematics, Engineering, Computational or related field.</li><li>2+ years in external clinical data acquisition or management.</li><li>Experience managing clinical data types such as biomarker, eCOA, imaging, ECG, PK, genomics and laboratory data.</li><li>Knowledge of 21 CFR Part 11, ICH-GCP and CDISC standards.</li><li>Experience extracting data into SAS, CSV and XML formats.</li><li>Knowledge of EDC platforms and external data reconciliation processes.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development IT & Digital]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45997]]></requisitionid>
    <referencenumber><![CDATA[R45997]]></referencenumber>
    <apijobid><![CDATA[r45997]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45997/senior-manager-global-development-it-digital/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong> Tokyo, Japan</p><p>We are seeking a dedicated and innovative <strong>Global Development IT & Digital Manager</strong> to join our team in Tokyo. This pivotal role supports our Global Clinical Development, Patient Safety, Regulatory Affairs, and Medical Affairs organizations by leveraging IT solutions to drive high business value. As a trusted partner, you will collaborate across diverse teams, blending technical expertise with a deep understanding of pharmaceutical industry processes to deliver impactful results.</p><p>If you are passionate about IT, thrive on solving complex challenges, and are eager to make a meaningful difference in the pharmaceutical space, this role offers an exciting opportunity to grow and lead in a globally connected environment.</p><p><strong>A Typical Day:</strong><br>In this role, you will:</p><ul><li>Develop and implement IT action plans aligned with global and local business strategies.</li><li>Collaborate with local business units to understand and address goals, challenges, and regulatory requirements.</li><li>Manage IT projects and products, ensuring compliance with GxP regulations.</li><li>Promote IT-based business improvements using automation, data utilization, and cloud technologies.</li><li>Drive digital transformation initiatives leveraging AI, cloud, and data analytics.</li><li>Facilitate meetings and presentations in business-level English while coordinating with international teams.</li><li>Build and maintain a stable IT infrastructure, ensuring operational excellence.</li><li>Utilize development methodologies (agile, waterfall, hybrid) tailored to business needs.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You enjoy connecting IT with business needs and bridging different viewpoints through structured thinking and effective communication.</li><li>You have a curious and open mindset toward understanding multiple business domains and perspectives.</li><li>You thrive in collaborative environments and build trusted relationships with stakeholders.</li><li>You excel at problem-solving and are motivated by continuous improvement.</li><li>You are detail-oriented and capable of translating complex ideas into clear, actionable plans.</li><li>You are proficient in business-level English and skilled in facilitating conferences and delivering impactful presentations.</li></ul><p><strong>To Be Considered:</strong><br>You must have:</p><ul><li>Over five years of experience in the pharmaceutical industry, specifically in IT for development and medical departments.</li><li>A solid understanding of operational processes in drug development, clinical trials, and medical affairs.</li><li>Proven experience as an IT business analyst, IT project manager, or IT product manager.</li><li>Knowledge of GxP, regulatory compliance, and Computer System Validation (CSV).</li><li>Basic programming knowledge and familiarity with IT infrastructure (hardware, software, databases, networks, cloud).</li><li>Experience with agile and waterfall development methodologies.</li></ul><p>Preferred qualifications include:</p><ul><li>Execution and stakeholder management skills demonstrated through collaboration and accountability.</li><li>A constructive, positive approach to challenges and problem-solving.</li></ul><p>Join us to shape the future of IT-driven innovation in the pharmaceutical industry. Apply today to become part of a team that values curiosity, collaboration, and excellence.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Patient Advocacy]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48174]]></requisitionid>
    <referencenumber><![CDATA[R48174]]></referencenumber>
    <apijobid><![CDATA[r48174]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48174/senior-director-patient-advocacy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're looking for a Senior Director, Patient Advocacy to join our Patient Advocacy team, shaping enterprise-wide strategy across discovery, development, and commercialization from our Sleepy Hollow, NY campus. In this role, you'll build the operating model that brings the patient voice into executive decision-making, partnering closely with Medical, Commercial, Market Access, Policy, and Clinical Development. This position offers the opportunity to shape how a fast-growing, science-driven organization listens to and acts on patient needs, making a meaningful difference for people living with serious diseases worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Sleepy Hollow, NY</li><li>Work model/flexibility: Hybrid — onsite 4 days per week</li></ul><p><strong>Discover your role:</strong></p><ul><li>Shape Regeneron’s enterprise-wide patient advocacy strategy, connecting the patient voice to discovery, development, and commercialization.</li><li>Build the standards and governance that guide how we engage advocacy and professional organizations.</li><li>Partner with Medical, Commercial, Market Access, Policy, and Clinical Development to set a multi-year advocacy roadmap.</li><li>Drive measurable outcomes — faster diagnosis, stronger trial awareness, broader access, and a better patient experience.</li><li>Move fluidly between big-picture strategy and hands-on execution, leading through influence across teams.</li><li>Turn corporate priorities into focused, therapeutic-area plans with clear decision rights.</li><li>Read external trends and policy shifts early, and recommend the moves that keep patient impact and business goals aligned.</li><li>Report progress through KPIs, dashboards, and board-ready materials that keep senior leaders informed.</li></ul><p><strong><em>This role might be for you if:</em></strong></p><ul><li>You've built enterprise-level programs from the ground up and know how to earn buy-in across an organization.</li><li>You're comfortable being a visible advisor to senior leaders and advocacy partners alike.</li><li>You bring structure to ambiguity, turning broad strategy into clear, repeatable processes.</li><li>You communicate with precision — able to distill complex work into a concise, data-driven story.</li><li>You’ve partnered across Medical, Commercial, Market Access, and Policy functions and understand the compliance considerations that come with advocacy work.</li><li>You put patients first, and let that perspective shape decisions, budgets, and partnerships.</li><li>You're energized by leading through influence rather than direct authority.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree and 12+ years of relevant experience, including 10+ years leading multi-stakeholder patient advocacy programs</li><li>A track record of building enterprise-wide, cross-functional programs with visible business impact</li><li>Strong executive presence and communication skills, with experience preparing board-ready materials</li><li>Experience partnering with Medical, Commercial, Market Access, and Policy teams, with working knowledge of compliance in advocacy</li><li>Preferred: experience in rare disease, oncology, hematology, ophthalmology, immunology, or cardio-metabolic disease</li><li>Preferred: experience operating in complex, matrixed, or global organizations; alliance management experience is a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician (Overnights)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46909]]></requisitionid>
    <referencenumber><![CDATA[R46909]]></referencenumber>
    <apijobid><![CDATA[r46909]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46909/hvac-technician-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an HVAC Technician to join our Facilities Maintenance team. In this role, you will be responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Working hours: Saturday-Wednesday 10:00pm-8:30am</li><li>Training hours: Monday-Friday 7:00am-3:30pm</li><li>Location: Rensselaer, NY</li></ul><h3>Discover your role:</h3><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers.</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work.</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC equipment</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Coordinating with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li></ul><br><h3>This role requires:</h3><ul><li>AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level:</li><li>HVAC Technician II: AAS with 2+ years or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years or equivalent combination of education and experience</li><li>HVAC Technician IV: AAS with 8+ years or equivalent combination of education</li><li>Solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>EPA certified for refrigeration gases</li><li>Able to become fully gown qualified to work in production areas</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs (Standard Operating Procedures, cGMPs (current Good Manufacturing Processes), GDPs (Good Documentation Practices) and quality standards</li><li>Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Real-World Data and Analytics (HEOR)]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49658]]></requisitionid>
    <referencenumber><![CDATA[R49658]]></referencenumber>
    <apijobid><![CDATA[r49658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49658/manager-real-world-data-and-analytics-heor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Real-World Data and Analytics (RWDnA) to support the generation of real-world evidence (RWE) in oncology through the analysis of real-world data (RWD). Under the guidance of senior team members, you will be programming on internal RWD assets to support RWE generation to address research questions.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Sleepy Hollow, NY</p><p><br><strong>Discover your role:</strong><br>• Support the development of RWE queries, protocols, and SAPs in the oncology therapeutic area.<br>• Perform analyses of RWD using established methodologies and communicate findings to project teams and RWDnA colleagues.<br>• Support the preparation of presentations, publications, and other communication materials that summarize RWE findings.<br>• Provide operational support for interactions with external analytics vendors, including tracking deliverables and coordinating project activities.</p><p><strong>This role requires:</strong><br>• Doctoral degree in a quantitative field applying data science to healthcare data, or a Master's in a related field with 3+ years of relevant hands-on programming experience<br>• Advanced programming skills in SAS and R<br>• Hands-on experience with real-world data sources such as large-scale administrative claims data (e.g., Optum, Medicare, Komodo) and electronic health records<br>• Proficiency in statistical methods including survival analysis, propensity score methods, and generalized linear models<br>• Ability to work collaboratively in cross-functional environments.<br>• Oncology experience would be preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Neurology (Mountain West)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46426]]></requisitionid>
    <referencenumber><![CDATA[R46426]]></referencenumber>
    <apijobid><![CDATA[r46426]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46426/associate-director-field-medical-affairs-neurology-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs (Medical Science Liaison) to engage in the exchange of scientific data and other medical and/or scientific information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. As a scientific expert in your territory, you will demonstrate a thorough understanding of Neurology aligning with our strategic medical plans. The position will bring relevant insights from the field on research developments, treatment landscape and other opportunities to shape our medical strategy. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location/Territory: Kansas City, Minnesota, Colorado, Oklahoma<br>• Travel: (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends.<br>Discover your role:<br>• Establishing, fostering, cultivating and maintain peer relationships with KOLs in Neurology<br>• Acting as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding.<br>• Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.<br>• Support evidence generation (company sponsored trials and investigator-initiated studies) research initiatives.<br>• Identify and report medical insights.<br>• Identifies gaps in research and educational needs to inform medical strategy.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.<br>• Performs disease management and therapeutic area education with identified practitioners, payers and researchers.<br>• Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><p><strong>This role requires:</strong><br>• A Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) with a minimum 8 years of experience, including 4+ years working as a Medical Science Liaison in the pharmaceutical industry. <br>• Experience as a Neurology MSL or in Neurology is preferred. <br>• Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs is required. <br>• Established relationships with KOLs in neuromuscular centers is preferred, as is product launch experience. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. </p><p>#msl #medicalscienceliaison<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48340]]></requisitionid>
    <referencenumber><![CDATA[R48340]]></referencenumber>
    <apijobid><![CDATA[r48340]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48340/associate-biotech-production-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Within this role you will be working as part of the Manufacturing Team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors.<br> </p></div><div><p><strong>Where: </strong></p><ul><li><p>Location: Raheen, Limerick</p></li><li><p>Shift: 24/7</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors</p></li><li><p>Monitoring production processes</p></li><li><p>Participating in equipment start-up, commissioning, and validation activities</p></li><li><p>Assisting with troubleshooting in case of equipment failure</p></li><li><p>Performing manufacturing level maintenance on equipment</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Reviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standards</p></li><li><p>Maintaining housekeeping in designated area and adhering to the clean standards of the facility</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You possess excellent verbal and written communication skills</p></li><li><p>You enjoy problem solving</p></li><li><p>You demonstrate a can-do attitude</p></li><li><p>You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook</p></li><li><p>You demonstrate an ability to work within a successful team</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>To be considered for this opportunity you should have a BS/BA in Life Sciences or a related field. Relevant experience may be substituted in lieu of the educational requirement</p></li><li><p>Our site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyle</p></li></ul><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#LI-Onsite #JOBSIEST #REGNIELSM #IRELIM</strong></p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€16.42 - €25.59]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, RNA Therapeutics]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48808]]></requisitionid>
    <referencenumber><![CDATA[R48808]]></referencenumber>
    <apijobid><![CDATA[r48808]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48808/senior-associate-scientist-rna-therapeutics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist/Senior Associate Scientist to join our Nucleic Acid Therapeutics group, supporting drug discovery and technology development in the field of oligonucleotide therapeutics such as siRNAs and antisense oligonucleotides. In this role, you will develop assays and execute high-throughput screenings of hundreds to thousands of candidate molecules, while collaborating with your team to advance oligonucleotide therapeutic programs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop assays to enable high-throughput oligonucleotide library screenings</li><li>Execute high-throughput screening of hundreds to thousands of candidate molecules</li><li>Perform cell culture optimization, bDNA, RT-qPCR, cell line generation, and transfection optimization</li><li>Design probes and conduct compatibility tests, along with western blot analysis</li><li>Work with automated or semi-automated processes, including liquid handlers and instruments such as KingFisher and QuantStudio</li><li>Independently execute and refine techniques and technologies with general guidance</li><li>Multi-task and shift priorities based on communicated department needs</li><li>Thrive in a fast-paced environment, staying detail-oriented, organized, and eager to learn new techniques</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree required; Master's degree preferred</li><li>2+ years of industrial experience in a relevant field highly appreciated</li><li>Ability to independently execute and refine techniques with general guidance, multi-tasking across shifting priorities</li><li>Strong organizational and communication skills, with the ability to work well in a team</li><li>Preferred: experience with automated/semi-automated liquid handlers, KingFisher, and QuantStudio</li><li>Preferred: knowledge of oligonucleotide chemistry and RNA biology</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Preclinical & Translational Pharmacokinetics/Pharmacodynamics]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49723]]></requisitionid>
    <referencenumber><![CDATA[R49723]]></referencenumber>
    <apijobid><![CDATA[r49723]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49723/associate-director-preclinical-translational-pharmacokineticspharmacodynamics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Associate Director role involves supporting Pharmacokinetics (PK) and Pharmacokinetics/Pharmacodynamics (PK/PD) requirements for early-stage drug discovery and IND projects. Responsibilities include providing input and oversight for preclinical in vivo studies, coordinating with and influencing scientific teams conducting these studies, managing nonclinical Pharmacokinetics studies, analyzing and presenting PK/PD data to project teams and senior management, and preparing summary reports for regulatory submissions</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: 4 days per week onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Serving as a subject matter expert on Preclinical PK/PD within Discovery-stage project teams and guiding the design of preclinical PK/pharmacology studies.</p></li><li><p>Collaborating with various internal groups such as Therapeutic Proteins, Therapeutic Function Areas, Assay Development, Precision Medicine, Preclinical Operations, and PPK/PD management to develop and execute PK strategies for projects.</p></li><li><p>Effectively communicating project team queries, expectations, and timelines to management.</p></li><li><p>Conducting and reporting PK/PD analyses based on data from preclinical studies.</p></li><li><p>Working closely with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams within the Drug Safety and Pharmacometrics department to deliver data and regulatory documents supporting project progression.</p></li><li><p>Maintaining current knowledge of scientific literature, regulatory guidance, and best practices related to PK/PD.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry with more than 8 to 10 years of relevant experience in biotech or pharma.</p></li><li><p>Deep theoretical and applied understanding of PK and PD to interpret the pharmacology and biology of therapeutic proteins. Experience with other modalities such as siRNA, CRISPR-based therapeutics, and cell therapies is highly beneficial.</p></li><li><p>Proven ability to plan, coordinate, lead PK and/or PK/PD studies, and analyze related data.</p></li><li><p>Familiarity with PK/PD (e.g., WinNonLin), data visualization and AI software and experience writing scientific reports and regulatory summaries.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49413]]></requisitionid>
    <referencenumber><![CDATA[R49413]]></referencenumber>
    <apijobid><![CDATA[r49413]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49413/manager-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager</strong> to join our <strong>Regulatory Affairs Strategy Oncology</strong> team. The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations. </p><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul></div></div><div><p><strong>Discover your role:</strong></p><ul><li><p>Coordinate the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure </p></li><li><p>Assist in coordination and preparation for Agency meetings and associated briefing document preparation </p></li><li><p>Leads and tracks queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments </p></li><li><p>Provide representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum MD, PhD or PharmD degree along with 2+ years of regulatory experience.</p></li><li><p>We expect to see individuals have worked on filings, helped with developing regulatory related documents and engaged with external partners and authorities. </p></li><li><p>If you bring good understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices. </p></li><li><p>If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred </p></li><li><p>If you have a high attention to detail; ability to coordinate and prioritize assigned projects according to company goals </p></li><li><p>You bring strong interpersonal skills both written and verbally </p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Analytical Scientist (Automation)]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48399]]></requisitionid>
    <referencenumber><![CDATA[R48399]]></referencenumber>
    <apijobid><![CDATA[r48399]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48399/principal-analytical-scientist-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Analytical Scientist to join our Quality Control team in Rensselaer, NY, supporting our IOPS organization on-site. In this role, you will shape the future of QC analytical testing by designing, developing, and scaling automated assay workflows across advanced laboratory platforms, while mentoring scientists and fostering a culture of technical growth and innovation. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><div></div><p><strong>When & where</strong></p><p><strong>Location: </strong>Rensselaer, NY (Tempel Lane)</p><p><strong>Work Shift: </strong>Monday-Friday 1st shift</p><p><strong>Discover your role</strong>:</p><ul><li>Lead the design, implementation, and optimization of automated assay workflows across modern laboratory platforms, applying deep expertise in mass spectrometry, chromatography, bioassay, electrophoresis, and ELISA.</li><li>Mentor and develop junior and mid-level scientists, building team capability in analytical science and laboratory automation.</li><li>Set priorities, coordinate work, and track progress on analytical and automation initiatives against key milestones.</li><li>Independently design and execute studies to evaluate emerging automation technologies and troubleshoot existing systems with limited supervision.</li><li>Lead complex investigations into automated method performance, supporting verification activities and driving continuous improvement.</li><li>Transfer automated workflows to QC and partner functions by developing training materials, transfer plans, and acceptance criteria.</li><li>Engage cross-functional collaborators and equipment vendors to evaluate new technologies and assess their fit for QC applications.</li><li>Prepare clear scientific reports, automation procedures, and SOPs; communicate findings, risks, and mitigation strategies to management and cross-functional teams.</li><li>Bring hands-on experience programming and optimizing automated liquid handling systems (e.g., Hamilton/Venus, Andrew+/OneLab, or Cellario) and scripting in Python, R, or VBA.</li><li>Apply strong troubleshooting skills across both analytical methods and automated instrumentation to resolve complex technical challenges.</li><li>Make sound, independent decisions and proactively recommend experiments or solutions based on deep expertise in analytical science and automation.</li></ul><p><strong>This role requires</strong>:</p><ul><li>8+ years of industry experience in analytical development, laboratory automation, and QC method lifecycle management (or equivalent combination of education and experience).</li><li>Demonstrated hands-on expertise in automated liquid handling platforms and associated software programming.</li><li>Proficiency in scripting languages (Python, R, or VBA) for data analysis, workflow automation, or system integration.</li><li>Deep knowledge of QC analytical techniques including mass spectrometry, chromatography, electrophoresis, bioassay, or ELISA.</li><li>Proven ability to work independently, design scientifically sound studies from broad objectives, and drive projects to completion.</li><li><em>Level will be determined based on qualifications at the time of offer.</em></li></ul><p><strong>Preferred:</strong></p><ul><li>PhD in Chemistry, Biochemistry, Biology, or a related field.</li><li>Previous experience working in a cGMP or cGLP regulated environment.</li><li>Familiarity with Cellario, Venus (Hamilton), or OneLab (Andrew+) automation platforms.</li><li>Experience developing and executing technology transfer plans across QC or partner functions.</li></ul><p><strong>Physical Requirements: </strong>Ability to work in a laboratory environment, including standing for extended periods and handling laboratory equipment.</p><p><strong>Gowning & Environment: </strong>This role operates in a GMP analytical laboratory. Appropriate gowning and PPE are required in designated areas.</p><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior QA Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49282]]></requisitionid>
    <referencenumber><![CDATA[R49282]]></referencenumber>
    <apijobid><![CDATA[r49282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49282/senior-qa-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior QA Specialist </strong>to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Leading and supporting Quality Assurance activities associated with technology transfer projects, ensuring effective knowledge transfer, risk management, and implementation of quality requirements.</p></li><li><p>Providing Quality Assurance project leadership and oversight for the introduction of new manufacturing technologies, equipment, computerized systems, and digital solutions.</p></li><li><p>Partnering with Manufacturing, Engineering, IT, Validation, Supply Chain, and other cross-functional stakeholders to support projects and initiatives across IOPS.</p></li><li><p>Facilitating project governance, risk assessments, and quality decision-making for technology implementation and digitalization programs.</p></li><li><p>Driving the adoption of data-driven and digital approaches that enhance quality processes, visibility, review efficiency, compliance, and operational performance.</p></li><li><p>Supporting the implementation of systems and technologies including Manufacturing Execution Systems (MES), electronic batch records, automation solutions, data integration platforms, and advanced manufacturing technologies.</p></li><li><p>Finding opportunities for process simplification, automation, and digital innovation while ensuring compliance with applicable regulatory requirements and company procedures.</p></li><li><p>Supporting the development of quality strategies, procedures, training materials, and governance frameworks associated with new technologies and digital initiatives.</p></li><li><p>Monitoring project progress, quality risks, and key performance indicators associated with technology transfer, digitalization, and business transformation programs.</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Excellent project, time, and priority management skills, with the ability to independently manage multiple complex assignments simultaneously, adapt to changing priorities, and drive tasks through to successful completion with minimal supervision.</p></li><li><p>Solid understanding of technology transfer principles and lifecycle management within a GMP-regulated environment.</p></li><li><p>Understanding of computerized system implementation, validation principles, data integrity requirements, and applicable regulations including 21 CFR Part 11, Annex 11, and GxP expectations.</p></li><li><p>Familiarity with digital manufacturing systems and technologies, including MES, electronic batch records, automation platforms, data historians, analytics tools, and system integrations.</p></li><li><p>Knowledge of quality risk management methodologies and their application to new technology implementation and process changes.</p></li><li><p>Ability to work optimally across technical and business functions to deliver complex transformation initiatives.</p></li><li><p>Experience supporting continuous improvement, digital transformation, operational excellence, or innovation programs within a regulated industry.</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>BS/BA in scientific discipline or related field with 5+ years or MS 4+ years of relevant work experience in pharmaceutical or related industry or equivalent combination of education and experience.</p></li><li><p>Specialist: 2 years experience</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNQA</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Publications]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49903]]></requisitionid>
    <referencenumber><![CDATA[R49903]]></referencenumber>
    <apijobid><![CDATA[r49903]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49903/associate-director-publications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Publications to lead the development and execution of aligned dissemination plans across clinical, HEOR/RWE, PKPD, and disease state publications, while collaborating with cross-functional teams, alliance partners, and leading medical and scientific experts to ensure our research reaches the community accurately and on time.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Warren, NJ or Sleepy Hollow, NY<br>• Work model/flexibility: On-site, 4 days/week (relocation benefits available if eligible; hybrid or fully remote not offered)</p><p><strong>Discover your role:</strong><br>• Lead the development of scientific, clinical, and health-outcomes publications, ensuring accuracy, readability, and timely delivery<br>• Shape the scientific narrative and lexicon behind our data, translating statistical findings into clear strategic communication<br>• Guide cross-functional and alliance-wide publication teams through collaborative discussion, independent research, and strategic alignment<br>• Oversee budget, forecasting, and resource allocation, tracking expenditures and flagging issues early<br>• Partner across functions to identify gaps and opportunities that continually evolve our publication strategy<br>• Accurate and timely reporting of post-publications metrics, compliant maintenance of records in the Publication Management Tool (e.g., iEnvision), vendor and budget management. <br>• Manage timelines, quality, and efficiency across publication activities<br>• Track and report post-publication metrics, maintaining compliant, well-documented records<br>• Review and submit manuscripts, abstracts, and presentations in partnership with cross-functional colleagues</p><p><strong>This role requires:</strong><br>• Master's degree in science with 8+ years of related experience, or PhD/PharmD/MD with 5+ years of experience in medical affairs, publications, or scientific communications<br>• Strong publication, writing, and editing skills<br>• Working knowledge of Good Publication Practice (GPP 22), ICMJE, OIG, PhRMA code, Sunshine Act, and copyright/permission guidelines<br>• Experience collaborating within multi-disciplinary teams and alliances with drug development partners<br>• Oncology, ophthalmology or hematology experience preferred<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr QA Validation Specialist]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49428]]></requisitionid>
    <referencenumber><![CDATA[R49428]]></referencenumber>
    <apijobid><![CDATA[r49428]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49428/sr-qa-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>Senior QA Validation Specialist</strong> to join our <strong>Quality Assurance </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick</li><li>Some travel may be required.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Supervising the end-to-end qualification process ensuring each piece of equipment fits for the intended use that contribute to 365 inspection readiness program</li><li>Following, fostering and implementing a quality culture and other company manufacturing standards, policies and procedures</li><li>Scheduling, executing, reviewing and approving qualification activities</li><li>Assessing executed change controls and deviations for impact to the qualified state for conformance to regulations, SOPs, specifications, and other applicable acceptance criteria</li><li>Investigating and troubleshooting problems which occur and determining solutions or recommendations for changes and/or improvements</li><li>Reviewing, editing, and approving deviation notifications, deviation investigations and corrective actions, change controls, SOPs, reports and other documentation</li><li>Coordinating with other departments and outside contractors/vendors to complete validation tasks</li><li>Managing and driving projects</li><li>Supervising, providing direction and assigning work to less experienced full-time employees (e.g. validation specialists) and/or contingent workers to meet goals and deadlines</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Ability to work independently or as part of a team</li><li>Strong knowledge and understanding of the equipment used for QC analysis and operations</li><li>Ability to communicate with transparency</li><li>Meets commitments on scope and on time</li><li>You have strong knowledge of Data Integrity</li><li>Ability to prioritize and balance multiple tasks simultaneously</li><li>You have project management experience</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>To be considered for this opportunity you must have a BS/BA in Engineering, Chemistry or Life Science and requires at least 5 – 8+ years’ proven experience within the field preferred; may substitute relevant experience for education.</li><li>Previous experience as a SME in a highly regulated environment (e.g. pharma, biotech, medical devices) in both internal and external regulatory audits</li><li>Strong background in site change controls, risk management and data integrity initiatives/programs</li><li>You have expert knowledge of EU annex 11 and FDA 21 CFR Part 11</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQA #REGNQA</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Digital & Technology, Portfolio & Financial Management]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50013]]></requisitionid>
    <referencenumber><![CDATA[R50013]]></referencenumber>
    <apijobid><![CDATA[r50013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50013/senior-director-digital-technology-portfolio-financial-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together:</strong></p><p>We are seeking a Senior Director, Portfolio & Financial Management to join our Digital & Technology, Commercial and G&A Leadership Team. In this role you will establish the strategy, governance, and operating model for portfolio and financial management while driving investment prioritization, value realization, and organizational effectiveness across the technology portfolio. The role also serves as Chief of Staff to the SVP of Commercial and G&A Digital & Technology, acting as a trusted advisor responsible for leadership planning, communications, and execution of key strategic initiatives. Working closely with senior technology, finance, and business leaders, this individual will influence major investment decisions and help ensure technology investments deliver measurable business outcomes.</p><p><strong>When and Where:</strong></p><p><em>This role can sit on-site in our Sleepy Hollow, NY, Rensselaer, NY, or Warren, NJ offices a minimum of 4 days/week. Regular attendance for meetings in Sleepy Hollow is required.</em></p><p><strong>Discover Your Role:</strong></p><ul><li>Lead enterprise technology portfolio management across Commercial and G&A D&T, overseeing intake, prioritization, planning, and investment sequencing based on business value, risk, and delivery capacity.</li><li>Own IT financial management, including budgeting, forecasting, cost transparency, chargeback/allocation models, and technology investment value realization.</li><li>Lead value realization across the Digital & Technology portfolio by developing business cases, defining success metrics, and tracking, monitoring, and reporting realized business value against investment objectives.</li><li>Establish and govern enterprise portfolio and financial management standards, including intake processes, stage-gate reviews, investment frameworks, and governance forums.</li><li>Direct annual and ongoing technology planning cycles, aligning budgets, resource capacity, and prioritization with enterprise strategy and performance objectives.</li><li>Build and mature Technology Business Management (TBM) capabilities, leveraging cost and performance data to improve executive decision-making and demonstrate technology value.</li><li>Lead and develop a high-performing team while driving improvements in portfolio predictability, forecast accuracy, resource utilization, cost visibility, and executive reporting.</li><li>Serve as Chief of Staff to the SVP, managing leadership operating rhythms, strategic initiatives, executive communications, stakeholder engagement preparation, standardized executive reporting, AI-enabled portfolio management initiatives, and key vendor relationships.</li></ul><p><strong>This Role Requires:</strong></p><ul><li>BS/BA in Information Systems, Finance, Business, or a related field required; MS or MBA preferred.</li><li>15+ years of progressive leadership across technology portfolio management, PMO, or IT financial management, ideally within a complex, matrixed enterprise.</li><li>Experience with Planview software is a plus.</li><li>Strong command of portfolio and financial management disciplines (platform-agnostic, e.g., PPM/SPM, technology business management, and stage-gate governance frameworks).</li><li>Experience designing and facilitating executive governance forums, such as steering committees and investment review boards, and driving decisions among senior stakeholders.</li><li>Experience partnering directly with a senior executive in a chief-of-staff, business-management, or executive-office capacity, including executive communications and board-level preparation, is strongly preferred.</li><li>Comfort operating with a high degree of autonomy and discretion, exercising sound judgment on behalf of senior leadership. Proven ability to influence senior leaders, drive accountability across functional areas, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Program & Portfolio Operations]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49876]]></requisitionid>
    <referencenumber><![CDATA[R49876]]></referencenumber>
    <apijobid><![CDATA[r49876]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49876/associate-director-program-portfolio-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The <strong>Associate Director,</strong> <strong>Program Budget Delivery Lead</strong> is a content-level leadership role embedded within Program & Portfolio Operations (PPO), created to accelerate the consistent, decision-ready delivery of Program Budgets — one of the most critical Strategic Program Team (SPT) deliverables that translate program vision into an actionable, resourced, and costed plan. Deployed selectively alongside SPTs, this role partners directly with the Development Program Manager (DPM) and Program Finance to co-develop key strategic planning deliverables, bringing the drug-development and financial acumen needed to elevate portfolio-level signal and support confident investment decisions.</p><p>This role builds strong, trusted relationships at all levels of the organization, provides content-level leadership that improves consistency and comparability of SPT deliverables, and facilitates decision-making across Development, Research, Commercial, and Manufacturing. Over time, the role is expected to extend its expertise to future high-judgment SPT deliverables while contributing to longer-term capability building across the organization.</p><br><h3>When & where:</h3><ul><li>Location: Tarrytown NY or Warren, NJ</li><li>Travel percentage: <10%</li></ul><br><h3>Discover your role:</h3><ul><li>Partner directly with DPMs, Program Finance and SPTs to co-develop high-quality, decision-ready Program Budgets, embedding drug-development and financial expertise directly within program teams</li><li>Own the quality and timeliness of Program Budget outputs at the CDU and portfolio level, while the DPM retains overall accountability for Program Budget development</li><li>Accurately forecast resource capacity and costs, and build end-to-end development plans and associated costs from IND through lifecycle management (LCM)</li><li>Enable comparison of programs across the portfolio and support portfolio-level investment and prioritization decisions through consistent, comparable outputs</li><li>Manage timely entry and exit points for initial and subsequent Program Budget updates, working in close, ongoing collaboration with the DPM and Program Finance</li><li>Facilitate decision-making and guide SPTs through the strategic planning process, improving consistency and comparability of deliverables across the organization</li><li>Serve as a near-term force multiplier to expedite implementation of Program Budgets with consistent quality, while contributing to longer-term capability building across Program & Portfolio Operations</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor’s degree and 10+ years industry experience with a minimum of 5+ years in project management experience required. MBA preferred.</li><li>Significant experience in the biotechnology or pharmaceutical industry with a strong understanding of drug development activities from early development through lifecycle management</li><li>Strong financial competence with proven experience building and evaluating program budgets, resource forecasts, and development costs</li><li>Proven strategic planning and portfolio management experience, with the ability to synthesize complex program information into clear, decision-ready outputs</li><li>Proven ability to operate as an embedded content expert and thought partner to program leadership, without formal programmatic authority</li><li>Strong organizational and multitasking abilities, supporting multiple programs and SPTs simultaneously under compressed timelines</li><li>Excellent interpersonal skills with a proven ability to negotiate, influence and work effectively with individuals at all levels of the organization, including senior leadership</li><li>Excellent communication skills (written/verbal), including presenting complex financial and strategic information clearly</li><li>IT proficiency with MS software (including Excel-based financial modeling), project management tools and process mapping tools</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager GD GCP Auditing (UK)]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50349]]></requisitionid>
    <referencenumber><![CDATA[R50349]]></referencenumber>
    <apijobid><![CDATA[r50349]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50349/senior-manager-gd-gcp-auditing-uk/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager GD GCP Auditing </strong>to join our Global Development Quality Assurance team, supporting our global development organization in a remote work model. In this role, you will lead risk-based quality auditing activities and strengthen GCP compliance while collaborating with Global Development teams, external partners, and quality stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: United Kingdom</p><p>Work model: Remote</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead end-to-end GCP audits across internal and external global activities.</p></li><li><p>Schedule, conduct, report, and follow up on routine and directed audits.</p></li><li><p>Develop and execute risk-based audit programs for assigned clinical studies.</p></li><li><p>Identify compliance issues and drive process improvements and standardization.</p></li><li><p>Representing Quality Assurance on complex compliance projects and initiatives.</p></li><li><p>Interpret policies, standards, and regulations to address critical issues.</p></li><li><p>Support regulatory inspections and inspection room activities.</p></li><li><p>You thrive in a dynamic environment and build trusted stakeholder partnerships.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree with 8+ years of relevant industry experience; Master’s degree preferred.</p></li><li><p>At least 5 years of direct Good Clinical Practice audit experience.</p></li><li><p>Expert knowledge of FDA regulations, European Union regulations, ICH guidance, and GCP requirements.</p></li><li><p>Experience conducting audit types including process, site, vendor, and partner audits.</p></li><li><p>Experience with regulatory inspections involving investigator sites, sponsors, or Contract Research Organizations.</p></li><li><p>Ability to independently manage complex GxP compliance issues and high-value priorities.</p></li><li><p>Strong leadership skills with experience interfacing with senior leaders.</p></li><li><p>Excellent project management, stakeholder management, collaboration, and negotiation skills.</p></li><li><p>Strong problem-solving, written, and verbal communication skills.</p></li><li><p>Ability to work independently, take initiative, and perform effectively in ambiguous environments.</p></li><li><p>High attention to detail, accuracy, and organizational awareness.</p></li><li><p>Willingness to travel 30-40% domestically and internationally.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - RGM Chemistry]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49786]]></requisitionid>
    <referencenumber><![CDATA[R49786]]></referencenumber>
    <apijobid><![CDATA[r49786]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49786/senior-associate-scientist-rgm-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron Genetic Medicines, we are driven by a mission to transform the treatment of serious diseases through groundbreaking genetic therapies. Our team is at the forefront of innovation, applying cutting-edge science to improve patient outcomes and redefine the future of medicine.</p><p>We are seeking a highly motivated and detail-oriented Senior Associate Scientist to join the RGM R&D Chemistry team with a focus on oligomer and oligonucleotide synthesis, purification, and analytical characterization. The successful candidate will support the design and execution of solid-phase synthesis workflows, contribute to the preparation of modified RNA-related materials, and generate high-quality analytical data to guide platform research and development. This role offers an opportunity to work at the interface of synthetic chemistry, analytical characterization, and RNA therapeutic innovation while contributing to programs that may meaningfully advance future medicines.</p><p><strong> </strong></p><p><strong>What You'll Do:</strong></p><p>Sr. Associate Scientist focused on oligomer synthesis and characterization:</p><ul><li>Execute solid-phase oligomer and oligonucleotide synthesis using automated synthesis platforms, including preparation of reagents, setup of synthesis cycles, incorporation of standard and chemically modified amidites, and on-bead or post-synthetic modifications as needed.</li><li>Support synthesis of RNA-related constructs of varied lengths, formats, and chemical modification to enable discovery, platform development, and cross-functional program needs.</li><li>Develop, optimize, and troubleshoot synthetic workflows to improve yield, purity, reproducibility, and process efficiency.</li><li>Perform purification of synthesized oligomers using appropriate chromatographic techniques, including size-exclusion, anion-exchange, reverse-phase, and ion-pair reverse-phase methods.</li><li>Characterize purified materials using analytical methods such as LC-MS, HPLC/UPLC, UV-Vis, and other orthogonal techniques to confirm identity, purity, concentration, and product quality.</li><li>Analyze and interpret experimental results, summarize findings clearly, and recommend next steps to support iterative chemistry design and platform advancement.</li><li>Maintain accurate, complete, and timely experimental records in accordance with laboratory standards, safety expectations, and internal documentation practices.</li><li>Support routine operation, maintenance, troubleshooting, and inventory management for key synthesis and analytical instrumentation, reagents, and laboratory supplies.</li><li>Collaborate effectively with chemists, biologists, analytical scientists, and project teams to advance RGM Chemistry objectives and communicate technical progress in team discussions.</li></ul><p><strong>Let's Find Out If We're a Fit:</strong></p><ul><li>B.S. in chemistry, biochemistry, chemical biology, biology, or a related scientific discipline is required; Masters degree is preferred</li><li>Minimum of 5 years with BS / 3 years with MS in relevant undergraduate research, internship, or industry experience required.</li><li>Hands-on experience with solid-phase organic synthesis is preferred, particularly oligonucleotide, peptide, oligomer, or related polymer/biopolymer synthesis workflows.</li><li>Nice to have - familiarity with automated synthesis platforms such as MerMade, OligoSynt, or comparable oligonucleotide/oligomer synthesizers is highly desirable. Experience with purification and analytical characterization methods, including SEC, AEX, RP-HPLC or RPIP-HPLC, and LC-MS.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associates Scientist - Genotyping]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50202]]></requisitionid>
    <referencenumber><![CDATA[R50202]]></referencenumber>
    <apijobid><![CDATA[r50202]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50202/senior-associates-scientist-genotyping/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are looking for a motivated Scientist to join the Genotyping Group at VelociGene. As a Scientist, your primary responsibility will be genotyping complex genetically modified models utilizing state-of-the-art technology platforms to support our R&D and Technology Development efforts for drug discovery.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY United States</p><p><strong>Discover your role:</strong></p><ul><li>Processing biopsy samples for downstream extraction and genotyping analysis.</li><li>Using high-throughput automation for DNA isolation from embryonic stem cells and rodent biopsies.</li><li>Strategically selecting and implementing genotyping methodologies to establish workflow priorities.</li><li>Operating applications that create worklists for qPCR assay retrieval and bulk master mix preparation on Hamilton Liquid Handler.</li><li>Orchestrating multiple processes to begin the aliquoting of qPCR master mixes.</li><li>Setting up complex qPCR reactions across multiple Beckman i7 Liquid Handlers.</li><li>Initiating qPCR using the state-of-the-art customized cycling platform.</li><li>Collecting, organizing, and analyzing raw data files with custom data analysis tools.</li><li>Reporting genotyping results through LIMS and initiating discussions with collaborators if needed.</li><li>Performing conventional PCR or Southern Blotting Techniques as a genotyping alternative to qPCR.</li><li>Maintaining comprehensive sample management systems and assay inventory effectively.</li></ul><p><strong>This role requires:</strong></p><ul><li>Can multi-task assignments and operate effectively in the face of ambiguity and change.</li><li>Bachelor’s or Master’s degree in biology, molecular biology, or related biological sciences with a minimum of 3 years of experience.</li><li>Are highly motivated with a genuine curiosity for rodent genetics.</li><li>Maintain scientific rigor and familiarity with best practices.</li><li>Leverage automation to drive scientific advancement.</li><li>Drive innovation by developing novel approaches and optimizing existing platforms to increase efficiency and data quality.</li><li>Preferred: Prior experience in a screening laboratory and/or automation laboratory.</li><li>Preferred: Knowledge of coding languages (R, Python, Shiny web framework).</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Customer Insights - Oncology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50373]]></requisitionid>
    <referencenumber><![CDATA[R50373]]></referencenumber>
    <apijobid><![CDATA[r50373]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50373/associate-director-customer-insights-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director</strong> to join our <strong>Customer Insights Oncology</strong> team. The Associate Director, Customer Insights - Oncology, will report to the Senior Director, Insights & Analytics (I&A), Oncology, within the Commercial Intelligence & Operations (CI&O) department. This highly visible role will lead Customer Insights activities for Regeneron's US Oncology team with focus on solid tumors and lung cancer. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>4 days per week on site</p></li><li><p>10% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p>The role will partner with and serve as a strategic advisor for the Oncology Commercial Business Unit (CBU) stakeholders to inform and shape business decisions, specifically focused on solid tumors and lung cancer. The individual will require a strong understanding of how and when to use specific market research methodologies to drive a high-resolution and up-to-date market understanding, to inform commercial strategy and brand planning.</p><p><em>Lead</em></p><ul><li><p>Lead market research plans and individual projects, that generate meaningful insights, inform and shape business decisions and strategy for Oncology, including US HCP/patient initiatives</p></li><li><p>In collaboration with Oncology CBU team members and the Senior Director, I&A, lead market research vendors, budgets, plans, insights to maximize Insights and Analytics (I&A) investments that align with business priorities and help drive brand decisions and growth</p></li></ul><p><em>Develop</em></p><ul><li><p>Develop innovative Customer Insights plans that align with strategic imperatives for Oncology, demonstrating an ability to translate insights gaps into key business questions and timely inform the optimal research approach</p></li><li><p>Proactively recommend studies that inform critical brand decision-points and address brand opportunities and challenges; proactively champion implementation of innovative/AI driven primary market research approach and analysis in a compliant manner</p></li></ul><p><em>Partnership and collaboration</em></p><ul><li><p>Develop and maintain a mutually beneficial partnership with stakeholders across Oncology CBU, CI&O and Global teams; strike a balance between project rigor, timelines and ability to influence decisions</p></li><li><p>Manage market research suppliers to design, scope, execute and analyze research results and develop business implications</p></li><li><p>Collaborate with the Oncology CBU, CI&O colleagues and other stakeholders, to influence data capabilities; stay informed and share market landscape and competitive outlook</p></li><li><p>Work closely with Advanced Analytics and global partners as needed, to effectively measure brand performance using various data sources; address related questions from senior leadership</p></li></ul><p><em>Execute</em></p><ul><li><p>Demonstrate proficiency and drive continuous improvement in primary research designs and analysis (qualitative and quantitative), and develop customized innovative research solutions to address complex strategic issues across HCPs, patients, accounts etc.</p></li><li><p>Manage all primary research in accordance with internal compliance policies and best practices, with agreed upon preferred vendors</p></li><li><p>Recommend reasonable, evidence-driven business-building ideas, while encouraging the use of customer and market insights to inform strategic business decisions</p></li><li><p>Establish, manage and share outcomes from plans that measure and track performance against critical success factors</p></li><li><p>Synthesize insights and analyses from a variety of sources (marketing research, competitive intelligence, secondary data) to inform strategic choices and decisions; develop and present findings to business teams and senior management</p></li><li><p>Consolidate and integrate a variety of data and information into actionable and differentiating insights that identify business opportunities/strategies, keeping in mind portfolio implications</p></li><li><p>Create compelling presentations that communicate complex insights in a manner that is easily understood and actioned upon</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BA/BS required; MBA/MS preferred</p></li><li><p>10+ years of pharmaceutical/biotech commercial experience (or 7+ years for MBA/MS), in roles of increasing accountability; prior experience with leading brands preferred</p></li><li><p>Experience in biologic drugs and oncology (required); experience in lung cancer market preferred</p></li><li><p>Functional expertise in HCP/patient insights, primary research methods; with experience in analog forecast development, business analytics, competitive intelligence highly preferred</p></li><li><p>Demonstrated success in using market research to inform and influence important business decisions</p></li><li><p>Expertise in survey design, data analysis, managing suppliers, presenting results, and recommending courses of action supported by research findings</p></li><li><p>Strong experience in establishing strong partnership with brand teams, cross-functional communication and consensus building</p></li><li><p>Strong technical understanding of marketing research methodologies and knowledge across multiple research tools</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment related to product development and commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Demonstrated flexibility, leadership potential, influence and emotional intelligence in working across stakeholders and cross-functional teams</p></li><li><p>Experience managing multiple projects concurrently against stringent deadlines in a fast-paced, timeline-driven environment; strong project management experience required</p></li><li><p>Strong analytical skills and strategic thinking ability</p></li><li><p>Concise and impactful written and verbal communication skills</p></li><li><p>Expertise in data visualization and data storytelling of market research findings</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Precision Medicine (Clinical Diagnostics)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49933]]></requisitionid>
    <referencenumber><![CDATA[R49933]]></referencenumber>
    <apijobid><![CDATA[r49933]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49933/associate-director-precision-medicine-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution. This role owns CDx programs from early biomarker feasibility through clinical validation, regulatory submission, and launch — translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions. You'll work at the interface of biomarker science, clinical development, regulatory, and external In Vitro Diagnostic (IVD) partners to ensure diagnostics keep pace with therapeutic milestones. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Dublin, Ireland (multiple locations are being considered for this role.)</p></li><li><p>Work model/flexibility: 3 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles (TPPs), defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays). </p></li><li><p>Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics.</p></li><li><p>Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints. </p></li><li><p>Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. </p></li><li><p>Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. </p></li><li><p>Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment. </p></li><li><p>Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). </p></li><li><p>Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. </p></li><li><p>Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. </p></li><li><p>8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. </p></li><li><p>Track record translating biomarker science into validated assays supporting drug approvals. </p></li><li><p>Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). </p></li><li><p>Ability to translate complex scientific and clinical data for cross-functional and executive audiences. </p></li><li><p>Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. </p></li></ul><p>#PrecisionMedicineCDX</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €165,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Manhattan West]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50353]]></requisitionid>
    <referencenumber><![CDATA[R50353]]></referencenumber>
    <apijobid><![CDATA[r50353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50353/medical-specialist-i-dermatology-manhattan-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role</p></li><li><p>Location: Manhattan West</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus</p></li><li><p>A 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</p></li><li><p>Demonstrated success and consistent sales performance in complex markets across diverse customer segments</p></li><li><p>This role requires the ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager (Dermatology) - Charlotte, NC]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50474]]></requisitionid>
    <referencenumber><![CDATA[R50474]]></referencenumber>
    <apijobid><![CDATA[r50474]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50474/field-reimbursement-manager-dermatology-charlotte-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - North Carolina]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><h3>When & where:</h3><ul><li><p>Greater Charlotte, NC area</p></li><li><p>In the field 4 days a week</p></li></ul><h3>Discover your role:</h3><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><h3>This role requires:</h3><ul><li><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.</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 required.</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><li><p>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</p></li><li><p>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist, Cardiac Vascular - In Vivo]]></title>
    <date><![CDATA[Tue, 15 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49817]]></requisitionid>
    <referencenumber><![CDATA[R49817]]></referencenumber>
    <apijobid><![CDATA[r49817]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49817/scientist-cardiac-vascular-in-vivo/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Cardiac and Vascular Rodent Surgeon to join our cardiovascular research team, serving as a key contributor to the design and execution of longitudinal in-vivo rodent studies supporting our cardiovascular disease programs. In this role, you will perform advanced surgical models of cardiac disease, conduct precision dosing and physiological monitoring, and generate high-quality functional and molecular data to support target validation and therapeutic development.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Perform surgical models of cardiac and vascular disease in mice and rats, including transverse aortic constriction (TAC), myocardial infarction (MI), and renal/kidney models (RKM)</p></li><li><p>Administer test articles via multiple routes (IV, SC, IM) or osmotic minipump implantation with precision and consistency across longitudinal study timelines</p></li><li><p>Implant and manage telemetry devices for continuous blood pressure and ECG monitoring in conscious, freely moving rodents</p></li><li><p>Conduct invasive hemodynamic assessments using PV-loop methodology to quantify cardiac function</p></li><li><p>Perform ex-vivo tissue collection and processing, including cardiac dissociation via Langendorff perfusion</p></li><li><p>Manage end-to-end in-vivo study logistics, including animal health monitoring, surgical scheduling, and post-operative care</p></li><li><p>Analyze and interpret physiological, hemodynamic, and functional data using PRISM, PONEMAH, and other relevant analysis software</p></li><li><p>Generate high-quality figures, reports, and data summaries for internal presentations, regulatory packages, and peer-reviewed publications</p></li><li><p>Maintain rigorous records of surgical procedures, animal welfare documentation, and study protocols in compliance with institutional and regulatory standards</p></li><li><p>Collaborate closely with study directors, therapeutic area scientists, and cross-functional teams to align surgical and analytical approaches with program goals</p></li><li><p>Proactively flag capacity constraints, scheduling conflicts, or technical challenges to stakeholders</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS with 10+ years, MS with 6+ years with relevant experience in a related field (e.g., Physiology, Biomedical Sciences, Veterinary Science, or similar)</p></li><li><p>Demonstrated hands-on expertise in rodent cardiac and vascular surgical models (TAC, MI, RKM)</p></li><li><p>Proficiency in rodent dosing techniques (IV, SC, IM) and telemetry implantation for blood pressure and ECG monitoring</p></li><li><p>Experience with invasive hemodynamic measurement techniques, including PV-loop analysis</p></li><li><p>Hands-on experience with Langendorff perfusion and cardiac tissue dissociation</p></li><li><p>Proficiency with data analysis software such as PRISM and PONEMAH</p></li><li><p>Strong understanding of rodent anatomy, physiology, and survival surgery best practices</p></li><li><p>Excellent organizational skills, with the ability to manage multiple longitudinal studies and competing priorities simultaneously</p></li><li><p>Strong attention to detail and commitment to scientific rigor and animal welfare standards</p></li><li><p>Excellent oral and written communication skills</p></li><li><p>Preferred: experience with additional cardiovascular functional assessment techniques or prior work in a GLP/regulated research environment</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 16 Sep 2026 11:56:14 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Visual Inspection Engineer]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50560]]></requisitionid>
    <referencenumber><![CDATA[R50560]]></referencenumber>
    <apijobid><![CDATA[r50560]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50560/principal-visual-inspection-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Visual Inspection Engineer to join our Internal Fill/Finish Manufacturing team. In this role, the Principal Visual Inspection Engineer specializing in visual inspection (fully automated); leads equipment selection and process development; establishes and optimizes the visual inspection program and product-specific recipes; develops KNAPP/test sets and training/qualification content; provides hands-on support during tech transfer, cGMP start-up, and routine manufacturing; and drives validation and operator training for assigned equipment and processes.</p><h3>When & where:</h3><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: Monday-Friday, 8:00am-4:30pm</p></li><li><p>Travel: 10% international & domestic</p></li></ul><br><h3>Discover your role:</h3><ul><li><p>Acts as a technical SME for assigned visual inspection equipment and processes</p></li><li><p>Responsible for recipe development, vision system tuning, and life cycle management of semi-automated and automated processes and associated vision systems</p></li><li><p>Supports Project Engineering, QA Validation, and Process Validation in new equipment startup, commissioning, and qualification/validation activities</p></li><li><p>Supports technology transfer/new product introduction and the development or revision of defect classifications and manuals</p></li><li><p>Partners cross functionally to implement or revise policies and procedures for the visual inspection program</p></li><li><p>Gathers, trends, and analyzes process-generated data and implements continual improvements</p></li></ul><br><h3>This role requires:</h3><ul><li><p>BS/BA in Life Sciences, Engineering or related field; or equivalent combination of education and experience</p></li><li><p>Principal VI Engineer: 8+ years of relevant experience</p></li><li><p>Staff VI Engineer: 10+ years of relevant experience</p></li><li><p>Level will be determined based on experience</p></li><li><p>Experience in pharmaceutical automated visual inspection and camera tuning</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Life Cycle Management Lead - Oncology]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49562]]></requisitionid>
    <referencenumber><![CDATA[R49562]]></referencenumber>
    <apijobid><![CDATA[r49562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49562/senior-director-life-cycle-management-lead-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Senior Director, Global Skin Cancer Life Cycle Management (LCM) Lead is a member of the Oncology Business Unit at Regeneron, responsible for leading life cycle management strategy and planning for all in-line oncology assets within the Skin Cancer tumor area. This leader is a highly strategic, business-focused expert who assesses opportunities and threats for brands in a fast-paced, complex market.</p><p>This role reports directly to the Executive Director of Global Skin Cancer Marketing. The LCM Lead will collaborate closely with cross-functional teams and support the overall strategic goals of the portfolio, playing a critical role in Commercial/Clinical cross-functional forums.</p><p>This individual needs to have strong communication and collaboration skills and will be in involved with leading activities across indications. Based on business needs, support of programming and process across total brand indications is required, which includes managing timelines and eliciting content from the Lung franchise for overall deliverable completion. Examples of select content includes summary reports and planning documents that are applicable across brand indications which are evaluated on a case-by-case basis.</p><p><strong>When & where:</strong></p><ul><li>On site in Sleepy Hollow, NY for 4 days a week</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Facilitate development of and evolution of the global life cycle management strategy (e.g., indication sequencing, geographic expansion) for all in-line oncology assets with Skin Cancer indications to maintain competitive advantage.</li><li>Shape asset plans within Skin Cancer indications in coordination with the Executive Director of Global Skin Cancer Marketing, Regulatory, Clinical, Competitive Intelligence (CI), and other cross-functional partners; partner with US and international marketers to inform and align on the LCM plan.</li><li>Maintain up-to-date tumor landscape outlooks for our portfolio and potential competitors in relevant current and future areas, working with Clinical, CI, and Commercial Insights.</li><li>Share current CI with Global, US, and international marketers and country teams; develop global action plans for competitive threats to be implemented at the country level; develop and deliver related content (e.g., action memos on competitor approvals).</li><li>Support the Executive Director of Global Skin Cancer Marketing in developing the Commercial perspective for Skin Cancer assets in decision-making forums (e.g., Commercial/Clinical cross-functional committees) and cross-tumor planning meetings; help prepare for these meetings and support follow-up actions.</li><li>Lead the Marketing team’s efforts to plan cross-functionally for new indication launches from early development through pre-launch readiness, following established internal processes including identifying working groups cross functionally and across global and country/international teams to facilitate plans and decisions</li><li>Inform Medical Affairs and related teams of key data needs and future development plans the organization will support.</li><li>Develop business analyses/cases for Business Development purposes, for assessing indication trials, and for senior management reviews.</li><li>Serve as the key Marketing point of contact for the Business Development team on Skin Cancer strategy.</li><li>Contribute to labeling review team preparations, providing commercial insights to inform labeling decisions.</li><li>Analyze customer insights, monitor brand performance and competitive dynamics, and translate findings into marketing strategy to address customer needs.</li><li>Leverage customer feedback through formal and informal channels (e.g., advisory boards, KOL meetings at congresses, market research, field intelligence) to shape strategy and competitive differentiation.</li><li>Serve as a member of the cross-functional team that develops and delivers the annual US/Global brand plan, including brand strategy, tactical plans, and budget.</li></ul><p><strong>Operational</strong></p><ul><li>Work closely with Legal and Compliance to ensure all activities meet compliance standards.</li><li>Lead launch-readiness efforts, including cross-organizational planning forum preparation; oversee decision-point team inputs across life cycle stages, track performance metrics, and mobilize functional teams to optimize brand impact.</li><li>Coordinate execution of life cycle levers (e.g., label expansion, access challenges, new formulations, delivery devices).</li><li>Engage regularly with Global Oncology Marketing Leadership, International teams, Clinical Development, Regulatory, Medical Affairs, Market Access, and Sales to align life cycle strategies across functions.</li><li>Provide regular updates on LCM strategy to senior leadership.</li><li>Deliver regular updates to tumor landscape outlook documents and the product strategy guide to align country teams with the long-term LCM strategy.</li><li>Collaborate as needed on globally developed promotional materials for country handoff, especially those aligned to landscape or competitive preparation.</li></ul><br><p><strong>Budgeting</strong></p><ul><li>Work cross-functionally to create, manage, and track US and global budgets within Skin Cancer, ensuring adherence to approved budgets and phasing.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; PhD, PharmD, or MBA preferred.</li><li>14+ years of progressive experience in pharmaceutical marketing, brand strategy, and execution. Oncology experience preferred; Skin cancer experience is a plus.</li><li>Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate.</li><li>Strong scientific acumen with deep knowledge of oncology; ability to understand, partner with, and provide commercial input to all functions within the project team.</li><li>Expertise in early- and late-stage life cycle management for pharmaceutical products, including in competitive environments.</li><li>Previous in-line product and/or indication launch experience required.</li><li>Experience with global, US, or country marketing and pre-approval planning of oncology and/or buy-and-bill drugs required.</li><li>Proven track record of market analysis and identifying growth opportunities on a global scale.</li><li>Ability to synthesize inputs from external and internal collaborators such as HCPs, field teams, country marketers, and market access colleagues.</li><li>Effective written and oral communication; experience delivering complex messages to diverse internal and external collaborators with a track record of influential presentations.</li><li>Ability to communicate and act promptly; demonstrated initiative and creativity; and the agility to work effectively in complex, rapidly changing environments.</li><li>Strong project and process management skills, with the ability to manage multiple tasks and effectively prioritize.</li><li>Proven standout colleague with the ability to navigate cross-functionally.</li><li>Strong analytical skills, both quantitative and qualitative.</li><li>Demonstrated track record of commercial success in roles with progressive responsibilities.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Employee Technology & Digital Workplace]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50605]]></requisitionid>
    <referencenumber><![CDATA[R50605]]></referencenumber>
    <apijobid><![CDATA[r50605]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50605/executive-director-employee-technology-digital-workplace/]]></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 role leads Employee Technology & Digital Workplace, a significant function within Digital and Technology, directing the Service Desk and ServiceNow ITSM platform, employee lifecycle technology (onboarding/offboarding), digital workplace engineering, field/deskside support, and M365 and collaboration platform delivery through subordinate management. The Executive Director determines the organizational structure and operational direction for the function and participates with senior management in developing the strategic plans and objectives that govern it, ensuring the function's direction remains tied to company-wide performance and responds effectively to Regeneron's constantly changing business needs. </p><p>The Executive Director brings in-depth knowledge of the functional area, Regeneron's business strategies, and the company's goals to reposition employee-facing IT as a modern, consumer-grade digital experience. Decisions on strategy, investment, and operating model in this function have a measurable, long-term effect on employee productivity, cost-to-serve, and the company's ability to attract and retain talent — the Executive Director is expected to bring strength and clarity to the function during periods of growth or major change, and to lead effectively even where direction is ambiguous. </p><p>This is the next iteration of IT service delivery at Regeneron — evolving the function from a ticket- and SLA-driven operation into a proactive, experience-led organization measured on employee sentiment, self-service adoption, and time-to-resolution, not just uptime. The Executive Director partners closely with Enterprise Architecture on technical standards and platform decisions, and with IT Strategy & Transformation, which sponsors chartered modernization initiatives into this tower without assuming direct reporting authority. </p><p><strong>Where and When</strong></p><p>This is an on-site position 4 days/week, primarily based at our Sleepy Hollow, NY or Warren, NJ office. If eligible, we can offer relocation benefits; we cannot offer a fully remote option.</p><p><strong>What You'll Lead</strong> </p><p><strong>Employee Technology Strategy & Digital Experience Vision</strong> </p><ul><li>Participate with senior IT and business leadership in developing the strategic plans and objectives for employee technology, ensuring the function's direction stays tied to company-wide performance and adapts to constantly changing business needs. </li></ul><ul><li>Define and own the vision, roadmap, and operating model for Employee Technology & Digital Workplace, positioning IT as a modern, consumer-grade digital experience rather than a traditional service organization. </li></ul><ul><li>Translate employee and business feedback into a prioritized modernization roadmap across service desk, ITSM, endpoint, and lifecycle technology. </li></ul><ul><li>Champion a "digital-first, self-service-first" philosophy, shifting volume away from live support and toward intuitive, automated, and AI-enabled experiences. </li></ul><ul><li>Partner with IT Strategy & Transformation to align sponsored modernization initiatives (e.g., virtual agent/AI deflection, unified employee portal) with this tower's operational roadmap and capacity. </li></ul><p><strong>Service Desk & ITSM Operations (ServiceNow)</strong> </p><ul><li>Own end-to-end Service Desk operations, including tiered support, major incident management, and escalation processes across a global, follow-the-sun model. </li></ul><ul><li>Drive continuous modernization of the ServiceNow platform — intelligent routing, virtual agent/chatbot deflection, knowledge management, and workflow automation — to reduce ticket volume and resolution time. </li></ul><ul><li>Establish and monitor experience-led metrics (CSAT, first-contact resolution, deflection rate, mean time to resolve) as the primary measures of success, alongside traditional SLAs. </li></ul><ul><li>Ensure ticketing, request, and knowledge processes are simple, consistent, and easy for employees to navigate regardless of how they choose to engage (portal, chat, phone, walk-up). </li></ul><ul><li>Own GRC, vendor risk management (VRM), and policy exception workflows on the ServiceNow platform, ensuring timely processing and audit-ready records. </li></ul><ul><li>Own portal and content management for the ServiceNow platform, ensuring employees can easily find and act on the right services and policies. </li></ul><p><strong>Employee Lifecycle Technology (Onboarding & Offboarding)</strong> </p><ul><li>Own the technology experience for onboarding, transfers, and offboarding, ensuring new hires are productive on day one and departures are secure and frictionless. </li></ul><ul><li>Modernize onboarding/offboarding into an automated, orchestrated workflow spanning identity, access provisioning, equipment, and collaboration tools — eliminating manual handoffs across HR, IT, and Security. </li></ul><ul><li>Partner with HR, Security, and Facilities to design a seamless, employee-centric lifecycle journey, with clear accountability for every step and status transparent to the employee and their manager. </li></ul><ul><li>Continuously reduce time-to-productivity for new hires and time-to-deprovision for departures, tracking both as core experience and risk metrics. </li></ul><p><strong>Digital Workplace Engineering & Endpoint Experience</strong> </p><ul><li>Own engineering and lifecycle management for employee-facing technology: endpoints, mobility, unified endpoint management (UEM), collaboration tools, and meeting room/AV technology. </li></ul><ul><li>Drive modernization of the digital workplace — proactive device health monitoring, zero-touch provisioning, self-healing endpoints, and simplified software deployment — to minimize disruption to employees. </li></ul><ul><li>Ensure collaboration and meeting technologies (video, conferencing, messaging) provide a consistently excellent experience across office, lab, and hybrid work settings. </li></ul><ul><li>Partner with Enterprise Architecture and Security to ensure digital workplace standards remain secure, scalable, and aligned to enterprise architecture principles. </li></ul><p><strong>M365 & Collaboration Platform Delivery</strong> </p><ul><li>Own service delivery for the M365 platform — Teams, SharePoint, Exchange, OneDrive, and Power Automate — including platform guardrails, governance, and adoption. </li></ul><ul><li>Own voice and unified communications service delivery, ensuring reliable, modern calling and conferencing capability across the enterprise. </li></ul><ul><li>Drive continuous improvement of collaboration tooling to reduce friction and support hybrid and global ways of working. </li></ul><ul><li>Partner with Enterprise Architecture on platform roadmap decisions and with Security on data governance within M365 workloads. </li></ul><p><strong>Field & Deskside Support Operations</strong> </p><ul><li>Own field and deskside support across all Regeneron sites, ensuring consistent, high-quality in-person support where self-service and remote resolution aren't sufficient. </li></ul><ul><li>Right-size the deskside support model as digital self-service and remote resolution capabilities mature, reallocating capacity toward higher-value, in-person needs (labs, executive support, events). </li></ul><ul><li>Ensure support models scale appropriately across site types (corporate, R&D/lab, manufacturing) with services tailored to how each site's population actually works. </li></ul><ul><li>Own end-to-end lifecycle management of end-user assets — procurement coordination, deployment, tracking, refresh cycles, and secure disposal/decommissioning. </li></ul><ul><li>Maintain accurate asset inventory and compliance reporting to support audit, cost management, and security requirements. </li></ul><p><strong>Experience Measurement & Continuous Improvement</strong> </p><ul><li>Establish a consistent employee experience measurement framework (CSAT, NPS, effort scores) across every touchpoint in this tower, replacing purely operational SLA reporting. </li></ul><ul><li>Run a continuous improvement cadence — mining ticket, sentiment, and usage data to identify friction points and prioritize fixes before they become recurring complaints. </li></ul><ul><li>Report employee technology experience trends and improvement outcomes to executive stakeholders, connecting operational data to business and workforce impact. </li></ul><p><strong>Vendor & Platform Management</strong> </p><ul><li>Own vendor relationships and contracts for service desk, ITSM, endpoint, and digital workplace tooling, ensuring value, performance, and roadmap alignment. </li></ul><ul><li>Establish a vendor governance cadence — performance scorecards, quarterly business reviews, and value/ROI tracking — holding vendors accountable to continuous improvement commitments rather than static contract terms. </li></ul><ul><li>Partner with Finance and Procurement to manage the cost-to-serve for employee technology, balancing experience improvements against operating budget discipline. </li></ul><ul><li>Evaluate emerging digital workplace and AI-enabled support technologies, building the business case for adoption where they meaningfully improve employee experience or reduce cost-to-serve. </li></ul><p><strong>People Leadership, Mentoring & Team Culture</strong> </p><ul><li>Determine the organizational structure and operational direction for the function, directing critical work through subordinate managers and senior leaders. </li></ul><ul><li>Build, lead, and develop a high-performing, globally distributed organization across service desk, lifecycle technology, digital workplace engineering, and field support. </li></ul><ul><li>Mentor and coach people leaders across the organization, investing in career growth, succession planning, and bench strength. </li></ul><ul><li>Model and reinforce a customer-obsessed, continuous-improvement culture, holding the team accountable to employee experience outcomes, not just ticket throughput. </li></ul><ul><li>Champion development and team culture within the function, fostering collaboration across a global, follow-the-sun operating model. </li></ul><p><strong>Key Working Relationships</strong> </p><p>This role is viewed across Regeneron as a role model for employee-centric technology delivery and is regularly sought out by leaders at all levels for advice on employee technology matters. Because much of this role's influence runs through governance and partnership rather than direct authority over every function it touches, it also serves as the principal spokesperson for employee technology and digital workplace matters on highly significant issues, and is expected to negotiate difficult matters with senior management and functional heads, both internally and externally. </p><p><strong>What You Bring</strong> </p><ul><li>Bachelor's degree in Information Technology, Business, Engineering, or a related field is required. A master's degree or MBA is preferred. </li></ul><ul><li>17+ years of progressive experience in IT service delivery, end-user computing, digital workplace, or IT operations leadership roles. </li></ul><ul><li>Deep expertise in ITIL or equivalent service management frameworks, and hands-on experience modernizing an ITSM platform (ServiceNow strongly preferred). </li></ul><ul><li>Proven experience redesigning employee lifecycle technology (onboarding/offboarding) into an automated, cross-functional workflow spanning IT, HR, and Security. </li></ul><ul><li>Strong grounding in digital workplace and end-user computing technologies — unified endpoint management, collaboration platforms, mobility, and AV/conferencing. </li></ul><ul><li>Track record of building and using experience metrics (CSAT, NPS, deflection rate, first-contact resolution) to drive continuous improvement, not just SLA compliance. </li></ul><ul><li>Experience leveraging automation, self-service, and AI/virtual agent technologies to reduce support volume and improve employee experience. </li></ul><ul><li>Proven ability to build, scale, and lead large, globally distributed service organizations, including hiring, developing, and retaining talent across a follow-the-sun model. </li></ul><ul><li>Experience operating in a matrixed, governance-driven environment — partnering with peers in Enterprise Architecture and IT Strategy & Transformation without direct authority over their teams. </li></ul><ul><li>Strong vendor and contract management experience, including negotiating and managing platform and outsourced support relationships, with a track record of driving ongoing vendor performance and value through structured governance (scorecards, business reviews). </li></ul><ul><li>Sound business and financial acumen, with experience managing cost-to-serve and building business cases for employee technology investment. </li></ul><ul><li>Proven ability to bring strength and clarity to a business during periods of growth or major change, exercising sound judgment and taking a positive leadership role amid ambiguity or limited direction. </li></ul><ul><li>Executive presence and the ability to communicate operational performance and improvement priorities clearly to senior business and technology leaders, and to negotiate difficult matters with senior management and functional heads internally and externally. </li></ul><ul><li>Strong collaboration skills across global, cross-functional, and cross-cultural stakeholder groups. </li></ul><ul><li>A relentless passion for improvement — constantly enhancing the end-user experience and continuously leveraging innovation to raise the bar rather than settling for steady-state. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Director Pharmacoepidemiology]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50776]]></requisitionid>
    <referencenumber><![CDATA[R50776]]></referencenumber>
    <apijobid><![CDATA[r50776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50776/temp-director-pharmacoepidemiology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>Within Regeneron, there are a growing number of diverse collaborations and alliances with external entities. This individual will help to build productive external partnerships across several key areas. The Director will support the identification, execution and management of overarching strategic relationships with various organizations and institutions to support the Global Clinical Development organization’s efforts to more effectively develop Regeneron’s product candidates and advance the company’s broader R&D objectives. The individual will function as a strategic and critical thinker, identifying and developing key external relationships and coordinating across a matrix of teams with the purposes of finding opportunities and streamlining external partnership initiation and maintenance. They will be focused on further building an internal capability on behalf of Regeneron that is highly-regarded by external partners and internal leaders. The individual will partner closely with other internal leaders embedded in the company who work with external partners to ensure collaboration, continuity and alignment. This role will be highly collaborative with other functions and will require thoughtful and inclusive leadership. This role will be tasked with not only identifying strategic partnerships, but facilitating the drafting and execution of contracts, as well as remaining connected to the overarching relationships, while helping to facilitate the components that live in specific areas throughout the life of the agreements.</p><p><br><br><strong>Discover your role:</strong></p><p>The Pharmacoepidemiologist with qualifications commensurate with the Director level will be accountable for development and implementation of pharmacoepidemiology strategy in the designated therapeutic area (TA), leading cross-functional project teams and epidemiology activities such as regulatory agency-required epidemiologic studies and generation of epidemiology data to support clinical development and regulatory filings and approval, in accordance with global regulations and Regeneron SOPs and working practices. The Pharmacoepidemiologist will serve as an in-house subject matter expert in epidemiology to other departments. The candidate should be knowledgeable in the latest epidemiologic methods and resources to be able to be responsive within cross functional teams and to influence decision making where needed.</p><p>Under supervision of the Pharmacoepidemiology Therapeutic Area (TA) lead for General Medicines:</p><ul><li>Responsible for pharmacoepidemiology strategy generation of real-world evidence (RWE), and conduct of regulatory agency required epidemiologic studies for post-marketing commitments (e.g., PASS, PAES, PMR, DUS, effectiveness of REMS and RMMs) in support of clinical development, regulatory filings, and post-marketing requirements</li></ul><ul><li>As a subject matter expert, contribute to other pharmacoepidemiology activities, including but not limited to: (Development) Risk Management Plans; Benefit-Risk analyses; signal management; responses to regulatory agency queries; regulatory filings</li><li>Working closely with Global Patient Safety (GPS) Leads, Safety Scientists, Clinical Scientists, Regulatory Affairs and other functions, provide timely epidemiological and risk management strategy and support to project and product teams of TAs including design, implementation and data analysis of epidemiological studies, review of study proposal from internal and external sources, and database activities such as exploring external electronic, patient-level database(s) (administrative claims/EMR/surveys/registries etc) to evaluate safety/benefit questions, mortality and morbidities/comorbidities, and other appropriate epidemiologic data in support of clinical development and regulatory filings</li><li>Represent Pharmacoepidemiology on cross-functional teams, including Safety Monitoring Teams (SMT), Clinical Study Teams (including with external partners), Regeneron Safety Oversight Committee, and Independent Data Monitoring Committees</li><li>Proactively lead non-compound specific pharmacoepidemiology activities (ex. literature review and database queries in support of regulatory filling)</li></ul><ul><li>Actively drive and participate in the development and maintenance of relevant SOPs and Working Instructions</li><li>Actively drive and participate in process improvement activities and strategic initiatives GPS and across Regeneron, as appropriate</li><li>Manage contractors, and external vendors, as appropriate.</li><li>Develop and maintain professional relationships and collaborations with external experts and opinion leaders to ensure high quality evidence generation</li></ul><p><br><br></p><p><strong>This role requires:</strong></p><ul><li>A results-oriented, collaborative style.</li><li>Ability to build consensus with leaders and colleagues to gain support for initiatives.</li><li>Proven track record of developing and maintaining relationships with partners at all levels of the organization.</li><li>Previous experience in and deep understanding of the drug development process.</li><li>Ability to manage and prioritize multiple tasks and projects with a sense of urgency and to navigate within a matrix organization.</li><li>Experienced in planning and execution; thinks strategically and executes tactically in order to deliver positive results for the business.</li><li>Strong business and financial management acumen.</li><li>Demonstrated resiliency; able and willing to explore different paths to achieve an outcome. Consistently demonstrates good judgment. Takes initiative to bring forward new ideas to improve processes and programs.</li><li>Outstanding verbal and written communication and presentation skills; ability to communicate accurately and concisely</li></ul><br><p>​<strong>Education:</strong> Minimum of a Bachelors degree and 8+ years of relevant industry related experience in Biotech/Pharma </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Applied AI, Advanced Informatics]]></title>
    <date><![CDATA[Thu, 24 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48861]]></requisitionid>
    <referencenumber><![CDATA[R48861]]></referencenumber>
    <apijobid><![CDATA[r48861]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48861/manager-applied-ai-advanced-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Applied AI to join our Advanced Informatics team, supporting health data systems and analytical pipelines across the organization. In this role, you will design and validate applied AI/ML solutions against complex health data and clinical ground truth, while collaborating with senior applied AI leaders, clinical informaticists, data engineers, and production ML engineers to build reusable analytical capabilities the broader informatics team depends on.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Tarrytown, NY, Armonk, NY, or Warren, NJ</p><p><strong>Discover your role:</strong><br>• Frame clinical and business informatics challenges into well-scoped AI/ML problem statements with clear success criteria<br>• Design and build ML pipelines — data ingestion, feature engineering, training, and evaluation — alongside production engineering<br>• Run experiments, benchmarks, and ablation studies to validate model performance and guide modeling decisions<br>• Partner across clinical informatics, data engineering, and ML engineering to bring models into real informatics workflows<br>• Track advances in foundation models, LLMs, and retrieval-augmented generation, and apply them to biomedical and health data<br>• Document research findings and contribute to internal reports, publications, or conference presentations<br>• Explain model behavior, limitations, and performance in terms both technical and non-technical team members can act on</p><p><strong>This role requires:</strong><br>• Bachelor's degree in Computer Science, Machine Learning, Data Science, Biomedical Informatics, Statistics, or related field; Master's or Ph.D. strongly preferred with 4–6 years + of progressive experience in applied AI/ML, with demonstrated ability to independently develop and evaluate models (Ph.D. graduates with relevant research experience may be considered) <br>• Solid grounding in supervised, unsupervised, and self-supervised learning, deep neural networks, and modern ML frameworks (PyTorch, TensorFlow, or equivalent)<br>• Strong Python skills across the scientific ML stack (scikit-learn, HuggingFace Transformers, pandas, NumPy)<br>• Experience designing and evaluating NLP or multimodal models, including LLM fine-tuning or prompt engineering<br>• Comfort with experiment tracking, model versioning, and reproducible research practices (MLflow, W&B, DVC, or similar)<br>• Familiarity with cloud-based ML infrastructure (AWS SageMaker, GCP Vertex AI, Azure ML, or equivalent).<br>• Experience with health or life sciences data — EHR/EMR, claims, clinical notes, genomic, or imaging data<br>• Familiarity with medical terminologies and ontologies (SNOMED CT, ICD-10/11, LOINC, RxNorm, OMOP CDM)<br>• Published work or open-source contributions in applied ML, NLP, or computational biomedicine<br>• Experience with MLOps, CI/CD for ML, or model observability in production<br>• Familiarity with federated learning, privacy-preserving ML, or regulated-environment data use agreements</p><p>#AAI</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 25 Sep 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician (Days)]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49755]]></requisitionid>
    <referencenumber><![CDATA[R49755]]></referencenumber>
    <apijobid><![CDATA[r49755]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49755/calibration-technician-days/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking to add a Calibration Technician to our growing team. Calibration Technicians support our manufacturing operations by performing mechanical, electrical, calibration, electronic, and utility-related tasks. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: East Greenbush, New York, United States</li><li>Working shifts available: <ul><li>Monday-Friday 8:00am-4:30pm</li><li>Sunday-Wednesday 6:00am-4:30pm</li><li>Wednesday-Saturday 6:00am-4:30pm</li></ul></li><li>Training shift: Monday-Friday 8:00am-4:30pm for approximately 6 months</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Calibrate various types of instrumentation including temperature, pressure, level, flow, and analytical instruments</li><li>Perform loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Work with medium and low voltages</li><li>Perform basic plumbing and tube bending jobs</li><li>Assist the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Perform daily Work Orders (WO) and Preventative Maintenance (PM), and efficiently coordinating the workflow and documentation of PMs and WOs</li><li>Communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work, as needed</li><li>Participate in compliance investigations if and when necessary</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum years of related experience for each level:<ul><li>Calibration Technician II: 2+ years or HSD/GED and 5+ years</li><li>Calibration Technician III: 5+ years or HSD/GED and 8+ years</li><li>Calibration Technician IV: 8+ years or HSD/GED and 11+ years</li></ul></li><li>Demonstrated basic problem-solving skills</li><li>Ability to learn and follow routine procedures independently as well as part of a team</li><li>The ability to lift, push, and pull at least 50 lbs</li><li>Participating in a rotating on-call schedule</li><li>Strong written and verbal communication skills</li><li>Ability to maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><br><h3><strong>Gowning and Environment:</strong></h3><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Las Palmas (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50493]]></requisitionid>
    <referencenumber><![CDATA[R50493]]></referencenumber>
    <apijobid><![CDATA[r50493]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50493/sales-representative-las-palmas-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Las Palmas</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Payroll Service Delivery Analyst (International)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50450]]></requisitionid>
    <referencenumber><![CDATA[R50450]]></referencenumber>
    <apijobid><![CDATA[r50450]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50450/sr-payroll-service-delivery-analyst-international/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, our Global Business Services organization plays a critical role in delivering efficient, compliant, and employee-focused operations that support our global workforce. We are seeking a <strong>Senior Payroll Service Delivery Analyst</strong> to join our Global Capability Center (GCC). In this role, you will support the accurate, timely, and compliant delivery of payroll services across multiple international locations while partnering with Global Payroll, HR, Finance, and external payroll providers. You will contribute to payroll operational excellence through data accuracy, process compliance, team member collaboration, and continuous improvement initiatives while developing expertise in global payroll service delivery within a dynamic and growing organization.</p><p><strong>When & Where</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role</strong></p><ul><li><p>Support the preparation and processing of payroll activities for assigned international countries, ensuring accurate and timely payroll delivery.</p></li><li><p>Validate payroll inputs, perform audit checks, reconciliations, and data reviews to maintain payroll accuracy, compliance, and data integrity.</p></li><li><p>Partner with Global Payroll, Human Resources, Finance teams, and external payroll vendors to ensure timely submission of payroll data and resolution of payroll-related inquiries.</p></li><li><p>Maintain payroll calendars, operational checklists, process documentation, and standard operating procedures to support payroll governance and service delivery.</p></li><li><p>Monitor statutory and regulatory changes impacting payroll operations and support implementation of required updates and compliance activities.</p></li><li><p>Prepare payroll reports, support month-end activities, and assist with payroll-related analysis and reconciliations.</p></li><li><p>Participate in payroll system enhancements, testing activities, process improvement initiatives, and GCC standardization efforts.</p></li><li><p>Support internal and external audit activities by providing documentation, responding to inquiries, and ensuring adherence to internal controls.</p></li><li><p>Contribute to operational excellence initiatives by identifying opportunities to improve payroll processes, efficiencies, and employee experience.</p></li><li><p>Maintain the highest standards of confidentiality, compliance, and data security while handling employee and payroll information.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Bachelor’s degree in Accounting, Finance, Human Resources, Business Administration, or a related field; equivalent experience considered.</p></li><li><p>5+ years of experience in payroll, HR operations, accounting, shared services, or related operational functions.</p></li><li><p>Understanding of payroll processes, payroll compliance requirements, controls, and operational standard methodologies.</p></li><li><p>Experience working with HRIS and payroll systems such as Workday, SAP, ADP, Oracle, or similar platforms.</p></li><li><p>Strong Microsoft Excel skills, including data analysis, reporting, reconciliations, and validation activities.</p></li><li><p>Demonstrated attention to detail with the ability to work accurately in a fast-paced, deadline-driven environment.</p></li><li><p>Strong analytical and problem-solving capabilities with the ability to identify discrepancies and support issue resolution.</p></li><li><p>Experience collaborating with cross-functional collaborators, external vendors, and global teams.</p></li><li><p>Effective communication, organizational, and stakeholder management skills.</p></li><li><p>Ability to manage multiple priorities while maintaining accuracy, compliance, and service excellence.</p></li><li><p>Experience supporting audits, compliance activities, and process improvement initiatives within a shared services environment preferred.</p></li><li><p>Exposure to multi-country payroll operations and global business services environments preferred.</p></li><li><p>Multilingual capabilities or experience working across diverse cultural environments preferred.</p></li><li><p>Ability to work a hybrid schedule and occasionally align with global time zones to support business requirements.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 01:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Downstream Purification & Process Characterization (IOPS)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50981]]></requisitionid>
    <referencenumber><![CDATA[R50981]]></referencenumber>
    <apijobid><![CDATA[r50981]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50981/2027-co-op-downstream-purification-process-characterization-iops/]]></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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Downstream Purification & Process Characterization (IOPS) to join our Process Characterization and Controls and Downstream Investigations (Raw Materials) teams within Regeneron Industrial Operations and Product Supply (IOPS) <strong>Process Sciences</strong> department.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Rensselaer, NY (Temple Lane)</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><em>This role typically runs from May through December only.</em></p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$25.50 per hour.</p><p><strong>What you’ll do:</strong></p><ul><li>Support purification and raw material characterization methods used to isolate, concentrate, and de-risk biologic drug substances</li></ul><ul><li>Conduct filtration and separations studies to establish reusable filter lifetimes</li></ul><ul><li>Investigate opportunities to extend hold times for filtration equipment</li></ul><ul><li>Establish acceptable reuse limits for filtration membranes used in antibody concentration and purification</li></ul><ul><li>Study raw material risk factors, including nitrosamine clearance and formation</li></ul><ul><li>Support hands-on purification and filtration operations</li></ul><ul><li>Contribute to nitrosamine risk assessment development</li></ul><ul><li>Document results that directly support regulatory filings</li></ul><p><strong> </strong></p><p><strong>Relevant majors: </strong>Chemical Engineering, Biomedical Engineering, Biochemistry, Chemistry</p><p><strong> </strong></p><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li></ul><ul><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li></ul><ul><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li></ul><ul><li>Cumulative GPA of 3.0 or higher preferred</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Quality Assurance Microbiology]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46191]]></requisitionid>
    <referencenumber><![CDATA[R46191]]></referencenumber>
    <apijobid><![CDATA[r46191]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46191/executive-director-quality-assurance-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director, QA Microbiology who leads the strategy, design, and operational execution of Regeneron's GMP contamination control program across aseptic and low-bioburden biopharmaceutical manufacturing operations. This individual provides technical and operational direction to ensure robust environmental control, sterility assurance, and microbial contamination risk management across the network, driving compliance with global regulatory expectations for sterile and non-sterile product manufacturing. This position guides functional areas in support of compliance and business objectives, ensures the contamination control strategy remains current with evolving industry and regulatory expectations, and serves as the key liaison with operational microbiology and manufacturing subject matter experts across the lines of business.</p><br><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, NY</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Design, implement, and continuously improve a holistic Contamination Control Strategy (CCS) grounded in sound microbiological science, aseptic processing principles, and applicable quality, regulatory, and legal requirements.</li><li>Provide expert vision in environmental monitoring (EM) programs, cleanroom classification, personnel qualification, gowning practices, and aseptic process simulation (media fill) performance across manufacturing sites.</li><li>Influence root cause investigations and risk assessments for microbial excursions, sterility failures, and environmental monitoring deviations, ensuring timely, science-based corrective and preventive actions.</li><li>Monitor contamination control program performance using meaningful operational metrics (e.g., EM trends, excursion rates, media fill success rates) and demonstrate a commitment to continuous improvement.</li><li>Embed quality risk management (QRM) tools—such as FMEA and contamination risk mapping—within microbiology and aseptic operations to proactively identify and mitigate contamination vectors.</li><li>Maintain current expertise in evolving regulatory expectations (e.g., EU Annex 1, FDA Aseptic Processing Guidance, USP <1116>, PIC/S) and proactively integrate emerging requirements into the contamination control program.</li><li>Apply quality and risk management tools to make timely, science-based decisions that protect patient safety and product sterility.</li><li>Partner closely with QA Operations, Manufacturing, Facilities/Engineering, and Microbiology Lab functions to translate contamination control strategy into robust, compliant aseptic practices on the floor.</li><li>Serve as the senior microbiological and contamination control decision-maker, exercising sound judgment under pressure to ensure product safety and efficacy.</li><li>Represent Regeneron as the subject matter authority on contamination control and sterility assurance to internal leadership, regulatory agencies, and corporate/external partners.</li><li>Translate contamination control vision and strategy into executable, resourced action plans across the manufacturing network.</li><li>Ensure the Contamination Control Strategy is transparent, well-documented, and that the broader organization is engaged and accountable for its execution.</li><li>Establish high standards for performance management and accountability to achieve microbiological, sterility assurance, and organizational objectives.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in Microbiology, Molecular Biology, Biology, Pharmaceutical Sciences, or related scientific discipline (advanced degree preferred), or equivalent combination of education and experience, and the following amount of progressive experience in pharmaceutical/biopharmaceutical microbiology, sterility assurance, or contamination control, including significant leadership experience in aseptic manufacturing environments, for each level:<ul><li>Senior Director – 15+ years</li><li>Executive Director – 18+ years</li><li>Level will be determined based on experience</li></ul></li></ul><ul><li>Deep operational expertise in aseptic processing and low-bioburden manufacturing, including cleanroom design/classification, HVAC airflow principles, personnel and material flow, gowning qualification, and aseptic technique.</li><li>Demonstrated hands-on ownership of a Contamination Control Strategy (CCS), including environmental monitoring program design, trending, and risk-based EM site selection.</li><li>Strong working knowledge of aseptic process simulation (media fill) design, execution, and failure investigation.</li><li>Expert-level understanding of global regulatory expectations and guidance, including EU Annex 1 (2022 revision), FDA Guidance for Industry: Sterile Drug Products Produced by Aseptic Processing, USP <1116>, PIC/S, and ISO 14644.</li><li>Proven track record leading root cause investigations, deviation management, and CAPA for microbial contamination events, sterility test failures, and environmental excursions.</li><li>Demonstrated ability to apply Quality Risk Management tools (FMEA, fishbone, risk mapping) to contamination control and microbiological decision-making.</li><li>Experience representing microbiological/contamination control positions directly to health authorities during inspections (FDA, EMA, MHRA) with a strong inspection track record.</li><li>Demonstrated success partnering cross-functionally with Manufacturing, Facilities/Engineering, QA Operations, and Microbiology Labs to translate strategy into floor-level execution.</li><li>Strong people leadership experience, including building and developing high-performing technical teams and driving accountability across a matrixed organization.</li><li>Excellent judgment and composure in high-stakes, time-sensitive decision-making affecting product disposition and patient safety.</li><li>Executive presence and communication skills suited to representing the company with regulators, corporate partners, and senior leadership.</li></ul><br><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$203,000.00 - $399,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Electrician]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49527]]></requisitionid>
    <referencenumber><![CDATA[R49527]]></referencenumber>
    <apijobid><![CDATA[r49527]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49527/electrician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking for an Electrician to join our growing team. Our Electricians are responsible for start-up, normal operation, monitoring, and shutdown of all electrical systems and emergency generator equipment; troubleshooting, preventative maintenance, and repair work of all facilities electrical equipment. We maintain the site's electrical distribution systems in a state of electrical code compliance. As an Electrician, you will truly be “keeping the lights on” to ensure continuous manufacturing of our life-saving products. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Working shift: Sunday-Wednesday 6:00am-4:30pm</li><li>Training shift: Monday-Friday 8:00am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Maintain electrical power systems and stand-by power generation equipment, as well as accurate electrical one-line drawings</li><li>Maintain an inventory of essential fuses and circuit breakers</li><li>Direct outside service providers to provide and install electrical work and PMs</li><li>Assist Mechanical Technicians on facility or process equipment electrical issues</li><li>Install lighting, electrical, and computer wiring when appropriate</li><li>Schedule work and maintain all preventative maintenance for on-site emergency generators utilizing contracted services</li><li>Schedule and maintain documentation on infrared scans for all electrical enclosures</li><li>Develop, establish, and conduct annual employee training classes on electrical safety procedures and practices</li></ul><p><strong>This role requires:</strong></p><ul><li>AAS in Engineering or Construction Technologies and the following minimum amounts of experience for each level; relevant Journeyman-level experience may be substituted for degree<ul><li>Electrician II: 2+ years, or an equivalent combination of education and experience</li><li>Electrician III: 5+ years, or an equivalent combination of education and experience</li></ul></li><li>Experience with high voltage is beneficial</li><li>Proficiency with electrical and mechanical schematics and blueprints</li><li>Ability to work independently in a constantly evolving, collaborative environment</li><li>Strong verbal and written communication skills, with the ability to build effective working relationships across the organization</li><li>Some exposure to MS Office Suite, specifically Excel</li><li>Participating in rotational on-call schedule</li><li>May involve working off-shift to support 24/7 coverage</li></ul><p>Level will be determined based on qualifications relevant to the role</p><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Gowning: Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, makeup and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but are not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 11:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Analyst, Commercial Finance]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50850]]></requisitionid>
    <referencenumber><![CDATA[R50850]]></referencenumber>
    <apijobid><![CDATA[r50850]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50850/sr-analyst-commercial-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Analyst Commercial Finance Oncology & Hematology to join our Commercial Finance team, supporting our US Commercial Finance organization in a hybrid work model. In this role, you will build demand and revenue forecasts, develop patient-based forecasting models, and translate market insights into business decisions while collaborating with Commercial Business Units, Commercial Operations, Market Access, Insights & Analytics, and Accounting teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Partner with US Commercial Finance teams to deliver demand and revenue estimates and analytical support across commercial functions.</li><li>Own commercial demand and revenue forecasting and the supporting analytics for assigned business areas.</li><li>Create and maintain driver-based forecasting models, budgets, rolling forecasts, strategic plans, scenario analyses, and assumptions documentation.</li><li>Translate primary research, secondary data, industry datasets, and market insights into quantified forecasting assumptions and model inputs.</li><li>Run sensitivity and scenario analyses for competitive entry, indication expansion, access and reimbursement changes, and pricing impacts.</li><li>Develop gross-to-net revenue estimates using channel and payer mix trends in partnership with Accounting and Market Access teams.</li><li>Lead forecast variance analyses and provide commentary against budget, forecast, and prior-year performance.</li><li>You bring a data-driven attitude and can confidently defend assumptions while collaborating effectively across time zones.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in pharma, life sciences, business, or a quantitative field.</li><li>5+ years of experience in commercial and strategic forecasting, preferably within pharma, biotech, or healthcare.</li><li>5+ years of progressive pharmaceutical industry experience, preferably within a Global Capability Center (GCC) or consulting environment.</li><li>Demonstrated experience building forecasting models from scratch, including patient-based and demand-based forecasting approaches such as time series and machine learning models.</li><li>In-depth knowledge of industry secondary datasets, including IQVIA or Symphony; experience with IQVIA assets such as NSP, DDD, NPA, Xponent, and Oncology Dynamics.</li><li>Experience with gross-to-net revenue mechanics and revenue translation methodologies.</li><li>Advanced Excel and data wrangling skills, including Power Query, Alteryx, and SQL.</li><li>Prior experience supporting cross-time-zone partners in a GCC or shared services environment is strongly preferred.</li><li>MBA or CFA qualification is a plus.</li><li>Effective verbal and written communication skills, with the ability to engage partners across multiple time zones.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Development Program Management]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51046]]></requisitionid>
    <referencenumber><![CDATA[R51046]]></referencenumber>
    <apijobid><![CDATA[r51046]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51046/director-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>This role (Director, Development Program Management) uses extensive program management knowledge and experience in the drug development industry to provide operational leadership, direction, and support to assigned development program(s) and/or portfolio(s). This individual is expected to drive the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and monitor the execution of these plans from preclinical through commercialization/lifecycle management. Responsibilities may also include coaching and mentorship of junior colleagues, managing direct reports, working with collaborators, and contributing to departmental initiatives. This is a leadership role within the department and organization thus this individual is expected to independently execute responsibilities, interact effectively with senior leadership, and influence the direction and outcomes of assignments. </p><br><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY</li><li>Additional Locations: Warren, NJ or Cambridge, MA</li></ul><br><p><strong>Discover your role:</strong></p><ul><li><strong>Development Teams: </strong>Partners with the Global Program Head to drive strategic program teams (SPT) and sub teams by leading key governance meetings. Uses broad knowledge of drug development and project/program management coupled with leadership and problem-solving skills to align development teams around an integrated project/program plans, timelines and budgets based on program vision. Ensures efficient delivery of plans. Proposes and aligns annual program goals with program strategy and Regeneron’s corporate goals. Monitors progress against program goals and ensures accurate and timely reporting of program progress to management. Anticipates issues and program risks and drives timely development of risk management plans and issue resolution.</li><li><strong>Business Acumen: </strong>Utilizes knowledge of industry trends to identify risks/threats/opportunities and translates these to actionable activities for the development teams. Able to leverage political savvy and awareness of team dynamics to effectively drive decision making and achieve desired outcomes. Is proficient in project management planning systems (MS Project, SharePoint) and tools/techniques. Understands how systems and tools can be leveraged to move the program and business forward.</li><li><strong>Communication:</strong> Effective and trusted communicator that will develop a proven track record across the organization. Works effectively with different styles and adapts approaches in a cross-functional matrix environment to drive results. Establishes a culture which promotes and encourages open communication, transparency, accountability and learning from mistakes.</li><li><strong>Problem Solving: </strong>Is proficient at proactively identifying and critically analyzing potential problems that may affect the project, processes, or the team. Uses extensive industry and professional experience and knowledge to develop viable, long-term solutions to cross-functional, project, process, or team issues, driving alignment with impacted stakeholders. Proactively implements lessons learned/best practices across programs/TA and department to help other teams preempt or mitigate problems.</li><li><strong>Leadership</strong>: Strengthens teams and continuously works to drive teams to be high performing and efficient. Ability to align team members towards a common goal through expertise with conflict management, self/social awareness, and diverse team dynamics.</li></ul><p><strong><br></strong></p><p><strong>This role requires:</strong></p><ul><li>Minimal educational requirements: Bachelor’s Degree </li><li>12+ years of relevant broad project / program management experience required, preferably in the pharmaceutical or related industry </li><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels both internal and external to the company in order to establish credibility with professionals on the project teams. </li></ul><ul><li>Understand and motivate others and build effective teams. </li></ul><ul><li>Have strong presentation and critical thinking skills. </li></ul><ul><li>Actively promote constructive interactions among team members in order to address difficult situations. </li></ul><ul><li>Resolve and negotiate conflicts or problems with tact, diplomacy and composure. </li></ul><ul><li>Handle multiple projects and priorities with exceptional organizational and time management skills (both project and self) </li></ul><ul><li>Thrive in fast paced entrepreneurial organizations; expert in dealing with ambiguity and uncertainty </li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager, Immunology – Pulmonology and Gastroenterology (Boston, N)]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51013]]></requisitionid>
    <referencenumber><![CDATA[R51013]]></referencenumber>
    <apijobid><![CDATA[r51013]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51013/field-reimbursement-manager-immunology-pulmonology-and-gastroenterology-boston-n/]]></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>Field Reimbursement Manager, Immunology – Pulmonology and Gastroenterology </strong></p><p><strong> </strong></p><p><strong>Build Our Future Together </strong></p><p><strong><br></strong>The Field Access & Reimbursement environment for specialty biologics has proven to be highly challenging for HCPs and Patients. Payer Formularies and restrictive Utilization Management Criteria including: Prior Authorization Processes, Step Edits, Appeals, detailed Clinical Documentation, Peer to Peer reviews etc., requires dedicated and focused customer facing support through the Reimbursement Management Team.<strong><br></strong></p><br><p><strong>When and Where</strong>: </p><p>Boston North </p><br><p><strong>Discover Your Role:</strong> </p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. The primary purpose of this role is to support Health Care Practitioner offices in obtaining appropriate access to Regeneron products for patients. Ensuring optimal access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron product portfolio. Support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate across multiple internal stakeholders, sales teams, Payer teams, Alliance partners, HUBs, etc. The Field Reimbursement Management reports to the District Manager of Field Market Access. </p><br><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. Complete 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><br><p>Complete established performance parameters and monitor personal performance against these agreed parameters: Work closely with partners as assigned; District Sales Managers, Medical Specialists, other FRM, Reimbursement, Marketing and Access team members in assigned geographical areas to insure efficient coverage and customer knowledge of this process and all REGN patient services within defined accounts</p><br><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, in efforts to streamline the coverage and specialty pharmacy processes to acquire alliance products</p><br><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p><p><strong><br></strong></p><p><strong>This Role Requires: </strong></p><br><p>You have biologic expertise (Specialty Pharmacy/Buy & Bill)</p><p>You are a standout colleague and able to collaborate</p><p>You can optimally communicate across multiple regions via different mediums</p><p>You can get results with your activity</p><p>You are capable with meeting the expectations of internal and external customers</p><br><p>To be considered for this role, we expect you to have a bachelor's degree and at least 5 years of experience in the pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience. We are also expecting you to have worked with products delivered through a Specialty Pharmacy network.</p><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Lab Project Management]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50795]]></requisitionid>
    <referencenumber><![CDATA[R50795]]></referencenumber>
    <apijobid><![CDATA[r50795]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50795/senior-manager-clinical-lab-project-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Precision Medicine Clinical Laboratory Operations will be responsible for Clinical Laboratory Project & Program management for various therapeutic areas working closely with Director, Precision Medicine Clinical Laboratory Operations and key cross-functional collaborators. The primary role will be to keep laboratory deliverables across the portfolio on track, ensuring that study start timelines are met, provide risk management. This will be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory Operations Management, Global Development colleagues and central and specialty testing laboratories to support early and late-stage programs within our pipeline. </p><br><p><strong>When & Where:</strong></p><p>This role can be based remotely (in the US) or sit on-site in our Warren, NJ or Armonk, NY office. If on-site, the role would be expected to be on-site four days per week.</p><br><p><strong>Discover Your Role:</strong></p><ul><li>Perform clinical laboratory portfolio management for Regeneron clinical trials and review clinical laboratory operations timelines and risks and be able to manage and communicate risks and ensure study starts and data delivery are aligned with expectations </li></ul><ul><li>Be a subject matter expert on central and specialty laboratory processes and leverage this knowledge to be a trusted collaborator and ensure clinical laboratory deliverables </li></ul><ul><li>Keep biomarker strategy delivery schedules for clinical development programs and studies on track, identifying and tracking risks and decisions, creating mitigation plans </li></ul><ul><li>Manage clinical laboratory operations goals, including progress, schedules of testing/data generation across the portfolio with clear objectives and deadlines </li></ul><ul><li>Manage strong relationships and trust with internal and cross functional partners, including Precision Medicine Clinical Lab Study Management, Precision Medicine Strategy Leads and others within Global Development to manage and implement program level clinical laboratory management </li></ul><ul><li>Demonstrate relevant knowledge and understanding of clinical laboratory trial requirements on the program and implement operational decisions. Ensure the laboratory portion of the studies are harmonized for assigned program from onset to final delivery </li></ul><ul><li>Be viewed as an operational subject matter expert to effectively communicate with clinical study teams on laboratory program direction. Demonstrate authority for the studies related to the program.</li></ul><ul><li>Create and communicate enhancements to Clinical Laboratory Project Management and connections through the matrix environment, design and develop processes to address identified gaps </li></ul><br><p><strong>This Role Requires:</strong></p><ul><li>Bachelors degree required, Masters degree preferred.</li><li>Minimum of 10 years experience preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. </li><li>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. </li><li>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. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Specialist, Medical Coding]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50669]]></requisitionid>
    <referencenumber><![CDATA[R50669]]></referencenumber>
    <apijobid><![CDATA[r50669]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50669/sr-specialist-medical-coding/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases.</p><br><p>We are seeking a Senior Specialist, Medical Coding to join our Clinical Data Management team. You will independently manage medical coding activities across assigned clinical studies using MedDRA and WHODrug dictionaries. You will help ensure accurate, consistent, and timely coding, support study setup and database lock activities, collaborate with cross-functional teams and CRO partners, and guide junior coding staff.</p><br><p><strong>When & where: </strong></p><p>Hyderabad (hybrid) </p><br><p><strong>Discover your role: </strong></p><ul><li>Independently manage medical coding activities for assigned studies and serve as the main contact for study-level coding questions and issues. </li></ul><ul><li>Perform and review coding using MedDRA and WHODrug dictionaries in line with company conventions and study requirements. </li></ul><ul><li>Develop Medical Coding Plans and support study setup within medical coding systems. </li></ul><ul><li>Review coding CRFs, data collection standards, coding configurations, and reports for accuracy and completeness. </li></ul><ul><li>Support dictionary version upgrades, synonym maintenance, impact assessments, and recoding activities. </li></ul><ul><li>Maintain study-specific coding guidelines and inspection-ready documentation. </li></ul><ul><li>Perform coding reconciliation with Clinical Data Management and Drug Safety teams. </li></ul><ul><li>Partner with Medical Monitors, Clinical Scientists, Drug Safety, Biostatistics, CROs, and other stakeholders to resolve coding issues. </li></ul><ul><li>Identify data quality risks, escalate concerns, and complete coding deliverables within database lock timelines. </li></ul><ul><li>Mentor junior staff and contribute to process improvements, automation tools, and AI-enabled coding solutions.</li></ul><p><strong>This role requires: </strong></p><ul><li>A bachelor's degree in Pharmacy, Life Sciences, Nursing, or a related healthcare field. </li></ul><ul><li>At least 5 years of medical coding experience within biotechnology, pharmaceutical, CRO, or a health-related industry. </li></ul><ul><li>Strong hands-on experience with MedDRA and WHODrug dictionaries, including coding conventions, hierarchies, version upgrades, impact assessments, and recoding. </li></ul><ul><li>Experience with medical coding systems such as Medidata Rave Coder, including coding workflows, study setup, configuration review, and report validation. </li></ul><ul><li>Strong knowledge of medical and medication terminology and its use in clinical development. </li></ul><ul><li>Experience developing Medical Coding Plans, reviewing coding CRFs, and supporting study setup and database lock activities. </li></ul><ul><li>Experience with coding reconciliation between Clinical Data Management and Drug Safety. </li></ul><ul><li>Working knowledge of 21 CFR Part 11, ICH-GCP, GxP, GDPR, and relevant regulatory requirements. </li></ul><ul><li>The ability to independently manage multiple studies, priorities, and timelines with minimal supervision. </li></ul><ul><li>Strong analytical, problem-solving, organizational, communication, and stakeholder management skills. </li></ul><ul><li>The ability to mentor less-experienced staff and work effectively in a fast-paced, cross-functional environment. </li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50972]]></requisitionid>
    <referencenumber><![CDATA[R50972]]></referencenumber>
    <apijobid><![CDATA[r50972]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50972/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[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Clinical Study Lead to join our Clinical Trial Management team, supporting our global, regional and country studies in a hybrid work mode. In this role, you will lead complex clinical trials from study design through close-out while collaborating with cross-functional study teams, vendors and clinical research organizations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Tokyo, Japan</p><p>Hybrid</p><p>Up to 25% travel.</p><h3><strong>Discover your role:</strong></h3><ul><li>Lead cross-functional teams and global, regional or country trial delivery from design through close-out.</li><li>Own timelines, budgets, risks, protocol input and study documentation under ICH/GCP and Regeneron SOPs.</li><li>Oversee CTMS, TMF, trial registry compliance, vendors, CROs and audit or inspection readiness.</li><li>Direct feasibility, site selection, activation, monitoring, investigator meetings and patient recruitment strategies.</li><li>Monitor data quality, queries, deviations, supplies, accountability and trial performance against agreed metrics.</li><li>Manage close-out, database lock, reconciliations, clinical study reports, CAPAs and lessons learned.</li><li>You drive continuous improvement, innovative study execution and effective cross-functional collaboration.</li><li>Lead CTM staff deliverables and, when assigned, supervision or unmasked study activities.</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree and at least eight years of relevant industry experience.</li><li>Extensive global clinical trial operations experience and knowledge of ICH/GCP and regulatory requirements.</li><li>Advanced project, budget and vendor management, cross-functional leadership and organizational skills.</li><li>Advanced proficiency with trial management systems, Microsoft applications, IVRS/IWRS and EDC.</li><li>Expert data-driven planning, problem-solving, negotiation, communication, prioritization and stakeholder influence.</li><li>Ability to build and develop study teams; line management experience is preferred.</li><li>Awareness of relevant industry trends and a proactive, self-disciplined approach.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Market Access Lead - Rare Diseases (Europe Region)]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50647]]></requisitionid>
    <referencenumber><![CDATA[R50647]]></referencenumber>
    <apijobid><![CDATA[r50647]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50647/director-market-access-lead-rare-diseases-europe-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Regional Market Access, Rare Diseases, Europe to join our market access function, supporting our Europe region in a hybrid work mode. In this role, you will shape pricing, reimbursement, and patient access strategies while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead rare disease access strategies aligned with global objectives and country needs.</p></li><li><p>Differentiate approaches across cost-effectiveness and list-price or free-pricing markets.</p></li><li><p>Monitor European policies, payer trends, and reimbursement frameworks.</p></li><li><p>Adapt global access tools and value propositions for regional stakeholders.</p></li><li><p>Manage health technology assessment dossiers, pricing negotiations, and reimbursement submissions.</p></li><li><p>Partner with medical affairs and access teams on evidence and health economics outcomes research plans.</p></li><li><p>Engage payers, policymakers, advocacy groups, and public affairs teams to advance access.</p></li><li><p>You build collaboration through advisory boards, market research, and landscape assessments.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>European rare disease pricing, reimbursement, launches, and approval experience.</p></li><li><p>Expertise in payer systems, economic models, and health technology assessment submissions.</p></li><li><p>Knowledge of NICE, ZIN, TLV, QALY frameworks, and free-pricing markets.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>English fluency; additional European languages are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix leadership, agility, and collaboration.</p></li><li><p>Healthcare policy shaping and multi-stakeholder engagement experience preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€100,275.00 - €167,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Statistical Programming - Oncology]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44717]]></requisitionid>
    <referencenumber><![CDATA[R44717]]></referencenumber>
    <apijobid><![CDATA[r44717]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44717/manager-statistical-programming-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables</li><li>Lead the development and quality control of tables, listings, and graphs in support of analysis requirements</li><li>Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests</li><li>Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch</li><li>Partner with management to determine resource requirements for your therapeutic area or department</li><li>Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles</li><li>Provide feedback to management on team members' contributions to support performance evaluations and goal-setting</li><li>Advise direct reports on procedures for data, records, and information retention</li><li>Enjoy working with minimal supervision and taking ownership of complex deliverables</li><li>Communicate clearly with cross-functional, multidisciplinary teams</li><li>Think analytically and stay organized when managing multiple priorities and timelines</li><li>Take initiative in developing deep expertise within a specialized area</li><li>Bring a collaborative mindset to hiring, feedback, and team development</li><li>Adapt easily to shifting priorities, including last-minute requests from senior leadership</li><li>Approach quality and documentation with rigor in a regulated environment</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)</li><li>Proven experience leading programming deliverables within a clinical study team</li><li>Experience providing input on hiring, feedback, and performance evaluation</li><li>Strong organizational and documentation skills within a regulated environment</li><li>Nice to have: SAS Certification</li></ul><br><p>#statprogregn</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Commercial Operations Lead, Associate Director]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49945]]></requisitionid>
    <referencenumber><![CDATA[R49945]]></referencenumber>
    <apijobid><![CDATA[r49945]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49945/commercial-operations-lead-associate-director/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are seeking an Associate Director, Commercial Operations Lead to join our Global Capability Center (GCC) Commercial Operations organization. This role will serve as a strategic partner to U.S., international, and global commercial leadership and will be responsible for establishing and scaling Commercial Operations capabilities across HCP Engagement, Marketing Enablement, and Marketing Project Management. Reporting to the Director, GCC Commercial Lead, this position will drive operational excellence, performance monitoring, stakeholder management, and capability-building initiatives that support global commercial strategies and execution across markets.</p><p><strong>When & Where:</strong></p><p><strong>Hyderabad, India (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Provide strategic and operational leadership to Global Commercial Operations and Global Marketing teams, ensuring alignment between global priorities and local execution.</p></li><li><p>Establish and scale the India-based Commercial Operations organization across multiple functional capability areas.</p></li><li><p>Lead and develop teams responsible for HCP Engagement Operations, Marketing Enablement, and Marketing Project Management.</p></li><li><p>Partner with global stakeholders to optimize omnichannel marketing campaigns and project management processes across products and indications.</p></li><li><p>Serve as the primary point of contact for U.S. and international commercial operations leadership regarding operational execution and customer engagement.</p></li><li><p>Drive content operations and marketing enablement initiatives, including MLR review processes, claims management, and digital asset management.</p></li><li><p>Collaborate with Marketing, IT, and in-market teams to localize and deploy promotional materials aligned with global standards and local needs.</p></li><li><p>Develop dashboards, scorecards, KPI tracking, and reporting tools to provide visibility into operational performance and support data-driven decision-making.</p></li><li><p>Monitor commercial operations performance, identify process improvement opportunities, and implement operational excellence initiatives.</p></li><li><p>Ensure compliance with internal policies, industry regulations, and audit requirements across commercial operations activities.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; MBA, Master's degree, or equivalent advanced degree preferred.</p></li><li><p>Minimum 10 years of pharmaceutical/biotech commercial experience, or 7+ years with an MBA/MS, demonstrating increasing levels of responsibility.</p></li><li><p>Proven experience in Commercial Marketing Operations, HCP Engagement Operations, Program Management, and Project Management.</p></li><li><p>Strong understanding of HCP engagement models, operational performance frameworks, metrics, and scorecards.</p></li><li><p>Experience translating global commercial strategies into localized operational plans and supporting execution across diverse international markets.</p></li><li><p>Hands-on experience with content operations, MLR processes, claims management, and Digital Asset Management (DAM).</p></li><li><p>Demonstrated success working with cross-functional and geographically dispersed teams in a global or regulated environment.</p></li><li><p>Experience driving operational excellence, process improvement, and business transformation initiatives.</p></li><li><p>Experience within Global Capability Centers (GCC) or global delivery models in pharmaceutical, biotech, or other regulated industries is preferred.</p></li><li><p>Strong leadership, stakeholder management, communication, and team development capabilities.</p></li><li><p>Strong analytical, problem-solving, and decision-making skills with a focus on continuous improvement and execution excellence</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 10 Oct 2026 02:56:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Technology Specialist]]></title>
    <date><![CDATA[Tue, 21 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42107]]></requisitionid>
    <referencenumber><![CDATA[R42107]]></referencenumber>
    <apijobid><![CDATA[r42107]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r42107/senior-it-technology-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior IT Technology Specialist to join our IOPS IT team, ensuring high-quality service delivery and driving IT and OT solutions across our industrial sites. In this role, you will serve as a Subject Matter Expert in IT/OT risk management, security, and operational excellence — identifying and mitigating risks, overseeing incident management, and ensuring compliance with regulatory and security standards — while collaborating with cross-functional teams, service providers, and third-party partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Develop and implement strategies to identify, assess, and mitigate risks within IT and OT operations, ensuring alignment with organizational goals, compliance standards, and regulatory requirements; advise management and business owners on critical issues</li><li>Monitor endpoint security posture, respond to incidents, and coordinate remediation efforts; support IT/OT network segmentation initiatives in alignment with industry frameworks such as IEC 62443</li><li>Contribute to Enterprise Cyber Resiliency projects, enhancing the organization's ability to withstand, detect, respond to, and recover from cybersecurity incidents across IT and OT environments</li><li>Provide oversight and guidance for major incidents, ensuring coordination of resolving parties, effective stakeholder communication, and thorough post-incident review</li><li>Partner with service providers and third-party teams to ensure quality of service, highest levels of availability and efficiency, and adherence to agreed SLAs benchmarked against industry standards</li><li>Provide direction and oversight across the full lifecycle of IT/OT solutions from initiation through transition, collaborating with internal and external teams to ensure successful delivery</li><li>Support audits and compliance reviews with detailed documentation and insights into IT/OT risk management practices; monitor emerging risks and recommend proactive measures to safeguard systems</li><li>Train and guide team members on risk management protocols, fostering a culture of risk awareness and continuous improvement across IT operations</li><li>Deep experience with ITIL disciplines and service management in large-scale, diverse environments including incident management and escalation procedures</li><li>Experience with operating systems including Microsoft Windows and Linux, and virtualization platforms such as VMware</li><li>Experience with monitoring and security tools such as Splunk, Claroty, and next-generation OT tools preferred</li><li>Proven problem determination and root cause analysis skills; excellent customer-facing, negotiation, and influencing skills with the ability to work effectively with global teams and third-party service providers</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology or a related field</li><li>Senior: 5 years of experience delivering IT/OT services.</li><li>Principal: 8 years of experience delivering IT/OT services.</li><li>Strong GxP experience and experience in highly regulated environments required.</li><li>May consider equivalent combination of education and experience; level determined based on qualifications ​</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$77,600.00 - $148,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Study Lead]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49337]]></requisitionid>
    <referencenumber><![CDATA[R49337]]></referencenumber>
    <apijobid><![CDATA[r49337]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49337/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p></div><div><p>The Manager, Clinical Study Lead may perform the following responsibilities with moderate oversight: accountable for the global execution of assigned smaller or less complex clinical trials from study design, through execution, to study close out. You are accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions</p></li><li><p>Provides operational input into protocol development; leads feasibility assessments to select relevant regions and countries; oversees or conducts site evaluation and selection; and leads investigator meeting preparation and execution</p></li><li><p>Oversees and contributes to study documentation, including case report forms, data management plan, monitoring plan, monitoring oversight plan, project-specific training plan, data review plan, statistical analysis plan, and related materials</p></li><li><p>Oversees set-up and maintenance of study systems (e.g., CTMS, TMF) and ensures compliance with clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs and leads vendor engagement, contracting, and management; ensures CROs and third-party vendors are aligned and delivering per scope of work</p></li><li><p>Provides input into baseline budget and timeline development and management; ensures accurate budget management and scope change control for internal and external studies</p></li><li><p>Leads study-level risk assessment and mitigation; monitors site activation and monitoring visits and acts on deviations; leads development and oversees implementation of patient recruitment and retention strategies and responds to deviations from plan; and monitors data entry and query resolution against agreed metrics</p></li><li><p>Manages study close-out activities, including database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability; contributes to clinical study report writing and review; and facilitates study-level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and have at least six years of relevant industry experience</p></li><li><p>Extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience</p></li><li><p>Strong technical proficiency with trial management systems and Microsoft applications is required, including Project, PowerPoint, Word, Excel, and platforms such as IVRS/IWRS and EDC</p></li><li><p>Experience in global clinical trial operations, including developing protocols and key study documents; solid knowledge of ICH/GCP and relevant regulatory guidelines and directives; and effective project management, cross-functional team leadership, and organizational skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - HEMATOLOGY - COLUMBIA, SC]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48924]]></requisitionid>
    <referencenumber><![CDATA[R48924]]></referencenumber>
    <apijobid><![CDATA[r48924]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48924/medical-account-specialist-ii-hematology-columbia-sc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong> </p><ul><li><p>Field Based</p></li></ul><ul><li><p>Location: Columbia, SC</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results-oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p><strong>To be considered for this opportunity you will have the following:</strong></p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47444]]></requisitionid>
    <referencenumber><![CDATA[R47444]]></referencenumber>
    <apijobid><![CDATA[r47444]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47444/senior-medical-director-clinical-development-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Ophthalmology Therapeutic Area, supporting clinical development programs from first-in-human through registration-enabling studies. In this role, you will serve as scientific and medical lead for clinical team(s), guiding development strategy and regulatory submissions while collaborating with Internal Medicine leadership, executive leadership, development partners, and global regulatory agencies. This role reports to the Vice President, Ophthalmology Therapeutic Area Lead.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY; Cambridge, MA; or Warren, NJ</p></li><li><p><strong>Travel:</strong> 10% to relevant conferences</p></li></ul><br><p><strong>Discover your role:</strong></p><ul><li><p>Act as medical expert and leader in interactions with external stakeholders, internal stakeholders, and decision boards</p></li><li><p>Develop innovative clinical strategies to shorten development cycles amid an evolving regulatory landscape</p></li><li><p>Design efficient, robust Phase 1, 2, and 3 programs</p></li><li><p>Partner with research and discovery teams to inform the next generation of targets in the field</p></li><li><p>Safeguard patient safety in clinical studies and support signal detection from post-marketing surveillance</p></li><li><p>Ensure the quality of clinical documents, including investigator brochures, protocols, study reports, and regulatory submission materials</p></li><li><p>Draft responses to regulatory agency questions and prepare regulatory submission documents</p></li><li><p>Build consensus and drive sound decision-making across dynamic, matrixed clinical teams</p></li></ul><br><p><strong>This role requires:</strong></p><ul><li><p>MD or equivalent medical degree, with board certification or eligibility in Ophthalmology</p></li><li><p>Minimum of 4 years of industry experience in early or late clinical development (candidates with strong academic backgrounds and less experience may be considered)</p></li><li><p>Experience leading proof-of-concept and/or registrational clinical trials, including protocol design and study execution</p></li><li><p>Solid knowledge of global regulatory requirements (ICH) for pharmaceutical development</p></li></ul><p>#MDJobs, #MDJOBSCD, #GDTherapeuticJobs, #Ophthalmology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology - PHILADELPHIA, PA]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49692]]></requisitionid>
    <referencenumber><![CDATA[R49692]]></referencenumber>
    <apijobid><![CDATA[r49692]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49692/medical-account-specialists-hematology-philadelphia-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Philadelphia]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong>: </p><p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to work closely with Reimbursement and Access Specialists, Regional Science Managers, to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li>Field Based</li></ul><ul><li>Location: <strong>Philadelphia, PA</strong></li></ul><p><strong>Discover your role: </strong></p><ul><li>Engage Oncology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of a bispecific agent to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory.</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads to appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identify approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrate dedication to compliance through understanding regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have proven advanced clinically based and account-based selling skills</li><li>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>You are results-oriented with a track record of success with product launches</li><li>You are a strong account manager with analytical, problem-solving and planning skills</li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelor’s degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr Global Procurement- Lab Consumables]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44951]]></requisitionid>
    <referencenumber><![CDATA[R44951]]></referencenumber>
    <apijobid><![CDATA[r44951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44951/sr-mgr-global-procurement-lab-consumables/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager of Global Procurement Lab Consumables role supporting our Research and Pre-Clinical Development. In this role, you will develop and manage sourcing strategies, lead strategic sourcing initiatives, and negotiate supplier agreements while collaborating with Procurement management, cross-functional stakeholders to drive cost savings, efficiency, and category performance.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Schedule: Mon-Fri 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Defines and implements the global Lab Consumables Category strategy to serve global and regional business needs</p></li><li><p>Aligns category priorities with Procurement management and cross-functional stakeholders through strategic sourcing initiatives</p></li><li><p>Manages negotiations, contracting, and supplier relationship management activities for the Lab Consumables category, in consultation with the Law department</p></li><li><p>Drives cost savings, cash flow improvement, and other efficiency gains through category management activities</p></li><li><p>Represents Global Procurement in organizational decisions with critical short- and long-term impact on category performance</p></li><li><p>Leverages market intelligence, benchmarking, and supplier engagement to strengthen Regeneron's knowledge of supply market dynamics</p></li><li><p>Applies data analytics, automation, and visualization tools to generate insights and communicate results to stakeholders and senior leadership</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Sr Manager Level: Bachelor's degree in a relevant field + 8+ years of progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma</p></li><li><p>In-depth knowledge of managing global category processes and suppliers</p></li><li><p>Proven success managing suppliers and category processes across a breadth of categories, driving results through effective sourcing, negotiations, contracting, and supplier relationship management</p></li><li><p>Preferred-Experience with sourcing and contracting tools, ERPs, and eRFx or sourcing platform systems (e.g., Oracle, Zycus, Ariba, LabViva, Zageno, Science Exchange, Scientist.com)</p></li><li><p>Preferred-Experience with data analytics and visualization tools (e.g., Power BI, Tableau, Power Automate)</p></li><li><p>Preferred/nice-to-have: Experience managing and implementing inventory management programs and technologies (e.g., RFID, QR codes, consignment, VMI solutions, single-use materials, biore</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Solid Tumor Oncology (GYN Oncology)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45090]]></requisitionid>
    <referencenumber><![CDATA[R45090]]></referencenumber>
    <apijobid><![CDATA[r45090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45090/medical-director-clinical-development-solid-tumor-oncology-gyn-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Sciences to join our Oncology team, supporting solid tumor drug development, including studies in ovarian cancer. In this role, you will design clinical study concepts, oversee the medical and scientific supervision of clinical trials, and lead the Clinical Team to deliver high-quality program milestones, while collaborating with Clinical Project Managers, Clinical Trial Managers, and Therapeutic Area Program Managers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY</p></li><li><p><strong>Travel: </strong>10% to relevant conferences</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Define clinical trial-related goals and objectives</p></li><li><p>Conduct literature and database research to inform trial design</p></li><li><p>Collaborate with Clinical Project Managers, Clinical Trial Managers, and the Therapeutic Area Program Manager</p></li><li><p>Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings</p></li><li><p>Lead and supervise the Clinical Team to deliver high-quality program milestones on schedule</p></li><li><p>Build and maintain relationships with key study investigators</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MD or MD/PhD with a minimum of 2 years of relevant research experience in industry or the academic research setting</p></li><li><p>Oncology clinical fellowship training with translational and/or clinical research experience strongly preferred</p></li></ul></div><div><div><div><div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs, #Oncology</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology (f/m/d)]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49973]]></requisitionid>
    <referencenumber><![CDATA[R49973]]></referencenumber>
    <apijobid><![CDATA[r49973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49973/director-international-commercialization-immunology-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Munich, Germany - multiple locations are being considered for this role</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>125.250,00 € - 208.750,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Developer - Research and Development]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48042]]></requisitionid>
    <referencenumber><![CDATA[R48042]]></referencenumber>
    <apijobid><![CDATA[r48042]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48042/senior-developer-research-and-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is seeking an outstanding Senior Developer to design, develop, and deliver informatics solutions that enable our research and preclinical development pipeline. This role focuses on LIMS/ELN platform development, scientific data integrations, and building AI-powered capabilities that accelerate scientific workflows. The ideal candidate brings a data-first perspective — approaching every problem by understanding the underlying data, its structure, and how it flows across systems before writing code. You will serve as a technical lead — driving architecture decisions, mentoring team members, and delivering high-quality solutions on COTS platforms including Sapio, Benchling, and Dotmatics.</p><p><strong>Where: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li><p>Own the design and development of server-side plugins, integrations, and workflows on LIMS/ELN platforms (Sapio preferred) using Java and Python</p></li><li><p>Architect and build AI/GenAI-enabled solutions (LLM agents, RAG pipelines, prompt-engineered workflows) to streamline R&pD informatics processes</p></li><li><p>Develop data pipelines and integrations between scientific instruments, LIMS/ELN systems, and enterprise data platforms — owning data modeling, transformation logic, and data quality validation end-to-end</p></li><li><p>Serve as technical lead on projects — defining technical approach, conducting code reviews, and mentoring developers</p></li><li><p>Partner with scientists, lab operations, and product owners to translate scientific requirements into scalable technical solutions</p></li><li><p>Evaluate and implement COTS platform capabilities (Sapio, Benchling, Dotmatics) to enhance out-of-the-box functionality before custom development</p></li><li><p>Design and develop REST APIs, webhooks, and middleware to enable interoperability across R&PD systems</p></li><li><p>Apply a data-first approach to problem-solving — analyze scientific datasets, identify data quality issues, build dashboards and reporting solutions, and translate data insights into actionable recommendations for scientific collaborators</p></li><li><p>Contribute to platform modernization initiatives, including cloud migration and containerized deployments</p></li><li><p>Ensure solutions meet GxP compliance requirements where applicable</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Computer Science, Bioinformatics, Life Sciences, or related field</p></li><li><p>2+ years of work experience in software development supporting life sciences R&D or laboratory informatics</p></li><li><p>Proficiency in Java (server-side development, plugin architectures)</p></li><li><p>Proficiency in Python (scripting, data pipelines, webhooks, automation)</p></li><li><p>Experience with at least one LIMS or ELN platform: Sapio, Benchling, or Dotmatics. Experience with Sapio LIMS/ELN (server-side plugins, workflows, data model configuration) is preferred.</p></li><li><p>Proven experience with AI/GenAI technologies: building LLM-powered agents, prompt engineering, retrieval-augmented generation (RAG), or AI-assisted workflow automation. Experience with AI agent frameworks (LangChain, LlamaIndex, Claude/Anthropic APIs, OpenAI APIs) is preferred.</p></li><li><p>Familiarity with containerization (Docker, Kubernetes) and CI/CD pipelines (Jenkins, GitHub Actions) is a plus</p></li><li><p>Experience with instrument integrations (TetraScience or direct instrument interfaces) is preferred</p></li><li><p>Experience with data analytics and visualization tools (Spotfire, Tableau, Power BI, or Jupyter notebooks) to support data-driven decision-making is a plus</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[AP Service Delivery Coordinator]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48262]]></requisitionid>
    <referencenumber><![CDATA[R48262]]></referencenumber>
    <apijobid><![CDATA[r48262]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48262/ap-service-delivery-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we are seeking an AP Service Coordinator to join our Finance team. In this role, you will be responsible for day-to-day invoice and credit memo processing within Accounts Payable workflow and ERP systems, supporting vendor management activities, resolving payment-related queries, and ensuring accurate and efficient AP operations. You will work closely with internal stakeholders and external vendors while leveraging automation, standard processes, and accounting fundamentals to deliver high-quality financial services.</p><p><strong>When & where:</strong></p><p><strong>Hyderabad (Hybrid)</strong></p><p><strong>Discover your role:</strong></p><ul><li>Process invoices and credit memos through AP workflow and ERP systems using 2-way and 3-way purchase order matching.</li><li>Compile, review, and analyze routine accounts payable transactions to support internal and external business requests.</li><li>Review and reconcile vendor statements, request missing invoices or credit notes, and coordinate resolution of discrepancies with vendors and internal teams.</li><li>Manage accounts payable inquiries, ensuring timely investigation and resolution of vendor and end-user issues.</li><li>Support departmental goals through execution of assigned AP-related activities and process improvements.</li><li>Utilize AP automation tools, accounting principles, and best practices to improve efficiency and accuracy.</li><li>Build and maintain strong working relationships with internal stakeholders and external vendors to facilitate timely issue resolution.</li><li>Provide backup support for AP Coordinator II responsibilities and assist with invoice entry as required.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Accounting, Finance, Commerce, or a related discipline.</li><li>0-2 years of Accounts Payable experience.</li><li>Basic understanding of accounting principles and strong English communication skills.</li><li>Excellent organizational skills with the ability to manage high volumes of work in a fast-paced environment.</li><li>Strong analytical, problem-solving, and attention-to-detail capabilities.</li><li>Ability to adapt quickly to changing priorities and business requirements.</li><li>Strong interpersonal and stakeholder management skills.</li><li>Proficiency in Microsoft Office applications, including Excel, Outlook, Word, and PowerPoint.</li><li>Experience with Oracle ERP systems, document scanning, and invoice workflow systems is preferred.</li><li>Advanced working knowledge of MS Excel and MS Outlook is highly desirable.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Plant Utilities Technician (Nights)]]></title>
    <date><![CDATA[Sun, 30 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48940]]></requisitionid>
    <referencenumber><![CDATA[R48940]]></referencenumber>
    <apijobid><![CDATA[r48940]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48940/plant-utilities-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking to add a Plant Utilities Technician to our team. 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. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Rensselaer, New York, United States</li><li>Working shift: Wednesday-Saturday 2:00pm-12:30am</li><li>Training shift: Monday-Friday 7:00am-3:30pm for approximately 3 months</li></ul><br><h3>What you’ll do:</h3><ul><li>Maintain high pressure steam and hot water boilers, controls, and associated equipment; maintain boiler and cooling tower chemical treatment program</li><li>Maintain all other Plant Utility equipment such as boiler pretreatment water, condensate return, natural gas, domestic potable water, tepid water, and wastewater</li><li>Review, monitor, respond to, and react to alarm notifications from the Building Automation Systems (BAS)</li><li>Perform Plant Utility monthly Preventative Maintenance</li><li>Plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Schedule, assign, complete, and review incursions specific to Plant Utility activities</li><li>Communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Maintain documents and records on all plant equipment and systems</li><li>Collaborate with other departments, contractors, and subject areas on scheduling repairs and maintenance of plant utility systems</li></ul><br><h3>This role requires:</h3><ul><li>AAS degree, preferably in an Engineering or Construction Technologies related area, and the following minimum amounts of experience for each level:<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><li>Plant Utilities Technician IV: 8+ years of related experience, or HSD/GED with 12+ years of related experience</li></ul></li><li>Experience with or knowledge of high-pressure boilers and waste neutralization</li><li>Working with chemicals and steam</li><li>Participating in rotational on-call schedule</li><li>Prior experience in the maintenance and operation of a large-scale utilities plant is preferred.</li></ul><p>Level will be determined based on qualifications relevant to the role</p><br><h3>The environment and physical rhythms of this role:</h3><ul><li>Gowning: Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, makeup and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but are not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Oncology Marketing - Austria, Switzerland  & Portugal]]></title>
    <date><![CDATA[Sat, 22 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47355]]></requisitionid>
    <referencenumber><![CDATA[R47355]]></referencenumber>
    <apijobid><![CDATA[r47355]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47355/senior-manager-oncology-marketing-austria-switzerland-portugal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><div><div><div><div><div><div><div><div><h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><div><div>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Oncology Marketing, DACH & Portugal to join our International Commercial team, supporting our oncology business across Austria, Switzerland, and Portugal in a hybrid work model. In this role, you will develop and deliver brand strategy across international markets while collaborating with Medical Affairs, global teams, agencies, and external partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</div></div><br><div><strong>When</strong> <strong>&</strong> <strong>where:</strong></div><div><div>Austria & Field Based </div></div><br><div><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></div><ul><li><div>Lead local brand marketing plan development and execution.</div></li><li><div>Analyse market dynamics to find opportunities and identify risks.</div></li><li><div>Shape brand strategy aligned with global direction.</div></li><li><div>Partner with Medical Affairs on market approaches.</div></li><li><div>Drive compliant promotional activities across channels.</div></li><li><div>Adapt global materials for local market use.</div></li><li><div>Plan congresses, healthcare professional engagement, and events.</div></li><li><div>You build positive relationships while balancing strategy and execution.</div></li></ul><br><div><strong>This</strong> <strong>role</strong> <strong>requires:</strong></div><ul><li><div>Bachelor’s degree in business, science, or a related field.</div></li><li><div>8-10+ years’ experience in pharmaceutical or biotechnology brand marketing.</div></li><li><div>Strong knowledge of the Austrian and Swiss healthcare markets.</div></li><li><div>Experience managing agencies and external partners.</div></li><li><div>Knowledge of healthcare compliance and promotional regulations.</div></li><li><div>Proficiency in English & German.</div></li><li><div>Willingness to travel approximately 30-40%.</div></li><li><div>Experience in oncology marketing, including immuno-oncology, preferred.</div></li><li><div>Product launch experience preferred.</div></li><li><div>Strong prioritization, relationship-building, and budget management skills.</div></li></ul></div></div></div></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€87,525.00 - €145,875.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Rare Disease Commercial Operations]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50152]]></requisitionid>
    <referencenumber><![CDATA[R50152]]></referencenumber>
    <apijobid><![CDATA[r50152]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50152/senior-manager-rare-disease-commercial-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Commercial Operations Rare Disease Japan to join our Commercial Operations team, supporting our Japan business in a hybrid work model. In this role, you will provide proactive commercial operations and analytics support while collaborating with Commercial, Corporate, HR, IT, and above-market teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Japan</p><p>Hybrid work model</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead customer targeting, segmentation analysis, and key account planning.</li><li>Create insights through reports and presentations to support decisions.</li><li>Develop patient cohorts, treatment journey mapping, and demand forecasts.</li><li>Manage commercial field communications and approval processes.</li><li>Maintain customer and activity data through CRM and master data processes.</li><li>Coordinate onboarding and offboarding with HR, IT, and key stakeholders.</li><li>Support HCP contracting, meetings, events, sponsorships, and memberships.</li><li>You thrive in changing environments and proactively solve operational challenges.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree and 8+ years of pharmaceutical or biotechnology commercial experience.</li><li>5 years of global collaboration experience in commercial operations or equivalent.</li><li>Understanding of Japan rare disease biopharmaceutical market dynamics, laws, and regulations.</li><li>Functional field support experience in the Japan market.</li><li>Expertise in data analysis and storytelling.</li><li>Proficiency with Microsoft Excel, PowerPoint, Word, Veeva, and analytical tools.</li><li>Experience managing multiple projects and delivering against deadlines.</li><li>Strong organizational, project management, change management, and presentation skills.</li><li>Strong interpersonal, facilitation, communication, problem-solving, and collaboration skills.</li><li>Intermediate English and native-level Japanese communication skills.</li><li>Experience in a biopharmaceutical field operations role, particularly in rare disease, is preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Facilities Engineer]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48619]]></requisitionid>
    <referencenumber><![CDATA[R48619]]></referencenumber>
    <apijobid><![CDATA[r48619]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48619/principal-facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Principal Facilities Engineer</strong> to join our Facilities Operations, Utilities & HVAC team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Designing and specifying cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</li><li>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</li><li>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</li><li>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and maintenance processes</li><li>Preparing engineering evaluations and test plans for and executes modification change control documentation</li><li>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</li><li>Maintaining company reputation by enforcing compliance with all relevant laws, policies and regulations</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have strong analytical and interpersonal skills</li><li>You are able to prioritise and re-prioritise as needed and adapt to change</li><li>You are comfortable working in a fast-paced setting</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><strong>Principal</strong> - Requires BS/BA in Mechanical engineering with 8+ years of relevant experience or equivalent combination of education and experience.</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€63,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Automation (Overnights)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49538]]></requisitionid>
    <referencenumber><![CDATA[R49538]]></referencenumber>
    <apijobid><![CDATA[r49538]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49538/supervisor-automation-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are looking to add a Supervisor Automation to our growing team, ensuring that automated manufacturing equipment, plant utilities, and packaging equipment are fully operational and reliable in order to support manufacturing operations. As a domain authority on automation equipment and systems you will supervise a team of Automation Technicians and contracted resources that support automation work. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Working model: Tuesday - Saturday 12AM - 8:30AM</p></li><li><p>Training shift: Monday - Friday 8:00AM - 4:30PM approximately 6 weeks</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Provide mentoring and development opportunities to Automation Technicians while also providing supervisory support of activities on the plant floor</p></li><li><p>Full gowning when entering and working on production floor</p></li><li><p>Plan, coordinate, and schedule required maintenance/repairs on automated systems</p></li><li><p>Communicate and coordinate automation issue resolution between Automation, Manufacturing and Facilities groups</p></li><li><p>Support team in maintaining, diagnosing, troubleshooting and repairing automation equipment and systems</p></li><li><p>Support deviation management process, including review of investigation reports, root cause analysis and corrective actions</p></li><li><p>You are well versed in automation concepts, possessing strong mechanical and electrical proficiency</p></li><li><p>Demonstrate experience in the operation and maintenance of automation equipment/systems and have working knowledge of Allen Bradley and/or Siemens PLCs, HMIs, and computerized systems</p></li><li><p>Have leadership/supervisory experience, with the ability to lead and mentor others</p></li><li><p>Possess strong critical thinking, communication, and technical troubleshooting skills</p></li><li><p>Take initiative and empower others in times of uncertainty, while balancing changing priorities in a dynamic environment</p></li><li><p>Possess a basic understanding of data integrity regulations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Must have an AS/AT/AAT degree in Engineering or a related field along with 5+ years of relevant experience or an equivalent combination of education and experience</p></li><li><p>Experience in a pharmaceutical or biopharmaceutical manufacturing facility is desired</p></li><li><p><strong>Gowning and Physical Requirements:</strong> </p></li><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) Ability to remove jewelry, makeup and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but are 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>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Madrid Oeste-Sur, Toledo, Ciudad Real, Cáceres]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50499]]></requisitionid>
    <referencenumber><![CDATA[R50499]]></referencenumber>
    <apijobid><![CDATA[r50499]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50499/sales-representative-madrid-oeste-sur-toledo-ciudad-real-caceres/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Gastroenterology business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Madrid Oeste-Sur, Toledo, Ciudad Real, Cáceres</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 11 Sep 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Product Management]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50115]]></requisitionid>
    <referencenumber><![CDATA[R50115]]></referencenumber>
    <apijobid><![CDATA[r50115]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50115/director-product-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Director Product Management </strong><strong>(Sleepy Hollow, NY)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks a Director Product Management (Sleepy Hollow, NY) to support day-to-day improvements, configuration, and setup changes in Oracle ERP to provide efficiency and support business operation’s needs, and be responsible for end-to-end delivery for any projects, improvements, and support. Act as a liaison to Finance and Supply Chain. Partner multi-functionally across SS&P, HR, Legal, and Manufacturing verticals to ensure systems integrate and operate as designed and intended to support global process execution to deliver the best stakeholder and customer experience. Utilize best practices for defining business capabilities, understanding core requirements, and handling vendors for implementation and ongoing support. Ensure and maintain Application, Integration, and Data architectures for responsible areas and overall ERP eco-system. Implement integrated and automated processes that drive efficiency. Establish and sustain knowledge continuity through appropriate level of documentation, cross training, and vendor management for not only System Configs (BR.100) but also Functional (MD.050) and technical specs (Md.070) including API Integrations and any data exchange with 3rd party systems. Establish governance and tight change control processes and ensure they are rigorously followed across the organization, with respect to Oracle System Configuration changes, setups, extensions and customizations, and integrations to always ensure ITGC SOX Controls. This includes all Finance-related applications, external and internal. Work with the development team to ensure that all software, platform, and SaaS including 3rd party software are up to date and patched up to mitigate any risk due to out-of-support software. Institute and maintain tight Identity and Access Controls across key and sensitive corporate systems (using RBAC / ABAC) to ensure we align with Regeneron’s Security controls and mitigate Security risks by removing excessive access rights. Streamline and standardize financial templates and deliverables. Two (2) Direct Reports in the positions of Product Manager. Local telecommuting permitted up to 1 day per week. 15% domestic travel required to attend conferences, business meetings and workshops, training, and other business-related activities and 10% international travel required.</p><p>WORK SCHEDULE: 40 hrs/wk, M-F (9:00am –5:00pm)</p><p>SALARY RANGE: $260,000 - $305,200 per year</p><p><strong>Job Requirements</strong><strong>:</strong></p><p>Requires a Bachelor’s degree in Computer Science, Industrial Engineering or a related field and 10 years of experience in Oracle or other IT applications. Must have 5 years of experience with: Analyzing supply chain-related business problems to develop Oracle-based computer solutions; Partnering and working with Global Order to Cash multi-functional workstreams, and business enablement functions on the implementation of new business capabilities enabled by IT such as Order Management, BOM, Inventory, Procure to Pay, Supplier Collaboration, VAT, or Intercompany. Must have experience with: 3PL; Order to Cash and Supply Chain touchpoints; Multiple best-in-class solutions like Oracle EBS Order to Cash, VAT, (EDI, Intercompany, AR/AP, Procurement, Sourcing, Cost Mgt, BOM, or Inventory) and Oracle Fusion; Migrating Oracle EBS 12.1.3 or 12.2 to Oracle Fusion; Analyzing business and data processing problems to implement and improve computer systems for Operations, Supply Chain, Logistics, and Procurement; Assisting Operations, Supply Chain, Logistics, and Procurement teams to solve computer-related problems, including day-to-day production support issues, and product/process leadership for all projects and enhancements; Leading solution design, testing, maintaining, and monitoring a company’s computer systems, specifically its Oracle software including Supply Chain, Inventory, iSupplier, Procure to Pay (P2P) process, and Electronic Data Interchange (EDI) Transactions; Adapting company’s IT systems to improve Supply Chain workflows by integrating Supply Chain data with Oracle applications</p><p>to manage regulatory and reporting needs; Practical knowledge of Supply Chain business processes to analyze user requirements, procedures, and problems to automate and improve a company’s existing systems and review its system capabilities; Recommending the most effective software needed to set up/modify systems and lead all configuration, best practice setup, and integration efforts for the Oracle Supply Chain, Inventory, and Procure to Pay modules; Analyzing information processing needs through document analysis, requirements workshops, scenarios, business analysis, and implementation to develop project scope and requirements to plan and design computer systems; Developing implementation plans for systems projects that maximize resource allocation, ensure timely delivery, and optimize technology solutions by collaborating with project managers; Preparing cost-benefit and return on investment analyses to aid in decisions on system implementation; Ensuring agreement on system principles and working closely with Supply Chain team to improve workflow, ensuring systems support delivery requirements; Leading, training, and mentoring functional users to work with IT systems and make appropriate business process and information delivery changes/decisions that deliver desired results; Conferring with internal clients regarding the nature of business needs to be addressed by computer systems and work with the business to build case justifications for Supply Chain and Procurement system initiative requests; Defining system goals by translating business requirements into functional specifications, describing logical operational steps of systems, and developing procedures for regression, and integration/QA testing; Developing, documenting, and revising standardized policies and procedures for new IT solutions, in accordance with established IT standards; Providing effective project control by monitoring progress and providing appropriate updates to senior management; Managing and mentoring SME resources in different business tracks; IT Product management and Inhouse IT product design; Project estimation and Project Management; Vendor management and project negotiation; Product delivery and life cycle management with Information security scope coordination; and Designing and enhancing external user facing tools with Agile methodology via Jira stories. 15% domestic travel required to attend conferences, business meetings and workshops, training, and other business-related activities and 10% international travel required.</p><h3>To apply for this position, visit <a href="https://careers.regeneron.com">https://careers.regeneron.com</a> Reference code: R50115.</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45803]]></requisitionid>
    <referencenumber><![CDATA[R45803]]></referencenumber>
    <apijobid><![CDATA[r45803]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45803/director-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director </strong>to join our <strong>Patient Safety</strong> team.</p><br><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><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA</li><li>4 days per week on site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>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.)</li><li>Leads cross-functional Safety Monitoring Team (SMT) activities</li><li>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)</li><li>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</li><li>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</li><li>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </li><li>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</li><li>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.</li><li>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.</li><li>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</li><li>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</li><li>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </li></ul><br><p><strong>This role requires:</strong></p><ul><li>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). </li><li>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</li><li>Clinical experience and/or industry experience in Oncology is a plus</li></ul><br><p>#MDJOBSPS #GDPSJobs</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Affairs,  Cutaneous Oncology (CA, NV, HI)]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50518]]></requisitionid>
    <referencenumber><![CDATA[R50518]]></referencenumber>
    <apijobid><![CDATA[r50518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50518/associate-director-medical-affairs-cutaneous-oncology-ca-nv-hi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs responsible for engaging in the exchange of scientific data and other medical and/or scientific information with key opinion leaders (KOLs), health care providers (HCPs), researchers, pharmacists and population-based decision makers. We demonstrate a thorough understanding of solid tumors, including cutaneous oncology, and other tumors of interest within clinical development and aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Field- CA, NV, HI (preference for candidates residing in San Francisco, Los Angeles, or San Diego areas</p><p>• Travel: approximately 50% of the time, including air travel, overnight and occasionally on weekends</p><p><strong>Discover your role: </strong></p><p>• Establish, foster, cultivate and maintain peer relationships with KOLs. <br>• Act as the primary clinical/scientific resource to HCPs for information pertaining to disease state and our product(s) to ensure awareness and understanding.<br>• Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.<br>• Support evidence generation (company sponsored trials and investigator initiated studies (IIS)) research initiatives<br>• Identify and report medical insights.<br>• Identifies gaps in research and educational needs to inform medical strategy.<br>• Responds to requests for information and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.<br>• Performs disease management and therapeutic area education with identified practitioners, payers and researchers.<br>• Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence with the purpose of informing internal partners.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><p><strong>This role requires:</strong> <br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience as an Oncology Medical Science Liaison function is required.<br>• Knowledge or experience in the Oncology therapeutic area is required, and experience in cutaneous oncology is preferred.<br>• Established relationships with KOLs in thoracic malignancies and knowledge of institutions focused on Solid Tumor Malignancies preferred.<br>• Drug launch experience is strongly preferred.<br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines.<br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.</p><p>#ofm #msl #medicalscienceliaison</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Auditor]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47018]]></requisitionid>
    <referencenumber><![CDATA[R47018]]></referencenumber>
    <apijobid><![CDATA[r47018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47018/senior-it-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior IT Auditor is responsible for contributing towards planning, executing, and reporting on operational IT audits, evaluating risks and controls, including application, infrastructure, cloud, data management, SDLC, change management, and IT operations, in accordance with IIA standards and department methodologies. Perform IT SOX control walkthroughs and testing, along with preparing the related documentation. Assess the effectiveness of cybersecurity controls, including identity and access management, vulnerability management, logging and monitoring, incident response, and security governance. <br> </p><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include the following:</strong> </p><div><ul><li><p>Review controls related to cloud computing (e.g., AWS, Azure), SaaS platforms, data lakes, and analytics environments, including shared responsibility models. </p></li></ul></div><div><ul><li><p>Design and execute data analytics‑driven audit procedures using tools such as Dataiku or equivalent, to identify anomalies, trends, and control gaps. </p></li></ul></div><div><ul><li><p>Apply automation, continuous auditing techniques, and responsible use of AI, where appropriate, to improve audit efficiency, coverage, and insight, including assessing AI‑enabled business processes and controls. </p></li></ul></div><div><ul><li><p>Manage timely completion of audit tasks, including communication of status to the auditee and the Manager/Director. </p></li></ul></div><div><ul><li><p>Identify, document, and communicate control deficiencies, root causes, technology risks, and opportunities for improvement, providing practical, actionable recommendations aligned with business objectives. </p></li></ul></div><div><ul><li><p>Present the results of audit work to Internal Audit Management and auditees, including practical recommendations to address identified risks and/or weaknesses in internal controls as well as opportunities to enhance operational efficiencies. </p></li></ul></div><div><ul><li><p>Prepare clear, concise, and professional audit reports and executive‑level presentations for Internal Audit leadership, management, and key stakeholders. </p></li></ul></div><p><strong>This role might be for you if have experience with :</strong></p><div><ul><li><p>Advanced knowledge of IT infrastructure, applications, cybersecurity, and automated controls </p></li></ul></div><div><ul><li><p>Strong understanding of SOX, COSO, COBIT, NIST, GxP, GDPR, and other relevant regulatory and governance frameworks. </p></li></ul></div><div><ul><li><p>Strong analytical, critical‑thinking, and problem‑solving skills, with the ability to independently assess risk and propose solutions. </p></li></ul></div><div><ul><li><p>Comfortable working and learning independently and as part of a team </p></li></ul></div><div><ul><li><p>Excellent interpersonal, communication and writing skills, strong organizational abilities, and attention to detail are required </p></li></ul></div><div><ul><li><p>Experience with data analytical tools (e.g. Dataiku, Alteryx, etc.) </p></li></ul></div><div><ul><li><p>Understanding of AI concepts, associated risks (e.g., model governance, data quality, access, ethical use), and internal controls relevant to AI‑enabled processes. </p></li></ul></div><p><strong>To be considered for this role</strong>, you must have a Bachelor's degree with a<strong> </strong>minimum of 3 - 4 years of progressive experience in IT audit, information security, or technology risk. CISA, CISM and/or CISSP certifications/license preferred. Experience auditing and evaluating infrastructure, cybersecurity risks/controls and auditing operating systems. Pharmaceutical, life sciences, or other regulated industry experience strongly preferred. Big 4 or public accounting experience preferred but not required. </p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences Delivery, Oncology]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50541]]></requisitionid>
    <referencenumber><![CDATA[R50541]]></referencenumber>
    <apijobid><![CDATA[r50541]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50541/director-global-patient-safety-sciences-delivery-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[[Unknown]]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director to join our Safety Sciences Delivery team, supporting our oncology portfolio in a hybrid model. In this role, you will lead compliant safety operations and serve as the primary oncology contact while collaborating with Safety Sciences Strategy and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Multiple locations are being considered for this role (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Standardise practices, processes, and templates for signal detection and safety-document authoring.</p></li><li><p>Ensure compliant Safety Sciences Delivery activities through regulations, standard operating procedures, and monitoring tools.</p></li><li><p>Lead oncology signal detection and management, including Safety Monitoring Teams, surveillance plans, and evaluation reports.</p></li><li><p>Integrate innovative technologies into core safety activities.</p></li><li><p>Analyse aggregate data with Safety Sciences Strategy to identify emerging safety issues and patterns.</p></li><li><p>Coordinate benefit-risk assessments and safety contributions across periodic reports and portfolio documents.</p></li><li><p>Develop standardised training curricula, proficiency matrices, and knowledge repositories across Strategy and Operations.</p></li><li><p>You build, coach, and scale teams through succession planning, talent pipelines, and leadership development.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced life sciences or healthcare degree with 12+ years of pharmacovigilance experience.</p></li><li><p>Safety Sciences experience, preferably within oncology.</p></li><li><p>Strong leadership, communication, organisation, workload planning, and detail orientation.</p></li><li><p>Ability to optimise safety operations and manage multiple projects.</p></li><li><p>Global patient safety operations oversight experience preferred.</p></li><li><p>Matrix leadership, people management, and artificial intelligence technology experience preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 11 Sep 2026 03:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development Quality Lead Japan]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45173]]></requisitionid>
    <referencenumber><![CDATA[R45173]]></referencenumber>
    <apijobid><![CDATA[r45173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45173/senior-manager-global-development-quality-lead-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Global Development Quality Lead – Japan, to join our Global Development Quality & Regulatory Compliance team, supporting our Japan affiliate in a hybrid work model. In this role, you will drive quality and compliance in local operations by providing expert guidance and leadership for the Regeneron quality management system supporting GCP, GVP, Medical and Regulatory Affairs. You will collaborate with cross-functional teams and key stakeholders across local and global functions. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Japan<br>Work model: Hybrid</p><p><strong>Discover your role:</strong></p><ul><li>Lead quality and compliance activities for GCP, GVP, Medical and Regulatory Affairs at the Japan affiliate.</li><li>Build strategic partnerships and drive proactive, risk-based quality initiatives, including audits, with key stakeholders.</li><li>Optimize inspection readiness and support inspection preparation for local affiliate operations.</li><li>Contribute to process improvement initiatives and lead projects aligned with quality objectives.</li><li>Manage issue resolution and escalate serious non-compliances through established processes.</li><li>Provide expert guidance, training, and support on international regulations and Regeneron standards.</li><li>Line manage, coach, and mentor junior team members or serve as process owner, as assigned.</li><li>You exemplify a quality mindset, professional conduct, and continuous learning in all interactions.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree (or equivalent experience) and at least 8 years of relevant healthcare/pharmaceutical industry experience.</li><li>Advanced knowledge and application of GCP guidelines, including managing complex quality and compliance issues.</li><li>Experience in quality/compliance or clinical development roles, with expertise in GCP.</li><li>Proven ability in training, supervising, line management, and staff development.</li><li>Strong project management, planning, prioritization, and time management skills.</li><li>Advanced digital literacy, including Microsoft Office suite.</li><li>Effective communication and stakeholder engagement skills, with ability to influence senior leaders.</li><li>Demonstrated ability to manage multiple priorities with urgency and attention to detail.</li><li>Understanding of risk-based quality management and process improvement.</li><li>Business level fluency in Japanese and English language</li><li>Behavioral strengths including integrity, adaptability, critical thinking, and collaborative problem solving.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Barcelona Tarragona (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50497]]></requisitionid>
    <referencenumber><![CDATA[R50497]]></referencenumber>
    <apijobid><![CDATA[r50497]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50497/sales-representative-barcelona-tarragona-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Barcelona Tarragona</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Toxicology]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50772]]></requisitionid>
    <referencenumber><![CDATA[R50772]]></referencenumber>
    <apijobid><![CDATA[r50772]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50772/senior-director-toxicology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Director, Toxicology to apply advanced knowledge of toxicology and pharmaceutical drug development to advance therapeutic assets through all stages of development. Working individually, or in collaboration with one or more direct reports, you will solve complex scientific and strategic/regulatory problems using extensive drug development experience, as well as state-of-the-art approaches in toxicology, pharmacology, and related disciplines. You'll communicate clearly and effectively at all levels of the organization and positively impact program strategy beyond the core discipline of Toxicology. You will also provide mentoring and management of junior scientific staff, offering relevant project-related guidance and career development, and will work with Toxicology leadership on the review and development of policies and procedures related to the conduct of toxicology research at Regeneron.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><br><ul><li>Full-time, standard business hours, with flexibility to support before- and after-hours executive meetings, town halls, and corporate events</li><li>Location: Tarrytown, NY</li></ul><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Applies advanced knowledge of pharmacology, toxicology, and related disciplines to the design and implementation of preclinical safety programs to support development of new products</li><li>Ensures effective communication with line-management on all ongoing project activities, status, and issues relating to programs and personnel</li><li>Writes and/or reviews relevant portions of INDs, BLAs, and other regulatory documents as needed to support program development</li><li>Communicates effectively with global regulatory authorities in writing, by teleconference, and during face-to-face meetings as necessary</li><li>Develops and maintains appropriate external contacts to further the advancement of development programs (e.g., contract research organizations, industry-wide scientific societies, regulatory agencies, academic research organizations)</li><li>Provides consultative toxicology support to scientists and colleagues in other functional areas</li><li>Maintains a deep understanding of industry trends and regulatory requirements across all major geographic regions and applicable therapeutic areas</li><li>Contributes as Toxicology representative to corporate due diligence activities when called upon</li><li>Contributes to the drafting and finalization of SOPs and working practices as requested</li><li>Provides mentoring and/or supervision to junior scientific staff or direct reports, as appropriate</li><li>May be called upon to recruit, interview, and hire new scientific staff to meet the needs of the department</li></ul><br><h3><strong>This role requires:</strong></h3><br><ul><li>Advanced degree (e.g., MS, PhD, DVM) in toxicology or a closely related biological science, along with 15+ years of experience, or a Master's Degree plus 20+ years, working in toxicology/safety assessment, drug development, or a contract research organization</li><li>Significant experience or training in the development of biologic therapeutics</li><li>Board Certification in Toxicology is desirable</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 13:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Specialist, Drug Product]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48374]]></requisitionid>
    <referencenumber><![CDATA[R48374]]></referencenumber>
    <apijobid><![CDATA[r48374]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48374/qa-specialist-drug-product/]]></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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support QA initiatives for a broad range of topics relative to the start-up and operations of a drug product facility. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p>When & where:</p><ul><li>1st shift, Monday-Friday, 8am-4:30pm</li><li>Location: Rensselaer, New York, United States</li></ul><p>What you’ll do:</p><ul><li>Work on and potentially lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team</li><li>Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures</li><li>Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.</li><li>Maintain project timelines to support the evolving business</li><li>Perform on-the-floor quality review of documents, such as: equipment logs, training records, testing results, batch records and supporting documents</li><li>Review and approval of documents (electronic and paper-based)</li><li>Provide mentorship during on-the-floor manufacturing</li><li>Support audits, inspections and investigations</li><li>Perform quarantine, segregation of material and line clearances</li><li>Contribute to the continuous improvement initiatives</li><li>Adjust schedule based on facility start up, filling, and manufacturing needs</li><li>Collaborate with cross-functional internal teams</li></ul><p>The environment and physical rhythms of this role:</p><ul><li>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Let’s find out if we’re a fit:</p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Assoc QA Specialist : 2+ years of experience</li><li>QA Specialist : 4 + years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p>Thrive today. Grow tomorrow.</p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family Care Benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Maintenance Technician (Nights)]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50594]]></requisitionid>
    <referencenumber><![CDATA[R50594]]></referencenumber>
    <apijobid><![CDATA[r50594]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50594/process-maintenance-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> </p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Process Technician to join our manufacturing operations team, supporting biopharmaceutical production onsite. In this role, you will keep manufacturing, utility, and building systems running safely and in strict cGMP compliance. You will work closely with Facilities Management and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p><br><p><strong>When & where: </strong> </p><ul><li>Location: East Greenbush, New York, United States</li><li>Working shift: Sunday-Wednesday 2:00pm-12:30am </li></ul><ul><li>Training shift: Monday-Friday 6:00am-2:30pm </li><li>On-call: Rotational on-call support required </li></ul><br><p><strong>What you’ll do:</strong> </p><ul><li>Perform daily operations, maintenance, and repairs on utility systems, manufacturing equipment, and building systems in a cGMP environment. </li></ul><ul><li>Ensure safe, hands-on maintenance of plant manufacturing and support equipment. </li></ul><ul><li>Identify off-nominal conditions and troubleshoot mechanical issues on manufacturing and utility equipment in a clean room environment. </li></ul><ul><li>Complete daily Work Orders and Preventive Maintenance, coordinating workflow and documentation. </li></ul><ul><li>Troubleshoot electrical equipment during off-nominal conditions, locating faults and performing repairs. </li></ul><ul><li>Coordinate with Facilities Management and other departments during planned and unplanned work events. </li></ul><ul><li>Bring a safety-minded focus and a drive for continuous improvement to everything you do. </li></ul><br><p><strong>The environment and physical rhythms of this role:</strong> </p><ul><li>Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </li></ul><ul><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </li></ul><ul><li>Ability to lift, push, and pull up to 50 pounds </li></ul><br><p><strong>Let’s find out if we’re a fit: </strong> </p><ul><li>AAS degree, preferably in Engineering or Construction Technologies with the following minimum years of related equipment maintenance experience for each level:<ul><li>Process Technician II: 2+ years or HSD/GED with 5+ years of related experience</li><li>Process Technician III: 5+ years or HSD/GED with 8+ years of related experience</li></ul></li></ul><ul><li>Ability to interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications. </li></ul><ul><li>Prior experience in equipment maintenance or a related role requiring mechanical skills. </li></ul><ul><li>Ability to fully gown and work on the production floor. </li></ul><ul><li>Commitment to compliance with regulatory, corporate, and site-specific policies and procedures.</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 13:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Tacoma, WA & Anchorage, AK]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50509]]></requisitionid>
    <referencenumber><![CDATA[R50509]]></referencenumber>
    <apijobid><![CDATA[r50509]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50509/medical-specialist-i-allergyent-tacoma-wa-anchorage-ak/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><br><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><br><p><strong>When & where:</strong></p><ul><li>Remote role</li><li>Location: <strong> Tacoma, Washington Allergy/ENT territory</strong></li><li><strong>Key Markets include </strong>Tacoma, Olympia, Anchorage, Fairbanks, Covington</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</li><li>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</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>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings, and medical conferences.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>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 </li><li>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</li><li>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments</li><li>This role requires the ability to travel and cover large geographic territories</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,743.00 - $209,358.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 25 Sep 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant - Temporary]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50685]]></requisitionid>
    <referencenumber><![CDATA[R50685]]></referencenumber>
    <apijobid><![CDATA[r50685]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50685/executive-assistant-temporary/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Administrative Coordinator Commercial Oncology Leadership International to join our Commercial Oncology team, supporting our International Oncology business in a hybrid work model. In this role, you will enable senior leaders and cross-functional teams to operate efficiently by coordinating business activities, managing priorities, facilitating global collaboration, and delivering seamless administrative support. Working closely with commercial leaders, internal partners, and external stakeholders, you will help create an organized, connected, and high-performing environment that supports business objectives. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Dublin</p><p>Work model: Hybrid</p><p>Temporary 6 months</p><br><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Coordinate complex meetings across multiple time zones, managing logistics, venues, technology, travel, and accommodations to ensure seamless execution.</li><li>Manage dynamic executive calendars, prioritize requests, schedule meetings, and support the efficient use of leadership time.</li><li>Arrange business travel and transfers while preparing and reconciling expense reports through established expense management processes.</li><li>Provide project coordination and administrative support, including document preparation, electronic filing, invoice handling, and general office administration.</li><li>Organize internal and visitor events, coordinating meeting rooms, catering, invitations, and end-to-end event logistics.</li><li>Partner with Facilities, Information Technology, Human Resources, and external vendors to address operational needs and support business continuity.</li><li>You anticipate needs, manage multiple priorities with confidence, and build trusted relationships across a diverse international organization.</li></ul><br><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>Experience providing administrative or executive support to senior leaders within a fast-paced, cross-functional business environment.</li><li>Experience with expense management systems; Concur experience is advantageous.</li><li>Strong technical proficiency with business technology, communication platforms, meeting room reservation systems, and mobile tools.</li><li>Proven ability to coordinate complex travel arrangements, meetings, events, and business administration activities.</li><li>Excellent organizational skills with the ability to manage multiple projects, deadlines, and competing priorities simultaneously.</li><li>Exceptional attention to detail, accuracy, and time management skills.</li><li>Ability to work independently with minimal supervision while exercising sound judgment and discretion.</li><li>Strong interpersonal skills with the ability to build effective relationships across functions, seniority levels, and external partners.</li><li>Ability to handle and commercially sensitive information with the highest level of professionalism and integrity.</li><li>Demonstrated flexibility, adaptability, proactivity, and a customer-focused approach to support.</li></ul><p><br><br></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 07:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs, Gastroenterology]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50708]]></requisitionid>
    <referencenumber><![CDATA[R50708]]></referencenumber>
    <apijobid><![CDATA[r50708]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50708/medical-director-medical-affairs-gastroenterology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Medical Affairs to join our Gastroenterology and Immunology team, supporting our US medical strategy across sites in Sleepy Hollow, NY, Warren, NJ, or Cambridge, MA. In this role, you will help shape and execute medical strategy for a key asset, oversee generation and dissemination of high-quality scientific data, and ensure medical activities are delivered with integrity and scientific rigor, while collaborating with field medical, medical operations, R&D, commercial, access & reimbursement, patient advocacy, and external clinical experts.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Sleepy Hollow, NY (preferred) or Warren, NJ or Cambridge, MA</li><li>Travel percentage: 30% U.S. travel, with occasional global travel</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Develop and oversee US medical strategy and tactics for a key asset, including publications, field communications, and expert collaborations</li><li>Apply deep therapeutic expertise to address current and future medical needs in clinical practice</li><li>Lead generation and dissemination of clinical and non-clinical data supporting the medical strategy</li><li>Partner across a cross-functional Medical Product Team, R&D, commercial, and access & reimbursement to drive alignment</li><li>Cultivate long-term strategic relationships with clinical experts, societies, advocacy groups, and alliance partners</li><li>Co-lead formation and execution of Phase 3b/4 plans where applicable</li><li>Champion high standards of compliance, ethics, and patient safety across all medical activities</li><li>Oversee medical review of promotional materials and training content for scientific accuracy</li></ul><h3><br></h3><h3><strong>This role requires:</strong></h3><ul><li>Medical degree (MD, MBBS, or equivalent) </li><li>Relevant residency or fellowship training in gastroenterology or allergy/immunology preferred</li><li>8+ years of relevant medical/scientific experience</li><li>Demonstrated ability to lead technical and business discussions with internal and external stakeholders</li><li>Strong presentation and communication skills, with the ability to deliver succinct, strategic insight to senior management</li><li>Thorough understanding of the healthcare environment and its external stakeholders</li></ul><br><p>#MDJOBS, #MDJOBSMA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 21:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Bioassay Development and Screening]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49884]]></requisitionid>
    <referencenumber><![CDATA[R49884]]></referencenumber>
    <apijobid><![CDATA[r49884]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49884/associate-scientist-bioassay-development-and-screening/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a highly motivated Associate Scientist to join our Bioassay Development and Screening group within the Therapeutic Proteins Department, supporting our VelocImmune antibody pipeline. In this role, you will develop and perform cell-based assays that reveal how antibodies act on molecular function and signaling, playing an integral role in the discovery and characterization of therapeutic molecules across diverse disease areas, while collaborating with scientists across neuroscience, immunology, and other therapeutic teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model: Onsite</li></ul><h3>Discover your role:</h3><ul><li>Develop and perform cell-based assays in support of the company's VelocImmune antibody pipeline</li><li>Contribute to the in vitro characterization and screening of therapeutic antibodies across neuroscience, immunology, and other disease areas</li><li>Develop cell lines and characterize them using cell engineering techniques such as transfection, transduction, and CRISPR</li><li>Apply flow cytometry and imaging to characterize cell-based systems</li><li>Develop and optimize bioassays, including luciferase reporter and internalization assays</li><li>Perform primary cell-based assays, including those involving immune cells</li><li>Run high-throughput functional screens using 96- and 384-well plate formats</li><li>Analyze data, organize results, and communicate findings clearly to your supervisor</li><li>Document experiments in an electronic notebook and present data effectively at team meetings</li></ul><h3>This role requires:</h3><ul><li>Bachelor's in biology or a related field with at least 3 years of relevant professional experience, or a Master's degree with 0-3 years of relevant experience</li><li>Proficiency in planning, executing, and analyzing experiments in addition to communicating clearly and presenting data to colleagues</li><li>Experience with mammalian cell culture and hands-on technical proficiency with in vitro and cell-based assays</li><li>Familiarity with in vitro assays interrogating molecular and cellular function and signal transduction pathways</li><li>Must thrive in a fast-paced, collaborative, and multi-tasking environment, and bring strong organizational skills to daily work</li><li>Preferred qualifications include: cell engineering experience, multi-well assay experience, cell-based functional assay experience, flow cytometry and imaging experience, immunology experience, antibody development experience and primary immune cell assay experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming - Hematology]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49371]]></requisitionid>
    <referencenumber><![CDATA[R49371]]></referencenumber>
    <apijobid><![CDATA[r49371]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49371/senior-manager-statistical-programming-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager, Statistical Programming</strong> to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In this role, you will drive high-quality programming deliverables from single studies through regulatory approval, product launch, and beyond, while collaborating with partnering functions, external service providers, and study teams.</p><br><p>This position offers the opportunity to shape department strategy and mentor talent within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location<strong>: </strong>Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Lead programming support across multiple studies, ensuring timely, high-quality deliverables</li><li>Coordinate programming documentation and specifications, following established standards</li><li>Champion company values through excellence, collaboration, and accountability</li><li>Communicate proactively with study and project teams to clarify requirements and guide programmers</li><li>Lead submission-ready programming deliverables for global regulatory authority filings</li><li>Drive department goals and serve as a subject matter expert on key topics</li><li>Guide the development of direct reports through goal-setting, coaching, and mentoring</li><li>Contribute to hiring by screening and interviewing programming candidates</li><li>You bring advanced SAS skills honed in a clinical data environment, ideally across multiple therapeutic areas</li><li>You understand pharmaceutical clinical development, statistical concepts, and regulatory submission requirements</li><li>You collaborate naturally across global, interdisciplinary teams</li><li>You juggle multiple projects and priorities without losing sight of quality</li><li>You solve problems with initiative, creativity, and a self-starter mindset</li><li>You enjoy influencing, mentoring, and coaching others toward strong results</li><li>You lead with accountability and hold yourself to a high bar</li><li>You're energized by both hands-on programming work and people leadership</li></ul><br><p><strong>This role requires:</strong></p><ul><li>MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline, with 10+ years (12+ for BS) of programming experience — preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including some project and people management experience</li><li>Advanced SAS programming expertise in a clinical data environment</li><li>Strong understanding of clinical trial principles and regulatory submission requirements</li><li>Proven ability to lead global, cross-functional teams</li><li>Experience managing multiple concurrent projects and priorities</li><li>Demonstrated mentoring or coaching experience with junior programmers</li><li>Preferred/nice to haves:<strong> </strong>Knowledge of additional programming languages such as R or Python</li></ul><br><p>#statprogregn</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Statistical Programming - Internal Medicine]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44853]]></requisitionid>
    <referencenumber><![CDATA[R44853]]></referencenumber>
    <apijobid><![CDATA[r44853]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44853/manager-statistical-programming-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables</li><li>Lead the development and quality control of tables, listings, and graphs in support of analysis requirements</li><li>Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests</li><li>Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch</li><li>Partner with management to determine resource requirements for your therapeutic area or department</li><li>Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles</li><li>Provide feedback to management on team members' contributions to support performance evaluations and goal-setting</li><li>Advise direct reports on procedures for data, records, and information retention</li><li>Enjoy working with minimal supervision and taking ownership of complex deliverables</li><li>Communicate clearly with cross-functional, multidisciplinary teams</li><li>Think analytically and stay organized when managing multiple priorities and timelines</li><li>Take initiative in developing deep expertise within a specialized area</li><li>Bring a collaborative mindset to hiring, feedback, and team development</li><li>Adapt easily to shifting priorities, including last-minute requests from senior leadership</li><li>Approach quality and documentation with rigor in a regulated environment</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 8-10 years of relevant work experience (or a Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 5+ years of relevant programming experience, including some project and people management experience)</li><li>Proven experience leading programming deliverables within a clinical study team</li><li>Experience providing input on hiring, feedback, and performance evaluation</li><li>Strong organizational and documentation skills within a regulated environment</li><li>Nice to have: SAS Certification</li></ul><br><p>#statprogregn</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Product Management — Enterprise AI Platforms & Tools]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48868]]></requisitionid>
    <referencenumber><![CDATA[R48868]]></referencenumber>
    <apijobid><![CDATA[r48868]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48868/senior-director-product-management-enterprise-ai-platforms-tools/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>Regeneron’s newly established Enterprise Data & AI organization is built to drive AI transformation and adoption at scale across every part of the enterprise. This is a high-visibility, high-velocity position where the work is directly tied to business and scientific impact. </p><br><p>As the product leader for Regeneron's AI platforms and tools, the successful candidate will have the potential for massive impact and help shape how the enterprise builds, accesses, and adopts AI capabilities. The Sr Director Product Management – Enterprise AI Platforms & Tools will set AI platform strategy and roadmap for the platforms and tools that put AI into the hands of colleagues across the organization, from internal AI assistants to secure data-connected applications to agentic solutions. They will translate business needs into clear technical requirements, frame decisions with a transparent view into their assumptions and the rigor behind them and proactively use data to inspire the next generation of capabilities.</p><br><p>The successful candidate will be part of the Enterprise Data & AI (ED&AI) team within the AI Center of Excellence (AICOE), working closely with the Chief AI Officer, the AI Innovation Leader, the Platform Engineering team, Delivery Managers, and BU IT partners. Together with this network, they will leverage Regeneron's rich data and state-of-the-art infrastructure to deliver platforms that are useful, trusted, and adopted at enterprise scale.<br></p><br><br><p><strong>When & where: </strong> </p><p>This position can be based in any of our Tri- State area campuses: Tarrytown, NY; Sleepy Hollow, NY; Armonk, NY or Warren, NJ.</p><br><p><strong>Discover your role:</strong></p><ul><li>Own the release strategy and roadmap for Regeneron's AI platforms and tools, aligned to the enterprise digital roadmap.</li></ul><ul><li>Build business cases to develop, acquire, or invest in new AI/ML capabilities, datasets, platforms, and tools.</li></ul><ul><li>Prioritize ruthlessly across competing demands, framing recommendations with clear assumptions and analytical rigor.</li></ul><ul><li>Develop deep insight into colleague and end-user pain points and identify the highest-value opportunities to improve their experience.</li><li>Define requirements for core platform capabilities — data access, model serving, search/ranking, automation pipelines, and self-serve tools.</li></ul><ul><li>Lead the technical product development of large-scale AI platforms, machine learning/AI models, and supporting tooling, partnering with engineering and Business Digital teams to ship high-quality deliverables.</li></ul><ul><li>Define requirements for core platform capabilities — data access, model serving, search/ranking, automation pipelines, and self-serve tools.</li></ul><ul><li>Guide the use of cloud technologies (AWS, Azure, GCP) for building and deploying automated ML and analytics pipelines.</li></ul><ul><li>Setting the evaluation framework and criteria, pilot, and deploy new technologies as appropriate, building toward an industry-leading internal AI ecosystem.</li></ul><ul><li>Drive product adoption: measure usage, gather feedback, and continuously improve.</li></ul><ul><li>Partner with GCC engineering teams to translate platform architecture decisions and product requirements into well-scoped, production-ready deliverables; maintain ongoing alignment on roadmap priorities, handoff standards, and delivery quality to ensure continuity between applied AI prototyping and GCC-led build and operate.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in related field required, Masters, MBA, or advanced degree preferred</li></ul><ul><li>15+ years of progressive experience in technical product management</li></ul><ul><li>Strong working knowledge of large language models (LLMs), foundation models, and modern generative AI — including their capabilities, limitations, and evaluation.</li></ul><ul><li>Familiarity with agentic AI: autonomous and multi-step agents, tool use, planning/orchestration, and human-in-the-loop design.</li></ul><ul><li>Hands-on understanding of emerging interoperability standards, including the Model Context Protocol (MCP) for connecting models to tools and data, and Agent-to-Agent (A2A) protocols for multi-agent coordination.</li></ul><ul><li>Experience with retrieval-augmented generation (RAG), vector databases, embeddings, and grounding models in enterprise data.</li></ul><ul><li>Familiarity with prompt engineering, context engineering, fine-tuning, and model customization techniques.</li></ul><ul><li>Understanding of AI evaluation and observability — building evals, measuring quality/safety, monitoring drift, and managing model/agent performance in production.</li></ul><ul><li>Awareness of responsible and secure AI practices: guardrails, access controls, data privacy, and AI governance frameworks.</li></ul><ul><li>Familiarity with MLOps/LLMOps tooling and orchestration frameworks for building, deploying, and maintaining AI applications and pipelines.</li></ul><ul><li>Translates ambiguous business needs into clear product requirements and measurable outcomes.</li></ul><ul><li>Balances technical depth with product judgment and stakeholder empathy.</li></ul><ul><li>Keen eye for detail and thoughtful scrutiny of data before relying upon it.</li></ul><ul><li>Drives consensus across engineering, data science, business, IT, and Legal.</li></ul><ul><li>Comfortable owning roadmap, budget, and outcomes end-to-end.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Talent Management]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48164]]></requisitionid>
    <referencenumber><![CDATA[R48164]]></referencenumber>
    <apijobid><![CDATA[r48164]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48164/director-talent-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Talent Management<strong> </strong>to join our Talent Management Team. In this role we are looking for a bold, strategic talent leader to shape how Regeneron grows its people — globally, intentionally, and at scale. You will build our career development framework and skills ontology and bring them to life in Workday. As the Director, Talent Management, you will architect the frameworks and programs that define how talent is onboarded and developed across our company. From leading the company-wide talent review process and translating data into decisions, to building a best-in-class career development philosophy and designing assimilation experiences that set people up to thrive from day one — your work will directly influence the capabilities and culture that power Regeneron’s mission for years to come.</p><br><p>This is a rare opportunity to do consequential work — building the talent infrastructure of a fast-growing, science-driven company that is changing the lives of patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Sleepy Hollow, New York, United States</li><li>Work model: Onsite 4 days per week</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Set the enterprise vision and strategy for career development and build the framework behind it — designing an integrated approach that spans early career pipelines, key talent acceleration, and long-term internal talent development, ensuring Regeneron always has the right capabilities ready for what’s next</li><li>Define and govern an enterprise skills ontology (taxonomy, skill relationships, proficiency, mapping to job profiles, and maintenance approach) and partner with HR Technology to build it, along with the career development framework, in Workday Talent Optimization (Career Hub, Skills Cloud) — powering talent decisions, internal mobility, and future skills-based initiatives</li><li>Own the company-wide talent review process for the global organization — leading end-to-end execution, building and managing a robust talent review data infrastructure, and translating outcomes and trends into actionable insights that surface leadership gaps, skill needs, and succession risks at the enterprise level</li><li>Lead the strategy and continuous improvement of enterprise onboarding and assimilation programs that accelerate integration — ensuring every employee, from individual contributor to senior leader, enters Regeneron connected, informed, and ready to contribute from day one</li><li>Build, lead, and continuously elevate Regeneron’s early career program — designing a cohesive, multi-program framework with the standards, experiences, and governance to consistently feed the organization’s most critical talent pipelines</li><li>Partner with business leaders and managers to identify stretch assignments and development pathways for employees, and design the IDP tools and accountability structures that turn development plans into real, measurable growth experiences for employees at every level</li><li>Champion internal mobility as a strategic priority — building the systems, frameworks, and cultural conditions that make it easy for employees to grow laterally and vertically, and leveraging stakeholder feedback, cross-functional partnerships, and technology to make opportunities visible and accessible across the global organization</li><li>Establish a disciplined approach to measuring program effectiveness — tracking talent movement, development outcomes, and emerging workforce trends, and presenting clear, compelling insights to senior leadership that drive confident, data-driven decision-making and continuous improvement</li><li>Cultivate trusted relationships with HR COEs and key customers across the global business — partnering to diagnose talent and skill gaps, align on strategic development plans, and build the ongoing feedback loops that keep Regeneron’s talent initiatives innovative, relevant, and ahead of the curve<br></li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in Human Resources, Business Administration, Organizational Development, or a related field; a Master’s degree or relevant professional certification (e.g., SHRM-SCP, ATD, or equivalent) is strongly preferred</li><li>10+ years of progressive experience in talent management, career development, or organizational effectiveness, including at least 5 years leading people or enterprise-wide programs in a complex, global organization</li><li>Experience leading a team of Talent Management professionals</li><li>Demonstrated success designing and scaling strategic career development and talent management programs, with a track record of driving measurable outcomes across multiple talent domains simultaneously</li><li>Deep knowledge of HR principles and talent management frameworks, with the ability to connect people strategy to business strategy in a meaningful and credible way</li><li>Exceptional communication, relationship-building, and executive presence skills, with the ability to influence and align stakeholders at all levels of the organization</li><li>Strong analytical mindset with demonstrated experience using talent data and workforce trends to inform strategy, identify risks, and guide investment decisions</li><li>Comfortable operating with ambiguity and agility in a fast-moving, science-driven environment — equally skilled at big-picture strategy and hands-on execution</li><li>Experience building a skills taxonomy or ontology and operationalizing it in a talent system; hands-on experience designing and building Workday Talent Optimization, specifically Career Hub and Skills Cloud (strongly preferred)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology (TN, AL, MS, AR)]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51169]]></requisitionid>
    <referencenumber><![CDATA[R51169]]></referencenumber>
    <apijobid><![CDATA[r51169]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51169/associate-director-field-medical-affairs-hematology-tn-al-ms-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location/Territory: Tennessee, Alabama, Mississippi and Arkansas (residency in the territory is required with a preference of TN and AL</p><p>Work model: Field</p><p>Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p><br><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><br><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. </p><p><br>#medicalscienceliaison #msl #HFM</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 18:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician (Days)]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49317]]></requisitionid>
    <referencenumber><![CDATA[R49317]]></referencenumber>
    <apijobid><![CDATA[r49317]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49317/calibration-technician-days/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking to add a Calibration Technician to our growing team. Calibration Technicians support our manufacturing operations by performing mechanical, electrical, calibration, electronic, and utility-related tasks. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Rensselaer, New York, United States</li><li>Working shift: Wednesday-Saturday 6:00am-4:30pm</li><li>Training shift: Monday-Friday 8:00am-4:30pm for approximately 6 months</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Calibrate various types of instrumentation including temperature, pressure, level, flow, and analytical instruments</li><li>Perform loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Work with medium and low voltages</li><li>Perform basic plumbing and tube bending jobs</li><li>Assist the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Perform daily Work Orders (WO) and Preventative Maintenance (PM), and efficiently coordinating the workflow and documentation of PMs and WOs</li><li>Communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work, as needed</li><li>Participate in compliance investigations if and when necessary</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum years of related experience for each level:<ul><li>Calibration Technician II: 2+ years or HSD/GED and 5+ years</li><li>Calibration Technician III: 5+ years or HSD/GED and 8+ years</li><li>Calibration Technician IV: 8+ years or HSD/GED and 11+ years</li></ul></li><li>Demonstrated basic problem-solving skills</li><li>Ability to learn and follow routine procedures independently as well as part of a team</li><li>The ability to lift, push, and pull at least 50 lbs</li><li>Participating in a rotating on-call schedule</li><li>Strong written and verbal communication skills</li><li>Ability to maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><br><h3><strong>Gowning and Environment:</strong></h3><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Fill Finish Manufacturing Engineer]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47889]]></requisitionid>
    <referencenumber><![CDATA[R47889]]></referencenumber>
    <apijobid><![CDATA[r47889]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47889/senior-fill-finish-manufacturing-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Fill/Finish Manufacturing Engineer to join our Manufacturing organization, supporting our fill/finish operations team on-site. In this role, you will serve as the technical subject matter expert for medical device and combination product assembly design and selection as well as process development activities. In this role you will be hands-on problem solving issues during technology transfer, cGMP start-up, and routine manufacturing for Regeneron internal process. This role will also support validation and training activities for targeted equipment, processes and operators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Travel percentage: Up to 15%</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Acts as the technical subject matter expert for assembly, labeling, and packaging processes</p></li><li><p>Serves as the primary interface between operations and Engineering, Combination Products, Validation, and Quality Assurance</p></li><li><p>Leads material and component selection, design, and approval in partnership with internal stakeholders and external vendors</p></li><li><p>Supports equipment and new technology design, installation, and qualification, along with technology transfer studies and investigations</p></li><li><p>Drives innovation in fill/finish manufacturing equipment and techniques, recommending capital investments to support continuous improvement</p></li><li><p>Represents manufacturing during regulatory and client audits</p></li><li><p>Fosters a positive team environment by listening closely to team members and stakeholders while driving toward shared goals</p></li><li><p>Brings strong interpersonal, cross-cultural, and communication skills alongside confidence, emotional intelligence, and creative problem-solving</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Sr Engineer: Bachelor's degree in Engineering with 5+ years of related experience (level determined based on qualifications)</p></li><li><p>Knowledge of cGMP manufacturing environments and familiarity with assembly, labeling, and packaging of liquid and lyophilized injectable products</p></li></ul><p><strong>Preferred qualifications:</strong></p><ul><li><p>Experience operating and qualifying highly automated equipment, including serialization systems</p></li><li><p>Technology transfer and equipment/process validation experience in aseptic, parenteral fill/finish operations</p></li><li><p>Previous experience providing technical support</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 14:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Finance Transformation]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50110]]></requisitionid>
    <referencenumber><![CDATA[R50110]]></referencenumber>
    <apijobid><![CDATA[r50110]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50110/associate-director-finance-transformation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>The Associate Director, Finance Transformation, is responsible for driving strategic initiatives that improve the effectiveness, scalability, and operational performance of Finance. This role partners with Finance Operations, Shared Services, IT, and business stakeholders to lead process optimization, technology enablement, standardization, and continuous improvement efforts across the organization.</p><br><p>The Associate Director will identify opportunities to simplify and modernize finance processes, enhance service delivery, strengthen controls, and support enterprise transformation initiatives. Success in this role requires a deep understanding of finance operations, strong leadership capabilities, and experience leveraging key Finance technologies including Oracle Fusion, Hyperion, Tableau, BI Publisher, and other enterprise platforms to improve business outcomes.</p><br><p><strong>When & Where</strong></p><p>This role is based in our Sleepy Hollow, NY office and is required to be on-site 4 days per week.</p><br><p><strong>Discover Your Role</strong></p><ul><li><strong>Finance Operations Leadership:</strong> Leads Finance operational excellence initiatives by driving process standardization, performance improvement, scalability, risk reduction, and service delivery enhancements aligned with business priorities.</li><li><strong>Process Improvement & Transformation:</strong> Oversees Finance process transformation efforts through continuous improvement, automation, and change management to increase efficiency, controls, and scalability.</li><li><strong>Technology Enablement:</strong> Partners with Finance and IT teams to optimize and implement enterprise technologies, leveraging automation, AI, and analytics platforms to improve business performance and decision support.</li><li><strong>Reporting, Analytics & Decision Support:</strong> Delivers actionable financial and operational insights through standardized reporting, data governance, performance metrics, and trend analysis to support strategic decision-making.</li><li><strong>Stakeholder Management:</strong> Builds and manages cross-functional partnerships, driving collaboration, executive communication, and data-driven recommendations to achieve operational and transformation objectives.</li></ul><br><p><strong>This Role Requires</strong></p><ul><li>Bachelor's degree required in Finance, Accounting, Business Administration, Information Systems, or a related field. MBA preferred.</li><li>10+ years of progressive experience in Finance Operations, Shared Services, Finance Transformation, or related disciplines.</li><li>5+ years of leadership experience managing teams and complex cross-functional initiatives.</li><li>Demonstrated experience leading process improvement, operational excellence, and technology-enabled transformation initiatives.</li><li>Strong understanding of finance processes, controls, and enterprise operations.</li><li>CPA, CMA, PMP, Lean Six Sigma, or equivalent certification are preferred</li><li>Experience supporting large-scale Finance Transformation or ERP initiatives.</li><li>Knowledge of Oracle Fusion, Hyperion, Tableau, BI Publisher, Power BI, automation platforms, and AI-enabled technologies.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp QA Specialist]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51045]]></requisitionid>
    <referencenumber><![CDATA[R51045]]></referencenumber>
    <apijobid><![CDATA[r51045]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51045/temp-qa-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temp QA Specialist </strong>to join our <strong>QA Raw Materials </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Providing QA oversight and support for manufacturing operations, serving as the primary quality representative within production areas</li><li>Partnering with cross-functional teams to facilitate issue resolution, including troubleshooting equipment, process, and schedule disruptions, while ensuring appropriate documentation and quality oversight</li><li>Assessing and triaging potential non-conformances in real time, ensuring required information and documentation are secured to support investigations</li><li>Reviewing and approving documentation associated with routine and non-routine manufacturing activities, including area clearances, incursions, changeovers, and other operational events</li><li>Participating in shift meetings and operational discussions, providing quality mentorship, observations, and recommendations related to ongoing activities and containment actions</li><li>Providing quality consultation and guidance in alignment with QA policies, procedures, and regulatory expectations</li><li>Representing Quality Assurance in the management of complex deviations, change controls, CAPAs, and other quality systems, including active participation in investigations, root cause analysis, and corrective action implementation</li><li>Supporting employee development through training, coaching, and mentoring on QA processes, procedures, and standards</li><li>Performing activities related to product disposition and release, including review of manufacturing records and supporting documentation</li><li>Reviewing and approving investigations associated with product, process, and manufacturing events</li><li>Identifying opportunities for continuous improvement and support initiatives that improve product quality, compliance, and operational efficiency</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Excellent organisational skills and attention to detail</li><li>You have the ability to learn and utilise computerised systems for daily performance of tasks</li><li>Strong written, verbal and interpersonal communication skills and can optimally interact cross functionally</li><li>You have the ability to prioritise, manage multiple tasks, and meet deadlines</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><strong>Assoc Specialist </strong>- BS/BA in scientific discipline or related field or equivalent combination of education and experience</li><li><strong>Specialist </strong>- BS/BA in scientific discipline or related field with min 3 years of relevant work experience in pharmaceutical or related industry or equivalent combination of education and experience</li><li><strong>Sr Specialist </strong>- BS/BA in scientific discipline or related field with 5+ years or MS 4+ years of relevant work experience in pharmaceutical or related industry or equivalent combination of education and experience</li></ul><p>Thrive today. Grow tomorrow.</p><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLQA #REGNQA</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor, Quality Assurance Specialist]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50076]]></requisitionid>
    <referencenumber><![CDATA[R50076]]></referencenumber>
    <apijobid><![CDATA[r50076]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50076/supervisor-quality-assurance-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Quality Assurance Specialist 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.</p><p><strong>Where & Where:</strong></p><br><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Wednesday-Sunday, 3rd shift, 10:00 PM - 8:30 AM</li></ul><p><strong>Discover your role:</strong></p><br><ul><li>Represent Quality Assurance in support of complex and/or significant Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</li><li>Represents the organization on behalf of QA with external partners to communicate QA policy and procedures; liaise with external partners and provide input on regulatory communication</li><li>Train and/or mentor employees, including providing insights and education on processes and procedures, and conveying expectations of QA organization</li><li>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</li><li>Perform activities associated with disposition of product (e.g., manufacturing record review, document review, source data review etc.). </li><li>Review, edit, or approve Regeneron controlled documents</li><li>Review and approve investigations associated with product or processes</li><li>Continually evaluating Regeneron processes and procedures with an eye toward continuous improvement</li><li>Supervising direct reports</li><li>Participates with employee training to ensure that all requirements are met.</li><li>Performs, minimally, monthly performance feedback meetings with direct reports.</li></ul><br><p><strong> </strong><strong>This role requires:</strong></p><br><ul><li>BS/BA in Life Sciences, Engineering or related field; or equivalent combination of education and experience </li><li>Principal QA Specialist: 6+ years of relevant experience </li><li>Staff QA Specialist: 8+ years of relevant experience </li><li>Experience with sterile drug product manufacturing, fill finish and/or quality control testing</li><li>Level will be determined based on experience</li></ul><br><p><strong>This role may be for you if you</strong>:</p><br><ul><li>Excel in a quality driven organization</li><li>Have an understanding of biologics manufacturing operations</li><li>Are organized and have an attention to detail</li><li>Can prioritize multiple assignments and changing priorities</li><li>Are able to stand for periods of time when performing tasks on the floor</li></ul><p><strong>Gowning and Environment:</strong></p><br><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Commercial GCC Lead - Director Insights and Analytics]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49944]]></requisitionid>
    <referencenumber><![CDATA[R49944]]></referencenumber>
    <apijobid><![CDATA[r49944]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49944/commercial-gcc-lead-director-insights-and-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, GCC Commercial Lead to join our Global Capability Center (GCC) in Hyderabad. This role is a foundational member of Regeneron's first GCC and will drive the expansion and scaling of commercial capabilities across Insights & Analytics, Commercial Operations, and Market Access. The successful candidate will establish best practices, build high-performing teams, and enable a data-driven, customer-centric commercial model while working closely with U.S.-based commercial leadership.</p><p><strong>When & where:</strong></p><p><strong>Location:</strong> Hyderabad, India (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Lead and scale the India-based GCC commercial organization, driving innovation, best practices, and collaboration across teams.</li><li>Serve as a member of the GCC leadership team and contribute to the overall success of the Global Capability Center.</li><li>Build, develop, and mentor high-performing teams through hiring, capability development, and leadership coaching.</li><li>Oversee leaders responsible for Insights & Analytics, Commercial Operations, and Market Access functions.</li></ul><ul><li>Collaborate with global commercial leadership to define and implement the commercial capability roadmap aligned with enterprise strategy and business priorities.</li><li>Partner with U.S.-based commercial leaders to align priorities, manage stakeholder expectations, and ensure seamless execution across time zones.</li><li>Establish knowledge transfer programs with VP-level commercial leaders to support transition, localization of methodologies, and capability building within the GCC.</li><li>Build strong relationships with senior stakeholders and influence strategic business decisions.</li></ul><ul><li>Drive integration of analytics, insights, and operations to support data-driven decision-making and commercial excellence.</li><li>Establish governance frameworks, operating models, and delivery standards across Commercial GCC teams.</li><li>Oversee delivery of analytics, reporting, campaign execution, and operational support across multiple global markets, including the U.S., EU5, and Japan.</li><li>Ensure compliance with regulatory, legal, and internal quality standards across all commercial activities.</li><li>Lead continuous improvement initiatives to enhance efficiency, scalability, and quality of commercial capabilities.</li></ul><p><strong>This role requires:</strong></p><ul><li>Strong understanding of the end-to-end pharmaceutical commercial ecosystem, including Insights & Analytics, Market Access, Sales Operations, Marketing, and Patient Engagement.</li><li>Deep familiarity with commercial data domains including patient, HCP, claims, prescription, payer, CRM, and market datasets.</li><li>Experience using advanced analytics, customer segmentation, performance analytics, and forecasting to support business decisions.</li><li>Knowledge of data strategy, governance, quality, standardization, and scalable data management frameworks.</li><li>Understanding of digital, CRM, and omnichannel engagement ecosystems, including campaign measurement and customer engagement strategies.</li><li>Experience with business intelligence and visualization tools such as Power BI and Tableau.</li><li>Familiarity with commercial operations processes including campaign execution, incentive compensation, territory alignment, and program delivery.</li><li>Understanding of data integration, architecture concepts, multi-source data environments, ETL processes, and analytics enablement.</li><li>Knowledge of regulatory, compliance, and review processes impacting commercial content and engagement.</li><li>Experience building and scaling global capability models, operating frameworks, and service delivery structures.</li></ul><ul><li>Proven leadership experience managing large, cross-functional teams.</li><li>Strong strategic thinking with the ability to translate business priorities into execution.</li><li>Excellent stakeholder management skills, including experience working with senior leadership teams.</li><li>Strong communication and influencing skills across all organizational levels.</li><li>Ability to thrive in high-growth, evolving environments and lead organizational transformation.</li><li>Strong problem-solving and continuous improvement attitude.</li><li>Comfortable working across global time zones and collaborating with U.S.-based leadership.</li><li>10+ years of experience in pharmaceutical or biotechnology commercial functions, including significant leadership experience across Insights & Analytics, Commercial Operations, Market Access, or related domains.</li><li>Demonstrated success in building and scaling high-performing teams.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 10 Oct 2026 06:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Marketing Enablement Program Manager - Pod Lead]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51052]]></requisitionid>
    <referencenumber><![CDATA[R51052]]></referencenumber>
    <apijobid><![CDATA[r51052]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51052/marketing-enablement-program-manager-pod-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><br><p>At Regeneron, we are seeking a Marketing Enablement Program Manager - Pod Lead to join our Hyderabad Global Capability Center (GCC). As a founding member of the GCC, you will lead a team supporting U.S. and Global Marketing organizations through marketing coordination, omnichannel enablement, promotional review support, launch readiness activities, and operational excellence initiatives. This role provides an opportunity to build scalable processes, drive marketing effectiveness, and lead a high-performing team within a global, highly matrixed organization.</p><br><h3>When & Where:</h3><p>Hyderabad, India (Hybrid)</p><br><h3>Discover your role:</h3><ul><li>Lead and manage a team of 3 Senior Analysts, assigning resources, balancing workloads, and ensuring quality control across deliverables.</li><li>Oversee budget management, forecasting, launch readiness reviews, and marketing performance monitoring activities.</li><li>Manage multiple concurrent projects across omnichannel initiatives, promotional material updates, and market implementation activities.</li><li>Drive omnichannel optimization efforts to ensure consistency and effectiveness across marketing assets and tactics.</li><li>Lead Veeva workflow management and JRC (Joint Review Committee) sponsorship activities, ensuring timely review and approval processes.</li><li>Support marketing excellence initiatives, brand stewardship activities, patient-focused programs, and overall brand strategy execution.</li><li>Own consolidated budget reporting, project documentation, and stakeholder communications across marketing workstreams</li><li>Guide content creation, editorial support, and tactical communications development.</li><li>Establish operating procedures, documentation standards, and scalable frameworks for marketing enablement within the Hyderabad GCC.</li><li>Partner with Global and local market teams to support launch readiness, competitor intelligence, sales meetings, congress activities, and affiliate engagement.</li><li>Coordinate knowledge transfer initiatives and transition plans to successfully localize marketing operations into the GCC.</li><li>Build and scale repeatable workflows, templates, and playbooks to improve efficiency, quality, and marketing execution excellence.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree in Marketing, Communications, Life Sciences, or a related field. MBA from a Tier-1 institution or PMP certification preferred.</li><li>7+ years of experience in pharmaceutical or biotechnology marketing.</li><li>Minimum 2 years of people leadership experience managing marketing coordination or enablement teams.</li><li>Demonstrated experience working in highly matrixed, global organizations.</li><li>Strong project management, stakeholder management, and organizational skills.</li><li>Ability to manage multiple priorities while maintaining quality and delivery timelines.</li><li>Strong written and verbal communication skills and the ability to collaborate effectively across global teams and time zones.</li><li>Experience with Veeva Vault PromoMats and pharmaceutical promotional review processes (JRC/MLR).</li><li>Strong understanding of omnichannel marketing, digital asset management, and marketing performance measurement.</li><li>Experience with budget management, compliance oversight, and marketing operations support.</li><li>Familiarity with AI-enabled content solutions and emerging marketing technologies.</li><li>Experience tracking delivery metrics, asset quality, team utilization, and operational performance indicators.</li><li>Proven leadership capabilities with experience coaching, developing, and retaining talent.</li><li>Excellent problem-solving and decision-making skills in a fast-paced environment.</li><li>Strong cross-functional collaboration skills with the ability to influence stakeholders across multiple functions and regions.</li><li>Ability to work in a hybrid IST/US EST model and effectively partner with U.S.-based teams and agency partners.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 05:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Data Management Lead]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51349]]></requisitionid>
    <referencenumber><![CDATA[R51349]]></referencenumber>
    <apijobid><![CDATA[r51349]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51349/senior-manager-data-management-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><br><p>At Regeneron, we are building our first Global Capability Center (GCC) in Hyderabad, creating new opportunities to shape the future of commercial data management and analytics. We are seeking a Senior Manager, Data Management Lead to join our Commercial Data Management organization. In this role, you will lead the prioritization, execution, and enhancement of enterprise commercial data platforms, ensuring the delivery of analytics-ready data solutions that support business decision-making. You will collaborate closely with US-based Commercial and Technology teams, drive data transformation initiatives, and help establish operational excellence within the Hyderabad GCC.</p><br><p><strong>When & Where:</strong></p><p>Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead the prioritization, execution, and deployment of features across commercial data platform product teams in alignment with platform governance and business priorities.</li><li>Oversee cloud-based commercial data platform infrastructure, ensuring data quality, accessibility, performance, and cost optimization.</li><li>Integrate licensed and internal commercial data assets to provide analytics-ready datasets for business stakeholders.</li><li>Evaluate, recommend, and implement next-generation platform capabilities, including automated anomaly detection, knowledge management, searchability solutions, and Generative AI/LLM applications.</li><li>Establish and enhance data management operating procedures, workflows, and governance standards within the Hyderabad GCC.</li><li>Lead data transformation and operational transition activities, including insourcing services from external vendors while ensuring business continuity and effective knowledge transfer.</li><li>Partner with Commercial Data Management pillars including Data Operations, Customer Master Data, Data Strategy, Patient & Channel teams to deliver aligned solutions.</li><li>Collaborate with Technology, Commercial, and Analytics stakeholders to design and implement scalable data solutions for business needs.</li><li>Drive continuous improvement initiatives across data management processes, platform operations, and data governance practices.</li><li>Mentor team members and contribute to the development of a high-performing, collaborative data management organization.</li></ul><br><p><strong>This role requires</strong></p><ul><li>Bachelor’s degree in Computer Science, Information Systems, Data Science, or a related technical field; advanced degree preferred.</li><li>10+ years of relevant data management experience, including leading data platform, data governance, or enterprise data transformation initiatives.</li><li>Hands-on experience with data analysis platforms and technologies, preferably Snowflake.</li><li>Strong knowledge of data architecture, data modeling, data profiling, and end-to-end data flow design.</li><li>Experience with cloud-based data platforms and large-scale data operations.</li><li>Expertise in root cause analysis, issue remediation, and platform enhancement delivery.</li><li>Understanding of syndicated commercial datasets, patient data, and commercial analytics use cases.</li><li>Familiarity with Generative AI and advanced analytics capabilities applied to data and document management.</li><li>Proven track record leading complex, global data transformation programs across cross-functional teams.</li><li>Strong stakeholder management and collaboration skills across business and technology organizations.</li><li>Excellent verbal and written communication skills with the ability to simplify complex technical concepts.</li><li>Strong learning agility, problem-solving abilities, and continuous improvement mindset.</li><li>Working knowledge of data privacy, compliance, and regulatory requirements related to commercial and patient data.</li><li>Ability to work effectively across time zones in a global, matrixed, and fast-paced environment.</li><li>Experience supporting Global Capability Center (GCC) operations and operating model development.</li><li>Experience working with Agile product teams and phased platform delivery models.</li><li>Prior experience leading vendor transition and insourcing initiatives.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Mountain West]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48154]]></requisitionid>
    <referencenumber><![CDATA[R48154]]></referencenumber>
    <apijobid><![CDATA[r48154]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48154/neurology-account-director-mountain-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Minnesota]]></city>
    <state><![CDATA[Minnesota]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Mountain West (Minnesota, Iowa, Missouri, Kansas, Idaho, Colorado, New Mexico and Arizona)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Medical Review]]></title>
    <date><![CDATA[Mon, 15 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47767]]></requisitionid>
    <referencenumber><![CDATA[R47767]]></referencenumber>
    <apijobid><![CDATA[r47767]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47767/senior-manager-medical-review/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Pharmacovigilance Medical Review, India to join our Global Patient Safety team, supporting our global development programs and marketed products in a hybrid role. In this role, you will lead the medical review of safety cases to ensure every report is scientifically sound and inspection-ready before health authority submission, while collaborating with triage, pharmacovigilance, risk management, and clinical development partners across India, the US, and the EU. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad (Hybrid)</p><br><h3><strong>Discover your role:</strong></h3><ul><li><p>Act as team lead, owning end-to-end case quality from coding through causality to final company comment</p></li><li><p>Perform and oversee medical review of ICSRs within defined time standards, ensuring accuracy in Argus</p></li><li><p>Author and review case narratives, analysis of similar events, and company causality rationale</p></li><li><p>Code adverse events and medical history using MedDRA in line with global safety standards</p></li><li><p>Partner with triage, PV, risk management, and clinical development teams on inspection-ready documentation</p></li><li><p>Serve as the medical resource for assigned compounds, resolving and escalating complex case issues</p></li><li><p>Drive SOP development, process improvement, and integration of new technologies including AI</p></li><li><p>You mentor Managers and junior reviewers to ensure consistent application of medical and regulatory standards</p></li></ul><br><h3><strong>This role requires:</strong></h3><ul><li><p>MD or MBBS with active registration, or eligibility for registration, with the relevant Indian professional regulatory body</p></li><li><p>Minimum 8–10 years of pharmacovigilance experience with hands-on ICSR medical review, including narrative authoring, causality assessment, and expectedness determination</p></li><li><p>Strong knowledge of ICH E2A, E2B, and E2D guidelines and FDA/EMA pharmacovigilance regulations</p></li><li><p>Proficiency with Argus Safety or an equivalent safety database and MedDRA coding</p></li><li><p>Sound clinical judgment with the ability to assess complex cases and communicate reasoning clearly in writing</p></li><li><p>Experience within global development programs or on marketed products preferred</p></li><li><p>Exposure to AI or generative AI tools in pharmacovigilance or clinical documentation a plus</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Tampa Central]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49126]]></requisitionid>
    <referencenumber><![CDATA[R49126]]></referencenumber>
    <apijobid><![CDATA[r49126]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49126/medical-specialist-i-allergyent-tampa-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tampa]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US</p><p>The MS is responsible for developing strategy and executing tactics within key allergists in the Dermatology and Respiratory therapeutic areas to generate product utilization. The MS will develop strong working relationships with experts and all Allergists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Tampa Central</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Dermatology or Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Medical Affairs, Hematology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49776]]></requisitionid>
    <referencenumber><![CDATA[R49776]]></referencenumber>
    <apijobid><![CDATA[r49776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49776/director-medical-affairs-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director Medical Affairs Hematology Strategy Japan to join our Global Medical Affairs team, supporting our Japan business in a hybrid work model. In this role, you will provide scientific and medical leadership for our hematology portfolio and pipeline while collaborating with global, regional, local, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Tokyo</li><li>Work model: Hybrid</li></ul><br><h3>Discover your role:</h3><ul><li>Serve as the in-country medical lead for hematology assets and pipeline activities.</li><li>Represent Medical Affairs in cross-functional planning with regional and global partners.</li><li>Direct Field Medical execution, insight generation, and external scientific engagement.</li><li>Coach and develop Field Medical colleagues through onboarding, feedback, and guidance.</li><li>Support clinical development, research, investigator engagement, and site identification.</li><li>Lead medical strategy for congresses, symposia, advisory boards, and educational activities.</li><li>Deliver scientific presentations to healthcare professionals and key stakeholders.</li><li>You build trusted relationships and bring local patient and physician insights forward.</li></ul><br><h3>This role requires:</h3><ul><li>MD or PhD with strong scientific expertise and extensive hematology experience.</li><li>More than 10-15 years of relevant pharmaceutical or biotechnology industry experience.</li><li>Strong knowledge of Medical Affairs, Clinical Development, and Japan regulatory requirements.</li><li>Solid experience in drug development and lifecycle management.</li><li>Experience leading people and directing Field Medical activities.</li><li>Deep knowledge of solid tumors; immuno-hematology experience preferred.</li><li>Experience in matrix organizations and cross-functional collaboration.</li><li>Thorough understanding of the Japanese healthcare environment.</li><li>Ability to shape strategic and tactical planning opportunities.</li><li>Excellent medical communication, analytical, and stakeholder management skills.</li><li>Publication record and translational or basic research experience are a plus.</li><li>Business-level Japanese and English proficiency.</li><li>Ability to manage multiple priorities while maintaining compliance standards.</li><li>Willingness to travel approximately 10-20%.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Accountant, Corporate Accounting]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47371]]></requisitionid>
    <referencenumber><![CDATA[R47371]]></referencenumber>
    <apijobid><![CDATA[r47371]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47371/staff-accountant-corporate-accounting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Join Regeneron's Corporate Accounting team as a Staff Accountant with high visibility across Product Revenue and general ledger accounting. This role owns core close-process responsibilities — journal entries, account reconciliations, and variance analysis — and works directly with Accounting, Finance, Commercial, and Trade on GAAP-based accounting for the business.</p><p>We are looking for a Staff Accountant who is a collaborative team member, communicates effectively with colleagues, thrives in a dynamic environment, and is eager to take on challenges and contribute to Regeneron's growth.</p><p><strong>Discover your role:</strong></p><ul><li>Perform Product Revenue accounting activities, including journal entries for sales, gross to net deductions, and receivables; balance sheet reconciliations; and detailed trend analysis of product sales related deductions</li><li>Own preparation and analysis of Corporate Accounting schedules and balance sheet account reconciliations for assigned areas ensuring completeness, accuracy, and timely resolution of reconciling items</li><li>Partner with Finance to ensure completeness and accuracy of accruals and reclasses</li><li>Participate in the Oracle Fusion Cloud Financials ERP implementation and ongoing optimization efforts, including user acceptance testing (UAT), process design activities, updates to process documentation, and identification of automation opportunities</li><li>Support accounting transformation and process improvement initiatives by leveraging technology, automation, and data analytics to improve reporting and operational efficiency</li><li>Analyze financial results, investigate period-over-period fluctuations, and prepare meaningful variance explanations for Management</li><li>Maintain knowledge of and compliance with Company accounting policies and internal controls</li><li>Ensure compliance with the Company’s Prepaid Expense Accounting Policy and other relevant accounting policies</li><li>Support compliance with Sarbanes Oxley (SOX) requirements, including maintaining documentation and supporting control execution and assist with internal and external audit requests</li><li>Assist with special projects, financial analyses, and continuous improvement initiatives</li></ul><p><strong>This Role May Be for You If You:</strong></p><ul><li>Bachelors degree in Accounting or Finance. CPA or active pursuit of CPA licensure is preferred.</li><li>Have 1-3 years of general ledger accounting, audit, or corporate accounting experience within public accounting experience (Big 4 or national firm) and/or publicly traded company environment are considered strong assets.</li><li>Experience with ERP systems, financial reporting tools, and large datasets is preferred. Experience with Oracle GL, Oracle Fusion, SmartView, Hubble, or similar reporting tools is a plus.</li><li>Are a team player who collaborates effectively, thinks independently, and proactively proposes solutions with a continuous improvement mindset</li><li>Have a solid grasp of GAAP and enjoy applying it to real operational challenges</li><li>Are analytical and comfortable working with large data sets to reach sound accounting conclusions</li><li>Bring strong organizational skills and attention to detail</li><li>Can operate in a fast‑paced environment and comfortably manage multiple priorities</li><li>Have strong written and verbal communication skills</li><li>Enjoy partnering with cross-functional teams and learning how accounting supports business decision-making</li><li>Have an interest in leveraging technology, automation, and data analytics to improve accounting processes</li><li>Are seeking opportunities for professional growth, expanded responsibilities, and career progression within Finance and Accounting</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Engineer]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49773]]></requisitionid>
    <referencenumber><![CDATA[R49773]]></referencenumber>
    <apijobid><![CDATA[r49773]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49773/project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><strong>Build our future together:</strong></div><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Project Engineer </strong>to join our <strong>Project Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Designing and specifying cGMP process equipment, piping, and/or controls</p></li><li><p>Managing small projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li><li><p>Preparing process and instrument drawings and other related drawings</p></li><li><p>Developing Process Flow Diagrams for manufacturing processes.</p></li><li><p>Supporting the validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Assisting in investigations of process equipment and control system anomalies</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations for and executes modification change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>Problem-solving and continuous improvement skills</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>To be considered for this opportunity you should have a BS/BEng or higher in Chemical/Process/Mechanical engineering with 2+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li><li><p><strong>Senior Project Engineer:</strong> BS/BEng or higher in chemical/process/mechanical engineering with 5+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager - Hematology (f/m/d) - Germany North-West]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49846]]></requisitionid>
    <referencenumber><![CDATA[R49846]]></referencenumber>
    <apijobid><![CDATA[r49846]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49846/key-account-manager-hematology-fmd-germany-north-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Key Account Manager Hematology to join our International Hematology team, supporting Germany in a field-based work mode. In this role, you will drive account performance and regional contracting activities for our hematology portfolio while collaborating with Medical colleagues, pharmacists, hospital stakeholders, and commercial teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Field-based in Germany North-West</p><p><strong>Discover your role:</strong></p><ul><li><p>Establish high-quality healthcare professional relationships across the territory</p></li><li><p>Develop referral networks spanning hospital, outpatient, and office-based settings</p></li><li><p>Deliver portfolio value messages through face-to-face, remote, and digital engagement</p></li><li><p>Partner with Medical on regional programs and healthcare professional activities</p></li><li><p>Manage account planning, segmentation, targeting, and local account plans</p></li><li><p>Support regional contracting activities and adapt contract models to local needs</p></li><li><p>Analyze market trends and competitor activity to inform negotiations</p></li><li><p>Thrive in an agile environment and adjust priorities to account needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or recognized equivalent for sales professionals</p></li><li><p>5-7 years of progressive pharmaceutical or biotechnology sales experience</p></li><li><p>Knowledge of the German healthcare system and regional market structures</p></li><li><p>Experience using data, customer relationship management systems, and multiple business systems</p></li><li><p>Qualification in applicable pharmaceutical industry codes, including EFPIA Code or VFA Pharmakodex</p></li><li><p>Fluency in German and good working knowledge of English</p></li><li><p>Ability to manage a large territory independently with frequent travel</p></li><li><p>Strong customer engagement, negotiation, and communication skills</p></li><li><p>High integrity and ethical standards in all interactions</p></li><li><p>Hematology sales experience and an established network strongly preferred</p></li><li><p>Experience supporting hospital, purchasing group, or payer contract negotiations preferred</p></li><li><p>Product launch experience preferred</p></li></ul><p>Salary range (annually)</p><p>73,125 -121,875 €</p></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist-Raleigh & Durham, NC]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49458]]></requisitionid>
    <referencenumber><![CDATA[R49458]]></referencenumber>
    <apijobid><![CDATA[r49458]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49458/oncology-account-specialist-raleigh-durham-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Raleigh & Durham, NC</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identifies business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC experience Preferred).</p></li><li><p>Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC thought leaders or high influence customers in group practices, academic hospitals, key institutions.</p></li><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines.</p></li><li><p>You are results oriented with a track record of success with product launches.</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49912]]></requisitionid>
    <referencenumber><![CDATA[R49912]]></referencenumber>
    <apijobid><![CDATA[r49912]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49912/director-international-commercialization-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Uxbridge, UK - multiple locations are being considered for this role</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs - Hematology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49777]]></requisitionid>
    <referencenumber><![CDATA[R49777]]></referencenumber>
    <apijobid><![CDATA[r49777]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49777/senior-manager-field-medical-affairs-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Field Medical Hematology Japan to join our Global Medical Affairs team, supporting our Hematology business area in a field-based work model. In this role, you will advance scientific engagement, generate actionable field insights, and support Medical Affairs execution while collaborating with Medical Affairs colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Japan</p><p>Work model: Field-based</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead compliant scientific engagement with external experts across Hematology.</li><li>Gather and communicate field insights from clinical practice and congress activities.</li><li>Own complex field medical activities aligned with Medical Affairs strategy.</li><li>Maintain expert, investigator, and engagement-priority mapping.</li><li>Deliver disease-state education to practitioners and researchers in Hematology.</li><li>Contribute to evidence generation, medical education, and scientific communication.</li><li>Lead selected Medical Affairs projects and support IIS and clinical-trial activities.</li><li>You build trusted relationships and translate scientific exchange into actionable insights.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>MD, PhD, or PharmD preferred; Master's degree with substantial Hematology experience may be considered.</li><li>Deep scientific expertise in Hematology and solid tumors; hemato-oncology or immuno-Hematology experience preferred.</li><li>6+ years in pharmaceutical, clinical research, clinical practice, Medical Affairs, or related scientific roles.</li><li>Ability to independently deliver advanced scientific engagement and high-quality field outcomes.</li><li>Strong scientific communication and presentation skills with external and internal stakeholders.</li><li>Experience building relationships with academic and clinical experts.</li><li>Experience working in matrix organizations; partnership experience is valued.</li><li>Understanding of compliance requirements governing non-promotional Field Medical activities.</li><li>Experience supporting evidence generation, medical education, scientific communication, or Medical Affairs projects preferred.</li><li>Prior Field Medical or Medical Science Liaison experience in Hematology preferred.</li><li>Fluency in Japanese and English.</li><li>Ability and willingness to travel approximately 40–60%.</li><li>Strong teamwork, integrity, ownership, judgment, adaptability, and follow-through.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Hematology Thought Leader Liaison (Midwest)]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48325]]></requisitionid>
    <referencenumber><![CDATA[R48325]]></referencenumber>
    <apijobid><![CDATA[r48325]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48325/associate-director-hematology-thought-leader-liaison-midwest/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Michigan]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Hematology Thought Leader Liaison (TLL), Midwest is a field-based, non-sales position on Regeneron’s Commercial Hematology Marketing team. It will be focused on enhancing and improving interactions with key external US hematology thought leaders at academic centers and leading community practices for our Hematology bispecific.</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Market Access, and the Oncology/Hematology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to execute key initiatives.</p><h3>When & where:</h3><ul><li>Must reside in one of the following states:</li><li>North Dakota, South Dakota, Nebraska, Minnesota, Iowa, Michigan, Wisconsin, Ohio, Indiana, and Kentucky</li><li>Must be able to travel 60%-80% of time within the territory</li></ul><h3>Discover your role:</h3><ul><li>The Hematology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or in the course of day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Assist with thought leader development</li><li>Support speaker bureau program placement and execution, which may include identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification a plus</li><li>Specialty pharmaceutical/biopharmaceutical experience, with a minimum of 10 years of work experience in 2 or more of the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience, experience in hematology/oncology markets strongly preferred</li><li>Demonstrated expertise in marketing strategies within the pharmaceutical industry</li><li>Experience with physician-administered biologics preferred</li><li>Strong organizational skills and project management experience</li><li>A proven team player with an in-depth knowledge of industry regulations and compliance guidelines</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Triage and Medical Review]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47768]]></requisitionid>
    <referencenumber><![CDATA[R47768]]></referencenumber>
    <apijobid><![CDATA[r47768]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47768/associate-director-triage-and-medical-review/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Global Patient Safety POD, supporting our global programmes in a hybrid role. In this role, you will lead end-to-end ICSR triage and medical review while collaborating with global safety and clinical development teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (Hybrid - three days a week on site)<br> </p><p><strong>Discover your role:</strong></p><ul><li><p>Oversee Individual Case Safety Report medical review and accurate data capture in Argus.</p></li><li><p>Lead triage harmonisation and end-to-end case quality across the India POD.</p></li><li><p>Review narratives, author analyses, causality rationale, and reporting decisions.</p></li><li><p>Guide expectedness determinations against programmes, products, and approved labelling.</p></li><li><p>Oversee clinically appropriate MedDRA coding for adverse events and medical history.</p></li><li><p>Partner with pharmacovigilance, risk management, and clinical teams before regulatory submissions.</p></li><li><p>Support compounds, case issue resolution, SOP development, process improvements, and inspection readiness.</p></li><li><p>You explore artificial intelligence technologies to strengthen pharmacovigilance activities.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MD or MBBS with active Indian registration or eligibility.</p></li><li><p>10+ years’ industry experience, including 7+ years in pharmacovigilance.</p></li><li><p>Hands-on ICSR review, narrative authoring, causality assessment, expectedness determination, and MedDRA coding.</p></li><li><p>Expert knowledge of ICH E2A, E2B, E2D, and FDA/EMA pharmacovigilance regulations.</p></li><li><p>Proficiency with Argus Safety or equivalent safety databases.</p></li><li><p>Strong clinical judgement and clear written rationale.</p></li><li><p>Global development or marketed product experience preferred.</p></li><li><p>GPS POD or insourced pharmacovigilance experience is advantageous.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) -Oncology *Hokkaido Area]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50238]]></requisitionid>
    <referencenumber><![CDATA[R50238]]></referencenumber>
    <apijobid><![CDATA[r50238]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50238/medical-representative-mr-oncology-starhokkaido-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist, Oncology to join our Oncology Sales team, supporting our oncology business area in a field-based role. In this role, you will drive the adoption of our oncology product portfolio while collaborating with healthcare professionals and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>You will be responsible for the Hokkaido area.</p><p>Your residence is expected to be in Sapporo.</p><br><p><strong>Discover your role:</strong></p><ul><li>Drive sales and adoption of the oncology product portfolio within assigned territory</li><li>Develop and execute territory business plans to achieve sales targets</li><li>Build and maintain relationships with healthcare professionals and key accounts</li><li>Deliver approved scientific and clinical information to support customer decisions</li><li>Identify and engage new business opportunities in the oncology space</li><li>Collaborate with cross-functional teams to support customer needs</li><li>You adapt to evolving priorities and thrive in a results-driven environment</li><li>You demonstrate strong communication and relationship-building skills</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in life sciences, business, or related field</li><li>Proven sales experience in the pharmaceutical, biotech, or healthcare industry</li><li>Knowledge of oncology or related therapeutic area</li><li>Strong communication, presentation, and negotiation skills</li><li>Ability to travel within assigned territory as required</li><li>Driver license and MR certification</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Precision Medicine (Clinical Diagnostics)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49845]]></requisitionid>
    <referencenumber><![CDATA[R49845]]></referencenumber>
    <apijobid><![CDATA[r49845]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49845/associate-director-precision-medicine-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution. This role owns CDx programs from early biomarker feasibility through clinical validation, regulatory submission, and launch — translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions. You'll work at the interface of biomarker science, clinical development, regulatory, and external IVD partners to ensure diagnostics keep pace with therapeutic milestones. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Armonk, NY, Cambridge, MA, Warren, NJ</p></li><li><p>Work model/flexibility: 4 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles (TPPs), defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays). </p></li><li><p>Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics.</p></li><li><p>Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints. </p></li><li><p>Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. </p></li><li><p>Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. </p></li><li><p>Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment. </p></li><li><p>Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). </p></li><li><p>Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. </p></li><li><p>Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. </p></li><li><p>8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. </p></li><li><p>Track record translating biomarker science into validated assays supporting drug approvals. </p></li><li><p>Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). </p></li><li><p>Ability to translate complex scientific and clinical data for cross-functional and executive audiences. </p></li><li><p>Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. </p></li></ul><p>#PrecisionMedicineCDX</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50300]]></requisitionid>
    <referencenumber><![CDATA[R50300]]></referencenumber>
    <apijobid><![CDATA[r50300]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50300/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[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Scientist to join our Clinical Sciences team, supporting rare hematologic conditions and/or immunologic diseases. In this role, you will lead the design, execution, and interpretation of clinical studies within a cross-functional matrix environment while collaborating closely with Medical Directors, Clinical Study Teams, and Global Clinical SubTeams to advance early- and late-stage development programs. This position will support rare hematologic conditions and/or immunologic diseases.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Work model/flexibility: Primarily on-site with hybrid flexibility</p></li></ul><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead clinical study design, execution, and data interpretation across a full development program</p></li><li><p>Partner with Medical Directors and cross-functional teams to shape study strategy and scientific direction</p></li><li><p>Author and review key clinical documents, including protocols, amendments, and clinical study reports</p></li><li><p>Drive medical and safety data review to protect patient safety throughout the trial lifecycle</p></li><li><p>Apply deep therapeutic area knowledge to inform study design and risk mitigation</p></li><li><p>Represent Clinical Sciences in scientific advisory boards, steering committees, and safety monitoring meetings</p></li><li><p>Mentor and guide junior team members as part of a growing Clinical Sciences function</p></li><li><p>Ensure compliance with FDA, EMEA, ICH, and GCP standards across all study activities</p></li></ul><h3><strong>This role might be for you:</strong></h3><ul><li><p>Bachelor's degree required; advanced degree (PhD/MD/PharmD/MSc) in life sciences or healthcare preferred</p></li><li><p>8+ years of pharmaceutical clinical drug development experience</p></li><li><p>Experience in rare hematologic conditions and/or immunologic diseases preferred</p></li><li><p>Demonstrated knowledge of GCP, clinical study design, and clinical research methodology</p></li><li><p>Proven track record driving clinical trial process improvements</p></li><li><p>Bring strong scientific and analytical skills to complex clinical development challenges</p></li><li><p>Are energized by contributing to therapies for rare and underserved patient populations</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Clinical Trial Liaison Strategy]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50397]]></requisitionid>
    <referencenumber><![CDATA[R50397]]></referencenumber>
    <apijobid><![CDATA[r50397]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50397/senior-director-clinical-trial-liaison-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Head of Clinical Trial Liaison to join our Global Site Management team within Global Clinical Operations. As a senior leader within Global Clinical Operations, you will work with abstract ideas and objectives to solve complex, often precedent-setting problems, directing strategy implementation for a broad, business-critical function spanning multiple disciplines, regions, and study teams. You will lead the activities of a diverse, global team, building and sustaining an industry-leading, field-based operational capability enabled by people, process, and technology, and own line management of Director, CTL Regional Heads. You will partner closely with cross-functional stakeholders and senior leaders across Global Development to align and execute a portfolio-wide, multi-year operational strategy for field-based clinical trial support, reporting into the Head of Global Site Management.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: Preferred: Tarrytown, NY, Warren, NJ, Cambridge, MA, or Remote</li><li>Work model/flexibility: Primarily on-site with hybrid flexibility</li><li>Travel percentage: 30-40%</li></ul><h3>Discover your role:</h3><ul><li>Direct strategy implementation for a business-critical, multi-disciplinary field-based operations capability spanning multiple regions</li><li>Lead the activities of a diverse, global team; own individual career development, performance management, and succession planning for the CTL organization</li><li>Establish broad, function-wide objectives and develop, modify, and oversee organization-wide policies and processes</li><li>Provide strategic business oversight of the FSP relationship, ensuring optimum operational effectiveness and quality deliverables</li><li>Act as the senior point of escalation on complex, often precedent-setting issues</li><li>Represent Global Site Management and the CTL function across key forums including the GSM Leadership Team, CRO Joint Operating Committee, Clinical Operations Review, and Global Development Compliance and Quality Meeting</li><li>Maintain a field-facing presence, engaging in site visits with investigator site staff and CRO representatives</li><li>Apply advanced negotiation and interpersonal skills to secure budgets, resources, and executive sponsorship for CTL initiatives, including Agentic/AI-enabled and technology-driven process innovation</li></ul><h3>This role requires:</h3><ul><li>Bachelor's Degree and 18+ years of relevant industry and/or CRO experience, including significant experience leading global, multi-disciplinary teams at a senior management level; Master's Degree, MD, or PhD preferred</li><li>Extensive, expert-level experience in global clinical trial operations, with responsibility for managing financial and people resources across multiple Job Family groups/disciplines</li><li>Extensive medical and scientific knowledge and clinical development understanding</li><li>Strong organizational skills, with demonstrated ability to establish org-wide policies and manage large-scale, multi-project portfolios</li><li>Working knowledge of ICH/GCP and current regulatory guidance (e.g., ICH E6(R3), RBQM guidance)</li><li>Advanced negotiation and interpersonal skills, with demonstrated ability to work independently and collaboratively across a matrixed, global organization</li><li>Excellent communicator, able to synthesize complex information and present it to a wide variety of senior audiences, internal and external</li><li>Ability to build and sustain relationships with the external medical, investigator, and vendor community</li><li>Cross-cultural awareness and fluency in business English; experience operating across EMEA, JAPAC, US/CA, and/or LATAM regions is highly desirable</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 11 Sep 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Safety Scientist Lead - Rare Disease]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50272]]></requisitionid>
    <referencenumber><![CDATA[R50272]]></referencenumber>
    <apijobid><![CDATA[r50272]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50272/director-safety-scientist-lead-rare-disease/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global Patient Safety Sciences Delivery </strong>team.</p><p>The Director, Global Patient Safety Sciences Delivery, Rare Disease, serves as the first point of contact for all Rare Disease operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness. This role is responsible for high quality, compliant execution of safety surveillance, signal management, and aggregate reporting activities across the portfolio. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>The Director is responsible for the development of their team, which is comprised of Safety Scientists. The Director will also be expected to work closely with other Directors on driving standardization and consistency in execution of signal detection activities in partnership. This role will report to the ED, Global Patient Safety Sciences Delivery. </p></li><li><p>Develop common practices, processes and templates to drive standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs </p></li><li><p>Ensure compliance and quality management of Safety Sciences Delivery activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Lead all aspects of signal detection coordination and signal management process across Rare Disease, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies,</p></li><li><p>Analyze aggregate safety data to identify emerging safety issues and patterns, in partnership with Safety Sciences Strategy </p></li><li><p>Support cross-functional coordination to support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Drive development and implementation of relevant training programs for GPS staff, including maintenance of a standardized Safety Sciences training curriculum, proficiency matrix, and knowledge management repository across both Strategy and Delivery </p></li><li><p>Serve as main point of contact to liaise with Safety Sciences Strategy Rare Disease GPS Leads </p></li><li><p>Collaborate with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Implement talent strategy and leadership development initiatives that raise capabilities across the organization </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced Degree required in life sciences or healthcare with 12+ years of PV experience, preferably with a focus on Safety Sciences and Rare Disease experience</p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Preferred experience leading a matrixed role working across multiple areas of an organization and people management experience </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Business Analysis]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46273]]></requisitionid>
    <referencenumber><![CDATA[R46273]]></referencenumber>
    <apijobid><![CDATA[r46273]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46273/associate-director-business-analysis/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director Business Analysis </strong><strong>(Sleepy Hollow, NY)</strong></p><p>Regeneron Healthcare Solutions, Inc. seeks an Associate Director Business Analysis (Sleepy Hollow, NY) to support the Rare Disease Commercial Business Unit through the application of end-to-end analyses and insights, and the application of analytical expertise to drive strategic choices, tactical execution, and commercial excellence. Collaborate on the rare disease data strategy, the procurement of various datasets, build and implement the analytics plan, inform business decisions, and design and implement analytical solutions to support business opportunities. Conduct primary and secondary market research and provide integrated insights for the business unit. Develop and execute analytics plans to support business objectives and strategic initiatives. Generate performance reporting and interpret results based on key strategic imperatives, business questions and definition of success. Identify business needs and propose potential analytical approaches for solutions. Conduct subnational analyses and champion the use of local customer insights. Identify and evaluate business opportunities leveraging descriptive, prescriptive and predictive analytics (e.g., patient finder, next best HCP, etc.). Deliver the analytics necessary for Integrated business reviews, Quarterly business reviews support, and strategic planning. 2 Direct Reports in the position of Contractor Analysts. Local telecommuting permitted up to 1 day per week. 5% domestic travel required.</p><p>SALARY RANGE: $224,640 - $256,600 per year</p><p><strong>Job Requirements</strong><strong>:</strong></p><p>Requires a Bachelor’s degree in Statistics, Econometrics, Mathematics, Electrical Engineering, Electronics Engineering or related field, and 4 years of experience in advanced Analytics and Customer Insights within the biopharmaceutical healthcare market. Must have experience with: Leading analytics and market research initiatives targeting healthcare providers, patients, caregivers, payers, and other critical stakeholders; Data Mining of syndicated pharma data sources such as IQVIA, Komodo, and MMIT to analytically derive insights to inform Business Questions and Key decisions; Assessing and implementing novel methodologies and frameworks that address rare disease challenges, such as identifying meaningful insights for rare disease patient journeys, improving diagnostic pathways, and enhancing brand differentiation throughout the product lifecycle; Developing and operationalizing diagnostic funnel and patient journey models specific to rare disease indications, focusing on the unique challenges of disease awareness, diagnosis, and treatment pathways; Coding in SQL, Python, R and/or SAS (BASE, STAT, SQL, or Macros) in cloud-based data platforms such as Snowflake; Hands-on Working Knowledge of Business Reporting Intelligence tools such as Tableau, PowerBI, and MicroStrategy to report Brand Performance and Execution Metrics in Rare Disease Space; Applying Artificial Intelligence and Machine Learning Based models on top of De-identified Patient and Physician datasets such as Claims, and EMR for Patient Identification, Customer Targeting, Leads and Triggers Generation, and Customer Insights; Conducting Primary Market Research Studies in Rare Disease Space to inform Clinical Message Effectiveness and Brand – Performance, Positioning, Perceptions, Access, and Treatment related questions; Working on Commercial Mix Modelling, Field Alignment, Incentive Compensation and Call Planning to Design Sales Force Commercial Effectiveness Strategy; Major CRM Tools such as Veeva and Salesforce, and leveraging them to develop key capabilities for Omnichannel Engagement Strategy; and Developing Analytics Framework for New Product Launches working with different stakeholders in Commercial Organization.</p><h3>To apply for this position, visit <a href="https://careers.regeneron.com">https://careers.regeneron.com</a> Reference code: R46273.</h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Toxicologist]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50779]]></requisitionid>
    <referencenumber><![CDATA[R50779]]></referencenumber>
    <apijobid><![CDATA[r50779]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50779/principal-toxicologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Principal Toxicologist </strong>to join our Toxicology group within Drug Safety and Pharmacometrics, applying scientific and regulatory expertise to lead nonclinical development programs with minimal supervision. You'll have a deep understanding of global regulatory guidelines to ensure all aspects of nonclinical safety are met, enabling progression of assigned programs across the life cycle of a therapeutic asset. You'll manage all aspects of multiple programs across therapeutic classes, demonstrating the ability to prioritize and meet deadlines with high-quality deliverables, and will work in collaboration with other members of the toxicology group to develop policies and procedures related to the conduct of toxicology research at Regeneron. Candidates with experience across diverse therapeutic modalities, such as monoclonal antibodies, oligonucleotides, and gene therapies, are preferred. Prior experience providing toxicology and nonclinical safety support for Ophthalmology, Oncology, and/or Infectious Diseases programs is a plus.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><br><ul><li>Location: On-site in Tarrytown, NY</li></ul><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Represents toxicology on global research and development project teams, communicating non-clinical safety strategy</li><li>Develops regulatory risk assessment strategies and contributes to program planning, budgeting, and the execution of toxicology studies to support regulatory and clinical development milestones</li><li>Collaborates with cross-functional subject matter experts to design and execute nonclinical safety programs that support drug development and clinical advancement</li><li>Provides scientific oversight of CRO activities, including study design, conduct, monitoring, data interpretation, and reporting</li><li>Communicates nonclinical safety data, risk assessments, and development strategies to internal and external stakeholders, including regulatory agencies</li><li>Authors and reviews nonclinical safety content for global regulatory submissions and provides toxicology expertise in interactions with health authorities</li><li>Collaborates with external partners and consultants to advance nonclinical safety strategies and support drug development programs</li><li>Maintains currency with GLP regulations and ICH, FDA, and EMEA non-clinical safety guidelines</li><li>Keeps up with the latest scientific developments by reading current literature and attending conferences</li><li>Drives continuous improvement initiatives and mentors junior scientists to promote scientific excellence and professional development</li></ul><br><h3><strong>This role requires:</strong></h3><br><ul><li>Advanced Degree (e.g., PhD, DVM) in Toxicology or a closely related discipline, plus 5+ years, or a Master's Degree plus 15+ years, of relevant pharmaceutical industry experience</li><li>Demonstrated expertise in the design, oversight, interpretation, and reporting of nonclinical safety assessment studies supporting drug development</li><li>Proven experience serving as the nonclinical safety representative on cross-functional drug development teams and contributing to regulatory submissions (e.g., INDs, CTAs, BLAs/MAAs)</li><li>Strong knowledge of global regulatory requirements and nonclinical safety strategies across all stages of pharmaceutical development</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Instrument Engineer]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49607]]></requisitionid>
    <referencenumber><![CDATA[R49607]]></referencenumber>
    <apijobid><![CDATA[r49607]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49607/instrument-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are looking for an experienced Instrument Engineer to join our team! Our Instrument Engineers support projects for new and/or replacement instruments and assure they are fit-for-purpose. We support investigations where measurement issues may be a contributing root cause, and we develop specifications and standards for instruments. In this role, you will support authoring and maintain configuration specifications for manufacturing equipment for the production of our life-changing products. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Onsite Monday-Friday, 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Operate as a project manager; plan, execute, and close projects within scope, time, and budget constraints</li><li>Specify cGMP process instrumentation, components, and spare parts</li><li>Set priorities for and complete Calibration Range and Tolerance Justifications forms for new instruments</li><li>Evaluate new instruments for Functional Equivalence to existing instrumentation that has become obsolete</li><li>Review and approve input/output lists for automated systems</li><li>Conduct troubleshooting and root cause analysis for complex instrumentation and associated systems</li><li>Create and maintain configuration specifications for cGMP manufacturing equipment</li><li>Assist in the design review of equipment, and approved supplier lists for instrumentation</li><li>Write and execute test plans to demonstrate instrument suitability</li><li>Implement corrective/preventative actions for existing equipment</li><li>Prepare engineering evaluations and test plans for change control documentation</li><li>Possibly supervise engineering contractors</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA in Engineering; Electrical Engineering preferred and the following minimum years of relevant experience engineering experience for each level:<ul><li>Instrument Engineer: 2+ years</li><li>Senior Instrument Engineer: 5+ years</li></ul></li><li>Understanding of common process instrumentation, including load cells, pressure transmitters/gauges, pH sensors, dissolved oxygen sensors, temperature sensors, mass flow meters, UV analyzers, conductivity sensors, TOC analyzers, and level sensors</li><li>Demonstrated ability to guide the prioritization, coordination, and completion of multiple projects within tight timeframes, while maintaining a high level of attention to detail</li><li>Ability to think independently to make quality decisions based on analyzing available and potentially limited information</li><li>Experience utilizing advanced problem-solving methods and leadership for investigations</li><li>Direct experience with biopharmaceutical process equipment is highly desirable</li><li>Understanding of process control systems and automation is preferred</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $123,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 13:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Equipment Engineer]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49526]]></requisitionid>
    <referencenumber><![CDATA[R49526]]></referencenumber>
    <apijobid><![CDATA[r49526]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49526/principal-equipment-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Our Equipment Engineers specify and commission small equipment and equipment components for biopharmaceutical process systems. We evaluate functional equivalence of equipment and components and author test plans to demonstrate suitability of replacement equipment. This team works across the business supporting the manufacturing process, ensuring our equipment is functioning properly for the production of our life-changing products. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Onsite Monday-Friday 8:00am-4:30pm</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Specify cGMP process equipment, components, and spare parts</li><li>Evaluate equipment for Functional Equivalence to existing equipment</li><li>Assist in the design review, site acceptance, and installation of equipment</li><li>Write and execute test plans demonstrating equipment suitability</li><li>Support QA Validation department by preparing design documents and assisting in protocol execution</li><li>Author, review, and revise Standard Equipment Specifications</li><li>Implement corrective/preventative actions for existing equipment</li><li>Prepare engineering evaluations and test plans for change control documentation</li><li>Support large capital projects in a spare parts capacity</li></ul><br><p><strong>This role requires:</strong></p><ul><li>BS/BA in engineering and the minimum years of relevant experience listed below for each level. Chemical, biochemical, or mechanical engineering degree preferred<ul><li>Senior Equipment Engineer: 5+ years</li><li>Principal Equipment Engineer: 8+ years </li></ul></li><li>Direct experience in equipment engineering and with biopharmaceutical process equipment is highly desirable</li><li>Intermediate level knowledge of CAD software and drafting principles</li><li>Ability to think independently to make quality decisions based on analyzing available and potentially limited information</li><li>Ability to understand and implement project plans and schedules</li><li>Outstanding written, verbal, and interpersonal communication skills, with the ability to effectively interact with team members with tact and diplomacy</li><li><strong>Gowning and Physical Requirements: </strong></li><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Control Visual Inspection Technician]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50212]]></requisitionid>
    <referencenumber><![CDATA[R50212]]></referencenumber>
    <apijobid><![CDATA[r50212]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50212/quality-control-visual-inspection-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>Build our future together:</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking for a Quality Control Visual Inspection Technician. This position performs manual visual inspection of incoming drug product packaging and medical device components to ensure materials meet quality standards prior to use in drug product manufacturing. This role supports product quality and patient safety by identifying defects, ensuring compliance with cGMP requirements, and maintaining accurate documentation. The position requires sustained attention to detail and adherence to established inspection procedures. Typically, 80% or more of each shift is spent performing visual inspection.</p><br><p>When & where:</p><ul><li>Location: Rensselaer, New York, United States</li><li>Working shift: Sunday-Thursday 8:00am-4:30pm</li><li>Training shift: Monday-Friday 8:00am-4:30pm</li></ul><br><p>Discover your role:</p><ul><li>Conducts manual visual inspection of drug product packaging and medical device components primarily using light boxes and partially using microscopes to identify defects and ensure material quality.</li><li>Uses inspection tools (e.g., magnifiers, size estimation charts, optical comparators) to evaluate and characterize defects accurately.</li><li>Completes, reviews, and reconciles inspection records and logbooks to ensure compliance with cGMP standards and internal procedures.</li><li>Maintains laboratory supplies and performs routine laboratory maintenance to support continuous operations.</li><li>Participates in training and competency assessments for visual inspection.</li><li>Adheres to cGMP, safety, and gowning/PPE requirements to maintain a safe working environment.</li><li>Supports high-throughput inspection activities, sustaining focus and accuracy for extended periods.</li><li>Uses computerized systems to perform daily tasks and document inspection results.</li><li>Collaborates with team members and communicates inspection findings to ensure alignment and timely resolution of quality issues.</li></ul><br><p>This role requires:</p><ul><li>High school degree, Associates degree in a physical or biological science preferred, and the following minimum amounts of experience for each level;<ul><li>Technician II: 2+ years</li><li>Technician III: 5+ years</li><li>Level will be determined based on qualifications relevant to the role</li></ul></li><li>Prior experience in a quality control, laboratory, or manufacturing environment preferred but not required.</li><li>Have the ability to pass a visual acuity exam according to SOP requirements</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$18.94 - $33.99]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Associate Process Scientist]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50805]]></requisitionid>
    <referencenumber><![CDATA[R50805]]></referencenumber>
    <apijobid><![CDATA[r50805]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50805/temp-associate-process-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temporary Associate Process Scientist </strong>to join our <strong>Process Sciences Lab </strong>team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Raheen, Limerick.</li><li>This is a 12-month contract position.</li></ul><br><h3><strong>What you’ll do:</strong></h3><ul><li>Supporting the delivery of process solutions to IOPS and contributing to best-in-class laboratory and process validation report packages.</li><li>Assisting in the root cause analysis of process related deviations using scientific data–driven rationale.</li><li>Participating in cross functional teams to understand process issues in technical and laboratory investigations.</li><li>Contributing to the knowledge-based reports summarising conclusion of studies, investigations and process improvements.</li><li>Presenting findings at group meetings.</li><li>Producing and maintaining accurate records in accordance with site procedures and guidelines.</li></ul><br><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Ability to work well in a team environment.</li><li>You can demonstrate strong communication and interpersonal skills.</li><li>You possess logical troubleshooting and problem-solving skills.</li><li>You have strong written and report writing skills.</li></ul><br><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Assoc Process Scientist: BSc/MSc Biotechnology, Biochemistry, or related field will be considered or equivalent combination education and experience.</li><li>Process Scientist: BSc Biotechnology, Biochemistry, or related field with 2 years’ experience; MSc Biotechnology, Biochemistry, or related field with 1 year experience.</li></ul><br><h3>Thrive today. Grow tomorrow.</h3><br><h3>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLPS</h3><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 05:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Technician (Days)]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50307]]></requisitionid>
    <referencenumber><![CDATA[R50307]]></referencenumber>
    <apijobid><![CDATA[r50307]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50307/process-technician-days/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> </p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Process Technician to join our manufacturing operations team, supporting biopharmaceutical production onsite. In this role, you will keep manufacturing, utility, and building systems running safely and in strict cGMP compliance. You will work closely with Facilities Management and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p><br><p><strong>When & where: </strong> </p><ul><li>Location: Rensselaer, New York, United States</li><li>Working shift: Wednesday-Saturday 6:00am-4:30pm </li></ul><ul><li>On-call: Rotational on-call support required </li></ul><br><p><strong>What you’ll do:</strong> </p><ul><li>Perform daily operations, maintenance, and repairs on utility systems, manufacturing equipment, and building systems in a cGMP environment</li></ul><ul><li>Ensure safe, hands-on maintenance of plant manufacturing and support equipment</li></ul><ul><li>Identify off-nominal conditions and troubleshoot mechanical issues on manufacturing and utility equipment in a clean room environment</li></ul><ul><li>Complete daily Work Orders and Preventive Maintenance, coordinating workflow and documentation</li></ul><ul><li>Troubleshoot electrical equipment during off-nominal conditions, locating faults and performing repairs</li></ul><ul><li>Coordinate with Facilities Management and other departments during planned and unplanned work events</li></ul><ul><li>Bring a safety-minded focus and a drive for continuous improvement to everything you do</li></ul><br><p><strong>The environment and physical rhythms of this role:</strong> </p><ul><li>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </li></ul><ul><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </li></ul><ul><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><br><p><strong>Let’s find out if we’re a fit: </strong> </p><ul><li>AAS degree, preferably in Engineering or Construction Technologies with 2+ years of related equipment maintenance experience or HSD/GED with 5+ years of related experience</li><li>Ability to interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications</li></ul><ul><li>Prior experience in equipment maintenance or a related role requiring mechanical skills</li><li>Commitment to compliance with regulatory, corporate, and site-specific policies and procedures</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, R&D Chemistry, Peptidomimetic Purification]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48140]]></requisitionid>
    <referencenumber><![CDATA[R48140]]></referencenumber>
    <apijobid><![CDATA[r48140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48140/sr-associate-scientist-rd-chemistry-peptidomimetic-purification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>We are currently seeking a lab-centric peptide purification chemist to join the R&D (Research & Development) Chemistry group. In this position, they will play a key role in Regeneron’s peptidomimetic antibody-conjugate drug discovery capabilities to enable seamless combination with the company’s existing expertise in biologics and novel genetic medicines. The candidate will drive the purification of peptidomimetic payloads and linker payloads for antibody conjugate drug therapeutics across diverse research areas. Cultural fit with the Regeneron cross-functional teams will be a key driver for success. The R&D Chemistry team is primarily composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have a peptide/peptidomimetic purification background and will require a firm understanding of the latest techniques, strategies and instrumentation for HT peptide purification and isolation. We expect they will act as an inspiring and motivating colleague, effective communicator, and strong project team collaborator to help develop novel antibody-conjugated peptidomimetic therapeutics.</p><p><strong> </strong></p><p><strong>Discover Your Role</strong></p><ul><li>Actively participate and collaborate in the day-to-day activities of the R&D Chemistry Peptidomimetic purification team.</li><li>Perform mass-triggered HPLC purification of novel peptidomimetic drug modalities, using modern purification instrumentation/detection and techniques</li><li>Troubleshoot and optimize peptide purification methods and enable high throughput purification and isolation.</li><li>Identify new strategies and technologies for peptidomimetic purification to improve on existing Regeneron techniques</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic purification team.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required, Master’s degree preferred in peptide, peptidomimetic, small molecule purification</li><li>Minimum of 5 years of industry experience.</li><li>Extensive hands-on experience of the HPLC purification/detection and method troubleshooting of peptidomimetics</li><li>Hands-on experience with Waters and/or Agilent purifications systems preferred</li><li>Hands-on experience with mass-triggered collection preferred</li><li>Experience with high throughput purification</li><li>Extensive experience running modern purification/isolation equipment and instrumentation </li><li>A track record of success in the field of either peptidomimetics or small molecules purification is required. </li><li>Working collaboratively with both internal and external organizations (e.g., CROs) is essential.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Applications Analyst, Oracle EBS]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46999]]></requisitionid>
    <referencenumber><![CDATA[R46999]]></referencenumber>
    <apijobid><![CDATA[r46999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46999/principal-it-applications-analyst-oracle-ebs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Analyst (Senior or Principal) to join our IOPS IT team, supporting the configuration, implementation, and ongoing management of Oracle Supply Chain applications and ERP systems. In this role, you will serve as a technical expert and strategic partner — leading system integrations, driving continuous improvement, and delivering scalable solutions that enhance operational efficiency and user experience — while collaborating with IT, business partners, and vendors across the enterprise. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead technical configuration and deployment of Oracle Supply Chain modules within Oracle ERP, ensuring alignment with business requirements and compliance with regulatory standards</li><li>Design and implement scalable solutions including customizations, extensions, and workflows using Oracle ADF, BPM, and other Oracle tools; develop supporting technical documentation, test plans, and deployment strategies</li><li>Manage system integrations with enterprise applications including middleware tools, APIs, and EDI configurations; coordinate application upgrades, patches, and security configurations in adherence with change management protocols</li><li>Monitor system performance and availability, proactively identifying and resolving issues; provide root cause analysis and technical guidance for complex system problems</li><li>Partner with IT and business teams to develop and drive a strategic application roadmap; work with business partners to deploy system functionality to applicable user communities</li><li>Manage vendor relationships and contracts; may serve as IOPS IT SME or spokesperson during regulatory inspections and audits</li><li>Oversee a small team of specialists on department projects and initiatives; provide leadership in continuous improvement of GMP training programs including SOP assessments and OJT delivery</li><li>Follow and uphold IOPS IT methodologies, standards, and compliance guidelines across all project documentation and implementation activities</li><li>Advanced knowledge of Oracle EBS or Fusion ERP including Supply Chain modules such as Procurement, Inventory, Order Management, and Manufacturing</li><li>Expertise in Oracle SQL, PL/SQL, and reporting tools such as Oracle BI Publisher and OTBI</li><li>Experience with integration platforms such as Oracle Integration Cloud (OIC), middleware, and APIs</li><li>Strong understanding of GMP compliance requirements; experience supporting audits and regulatory inspections and pharmaceutical, life sciences, or medical device manufacturing industry experience highly preferred</li><li>Proven track record delivering complex ERP upgrades, integrations, and customizations in a regulated environment</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>BS/BA in Information Technology or a related field;</li><li>Senior Analyst: 5+ years of experience</li><li>Principal Analyst: 8+ years experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oracle EPM Manager (temporary)]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50691]]></requisitionid>
    <referencenumber><![CDATA[R50691]]></referencenumber>
    <apijobid><![CDATA[r50691]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50691/oracle-epm-manager-temporary/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a temporary <strong>Manager, Enterprise Performance Management (EPM)</strong> to drive the company's forecasting process, working in close partnership with Finance and FP&A stakeholders. This role sits at the intersection of finance operations and systems, owning the EPM platform (e.g., Oracle EPM/Hyperion) that powers budgeting, forecasting, and reporting across the organization. The ideal candidate combines strong financial acumen with hands-on systems expertise to streamline and scale the forecast cycle.</p><br><p><strong>When & Where</strong></p><p>This is a contract position approved for 12 months. The role will site on-site in Sleepy Hollow, NY and needs to be in the office four days per week.</p><br><p><strong>Discover Your Role</strong> </p><ul><li>Manages the end-to-end <strong>rolling forecast process</strong>, coordinating timelines, templates, and submissions across Finance and business unit stakeholders.</li><li>Partner closely with <strong>FP&A, Accounting, and business leaders</strong> to gather assumptions, validate inputs, and ensure forecast accuracy and consistency.</li><li>Administer and continuously improve the <strong>EPM platform</strong>, including model builds, metadata management, workflow automation, and data integrations with ERP/GL systems.</li><li>Design and maintain <strong>forecast models, dashboards, and reporting templates</strong> that support monthly/quarterly forecast cycles, annual budgeting, and long-range planning.</li><li>Conduct <strong>variance analysis</strong> comparing forecast vs. actuals vs. budget, and deliver clear, actionable insights to Finance leadership.</li><li>Drive <strong>process improvement and automation</strong> initiatives to reduce cycle time and manual effort in the forecast and planning process.</li><li>Ensure <strong>data integrity and governance</strong> across the EPM environment, including security, access controls, and audit trails.</li><li>Manage relationships with <strong>EPM software vendors</strong> and coordinate system upgrades, patches, and enhancements.</li></ul><p><strong> </strong></p><p><strong>This Role Requires</strong></p><ul><li>Bachelor's degree in Finance, Accounting, Business, Information Systems, or related field.</li><li>5-9+ years of experience in FP&A, corporate finance, or financial systems, with direct experience running forecast/budget cycles.</li><li>Hands-on experience administering an EPM platform (e.g., <strong>Oracle EPM/Hyperion Planning)</strong>.</li><li>Strong understanding of financial forecasting, budgeting, and variance analysis concepts.</li><li>Advanced Excel skills; experience with SQL or data visualization tools (Power BI, Tableau) a plus.</li><li>Excellent stakeholder management and communication skills — able to translate finance requirements into system design and vice versa.</li></ul><p><strong>Preferred:</strong></p><ul><li>Prior experience leading an EPM implementation or major system upgrade.</li><li>Experience integrating EPM systems with ERP platforms (e.g., NetSuite, SAP, Oracle Fusion, Workday Financials).</li><li>CPA, CFA, or MBA a plus but not required.</li></ul><p><strong>What Success Looks Like</strong></p><ul><li>The forecast cycle runs on time, with high data accuracy and minimal manual rework.</li><li>Finance stakeholders trust the EPM system as the single source of truth for forecast data.</li><li>Continuous improvements reduce cycle time and increase self-service reporting capability across the business.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, Business Intelligence Architect]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50836]]></requisitionid>
    <referencenumber><![CDATA[R50836]]></referencenumber>
    <apijobid><![CDATA[r50836]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50836/specialist-business-intelligence-architect/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist Business Intelligence Architecture Analytics to join our Data, Tech, and Innovation function, supporting our Global Development analytics initiatives in a hybrid work model. In this role, you will build and maintain analytical datasets, data models, and data products while collaborating with Business Intelligence Architecture, reporting, analytics, and downstream stakeholder teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Build, refine, and maintain data pipelines and transformation workflows in Databricks and Snowflake using SQL and PySpark.</li><li>Develop, test, and support analytical data models and curated datasets for Global Development analytics initiatives and workflow migrations.</li><li>Implement reusable, well-structured code aligned with established development standards, naming conventions, and architecture patterns.</li><li>Create data products that support analytics, dashboarding, and artificial intelligence/machine learning use cases.</li><li>Validate data accuracy and completeness through data quality checks, discrepancy analysis, and root cause investigation.</li><li>Prepare structured documentation for datasets, transformations, and business logic to support downstream reporting and analytics teams.</li><li>You bring a collaborative attitude and work effectively with technical and business partners to deliver project outcomes.</li><li>You approach complex data challenges with curiosity, attention to detail, and a commitment to high-quality execution.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree with 3+ years of relevant experience, or Master’s degree in Data Science, Analytics, Computer Science, or a related field.</li><li>Experience in data analytics, data engineering, business intelligence, or a related discipline.</li><li>Hands-on experience with Snowflake for data engineering and analytics workflows; experience with Databricks is preferred.</li><li>Proficiency in SQL and Python for data transformation, engineering, and analysis.</li><li>Experience supporting Tableau dashboards and data visualizations.</li><li>Familiarity with cloud-based data platforms and tools.</li><li>Strong analytical and problem-solving skills with the ability to understand and interpret complex datasets.</li><li>Experience developing datasets for downstream artificial intelligence and machine learning use cases preferred.</li><li>Knowledge of advanced analytics techniques, including machine learning, statistical modeling, and data mining preferred.</li><li>Familiarity with clinical trial operational data preferred.</li><li>Strong communication skills with the ability to translate technical insights into business value.</li><li>Ability to work collaboratively in a team-oriented, fast-paced environment with strong attention to detail and commitment to delivering high-quality work.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Product Manager, Predictive Analytics]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48512]]></requisitionid>
    <referencenumber><![CDATA[R48512]]></referencenumber>
    <apijobid><![CDATA[r48512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48512/senior-product-manager-predictive-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>We are seeking a highly motivated and skilled Senior Product Manager to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop products based on the world’s largest integrated datasets of genomics, proteomics, and electronic medical records. </p><br><p>The role involves partnering with cross-functional teams, including Business Development, Laboratory staff, and other scientific groups, to foster collaboration and advance key initiatives. Excellent communication and interpersonal skills are also required as this candidate will be encouraged to work efficiently in a collaborative, team working environment.</p><br><p><strong>When & where: </strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: 4 days onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Mock up products based on proteomic, electronic medical record, and/or genomic datasets</li><li>Draft specifications for software to display disease risk predictions, use AI tools to implement the specifications, and evaluate the results</li><li>Turn disease prediction ideas from other teams and collaborators into concrete project/budget proposals</li><li>Stay informed on emerging market trends in disease prediction and applications of genomics data to continuously refine product directions</li><li>Deliver clear and concise presentations of genomics and proteomic use cases to leadership, ensuring alignment with organizational goals and priorities</li><li>Assist in the design of clinical validation programs for products</li><li>Leader partner and customer discussions to test hypotheses about the value of new products, and summarize this feedback to leadership </li></ul><br><p><strong>Discover your role: </strong></p><ul><li>A bachelor's degree in a relevant field (software engineering, computational biology, etc.) with at least 13+ years of relevant industry experience (or a PhD and +7 years of experience as an equivalent)</li><li>Demonstrated expertise in software engineering or product design </li><li>Proven skills for translating scientific results into product prototypes</li><li>Proven track record to independently lead and run research projects from conception to completion.</li><li>Excellent communication and collaboration skills, with a track record of working effectively in interdisciplinary teams</li><li>Proven ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</li></ul><br><p>#RGC</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 08:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Neuroscience / Genetic Medicine]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50139]]></requisitionid>
    <referencenumber><![CDATA[R50139]]></referencenumber>
    <apijobid><![CDATA[r50139]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50139/principal-scientist-neuroscience-genetic-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Scientist to join our Genetic Medicines team, helping advance the preclinical development of targeted genetic medicines for disorders of the central nervous system. In this role, you will design and lead experiments across CNS disease models, working as part of a collaborative, multidisciplinary team spanning platform technology, disease biology, and early clinical development.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Design experiments to evaluate the efficacy, target engagement, and delivery efficiency of viral and non-viral therapeutic candidates across CNS disease models</li><li>Design AAV transgene cassettes to optimize therapeutic efficacy</li><li>Lead a team of associates in the execution of experiments and analysis of primary data</li><li>Interpret complex datasets, integrating findings with current scientific literature to propose data-driven next steps</li><li>Communicate project strategy, scientific vision, and data updates to senior leaders</li><li>Author and review preclinical study reports to support regulatory submissions</li><li>Approach scientific problems with an engineering mindset and a design-build-test-learn framework</li><li>Coach and mentor junior scientists within a multidisciplinary team environment</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Experience evaluating DNA- or RNA-based therapeutics in small-animal models</li><li>Hands-on experience with molecular biology techniques</li><li>Experience mentoring and managing research associates</li><li>Excellent communication and presentation skills</li><li>Preferred: Ph.D. in neuroscience, gene therapy, or a related discipline</li><li>Preferred: 5+ years of combined postdoctoral and industry experience in biotechnology, genetic medicines, or CNS drug discovery</li><li>Preferred: knowledge of both viral and non-viral genetic medicine delivery modalities</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Specialist, Lab Support]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49487]]></requisitionid>
    <referencenumber><![CDATA[R49487]]></referencenumber>
    <apijobid><![CDATA[r49487]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49487/quality-assurance-specialist-lab-support/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Quality Assurance (QA) Specialist to focus on lab support for our fill finish facility and quality control laboratory areas. They will ensure compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>What you’ll do: </strong></p><ul><li>Communicates QA policy and procedures; liaises with Quality Control laboratories, support laboratories, facilities, internal or external partners and stakeholders to ensure a successful compliance profile</li><li>Represents Quality Assurance in support of complex Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</li><li>Actively participates in QC laboratory oversight activities such as data review and laboratory walkthroughs</li><li>Performs activities associated with review, edit, and approval of QC generated documentation. Activities may be on the floor or at a desk</li><li>Collaborates with key partners in the business to proactively identify areas for improvement and develop solution strategies</li><li>Trains and/or mentors junior employees, including providing insights and education on processes and procedures</li><li>Provides consultation or advice in alignment with QA policies</li><li>Adheres to Regeneron processes and procedures and may lead Continuous Improvement initiatives</li><li>Demonstrate good understanding of analytical laboratory and biologics manufacturing operations is preferred</li></ul><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>Associate Quality Assurance Specialist: 2+ years of experience</li><li>Quality Assurance Specialist: 4+ years of experience</li><li>Senior Quality Assurance Specialist: 6+ years of experience</li></ul></li></ul><ul><li>Level will be determined based on experience</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Biotech Production]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50706]]></requisitionid>
    <referencenumber><![CDATA[R50706]]></referencenumber>
    <apijobid><![CDATA[r50706]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50706/manager-biotech-production/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Saratoga Springs]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is currently seeking a Manager Biotech Production to join our Global Manufacturing team. In this role you will provide direction and leadership for all manufacturing programs through startup of the Saratoga Springs bulk biologics facility. This manufacturing site is in the early stages and we are looking for an experienced biologics manufacturing operations leader to help build out the team and facility. This role will oversee implementation of both clinical and commercial manufacturing production schedules. This is an opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location:<ul><li>Initial: Rensselaer, New York, United States</li><li>Permanent: Saratoga Springs, New York, United States</li></ul></li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong> </strong></p><p><strong>Discover your role:</strong></p><ul><li>Manages all aspects of production operations in a GMP biologics drug substance facility</li><li>Leads the manufacturing implantation of technology transfer</li><li>Drafts and implements long-term planning for the process, staff, and budget</li><li>Performs personnel management functions (i.e. annual employee evaluations, coaching, disciplining, etc.)</li><li>Prepares reports by collecting, analyzing, and summarizing information and trends</li><li>Makes decisions; develops and implements policies</li><li>Ensures that policies and procedures are effectively administered and that they comply with regulatory requirements</li><li>Working with, designing, and implementing single-use process equipment</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li>BS/BA in Life Sciences or related field and 5+ years of relevant experience in GMP biologics manufacturing and 3+ years of supervisory experience; or equivalent combination of education and experience</li><li>Experience with MES, DCS, and advanced process control systems</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Quality Assurance, Medical Device (Sustaining)]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47283]]></requisitionid>
    <referencenumber><![CDATA[R47283]]></referencenumber>
    <apijobid><![CDATA[r47283]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47283/senior-manager-quality-assurance-medical-device-sustaining/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is currently seeking a Senior Manager, Medical Device Quality Assurance (QA) to join our Medical Device QA team. This expanded leadership role will provide QA oversight across two critical functions: Combination Products Sustaining Engineering and Compliance. The position will lead a team of engineers and quality specialists.</p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Manage, mentor, and develop quality engineering and compliance teams</li><li>Standardize, streamline, and improve processes across sustaining and compliance</li><li>Implement digital, data-driven tools for accurate, consistent, and timely reporting</li><li>Lead teams through complex, ambiguous challenges in a pharmaceutical/medical device environment</li><li>Sustaining Engineering Support:<ul><li>Support sustaining engineering programs through risk assessment, design change management, and maintenance of the Design History File and Risk Management File</li><li>Advice and actively participate in Design Reviews associated with combination products</li><li>Provide QA and technical support to quality engineers and project teams during ongoing maintenance of the combination product</li><li>Interact with partners and contract organizations to ensure accurate completion of project milestones, including post-commercialization activities</li></ul></li></ul><ul><li>Combination Product Support:<ul><li>Act as Management Representative for the combination products QMS; own policies and procedures</li><li>Support regulatory inspections and partner audits for combination products</li><li>Keep the QMS current and inspection-ready via monitoring, gap assessments, and updates</li></ul></li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering and 8+ years of experience; including combination product or medical device experience; or equivalent combination of education & experience</li><li>Previous supervisory/ people leadership experience</li><li>Knowledge of the combination device development and lifecycle process</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Study Specialist]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50974]]></requisitionid>
    <referencenumber><![CDATA[R50974]]></referencenumber>
    <apijobid><![CDATA[r50974]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50974/clinical-study-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Specialist to join our clinical study team, supporting our Japan business in a hybrid work mode. In this role, you will support clinical trial execution while collaborating with clinical study leads, sites, and Clinical Research Organizations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Tokyo, Japan.</p><p>Hybrid.</p><p>Travel may be required up to 25%.</p><h3><strong>Discover your role:</strong></h3><ul><li>Deliver analyzable study reports and metrics to clinical study leads.</li><li>Coordinate study meetings, materials, minutes, training, and investigator meetings.</li><li>Collate feasibility and site-selection data, reviewing site usability information.</li><li>Review study documents and maintain version-controlled manuals under standard operating procedures.</li><li>Track activation, enrollment, monitoring, site status, registry postings, reconciliations, required reports, and close-out activities.</li><li>You proactively identify issues, investigate trial impacts, recommend improvements, and support departmental initiatives.</li><li>Maintain SharePoint, shared drives, site contacts, line-listing reviews, and third-party vendor oversight.</li><li> </li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree with 2+ years of relevant experience.</li><li>Associate degree with 5+ years of relevant experience may substitute for a bachelor’s degree.</li><li>Awareness of International Council for Harmonisation and Good Clinical Practice requirements.</li><li>Basic familiarity with medical terminology and clinical drug development.</li><li>Working knowledge of trial management systems and Microsoft applications, including Project, PowerPoint, Word, and Excel.</li><li>Ability to acquire working knowledge of IVRS/IWRS, EDC, and Trial Master File systems.</li><li>Attention to detail, problem-solving, prioritization, deadline management, and proactive information assessment.</li><li>Strong communication and interpersonal skills, with resourcefulness, self-discipline, and relationship-building ability.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Financial Analyst, SOX Compliance]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47488]]></requisitionid>
    <referencenumber><![CDATA[R47488]]></referencenumber>
    <apijobid><![CDATA[r47488]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47488/senior-financial-analyst-sox-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>As our Senior Financial Analyst, SOX Compliance, you'll be the go-to expert connecting Program Finance with our Global Development organization, making sure our clinical trial finances run smoothly, transparently, and in full compliance with SOX requirements. You'll build and refine the tools, processes, and guidelines that keep our financial operations efficient, audit-ready, and aligned with how the business actually works.</p><br><p><strong>When & Where:</strong></p><p>This role will be based on-site in our Sleepy Hollow, NY or Warren, NJ office and is expected to be in office four days per week.</p><br><h3><strong>What You'll Do:</strong></h3><ul><li>Ensure financial controls are executed in line with the Company's SOX requirements.</li><li>Partner with the Head of Program Finance to present process changes to the SOX Committee and keep SOX documentation (narratives) current.</li><li>Lead the annual SOX audit process — running walkthroughs with internal and external auditors and preparing documentation for Study Budget and Study Requisition approvals as part of key controls testing.</li><li>Advise Program Finance and Global Development teams on SOX key controls for Study Budget and Study Requisition approvals.</li><li>Conduct ad-hoc reviews of Program Trial Finance (PTF) analysts' documentation, spotting gaps or weaknesses and recommending improvements to strengthen controls.</li><li>Champion operational improvements that cut unnecessary work and streamline processes — always within SOX guardrails.</li><li>Take a continuous-improvement mindset to clinical trial, program budget, and study-level requisition processes, including:</li><li>Submitting and updating approved budget information in Hyperion.</li><li>Reviewing budget dashboards to confirm accurate reporting of approved budgets.</li><li>Reviewing custom hierarchies for clinical trials and required approvers.</li><li>Administering and maintaining study budget approval workflows and QlikView dashboards that support SOX compliance via partnership with IT support teams.</li><li>Periodically reviewing budget values in Hyperion to keep QlikView budget dashboards accurate and up to date.</li></ul><br><h3><strong>This Role Requires:</strong></h3><ul><li>Bachelor's degree in Finance, Accounting, or a related quantitative field; an MBA is a plus.</li><li>5+ years of experience in compliance, forecasting, budgeting, and/or business partnering — ideally within a science- or research-driven organization.</li><li>A proven track record spanning both audit and finance functions.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Internal Medicine]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50979]]></requisitionid>
    <referencenumber><![CDATA[R50979]]></referencenumber>
    <apijobid><![CDATA[r50979]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50979/manager-clinical-scientist-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><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting our cardiovascular, renal, and metabolic disease programs. In this role, you will help design, execute, and interpret clinical studies that advance our development pipeline while collaborating with Medical Directors and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model: Primarily on-site with hybrid flexibility</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Support the planning, execution, and evaluation of early- and late-phase clinical studies</li><li>Partner with Medical Directors to deliver scientific expertise for study and program design</li><li>Contribute to program team meetings, advisory boards, steering committees, and safety monitoring meetings</li><li>Develop a deep understanding of the disease area, drug mechanism, and competitive landscape</li><li>Author and review key study documents, including protocol sections, monitoring plans, SAPs, informed consents, and Clinical Study Report components</li><li>Review clinical and safety data to protect patient safety and ensure data integrity</li><li>Identify study risks and propose practical mitigations</li><li>Work with internal teams and external vendors to uphold study quality and compliance with FDA, EMA, ICH, and GCP standards</li></ul><br><p><strong>This role requires:</strong></p><ul><li>MS, PhD, or PharmD in a related field</li><li>5+ years of pharmaceutical clinical drug development experience (other levels considered based on experience)</li><li>Working knowledge of the drug development process, GCP, study design, and clinical research methodology</li><li>Strong analytical, communication, and presentation skills, with the ability to influence within and across teams</li><li>Demonstrated ability to solve complex problems independently and work effectively in a matrix environment</li><li>Preferred: experience in cardiovascular, renal, or metabolic disease</li><li>Preferred: medical writing skills and a track record of clinical trial process improvements</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Clinical Imaging Informatics]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51015]]></requisitionid>
    <referencenumber><![CDATA[R51015]]></referencenumber>
    <apijobid><![CDATA[r51015]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51015/manager-clinical-imaging-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Manager, Imaging Informatics</strong></p><p><em>Clinical Imaging Informatics and Data Sciences</em></p><br><p><strong>Build our future together:</strong></p><p>We are seeking a Manager with a focus in imaging informatics to join our Clinical Imaging Informatics and Data Sciences team. You will maintain, support and enhance the tools our group uses to ingest, standardize, manage, analyze and visualize clinical imaging data, and develop new tools as those needs grow. Work closely with Clinical Imaging colleagues, Data Management, Biostatistics, IT and imaging vendors, with emphasis on reliable tools and analysis-ready imaging data.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY United States of America</p><br><p><strong>Discover your role:</strong></p><ul><li>Maintain and support the group's imaging informatics tools and analytical pipeline, including monitoring of dataflows and scheduled jobs, user access and support, upgrades and issue resolution.</li></ul><ul><li>Maintain clinical imaging databases and data pipelines, including routine loading of vendor imaging-derived data, standardization to internal and CDISC conventions, QC and reconciliation, and query support for study teams.</li></ul><ul><li>Develop new tools, scripts and automations that reduce manual effort in imaging operations, such as reconciliation of expected versus received deliverables, read progress tracking and assembly of analysis-ready datasets.</li></ul><ul><li>Execute and adapt quantitative image analysis workflows, including segmentation, registration and derived measurements, and deliver results in a documented and reproducible form.</li></ul><ul><li>Author and maintain documentation for the tools you support, including requirements, specifications, testing records and user guides.</li></ul><ul><li>Collaborate with IT, Data Management, Biostatistics and imaging vendors to troubleshoot dataflow issues and support evaluation of new imaging platforms and AI tools.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Work efficiently within a fast-paced, collaborative environment.</li></ul><ul><li>Enjoy owning tools end to end and take satisfaction in things running reliably.</li></ul><ul><li>Explain technical work clearly and come up with ideas that move solutions forward.</li></ul><ul><li>Desire to make a broader impact on developing medicines for patients with serious diseases.</li></ul><ul><li>A BS with 5+ years, MS with 3+ years, or PhD in imaging science, biomedical engineering, computer science, data science or a related field.</li></ul><ul><li>Hands-on programming ability in Python and SQL and practical experience building and maintaining relational databases.</li></ul><ul><li>Working knowledge of medical imaging fundamentals, including DICOM, image formats, modalities and analysis software, and demonstrated experience performing quantitative image analysis.</li></ul><ul><li>Preferred: Experience supporting clinical trial imaging in a regulated environment.</li></ul><ul><li>Preferred: Familiarity with ophthalmic and oncology modalities and with Linux, cloud and dashboard tools such as Tableau.</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Pharmacovigilance Hub - Americas]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51026]]></requisitionid>
    <referencenumber><![CDATA[R51026]]></referencenumber>
    <apijobid><![CDATA[r51026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51026/director-pharmacovigilance-hub-americas/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director, Pharmacovigilance Hub</strong> to join our <strong>Global Patient Safety Operations</strong> team. The Director, PV Hub oversees country and/or regional level PV execution within their assigned region and ensures that local safety activities are performed in accordance with global standards, local regulatory requirements are met, and all country-generated safety data are accurately and timely integrated into the global PV system. This role serves as the escalation point for local execution issues and as the conduit between local operations and global oversight functions. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY, Cambridge MA or Warren, NJ</li><li>4 days per week on site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Maintain a comprehensive understanding of local legislation and Health Authority requirements and keep Worldwide Operations Office (WWOO) leadership informed of updates or changes to local requirements or processes (e.g., SOP addenda, safety communications, labeling updates, and local submission requirements) in alignment with country-specific regulatory requirements </li><li>Track local process status, changes, and risks to drive consistency and continuous improvement for hub’s geographic markets, including maintaining and monitoring via common tool (e.g., tracker, dashboard) </li><li>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </li><li>Ensure country compliance with the global PV quality system, supporting inspections, audits, CAPAs, and timely resolution of deviations or non-compliance </li><li>Serve as local safety PoC to coordinate with global GPS (e.g., PV Enablement, CER, SS) and non-GPS (e.g., Med Affairs, Regulatory) teams to: </li><li>Guide and inform global teams on local requirements and ensure compliance with local legislations </li><li>Coordinate with other PV hub(s) as needed for contributions to activities and/or local documentation </li><li>Shape compliant programs that provide high quality adverse event reports </li><li>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </li></ul><p><strong>This role requires:</strong></p><ul><li>Minimum Bachelor’s Degree (Advanced Degree preferred) with 12+ years of PV experience and demonstrated achievements in patient safety</li><li>Experience supporting regulatory inspections, audits, and quality issue management at the country or regional level </li><li>Preferred experience with AI technologies </li><li>Ability to coordinate across functions and cultures, operating effectively as an execution and escalation lead rather than a policy owner </li><li>Strong organizational and communication skills, with the ability to surface local risks early and drive resolution through global governance channels </li><li>Experience working within LATAM, US and Canadian markets strong preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Study Specialist]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51364]]></requisitionid>
    <referencenumber><![CDATA[R51364]]></referencenumber>
    <apijobid><![CDATA[r51364]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51364/clinical-study-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Specialist to join our Clinical Trial Management team. In this role, you will provide technical and administrative support to clinical study teams executing trials across a program, helping ensure studies stay on track from site activation through close-out, while collaborating with Clinical Study Leads, Clinical Study Associate Managers, CROs, and study sites.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Armonk, NY, Warren, NJ</li><li>Work Model: Primarily on-site with hybrid flexibility </li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Organizes and delivers analyzable reports and metrics, and coordinates study team meetings, agendas, and minutes</li><li>Collates data for feasibility and site selection assessments, and contributes to review of study documents (e.g., informed consent forms, case report forms) and reference materials (e.g., regulatory, pharmacy, laboratory binders)</li><li>Tracks site activation, enrollment, and monitoring visits against projected plans, escalating issues or delays, and monitors investigator/site status and registry postings</li><li>Ensures timely receipt of scheduled reports (e.g., 1572s, financial disclosures) and performs TMF reconciliations with study lead guidance</li><li>Communicates with sites as directed, maintaining site contact information and strong relationships internally and externally</li><li>Contributes to close-out activities (e.g., 1572s, IP reconciliation, financial disclosures, CRA close-out visits) and supports oversight of third-party vendors as needed</li><li>Brings attention to detail, resourcefulness, and proactive problem-solving to assigned study activities, investigating impact on trials as new information arises</li><li>Participates in SOP revisions and departmental initiatives, proactively recommending process improvements</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree with 2+ years of industry-related work experience in a clinical setting</li><li>Ability to acquire working knowledge in trial management systems and MS applications (Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, TMF)</li><li>Basic familiarity with medical terms and clinical drug development</li><li>Awareness of ICH/GCP</li><li>Proactive, self-disciplined, and effective at managing deadlines and priorities</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director,  Program Operations Leader - Ophthalmology/Renal]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45092]]></requisitionid>
    <referencenumber><![CDATA[R45092]]></referencenumber>
    <apijobid><![CDATA[r45092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45092/director-program-operations-leader-ophthalmologyrenal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>For US Locations, this position is on-site 4 days per week and 1 day from home. A fully remote role is not possible for this position. </em></p><p>The Program Operations Leader (POL) is responsible for leadership of and setting and implementation of the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional strategy of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence.</p><p>In a typical day, you will:</p><ul><li>Be responsible for the overall success of the clinical study team(s) within a program(s)</li><li>Maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested</li><li>Provide operational insight into feasibility, timeline and cost estimates during clinical program/study development</li><li>Oversee clinical study timelines within a clinical program(s)</li><li>Provide input and operational insight into Clinical Study Concepts (CSC)</li><li>Be responsible for development and implementation of operational strategy, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol </li><li>Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency within the program and development of best practices within CTM</li><li>Oversee clinical study budgets within a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate</li><li>Ensure timely delivery of quality operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams within the clinical program(s). </li><li>Drive decision making and integrates all operational considerations for studies within a clinical program(s) to ensure goals are attainable prior to implementation</li><li>Act as point of contact for clinical program and study level escalation</li><li>Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress</li><li>Provide proactive creation and implementation of risk mitigation strategies</li><li>Provide innovative and flexible operational solutions and options to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges</li><li>Drives the strategy and oversight for vendor selection and management within a clinical program(s)</li><li>Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts</li><li>May require up to 25% travel</li></ul><p>To be considered, you must possess a Bachelor's degree and a minimum of 12 years of related in-house sponsor-side pharmaceutical experience, with 8 years in clinical operations.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Change Communications]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45838]]></requisitionid>
    <referencenumber><![CDATA[R45838]]></referencenumber>
    <apijobid><![CDATA[r45838]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45838/manager-internal-change-communications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an internal communications pro at the Manager level to help develop and drive communications targeting our 15,000+ colleagues globally. The successful candidate will join a dynamic and high-performing Internal Communications team that thinks strategically and executes at a high level to support our fast-growing company -- where colleagues are passionate about their work and our mission to bring important new medicines to patients in need. Internal Communications is part of the Corporate Affairs organization, which is focused on strengthening Regeneron’s reputation by developing strategies and programs that (1) distinguish our science, medicines and patient focus, (2) sustain culture and drive employee engagement, and (3) advance and differentiate our corporate responsibility commitments.</p><p><em><strong>This role will require 4 days per week onsite at our Global HQ Campus in Westchester, NY. This is not available as a fully remote / hybrid work.</strong></em></p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li><p>Support the development and execution of global communications programs that advance the goals of our key corporate functions (HR, IT, etc.) that are advancing critical innovation and digital transformation programs across the company.</p></li><li><p>Serve as trusted internal communications partner to leaders within G&A functions, advising on communications approaches that support enterprise priorities and initiatives.</p></li><li><p>Plan and coordinate key internal communications initiatives, demonstrating project management know-how and creative approaches that effectively inform, inspire and engage employees.</p></li><li><p>Draft compelling messaging – including project briefs, key messages, talking points, FAQ and other materials – that connect to company goals and priorities.</p></li><li><p>Develop informative and creative ways to communicate and engage employees about critical enterprise change initiatives, including digital transformation, global expansion, culture storytelling, and more.</p></li><li><p>Build strong relationships with colleagues at all levels of the organization to support collaboration.</p></li><li><p>Measure the effectiveness of communications and translate insights into actionable recommendations to improve reach, clarity and impact. </p></li><li><p>Identify and implement opportunities to elevate the strategic focus of communications, streamline processes, and improve overall efficiency and effectiveness.</p></li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li><p>Experienced in planning and executing communications initiatives, including storytelling and content management, that engage a busy, global employee base.</p></li><li><p>Knowledge and understanding of change communication principles that help employees navigate organizational change and connect to the opportunity that change presents.</p></li></ul><ul><li><p>Outstanding verbal and written communication skills, with the ability to translate complex topics into clear, accessible messaging tailored to diverse audiences.</p></li><li><p>Knowledge of and experience with channels, approaches and technologies that are used to communicate and connect with employees (intranets, enterprise social platforms, email distribution tools, etc.)</p></li><li><p>Ability to manage and prioritize multiple tasks and projects, adapt quickly to changing priorities and needs, and meet deadlines in a fast-paced environment.</p></li><li><p>Exceptional project management skills, strong attention to detail, sound judgment and curiosity to learn.</p></li></ul><p><strong>To be considered you must have a:</strong></p><ul><li><p>Bachelor's degree</p></li><li><p>Minimum 4+ relevant experience in internal communications and employee engagement.</p></li></ul><ul><li><p>Previous employment in a PR/Communications agency and/or the pharma/biotech industry preferred but not required.</p></li><li><p>Experience in a communications role supporting corporate or business functions, including HR, IT, etc.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Statistical Programming - Pharmacometrics]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47328]]></requisitionid>
    <referencenumber><![CDATA[R47328]]></referencenumber>
    <apijobid><![CDATA[r47328]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47328/associate-director-statistical-programming-pharmacometrics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director Pharmacometrics Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. Provides project leadership, resource planning/coordinating deliverables within project or across multiple projects. Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement and programming specifications using internal standards and guidelines. Providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. The incumbent is responsible for addressing administrative functions required for project management such as compilation of resource requirements and milestones, identifying/communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies.</p><p><strong><em>This position requires 4 days onsite presence based out of our Tarrytown, NY or Warren, NJ location.</em></strong></p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Lead the programming and QC of analysis datasets, TFL's across multiple projects or standard tools following Regeneron standard data models or user requirements. Representation of PMX programming functions and coordination of activities with cross line functions and support planning/coordinating timelines in data exchange, deliverables. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.</p></li><li><p>Lead the integration of data across studies in support of Exposure-response, PopPK and PopPKPD analysis and 2.7.2.</p></li><li><p>Provide programming support for all PMX deliverable in HAR request, data driven analysis, publications, conference</p></li><li><p>Plan and lead the creation and validation of electronic submission requirements (i.e. annotated CRF, data export files, define documents).</p></li><li><p>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Expert SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment</p></li><li><p>Understanding of relational database structure and reporting systems utilizing multiple data delivery applications</p></li><li><p>Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards.</p></li><li><p>Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis), experienced in data handling, process and analysis and able to understand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner</p></li><li><p>Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.</p></li><li><p>Good Skilled in use of relevant software, including Window SAS, SAS studio (Base, Stat, Macro, graph), MS-Excel, R programming and/or Python.</p></li><li><p>Good knowledges in AI use case in statistical programming and data sciences.</p></li></ul><p><strong>To be considered for this opportunity</strong> you must have a Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline. 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. Experience in project and people management, and expertise in one or more therapeutic areas is also preferred. SAS Certification desirable in statistics, computer science.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Finance Service Delivery Analyst]]></title>
    <date><![CDATA[Wed, 24 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47446]]></requisitionid>
    <referencenumber><![CDATA[R47446]]></referencenumber>
    <apijobid><![CDATA[r47446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47446/finance-service-delivery-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Finance Service Delivery Analyst to join our Financial Shared Services team, supporting our global payroll and accounting operations in a hybrid work model. In this role, you will support standardized financial processes, ensure accurate reporting, and drive efficiency across global operations while collaborating with international teams and stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Perform reconciliations between enterprise systems and external vendor systems to ensure data accuracy</p></li><li><p>Prepare and reconcile payroll data templates supporting processing across multiple global countries</p></li><li><p>Implement established payroll and accounting procedures consistently to support centralized operations</p></li><li><p>Coordinate and support month-end, quarter-end, and year-end close processes, including preparation of schedules impacting reporting</p></li><li><p>Assist in preparing reports, audit documentation, and materials for compliance reviews</p></li><li><p>Collaborate with international teams to deliver operational support and ensure seamless service delivery across regions</p></li><li><p>Maintain process documentation, mappings, and Standard Operating Procedures (SOPs) while ensuring adherence to governance practices and internal controls</p></li><li><p>You proactively identify and drive opportunities to improve efficiency and consistency within financial operations.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in Accounting, Finance, Business, Data Analytics, or related field (B.Com or BBM preferred)</p></li><li><p>Minimum 2+ years of experience in payroll, accounting, or data analysis</p></li><li><p>Experience performing reconciliations between enterprise systems and external vendor systems</p></li><li><p>Experience preparing and reconciling payroll data templates across multiple global countries</p></li><li><p>Knowledge of accounting month-end close processes and financial reporting schedules</p></li><li><p>Experience supporting audit preparation and compliance documentation</p></li><li><p>Understanding of governance practices, internal controls, and regulatory compliance requirements</p></li><li><p>Strong customer service and stakeholder communication skills when addressing associate inquiries</p></li><li><p>Ability to collaborate effectively with international, cross-regional teams</p></li><li><p>Proactive approach to identifying process improvements and driving operational efficiencies</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Thu, 11 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48310]]></requisitionid>
    <referencenumber><![CDATA[R48310]]></referencenumber>
    <apijobid><![CDATA[r48310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48310/senior-specialist-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Specialist, External Data Acquisition and Delivery to join our Clinical Data Management team in a hybrid role. In this role, you will manage end-to-end non-Case Report Form data across assigned studies or Clinical Development Units - developing or amending Data Transfer Specifications of low to medium complexity with minimal supervision, performing external data reconciliation and ensuring vendor data is accurately transferred and cleaned in accordance with study protocols and Data Management Plan - while collaborating with external data vendors, CRO partners and cross-functional stakeholders. Ensure compliance with Regeneron SOPs, regulatory requirements, and industry best practices. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Develop Data Transfer Specifications (DTS) for assigned studies or Clinical Development Units as per study timelines.</li><li>Author and maintain DTS documents using standard templates and CDISC requirements, in collaboration with internal and external stakeholders.</li><li>Act as the primary technical point of contact between clinical data management and vendors.</li><li>Respond to vendor and stakeholder queries to ensure external data is complete, correctly structured and delivered in the required format.</li><li>Track DTS status, milestones and deliverables across data types and programs, escalating issues and following through to resolution.</li><li>Process change requests, support data structure issue resolution and facilitate the creation of new test codes where required.</li><li>Reconcile external vendor data against clinical database to ensure accurate transfer, completeness and consistency across all data sources.</li><li>Support data locking, archival, reconciliation documentation, eTMF maintenance and ensure inspection readiness standards.</li><li> Provide review of protocol requirements, vendor specifications, and operational data flows with minimal supervision.</li><li>You guide CROs, vendors and cross-functional partners with clear technical direction while identifying areas for process improvement.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Science, Health, Mathematics, Engineering, Computational or related field.</li><li>4+ years in external clinical data acquisition or management within biotechnology, pharmaceutical or a health-related industry.</li><li>Experience managing multiple clinical data types and formats such as biomarker, eCOA, imaging, ECG, PK, genomics and laboratory data.</li><li>Knowledge of 21 CFR Part 11, ICH-GCP guidelines and CDISC standards for data collection.</li><li>Proficiency extracting data into SAS, CSV and XML formats.</li><li>Experience with EDC platforms such as Medidata Rave, Veeva or Oracle Inform, and external data reconciliation and query processes between EDC and vendor systems.</li><li>Basic knowledge of database structures and protocol review as relevant to clinical data management is preferred.</li><li> Ability to draw from wide-ranging experience to resolve complex issues.</li><li> Strategic thinking, creativity, and problem-solving skills essential</li><li> Ability to work effectively with and motivate virtual teams in a matrix environment.</li><li>Good interpersonal, oral, and written communication skills.</li><li>Society of Clinical Data Management certification is recommended.</li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42183]]></requisitionid>
    <referencenumber><![CDATA[R42183]]></referencenumber>
    <apijobid><![CDATA[r42183]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r42183/associate-director-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Clinical Data Management</strong> team.</p><p>As an Associate Director, External Data Acquisition and Delivery (EDAD), you will provide strategic oversight and operational leadership for External Data Acquisition and Delivery activities across Regeneron’s clinical trial portfolio and initiatives. You will ensure readiness of external data collection platforms, data conformance tools, reconciliation processes, and the delivery of high-quality, compliant external data from third-party vendors including laboratory, biomarker, Digital Health Technologies, imaging, ECG, PK, genomics, and specialty data. You will partner closely with Clinical Data Management, CROs, external vendors, and cross-functional partners to drive external data strategy, operational excellence, vendor oversight, digital transformation initiatives, and process improvements.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Warren, NJ</p></li><li><p>Hybrid; 4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leading External Data Acquisition, integration, quality oversight, and delivery strategy across the clinical trial portfolio</p></li><li><p>Serving as a portfolio-level lead for external data quality and clinical-data operational strategy</p></li><li><p>Reviewing protocol requirements, vendor specifications, and operational data flows</p></li><li><p>Leading all aspects of development and maintenance of Data Transfer Specification (DTS) documents to ensure compliance with Regeneron standards and timelines</p></li><li><p>Providing expert mentorship on external data services including biomarker, eSource, eCOA, imaging, ECG, PK, genomics, and laboratory data</p></li><li><p>Driving external vendor oversight, onboarding, qualification, governance, and ongoing performance monitoring</p></li><li><p>Establishing and handling vendor KPIs, SLAs, and quality metrics</p></li><li><p>Governing reconciliation activities between EDC systems and vendor data platforms to ensure data integrity and consistency</p></li><li><p>Monitoring reconciliation metrics, discrepancy trends, and resolution timelines across studies</p></li><li><p>Collaborating with Database Development, Biostatistics, Study Data Managers, and external vendors to resolve complex data discrepancies</p></li><li><p>Leading process improvement initiatives, automation opportunities, and implementation of innovative external data solutions</p></li><li><p>Managing and developing a team of EDAD Managers, Specialists, and associates through coaching, mentoring, and performance management</p></li><li><p>Supporting SOP development, inspection readiness, audit activities, and regulatory compliance</p></li><li><p>Representing EDAD in leadership forums, governance committees, and technology discussions</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10+ years of experience in Clinical Data Acquisition/Management within biotechnology, pharmaceutical, or healthcare industries</p></li><li><p>Minimum 4+ years of people management experience</p></li><li><p>Demonstrated experience overseeing external data reconciliation activities between EDC systems and vendor platforms</p></li><li><p>Experience driving process improvements and vendor oversight in supervised environments</p></li><li><p>Bachelor’s degree in Science, Health, Mathematics, Computing, Information Systems, or a related field</p></li><li><p>Advanced degree preferred</p></li><li><p>Strong expertise managing multiple clinical external data types including biomarker, imaging, eCOA, ECG, PK, genomics, laboratory, and Digital Health Technology data</p></li><li><p>Advanced knowledge of external data reconciliation processes and EDC platforms such as Medidata Rave, Veeva, or Oracle Inform</p></li><li><p>Experience working with SAS, CSV, and XML data formats</p></li><li><p>Strong understanding of industry regulations including 21 CFR Part 11, ICH-GCP, and CDISC standards</p></li><li><p>Proven experience handling external vendor relationships and driving accountability for quality deliverables</p></li><li><p>Strong leadership, people management, coaching, and mentoring capabilities</p></li><li><p>Strategic thinking, creativity, problem-solving, and analytical skills</p></li><li><p>Strong project management and stakeholder management capabilities</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Ability to work effectively in a fast-paced, matrixed, and global environment</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement - Direct Materials]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47496]]></requisitionid>
    <referencenumber><![CDATA[R47496]]></referencenumber>
    <apijobid><![CDATA[r47496]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47496/director-global-procurement-direct-materials/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As the Director, Global Procurement you will be developing and leading procurement strategies within the managed spend areas. You will work to build the foundation for continued success in Global Procurement by simplifying, accelerating, and clarifying ways of working. </p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Applying advanced judgement, planning, and independent thought leadership in order to influence positive business program outcomes and drive the procurement team deliverables</p></li><li><p>Either directly, or through a matrix, manages an organization of procurement professionals responsible for carrying out category management and sourcing projects</p></li><li><p>Developing and presenting functional strategy and objectives for procurement in alignment with the category business strategy and operational requirements</p></li><li><p>As part of a business team, influences the strategic direction of how Regeneron employs service providers</p></li><li><p>Directing a team responsible for activities associated with the development and execution of contracts covering spend under management</p></li><li><p>Liaising with finance to ensure all sourcing activities align with Regeneron’s financial controls, ensures ongoing engagement with finance throughout a program’s lifecycle for appropriate levels of contract, savings, and budgetary oversight</p></li><li><p>Providing mentorship, support, and overall leadership to the team to ensure goals are achieved</p></li><li><p>Advises, consults, and drives the global category management program for spend categories under management</p></li><li><p>Reviewing major contracts and acts as an expert resource for planning and leading complex negotiations using leader level mastery skills</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in a relevant area along with 12 years of relevant, progressive experience within procurement, preferably including 9 years directly in sourcing Pharma/Biotech</p></li><li><p>Senior Manager: BS/BA plus 10 years experience</p></li><li><p>Associate Director: BS/BA plus 10 years experience</p></li></ul><p><strong>#IRELIM #JOBSIEST #LI-Onsite</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Regulatory Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49492]]></requisitionid>
    <referencenumber><![CDATA[R49492]]></referencenumber>
    <apijobid><![CDATA[r49492]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49492/associate-manager-regulatory-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Manager </strong>to join our <strong>Regulatory Affairs Advertising and Promotion</strong> team.</p><p>The Associate Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). Provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Associate Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Contribute to the management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Assist with providing timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Assist with providing review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Ability to collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Contributes to the working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Assist with interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, assist with helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; help assess the potential impact of enforcement activities on the company policies.</p></li><li><p>Knowledge of process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Knowledge of products/indications to help provide continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>Knowledge of the input provided during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Ability to understand and work with management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 1 to 2 years within regulatory affairs, preferably within advertising and promotion or completion of a Post-Doctoral Fellowship Program with related experience focused on Regulatory Affairs, including Advertising and Promotion</p></li><li><p>Requires advanced scientific degree (i.e., Masters, PharmD, Ph.D) or at minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences.</p></li><li><p>Fundamental understanding of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products is highly preferred, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is desirable</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and help support launch products/campaigns, while maintaining excellent written/verbal communication skill</p></li><li><p>Familiarity with global promotional review, clinical trial recruitment materials, and labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II - Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Sun, 30 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50358]]></requisitionid>
    <referencenumber><![CDATA[R50358]]></referencenumber>
    <apijobid><![CDATA[r50358]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50358/process-development-engineer-ii-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together: </strong></h3><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Process Development Engineer II to join our Preclinical Manufacturing & Process Development (PMPD) group, supporting the new Synthetic and Bioconjugation Scale-up Technologies (SBST) team. You'll develop conjugation and purification processes for bioconjugation of proteins to a diverse range of synthetic molecules, working closely with cross-functional teams to apply Quality by Design (QbD) principles that make processes suitable for GMP production. You'll also support process scale-up and technology transfer of manufacturing workflows to Contract Development and Manufacturing Organizations (CDMOs) or Regeneron-based manufacturing suites, helping ensure timely and reliable progress from clinic to commercialization.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p><br>Location: Tarrytown, NY</p><p>Work model/flexibility: Onsite, full-time</p><h3><strong>Discover your role:</strong></h3><ul><li>Works at the bench to design and develop scalable, robust and controlled GMP-ready bioconjugation and purification processes</li><li>Collaborates with analytical groups within or outside the organization to establish supportive analytical characterization techniques</li><li>Discusses plans and data in cross-functional teams to evaluate processes and determine developmental goals, ensuring integrated program success</li><li>Proactively complies with lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as the FDA and Department of Transportation (DoT)</li><li>Uses statistical design of experiments (DOE) to optimize bioconjugation processes, including conjugation reactions, purification operations, and analytical characterization</li><li>Partners with the External Manufacturing group and other key partners at Regeneron's IOPS organization to provide technical assessment of CDMOs intended for GMP production, successfully transferring processes with immediate, first-time success</li><li>Researches, identifies, and develops new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT)</li><li>Authors robust technology transfer documentation and supports production with onsite presence during scale-up/GMP manufacturing activities</li><li>Analyzes and presents data in a clear and cohesive manner to a broad audience, facilitating data-driven decision making</li><li>Authors, reviews, or provides domain expertise for publications, reports, tech transfer documents, regulatory support documents, and patents</li><li>Acts as a responsible lab citizen by ensuring timely maintenance of lab equipment, keeping the lab tidy and organized, and proactively planning for lab resources</li><li>Coaches and mentors junior team members of the organization as needed</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree + 5-6 years relevant experience, or Master's degree + 3-4 years relevant experience, in chemical/biochemical engineering or a related field</li><li>Experience with antibodies in the bioconjugates space is highly preferable</li><li>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, and membrane technologies is preferred</li><li>Experience with a variety of analytical characterization tools such as electrophoresis, mass spectrometry, high-performance liquid chromatography (HPLC), and UV spectroscopy is preferred</li><li>Strong initiative with the drive to complete challenging tasks and learn new technologies</li><li>Strong fundamental understanding of protein purification and technology transfer principles</li><li>Capable of multi-tasking and working both independently and in a collaborative, cross-functional environment</li><li>Excellent interpersonal, verbal, and written communication skills</li><li>Strong critical thinking and problem-solving skills</li></ul><h3><strong>#pmpd</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[AI/MLOps SRE Lead Engineer]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50034]]></requisitionid>
    <referencenumber><![CDATA[R50034]]></referencenumber>
    <apijobid><![CDATA[r50034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50034/aimlops-sre-lead-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron Digital & Technology, we are expanding our AI and Platform Engineering capabilities to support next-generation intelligent systems, machine learning platforms, and cloud-native technologies. We are seeking an AI-MLOps SRE Lead Engineer to drive reliability, scalability, observability, and operational excellence across our AI, ML, and cloud ecosystem. This role will lead the design and operation of resilient platforms supporting machine learning workloads, LLMs, AI Agents, and enterprise-scale automation while enabling engineering teams to innovate with speed and confidence.</p><p><strong>When & Where</strong></p><p><strong>Hyderabad (Hybrid)</strong></p><p><strong>Discover your role</strong></p><ul><li><p>Drive service reliability, availability, and performance across multi-cloud environments, establishing SLOs, SLIs, error budgets, and reliability standard methodologies.</p></li><li><p>Design, build, and scale enterprise ML platform infrastructure using technologies such as Dataiku, Amazon SageMaker AI, Databricks, and Google Vertex AI.</p></li><li><p>Develop AI-driven observability capabilities using anomaly detection, predictive analytics, and automated remediation solutions to proactively identify and resolve operational issues.</p></li><li><p>Lead the implementation and monitoring of LLM, SLM, RAG, and AI Agent platforms, ensuring performance, governance, operational efficiency, and scalability.</p></li><li><p>Design and implement Infrastructure as Code, CI/CD pipelines, self-healing systems, and platform automation capabilities to improve engineering productivity and operational resilience.</p></li><li><p>Architect enterprise ChatOps solutions that integrate operational events, AI workflows, observability platforms, and automated remediation capabilities.</p></li><li><p>Partner with Data Science, AI Engineering, and Platform teams to deliver secure, scalable, and production-ready AI/ML solutions.</p></li><li><p>Evaluate emerging AI-native operational technologies and integrate innovative solutions that enhance platform reliability, engineering efficiency, and business value.</p></li><li><p>Conduct technical debt assessments, identify architectural risks, and provide strategic recommendations to improve enterprise platform maturity.</p></li><li><p>Serve as a technical leader and trusted advisor, mentoring engineers and influencing reliability engineering, MLOps, and cloud platform strategy across the organization.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Bachelor's degree in Computer Science, Information Technology, Engineering, Data Science, Artificial Intelligence, or a related subject area; Master's degree preferred.</p></li><li><p>6-8 years of experience in Site Reliability Engineering, Platform Engineering, DevOps, or related technology fields with enterprise-scale delivery experience.</p></li><li><p>Strong hands-on experience operating across two or more major cloud platforms, including AWS, GCP, or Azure.</p></li><li><p>Deep expertise with ML platform technologies including Databricks, Amazon SageMaker AI, Dataiku, and Google Vertex AI.</p></li><li><p>Proven experience implementing end-to-end ML workflows including model training, deployment, experiment tracking, monitoring, and pipeline orchestration.</p></li><li><p>Advanced proficiency in Infrastructure as Code tools such as Terraform, Pulumi, AWS CDK, and modern CI/CD automation practices.</p></li><li><p>Strong programming and scripting skills in Python, Go, Bash, or similar languages.</p></li><li><p>Experience building enterprise observability solutions using Prometheus, Grafana, Datadog, OpenTelemetry, distributed tracing, metrics, and logging platforms.</p></li><li><p>Demonstrated expertise in anomaly detection, predictive analytics, automated remediation, and AI-assisted operational capabilities.</p></li><li><p>Proven experience designing and implementing enterprise ChatOps solutions and AI-enabled operational workflows.</p></li><li><p>Strong ability to assess technical debt, influence technical strategy, and drive platform modernization initiatives.</p></li><li><p>Experience using AI tools, LLM-powered assistants, and AI Agents to enhance engineering operations and productivity.</p></li><li><p>Experience with Kubernetes and container orchestration platforms such as EKS, GKE, or AKS preferred.</p></li><li><p>Familiarity with MLOps technologies including Kubeflow, Feast, MLflow, and model evaluation frameworks such as LangSmith, RAGAS, Evidently AI, or Weights & Biases preferred.</p></li><li><p>Knowledge of cloud cost optimization, policy-as-code, compliance automation, and multi-cloud governance practices preferred.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Preclinical and Translational PK/PD]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50217]]></requisitionid>
    <referencenumber><![CDATA[R50217]]></referencenumber>
    <apijobid><![CDATA[r50217]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50217/associate-director-preclinical-and-translational-pkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><strong>Build Our Future Together</strong></div><div><div><div><div><div><div><div><div><div><p>The Associate Director role involves supporting PK and PK/PD requirements for early-stage drug discovery and IND projects. Responsibilities include providing input and oversight for preclinical in vivo studies, coordinating with and influencing scientific teams conducting these studies, managing nonclinical PK studies, analyzing and presenting PK/PD data to project teams and senior management, and preparing summary reports for regulatory submissions</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY</p></li><li><p>Four days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Serving as a subject matter expert on Preclinical PK/PD within Discovery-stage project teams and guiding the design of preclinical PK/pharmacology studies.</p></li><li><p>Collaborating with various internal groups such as Therapeutic Proteins, Therapeutic Function Areas, Assay Development, Precision Medicine, Preclinical Operations, and PPK/PD management to develop and execute PK strategies for projects.</p></li><li><p>Effectively communicating project team queries, expectations, and timelines to management.</p></li><li><p>Conducting and reporting PK/PD analyses based on data from preclinical studies.</p></li><li><p>Working closely with Toxicology, Pathology, Clinical Pharmacology, and Quantitative Pharmacology teams within the Drug Safety and Pharmacometrics department to deliver data and regulatory documents supporting project progression.</p></li><li><p>Maintaining current knowledge of scientific literature, regulatory guidance, and best practices related to PK/PD.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD in Pharmacology, Pharmacokinetics, Biology/Molecular Biology, or Biochemistry with more than 8 to 10 years of relevant experience in biotech or pharma.</p></li><li><p>Deep theoretical and applied understanding of PK and PD to interpret the pharmacology and biology of therapeutic proteins. Experience with other modalities such as siRNA, CRISPR-based therapeutics, and cell therapies is highly beneficial.</p></li><li><p>Proven ability to plan, coordinate, lead PK and/or PK/PD studies, and analyze related data.</p></li><li><p>Familiarity with PK/PD (e.g., WinNonLin), data visualization and AI software and experience writing scientific reports and regulatory summaries.</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Regulatory Affairs]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50617]]></requisitionid>
    <referencenumber><![CDATA[R50617]]></referencenumber>
    <apijobid><![CDATA[r50617]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50617/senior-director-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan business in a hybrid work mode. In this role, you will lead regulatory strategies and submissions across multiple therapeutic areas while collaborating with global regulatory teams and cross-functional colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Tokyo, Japan</li><li>Work model/flexibility: Hybrid</li></ul><br><h3>Discover your role:</h3><ul><li>Plan and execute Japan regulatory strategies, including Japan NDA and PMDA consultations.</li><li>Lead NDA, approval, and post-approval change/life cycle management.</li><li>Support management of the Japan Regulatory Affairs function with local and global leadership.</li><li>Oversee interactions with Japanese regulatory authorities alongside Japan Regulatory Leads.</li><li>Lead or support clinical trial notification submissions to PMDA.</li><li>Represent Regulatory Affairs on multidisciplinary teams across clinical, medical, commercial, and patient safety functions.</li><li>Develop local labeling, patient information, and promotional material reviews.</li><li>Build strong partnerships across global matrix teams.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree in a scientific discipline; Master's degree preferred; Doctor’s degree advantaged.</li><li>Strong experience in Development and Regulatory Strategies roles with demonstrated track record of delivery of Japan NDA</li><li>People management experience preferred</li><li>Deep knowledge of Japan clinical development requirements</li><li>Expertise in Japan submission requirements, regulations, and local standards</li><li>Business level English fluency</li><li>Strategic thinking, commercial awareness, strong written and verbal communication skills, and success in global matrix environments</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 04:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Safety Scientist Lead - General Medicine]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50270]]></requisitionid>
    <referencenumber><![CDATA[R50270]]></referencenumber>
    <apijobid><![CDATA[r50270]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50270/director-safety-scientist-lead-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global Patient Safety Sciences Delivery </strong>team.</p><p>The Director, Global Patient Safety Sciences Delivery, General Medicine, serves as the first point of contact for all General Medicine operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness. This role is responsible for high quality, compliant execution of safety surveillance, signal management, and aggregate reporting activities across the portfolio. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>The Director is responsible for the development of their team, which is comprised of Safety Scientists. The Director will also be expected to work closely with other Directors on driving standardization and consistency in execution of signal detection activities in partnership. This role will report to the ED, Global Patient Safety Sciences Delivery. </p></li><li><p>Develop common practices, processes and templates to drive standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs </p></li><li><p>Ensure compliance and quality management of Safety Sciences Delivery activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Lead all aspects of signal detection coordination and signal management process across General Medicine, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies,</p></li><li><p>Analyze aggregate safety data to identify emerging safety issues and patterns, in partnership with Safety Sciences Strategy </p></li><li><p>Support cross-functional coordination to support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Drive development and implementation of relevant training programs for GPS staff, including maintenance of a standardized Safety Sciences training curriculum, proficiency matrix, and knowledge management repository across both Strategy and Delivery </p></li><li><p>Serve as main point of contact to liaise with Safety Sciences Strategy General Medicine GPS Leads </p></li><li><p>Collaborate with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Implement talent strategy and leadership development initiatives that raise capabilities across the organization </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced Degree required in life sciences or healthcare with 12+ years of PV experience, preferably with a focus on Safety Sciences and General Medicine experience</p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Preferred experience leading a matrixed role working across multiple areas of an organization and people management experience </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Safety Scientist Lead - Rare Disease]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50470]]></requisitionid>
    <referencenumber><![CDATA[R50470]]></referencenumber>
    <apijobid><![CDATA[r50470]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50470/director-safety-scientist-lead-rare-disease/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global Patient Safety Sciences Delivery </strong>team.</p><p>The Director, Global Patient Safety Sciences Delivery, Rare Disease, serves as the first point of contact for all Rare Disease operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness. This role is responsible for high quality, compliant execution of safety surveillance, signal management, and aggregate reporting activities across the portfolio. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Dublin, IRE</p></li><li><p>3 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>The Director is responsible for the development of their team, which is comprised of Safety Scientists. The Director will also be expected to work closely with other Directors on driving standardization and consistency in execution of signal detection activities in partnership. This role will report to the ED, Global Patient Safety Sciences Delivery. </p></li><li><p>Develop common practices, processes and templates to drive standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs </p></li><li><p>Ensure compliance and quality management of Safety Sciences Delivery activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Lead all aspects of signal detection coordination and signal management process across Rare Disease, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies,</p></li><li><p>Analyze aggregate safety data to identify emerging safety issues and patterns, in partnership with Safety Sciences Strategy </p></li><li><p>Support cross-functional coordination to support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Drive development and implementation of relevant training programs for GPS staff, including maintenance of a standardized Safety Sciences training curriculum, proficiency matrix, and knowledge management repository across both Strategy and Delivery </p></li><li><p>Serve as main point of contact to liaise with Safety Sciences Strategy Rare Disease GPS Leads </p></li><li><p>Collaborate with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Implement talent strategy and leadership development initiatives that raise capabilities across the organization </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced Degree required in life sciences or healthcare with 12+ years of PV experience, preferably with a focus on Safety Sciences and Rare Disease experience</p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Preferred experience leading a matrixed role working across multiple areas of an organization and people management experience </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€119,900.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Quality Assurance (On the floor)]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49833]]></requisitionid>
    <referencenumber><![CDATA[R49833]]></referencenumber>
    <apijobid><![CDATA[r49833]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49833/manager-quality-assurance-on-the-floor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager to join our Quality Assurance (QA) on the floor team. This operational position is responsible for the leadership, development, and oversight of the QA team supporting visual Inspection, assembly, labeling, and packaging operations performed at Regeneron’s internal Fill/Finish facility. </p><p><strong>When & where:</strong></p><ul><li>Location: East Greenbush, New York, United States</li><li>Work model, available shifts:<ul><li>Monday-Friday, 8am-4:30pm</li><li>Monday-Friday, 2-10:30pm</li></ul></li></ul><p><strong>Discover your role: </strong></p><ul><li>Manage direct reports, including performance management</li><li>Provide first response for quality and compliance issues encountered on the manufacturing floor</li><li>Lead, set expectations, schedule, and monitor performance standards and goals of assigned team(s) to ensure optimal performance.</li><li>Ensure teams possess the required skills and knowledge, and are appropriately trained, to support plant operations</li><li>Ensure compliance with all regulatory requirements and good documentation practices to provide a safe, quality, and effective product</li><li>Represent Quality function and speak to area processes and responsibilities in regulatory inspections</li><li>Monitor and update area procedures to ensure alignment with policies and operational requirements to ensure quality standards are maintained</li><li>Represent Quality Assurance in support of Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</li><li>Review, edit, or approve Regeneron controlled documents; may review or approve master batch records in electronic execution system</li><li>Influence standards, challenge the status quo, and influence others to achieve results</li><li>May oversee and administer visual inspection training and qualification programs</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Life Sciences or related field; or equivalent combination of education and experience<ul><li>Associate Manager QA: 6+ years of relevant experience</li><li>Manager QA 7+ years of relevant experience</li><li>Level will be determined based on experience</li></ul></li><li>Previous people leadership/supervisory experience</li><li>Knowledge of visual inspection, assembly, labeling, and packaging operations is preferred</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 13:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Associate Scientist, Histology]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48549]]></requisitionid>
    <referencenumber><![CDATA[R48549]]></referencenumber>
    <apijobid><![CDATA[r48549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48549/sr-associate-scientist-histology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Associate Scientist to join our Obesity, Metabolism and Muscle Diseases Group, serving as a central histological resource providing expert tissue processing and staining services across multiple research programs simultaneously. In this role, you will manage end-to-end histological workflows spanning a broad range of tissue types, maintaining rigorous quality standards while navigating competing program demands to deliver high-quality data on time.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Process tissue samples from multiple tissue types (e.g., liver, heart, brain, muscle, adipose), including fixation, dehydration, clearing, embedding, and sectioning</p></li><li><p>Perform routine and special histological staining according to program needs</p></li><li><p>Conduct IHC and IF, developing, optimizing, and validating new protocols, antibody titrations, and antigen retrieval conditions</p></li><li><p>Apply in situ hybridization (ISH/RNAscope) techniques for gene expression localization where required</p></li><li><p>Perform image acquisition using various scanning platforms and manage image data repositories</p></li><li><p>Perform quantitative image analysis, developing and applying customized algorithms as needed</p></li><li><p>Generate high-quality figures and data summaries for internal reports, regulatory packages, and peer-reviewed publications</p></li><li><p>Maintain and communicate a dynamic workload tracker, proactively flagging capacity constraints or scheduling conflicts to stakeholders</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS with 5+ years or MS with 2+ years of relevant experience</p></li><li><p>Proficiency in standard and special histochemical staining techniques across multiple tissue types</p></li><li><p>Demonstrated IHC/IF assay development, optimization, and troubleshooting experience</p></li><li><p>Proficiency with whole-slide imaging systems and digital pathology image analysis software (e.g., HALO)</p></li><li><p>Strong organizational and record-keeping skills, with the ability to manage and prioritize simultaneous requests from multiple stakeholders</p></li><li><p>Excellent oral and written communication skills</p></li><li><p>Preferred: experience with in situ hybridization platforms (RNAscope, BaseScope, FISH)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Obesity, Muscle and Metabolism]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47998]]></requisitionid>
    <referencenumber><![CDATA[R47998]]></referencenumber>
    <apijobid><![CDATA[r47998]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47998/associate-scientist-obesity-muscle-and-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Obesity, Muscle and Metabolism group is seeking a highly motivated Associate Scientist to support the development of therapeutics for muscle diseases. This role involves joining a productive and collaborative team working on treatments for muscular dystrophies, myopathies, and myositis, with the opportunity to engage in cutting edge tissue engineering, disease modeling research as a part of our discovery efforts.</p><p>This is a lab-focused role suited for a bench scientist with a strong foundation in cell biology and physiology, as well as experience in cell culture and tissue engineering. You will be developing assays for validating molecular and functional readouts for our therapeutic programs.</p><p>As an Associate Scientist in the Obesity, Muscle and Metabolism group, your typical day might include:</p><ul><li><p>Maintaining, expanding, and modulating cells in vitro</p></li><li><p>Generation of engineered muscle tissue from primary or iPSC-derived progenitor cells</p></li><li><p>Optimization of cellular assays, and development of readouts for muscle function</p></li><li><p>Handling and caring for mice, including performing procedures such as blood and tissue sample collection</p></li><li><p>Processing of tissue samples for molecular and histological assessments</p></li><li><p>Close collaborative interactions with teams across the organization</p></li><li><p>Analysis of data using biological and statistical software such as ImageJ, Flowjo, Excel, Prism</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Enjoy working in an innovative and team-driven environment</p></li><li><p>Are highly organized, detail-oriented, and motivated, with a creative approach to problem-solving</p></li><li><p>Are adaptable, flexible, and enjoy learning new techniques or switching tasks as needed</p></li><li><p>Are excited to contribute to the development of novel therapeutics</p></li><li><p>Communicate openly and frequently with manager and team members</p></li></ul><p><strong>To be considered for this role, you should have</strong></p><ul><li><p>B.S. or M.S. degree in a relevant field with 1-2 years of experience in muscle biology or a related discipline</p></li><li><p>Experience in tissue culture, cell-based assays, flow cytometry, and histology (e.g. IHC, IF) is highly preferred</p></li><li><p>Experience in mouse handling is highly preferred</p></li><li><p>Proficiency in basic computer applications and experience with biological data collection and analysis is highly preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Corporate Strategy]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47067]]></requisitionid>
    <referencenumber><![CDATA[R47067]]></referencenumber>
    <apijobid><![CDATA[r47067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47067/manager-corporate-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>Our Corporate Strategy team is responsible for conceiving and conducting analyses to help senior leadership make critical decisions for our business. We are looking for a <strong>Manager of Corporate Strategy</strong> who will play a key role in collaborating with functions across Regeneron to drive projects forward from start to finish, building models to assess different business options, and developing actionable insights for presentation to senior leadership.</p><p>This role requires strong analytical and communication skills and the ability to generate clear insights from complex information for leaders across the organization.</p><h3>When & where:</h3><ul><li>Location: Global HQ campus in Tarrytown, NY</li><li>Work model/flexibility: On-site; not eligible for remote or hybrid work arrangements</li><li>Travel percentage: Occasional travel may be required</li></ul><h3>Discover your role:</h3><ul><li>Collaborate with all key functions of the company to gather information and data about our business</li><li>Lead discussions with research, development, and commercial leaders to better understand specific challenges, and help find solutions</li><li>Investigate emerging issues in the external landscape and how other biopharmaceutical companies are reacting to it</li><li>Assess market opportunities and potential return for key R&D investment decisions</li><li>Model future scenarios at the program and corporate level to inform internal business decisions and potential business development deals</li><li>Contribute to the development of our annual long-term corporate outlook presentation to help senior management and the Board of Directors understand the consequences of the company's strategies</li><li>Communicate conclusions and recommendations of analyses to senior management.</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree in a relevant field</li><li>5+ years of work experience in consulting, equity research, or investment banking, or in a strategy role within the biopharmaceutical industry</li><li>Strong analytical skills, including extensive experience using Microsoft Excel and PowerPoint and strong command of financial modeling and valuation</li><li>Problem-solving skills and the ability to think through complex business problems and propose a path to a solution</li><li>Strong interest in understanding “the big picture” of how drugs are developed and deliver meaningful impact to patients</li><li>Comfort working independently and taking action on projects when limited guidance has been provided</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Safety Standards & Training]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50968]]></requisitionid>
    <referencenumber><![CDATA[R50968]]></referencenumber>
    <apijobid><![CDATA[r50968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50968/associate-director-global-patient-safety-standards-training/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Global Patient Safety Standards & Training</strong> team.</p><br><p>Reporting to the Head of Global Patient Safety (GPS) Standards & Training, this position is responsible for establishing and maintaining procedures and policies consistent with Pharmacovigilance regulatory requirements and industry standards. A key part of the role is close collaboration with the Process and Procedures (P&P) team and support of the Process Owner Network (PONs). The responsibilities of this job are foundational in the creation and maintenance of the Pharmacovigilance (PV) System that is essential in enabling the department, and therefore the company, to comply with regulatory PV requirements in all relevant territories worldwide, and to operate efficiently and effectively in alignment with established industry practices. The role supports GPS activities and ensures procedures remain compliant with applicable global regulations as they evolve.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Uxbridge, UK</li><li>3 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Ensure that PV Intelligence updates are systematically assessed and reflected in GPS procedures, so that documented processes remain aligned with current regulatory expectations and the procedural framework is maintained in a state of audit and inspection readiness at all times.</li><li>Act as a key liaison to Process & Procedures (P&P) and the Learning Centre of Excellence (LCoE) for procedural updates, so that procedural changes are accurately captured, appropriately sequenced, and correctly reflected in the associated training curriculum.</li><li>As an SME, partner with the Head of GPS Safety Operations to validate that procedures are fit for purpose against safety practices, closing gaps between documented process and operational execution, including the mapping of procedural documents to regulations and to the training curriculum.</li><li>Apply deep PV process design expertise to develop, implement, and maintain GPS procedures in alignment with regulations, Regeneron Standards, and industry best practices — in partnership with Process & Procedures (P&P), Process Owners, and SMEs — and lead the assessment of evolving global PV regulations.</li><li>As a primary liaison to P&P, partner to set risk-based prioritization and sequencing in managing procedural updates across the GPS framework, in partnership with PONs and GPS Functional Leads.</li><li>Assist in ensuring the correct procedural documents are assigned to the relevant training curriculum.</li><li>Maintain oversight of and support for GPS Planned Process Deviations (PPDs), including guiding SMEs on meeting Global Development Quality (GDQ) approval criteria.</li><li>Coordinate with P&P to align PPD expiration dates with queued procedure projects, adjusting prioritization as needed.</li><li>Serve as GPS's escalation point for internal process and quality-event alignment challenges related to procedural updates, working in alignment with senior management and key stakeholders to investigate and resolve non-compliance.</li><li>Manage, alongside the Process Owners, the content of procedures for GPS, escalating material gaps to senior management, including the maintenance and accuracy of PSMF Annex E in relation to GPS procedures.</li><li>Maintain an overview of CAPAs associated with procedures, including those arising from both audits and inspections, and work closely with SMEs, PONs and the P&P team to ensure timely CAPA closure, including allowing appropriate time for associated training.</li><li>Provide regular metrics on CAPAs, process deviations, and training compliance to GPS department leadership.</li><li>Lead initiatives to enhance GPS process effectiveness and efficiency, including the analytical framework for performance metrics, and present findings and recommendations to leadership.</li><li>Liaise regularly with other functional teams e.g. Corporate and Clinical QA on potential impacts to GPS Processes or GXP-related activities.</li><li>Represent Standards & Training in audits and inspections.</li><li>Serve as the back-up GPS Standards & Training liaison to LCoE.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Minimum Bachelor's degree is required. Education in the life sciences is a strong plus.</li><li>7+ years' experience of Pharmacovigilance/Drug Safety, Regulatory Affairs or Quality Assurance in the pharmaceutical/biotech industry.</li><li>Thorough understanding of Pharmacovigilance/Drug Safety regulations and PV Quality Management Systems.</li><li>Extensive experience managing procedural updates.</li><li>Experience in PV process design and optimization.</li><li>Track record of successful project management relevant to document management.</li><li>Strong organizational skills.</li><li>Ability to write procedural documents to accepted standards of quality.</li><li>Experience presenting in audits and inspections.</li><li>Ability to work collaboratively across functions with SMEs, process owners and cross-functional partners.</li><li>Experience with Data Privacy is a plus</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 13:26:18 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50746]]></requisitionid>
    <referencenumber><![CDATA[R50746]]></referencenumber>
    <apijobid><![CDATA[r50746]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50746/senior-manager-global-patient-safety-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager</strong> to join our <strong>Patient Safety</strong> team. The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><br><ul><li>Work Location: Uxbridge, UK</li><li>3 days per week on site</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Complete signal detection activities in line with approved safety surveillance plan</li><li>Perform signal evaluation for any identified signals and author the safety evaluation reports</li><li>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</li><li>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned compounds</li><li>Participate in other risk management activities as appropriate for assigned compounds</li><li>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</li><li>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</li></ul><br><p><strong>This role requires:</strong></p><p>​</p><ul><li>Minimum a Master's, PhD, or PharmD</li><li>Offers 7+ years of relevant risk management experience in the pharmaceutical/ biotech industry or health authority</li><li>Ability to apply relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments</li><li>Ability to work with a safety system database for purposes of medical case review and simple queries</li><li>Able to be proactive and self-disciplined, you can meet deliverables, and effectively use your time and prioritize</li><li>Ability to effectively communicate (verbal and written) safety findings</li></ul><br><p>#GDPSJobs </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50747]]></requisitionid>
    <referencenumber><![CDATA[R50747]]></referencenumber>
    <apijobid><![CDATA[r50747]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50747/senior-manager-global-patient-safety-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager</strong> to join our <strong>Patient Safety</strong> team. The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Dublin, IRE</li><li>3 days per week on site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Complete signal detection activities in line with approved safety surveillance plan</li><li>Perform signal evaluation for any identified signals and author the safety evaluation reports</li><li>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</li><li>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned compounds</li><li>Participate in other risk management activities as appropriate for assigned compounds</li><li>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</li><li>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</li></ul><br><p><strong>This role requires:</strong>​</p><ul><li>Minimum a Master's, PhD, or PharmD</li><li>Offers 7+ years of relevant risk management experience in the pharmaceutical/ biotech industry or health authority</li><li>Ability to apply relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments</li><li>Ability to work with a safety system database for purposes of medical case review and simple queries</li><li>Able to be proactive and self-disciplined, you can meet deliverables, and effectively use your time and prioritize</li><li>Ability to effectively communicate (verbal and written) safety findings</li></ul><br><p>#GDPSJobs </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager - Data Quality & Governance]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50556]]></requisitionid>
    <referencenumber><![CDATA[R50556]]></referencenumber>
    <apijobid><![CDATA[r50556]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50556/associate-manager-data-quality-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager Data Quality & Governance Operations to join our Data Governance team, supporting our Data Analytics and Data Science organization in a hybrid work model. In this role, you will drive the delivery of data quality controls, data cataloguing, lineage management, and access governance capabilities on the Snowflake platform while collaborating with Data Governance, IT, Analytics, Data Science, and business partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead data quality workstreams within Snowflake, designing, implementing, and monitoring controls for assigned data domains while coordinating thresholds and remediation with data owners.</li><li>Design and maintain auditable, version-controlled data quality rules using Snowflake Data Metric Functions, Dynamic Data Masking, and Row Access Policies aligned to business requirements.</li><li>Monitor rule execution results, triage failures, and deliver exception reports and stakeholder dashboards that provide actionable insights to business teams, data stewards, and data owners.</li><li>Maintain Data Quality Rule Registers and governance documentation that is current, audit-ready, and aligned to enterprise data governance standards.</li><li>Lead catalogue maintenance and metadata management for assigned Snowflake assets within Horizon, ensuring consistent, business-meaningful documentation and inspection-ready lineage records.</li><li>Produce lineage and provenance outputs that help Analytics and Data Science teams understand metric derivation, trustworthiness, and data usage.</li><li>Manage day-to-day access governance activities for Snowflake role-based access control (RBAC) and attribute-based access control (ABAC) structures, supporting certification reviews, audit evidence preparation, and governed Data Marketplace operations.</li><li>You proactively identify risks, continuously improve governance processes, and build productive relationships across technical and business teams while supporting leadership and team development.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree and 7+ years of relevant experience; advanced degree may be considered with 6+ years of relevant experience.</li><li>Solid hands-on experience with Snowflake, including Data Metric Functions, Dynamic Data Masking, Row Access Policies, Tasks, Streams, and Snowpark.</li><li>Strong SQL proficiency with the ability to write, review, and optimize data quality rules, logic, and data transformations.</li><li>Experience designing and implementing data quality controls within a structured governance, compliance, or regulated environment.</li><li>Strong understanding of data governance principles, including data quality dimensions, data ownership models, metadata management, and governance frameworks.</li><li>Experience maintaining data catalogues and business and technical metadata standards, including data lineage documentation and validation.</li><li>Experience managing Snowflake access governance, including RBAC, ABAC, access certification activities, and audit-ready documentation.</li><li>Ability to manage defined workstreams and coordinate delivery across multiple collaborator groups with limited supervision.</li><li>Clear communication skills with the ability to explain data quality, governance, and lineage concepts to non-technical audiences.</li><li>Experience in a regulated industry, preferably pharmaceutical, with familiarity with GxP data integrity requirements or equivalent frameworks.</li><li>Snowflake SnowPro Core certification or equivalent demonstrated experience.</li><li>Familiarity with Snowflake Horizon capabilities, including classification, governance policies, data sharing features, and metadata governance.</li><li>Experience with Python or dbt for Snowflake-based data quality automation.</li><li>Exposure to Data Marketplace or data-as-a-product operating models.</li><li>Familiarity with enterprise data governance tooling.</li><li>Diligent and dependable, with a commitment to delivering accurate, well-documented, audit-ready governance outputs.</li><li>Strong problem-solving, risk identification, and continuous improvement attitude, with the ability to collaborate effectively across Data Governance, IT, Analytics, and business teams and support more junior colleagues.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Automation]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49323]]></requisitionid>
    <referencenumber><![CDATA[R49323]]></referencenumber>
    <apijobid><![CDATA[r49323]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49323/senior-manager-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><strong>Build our future together:</strong></p><p>Our automation systems play a critical role in manufacturing operations. As a Senior Manager, Automation Engineering, you will lead a team responsible for supporting those systems while helping the organization deliver safe, reliable, and compliant manufacturing results. We're looking for a people-focused leader with a strong technical foundation who enjoys developing others, setting clear priorities, and creating an environment where teams can do their best work. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: Monday - Friday 08:00AM - 4:30PM</p></li></ul><p><strong>Discover your role:</strong></p><p>In this role, you will lead a team of Automation Engineers and Supervisors supporting and improving manufacturing automation systems across the site. You will:</p><ul><li><p>Lead, coach, and develop a highly skilled group of technical professionals</p></li><li><p>Set priorities, delegate workload, and help the team deliver work accurately and on time</p></li><li><p>Cultivate a collaborative environment built on trust, respect, and accountability</p></li><li><p>Conduct regular one-on-one meetings, performance discussions, and development planning conversations</p></li><li><p>Lead vendor relationships that support automation systems, infrastructure, and external service providers</p></li><li><p>Partner with Manufacturing, Quality, Validation, Engineering, and IT teams to resolve issues and improve system performance</p></li><li><p>Lead projects that improve reliability, efficiency, and operational performance</p></li><li><p>Support validation activities including design reviews, testing, and implementation of automation changes</p></li><li><p>Supervise GxP-regulated software and automation systems, including change control, investigations, and corrective actions</p></li><li><p>Participate in an on-call rotation approximately every fourth week and remain available to support critical business needs</p></li><li><p>Provide technical and automation support for manufacturing operations and business-critical systems</p></li><li><p>Be responsible for periodic evaluations of automated systems used in commercial manufacturing</p></li><li><p>Develop an understanding of the site's automation landscape, including more than 400 servers and 22 manufacturing unit operations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Engineering, Computer Science, Automation, or a related technical field; equivalent experience may be considered</p></li><li><p>8+ years of experience supporting automation, controls, manufacturing systems, or related technologies</p></li><li><p>At least one year of direct, hands-on experience designing, installing, maintaining, or troubleshooting automated control systems</p></li><li><p>Experience leading technical projects from planning through implementation</p></li><li><p>Strong organizational skills and the ability to manage multiple priorities in a fast-paced environment</p></li><li><p>Experience working within regulated environments with quality and compliance requirements</p></li><li><p><strong>Preferred Qualifications:</strong></p></li><li><p>Experience in pharmaceutical, biopharmaceutical, GxP-regulated manufacturing, nuclear, naval, or similarly structured technical environments</p></li><li><p>Knowledge of software change control, deviation investigations, CAPA, and automation quality systems</p></li><li><p>3+ years of people leadership experience, including management of teams of eight or more employees preferred</p></li><li><p>Leadership style that values collaboration, open communication, and employee development</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$141,400.00 - $231,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Project Manager, Facilities Engineering]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50732]]></requisitionid>
    <referencenumber><![CDATA[R50732]]></referencenumber>
    <apijobid><![CDATA[r50732]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50732/principal-project-manager-facilities-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Saratoga Springs]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We’re seeking a Principal Project Manager to join our facilities engineering department. The Principal Project Manager oversees highly complex design and construction projects. Projects include renovation and repurposing of existing space and may include complete design and construction of new buildings. Applies well developed and broad functional knowledge in a wide variety of complex situations on teams within IOPS.</p><br><br><p><strong>When & where:</strong></p><ul><li>Location: Saratoga Springs, New York, United States </li><li>Work model: Monday-Friday, 8am-4:30pm</li><li>Travel: 5% domestic</li></ul><p><strong>Discover your role:</strong></p><ul><li>Utilizes a high level of expertise in facility systems, designs, and operations to manage complex design and construction projects with minimal supervision</li><li>Proactively identifies and addresses issues throughout a project life cycle to minimize impact to cost and schedule.</li><li>Conducts preliminary surveys and prepares schematic, preliminary and work drawings for the construction and maintenance of new or remodeled facilities</li><li>Estimates cost of projects, writes contracts and specifications for labor materials, and equipment for construction projects, and secures bids from contractors</li><li>Evaluates and makes recommendations concerning changes in contract documents and ensures that authorized changes are implemented, in accordance with federal, state, and local building codes</li><li>Consults with architects, engineers, owners, and contractors regarding preliminary layout, construction procedures, and code requirements that apply to building projects</li><li>Manages cost, schedule, and scope of facilities related projects including renovations, new equipment installs, and new construction</li><li>Coordinates projects with other departments to minimize risk and impact to existing and ongoing operations<ul><li>Compiles required documents for seamless turnover of new or renovated space/equipment to area managers and facilities for maintenance</li><li>Supports equipment qualification efforts an executes new equipment commissioning</li><li>Enters data for new area/equipment into existing quality systems and databases as needed</li><li>Coordinates any necessary specialized training for new systems and equipment</li></ul></li><li>Completes complex analysis and determines project feasibility and design requirements<ul><li>Inspects existing facilities to ascertain their condition</li><li>Prepares reports depicting the condition, deficiencies observed, designs necessary for repairs, and estimated cost of repairs</li><li>Designs, prepares, and/or reviews plans of construction projects</li><li>Provides recommendations on growth direction with supporting justification</li></ul></li><li>Provides mentorship of junior and mid-level; manages a team of contractors</li><li>Designs and implements work in compliance with all safety, site cleanliness, and current good manufacturing practices (cGMP’s)</li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering, Construction management or other related field and 8+ years of relevant experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$103,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 20:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Global Procurement Associate – Leadership Development Rotational Program]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50461]]></requisitionid>
    <referencenumber><![CDATA[R50461]]></referencenumber>
    <apijobid><![CDATA[r50461]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50461/global-procurement-associate-leadership-development-rotational-program/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Global Procurement Associate to join our Future Leaders Development Program This is a full-time, two-and-a-half-year rotational program built to cultivate and develop recent university graduates. In this role, you will rotate through at least three assignments across our Global Category Teams, Center of Excellence, and International Markets teams, gaining hands-on experience while collaborating with internal stakeholders and external suppliers on strategic sourcing initiatives that support the goods and services critical to Regeneron's mission.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work model/flexibility: On-site</li></ul><ul><li>Program duration: Two-and-a-half years, including at least three distinct rotational assignments, with dedicated support from a program lead throughout</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Collaborates with stakeholders to gather business requirements and develop category strategies for strategic sourcing initiatives</li></ul><ul><li>Analyzes data and market trends to inform procurement strategies and business case development</li></ul><ul><li>Negotiates with suppliers to secure favorable terms and supports supplier performance management</li></ul><ul><li>Partners with international colleagues on global procurement efforts and process and system improvement projects</li></ul><ul><li>Assists in developing strategies to deliver goods and services aligned with Regeneron's business objectives</li></ul><ul><li>Supports supplier selection processes, including evaluation and contract drafting</li></ul><ul><li>Rotates through at least three procurement roles across Global Category Teams, the Center of Excellence, and International Markets</li></ul><ul><li>Builds procurement expertise through hands-on, cross-functional experience with guidance from a dedicated program lead</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Associate Level: A four-year degree in supply chain management, completed within the last 12 months or expected this spring</li></ul><ul><li>Strong analytical skills, with the ability to visualize, articulate, and derive insights from data</li></ul><ul><li>Established organizational, planning, and project management skills</li></ul><br><p><strong>Preferred qualifications:</strong></p><ul><li>Highly developed written and verbal communication skills</li></ul><ul><li>Comfort with business systems and technology, including proficiency in AI and MS Office (Word, Excel, PowerPoint)</li></ul><ul><li>Curiosity and a strong willingness to learn</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Genetics Medicine]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50546]]></requisitionid>
    <referencenumber><![CDATA[R50546]]></referencenumber>
    <apijobid><![CDATA[r50546]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50546/medical-director-clinical-development-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[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our MASH/Metabolism team, supporting genetic medicine programs from First in Human through Phase 3. In this role, you will lead cross-functional study teams to shape clinical development strategy and ensure the scientific integrity of trials, while collaborating closely with discovery scientists, translational researchers, and regulatory colleagues.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location: </strong>Tarrytown, NY</li><li><strong>Work model/flexibility: </strong>On-site four days per week</li><li><strong>Travel percentage: </strong>10% to relevant conferences/congresses</li></ul><br><h3>Discover your role:</h3><ul><li>Lead cross-functional teams to craft novel clinical development strategy for genetic medicines</li><li>Partner with discovery and translational scientists to understand emerging genetic targets across MASH, metabolism, rare diseases, and other therapeutic areas</li><li>Author and finalize protocols, amendments, monitoring plans, SAPs, and regulatory submissions</li><li>Evaluate the benefits and risks of assigned therapeutic candidates to inform program decisions</li><li>Oversee trial execution, including adverse event review and ongoing monitoring of patient health and data quality</li><li>Ensure team compliance with FDA, EMA, ICH, and GCP guidelines</li><li>Conduct literature reviews to identify development opportunities from mechanistic, pharmacological, and clinical perspectives</li><li>Represent clinical science in communications and meetings with regulatory agencies</li></ul><br><h3>This role requires:</h3><ul><li>M.D. degree (M.D./Ph.D. or prior research experience preferred)</li><li>Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred)</li><li>2-3+ years of clinical practice or industry experience preferred</li><li>Track record of success in clinical or scientific research settings</li></ul><br><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Lugo Orense Pontevedra (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50495]]></requisitionid>
    <referencenumber><![CDATA[R50495]]></referencenumber>
    <apijobid><![CDATA[r50495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50495/sales-representative-lugo-orense-pontevedra-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Lugo Orense Pontevedra</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Supply Chain & Clinical Drug Logistics]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51086]]></requisitionid>
    <referencenumber><![CDATA[R51086]]></referencenumber>
    <apijobid><![CDATA[r51086]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51086/2027-co-op-supply-chain-clinical-drug-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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Supply Chain & Clinical Drug Logistics to join our Global Development, Global Procurement, and other supply-chain-focused teams, which plan, package, and deliver investigational medicines to clinical trial sites worldwide while managing sourcing, procurement, and supply continuity across the organization.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Warren, NJ and Tarrytown / Sleepy Hollow, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January through May (Spring), January through August (Spring-Summer), and May/June-December (Summer-Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Build planning, forecasting, and inventory-management tools and dashboards to support clinical trial and supply chain operations</li><li>Develop interactive web applications and resource maps that improve visibility and efficiency across the supply chain</li><li>Support day-to-day clinical supply operations to help ensure the right medicine reaches the right trial site at the right time</li><li>Research and evaluate suppliers, materials, and sourcing opportunities to support procurement and supply continuity</li><li>Support supplier relationship management, category strategy development, and spend analytics activities</li><li>Analyze data and apply digital tools, including artificial intelligence (AI) and automation platforms, to streamline supply chain processes and decision-making</li><li>Document processes, maintain organized records, and contribute to continuous-improvement initiatives</li><li>Collaborate with cross-functional teams and present findings and recommendations</li></ul><br><p><strong>Relevant majors: </strong>Supply Chain, Industrial Engineering, Operations Management, Data Science/Analytics, Computer Science</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Product Biochemistry]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51034]]></requisitionid>
    <referencenumber><![CDATA[R51034]]></referencenumber>
    <apijobid><![CDATA[r51034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51034/2027-co-op-product-biochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops to join our Product Biochemistry team, which develops and applies analytical and biophysical characterization methods to understand the structure, stability, and function of Regeneron's biologic and oligonucleotide-based medicines.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><p>● Develop and apply analytical methods to characterize therapeutic proteins, antibodies, and oligonucleotide-based biotherapeutics</p><p>● Evaluate protein biophysical properties such as size, charge, and structural stability using light scattering, chromatography, and electrophoretic techniques</p><p>● Assess antibody developability properties, including hydrophobicity, surface charge, and self-association, using high-throughput screening assays</p><p>● Support structural studies of nucleic acid-based therapeutics using spectroscopic techniques</p><p>● Build automated workflows to streamline analytical data processing and reporting</p><p>● Analyze and interpret experimental data using statistical tools to support scientific decision-making</p><p>● Document experimental procedures, results, and method performance</p><p>● Collaborate with scientists across analytical development and drug discovery teams</p><br><p><strong>Relevant majors: </strong>Biology, Chemistry, Biomedical/Chemical Engineering</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Imaging Sciences]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51083]]></requisitionid>
    <referencenumber><![CDATA[R51083]]></referencenumber>
    <apijobid><![CDATA[r51083]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51083/2027-co-op-imaging-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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a 2027 Co-op to join our Imaging Sciences team, which supports assay development and biological discovery through advanced microscopy, automation, and image analysis.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>This position is full-time and onsite from January-August (Spring-Summer).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Work with widefield, confocal, and high-content imaging systems to support assay development and biological discovery</li><li>Optimize sample preparation workflows and acquire microscopy data</li><li>Implement cell segmentation strategies and generate morphology- and intensity-based metrics to quantitatively assess cellular responses</li><li>Apply artificial intelligence and machine learning (AI/ML) tools to image analysis and data interpretation</li><li>Troubleshoot challenges related to image acquisition, assay optimization, and data interpretation</li><li>Gain exposure to automated laboratory platforms and imaging instrumentation</li><li>Document experimental procedures and results</li><li>Collaborate with scientists across research teams to support imaging-based discovery projects</li></ul><br><p><strong>Relevant majors: </strong>Biology, Chemistry</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Purification Development (PMPD)]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48581]]></requisitionid>
    <referencenumber><![CDATA[R48581]]></referencenumber>
    <apijobid><![CDATA[r48581]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48581/process-development-engineer-iii-purification-development-pmpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build Our Future, Together.</strong></h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer III</strong> to join our Preclinical Manufacturing & Process Development (PMPD) group, on-site in Tarrytown, NY. In this exciting role, you will use your domain expertise in liquid chromatography separations to design, lead, and react to experiments and projects independently, while mentoring less experienced direct reports and team members within the Purification Development (PD) group.</p><br><p>This position offers the opportunity to act as an established authority in chromatography-based separation techniques, proactively identifying improvement opportunities and driving strategy across Regeneron in support of pipeline and assay development, and the release of clinical and commercial products.</p><br><h3><strong>When & where:</strong></h3><br><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site in Tarrytown, NY</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to maintain lab operations and support equipment</li></ul><br><h3><strong>What you'll do:</strong></h3><br><ul><li>Act as an established authority in chromatography-based separation techniques, demonstrating scientific acumen across Regeneron, and determine strategies for improvements</li><li>Begin to lead technology development independently, drive results, and onboard new technologies</li><li>Skillfully write and review complex technical documents typically reviewed by senior leadership</li><li>Take calculated risks to achieve goals, independently and accurately determining strategies to address gaps and implement them effectively</li><li>Ask pointed questions to eliminate ambiguity and provide appropriate solutions</li><li>Make science-based recommendations through novel incorporation of internal and external (literature) learnings</li><li>Maintain and continuously improve lab operations and relevant data or knowledge management systems within your area of expertise</li><li>Anticipate customer needs at an organizational level and proactively shape internal workflows to meet them</li><li>Prepare and deliver effective oral presentations in internal and external professional meetings, sharing cross-functional skills and knowledge</li><li>Collaborate across Regeneron and external groups, with regular interaction with PMPD Senior Leadership</li><li>Represent PMPD in external multi-functional meetings</li><li>Mentor peers, direct reports, and PMPD personnel directly or indirectly through leading, guiding, and assisting</li><li>Contribute to lab equipment maintenance and safety, anticipating and resolving potential problems with supplies and equipment</li><li>Keep up with SOP training and compliance responsibilities</li><li>Communicate relevant information to PMPD Senior Staff as departmental program team representative</li></ul><br><br><p><strong>Let's find out if we're a fit:</strong></p><br><p>Must-haves:</p><ul><li>Degree in an engineering discipline, with 0-2+ years of experience (PhD), 3-5+ years (MS), or 7-10+ years (BS) of industrial experience</li><li>Industrial experience in protein purification</li><li>Demonstrated ability to communicate complex messages clearly and credibly with multifaceted audiences, establishing multi-functional relationships that support proactive teamwork across the organization</li><li>Experience with specialized laboratory software and systems, including Empower, Unicorn, PI Historian, JMP, LIMS, Spotfire, RPES, and ELN</li></ul><br><br><p><strong>Thrive today. Grow tomorrow.</strong></p><br><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Integrated Data Review and Quality]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51027]]></requisitionid>
    <referencenumber><![CDATA[R51027]]></referencenumber>
    <apijobid><![CDATA[r51027]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51027/manager-integrated-data-review-and-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. </p><br><p>We are seeking a Manager, Integrated Data Review & Quality to provide operational leadership for integrated data review activities across our clinical development portfolio. You will manage and directly contribute to study-level data review, help identify and resolve data quality risks, and partner with cross-functional teams to deliver high-quality, inspection-ready clinical data. You may also lead and develop Integrated Data Review & Quality staff while supporting a culture of collaboration, accountability, and continuous improvement. </p><br><p><strong>When & where: </strong></p><p>Hyderabad (hybrid) </p><br><p><strong>Discover your role: </strong></p><ul><li>Manage Integrated Data Review activities in line with established methodologies, standards, processes, and governance requirements. </li></ul><ul><li>Develop, execute, and be responsible for Data Review Plans for assigned studies, ensuring data quality issues and risks are identified, tracked, escalated, and resolved. </li></ul><ul><li>Lead Data Review Team meetings and facilitate discussions on findings, discrepancies, trends, risks, actions, and issue resolution. </li></ul><ul><li>Review and interpret clinical, operational, safety, and external data using listings, visualizations, dashboards, patient profiles, analytical reports, and discrepancy reports. </li></ul><ul><li>Present data review findings, risks, trends, and recommendations to study teams and cross-functional stakeholders. </li></ul><ul><li>Manage study-level queries and discrepancies, including investigation, documentation, blocking issue, corrective action, resolution, and closure. </li></ul><ul><li>Support database readiness and database lock by ensuring data review activities and quality issues are completed and resolved on time. </li></ul><ul><li>Apply risk-based approaches to identify critical data and quality risks aligned with study objectives and critical-to-quality factors. </li></ul><ul><li>Act as a subject matter expert for Integrated Data Review, Data Review Plans, discrepancy management, risk identification, and data quality issue resolution. </li></ul><ul><li>Support SOPs, work instructions, templates, training materials, guidance, metrics, lessons learned, and process improvements. </li></ul><ul><li>Contribute to initiatives involving analytics, automation, AI-enabled solutions, and integrated review across clinical and external data domains. </li></ul><ul><li>Lead, coach, mentor, and develop team members, and support workload planning, resource allocation, priorities, and study deliverables, as applicable. </li></ul><br><p><strong>This role requires: </strong></p><ul><li>A bachelor's degree in Life Sciences, Statistics, Computer Science, or a related field. </li></ul><ul><li>At least 7 years of direct Clinical Data Management experience within biotechnology, pharmaceutical, CRO, or healthcare. </li></ul><ul><li>At least 4 years of experience in Integrated Data Review, Data Quality Management, Risk-Based Data Management, or related clinical data review activities. </li></ul><ul><li>At least 2 years of people management, team leadership, or equivalent experience leading study-level or cross-functional initiatives. </li></ul><ul><li>Strong knowledge of clinical data management, integrated data review, data quality management, issue management, and clinical trial data flow. </li></ul><ul><li>Experience developing and executing Data Review Plans and leading Data Review Team meetings. </li></ul><ul><li>Experience reviewing clinical, operational, safety, and external data to identify trends, anomalies, inconsistencies, and quality risks. </li></ul><ul><li>Experience leading study-level queries and discrepancies and driving root-cause analysis, corrective actions, and resolution. </li></ul><ul><li>Solid understanding of Risk-Based Data Management and Risk-Based Quality Management principles. </li></ul><ul><li>Solid understanding of ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, global data privacy requirements, and inspection readiness. </li></ul><ul><li>The ability to lead and influence in a matrix organization and build strong partnerships across clinical development functions. </li></ul><ul><li>Strong analytical, strategic, critical-thinking, stakeholder management, facilitation, negotiation, and communication skills. </li></ul><ul><li>The ability to manage multiple studies, priorities, and competing deliverables in a fast-paced environment. </li></ul><ul><li>Willingness to travel up to 25%, when required. </li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Summer 2027 MBA Interns | Business Leadership Development Program (BuiLD)]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49784]]></requisitionid>
    <referencenumber><![CDATA[R49784]]></referencenumber>
    <apijobid><![CDATA[r49784]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49784/summer-2027-mba-interns-business-leadership-development-program-build/]]></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>Tarrytown is where medicines are discovered. Our robust research and development engine allows us to discover therapies that could have a profound impact on patient health and scientific outcomes.</p><p>We generate ideas, explore them, and challenge them on their way to becoming life-changing medicines.<br><br>Our unique ability to repeatedly and consistently translate science into medicine has led to a robust pipeline of clinical-stage medicines, all of which were discovered in our laboratories. Our investigational treatments target allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neuromuscular diseases, infectious diseases, and rare diseases.<br><br>It’s a collegial place where science leads, and you’ll be supplied with what you need to do great work. We’re creative thinkers and rigorous workers. We never lose sight of the fact that the work we do here can change the world.<br><br>We are seeking 1st Year MBA students who are passionate about science and the business of biotechnology to join Regeneron’s MBA Summer internship program. Opportunities are available in the following areas:</p><ul><li><p>Corporate Strategy</p></li><li><p>Business Development</p></li><li><p>Market Access Strategy</p></li><li><p>New Products</p></li><li><p>Rare Disease Marketing ​​​ </p></li></ul><p><strong>In this role, a typical internship experience might include the following:</strong></p><ul><li><p>Working on meaningful, high-impact projects</p></li><li><p>Gaining exposure to senior leadership through Lunch & Learns and other events</p></li><li><p>Presenting a final project to senior leaders including the BuiLD board</p></li><li><p>Participating in team building and other fun events with the BuiLD community</p></li><li><p>Experiencing Regeneron’s amazing culture firsthand</p></li><li><p>Collaborating, learning, and growing from a world-class organization</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You are a self-starter with an entrepreneurial spirit</p></li><li><p>You are passionate about Regeneron’s mission of science to medicine</p></li><li><p>You can execute in a cross-functional environment</p></li><li><p>You possess strong project management skills</p></li><li><p>You have proven leadership skills in previous roles</p></li><li><p>You have strong problem-solving skills with the ability to think through complex business problems and propose a path toward arriving at a solution</p></li><li><p>You have integrity and a dedication to high ethical standards</p></li></ul><p><br>To be considered for this opportunity, you must be enrolled in a distinguished MBA program, anticipating graduating in the Spring/Summer of 2028. Experience in biotech, biotech consulting, or biotech investing is preferred.</p><p><strong>When applying, please include a resume and cover letter indicating which business area you are interested in applying (you may apply to more than one). </strong><strong>Applications accepted: October 1, 2026 – December 3, 2026.</strong></p><p><strong>Pay Rate for MBA Summer Interns is $70.40/hr.</strong><br> </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Data Manager Study Lead]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49901]]></requisitionid>
    <referencenumber><![CDATA[R49901]]></referencenumber>
    <apijobid><![CDATA[r49901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49901/manager-clinical-data-manager-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Manager Clinical Data Manager Study Lead , provides oversight of lead Data Manager(s) on assigned clinical data management studies in specific therapeutic areas to assure proper planning and execution for data management deliverables that meet Regeneron standards and within timelines. Assists in the development of SOPs, Working Practice, Data Management Plan, and other data management standards.</p><br><h3>When & where:</h3><ul><li>Location: Remote</li><li>Travel percentage: 25%</li></ul><br><h3>Discover your role:</h3><p>Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for 1 or more complex studies within a given TA. Oversee all DM activities across all stages of the trial from study start-up through archiving. To include but not limited to the following:</p><ul><li>Provide a high level of expertise in data management to support clinical studies.</li><li>Provide clear verbal or written information and hands-on support to project team members and to CROs related to eCRF and database design, data quality, and reporting of database / data quality status.</li><li>Oversee the implementation and execution of procedures for data quality review and data acceptance prior to data analyses and/or database lock.</li><li>Manage data transfers with CROs and third-party data sources, SAE/AE reconciliation and MedDRA/WHO-DD coding.</li><li>Support the transfer, locking, and archiving of study databases. Manage scheduling and time constrains across multiple projects.</li><li>Prepare recommendations for new or improved processes for data management and data flow.</li><li>Perform & document the oversight of CRO data management activities for assigned studies:</li><li>Ensure the design, implementation and maintenance of electronic case report forms, clinical trial database and electronic edit checks are performed according to SOPs and WIs.</li><li>Identify data quality, CRO performance, documentation, process execution gaps and is accountable for resolution.</li><li>Document DM sponsor oversight activities from protocol review through study close-out.</li></ul><p>Review and approve study documentation for assigned studies, (including, but not limited to):</p><ul><li>Data Management Plan or equivalent (includes: Data Review, Reconciliation and Cleaning, Coding, SAE Recon, Local Lab Handling activities for CRF and non-CRF data)</li><li>Case Report Form and Completion Guidelines</li><li>Validation specifications and data transfer specifications</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor Degree or equivalent experience in Mathematics, Science or a related field with at least 7 or more years of clinical data management experience in biotechnology, pharmaceutical or health related industry</li><li>Perform quality review and inspection readiness tasks to meet quarterly Inspection Readiness</li><li>Review (IRR) compliance</li><li>Follow through on gaps until resolution, escalating as necessary.</li><li>Lead/oversee all data management deliverables for assigned studies:</li><li>Ensure deliverable timelines are developed according to the business need and program objectives.</li><li>Ensure snapshot/lock plans are developed and collaborate with the CST for review and approval.</li><li>Ensure regular status updates with metrics are provided to CST.</li><li>Provide program level input to & monitor deliverable timelines.</li><li>Monitor data quality and assess progress of data issue remediation on an ongoing basis.</li><li>Identify risks, propose mitigations, proactively escalate operational or DM vendor or DM CRO issues.</li><li>May provide limited program level support for a small program with limited number of studies</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Physician Scientist, Neuroscience & Ophthalmology Genetics]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46973]]></requisitionid>
    <referencenumber><![CDATA[R46973]]></referencenumber>
    <apijobid><![CDATA[r46973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46973/physician-scientist-neuroscience-ophthalmology-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Physician Scientist to join our Neuroscience and Ophthalmology Therapeutic Area Genetics (TAG) team within the Regeneron Genetics Center. In this role, you will translate human genetic evidence into actionable insights across neurological, psychiatric, ophthalmological, hearing-, and aging-related diseases, designing and interpreting large, complex genetic studies while collaborating with Genome Informatics, Analytical Genomics, Clinical Informatics, and other RGC teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY</li></ul><br><h3>Discover your role:</h3><ul><li>Apply human genetics to target discovery, indication selection, and identification of patient subgroups likely to respond to treatment</li><li>Design, execute, and interpret genetics studies alongside human genetics scientists, bioinformaticians, and statistical geneticists</li><li>Partner with Therapeutic Area Genetics colleagues and RGC teams to deliver complex, high-quality scientific work</li><li>Generate, summarize, and present findings to internal and external audiences</li><li>Lead or contribute to scientific reports and publications</li><li>Represent the TAG team in cross-functional initiatives across RGC and Regeneron</li><li>Collaborate with external industry and academic partners in scientific consortia</li></ul><br><h3>This role requires:</h3><ul><li>MD or MD/PhD with a strong background in human genetics or genetic epidemiology</li><li>Experience designing and leading human genetics studies that deliver medically relevant findings</li><li>Knowledge of study designs and analyses such as GWAS, exome, or genome sequencing across cohort, case-control, or family-based studies</li><li>Strong communication skills, with the ability to present complex genetic findings to varied audiences</li><li>Familiarity with statistical genetics applications (e.g., polygenic risk scores, quantitative trait analyses, Mendelian randomization) and programming/statistical software (e.g., Python, R) preferred</li><li>Experience integrating genetics with other "omics" technologies (e.g., epigenetics, proteomics, RNA-seq) preferred</li></ul><br><p>#MDJobs, #MDJobsRGC, #Neurology, #Ophthalmology, #GWAS</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$243,600.00 - $329,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 12:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[German-speaking Recruiter (f/m/d)]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50958]]></requisitionid>
    <referencenumber><![CDATA[R50958]]></referencenumber>
    <apijobid><![CDATA[r50958]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50958/german-speaking-recruiter-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a German-speaking recruiter (f/m/d) to join our Talent Acquisition team, supporting our DACH markets as well as other international recruitment activities. In this role, you will deliver end-to-end recruitment for professional-level roles while collaborating with hiring managers, Human Resources Business Partners, and Talent Acquisition colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.<br></p><p><strong>When & where:</strong></p><p>Munich </p><p>Hybrid (3 days per week)<br></p><p><strong>Discover your role:</strong></p><br><ul><li>Manage full-cycle recruitment from job briefing through offer management and pre-boarding.</li><li>Source and engage passive talent through LinkedIn Recruiter, talent databases, networks, and events.</li><li>Develop sourcing strategies informed by German market trends, compensation benchmarks, and candidate drivers.</li><li>Partner with hiring managers and Human Resources Business Partners throughout the hiring process.</li><li>Deliver a high-quality candidate experience while representing the employer brand.</li><li>Maintain accurate recruitment data using applicant tracking, customer relationship management, and sourcing systems.</li><li>Provide hiring metrics, pipeline insights, and market intelligence to Talent Acquisition leadership.</li><li>You build trusted relationships and adapt candidate engagement to local market needs.</li></ul><p><br><br></p><p><strong>This role requires:</strong></p><br><ul><li>Bachelor’s degree in Human Resources or a related discipline and 2+ years of Talent Acquisition experience within corporate and/or life sciences agency recruitment environments.</li><li>Experience managing full-cycle recruitment for professional roles across German-speaking markets.</li><li>Proven success sourcing and engaging passive candidates through digital and non-digital channels.</li><li>Full professional proficiency in German, written and spoken.</li><li>Full professional proficiency in English, written and spoken.</li><li>Experience using LinkedIn Recruiter, professional networks, and industry events for sourcing.</li><li>Knowledge of DACH employment law, works council requirements, and General Data Protection Regulation (GDPR).</li><li>Ability to manage multiple requisitions with strong planning and attention to detail.</li><li>Ability to work independently while collaborating across a geographically dispersed Talent Acquisition team.</li><li>Strong communication skills and cultural awareness within the German market context.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€50,625.00 - €84,375.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (Skin) - North East]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46312]]></requisitionid>
    <referencenumber><![CDATA[R46312]]></referencenumber>
    <apijobid><![CDATA[r46312]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46312/sales-specialist-oncology-skin-north-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is growing its newly established International Oncology organisation and is seeking a <strong>Sales Specialist Oncology (Skin) – North East</strong> to join the UK sales team.</p><p>This field-facing role focuses on engaging oncology healthcare professionals, supporting effective clinical practice through high-quality scientific exchange, and representing Regeneron Oncology across the local healthcare system. You will have the opportunity to contribute to a developing oncology portfolio while working closely with cross-functional colleagues.</p><br><p><strong>When & where</strong></p><ul><li><strong>Territory:</strong> North East, UK</li><li><strong>Work model:</strong> Field-facing role</li><li><strong>Travel:</strong> Frequent travel required, including attendance at meetings and congresses.</li></ul><br><p><strong>Discover your role</strong></p><ul><li>Engage oncology healthcare professionals through compliant, scientific discussions.</li><li>Understand local healthcare environments and account context.</li><li>Communicate agreed brand messages to support business objectives.</li><li>Develop and implement territory and account plans using data and insights.</li><li>Manage key accounts in line with regional and country guidance.</li><li>Work closely with Medical colleagues on regional activities.</li><li>Represent Regeneron Oncology at national and international meetings.</li><li>Report performance and market insights to UK leadership.</li></ul><br><p><strong>This role requires</strong></p><ul><li>A Bachelor’s degree or recognised equivalent for sales professionals.</li><li>Experience in customer engagement and disease- or concept-led selling.</li><li>Ability to present effectively to a variety of audiences.</li><li>Strong planning, prioritisation, and territory management skills.</li><li>Confidence engaging customers through face-to-face, remote, and digital channels.</li><li>Competence using CRM systems and multiple IT platforms.</li><li>Qualification in the relevant pharmaceutical industry Code of Practice, such as ABPI or EFPIA.</li><li>Fluency in English.</li><li>Willingness to travel frequently.</li><li>Consistent adherence to industry codes and company procedures, with professional conduct grounded in integrity and ethics.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51124]]></requisitionid>
    <referencenumber><![CDATA[R51124]]></referencenumber>
    <apijobid><![CDATA[r51124]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51124/director-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, External Data Acquisition and Delivery to join our Clinical Data Management. This role provides senior leadership for vendor and provider oversight for data and tech, external data reconciliation, data transfer specifications, external data acquisition capabilities, external data integrity, and inspection readiness across all data types. In this role, you will shape how laboratory, biomarker, eCOA, imaging, genomics, and digital health data are acquired, reconciled, and delivered with quality and speed. You will collaborate with vendors, technology teams, Quality, Procurement, and cross-functional partners while developing a high-performing across multiple regions. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>• Location: Warren, NJ</p><p>• Work model/flexibility: Primarily onsite with hybrid flexibility</p><p>• Travel percentage: Up to 20%</p><br><p><strong>Discover your role:</strong></p><p>• Set the strategic direction for external data acquisition, integration, and reconciliation across all therapeutic areas</p><p>• Own portfolio-level governance of external data quality, data integrity, and risk</p><p>• Own and mature the model for data management, including qualification, onboarding, operational readiness, ongoing performance monitoring, and governance for clinical data management domain in collaboration with the cross-functional team.</p><p>• Guide Data Transfer Specifications, external data management plans, and review plans with cross-functional partners</p><p>• Set EDC-to-vendor reconciliation standards that keep our processes inspection-ready and compliant with ICH-GCP and 21 CFR Part 11</p><p>• Advance new data capabilities, digital health technologies, and automation with Digital & Tech and Data Technology and Innovation</p><p>• Lead, coach, and develop a global team of Associate Directors, managers, specialists, and associates</p><p>• Represent Regeneron in industry forums such as CDISC and SCDM, and deputize for the Global Head as needed</p><br><p><strong>This role requires:</strong></p><p>• Bachelor's degree (advanced degree preferred) in Science, Health, Mathematics, Computing, Information Systems, Data Management, or a related field with 12+ years of progressive experience in clinical data acquisition/management, external data operations. </p><p>• 5+ years of people leadership, including managing managers or senior professionals</p><p>• Experience leading external data vendor oversight, data transfer specification governance, and external data reconciliation in a regulated environment</p><p>• Advanced knowledge of ICH-GCP, 21 CFR Part 11, CDISC standards, and EDC platforms such as Medidata Rave, Veeva, or Oracle InForm</p><p>• Society of Clinical Data Management or ACRP-CP certification is recommended</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Corporate Affairs]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51208]]></requisitionid>
    <referencenumber><![CDATA[R51208]]></referencenumber>
    <apijobid><![CDATA[r51208]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51208/senior-manager-corporate-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Corporate Affairs to join our team - a dynamic role that puts you at the intersection of manufacturing excellence and global enterprise communications. You will be supporting our Manufacturing site in Limerick in an onsite position. If you are a strategic communications professional ready to make your mark at one of the world's leading biotechnology companies, this could be the role for you. </p><br><p>In this role, you will help develop and drive compelling communications and engagement programming, working in partnership with business group leaders, while also advancing enterprise programs targeting our global employee base, with a focus on our international markets outside the U.S. The successful candidate will join a dynamic and high-performing global Corporate Affairs team that drives strategic programs aligned with Regeneron’s mission to turn science into medicine to bring important new medicines to patients in need. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><br><ul><li>Location: Limerick</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Partner and support the global manufacturing strategy for the Raheen site to strengthen alignment, reinforce a “One IOPS” culture and bring the IOPS story to life</li><li>Serve as the international communications lead for all-company events, ensuring a consistent and engaging employee experience across sites</li><li>Serve as international content lead and liaison, building and managing processes to source updates and stories, working in partnership with colleagues across Corporate Affairs and key contacts across our international sites (EU, UK, Japan, India, and Canada)</li><li>Support site director meetings by helping leadership shape agenda and develop content aligned with IOPS business messaging </li><li>Manage execution of our global social impact strategy, including Day for Doing Good, our annual days of service, and local STEM-related activities throughout the year</li><li>Manage local vendor partners that support key communications and engagement initiatives</li><li>Extend enterprise communications strategy and messaging into local international channels, tailoring as needed</li><li>Develop, socialize, and maintain the International Communications Best Practices Playbook(s)</li></ul><br><br><p><strong>This role requires:</strong></p><br><ul><li>7+ years of communications experience, including experience in employee communications </li><li>BS/BA in communications, public relations, journalism, or a related field </li><li>Demonstrated experience in communications planning, project management, and event coordination </li><li>Excellent writing, editing, and storytelling skills </li><li>Ability to build relationships across all levels of the organization </li><li>Ability to prioritize workload for multiple stakeholders and navigate ambiguity </li><li>Cultural fluency; a collaborative, inclusive mindset </li><li>Experience with digital media platforms </li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€86,800.00 - €141,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 03:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Medical Affairs Operations - Uxbridge, UK]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51098]]></requisitionid>
    <referencenumber><![CDATA[R51098]]></referencenumber>
    <apijobid><![CDATA[r51098]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51098/manager-medical-affairs-operations-uxbridge-uk/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Manager, Medical Affairs Operations</strong></p><br><p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager, Medical Affairs Operations, located in UK</strong> to join our Medical Affairs team in charge of our Hub Markets, supporting our country organisation in a hybrid work mode. In this role, you will deliver compliant country Medical Affairs activities while collaborating with local Medical Affairs colleagues and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When</strong> <strong>&</strong> <strong>where:</strong> </p><ul><li>Uxbridge</li><li>Office-based - Hybrid</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Maintain audit readiness through documentation, tracking, and records management.</li><li>Optimise transparency reporting, Anti-Bribery and Anti-Corruption documentation, and compliance processes.</li><li>Complete assigned medical activities in local systems through regulatory and GxP completion.</li><li>Localize global, regional, and local standard operating procedures and work instructions.</li><li>Handle vendor onboarding, contracts, purchase orders, budgets, and expense reconciliation.</li><li>Coordinate medical meetings, congress logistics, agenda flow, actions, and follow-up.</li><li>You bring structure and service focus to cross-functional Medical Affairs operations.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in life sciences, business, or a related field, or equivalent experience.</li><li>7+ years in Medical Affairs operations, coordination, project support, or administration.</li><li>Pharmaceutical or biotech environment experience.</li><li>Experience in a country organization or local operating company.</li><li>Solid understanding of compliance, transparency, and regulated country-level processes.</li><li>Fluency in French, with business-proficient English preferred.</li><li>Microsoft Office and relevant systems experience, including Veeva CRM, Vault Medical, PromoMats, and procurement tools.</li><li>Occasional business travel as required.</li><li>Country Medical Affairs operations experience, including event and congress planning.</li><li>Contract and procurement systems knowledge, such as iCertis or SAP.</li><li>Experience partnering with Finance and Procurement teams.</li><li>Commercial operations experience desirable.</li><li>Strong organization, communication, stakeholder management, and cross-functional collaboration skills.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Development Program Management]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51071]]></requisitionid>
    <referencenumber><![CDATA[R51071]]></referencenumber>
    <apijobid><![CDATA[r51071]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51071/senior-manager-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>With guidance, this role (Senior Manager, Development Program Management) uses program management knowledge and experience in the drug development industry to provide operational leadership and manage development program(s). This individual contributes to the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and monitor the execution of these plans from preclinical through commercialization/lifecycle management. </p><br><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY</li></ul><br><p><strong>Discover your role:</strong></p><ul><li><strong>Development Teams: </strong>In partnership with lead DPM and Global Program head (GPH), contributes to strategic program teams (SPT) and sub teams, and participates in key governance meetings. Uses knowledge of drug development and project/program management to work with cross functional team members to coordinate development of and track integrated project/program plans, timelines and budgets based on program vision. Assists in the identification and assessment of risks to the project, tracks risks and issues, and contributes to the development of risk management plans.</li><li><strong>Business Acumen: </strong>With oversight can identify, manage and handle relevant business situations arising on Development Teams, and can facilitate a positive outcome. Manages project management planning systems (MS Project, SharePoint) for assigned programs/projects. Leverages systems and tools to move the program and business forward.</li><li><strong>Communication:</strong> Tailors communication based on audience, effectively framing and communicating nuanced context for stakeholders and summarizing key decisions and actions. Contributes to a culture which promotes and encourages open communication, transparency, accountability and learning from mistakes.</li><li><strong>Problem Solving: </strong>Works with team to proactively identify, develop and implement viable long-term solutions to project issues. Develops tools and mechanisms for documenting and monitoring progress of solution implementation. Escalates complex problems or issues to lead DPM in a timely and appropriate manner.</li><li><strong>Leadership</strong>: Influences teams and may influence across functions. Keeps manager and key stakeholders informed to ensure alignment. May represent function in collaborative activities with other departments. With support, identifies and manages conflict.<br></li></ul><p><strong>This role requires:</strong></p><ul><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels, both internal and external to the company, in order to establish credibility with all project stakeholders.</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 facilitate strong cross-functional collaboration, </li><li>Resolve and negotiate conflicts or issues 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 entrepreneurial organizations; expert in dealing with ambiguity and uncertainty. </li></ul><br><p><strong>MINIMAL EDUCATIONAL REQUIREMENTS:</strong></p><p>High School Diploma</p><p>Associates Degree</p><p>Bachelor's Degree</p><br><p><strong>MINIMUM YEARS OF EXPERIENCE:</strong> 7+ years of relevant broad project / program management experience required, preferably in the pharmaceutical or related industry.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Site Management]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51041]]></requisitionid>
    <referencenumber><![CDATA[R51041]]></referencenumber>
    <apijobid><![CDATA[r51041]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51041/senior-manager-global-site-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[<h3>Build Our Future Together</h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager, Global Site Management</strong> to join our <strong>Global Development team</strong> in a hybrid role supporting our global clinical trial portfolio. In this position, you will play a meaningful role in designing and leading all aspects of risk-based monitoring strategies, ensuring high-quality site management and operational execution across clinical studies. Working closely with Clinical Trial Management, Central Monitoring, Quality, and external partners, you will help drive inspection readiness, study performance, and patient-focused outcomes. This is an opportunity to supply to a science-driven organization committed to advancing innovative therapies for patients worldwide!</p><h3><br></h3><h3>When & Where:</h3><ul><li><strong>Location:</strong> Warren, NJ or Armonk, NY</li><li><strong>Work Model/Flexibility:</strong> Hybrid 3 days a week</li><li><strong>Shift Requirements:</strong> Standard business hours</li><li><strong>Travel:</strong> Up to 25%</li></ul><br><h3>Discover Your Role</h3><br><ul><li>Lead the development and implementation of study-specific risk-based monitoring and site management strategies across global clinical programs.</li><li>Partner with Clinical Trial Management teams to identify critical data, key study risks, and appropriate monitoring approaches.</li><li>Provide oversight of CRO and FSP monitoring activities to ensure quality, compliance, and study execution objectives are achieved.</li><li>Evaluate performance metrics, key risk indicators, and operational trends to proactively identify and mitigate study risks.</li><li>Collaborate with cross-functional partners to support study planning, budget forecasting, inspection readiness, and operational excellence.</li><li>Establish productive relationships with investigator sites, CRO partners, and internal stakeholders to drive study performance and data quality.</li><li>Act as a subject matter expert in risk-based quality management (RBQM), monitoring strategy, and site management standards.</li><li>Contribute to process improvement initiatives and innovation efforts that enhance clinical trial delivery and operational efficiency.</li></ul><br><h3>This Role Requires</h3><br><ul><li>Bachelor's degree and <strong>8+ years of proven experience</strong> in clinical research, clinical operations, site management, monitoring, or related pharmaceutical/biotechnology environments.</li><li>Strong knowledge of clinical trial operations, risk-based monitoring methodologies, and site management practices.</li><li>Experience working within a Risk-Based Quality Management (RBQM) framework.</li><li>Working knowledge of ICH-GCP guidelines and applicable regulatory requirements.</li><li>Demonstrated experience managing and overseeing CROs, Functional Service Providers (FSPs), or external clinical partners.</li><li>Excellent communication, collaboration, organizational, and stakeholder management skills.</li></ul><br><h3>Preferred Qualifications</h3><br><ul><li>Experience developing monitoring plans, critical data identification strategies, and targeted Source Data Verification (tSDV) approaches.</li><li>Experience supporting global clinical studies across multiple countries and regions.</li><li>Familiarity with performance metrics, Key Risk Indicators (KRIs), and operational risk management processes.</li><li>Proven ability to influence cross-functional teams and drive process improvement initiatives.</li><li>Experience participating in regulatory inspections, audits, and inspection readiness activities.</li><li>Strong critical thinking, problem-solving, and decision-making capabilities in complex clinical development environments.</li></ul><p><br><br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Financial Analyst, R&D Finance]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51338]]></requisitionid>
    <referencenumber><![CDATA[R51338]]></referencenumber>
    <apijobid><![CDATA[r51338]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51338/senior-financial-analyst-rd-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>Regeneron's Finance group is looking for an energetic Sr. Financial Analyst to become an integral part of the Program Finance team. Program Finance is supporting development programs within multiple therapeutic areas, providing analyses and interpretation for relevant stakeholders including Senior Management, Program Management, Development teams, Clinical Project Managers, Strategic Alliance Management, and external collaborators.</p><p>In this exciting role, you will also play a critical part in program budget planning and forecasting and maintain a solid command of all aspects of programs. You will support Global Development (GD) cost center reporting and tracking, producing monthly spend and variance analyses, partnering with functional owners to explain drivers, and maintaining governance-aligned budget tracking.</p><br><p><strong>When & Where</strong></p><p>This role is going to be based on-site in Sleepy Hollow, NY and is required to be on-site 4 days per week.</p><br><p><strong>Discover Your Role</strong></p><ul><li>Own and lead the financial support for assigned programs and collaborations including preparing quarterly forecasts and monthly actuals reporting and effectively communicating the status of each program's financial execution and variances to plan/forecast</li><li>Support clinical teams with building detailed budgets for clinical trials, and track and monitor clinical trial financials through study completion</li><li>Translate operational components of development plans to detailed forecasts for internal and external clinical costs and load into Hyperion</li><li>Work with cross-functional teams, subject matter experts and external collaboration partners to manage and communicate P&L implications, including working with the Accounting group to ensure completeness and accuracy of actuals and clinical trial accruals</li><li>Lead and participate in departmental initiatives to improve ways of working including process streamlining, best practice identification and implementation, and standardization of financial templates and deliverables</li><li>Perform ad hoc projects and financial analyses to solve business problems and effectively communicate findings and recommendations to senior management and other stakeholders</li></ul><p><strong>This Role Requires</strong></p><ul><li>Bachelor’s degree in a finance, business, scientific, or quantitative field with </li><li>At least 5+ years of experience with forecasting, budgeting and/or business partnering, ideally in a science or research-driven environment.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Associate Scientist - Analytical Development, Regeneron Cell Medicines (RCM)]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47761]]></requisitionid>
    <referencenumber><![CDATA[R47761]]></referencenumber>
    <apijobid><![CDATA[r47761]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47761/sr-associate-scientist-analytical-development-regeneron-cell-medicines-rcm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sr Associate Scientist, RCM Analytical Development</strong> to join our Regeneron Cell Medicines (RCM) team. In this role, you will support cell therapy programs by developing, optimizing, and executing biophysical assays to characterize lentiviral vectors, planning and performing experiments, developing new assay protocols, and analyzing and communicating results to advance therapies for patients.</p><p>This position offers the opportunity to partner cross-functionally across RCM to meet program timelines and deliver high-quality analytical data in a fast-paced, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Shift Requirements: Full-time, standard business hours</li><li>Location: On-site laboratory setting</li><li>Flexibility & travel: Minimal to no travel; on-site presence required to support lab operations, instrument maintenance, and assay execution</li></ul><br><p><strong>What you'll do:</strong></p><ul><li>Advance analytical development for cell therapy programs, with a primary focus on lentiviral vectors (LVVs)</li><li>Strengthen existing and establish new biophysical methods to characterize LVVs</li><li>Analyze, interpret, and clearly present complex datasets to technical and cross-functional audiences</li><li>Partner with cross-functional teams across RCM to troubleshoot challenges, align on priorities, and support program execution</li><li>Author and review technical documentation, including assay protocols, method development reports, and data summaries</li><li>Maintain complete, timely, and compliant electronic lab notebook records, support instrument upkeep, and independently troubleshoot equipment and assays</li></ul><br><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>This is a hands-on, on-site laboratory role focused on biophysical characterization work, requiring independent design and execution of experiments alongside routine laboratory operations and instrument maintenance.</li><li>Flexibility to thrive in a fast-paced, collaborative environment, quickly learn new technologies, and prioritize effectively with minimal supervision is required.</li></ul><br><p><strong>Let's find out if we're a fit:</strong></p><p>Must-haves:</p><ul><li>Bachelor's or Master's degree in Biophysics, Biochemistry, Molecular Biology, or a related field, with 4-6+ years of proven experience characterizing and quantitatively analyzing lentiviral vectors</li><li>Ability to work independently to design experiments, as well as interpret, document, and communicate results</li><li>Self-motivated and proactive, with the ability to prioritize effectively and drive work forward with minimal supervision</li></ul><br><p>Preferred / nice-to-haves:</p><ul><li>Experience with biophysical characterization techniques for sizing and counting particles, such as DLS, MRPS, and fluorescent labeling assays</li><li>Understanding and knowledge of viral vector biology, design, process, and gene delivery mechanisms</li></ul><br><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Production AI/ML Engineering, Advanced Informatics]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48875]]></requisitionid>
    <referencenumber><![CDATA[R48875]]></referencenumber>
    <apijobid><![CDATA[r48875]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48875/associate-manager-production-aiml-engineering-advanced-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, Production AI/ML Engineering to join our Advanced Informatics team. In this role, you will architect and scale the computational ecosystem that powers our AI/ML applications — transforming population-scale clinical and claims data into reliable, production-grade model inference — while collaborating closely with Applied AI managers, clinical informaticists, and data governance partners. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Tarrytown or Armonk, NY or Warren, NJ</p><p><strong>Discover your role:</strong><br>• Architect and maintain a scalable AWS/Kubernetes ecosystem supporting model training, batch inference, and real-time serving<br>• Design and maintain production-grade ML pipelines over population-scale clinical and claims data, including ingestion, normalization, and transformation across controlled terminologies (SNOMED CT, ICD-10/11, LOINC, RxNorm, OMOP CDM).<br>• Develop RESTful APIs that reliably expose model inference to downstream teams and applications<br>• Operationalize models from the Applied AI team — owning deployment, versioning, rollback, and A/B testing<br>• Build MLOps infrastructure (CI/CD, feature stores, model registries) and champion engineering best practices<br>• Own monitoring, alerting, and incident response for production ML systems<br>• Partner with data governance and compliance to ensure pipelines and deployments adhere to data use agreements and de-identification standards.<br>• Shape capacity planning and the long-term technical roadmap for the team's AI/ML platform</p><p><strong>This role requires:</strong><br>• Bachelor's degree in Computer Science, Software Engineering, Data Science, Biomedical Informatics, or related (Master's preferred) with 7–9 years of progressive ML/platform/software engineering experience with an infrastructure focus<br>• Proven experience designing and operating ML infrastructure at enterprise scale on AWS (SageMaker, ECS, EC2, S3, Lambda, or equivalent).<br>• Strong Kubernetes expertise: cluster management, workload scheduling, autoscaling, and deploying containerized ML services in production.<br>• Proficiency building and maintaining RESTful APIs; experience with API design, versioning, performance tuning, and integration with ML serving frameworks.<br>• Hands-on experience with Postgres: schema design, query optimization, and integration into data and ML pipelines.<br>• Expert-level Python and SQL; strong software engineering fundamentals including Git, modular design, testing, and CI/CD.<br>• Proficiency with MLOps tooling: experiment tracking (MLflow, W&B), model registries, containerization (Docker), and pipeline orchestration (Airflow, Prefect, or similar).<br>• Informatics knowledge with health or life sciences data — EHR/EMR records, claims data, clinical notes, or administrative data is preferred. </p><p>#AAI<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Manufacturing Technical Services]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49659]]></requisitionid>
    <referencenumber><![CDATA[R49659]]></referencenumber>
    <apijobid><![CDATA[r49659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49659/senior-director-manufacturing-technical-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Manufacturing Technical Services (MTS) to join our team, supporting our fill/finish clinical and commercial drug product manufacturing operations. In this role, you will provide technical leadership across equipment characterization, cycle development, tech transfer, and troubleshooting for our aseptic fill/finish value stream, while collaborating with Quality, Engineering, Automation, and Validation to keep our fill/finish equipment and processes in a state of control.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Monday- Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads technical characterization, cycle development, and troubleshooting for aseptic fill/finish equipment, including filling systems, isolators, stoppering, capping, visual inspection, device assembly, labeling, and packaging</p></li><li><p>Directs tech transfer activities, including clinical and new product introductions, site-to-site transfers, and scale-up/scale-down</p></li><li><p>Owns the visual inspection program, spanning manual inspector qualification/AQL and automated inspection (AVI) systems, including defect library development and camera/algorithm optimization</p></li><li><p>Oversees alarm management and process monitoring strategy, including PAT, continuous monitoring, and alarm rationalization</p></li><li><p>Serves as a key technical resource during regulatory inspections and health authority interactions, authoring and defending technical justifications</p></li><li><p>Owns CAPA and root cause investigations for deviations and complaints tied to fill/finish equipment or process</p></li><li><p>Builds and develops a multi-faceted technical team, growing the maturity of the MTS function over time</p></li><li><p>Communicates technical and equipment risk clearly to senior leadership, translating it into executable steps for manufacturing operations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Director Level: Bachelor's or advanced degree in Engineering, Life Sciences, or a related technical field and 10+ years of biopharmaceutical manufacturing experience, including 5+ years in aseptic fill/finish or equivalent combination or education and experience</p></li><li><p>Senior Director Level: Bachelor's or advanced degree in Engineering, Life Sciences, or a related technical field and 15+ years of biopharmaceutical manufacturing experience, including 8+ years in aseptic fill/finish or equivalent combination or education and experience</p></li><li><p>Deep expertise in aseptic fill/finish equipment characterization and troubleshooting for commercial and clinical manufacturing lines</p></li><li><p>Strong regulatory and quality acumen, with the ability to support inspections and defend technical positions to health authorities</p></li><li><p>Platform experience with Bausch+Ströbel (VarioSys, CombiSys), Seidenader Inspection, Harro Hofliger assembly, or Körber (Dividella/Pester) packaging preferred</p></li><li><p> Automation/data historian familiarity (PAS-X, FactoryTalk, PI Vision) preferred</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$172,200.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45310]]></requisitionid>
    <referencenumber><![CDATA[R45310]]></referencenumber>
    <apijobid><![CDATA[r45310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45310/medical-director-clinical-development-oncology-lung-breast-colorectal-gastric-cancers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Oncology team, supporting solid tumor drug development on-site in Tarrytown, NY or Warren, NJ. In this role, you will design clinical study concepts, oversee the medical and scientific integrity of clinical trials, and ensure patient safety across trial activities while collaborating with the Global Clinical Study Team and key investigators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li><p><strong>Location:</strong> Tarrytown, NY</p></li><li><p><strong>Travel: </strong>10% to relevant conferences</p></li></ul><br><h3>Discover your role:</h3><ul><li><p>Define clinical trial-related goals and objectives</p></li><li><p>Conduct literature and database research to inform trial design</p></li><li><p>Ensure the scientific accuracy of clinical study concepts through rigorous review and consultation with internal and external experts</p></li><li><p>Oversee the medical content of clinical study reports and the analysis of clinical data, including safety monitoring</p></li><li><p>Safeguard patient safety across all trial activities and procedures</p></li><li><p>Lead and supervise the Global Clinical Study Team to deliver high-quality program milestones on schedule</p></li><li><p>Build and maintain relationships with key study investigators</p></li></ul><br><h3>This role requires:</h3><ul><li><p>MD or MD/PhD degree or the equivalent</p></li><li><p>Oncology clinical fellowship training strongly preferred</p></li><li><p>At least 2 years of translational and/or clinical research experience in academia or industry</p></li></ul><p>#MDJobs, #MDJobsCD, #GDTherapeuticJobs, #Oncology</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Dermatology-Bronx, NY]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49767]]></requisitionid>
    <referencenumber><![CDATA[R49767]]></referencenumber>
    <apijobid><![CDATA[r49767]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49767/medical-specialist-i-dermatology-bronx-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Bronx, NY</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus</p></li><li><p>The successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience</p></li><li><p>A minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred</p></li><li><p>This role requires the ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45490]]></requisitionid>
    <referencenumber><![CDATA[R45490]]></referencenumber>
    <apijobid><![CDATA[r45490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45490/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager </strong>to join our<strong> Regulatory Affairs Advertising and Promotion</strong> team. In this role, you will apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I – Allergy/ENT – Manhattan North, NY]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49970]]></requisitionid>
    <referencenumber><![CDATA[R49970]]></referencenumber>
    <apijobid><![CDATA[r49970]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49970/medical-specialist-i-allergyent-manhattan-north-ny/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Manhattan]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p><strong> </strong></p><p>The Medical Specialist (Sales Representative), Allergy/ENT (MS) will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists, Otolaryngologists (ENT) and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently deliver product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Allergy and Otolaryngology (ENT) therapeutic areas to generate product utilization. The MS will develop strong working relationships with Allergy/ENT experts and clinicians in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate in and help lead initiatives to support sales success as assigned (e.g. participate in industry-related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Manhattan North</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven history of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Allergy/ENT/Dermatology market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Scientist, Immunology]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50049]]></requisitionid>
    <referencenumber><![CDATA[R50049]]></referencenumber>
    <apijobid><![CDATA[r50049]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50049/senior-manager-clinical-scientist-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Clinical Sciences team, supporting our Immune/Inflammatory clinical development programs. In this role, you will help lead the design, execution, and interpretation of clinical studies, partnering closely with Medical Directors and cross-functional study teams to advance candidates through early and/or late phase development. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li><strong>Location:</strong> Tarrytown, NY, Cambridge, MA, or Warren, NJ</li></ul><h3>Discover your role:</h3><ul><li>Lead the scientific strategy behind clinical studies from design through execution and reporting</li><li>Partner with Medical Directors and cross-functional teams to shape protocols, amendments, and study conduct</li><li>Build deep expertise in disease biology, compound mechanism of action, and the competitive treatment landscape</li><li>Author and review key trial documents, including expanded synopses, monitoring plans, and study reports</li><li>Safeguard patient safety through ongoing clinical and medical data review</li><li>Identify risks to study integrity early and drive practical mitigation strategies</li><li>Represent Clinical Sciences on program teams, steering committees, and safety monitoring boards</li><li>Champion consistent, high-quality data review practices across assigned studies</li></ul><h3>This role requires:</h3><ul><li>MS, PhD, or PharmD in a related scientific field, plus 8+ years of pharmaceutical clinical drug development experience (other levels considered based on experience)</li><li>Proven knowledge of GCP, ICH guidelines, clinical trial design, and regulatory requirements</li><li>Strong medical writing skills and clinical research methodology expertise</li><li>Experience in Immune/Inflammatory clinical trials preferred</li><li>Demonstrated success working cross-functionally in a matrix organization</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead AI Engineer]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50147]]></requisitionid>
    <referencenumber><![CDATA[R50147]]></referencenumber>
    <apijobid><![CDATA[r50147]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50147/lead-ai-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Job Title: </strong>Lead AI Engineer</p><p><strong>Department: </strong>Digital Transformation – AI Strategy & Execution</p><p><strong>Location: </strong>Sleepy Hollow, New York</p><p><strong>Employment Type: </strong>Full-Time</p><p><strong>Experience Required: </strong>7–10 Years</p><h3>About Regeneron</h3><p>Regeneron is a leading biotechnology company headquartered in Tarrytown, New York, renowned for its innovative research and development of life-changing therapies. With a strong focus on ophthalmology, oncology, inflammation, cardiovascular diseases, and infectious diseases, Regeneron has brought groundbreaking medicines to market — including EYLEA® and the REGEN-COV™ monoclonal antibody cocktail. Our commitment to scientific excellence, cutting-edge technology, and patient impact has positioned Regeneron as a global leader in biotechnology.</p><h3>Position Overview</h3><p>Regeneron is seeking an experienced Lead AI Engineer to serve as a technical leader within the AI Strategy & Execution organization. In this role, you will architect and deliver enterprise-scale AI capabilities — spanning intelligent agents, LLM-powered applications, and AI platform services — that accelerate drug discovery, clinical research, and enterprise productivity. You will lead a team of engineers, drive cross-functional collaboration, and communicate AI strategy to senior stakeholders, all while maintaining a strong hands-on presence in Python development and AI systems design.</p><h3>Key Responsibilities</h3><h3>AI Engineering & Intelligent Systems</h3><ul><li>Lead end-to-end design, development, and deployment of enterprise AI applications and LLM-powered systems, ensuring production-grade quality, security, and scalability.</li></ul><ul><li>Design and build AI Agents and autonomous systems using agentic frameworks including LangChain, LangGraph, Strands, and CrewAI, applying ReAct, tool-use, planning, and memory management patterns.</li></ul><ul><li>Develop and operate MCP (Model Context Protocol) servers for standardized, secure integration between AI agents and enterprise data sources.</li></ul><ul><li>Apply advanced LLM techniques — prompt engineering, fine-tuning, and retrieval-augmented generation (RAG) — to build intelligent, context-aware applications.</li></ul><ul><li>Architect and manage vector database solutions (Milvus DB preferred) supporting semantic search, knowledge retrieval, and RAG pipelines.</li></ul><ul><li>Architect RESTful APIs that expose AI capabilities to internal platforms and downstream business applications.</li></ul><h3>LLM & AI Platform Management</h3><ul><li>Administer and continuously evolve the enterprise LLM and AI Gateway platform, including model routing, access controls, rate limiting, usage observability, and multi-model orchestration.</li></ul><ul><li>Evaluate and onboard new foundation models (OpenAI, Anthropic, AWS Bedrock, and others) in alignment with enterprise security and compliance standards.</li></ul><h3>Technical Leadership & Team Management</h3><ul><li>Lead, mentor, and manage a team of AI engineers, conducting code reviews, setting technical standards, and fostering a culture of engineering excellence.</li></ul><ul><li>Contribute to the organization’s AI roadmap through architectural design reviews, technical strategy, and proof-of-concept development.</li></ul><ul><li>Troubleshoot complex issues across AI model serving, APIs, and platform layers.</li></ul><h3>Cross-Functional Collaboration & Stakeholder Engagement</h3><ul><li>Partner with business units, data scientists, and clinical research teams to identify AI opportunities and translate them into scalable technical solutions.</li></ul><ul><li>Serve as the primary technical point of contact for enterprise AI platform discussions, presenting findings and recommendations to senior leadership.</li></ul><ul><li>Engage with external vendors, cloud providers, and AI research organizations to evaluate and integrate emerging capabilities.</li></ul><h3>Requirements & Qualifications</h3><h3>Education</h3><ul><li>Bachelor’s, Master’s, or Ph.D. in Computer Science, Computer Engineering, Artificial Intelligence or a related technical field.</li></ul><h3>Experience</h3><ul><li>7–10 years of progressive software and AI engineering experience, with at least 3 years in a technical lead or senior individual contributor role.</li></ul><ul><li>Expert-level Python development skills, including production REST API development with FastAPI.</li></ul><ul><li>Proven hands-on experience building AI Agents, MCP Servers, and LLM-powered applications using frameworks such as LangChain, LangGraph, Strands, or CrewAI.</li></ul><ul><li>Hands-on experience with vector databases (Milvus DB preferred) for RAG and semantic search pipelines.</li></ul><ul><li>Experience administering LLM API gateway platforms, including model routing, observability, access governance, and multi-model orchestration.</li></ul><ul><li>Experience with foundation models from OpenAI, Anthropic, AWS Bedrock, and other major providers.</li></ul><ul><li>Working knowledge of AWS cloud services relevant to AI workloads (SageMaker, Bedrock, EKS, Lambda, S3); Kubernetes and CI/CD experience is a plus.</li></ul><ul><li>Experience in the biotechnology, pharmaceutical, or healthcare industry preferred.</li></ul><h3>Technical Competencies</h3><ul><li>Programming: Python (expert-level).</li></ul><ul><li>AI Frameworks & Runtimes: LangChain, LangGraph, Strands, CrewAI; AWS Bedrock AgentCore.</li></ul><ul><li>LLM Techniques: Prompt engineering, fine-tuning, RAG, vector databases (Milvus DB preferred).</li></ul><ul><li>AI Platform: LLM Gateway management, model routing, multi-model orchestration, TensorFlow, PyTorch.</li></ul><ul><li>API Development: RESTful API design, FastAPI, OpenAPI/Swagger.</li></ul><ul><li>Cloud & Infrastructure (supporting): AWS (SageMaker, Bedrock, EKS, Lambda, S3), Kubernetes, Docker, Terraform, CI/CD pipelines.</li></ul><ul><li>Data & Analytics: Databricks, Dataiku, Postgres, Redis, NoSQL databases.</li></ul><ul><li>Observability: Monitoring, logging, and distributed tracing for AI workloads.</li></ul><h3>Certifications</h3><p><strong>Required:</strong></p><ul><li>AWS Certified Machine Learning – Specialty</li></ul><p><strong>Nice to Have:</strong></p><ul><li>AWS Certified Solutions Architect – Professional</li></ul><ul><li>Certified Kubernetes Administrator (CKA)</li></ul><h3>Soft Skills & Leadership</h3><ul><li>Exceptional communication skills with the ability to present AI concepts to both engineering teams and executive stakeholders.</li></ul><ul><li>Proven track record of leading engineering teams and managing delivery across cross-functional groups.</li></ul><ul><li>Strong problem-solving mindset with a bias toward pragmatic, production-ready AI solutions.</li></ul><ul><li>Collaborative and proactive in engaging with business units, compliance, and external partners.</li></ul><p><em>Joining Regeneron as a Lead AI Engineer offers a unique opportunity to shape enterprise AI strategy, build transformative platforms, and make a meaningful impact on the advancement of global healthcare. If you are a driven technical leader with deep expertise in AI systems and a passion for innovation in a regulated environment, we invite you to apply.</em>Please copy and paste the desired job description for this role here. If you need a copy of an existing job description please reach out to TA or work with your HR Business Partner to develop one for a new role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global & US Oncology Marketing Strategy & Operations Lead]]></title>
    <date><![CDATA[Wed, 26 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50280]]></requisitionid>
    <referencenumber><![CDATA[R50280]]></referencenumber>
    <apijobid><![CDATA[r50280]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50280/associate-director-global-us-oncology-marketing-strategy-operations-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[<h3>Build our future together:</h3><p>The Global & US Oncology Strategy & Operations Lead is responsible for enabling operating infrastructure and supporting effective governance, operational cadence, and coordinating performance monitoring for the Solid Tumor Marketing organization. An integral member of the Solid Tumor Marketing Leadership Team, the Strategy & Operations Lead reports to the Vice President, Global & US Solid Tumor Marketing and supports the VP in initiatives related to leading marketing strategy, driving performance for the Solid Tumor franchise, and fostering collaboration across Regeneron functions who marketing teams work with regularly. The Strategy & Operations Lead also supports the VP in establishing and maintaining effective processes and ways of working within the Solid Tumor Marketing Team to enhance team efficiency and culture.</p><br><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY Office 4 Days a week</li><li>Ability to travel US and globally as required 30-50%, some on weekends for conferences and meetings.</li></ul><br><h3>Discover your role:</h3><ul><li>Build Marketing developmental focus areas with VP, and execute initiatives related to these focus areas for the marketing team to fortify team culture and ways of working</li><li>With input from the VP and solid tumor marketing team, maintain platforms and processes that enable team transparency and effective coordination (e.g., central Marketing calendar, budget review processes)</li><li>Establish and coordinate workstreams to develop and measure key performance indicators, including supporting evolution of analytics and insights reporting processes in collaboration with the brand team and Insights & Analytics teams</li><li>Manage recurring Marketing team meeting agenda and logistics, including Monthly Full Marketing Team meetings, Marketing Leadership meetings, and team building initiatives with direction on behalf of the Vice President, Global & US Solid Tumor Marketing</li><li>Support and lead special projects related to a variety of marketing initiatives. Develop and support communication efforts within and outside of Commercial Business Unit.</li><li>Actively support continued evolution of worldwide commercial presence for product team, including supporting VP in regular communication with key international stakeholders.</li><li>Support VP in preparation for senior leadership reporting and presentation forums</li><li>Support and build cross-functional relationships with key functional partners across the organization</li><li>Maintain the highest ethical and compliance standards, personally and throughout the marketing team. Handles and maintains highly confidential and sensitive information</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree required with preference for science background.</li><li>10 years of biotech/pharma brand marketing or related experience</li><li>Successful record of driving brand or organizational performance and effectively impacting commercial responsibilities.</li><li>Ability to communicate and act promptly; demonstrated initiative, creativity, and ability to work effectively in complex, rapidly changing environments.</li><li>Excellent planning, prioritization, communication, and presentation skills</li><li>Comfortable working in ambiguity, growth mindset</li><li>Strong integrity and ethics in behaviors, actions, and communications.</li><li>Working knowledge of how BioPharma commercial organizations are structured and planning cycles</li></ul><p><br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quality Assurance Specialist, On the floor (Overnights)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49584]]></requisitionid>
    <referencenumber><![CDATA[R49584]]></referencenumber>
    <apijobid><![CDATA[r49584]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49584/senior-quality-assurance-specialist-on-the-floor-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Senior Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support QA initiatives for a broad range of topics relative to the start-up and operations of a drug product facility. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work model: 3rd shift, Friday-Tuesday, 10pm-8:30am</p></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Work on and potentially lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team</p></li><li><p>Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures</p></li><li><p>Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.</p></li><li><p>Maintain project timelines to support the evolving business</p></li><li><p>Perform on-the-floor quality review of documents, such as: equipment logs, training records, testing results, batch records and supporting documents</p></li><li><p>Review and approval of documents (electronic and paper-based)</p></li><li><p>Provide mentorship during on-the-floor manufacturing</p></li><li><p>Support audits, inspections and investigations</p></li><li><p>Perform quarantine, segregation of material and line clearances</p></li><li><p>Contribute to the continuous improvement initiatives</p></li><li><p>Adjust schedule based on facility start up, filling, and manufacturing needs</p></li><li><p>Collaborate with cross-functional internal teams</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Requires B.S in life sciences or related field and 6+ years of experience; may substitute proven experience for education requirement</p></li><li><p>Level will be determined based on experience</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family Care Benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, NSCLC Scientific Marketing]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50310]]></requisitionid>
    <referencenumber><![CDATA[R50310]]></referencenumber>
    <apijobid><![CDATA[r50310]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50310/associate-director-nsclc-scientific-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><strong>BUILD OUR FUTURE TOGETHER:</strong></p><p>The Associate Director, NSCLC Scientific Marketing is a critical role within Regeneron’s US Oncology Commercial organization, reporting to the Director, NSCLC Scientific Marketing Lead. This role is responsible for the tactical execution of the lung scientific marketing strategy serving as a critical link between the commercial organization and the external scientific community to drive awareness, education, and engagement.</p><p>You will work closely with cross-functional partners across Marketing, Sales, Medical Affairs, and external agency partners to ensure alignment on strategy, execution excellence, and compliant delivery of key initiatives. Success in this role requires strong collaboration, strategic thinking, and the ability to manage complex programs while delivering measurable impact.</p><p><strong>WHEN & WHERE:</strong></p><p>In the Sleepy Hollow, NY office for 4 days a week with 25% travel for business meetings, POA, Ad Boards, and conferences, including occasional weekend travel/meetings as business needs require</p><p><strong>DISCOVER YOUR ROLE:</strong></p><ul><li>Plan and execute key US Lung congresses, including booth strategy, content creation, and on-site activation</li><li>Serve as the Scientific Marketing Agency of Record (AOR) liaison, managing agency partners, budgets, SOWs, and deliverables</li><li>Oversee Speaker deck content development and that it aligns to current and future strategic opportunities</li><li>Lead US congress and sponsorship execution, including product theater placement, integrated engagement planning, and cross-functional alignment to deliver prioritized activities, ensure seamless execution, and develop executive briefing materials for senior leadership</li><li>Manage agency partners and project timelines to deliver high-quality programs on schedule</li><li>Track and monitor program KPIs to ensure cost-effective execution and continuous performance optimization</li><li>Analyze customer insights, brand performance, and competitive dynamics to inform marketing strategy and planning</li><li>Support TLL team Leader with KOL engagement strategy, including mapping, outreach initiatives, and scientific exchange programs</li><li>Contribute to Brand Team activities, including POA and NFM planning cycles</li><li>Ensure all programs and materials comply with corporate, legal, regulatory, and ethical guidelines</li><li>Partner cross-functionally to manage budgets and ensure delivery within approved financial parameters</li></ul><p><strong>THIS ROLE REQUIRES: </strong></p><ul><li>Bachelor’s degree required</li><li>10 years of experience in pharmaceutical/biotech marketing, scientific marketing, or related field</li><li>Demonstrated experience in oncology strongly preferred (lung cancer or solid tumors)</li><li>Proven experience in congress planning, speaker deck content creation, and KOL engagement strategies</li><li>Experience managing agency partners and overseeing budgets and project delivery</li><li>Strong understanding of pharmaceutical regulatory, legal, and compliance requirements</li><li>Excellent project management, organizational, and communication skills</li><li>Ability to work cross-functionally and influence without direct authority</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager International Payroll]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50096]]></requisitionid>
    <referencenumber><![CDATA[R50096]]></referencenumber>
    <apijobid><![CDATA[r50096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50096/manager-international-payroll/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The International Payroll Manager is responsible for the accurate, compliant, and timely delivery of payroll across multiple international locations. This role oversees end-to-end payroll operations, manages third-party payroll vendors, drives process standardization, and partners closely with HR, Finance, Tax, Mobility, Benefits, and Technology teams to ensure payroll excellence and regulatory compliance.</p><p>The ideal candidate is an experienced payroll leader with deep international payroll expertise, strong analytical skills, and a proven ability to manage complex payroll environments while supporting transformation initiatives, system implementations, and process improvements across a global organization.</p><p><em>This role will be based in our Sleepy Hollow, NY offices and requires 4 days per week on-site.</em></p><p><strong>Key Responsibilities</strong></p><div><ul><li><p><strong>International Payroll Operations:</strong> Oversees accurate, compliant end-to-end payroll processing across multiple international regions and countries.</p></li><li><p><strong>Vendor Management:</strong> Manages relationships and performance of global payroll providers while supporting vendor implementations and process improvements.</p></li><li><p><strong>Compliance, Controls & Audit:</strong> Ensures payroll compliance with regulatory requirements, internal controls, audits, and governance standards.</p></li><li><p><strong>Payroll Transformation & Technology:</strong> Leads payroll technology enhancements and transformation initiatives to improve efficiency, accuracy, and scalability.</p></li><li><p><strong>Cross-Functional Partnership:</strong> Collaborates with internal stakeholders to support payroll operations, financial reporting, employee services, and business growth initiatives.</p></li><li><p><strong>Team Leadership:</strong> Develops and leads payroll team members while driving accountability, service excellence, and continuous improvement.</p></li></ul></div><p><strong>Let's See If We're a Fit:</strong></p><ul><li>Bachelor's degree in Accounting, Finance, Business Administration, Human Resources, or related field.</li><li>8+ years of progressive payroll experience with significant international payroll exposure.</li><li>3+ years of people leadership experience.</li><li>This global role is primarily aligned to U.S. business hours and leads payroll operations across Europe and India, requiring flexibility to collaborate across multiple time zones and provide occasional support outside standard working hours to ensure successful payroll delivery and business continuity.</li><li>Strong knowledge of international payroll regulations, taxation, and compliance requirements.</li><li>Experience managing payroll vendors across multiple countries.</li><li>Advanced Excel and analytical skills (pivot tables etc.)</li><li>Strong project management and stakeholder management capabilities.</li><li>International experience with preferred concentration in Europe, India, and Japan.</li></ul><p>Preferred</p><ul><li>Certified Payroll Professional (CPP), IPASS, or equivalent payroll certification.</li><li>Experience with Workday, Oracle Fusion, SAP, ADP GlobalView, CloudPay, or similar global payroll platforms.</li><li>Experience supporting payroll transformation, shared services, or Global Capability Center environments.</li><li>Experience with global mobility, equity, and payroll-related tax processes.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49722]]></requisitionid>
    <referencenumber><![CDATA[R49722]]></referencenumber>
    <apijobid><![CDATA[r49722]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49722/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together: </strong></p></div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Automation Engineer to join our Automation Engineering team to keep our groundbreaking process controls and process monitoring systems running at peak efficiency. In this role, you will build, develop, and optimize systems for our sophisticated biopharmaceutical manufacturing processes. You will collaborate closely with multiple teams to include Manufacturing, Quality Control, and Facilities. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide. </p></div><div><p><strong>When & where: </strong></p></div><div><ul><li><p>Location: Rensselaer, New York, United States </p></li></ul></div><div><ul><li><p>Shift Requirements: Monday - Friday 8:00AM - 4:30PM </p></li></ul></div><div><p><strong>Discover your role: </strong></p></div><div><ul><li><p>Design, develop, and implement software and hardware improvements to automated and new equipment under change control. </p></li></ul></div><div><ul><li><p>Provide PLC- and HMI-based technical support to various departments per established SOPs. </p></li></ul></div><div><ul><li><p>Identify, investigate, and resolve manufacturing deviations tied to automated control systems. </p></li></ul></div><div><ul><li><p>Develop engineering design documents, technical evaluations, and test plans in line with GAMP 5. </p></li></ul></div><div><ul><li><p>Support process control and monitoring equipment through software design, commissioning, testing, and corrective action. </p></li></ul></div><div><ul><li><p>Support small manufacturing, engineering, and validation projects. </p></li></ul></div><div><ul><li><p>Author and execute Factory Acceptance Test and Site Acceptance Test protocols and system specifications. </p></li></ul></div><div><ul><li><p>Champion continuous improvement as an everyday outlook, not just a metric. </p></li></ul></div><div><p><strong>This role requires: </strong></p></div><div><ul><li><p>BS in Engineering or a related field, with 5+ years of relevant experience; equivalent combination of education and experience may be considered. </p></li></ul></div><div><ul><li><p>Experience in the design and maintenance of process control and/or data acquisition systems is required. </p></li></ul></div><div><ul><li><p>Experience programming and troubleshooting the DeltaV DCS as well as PLCs. Experience with Allen-Bradley and Siemens control system products and video graphic chart recorders is ideal. </p></li></ul></div><div><ul><li><p>Experience in a regulated manufacturing environment is ideal </p></li></ul></div><div><ul><li><p><strong>Gowning and Physical Requirements:</strong> </p></li></ul></div></div><div><div><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></ul></div><div><ul><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire is required </p></li></ul></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$75,300.00 - $123,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Specialist, Global Partnerships & Trial Optimization]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49808]]></requisitionid>
    <referencenumber><![CDATA[R49808]]></referencenumber>
    <apijobid><![CDATA[r49808]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49808/senior-specialist-global-partnerships-trial-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases.We are seeking a Senior Specialist, Global Partnerships & Trial Optimization (GPTO) to join our Global Clinical Trial Services team in Hyderabad. In this role, you will support portfolio and study-level trial optimization initiatives across the Global Development organization by leveraging data, analytics, feasibility insights, and recruitment strategies to improve clinical trial execution. You will collaborate with cross-functional stakeholders to drive operational efficiencies, support technology-enabled solutions, maintain key performance metrics, and contribute to innovative approaches that enhance study feasibility, enrollment planning, and patient recruitment efforts.</p><br><h3><strong>When & where:</strong></h3><p><strong>Hyderabad, India (Hybrid)</strong></p><br><h3><strong>Discover your role:</strong></h3><ul><li>Support portfolio and study-level feasibility, enrollment planning, and patient recruitment strategy activities across Global Development programs.</li><li>Serve as a GPTO technical and functional liaison, partnering with Global Development teams and supporting functions to address business and operational needs.</li><li>Manage technical insight generation, data quality initiatives, reporting activities, and operational planning to improve team efficiency and effectiveness.</li><li>Perform data entry, transformation, analysis, and reporting to support strategic clinical development and trial optimization decisions.</li><li>Maintain and monitor GPTO metrics, dashboards, KPIs, and vendor performance reporting to inform leadership decision-making.</li><li>Track portfolio, project, and pipeline activities proactively to support resource planning and operational efficiency.</li><li>Build and maintain strong partnerships with internal stakeholders while fostering collaboration and continuous improvement.</li><li>Support the development and implementation of technology-driven solutions and evolving data systems used within GPTO.</li><li>Develop scalable processes, tools, templates, and training materials to ensure consistent execution across the GPTO team.</li><li>Identify opportunities to enhance feasibility methodologies, analytical approaches, and data sources while ensuring compliance with ICH-GCP guidelines and Regeneron SOPs.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in Life Sciences, Clinical Research, Data Analytics, Business, Healthcare, or a related field.</li><li>Bachelor's degree with 5+ years of relevant experience, or Master's degree with 3+ years of relevant experience.</li><li>3+ years of experience using databases and systems to manage, analyze, and report clinical or operational data.</li><li>Proficiency in SQL and experience working with complex data sources.</li><li>2+ years of experience with Power BI, Power Query, data visualization, and analytical reporting tools.</li><li>Strong technical skills in Microsoft Excel, PowerPoint, Word, and related business applications.</li><li>Knowledge of clinical development processes, feasibility assessments, patient recruitment, and enrollment planning.</li><li>Ability to learn new technologies, systems, and data platforms independently.</li><li>Strong analytical, problem-solving, and data-driven decision-making capabilities.</li><li>Effective communication and stakeholder management skills with the ability to collaborate across matrixed teams.</li><li>Awareness of ICH-GCP guidelines and clinical research standards.</li><li>Experience with Tableau, Excel VBA, and advanced data visualization tools is preferred.</li><li>Willingness to travel up to 10% as business needs require</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44084]]></requisitionid>
    <referencenumber><![CDATA[R44084]]></referencenumber>
    <apijobid><![CDATA[r44084]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44084/calibration-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a 3rd shift Calibration Technician to our growing team. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</p><p><strong>When & Where:</strong></p><p><strong>Location: Rensselaer, NY</strong></p><p><strong>Hours: Working hours will be Sunday-Thursday 10:00pm-8:30am. </strong></p><p><strong>Training will take place Monday-Friday 8:00am-4:30pm for 3-6 months based on experience level. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p><strong>Discover Your Role:</strong></p><ul><li>Calibrating various types of instrumentation including temperature, pressure, level, flow and analytical instruments</li><li>Performing loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Working with medium and low voltages</li><li>Performing basic plumbing and tube bending jobs</li><li>Assisting the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Performing daily Work Orders (WO) and Preventative Maintenance (PM) and efficiently coordinate the workflow and documentation of PMs and WOs</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Following current Good Manufacturing Practices (cGMPs)</li><li>Occasionally working on other facility related work tasks/issues that are outside the calibration department’s normal work duties</li><li>May include planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</li><li>Participation in compliance investigations if and when necessary</li><li>Full gowning required when entering and working on production floor</li><li>Participating in rotation on-call schedule</li><li>Demonstrate basic problem-solving skills</li><li>Are able to learn and follow routine procedures independently as well as part of a team</li><li>Are comfortable and have the flexibility to work in a changing environment</li><li>Can lift, push, and pull at least 50lbs</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p><strong>This Role Requires:</strong></p><p>You must be willing and able to work a <strong>Sunday-Thursday 10:00pm-8:30am schedule.</strong></p><p>Applicants should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p><ul><li>Calibration Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li><li>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Marketing Manager Hematology]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50587]]></requisitionid>
    <referencenumber><![CDATA[R50587]]></referencenumber>
    <apijobid><![CDATA[r50587]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50587/senior-marketing-manager-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Marketing Manager Hematology Marketing Europe to join our Hematology International marketing team, supporting Austria, Switzerland and the Nordics. In this role, you will own the launch of key hematology assets, drive brand strategy and execution across multiple European markets, and collaborate with cross-functional and cross-regional stakeholders. This position offers the opportunity to contribute to a science-driven organization passionate about improving outcomes for patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Netherlands</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead the development and execution of hematology brand plans across Austria, Switzerland and the Nordics, aligning local priorities with global strategy.</li><li>Drive the launch of two hematology assets across six geographies, ensuring effective execution in competitive markets.</li><li>Analyze market dynamics, identify growth opportunities and risks, and develop differentiated messaging and action plans to support brand performance.</li><li>Partner with Medical Affairs and cross-functional teams to develop and implement market strategies, promotional activities and stakeholder engagement plans.</li><li>Adapt global campaigns and materials for local field and digital use while promoting consistency and best-practice sharing across markets.</li><li>Collaborate with Commercial Operations, Sales and external partners to implement field plans, communications, cycle meetings and customer engagement initiatives.</li><li>Manage promotional budgets, recommend investment priorities and monitor spending to support business objectives.</li><li>Build strong partnerships, gather customer insights and maintain high standards of compliance and ethical conduct.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree in Business, Science or a related field, with 8-10+ years of biotech or pharmaceutical brand marketing experience.</li><li>Significant oncology and/or hematology expertise, including successful launches of specialty medicines in competitive environments.</li><li>Experience developing and delivering brand strategies across multiple markets, managing budgets, agencies and external partners.</li><li>Experience in Multiple Myeloma, Follicular Lymphoma or Diffuse Large B-Cell Lymphoma, exposure to multiple European markets, and additional European language skills are advantageous.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€81,375.00 - €135,625.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director: Global Patient Safety Solutions Partner]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50627]]></requisitionid>
    <referencenumber><![CDATA[R50627]]></referencenumber>
    <apijobid><![CDATA[r50627]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50627/senior-director-global-patient-safety-solutions-partner/]]></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 Director, GPS Business Solution Lead will serve as the key interface between GPS business leadership and Digital & Technology, orchestrating D&T capabilities to deliver on Regeneron's Global Patient Safety (GPS) objectives and priorities across platforms, including Argus (safety), PIVIT, Signal Management, aRMM/ARMM, and SRP. This role owns the platform strategy and roadmap, prioritizing investment in partnership with the business, and will lead a team of Directors delivering delivery governance and regulatory-compliant operations across the safety technology portfolio. The Business Solution Lead will partner closely with GPS business leadership, Enterprise IT, and Information Security to ensure safety systems support Regeneron's Global Patient Safety obligations and global regulatory commitments.</p><p>This role reports to the Executive Director, Global Development IT and will collaborate closely with GPS business leadership and Enterprise IT partners to shape the safety technology roadmap and ensure delivery excellence across the platform portfolio.</p><p><strong>Where and When</strong></p><p>This is an on-site position 4 days/week, primarily based at our Sleepy Hollow, NY or Warren, NJ office. If eligible, we can offer relocation benefits; we cannot offer a fully remote option.</p><p><strong>Key Responsibilities</strong></p><p>In this role, you will own platform strategy and delivery for Regeneron's Global Patient Safety technology portfolio, leading a team of Directors across the domain. Your day-to-day responsibilities will include:</p><p><strong>GPS Platform Strategy & Ownership</strong></p><ul><li>Partner with senior GPS leadership, to align technology and capabilities to deliver on Global Patient Safety objectives and enterprise priorities.</li></ul><ul><li>Own and prioritize, in partnership with the business, the multi-year platform strategy and roadmap for Argus (safety), PIVIT, Signal Management, aRMM/ARMM, and SRP, translating Global Patient Safety and regulatory priorities into a funded, prioritized delivery plan.</li></ul><ul><li>Own the organizational design of the GPS Business Solution function, including structure, role allocation, and resourcing across Directors and Managers assigned to the domain.</li></ul><ul><li>Establish governance frameworks, standards, and validation practices for GPS platform delivery, ensuring consistency across teams and vendor engagements.</li></ul><ul><li>Own budget, forecast, and vendor contract accountability for the GPS platform portfolio, including software licensing and services agreements.</li></ul><p><strong>Delivery Oversight & Team Leadership</strong></p><ul><li>Serve as the escalation and quality-assurance point for planning, prioritization, and execution of safety platform initiatives led by direct reports.</li></ul><ul><li>Oversee product backlog, incident management, and release governance across the GPS platform portfolio, ensuring consistent reporting of value delivered against plan.</li></ul><ul><li>Coach and develop Directors and Managers, ensuring delivery commitments are met and domain capabilities continue to mature.</li></ul><ul><li>Manage steering committee meetings, working groups, and issue/release management for upgrades to existing safety platforms.</li></ul><p><strong>Data Governance & Regulatory Compliance</strong></p><ul><li>Partner with GPS business leadership, Regulatory Affairs, and Quality organizations to ensure safety platforms meet GxP validation, data integrity, and audit-readiness standards.</li></ul><ul><li>Own data classification, access, and quality standards for safety-related data, ensuring compliance with global safety reporting obligations (e.g., FDA, EMA).</li></ul><ul><li>Maintain oversight of case processing, signal detection, and risk management workflows to ensure platforms support timely and accurate regulatory reporting.</li></ul><p><strong>Cross-Functional & Vendor Partnership</strong></p><ul><li>Partner with Enterprise IT, Enterprise Architecture, and Information Security to align safety platform investments with enterprise standards and security requirements.</li></ul><ul><li>Build and maintain relationships with key platform vendors to clarify demands, resolve conflicts, and align technology roadmaps to business needs.</li></ul><ul><li>Represent GPS technology priorities in enterprise architecture and governance forums, ensuring alignment with enterprise-wide standards.</li></ul><p><strong>Executive & Stakeholder Engagement</strong></p><ul><li>Serve as the primary point of contact for senior GPS and IT leadership on matters requiring negotiation of complex or ambiguous issues.</li></ul><ul><li>Build relationships with key GPS business leaders to clarify demands, resolve conflicts, and align technology roadmaps with pharmacovigilance priorities.</li></ul><ul><li>Monitor industry trends in drug safety technology and regulatory reporting, bringing forward innovative approaches to senior leadership.</li></ul><ul><li>Prepare and deliver executive-level materials on the health and roadmap of the GPS platform portfolio for governance forums and senior leadership.</li></ul><p><strong>Qualifications and Requirements</strong></p><p><strong>Education & Experience</strong></p><ul><li>Bachelor’s degree in Computer Science, Information Systems, Business Administration, or a related field (Master’s degree preferred).</li></ul><ul><li>15+ years of progressive industry/relevant professional experience, including significant experience managing enterprise-scale Global Patient Safety, drug safety, or regulatory technology platforms.</li></ul><ul><li>Experience in the biotech, pharma, or life sciences industry strongly preferred.</li></ul><ul><li>Proven experience leading a multi-disciplinary team of Directors and Managers, including budget and vendor contract accountability for a major function.</li></ul><p><strong>Technical Expertise</strong></p><ul><li>Deep expertise in patient safety and drug safety systems (e.g., Oracle Argus Safety, signal management, and risk management platforms).</li></ul><ul><li>Experience with global safety reporting standards and regulatory requirements (e.g., E2B, ICSR, FDA, EMA).</li></ul><ul><li>Strong knowledge of GxP validation practices and solution delivery life cycle management.</li></ul><ul><li>Experience managing technology capability identification, selection, and implementation across multiple simultaneous safety platform initiatives.</li></ul><p><strong>Skills & Competencies</strong></p><ul><li>Proven track record of budget and vendor management for a department or major function.</li></ul><ul><li>Strong stakeholder management and negotiation skills, with experience influencing senior management internally and externally.</li></ul><ul><li>Demonstrated ability to grow, motivate, and develop teams, coaching Directors and Managers through career milestones and progression.</li></ul><ul><li>Strategic mindset with the ability to define organizational structure and set long-term goals and objectives for a major function.</li></ul><ul><li>Exceptional executive communication skills, with experience engaging senior/executive leadership on sensitive or ambiguous matters.</li></ul><p><strong>Certifications (Preferred)</strong></p><ul><li>PMP or equivalent project/program management certification.</li></ul><ul><li>ITIL or SAFe Agile certification.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, PV Case Operations]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50288]]></requisitionid>
    <referencenumber><![CDATA[R50288]]></referencenumber>
    <apijobid><![CDATA[r50288]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50288/associate-director-pv-case-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director</strong> to join our <strong>PV Case Operations</strong> team.</p><p><br>Responsible for providing oversight of pharmacovigilance (PV) operations in the successful management of vendor and case processing deliverables in accordance with applicable regulations and agreements. Responsible for ensuring that assigned staff are appropriately prepared to support current and anticipated activities for receipt, processing, distribution/ submission of reports from global development programs and globally marketed products. Responsible for ensuring inspection readiness; monitoring quality of PV deliverables; and monitoring compliance with case submission timelines as per regulatory requirements and agreements with License Partners and other parties. Incumbent may have a central role in audits and health authority inspections. This role has primary accountability for ICSR quality standards, CAPA ownership, KPI governance, and metrics-driven operational oversight across all case processing activities.py and paste the desired job description for this role here. If you need a copy of an existing job description, please reach out to TA or work with your HR Business Partner to develop one for a new role.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Warren, NJ, Tarrytown, NY or Cambridge, MA</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Responsible for accurate and timely case processing deliverables across global development programs and marketed products. </p></li><li><p>Oversee ICSR quality review processes, including narrative quality, case validity, completeness of assessments, and source document reconciliation. </p></li><li><p>Establish and maintain tiered quality review frameworks and quality sampling strategies appropriate to case complexity, risk level, and product lifecycle stage. </p></li><li><p>Drive continuous improvement in ICSR quality by identifying trends, root causes of recurring errors, and implementing targeted remediation. </p></li><li><p>Assume a supporting role in interactions with auditors and Health Authority inspectors. </p></li><li><p>Assume a central role in responding to audit / inspection findings </p></li><li><p>Lead root cause analysis (RCA) for quality deviations, case processing errors, and compliance failures; ensure findings are well-documented and actionable. </p></li><li><p>Develop, own, and track Corrective and Preventive Actions (CAPAs) to closure, including scheduling and conducting effectiveness checks post-implementation. </p></li><li><p>Ensure CAPA commitments made to health authorities, auditors, or internal quality teams are met within agreed timelines; escalate risks proactively. </p></li><li><p>Track and analyze operational metrics including case volumes, processing cycle times, resource utilization, overtime trends, and vendor performance benchmarks. </p></li><li><p>Develop and maintain vendor performance metrics frameworks; conduct regular governance meetings to review performance against contractual SLAs. </p></li><li><p>Ensure compliance with all regulations, guidelines, guidances and Regeneron SOPs and Working Instructions governing pharmacovigilance. </p></li><li><p>Responsible for mentorship and active support of assigned staff. </p></li><li><p>Responsible for ensuring deliverables and interests are communicated to senior management, internal partners, and external partners in a timely manner. </p></li><li><p>Skillful management and resolution of issues, which may, depending on complexity, require effective escalation. </p></li><li><p>Manage workload in meeting compliance objectives, optimizing job performance/ contributions, and achieving high levels of work quality.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum Bachelors Degree, Advanced Degree preferred; with 10 years of Pharmacovigilance/Drug Safety/PV Quality experience.</p></li><li><p>Previous Pharmacovigilance/Drug Safety experience in pharmaceutical / biotech industry</p></li><li><p>Well informed on 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>Experience with managing and supervising teams on complex projects. Demonstrated success in working on cross-functional teams</p></li><li><p>Contributes to and manages organizational projects and goals to support their timely completion.</p></li><li><p>Assist group members with their activities, as needed. Generally, accomplishes tasks through Individual Contributors or other managers.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 10 Sep 2026 10:26:36 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, Advanced Therapy Project Management (ATPM)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47142]]></requisitionid>
    <referencenumber><![CDATA[R47142]]></referencenumber>
    <apijobid><![CDATA[r47142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47142/process-development-engineer-ii-advanced-therapy-project-management-atpm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Associate</strong> to join our Advanced Therapy Project Management (AT-PM) group within Product, Analytical, and Process Development Operations (PAPD Ops) in an on-site capacity. In this role, you will support project management, technology transfer, and business operations for Regeneron's Advanced Therapy Programs, helping drive successful development and tech transfer of advanced therapies (e.g., AAV, bioconjugates, and synthetic chemistry programs), while collaborating with internal partners and Contract Development & Manufacturing Organizations (CDMOs) to enable clear cross-functional ways of working and operational excellence.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: On-site in Tarrytown, NY</li><li>Work model/flexibility: Onsite, full-time</li></ul><h3><strong>What you'll do:</strong></h3><ul><li>Lead cross-functional tech transfer teams and independently own workstreams to establish production processes at CDMOs</li><li>Drive readiness for manufacturing start-up by clarifying scope, securing inputs and approvals, tracking deliverables, and escalating risks with proposed mitigations</li><li>Own communication strategy and operating cadence for assigned programs, providing concise, decision-ready status reporting to audiences ranging from core teams to senior stakeholders</li><li>Build, maintain, and continuously improve integrated plans across development and transfer activities, facilitating scenario planning to protect key milestones</li><li>Anticipate and address risks to manufacturing readiness, defining mitigation plans to support rigorous CDMO campaign execution</li><li>Lead recurring and ad-hoc technical forums to drive timely decisions, resolve issues, and capture lessons learned</li><li>Lead continuous improvement initiatives to mature AT-PM ways of working</li><li>Partner with procurement, finance, legal, and internal stakeholders to support CDMO engagement, including RFPs, scope alignment, and contracting coordination</li></ul><h3><strong>This role might be for you if:</strong></h3><ul><li>You take initiative, reliably follow through, and thrive in non-structured environments, navigating ambiguity and changing priorities with a strategic, action-oriented mindset</li><li>You enjoy and excel at problem solving, breaking down complex technical and operational challenges into well-thought-out plans</li><li>You like building structure and scalable frameworks that help cross-functional teams execute efficiently</li><li>You proactively identify risks and roadblocks, communicate tradeoffs, and know when and how to escalate</li><li>You're willing to try, learn, and iterate to keep programs moving forward and partners aligned</li></ul><h3><strong>This role requires:</strong></h3><ul><li>B.Sc. in Biochemistry, Chemical/Biochemical Engineering, or a related field, with 6-8+ years of experience or a MS w/3-6+, including demonstrated ownership of cross-functional deliverables</li><li>A strong customer-service mindset</li><li>Ability to independently facilitate team collaboration, build and maintain integrated plans, and design/improve repeatable business processes</li></ul><h3><strong>Preferred / nice-to-haves:</strong></h3><ul><li>Experience supporting CMC development and/or technology transfer to CDMOs (e.g., process development, analytics, documentation readiness)</li><li>Experience or knowledge of bioconjugation, gene therapy/AAV, or</li></ul><p><strong>#pmpd</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 10 Sep 2026 17:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Field Medical Affairs-Thoracic Oncology/Pan Tumor (NY, VT, NH, ME)]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50439]]></requisitionid>
    <referencenumber><![CDATA[R50439]]></referencenumber>
    <apijobid><![CDATA[r50439]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50439/associate-director-field-medical-affairs-thoracic-oncologypan-tumor-ny-vt-nh-me/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs responsible for engaging in the exchange of scientific data and other medical and/or scientific information with key opinion leaders (KOLs), health care providers (HCPs), researchers, pharmacists and population-based decision makers. We demonstrate a thorough understanding of solid tumors, including thoracic malignancies, and other tumors of interest within clinical development and aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Field- NY, VT, NH, ME</p><p>• Travel: approximately 50% of the time, including air travel, overnight and occasionally on weekends</p><p><strong>Discover your role: </strong></p><p>• Establish, foster, cultivate and maintain peer relationships with KOLs. <br>• Act as the primary clinical/scientific resource to HCPs for information pertaining to disease state and our product(s) to ensure awareness and understanding.<br>• Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.<br>• Support evidence generation (company sponsored trials and investigator initiated studies (IIS)) research initiatives<br>• Identify and report medical insights.<br>• Identifies gaps in research and educational needs to inform medical strategy.<br>• Responds to requests for information and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.<br>• Performs disease management and therapeutic area education with identified practitioners, payers and researchers.<br>• Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence with the purpose of informing internal partners.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><p><strong>This role requires:</strong> <br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience as an Oncology Medical Science Liaison function is required.<br>• Knowledge or experience in the Oncology therapeutic area is required, and experience in thoracic malignancies preferred.<br>• Established relationships with KOLs in thoracic malignancies and knowledge of institutions focused on Solid Tumor Malignancies preferred.<br>• Drug launch experience is strongly preferred.<br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines.<br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.</p><p>#ofm #msl #medicalscienceliaison<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Payroll Service Delivery Analyst (International)]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50458]]></requisitionid>
    <referencenumber><![CDATA[R50458]]></referencenumber>
    <apijobid><![CDATA[r50458]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50458/payroll-service-delivery-analyst-international/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is built on the belief that the right idea, coupled with the right team, can transform lives. Our mission is to invent, develop, and commercialize life-transforming medicines for people with serious diseases. Through scientific innovation, operational excellence, and a commitment to patients, we continue to redefine what is possible.</p><p>The Global Payroll team plays a critical role in supporting Regeneron's worldwide workforce through accurate, compliant, and efficient payroll operations. We are seeking a <strong>Payroll Service Delivery Analyst</strong> to join our Global Capability Center (GCC) in Hyderabad. In this role, you will support payroll delivery across multiple countries, collaborate with global collaborators, and contribute to a positive employee experience while developing expertise in international payroll operations and shared services.</p><p><strong>When & Where</strong></p><p>Hyderabad, India (Hybrid)</p><p><strong>Discover your role</strong></p><p>As a Payroll Service Delivery Analyst, you will:</p><ul><li><p>Support the preparation and processing of payroll for assigned international countries by collecting, validating, and maintaining employee payroll data.</p></li><li><p>Perform payroll audits, reconciliations, and data reviews to ensure accuracy, compliance, and adherence to internal controls.</p></li><li><p>Maintain payroll calendars, process documentation, and operational checklists to support timely payroll delivery.</p></li><li><p>Partner with Global Payroll, Human Resources, and Finance teams to ensure data integrity and timely submission of payroll inputs.</p></li><li><p>Coordinate with external payroll vendors to submit data, track deliverables, and resolve payroll-related inquiries.</p></li><li><p>Support statutory compliance activities and assist in implementing payroll-related regulatory updates.</p></li><li><p>Generate payroll reports and support month-end activities, analysis, and operational reporting requirements.</p></li><li><p>Participate in payroll system updates, process improvements, and GCC standardization initiatives to drive operational excellence.</p></li><li><p>Ensure strict confidentiality of employee information while maintaining compliance with company policies and controls.</p></li><li><p>Collaborate across teams to support service delivery objectives in a fast-paced global environment.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Hold a Bachelor's degree in Business, Human Resources, Accounting, Finance, or a related field; equivalent experience considered.</p></li><li><p>Have 4+ years of experience in payroll, HR operations, accounting, shared services, or a related field.</p></li><li><p>Demonstrate proven attention to detail and accuracy while working with payroll data and financial information.</p></li><li><p>Possess strong analytical, organizational, and problem-solving skills in a deadline-driven environment.</p></li><li><p>Have excellent communication and stakeholder management skills with the ability to collaborate across teams and regions.</p></li><li><p>Are proficient in Microsoft Excel and comfortable learning and using new technologies and systems.</p></li><li><p>Have experience with payroll or HRIS platforms such as Workday, SAP, ADP, or similar solutions.</p></li><li><p>Bring a customer-focused approach and commitment to delivering high-quality employee support.</p></li><li><p>Demonstrate strong learning agility and an interest in global payroll operations and shared services.</p></li><li><p>Thrive in a collaborative, fast-paced environment with a continuous improvement approach.</p></li><li><p>Experience supporting global or multi-country payroll operations.</p></li><li><p>Exposure to Shared Services or Global Capability Center environments.</p></li><li><p>Multilingual skills or experience working with culturally diverse global teams.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 03:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II Ophthalmology- LA, MS, AR]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50690]]></requisitionid>
    <referencenumber><![CDATA[R50690]]></referencenumber>
    <apijobid><![CDATA[r50690]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50690/medical-specialist-ii-ophthalmology-la-ms-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Louisiana]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p>The Medical Specialist will report to the Regional Director and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>When & where: </strong></p><ul><li><p>Hybrid role</p></li><li><p>Location: Louisiana, Mississippi or Arkansas</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Experience in biologics and buy and bill products</p></li><li><p>Demonstrated history of high sales performance</p></li><li><p>Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>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</p></li><li><p>Buy and Bill experience</p></li><li><p>Ophthalmology with relevant retina experience is preferred</p></li><li><p>Must be based in or located in close proximity to the assigned territory (relocation will not be provided)</p></li><li><p>Ability to travel (40-60%)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 17:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Facilities Engineer]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47620]]></requisitionid>
    <referencenumber><![CDATA[R47620]]></referencenumber>
    <apijobid><![CDATA[r47620]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47620/facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>Where:</strong></p><ul><li><p>Location: Raheen, Limerick</p></li></ul><br><p><strong>What you’ll do:</strong></p><ul><li><p>Building and specifying cGMP clean/grey utilities, & HVAC equipment, piping, ducting and/or controls</p></li><li><p>Managing small-to-mid sized projects related to utilities & HVAC equipment & services</p></li><li><p>Conducting troubleshooting for complex issues with plant equipment issues and associated systems, identifying and recommending corrective actions</p></li><li><p>Assisting in the design review, site acceptance and installation of equipment</p></li><li><p>Supporting the QA Validation department by preparation of design documents and assists in protocol execution</p></li><li><p>Assisting in investigations of utility systems, and control system anomalies as well as safety incidents</p></li><li><p>Implementing corrective/preventative actions for existing equipment and maintenance processes</p></li><li><p>Preparing engineering evaluations and test plans for and executing modification change control documentation</p></li><li><p>Interpreting P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</p></li><li><p>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>You have strong analytical and interpersonal skills</p></li><li><p>You are able to prioritise and re-prioritise as needed and adapt to change</p></li><li><p>You are comfortable working in a fast-paced setting</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>To be considered for this position you should have a BS/BA in Mechanical Engineering or equivalent, with 5 years of relevant experience preferably in the Pharma/Biotech industry.</p></li><li><p>Senior Engineer: BS/BA in Mechanical Engineering with 5 years' minimum experience</p></li><li><p>Engineer: BS/BA in Mechanical Engineering with 2 years' minimum experience</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLTO</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 11 Sep 2026 03:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Quality Control Microbiology]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49545]]></requisitionid>
    <referencenumber><![CDATA[R49545]]></referencenumber>
    <apijobid><![CDATA[r49545]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49545/supervisor-quality-control-microbiology/]]></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 2nd shift Quality Control Supervisor focused in Microbiology. Our Quality Control Microbiology Department is responsible for activities related to pharmaceutical microbiology including environmental, personnel and utility monitoring, raw material, in-process, and product release testing. This position will be responsible for ensuring daily operations are completed accurately, timely, and reliably to ensure our medicines are safe and effective before reaching patients around the world. This is an excellent opportunity to join a select group of colleagues while working on molecules that help improve patients’ lives.</p><p><strong>When & Where:</strong></p><ul><li>2nd shift Tuesday- Saturday, 2 PM - 10:30 PM</li><li>Location: Rensselaer, New York, United States</li></ul><p><strong>Discover your role:</strong></p><ul><li>Coordinate testing and monitoring activities within the QC lab and manufacturing facility.</li><li>Review test results, procedures, protocols, and quality system records.</li><li>Attend cross-functional meetings to remain informed of business needs.</li><li>Organize lab investigations and assay troubleshooting as needed.</li><li>Support internal and regulatory audits.</li><li>Ensure safety and current Good Manufacturing Practice standards are maintained.</li><li>Execute personnel management functions including performance evaluations, personnel development, and scheduling time off.</li><li>Communicate effectively with management on complex matters; support laboratory management in mid to long range team goals.</li><li>Drive and manage projects within the group.</li><li>Coach team members in troubleshooting microbiology methods, Environmental Monitoring, aseptic techniques and equipment.</li></ul><p><strong>This role requires:</strong></p><ul><li>A BS/BA in Life Sciences or related field, with 5+ years of progressive, relevant experience, preferably within pharmaceutical microbiology.</li><li>Must be able to work <strong>2nd shift Tuesday- Saturday, 2 PM - 10:30 PM</strong></li><li>Supervisory/leadership experience required.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Principal Scientist - Microscopy]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50210]]></requisitionid>
    <referencenumber><![CDATA[R50210]]></referencenumber>
    <apijobid><![CDATA[r50210]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50210/senior-principal-scientist-microscopy/]]></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>Senior Principal Scientist of Microscopy</strong></p><br><p><strong>Build our future together:</strong></p><p>Regeneron is seeking an accomplished and innovative scientist to lead the Microscopy function within Imaging Sciences. The successful candidate will be a recognized expert in microscopy with deep expertise in cell biology, advanced optical imaging technologies, quantitative image analysis, and scientific leadership.</p><br><p>This individual will provide scientific and strategic leadership for a multidisciplinary microscopy team supporting discovery research, technology development, translational science, and early therapeutic programs across Regeneron's research portfolio. The role will build upon the core's current capabilities while driving the future vision of imaging sciences through the adoption of emerging microscopy technologies, automation, AI-enabled analytics, multidimensional imaging workflows, and integrated imaging solutions.</p><br><p>The ideal candidate combines outstanding scientific credentials as a practicing microscopist with a demonstrated track record of managing and growing a microscopy core facility, mentoring staff scientists, and partnering effectively with researchers across diverse therapeutic areas.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY United States – On-site</p><br><p><strong>Discover your role:</strong></p><ul><li>Advance the scientific direction for microscopy and cellular imaging across Regeneron Research, aligning capabilities with priority biological and therapeutic questions.</li></ul><ul><li>Identify, evaluate, validate, and adopt emerging technologies based on scientific value, technical performance, scalability, and portfolio need.</li></ul><ul><li>Provide senior consultation that translates complex biological questions into fit-for-purpose imaging strategies, experimental designs, and quantitative readouts.</li></ul><ul><li>Lead, develop, and retain a high-performing multidisciplinary microscopy team and foster a culture of scientific rigor, collaboration, innovation, and continuous learning.</li></ul><ul><li>Oversee annual strategic, operational, workforce, and capital-equipment plans for the microscopy function.</li></ul><ul><li>Establish governance, metrics, workflows, training, and service models that improve quality, accessibility, reliability, turnaround time, and scientific impact.</li></ul><ul><li>Provide scientific leadership across advanced optical, super-resolution, spectral, lifetime, label-free, live-cell, 3D, high-content, high-throughput, spatial, and translational microscopy approaches.</li></ul><ul><li>Guide method selection, assay development, experimental design, technology troubleshooting, and quantitative image analysis, including machine-learning-enabled approaches.</li></ul><ul><li>Develop scalable imaging infrastructure spanning laboratory automation, robotic image acquisition, image-data management, cloud analytics, AI applications, and digital microscopy.</li></ul><ul><li>Integrate microscopy with molecular imaging, histology, pathology, spatial biology, and other Imaging Sciences platforms to generate coherent, cross-scale evidence.</li></ul><ul><li>Partner with discovery, translational, platform, engineering, data science, and technology teams to deliver imaging strategies that inform target validation, mechanism-of-action studies, biomarker development, candidate selection, and translational planning.</li></ul><ul><li>Mentor microscopy scientists and imaging specialists, build technical depth and scientific leadership, and train researchers in microscopy best practices and experimental design.</li></ul><p><br><br></p><p><strong>This role requires:</strong></p><ul><li>A Ph.D. in Cell Biology, Cellular Physiology, Developmental Biology, Molecular Biology, Bioengineering, Biophysics, or related discipline.</li></ul><ul><li>Minimum 5 years of relevant postdoctoral and/or industry experience.</li></ul><ul><li>Minimum 5 years leading a microscopy core facility or equivalent scientific organization.</li></ul><ul><li>Demonstrated expertise developing and applying advanced microscopy methodologies to answer complex biological questions.</li></ul><ul><li>A strong publication record with evidence of leadership as a primary or senior contributor in microscopy-driven research.</li></ul><ul><li>Deep understanding of cell biology, optical physics, microscopy instrumentation and mechanics, image formation, fluorescent probes and reporters, automation, and quantitative image analysis.</li></ul><ul><li>Experience selecting, implementing, and optimizing advanced microscopy imaging platforms.</li></ul><ul><li>Demonstrated success managing scientific staff and multidisciplinary teams.</li></ul><ul><li>Strong project management and stakeholder engagement experience.</li></ul><ul><li>Preferred: Recognized external reputation in biological microscopy or imaging sciences.</li></ul><ul><li>Preferred: Experience building or transforming an imaging core facility.</li></ul><ul><li>Preferred: Working knowledge of machine learning and AI-driven image analysis.</li></ul><ul><li>Preferred: Experience with spatial omics and multiplexed imaging platforms is desirable but not required.</li></ul><ul><li>Preferred: Experience integrating microscopy with in vivo imaging, pathology, and translational biomarker efforts.</li></ul><ul><li>Preferred: Record of successful strategic technology adoption and innovation.</li></ul><br><p><strong>Success profile:</strong></p><p>Within the first several years, this individual will have:</p><ul><li>Established a clear strategic roadmap for the future of microscopy at Regeneron.</li></ul><ul><li>Developed and mentored a highly engaged, technically exceptional microscopy team.</li></ul><ul><li>Expanded the microscopy core from a service-oriented organization into a premier imaging innovation center whilst building strong partnerships across Regeneron research teams.</li></ul><ul><li>Enabled broad access to advanced microscopy imaging technologies and quantitative analysis workflows.</li></ul><p><br><br></p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Thu, 24 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50718]]></requisitionid>
    <referencenumber><![CDATA[R50718]]></referencenumber>
    <apijobid><![CDATA[r50718]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50718/associate-director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><br><p>We are seeking a highly motivated Associate Director to join the Quantitative Pharmacology (QP) group. The Associate Director will lead model-informed drug development strategies supporting one or more therapeutic areas across modalities including antibodies, siRNA, and gene therapies. This role combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY, Warren, NJ, Cambridge, MA or Remote, USA</li><li>Work model/flexibility: 4 days per week onsite or remote</li></ul><br><p><strong>Discover your role:</strong><br></p><ul><li>Proactively-identify and provide significant Pharmacometrics contribution potentially of a complex nature for research and development programs that address strategically important program needs, and that represent scientific advancements of one or more programs and/or aptly address significant regulatory hurdles.</li><li>Contribute to the overall strategic program development and is able to communicate complex Pharmacometrics strategies and results in an influential manner to the development team. </li><li>Independently design and conduct or otherwise oversee the development of PMx analysis plans and applies standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses.</li><li>Is responsible for the preparation and timely delivery of accurate and well-articulated nonclinical or clinical study reports and regulatory submission documents as appropriate.</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>PhD in Quantitative Pharmacology, Pharmacometrics, Engineering, or a related field with 7+ years of post-doctoral or industry experience; or MS with 9+ years of relevant experience.</li><li>Demonstrated expertise in population PK/PD, exposure–response, or mechanistic modeling (systems biology, or QSP) using tools such as NONMEM, Monolix, Simulx, MATLAB/Simbiology and R.</li><li>Proven track record of delivering analyses supporting regulatory submissions and engaging directly with agencies (e.g., FDA, EMA, PMDA).</li><li>Hands-on experience with a broad range of quantitative and computational tools and a strong publication record.</li><li>Exceptional communication and interpersonal skills, with the ability to influence and partner effectively across technical and non-technical teams.<br></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 25 Sep 2026 19:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs, Dermatology]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50722]]></requisitionid>
    <referencenumber><![CDATA[R50722]]></referencenumber>
    <apijobid><![CDATA[r50722]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50722/medical-director-medical-affairs-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Medical Affairs to join our Dermatology and Immunology team, supporting our Global & US medical strategy across sites in Sleepy Hollow, NY, Warren, NJ, or Cambridge, MA. In this role, you will help shape and execute medical strategy for a key asset, oversee generation and dissemination of high-quality scientific data, and ensure medical activities are delivered with integrity and scientific rigor, while collaborating with field medical, medical operations, R&D, commercial, access & reimbursement, patient advocacy, and external clinical experts.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Sleepy Hollow, NY (preferred), Warren, NJ, or Cambridge, MA</li><li>Travel percentage: 30% U.S. travel, with occasional global travel</li></ul><br><h3><strong>Discover your role:</strong></h3><ul><li>Develop and oversee Global & US medical strategy and tactics for a key asset, including publications, field communications, and expert collaborations</li><li>Apply deep therapeutic expertise to address current and future medical needs in clinical practice</li><li>Lead generation and dissemination of clinical and non-clinical data supporting the medical strategy</li><li>Partner across a cross-functional Medical Product Team, R&D, commercial, and access & reimbursement to drive alignment</li><li>Cultivate long-term strategic relationships with clinical experts, societies, advocacy groups, and alliance partners</li><li>Co-lead formation and execution of Phase 3b/4 plans where applicable</li><li>Champion high standards of compliance, ethics, and patient safety across all medical activities</li><li>Oversee medical review of promotional materials and training content for scientific accuracy</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Medical degree (MD, MBBS, or equivalent)</li><li>Relevant residency or fellowship training in dermatology or allergy/immunology preferred</li><li>8+ years of relevant medical/scientific experience</li><li>Demonstrated ability to lead technical and business discussions with internal and external stakeholders</li><li>Strong presentation and communication skills, with the ability to deliver succinct, strategic insight to senior management</li><li>Thorough understanding of the healthcare environment and its external stakeholders</li></ul><br><p>#MDJobs, #MDJobsMA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 21:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Mgr Global Patient Safety Sciences]]></title>
    <date><![CDATA[Mon, 21 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50637]]></requisitionid>
    <referencenumber><![CDATA[R50637]]></referencenumber>
    <apijobid><![CDATA[r50637]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50637/temp-mgr-global-patient-safety-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>SUMMARY: The Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><br><p>SCOPE:</p><p>N/A</p><br><p>JOB RESPONSIBILITIES:</p><ul><li>Complete signal detection activities in line with approved safety surveillance plan</li><li>Perform signal evaluation for any identified signals and author the safety evaluation reports</li><li>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</li><li>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned molecules compounds</li><li>Participate in other risk management activities as appropriate for assigned compounds</li><li>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</li><li>Experience in data manipulation and visualization (Excel, PIVOT tables, etc) for safety analysis</li><li>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</li></ul><br><p>JOB REQUIREMENTS:</p><p>Education</p><ul><li>Master of science degree, PhD, or PharmD.</li></ul><p>Experience</p><ul><li>Previous safety or relevant clinical experience in the pharmaceutical industry required, typically with at least 5+ years of risk management or relevant clinical experience in pharmaceutical/ biotech industry or health authority</li><li>Clinical experience and/or Industry experience in the TA of interest is a plus</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Commercial Business Operations & Systems]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51067]]></requisitionid>
    <referencenumber><![CDATA[R51067]]></referencenumber>
    <apijobid><![CDATA[r51067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51067/senior-director-commercial-business-operations-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><br><p>We are seeking a strategic and highly experienced leader to serve as Senior Director, Commercial Business Operations and Systems, reporting to the Executive Director, Field Enablement and Engagement Strategy. This individual will lead the Commercial Business Operations and Systems organization — including a US-based Director and an International Director— and will own the strategy, architecture, and end-to-end lifecycle of the organization's customer facing colleague platforms, systems, and processes.</p><br><p>The Senior Director is the organization's deepest functional expert on the systems, processes, and market-level requirements — both US and international — that shape how commercial technology and operational infrastructure come together to power field and customer engagement globally. This remit is a critical, direct feed into how strategy and roadmap decisions are made across the enterprise.</p><br><p>The ideal candidate is a systems thinker with deep commercial technology and process expertise across markets and a track record of driving enterprise-wide transformation — someone who can shape strategy at the enterprise level while leading a team that translates it into rigorous architecture, governance, and global execution for the business and our customer facing colleagues.</p><br><h3>When & where:</h3><br><ul><li>Location: In the Sleepy Hollow, NY Office 4 days a week</li></ul><br><h3>Discover your role:</h3><br><h3><strong>Commercial Platform & Systems Strategy</strong></h3><ul><li>Own the global strategy, architecture, and roadmap for the commercial organization's full customer facing colleague platforms — ensuring they are designed as an integrated, future-ready whole rather than a collection of point solutions.</li><li>Serve as the organization's deepest functional expert on commercial facing colleague platforms and systems — including the distinct requirements of US and international markets — and ensure that expertise directly shapes strategy and investment decisions, not just their execution.</li><li>Serve as the accountable leader for the health, evolution, and technical direction of these platforms and systems, making build-vs-buy, sequencing, and investment decisions that align to enterprise priorities.</li><li>Own the long-term, 3-5 year platform and systems roadmap, bringing market-level insight (US and international) on emerging technology, regulatory nuance, and competitive dynamics that informs where the roadmap should go.</li><li>Set standards and governance for platform architecture, data flows, and system interoperability across the commercial technology landscape.</li><li>Manage and optimize the commercial technology investment portfolio, ensuring prioritization is transparent, sequenced, and grounded in market-level cases.</li></ul><br><h3><strong>Process Strategy & Enterprise Design</strong></h3><ul><li>Lead the strategic design and continuous reinvention of the core commercial processes that govern how field and customer-facing teams engage, plan, and implement — including planning, engagement, and performance-management workflows — bringing deep knowledge of requirements to ensure these processes work in practice, not just on paper.</li><li>Establish global and regional process standards and operating models that balance enterprise consistency with the flexibility Business Units and individual markets need to compete effectively, serving as the primary voice for market-level requirements in how those standards are set.</li><li>Identify structural opportunities to simplify, automate, or reimagine commercial processes, using platforms and AI to remove friction and elevate field and customer experience.</li><li>Own the governance model that ensures platforms, systems, and processes evolve together as a coherent commercial operating model, rather than in silos.</li></ul><br><h3><strong>Strategic Leadership & Stakeholder Partnership</strong></h3><ul><li>Serve as a chief strategic commercial partner and co-owner on the commercial customer facing colleague technology and process agenda across Business Units, IT, Compliance, and Training.</li><li>Represent the platform and process strategy in senior governance forums, business reviews, and enterprise planning cycles, bringing the market and technical expertise needed to build consensus and secure investment.</li><li>Bring an external and forward-looking perspective — informed by industry trends, competitor capabilities, and emerging technology across both US and international markets — to continually challenge and elevate the organization's commercial platform strategy.</li><li>Build the argument for, and lead the change management around, major shifts in how the organization's commercial platforms and processes operate, partnering closely with training teams and ensuring end user capabilities and confidence in using these systems to meet customer needs and advance business priorities.</li></ul><br><h3><strong>Global Scale & Portfolio Leadership</strong></h3><ul><li>Lead the global portfolio of commercial customer facing colleague platform and process initiatives, ensuring strategic coherence, appropriate sequencing, and disciplined execution across regions and Business Units.</li><li>Partner with Enablement and Business Unit customers to ensure global platform and process strategy reflects real market-level needs and is adopted and adapted appropriately, without compromising enterprise scalability.</li><li>Define the metrics and success framework used to evaluate platform and process performance, and hold the organization accountable to measurable business outcomes.</li></ul><br><h3><strong>Team Leadership</strong></h3><ul><li>Build, lead, and develop the Commercial Business Operations and Systems team — including a direct-reporting US Director and International Director— fostering a culture of critical thinking, accountability, and high performance.</li><li>Ensure the US and International Director roles are structured so that market-specific requirements (regulatory, cultural, operational) are surfaced early and consistently into the broader strategy and roadmap, rather than treated as after-the-fact localization.</li><li>Serve as a key advisor on organizational design, capability-building, and resourcing needed to deliver the commercial platform and process strategy.</li></ul><br><h3>This role requires:</h3><br><ul><li>Bachelor's degree required; MBA or advanced degree preferred.</li><li>15+ years of progressive experience in commercial technology, business operations, or commercial strategy, ideally within pharmaceutical, biotech, or another regulated industry.</li><li>Demonstrated experience owning the strategy and architecture of commercial platforms and systems (CRM, digital engagement platforms) at an enterprise or global scale, including direct experience with both US and international market requirements.</li><li>Strong understanding of the market rules, regulations, and compliance requirements that govern commercial engagement across geographies (e.g., promotional regulations, data privacy standards, and HCP/customer engagement codes), and the ability to design platforms and processes that meet these requirements by design.</li><li>Proven ability to design a global vision and strategy while architecting harmonized, market- and region-specific programs — balancing enterprise-wide consistency with the flexibility individual regions or markets need to operate effectively and compliantly.</li><li>Strong track record of leading large-scale process transformation and operating-model design across a matrixed, multi-business-unit organization.</li><li>Systems-level thinking, with the ability to see across platforms, processes, and organizational boundaries to design a coherent commercial operating model.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 07:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Contract Development]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51095]]></requisitionid>
    <referencenumber><![CDATA[R51095]]></referencenumber>
    <apijobid><![CDATA[r51095]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51095/director-contract-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><br><p>The Director, Contract Development leads the team responsible for the drafting, negotiation, and enterprise-wide governance of contract language, templates, and terms and conditions supporting Regeneron’s commercial customer segments, including IDNs, GPOs, hospitals, and payers/PBMs. Partnering closely with the Contract Strategy leads, they translate approved contracting strategies into executable, compliant contract language and operate at the highest levels of autonomy in drafting, negotiating, and shaping contract language, including for the organization’s most complex and highest-value customer relationships. Working across Contract Strategy, Legal, Customer Engagement, Government Pricing, and Pricing & Contracting Operations, they deliver market-responsive, compliant, and risk-managed terms that balance commercial objectives, customer value, operational feasibility, and compliance. They serve as the senior technical expert and mentor for Contract Development, using discretion to determine appropriate escalation of final contract language, positions, and risk decisions to Market Access leadership.</p><br><h3>When & where:</h3><br><ul><li>Location: In the Sleepy Hollow, NY office 4 days a week</li></ul><br><h3>Discover your role:</h3><br><ul><li>Lead the drafting, negotiation, and execution of high-value, highly complex contract language for institutional and channel customers, translating approved contract strategy into executable terms and conditions.</li><li>Lead the drafting, negotiation, and execution of the organization’s most complex, highest-value agreements in support of Regeneron U.S. Commercial strategies, partnering with Contract Strategy on account strategy.</li><li>Drive innovation in contract language and constructs that create competitive advantage, assessing and managing legal and business risk.</li><li>Serve as the senior contract-language expert and primary point of knowledge on contractual terms and actual performance for all Institutional customers.</li><li>Lead Pricing Review Committee agenda and materials development within Regeneron as it relates to contract language, terms, and risk positioning.</li><li>Lead template governance, clause development, and the early-risk identification framework across the function.</li><li>Lead the ongoing development, governance, maintenance, and version control of contract templates, standard clauses, and agreement language, ensuring consistency and compliance across customer segments, partnering with Legal to enable scalable execution.</li><li>Lead the early-risk identification framework, converting cross-functional input into executive-level risk recommendations, recommending risk tolerance and mitigation approach.</li><li>Lead assessment of the impact of evolving healthcare laws and regulations on contract terms, recommending enterprise-wide template and policy updates.</li><li>Lead critical initiatives, including new template development and risk assessment for new customer segments and contracting channels, setting direction for how Contract Development scales into new areas.</li><li>Advise and influence leadership and partner cross-functionally to shape contractual positions.</li><li>Lead the translation of product, pricing, and customer strategy into executable contract language, partnering with Pricing & Commercial Operations, Contract Strategy, and Customer Engagement as the senior Contract Development authority.</li><li>Lead contract-language strategy and risk positioning within complex institutional negotiations, partnering with Contract Strategy and Customer Engagement to drive successful outcomes.</li><li>Lead efforts to ensure contract language, templates, and agreements align with legal, regulatory, and company policy requirements, partnering with Legal, and coordinate with Pricing and Contracting Operations to ensure operational feasibility and execution.</li><li>Set the standard for the function across tools, capability, and continuous improvement.</li><li>Drive development of analytical tools and frameworks that strengthen contract risk assessment and drafting decisions across the function.</li><li>Lead evaluation and adoption of innovative Contract Development platforms, tools, and enhanced AI capabilities across the contracting workflow.</li><li>Serve as the senior technical expert and mentor for Contract Development colleagues, setting the standard for and elevating drafting capability and consistency across the function.</li><li>Lead Contract Development process re-imaginations, driving continuous improvement of drafting standards, documentation, and governance practices.</li></ul><br><h3>This role requires:</h3><br><ul><li>Bachelor’s degree with a focus in Marketing, Business Administration, Science, Pharmacy, or Accounting/Finance preferred; paralegal degree or certification a plus.</li><li>12+ years of experience in US Pharma / biotech / healthcare industry, with experience in institutional or channel contracting, contract development / agreement drafting, pricing, and/or market access preferred, including a demonstrated track record of leading complex negotiations for high-value, strategically significant accounts.</li><li>Expert-level knowledge of contract drafting, agreement language, and industry-standard contracting terms, and of GPO, IDN, hospital, specialty pharmacy, specialty distributor, payer/PBM, trade, and/or retail customers.</li><li>Demonstrated track record of leading governance frameworks, driving cross-functional initiatives, and influencing senior partners, with strengths in risk assessment, analytical thinking, problem solving, and cross-functional collaboration.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 07:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50973]]></requisitionid>
    <referencenumber><![CDATA[R50973]]></referencenumber>
    <apijobid><![CDATA[r50973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50973/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[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Study Lead to join our Clinical Trial Management team, supporting our Japan operations in a hybrid work mode. In this role, you will lead assigned clinical trials from study design through close-out while collaborating with cross-functional study teams, vendors and leadership. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Tokyo, Japan</p><p>Hybrid</p><p>Up to 25% travel may be required.</p><h3><strong>Discover your role:</strong></h3><ul><li>Lead cross-functional study teams and global, regional or country execution of assigned clinical trials.</li><li>Shape protocols, study documentation, feasibility, site selection, investigator meetings and recruitment strategies.</li><li>Manage timelines, budgets, risks, vendors, supplies, study systems, activation, monitoring and data quality.</li><li>Maintain Clinical Trial Management System and Trial Master File readiness, including registry, audit and inspection compliance.</li><li>Escalate study issues and implement corrective actions with Program Operations Lead, Country Operations Lead and stakeholders.</li><li>Lead close-out, including database lock, vendor reconciliation, budgets, Trial Master File and study drug accountability.</li><li>Support study reports, lessons learned, staff deliverables, process improvement, unmasked activities and potential line management.</li><li>You use data-driven thinking to strengthen study execution and continuous improvement.</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree and at least six years of relevant industry experience.</li><li>Global clinical trial operations experience, including protocols, key study documents and budget and vendor management.</li><li>Knowledge of International Council for Harmonisation Good Clinical Practice and applicable regulatory guidelines.</li><li>Proficiency with trial management systems, Microsoft applications, Interactive Voice Response Systems and electronic data capture.</li><li>Project management, cross-functional leadership, organization, communication, influencing and negotiation skills.</li><li>Ability to implement operational strategy, meet deadlines, prioritize effectively and build productive study teams.</li><li>Industry awareness, proactive self-discipline and a data-driven approach to planning, execution and problem-solving.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 07:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist – Protein Expression Sciences (Antibody Discovery)]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48393]]></requisitionid>
    <referencenumber><![CDATA[R48393]]></referencenumber>
    <apijobid><![CDATA[r48393]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48393/senior-scientist-protein-expression-sciences-antibody-discovery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a highly motivated Senior Scientist to join our Antibody Discovery team within the Protein Expression Sciences department. This role is at the forefront of early therapeutic discovery, where you will drive ongoing programs and analyze complex datasets to enable the selection of next-generation therapeutic antibodies. The ideal candidate will thrive in a collaborative, cross-functional environment, coordinating screening campaigns, interpreting high-throughput data across multiple concurrent projects, and clearly communicating key findings to internal stakeholders. Strong analytical skills, attention to detail, and the ability to translate data into actionable insights are essential for success in this role. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>Location: Tarrytown, NY - On-site</p><p><strong>Discover your role:</strong></p><ul><li>Manages multiple projects simultaneously within a cross-functional team environment</li><li>Establishes and communicates timelines across research teams, both within and outside the department</li><li>Analyzes primary screening data using a variety of software tools and selects antibodies with desired functional properties</li><li>Ensures accurate and complete capture of experimental data in internal databases and repositories</li><li>Presents results from antibody discovery campaigns to team members, cross-functional partners, and senior leadership</li><li>Stays current with scientific advances in the field and contributes to team strategy</li><li>Mines and summarizes data to support process improvements and enhance discovery pipelines</li></ul><p><strong>This role requires:</strong></p><ul><li>Ph.D. in Molecular Biology, Cellular Biology, Biochemistry, Immunology, or a related field with 2–4 years of relevant experience</li><li>Enjoys working in a high-throughput environment focused on discovering innovative therapies for serious medical conditions</li><li>Brings a collaborative, agile mindset and leverages technology creatively to accelerate drug discovery</li><li>Has experience using modern data analysis and visualization tools (e.g., advanced Excel, GraphPad Prism, Spotfire, Power BI, or similar platforms) to explore datasets, generate insights, and communicate results</li><li>Demonstrates strong project management, analytical, and organizational skills</li><li>Familiarity with basic scripting or automation tools (e.g., Python, R, or workflow tools) is a plus but not required</li><li>Experience with laboratory automation and data management systems (e.g., LIMS) is a plus</li><li>A strong publication record in peer-reviewed journals is preferred</li></ul><p><strong>Additional qualifications:</strong></p><ul><li>Working knowledge of immunology, including antibody generation, structure, and characterization (strongly preferred)</li><li>Proven experience analyzing large datasets and synthesizing results into clear conclusions</li><li>Experience with multi-well assays used in drug screening and high-throughput data analysis (preferred)</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 10:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Process Management, Operations & Continuous Improvement]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51028]]></requisitionid>
    <referencenumber><![CDATA[R51028]]></referencenumber>
    <apijobid><![CDATA[r51028]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51028/2027-co-op-process-management-operations-continuous-improvement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Process Engineering, Operations & Continuous Improvement to join our Preclinical Manufacturing and Process Development (PMPD) team, which develops the manufacturing processes used to scale up and produce Regeneron's medicines.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support technology transfer projects between development and manufacturing teams</li></ul><ul><li>Lead or contribute to continuous improvement initiatives across process development</li></ul><ul><li>Build reporting and data-visualization tools to track project status across teams</li></ul><ul><li>Coordinate with upstream, downstream, and analytical teams to gather project information</li></ul><ul><li>Analyze operational data to identify opportunities for efficiency gains</li></ul><ul><li>Prepare presentations and updates for cross-functional stakeholders</li></ul><ul><li>Support project planning and timeline tracking</li></ul><ul><li>Collaborate with colleagues across the organization on operations</li></ul><br><p><strong>Relevant majors: </strong>Chemical/Biomedical Engineering, Industrial Engineering, Business, Supply Chain Management</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Indianapolis, IN]]></title>
    <date><![CDATA[Thu, 24 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50580]]></requisitionid>
    <referencenumber><![CDATA[R50580]]></referencenumber>
    <apijobid><![CDATA[r50580]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50580/medical-specialist-i-indianapolis-in/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Indianapolis]]></city>
    <state><![CDATA[Indiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>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>When & where: </strong></p><ul><li><p>Remote role</p></li><li><p>Location: Indianapolis, IN</p></li></ul><p><strong>Discover your role:</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 requires:</strong></p><ul><li><p>Possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus</p></li><li><p>We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience</p></li><li><p>Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred</p></li><li><p>We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments</p></li><li><p>This role requires the ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,743.00 - $209,358.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Scientific Writing Specialist]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50724]]></requisitionid>
    <referencenumber><![CDATA[R50724]]></referencenumber>
    <apijobid><![CDATA[r50724]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50724/sr-scientific-writing-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Scientific Writing Specialist to draft and manage reviews for Clinical Bioanalysis and Clinical Pharmacology submission documents across multiple therapeutic target areas (Cardiovascular & Metabolism, Oncology, General Medicine, Immunology & Inflammation, Genetic Medicine) and all phases of clinical development (Phase 1 through Phase 3). In this role, you will lead document meetings and timelines while collaborating with cross-functional program teams, with the opportunity to contribute to digital technology-based solutions for content generation.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><br><ul><li>Location: [Insert location]</li><li>Work model/flexibility: [Insert work model]</li></ul><br><p><strong>Discover your role:</strong></p><br><ul><li>Independently draft and manage review of reports and summaries for the Clinical Pharmacology and Clinical Bioanalysis functional areas</li><li>Lead Kickoff, Author, and Comment Reconciliation meetings for assigned documents</li><li>Attend cross-functional program meetings and report relevant strategic information back to the writing team and management</li><li>Manage multiple projects and timelines</li><li>Review data outputs for consistency with stylistic standards</li><li>Participate in the revision and maintenance of document templates or shells</li><li>Bring strong attention to detail and excellent interpersonal and communication skills</li><li>Stay curious about digital technology-based solutions that streamline content creation and daily workflows</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>BS degree with 2+ years of relevant experience, or MS/PhD/PharmD in a life science</li><li>1-2 years of relevant industry experience in a biotech/pharma setting</li><li>Strong attention to detail</li><li>Excellent interpersonal and communication skills (verbal and written)</li><li>Computer proficiency (Word, Excel, Adobe, and related software) and fluency in English</li><li>Preferred: experience using digital technology-based solutions (e.g., AI, PerfectIt) to streamline content creation or workflows</li><li>Preferred: basic understanding of the eCTD and drug development process</li><li>Preferred: strong background in protein therapeutics and/or gene therapy</li></ul><br><p>A cover letter is strongly encouraged.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 11:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[EH&S Specialist I]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51153]]></requisitionid>
    <referencenumber><![CDATA[R51153]]></referencenumber>
    <apijobid><![CDATA[r51153]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51153/ehs-specialist-i/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist to join our Environment, Health & Safety (EH&S) team in an on-site capacity. In this role, you will help protect the safety and health of our workforce by supporting regulatory compliance, inspections, incident response, and industrial hygiene programs while collaborating with laboratory, facilities, and departmental partners.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: On-site</li></ul><h3>Discover your role:</h3><ul><li>Support EH&S programs, procedures, and communications that promote regulatory compliance and safe work practices</li><li>Perform routine inspections, audits, and assessments of laboratories, facilities, and support areas</li><li>Coordinate environmental compliance activities, including spill kits, waste management support, and related documentation</li><li>Respond to EH&S incidents, alarms, and emergency events, including after-hours situations</li><li>Support industrial hygiene and occupational health through exposure monitoring, sampling, and ergonomic assessments</li><li>Manage calibration, maintenance, and logistics for EH&S monitoring and radiation safety equipment</li><li>Investigate near-misses and incidents, help identify corrective actions, and maintain EH&S records, inventories, and signage</li><li>Partner with assigned departments on risk mitigation, and support new construction, renovation, permits, and regulatory submissions</li></ul><h3> </h3><h3> </h3><h3>This role requires:</h3><ul><li>Bachelor's degree in Safety, Public Health, Industrial Hygiene, Science, or a related field</li><li>1-2 years of related work experience</li><li>Excellent written and verbal communication skills</li><li>Proficiency in computer skills, such as the Microsoft suite, and ability to learn specialized software and safety and industrial hygiene equipment</li><li>Preferred: Advanced degree and/or certifications (Certified Industrial Hygienist, Certified Safety Professional, Associate Safety Professional, Certified Hazardous Materials Manager, and/or Medical Emergency Technician)</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 12:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Pathologist]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47855]]></requisitionid>
    <referencenumber><![CDATA[R47855]]></referencenumber>
    <apijobid><![CDATA[r47855]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47855/associate-director-clinical-pathologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>Associate Director of Pathology has primary responsibility to support drug molecule efficacy and safety studies in a variety of therapeutic focus areas (TFAs). The successful candidate will also provide Clinical Pathology support for GLP toxicology and PK studies of Regeneron molecules. The Associate Director will be expected to manage Clinical Pathology support to selected TFAs, and mentor junior Pathologists. </p></div><div></div><div><p><strong>A Typical day in this role may look like:</strong> </p></div><div><ul><li><p>Serve as a scientific leader supporting nonclinical drug development across multiple therapeutic areas. </p></li></ul></div><div><ul><li><p>Work both independently and as a part of integrated discovery and development teams to interpret pharmacologic and toxicity related findings and help advance promising therapeutics through Regeneron’s pipeline. </p></li></ul></div><div><ul><li><p>Determining and evaluating clinical pathology-related endpoints in pharmacology and toxicology studies and guiding decision making. </p></li></ul></div><div><ul><li><p>Collaborate closely with anatomic pathologists, toxicologists, and researchers within Regeneron. </p></li></ul></div><div><ul><li><p>Partner with our CRO partners in providing scientific peer review of nonclinical safety studies. </p></li></ul></div><div></div><div><p><strong>This job might be for you if you have:</strong> </p></div><div><ul><li><p>Experience with integrating clinical and anatomic pathology data </p></li></ul></div><div><ul><li><p>Experience with animal models of human diseases </p></li></ul></div><div><ul><li><p>Clear, concise oral and written communication skills </p></li></ul></div><div><ul><li><p>Demonstrated ability to contribute to cross functional teams </p></li></ul></div><div><ul><li><p>Ability to contribute to scientific strategy, problem solving, and the broader understanding of pathology-related issues that influence drug development outcomes. </p></li></ul></div><div></div><div><p><strong>In order to be considered for this role, you must have</strong>: </p></div><div><ul><li>DVM (or equivalent) with ACVP certification in Clinical Pathology required, (strong preference for PhD in Pathology, Immunology, or related ) </li></ul></div><div><ul><li>Minimum 3 years of industry experience interpreting GLP and non GLP clinical pathology data in nonclinical studies and supporting discovery research in a pharma/ biotech or CRO setting. </li><li>Additional certification in Anatomic Pathology nice to have</li></ul></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Quality Control]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49639]]></requisitionid>
    <referencenumber><![CDATA[R49639]]></referencenumber>
    <apijobid><![CDATA[r49639]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49639/supervisor-quality-control/]]></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 looking for a 2nd shift Supervisor Quality Control. This role will be responsible for supporting the laboratory with testing and/or data review on release drug products, stability samples and non-routing samples in support of the company’s quality program. This position will also be responsible for providing on the floor support to the analyst. This position will have direct reports.</p><br><p><strong>When & Where:</strong></p><ul><li>2nd Shift, Sunday - Thursday 12PM - 8:30PM</li><li>Location: Rensselaer, New York, United States</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Supervise QC staff, assign and balance workload, and monitor progress against deadlines and priorities</li></ul><ul><li>Generate test results as well as review test results to ensure compliance with standards; reports any quality anomalies.</li></ul><ul><li>Calibrate and maintain laboratory equipment; participate in equipment qualifications.</li></ul><ul><li>Perform a review of testing performed within the laboratory to ensure compliance with standards.</li></ul><ul><li>Provides on-the-floor guidance and support to employees during routine testing.</li></ul><ul><li>Provide employees with support on laboratory investigations and participate in owning investigations.</li></ul><ul><li>Write, revise, and review controlled standard operating procedures.</li></ul><ul><li>Responsible for leading a cross functional project.</li></ul><ul><li>Completes, reviews, and reconciles logbooks to ensure compliance with cGMP standards and internal procedures.</li></ul><ul><li>Reviews and approve laboratory maintenance records to support daily laboratory operations.</li></ul><ul><li>Reviews and approve employees’ timesheets by end of the week.</li></ul><ul><li>Delivers training to employees and ensure requirements are met. Maintain up to date training records for self and direct reports.</li></ul><ul><li>Perform minimally monthly performance feedback meetings with direct reports.</li></ul><ul><li>Escalates all performance issues to management and/or HR.</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Chemistry, Biochemistry or related field required; MS preferred</li></ul><ul><li>5+ years of progressive, relevant QC experience, preferably within the pharmaceutical or biotechnology industry</li></ul><ul><li>Prior supervisory or leadership experience required</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II TN, AL, & Pensacola to Tallahassee, FL]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51306]]></requisitionid>
    <referencenumber><![CDATA[R51306]]></referencenumber>
    <apijobid><![CDATA[r51306]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51306/medical-specialist-ii-tn-al-pensacola-to-tallahassee-fl/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Alabama]]></city>
    <state><![CDATA[Alabama]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</p><p>At Regeneron, we are committed to transforming the lives of patients through science and innovation. As a leading biotechnology company, we discover, develop, manufacture, and commercialize medicines for serious diseases. We are seeking a <strong>Medical Specialist, Ophthalmology</strong> to join our Retina team, supporting the Tennessee, Alabama, Pensacola to Tallahassee, FL territory in a field-based role. In this position, you will help bring innovative retinal therapies to healthcare providers, build trusted partnerships with retina specialists and ophthalmology practices, and drive business results that improve patient outcomes. Working closely with customers and cross-functional partners, you will play a critical role in expanding access to life-changing treatments while contributing to a purpose-driven organization dedicated to advancing science and patient care.</p><p>When & where:</p><ul><li><strong>Location:</strong> Tennessee, Alabama, Pensacola to Tallahassee, FL</li><li><strong>Work model/flexibility:</strong> Field-based</li><li><strong>Travel percentage:</strong> Approximately 40-60%</li></ul><p>Discover your role:</p><ul><li>Develop and grow strategic relationships with retina specialists, ophthalmologists, and key customer accounts throughout the territory.</li><li>Execute territory business plans to achieve sales objectives and support the growth of Regeneron’s ophthalmology portfolio.</li><li>Educate healthcare providers on clinical data, product benefits, patient identification, and treatment pathways.</li><li>Partner with customers to identify opportunities that enhance patient access and improve treatment outcomes.</li><li>Navigate complex account environments using strong business acumen and strategic account management skills.</li><li>Collaborate cross-functionally to address customer needs and deliver valuable solutions that support practice success.</li><li>Analyze market trends, customer insights, and territory dynamics to inform business planning and prioritization.</li><li>Manage a geographically dispersed territory while balancing customer engagement, business objectives, and travel requirements.</li><li>Maintain expertise in the ophthalmology and retina landscape, including competitive, reimbursement, and market developments.</li></ul><p>This role requires:</p><ul><li>Bachelor’s degree and a minimum of 5 years of specialty sales experience within the pharmaceutical or biotechnology industry.</li><li>Demonstrated history of high sales performance and consistent achievement of territory goals and business objectives.</li><li>Experience selling biologics and buy-and-bill products within specialty healthcare settings.</li><li>Strong understanding of reimbursement programs, government programs, managed care, formulary processes, and contract negotiations.</li><li>Ophthalmology sales experience preferred, with retina-focused experience strongly preferred.</li><li>Proven ability to develop strategic relationships with physicians, retina specialists, and other key customer stakeholders.</li><li>Strong business acumen, account management capabilities, and the ability to navigate complex customer and market dynamics.</li><li>Excellent communication, customer engagement, and cross-functional collaboration skills.</li><li>Must reside within or near the assigned Tennessee, Alabama, Pensacola to Tallahassee, FL territory; relocation assistance is not provided.</li><li>Ability and willingness to travel approximately 40-60% of the time in support of customer and business needs.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$178,500.00 - $241,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 22:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Senior Administrative Coordinator]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51252]]></requisitionid>
    <referencenumber><![CDATA[R51252]]></referencenumber>
    <apijobid><![CDATA[r51252]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51252/temporary-senior-administrative-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Administrative Coordinator to join our Global Clinical Operations team, supporting Clinical Trial Management in a hybrid work environment. In this role, you will provide high-level administrative support to Vice Presidents and departmental leaders, enabling efficient day-to-day operations, streamlined processes, and effective team collaboration. Working closely with leadership, cross-functional partners, and department teams, you will help drive operational excellence while supporting key business activities. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Uxbridge</p><p>Hybrid (3 days on site)</p><p>Temporary 12 months role</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Manage complex calendars and scheduling activities, aligning priorities and resolving logistical challenges proactively.</li><li>Coordinate internal and external meetings, seminars, and events, including logistics, vendor engagement, budgeting, and contract support where applicable.</li><li>Support team activities including town halls, team-building events, agendas, presentations, catering coordination, and meeting materials distribution.</li><li>Assist employees and visitors with travel arrangements, expense reporting, and related administrative services.</li><li>Maintain department contact lists, organizational charts, dashboards, reports, SharePoint content, permissions, and version control.</li><li>Manage office supplies, purchase requisitions, purchase order tracking, and departmental expenses while supporting budget oversight.</li><li>Coordinate onboarding activities with Information Technology, Facilities, Procurement, and space planning teams for new hires and department needs.</li><li>You anticipate stakeholder needs, drive process improvements, communicate effectively, and collaborate across teams to deliver efficient administrative support.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Experience providing administrative support within Regeneron.</li><li>Experience supporting Vice President-level leaders and departmental leadership teams.</li><li>Experience managing calendars, travel logistics, expense reports, meetings, events, and administrative workflows.</li><li>Ability to create and maintain reports, dashboards, pivot tables, organizational charts, and departmental documentation.</li><li>Experience managing departmental content, permissions, and version control on SharePoint or internal platforms.</li><li>Ability to coordinate purchasing activities, requisitions, purchase orders, and budget-related administrative processes.</li><li>Strong written and verbal communication skills with the ability to interact effectively across all levels of the organization while maintaining confidentiality.</li><li>Ability to understand business priorities, exercise independent judgment, solve problems, manage ambiguity, and maintain high accuracy and attention to detail.</li><li>Demonstrated collaboration skills with the ability to build trusted relationships, work independently, manage projects, and adapt comfortably to change.</li></ul><br><br><br><br><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist - Bioanalytical Sciences]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50663]]></requisitionid>
    <referencenumber><![CDATA[R50663]]></referencenumber>
    <apijobid><![CDATA[r50663]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50663/principal-scientist-bioanalytical-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><br><p>Regeneron's Bioanalytical Sciences group, located in Tarrytown, NY, is looking for a Principal Scientist. In this role you will serve as the Bioanalytical Sciences Lead to manage bioanalytical strategy and oversee bioanalytical activities for clinical programs. Acts as the liaison between Bioanalytical Sciences (BAS) and clinical study teams to effectively manage pharmacokinetics (PK), immunogenicity, and biomarker deliverables and timelines for clinical studies. Supports regulatory submissions and interactions to ensure the completeness of sections related to immunogenicity and bioanalysis of PK and target biomarker samples. </p><br><p><strong>When & where: </strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: 4 days onsite</li></ul><br><p><strong>Discover your role: </strong></p><ul><li>Serve as the Bioanalytical Sciences Lead on clinical study teams and participates on project teams both internal and external to Regeneron to oversee bioanalysis for clinical studies. </li><li>Contributes to the development and management of bioanalytical strategy including immunogenicity risk assessment, assay selection, and sampling timepoints for clinical programs. </li><li>Act as a liaison between Bioanalytical Sciences (BAS) and the clinical development team, work closely with groups within BAS, as well as the Clinical Pharmacology group, Regulatory Affairs, clinical study teams, and other working groups to establish bioanalytical deliverables and timelines for multiple projects. </li><li>Review sample analysis documentation and clinical sample analysis reports. </li><li>Contribute to regulatory submissions and responses to regulatory inquiries. </li><li>Contribute to and review clinical study-related documents including expanded synopses, protocols, amendments, statistical analysis plan, and clinical study reports. </li><li>Review data, SOPs, publications, and guidelines to ensure the conduct of bioanalysis is compliant with industry practice and/or regulatory expectations. </li><li>Prepare and present scientific data at internal and external meetings. </li></ul><p><strong>This role requires: </strong></p><ul><li>PhD or BS/MS with 5+ years of experience in immunology, pharmaceutical sciences, or related field. </li><li>Experience with bioanalytical techniques, e.g., ELISA, ECL (MSD), LC-MS, PCR,flow cytometry, or immunogenicity assays.</li><li>Experience with writing/reviewing scientific documents, reports, and contributing to regulatory submissions.</li><li>Strong communication, project management, and interpersonal skills.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 10:56:34 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Statistical Programming - Internal Medicine]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51375]]></requisitionid>
    <referencenumber><![CDATA[R51375]]></referencenumber>
    <apijobid><![CDATA[r51375]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51375/manager-statistical-programming-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables</li><li>Lead the development and quality control of tables, listings, and graphs in support of analysis requirements</li><li>Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests</li><li>Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch</li><li>Partner with management to determine resource requirements for your therapeutic area or department</li><li>Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles</li><li>Provide feedback to management on team members' contributions to support performance evaluations and goal-setting</li><li>Advise direct reports on procedures for data, records, and information retention</li><li>Enjoy working with minimal supervision and taking ownership of complex deliverables</li><li>Communicate clearly with cross-functional, multidisciplinary teams</li><li>Think analytically and stay organized when managing multiple priorities and timelines</li><li>Take initiative in developing deep expertise within a specialized area</li><li>Bring a collaborative mindset to hiring, feedback, and team development</li><li>Adapt easily to shifting priorities, including last-minute requests from senior leadership</li><li>Approach quality and documentation with rigor in a regulated environment</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 6+ years (or BS 7+) of relevant work experience</li><li>Proven experience leading programming deliverables within a clinical study team</li><li>Experience providing input on hiring, feedback, and performance evaluation</li><li>Strong organizational and documentation skills within a regulated environment</li><li>Nice to have: SAS Certification</li></ul><br><p>#statprogregn</p><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Statistical Programming - Hematology]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48840]]></requisitionid>
    <referencenumber><![CDATA[R48840]]></referencenumber>
    <apijobid><![CDATA[r48840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48840/associate-director-statistical-programming-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Statistical Programming to join our Statistical Programming team, supporting our therapeutic area programs in a hybrid work model. In this role, you will oversee statistical programming activities across internal teams and functional service providers, ensuring high-quality deliverables while shaping departmental standards, processes, and training. You'll collaborate closely with study and project teams, programming leadership, and cross-functional stakeholders to meet therapeutic analysis and computing needs.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Lead and manage a statistical programming group, driving timely, high-quality deliverables across internal and outsourced work</li><li>Shape and implement programming standards, applications, processes, and training for your therapeutic area</li><li>Partner with study and project teams to clarify requirements and guide programmers through assignment execution</li><li>Represent Statistical Programming with partnering functions to ensure specifications and computing needs are met</li><li>Champion company values, modeling excellence, collaboration, ownership, and accountability</li><li>Drive department goals and lead subject-matter-expert initiatives</li><li>Set goals, manage performance, and mentor direct reports, supporting their growth and development</li><li>Contribute to hiring by screening and interviewing programming candidates</li><li>Bring proven experience managing programming teams and external service providers</li><li>Think strategically about department-wide standards, processes, and long-term goals</li><li>Communicate confidently across global, cross-functional teams</li><li>Solve problems independently and manage multiple priorities under tight timelines</li><li>Enjoy mentoring and developing junior staff and contractors</li><li>Take ownership of deliverables without close supervision</li><li>Bring a collaborative, respectful, and solutions-oriented mindset to complex projects</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline, with 10+ years of clinical programming experience</li><li>Advanced SAS programming skills (Base, Stat, Macro, Graph) within a clinical data environment</li><li>Demonstrated project and people management experience, including work across global, interdisciplinary teams</li><li>Expertise in one or more therapeutic areas and strong understanding of pharmaceutical clinical development and regulatory submissions</li><li>SAS certification (preferred)</li><li>Leadership experience supporting the hiring, development, and evaluation of junior staff and contractors (preferred)</li></ul><br><p>#statprogregn</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QC External Lab Coordinator]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51383]]></requisitionid>
    <referencenumber><![CDATA[R51383]]></referencenumber>
    <apijobid><![CDATA[r51383]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51383/qc-external-lab-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a <strong>QC External Laboratory Coordinator</strong>to join our <strong>Quality Control (QC) Support</strong> team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><br><ul><li><strong>Location:</strong> Raheen, Limerick, Ireland.</li><li><strong>Flexibility & Travel:</strong> Occasional travel may be required to support external laboratory partnerships and audits.</li><li><strong>Other Requirements:</strong> Ability to work cross-functionally in a highly regulated Good Manufacturing Practice (GMP) environment.</li></ul><br><h3><strong>What you’ll do:</strong></h3><br><ul><li>Coordinate sample management and method transfer activities with external laboratories supporting manufacturing and quality control operations.</li><li>Serve as a technical subject matter expert for analytical and microbiological method transfers, ensuring successful execution and compliance.</li><li>Partner with Quality Assurance, Manufacturing, and external laboratories to resolve quality issues, investigations, and technical challenges.</li><li>Review and approve method transfer documentation, quality records, and laboratory reports to support regulatory compliance.</li><li>Drive continuous improvement initiatives while maintaining quality systems, including change controls, corrective and preventive actions, and Standard Operating Procedures (SOPs).</li></ul><br><h3>The Environment and Physical Rhythms of This Role:</h3><br><ul><li>This role is primarily office and laboratory-based within a Good Manufacturing Practice (GMP) regulated environment.</li><li>May involve entering manufacturing, warehouse, or laboratory areas requiring appropriate gowning and personal protective equipment.</li><li>Requires routine use of computer systems and the ability to review technical documentation and laboratory data.</li></ul><br><h3><strong>Let’s find out if we’re a fit:</strong></h3><br><ul><li>Bachelor's degree in Biology, Chemistry, Microbiology, or a related scientific discipline, or equivalent relevant experience.</li><li>Experience in quality control, analytical testing, microbiology, or external laboratory management within a regulated industry.</li><li>Knowledge of Good Manufacturing Practice (GMP) requirements and quality systems.</li><li>Experience with method transfers, investigations, change controls, or contract laboratory oversight is preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>€18.34 - €28.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 04:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - South Central]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48156]]></requisitionid>
    <referencenumber><![CDATA[R48156]]></referencenumber>
    <apijobid><![CDATA[r48156]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48156/neurology-account-director-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: South Central (Texas, Arkansas and Louisiana)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, Clinical Data Reporting]]></title>
    <date><![CDATA[Tue, 23 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48587]]></requisitionid>
    <referencenumber><![CDATA[R48587]]></referencenumber>
    <apijobid><![CDATA[r48587]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48587/specialist-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Specialist, Clinical Data Reporting to join our Data Management team, supporting clinical trial oversight and study-level data review in a hybrid role. In this role, you will produce accurate and consistent reporting outputs that drive data cleaning, medical review, and operational decision-making, while collaborating with clinical data management, technology partners, and cross-functional teams to deliver study-level reports on schedule. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong> Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Program and maintain standardized clinical data reports and listings used for participant-level data review, data cleaning, and operational oversight</p></li><li><p>Translate study reporting requirements into technical specifications and implement outputs using established frameworks and data standards</p></li><li><p>Build and validate data review listings, exception reports, reconciliation outputs between EDC and external data, and operational performance reports</p></li><li><p>You communicate clearly with cross-functional partners to clarify reporting needs and deliver outputs on schedule</p></li><li><p>Partner with clinical data management and technology teams to leverage data sources including the Scientific Data Lake, EDC systems, and external data streams</p></li><li><p>Monitor routine data refreshes, troubleshoot issues with accuracy, completeness, and integration, and contribute to automation and workflow streamlining</p></li><li><p>Keep reporting documentation, specifications, and outputs audit- and inspection-ready in line with GCP, ICH, GDPR, SOPs, and internal quality standards</p></li><li><p>You stay curious about reporting tools and methodologies, sharing knowledge of standards and processes to support team learning and continuous improvement</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's or Master's degree in Data Science, Computer Science, Life Sciences, or a related field</p></li><li><p>2+ years of experience in clinical data, data visualization, or related disciplines, with a background in building interactive reporting solutions, KPIs, and metrics to support clinical trial oversight</p></li><li><p>Proficiency in EDC systems (e.g., Medidata RAVE) and analytics, reporting, and data visualization tools such as SAS, R, Python, JReview, elluminate, Tableau, Power BI, or Spotfire</p></li><li><p>Strong understanding of clinical trial processes, clinical data standards (e.g., CDISC), and regulatory requirements (GCP, GDPR, HIPAA)</p></li><li><p>Experience with risk-based data review concepts, data quality standards, and data lifecycle management in a regulated environment</p></li><li><p>Experience with data lakes, data pipelines, data integration, automation, and reporting and analytics in a clinical research environment</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, R&D Chemistry]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48744]]></requisitionid>
    <referencenumber><![CDATA[R48744]]></referencenumber>
    <apijobid><![CDATA[r48744]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48744/senior-associate-scientist-rd-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Senior Associate Scientist, R&D Chemistry Job Description</strong></p><p>We are currently seeking a synthetic organic chemist for the R&D (Research & Development) Chemistry group. In this position, they will play an important role in supporting Regeneron small molecule antibody-conjugate drug discovery capabilities, providing an important link with the company’s existing expertise in biologics and novel genetic medicines. The candidate will enable in-house laboratory-based synthetic chemistry activities towards the discovery and generation of novel small-molecule payloads and linkers for antibody-drug conjugate therapeutics across research areas of oncology, metabolic disease/obesity, infectious diseases, immunology and inflammation, neuroscience, and ophthalmology. Cultural fit with the Regeneron chemistry and cross-functional teams is a priority. The R&D Chemistry team is composed of synthetic organic, medicinal chemistry and bioconjugation scientists that work in a highly collaborative environment with other technology, biology and therapeutic area groups. Successful candidates will have small-molecule synthetic organic background and experience with the retrosynthetic analysis, synthetic route design, and hands-on execution of multistep synthetic protocols including compound isolation and characterization. A firm understanding of modern organic synthesis strategies and techniques and the ability to work independently while deploying them in a fit-for-purpose efficient approach to biologically active targets of interest will be the key. Ability to interpret spectroscopic data in the assignment/ confirmation of small molecule structures is required. Knowledge of the latest synthetic methods utilized in the antibody-conjugate linker generation is a plus.</p><p><strong>A day in the life of a Senior Associate Scientist – R&D Chemistry may look like:</strong></p><ul><li>Perform the day-to-day laboratory activities as part of the R&D Chemistry group, providing experimental execution of small-molecule syntheses and the associated compound isolation and characterization.</li><li>Troubleshoot, analyze data, interpret experimental results and propose synthetic approaches to new targets.</li><li>Discuss biological data and new targets within the existing projects to address structure-activity relationship directions.</li><li>Identify new strategies and technologies best suited for synthetic execution of the targets of interest.</li><li>Work within the priorities set by the cross-functional teams and your supervisor. Ensure successful progression of the group’s technology and pipeline projects.</li><li>Participate in departmental, cross-functional meetings to contribute expertise and to represent the goals of the R&D Chemistry group.</li><li>Interact broadly and collaboratively with other Regeneron groups.</li></ul><p><strong>This might be the right role for you if:</strong></p><ul><li>You are passionate and enthusiastic about the promise of small molecule-based, antibody-targeted therapeutics and appreciate the challenges of synthetic chemistry and drug design.</li><li>You enjoy developing solutions for synthesis and advancing structure-activity relationships within medicinal chemistry drug discovery programs.</li><li>You are comfortable working as part of a cross-functional team.</li><li>You want to be a part of the organizational culture that supports growth and development of its people and capabilities to drive forward the Regeneron pipeline.</li></ul><p><strong>To be considered for this role, you must:</strong></p><p>Have a M.Sc. in synthetic organic chemistry (or related), and familiarity with drug discovery processes and modern methods of synthetic organic and medicinal chemistry.</p><p>Bonus experience would include general understanding of the process of biological target validation, ADME/PK, PD/efficacy and of the ways that medicinal chemistry contributes to the progress in these areas.</p><p>A minimum of 5-7 years of industry drug discovery experience with small molecules is required. Familiarity with peptidomimetics or antibody-targeted therapeutics is a plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Okayama, Hiroshima Area]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47551]]></requisitionid>
    <referencenumber><![CDATA[R47551]]></referencenumber>
    <apijobid><![CDATA[r47551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47551/medical-representative-mr-dermatology-starokayama-hiroshima-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Sales Representative Dermatology Japan Region to join our commercial team, supporting Japan in a field-based work mode. In this role, you will achieve dermatology sales objectives and deliver customer value while collaborating with sales leadership, marketing teams, and alliance partners. This position offers the opportunity to supply to a fast-growing, science-driven organization making a relevant difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Okayama or Hiroshima, Japan</p><p>Work model: Field-based</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Achieve dermatology sales objectives through territory budget management.</li><li>Develop and update annual territory business plans using market insights.</li><li>Build territory action plans using key data sources.</li><li>Deliver disease-focused customer engagement and value-based solutions.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Partner with alliance teams to achieve shared business objectives.</li><li>Follow regulatory, legal, and company compliance requirements.</li><li>You act strategically and lead priorities to enhance customer impact.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree or equivalent.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Valid driver license and MR Certification.</li><li>Strong customer engagement skills with a focus on delivering value.</li><li>Technical proficiency and ability to conduct disease and concept selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and audience-focused communication skills.</li><li>Ability to implement strategic and tactical plans independently under tight timelines.</li><li>Computer proficiency in word processing, spreadsheets, databases, and email software.</li><li>Alliance partnership experience.</li><li>Dermatology knowledge and biologics sales experience preferred.</li><li>Current clinical knowledge of relevant therapy areas and competitor brands preferred.</li><li>Established Key Opinion Leader relationships within dermatology preferred.</li><li>English fluency is a plus.</li><li>Willingness to travel and work evenings or weekends when required.</li><li>Dedication to training completion, safe driving practices, and company policies.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Sun, 09 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49505]]></requisitionid>
    <referencenumber><![CDATA[R49505]]></referencenumber>
    <apijobid><![CDATA[r49505]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49505/associate-manager-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate</strong> <strong>Manager</strong> to join our <strong>Regulatory Affairs Strategy (Oncology) </strong>team.</p><p>The Associate Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Coordinating the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development in oncology therapeutic area, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure</p></li><li><p>Assisting in coordination and preparation for Agency meetings and associated briefing document preparation</p></li><li><p>Managing and tracking queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments</p></li><li><p>Providing representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings</p></li><li><p>Performing research to support the development of regulatory strategy for the assigned clinical development program</p></li><li><p>Maintaining knowledge of regulatory requirements up to current date, comments on draft regulatory guidance, and communicates changes in regulatory information as needed</p></li><li><p>Exercising discretion and independent judgment in the performance of the duties described above</p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum MD, PhD or PharmD degree along with relevant internship, fellowship, post-doc experience or industry experience</p></li><li><p>Experience in oncology preferred</p></li><li><p>Knowledgeable of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices.</p></li><li><p>Experience interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred</p></li><li><p>High attention to detail; ability to organize and prioritize assigned projects according to corporate goals</p></li><li><p>Ability to work in close collaboration with colleagues in regulatory department and throughout the development organization</p></li><li><p>Proficient in written, oral, and interpersonal communications in English</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44959]]></requisitionid>
    <referencenumber><![CDATA[R44959]]></referencenumber>
    <apijobid><![CDATA[r44959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44959/senior-manager-global-patient-safety-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager</strong> to join our <strong>Patient Safety</strong> team.The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><div><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Complete signal detection activities in line with approved safety surveillance plan</p></li><li><p>Perform signal evaluation for any identified signals and author the safety evaluation reports</p></li><li><p>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</p></li><li><p>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned compounds</p></li><li><p>Participate in other risk management activities as appropriate for assigned compounds</p></li><li><p>We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron</p></li><li><p>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</p></li></ul><p><strong>This role requires:</strong>​</p><ul><li><p>Minimum a Master's, PhD, or PharmD</p></li><li><p>Offers 7+ years of relevant risk management experience in the pharmaceutical/ biotech industry or health authority</p></li><li><p>Ability to apply relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments</p></li><li><p>Ability to work with a safety system database for purposes of medical case review and simple queries</p></li><li><p>Able to be proactive and self-disciplined, you can meet deliverables, and effectively use your time and prioritize</p></li><li><p>Ability to effectively communicate (verbal and written) safety findings</p></li></ul><p>#GDPSJobs </p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Management Process, Quality & Inspection Readiness]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48439]]></requisitionid>
    <referencenumber><![CDATA[R48439]]></referencenumber>
    <apijobid><![CDATA[r48439]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48439/director-data-management-process-quality-inspection-readiness/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Director, Data Management Process, Quality, and Inspection Readiness provides strategic leadership for Data Management quality, inspection readiness, and process excellence. This role is accountable for establishing and driving standardized approaches to Data Management quality, process frameworks, governance, compliance, and operational execution while ensuring compliance with global regulatory requirements, GCP, and industry best practices. The position serves as the primary Data Management lead for health authority inspections and audits, accountable for inspection preparation, response coordination, functional representation, and ensuring teams are prepared to effectively represent the function during regulatory inspections. In addition, the role also owns and drives the development, governance, and continuous improvement of Data Management processes, training programs, and operational frameworks to support standardized, scalable, compliant, and inspection-ready execution across the Data Management organization. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Warren, NJ, Tarrytown, NY or Armonk, NY</p></li><li><p>4 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Data Management Quality and Inspection Readiness</em></p><ul><li><p>Provide strategic leadership for Data Management quality and compliance, ensuring consistent application of quality standards and resolution of complex and systemic issues.</p></li><li><p>Develop Data Management quality frameworks, including CRO oversight, issue management, escalation pathways, and quality oversight processes to support proactive identification and management of operational quality issues and compliance gaps.</p></li><li><p>Ensure Data Management quality frameworks and operational activities are aligned with GCP, ICH guidelines, global regulatory requirements, and company quality standards.</p></li><li><p>Lead quality event and CAPA management activities, including root cause analysis, and implementation of sustainable corrective and preventive actions. Leverage insights to strengthen controls, improve processes, and enhance inspection readiness.</p></li><li><p>Collaborate with CRO partners and internal stakeholders on quality events, issue escalation, remediation activities, and CAPA implementation.</p></li><li><p>Lead Data Management inspection readiness and audit support; direct preparation, coordination, and response for health authority inspections.</p></li><li><p>Lead and conduct independent, risk-based reviews of study documentation and operational conduct at defined and ad hoc timepoints to identify gaps, strengthen compliance, and ensure sustained inspection readiness.</p></li><li><p>Establish Data Management quality review processes to identify process gaps and deficiencies, training needs, and the documentation of risks, enabling early remediation.</p></li><li><p>Establish and leverage Data Management KPI & KQI frameworks to provide visibility into performance, data quality, & compliance trends, driving proactive decision-making, continuous improvement, & innovation across the portfolio.</p></li><li><p>Define, monitor, and perform effectiveness checks measures for Data Management quality, compliance, inspection readiness, training and process performance to drive continuous improvement and operational excellence.</p></li><li><p>Lead impact assessments for new and evolving regulatory requirements, ensuring appropriate updates to Data Management processes, quality standards, and operational practices.</p></li><li><p>Educate and guide the Data Management organization on quality standards, regulatory expectations, and inspection readiness practices.</p></li><li><p>Establish and maintain strong partnerships with Inspection Management and Quality stakeholders to ensure alignment on inspection readiness activities, quality standards, compliance expectations, and remediation strategies.</p></li><li><p>Oversee Data Management SharePoint repositories to support centralized access to current quality and inspection readiness documentation.</p></li></ul><p><em>Data Management Process and Training</em></p><ul><li><p>Own and drive the development, governance, and continuous improvement of Data Management processes to support scalable, standardized, compliant, and inspection-ready execution.</p></li><li><p>Develop and execute robust implementation and change management plans for new and revised Data Management processes to ensure consistent adoption, operational effectiveness, and sustainable execution.</p></li><li><p>Establish & maintain training frameworks to support consistent implementation through development, maintenance, and delivery of role-based training and guidance.</p></li><li><p>Lead the Data Management SME network to ensure designated subject matter expertise, process ownership, and functional support coverage across Data Management.</p></li><li><p>Oversee Data Management SharePoint repositories to support centralized access to current process and training documentation.</p></li><li><p>Serve as a Data Management representative in the Global Development Process Owner Network.</p></li><li><p>Establish and maintain strong partnerships with the Process & Procedures, Learning Center of Excellence, Change Management functions to ensure alignment on Data Management processes and training.</p></li><li><p>Lead and contribute to cross-functional process improvement initiatives as required.</p></li></ul><p><em>People Management</em></p><ul><li><p>Responsible for line management and performance of direct reports, including the development of competencies, coaching, and assessment of annual performance.</p></li><li><p>Provide leadership, mentorship, and guidance to direct reports, fostering skill development, knowledge sharing, and operational excellence.</p></li><li><p>Foster a culture of accountability, collaboration, continuous improvement, and quality.</p></li><li><p>Support prioritization and workload management to ensure effective utilization.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Minimum Bachelor's Degree (Science, Health, Computing, or related field) with 12+ years in Clinical Data Management within the biotechnology, pharmaceutical or health related industry.</p></li><li><p>5+ years of people management, leadership, and mentoring</p></li><li><p>Expert knowledge of clinical data management principles, processes, quality frameworks, and inspection readiness practices within a global clinical development environment.</p></li><li><p>Deep understanding of global regulatory requirements and industry standards, including GCP, ICH guidelines, 21 CFR Part 11, ALCOA+ principles and inspection readiness expectations.</p></li><li><p>Demonstrated experience leading Data Management quality, compliance, inspection readiness, audit support and process governance activities.</p></li><li><p>Demonstrated experience developing, implementing, and continuously improving departmental processes, quality standards and frameworks, and operational controls.</p></li><li><p>Strong knowledge of quality management systems, CAPA processes, issue management, escalation frameworks, and continuous improvement methodologies.</p></li><li><p>Demonstrated experience supporting multiple health authority inspections across different health authorities (e.g., FDA, PMDA, MHRA, EMA, etc..) including inspection preparation, response coordination, remediation activities, and functional representation during regulatory inspections.</p></li><li><p>Experience establishing and leveraging KQI / KPI frameworks, effectiveness measures, and operational metrics to drive quality oversight, compliance monitoring, and process improvement.</p></li><li><p>Demonstrated ability to lead organizational change management initiatives, including implementation of new processes, quality standards, and operational frameworks.</p></li><li><p>Demonstrated success in solving complex business problems through strategic and critical thinking.</p></li><li><p>Proven ability to lead and influence within a matrix organization, driving alignment and outcomes with cross-functional stakeholders without direct authority</p></li><li><p>Proven ability to build strong collaborative relationships and influence alignment across key internal and external stakeholders.</p></li><li><p>Strong understanding of cross-functional activities and management of multiple and varied tasks with enthusiasm and attention to detail.</p></li><li><p>Excellent interpersonal, oral, and written communication skills.</p></li><li><p>Demonstrated ability to effectively lead and prioritize within a fast-paced, evolving, and highly regulated environment.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Ophthalmology]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48582]]></requisitionid>
    <referencenumber><![CDATA[R48582]]></referencenumber>
    <apijobid><![CDATA[r48582]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48582/associate-director-clinical-scientist-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director to join our Clinical Scientist, Internal Medicine team supporting Ophthalmology. In this role, you will contribute to the development, evaluation, planning and execution of Internal Medicine clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Work in a matrix environment as part of a cross-functional team (with internal and external vendor representation) and may contribute to candidate development projects through early and/or late phase development. You will report to the Sr Dir/Director, Clinical Science, Internal Medicine and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p><strong>Location: </strong>Tarrytown, NY, Warren, NJ, Cambridge, MA</p><h3><strong>Discover your role:</strong></h3><ul><li><p>May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Contributes to planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc)</p></li><li><p>≥ 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Ophthalmology</p></li><li><p>Proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills</p></li><li><p>Experience in all aspects of conducting global clinical trials and execution of clinical programs</p></li><li><p>We need an individual who is a strong team-player; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Regulatory Affairs]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50067]]></requisitionid>
    <referencenumber><![CDATA[R50067]]></referencenumber>
    <apijobid><![CDATA[r50067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50067/senior-manager-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Regulatory Strategy Oncology & Japan Affairs to join our Regulatory Affairs team, supporting our Japan business in a hybrid work model. In this role, you will lead Japan regulatory strategies across multiple therapeutic areas while collaborating with global regulatory teams and local cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Japan</p><p>Work model: Hybrid</p><br><p><strong>Discover your role:</strong></p><p>• Plan and execute Japan regulatory strategies and PMDA consultations for assigned programs<br>• Lead marketing application and post-approval change submissions<br>• Partner with local and global leadership to support Regulatory Affairs operations<br>• Manage interactions with PMDA and other Japanese health authorities<br>• Lead or support clinical trial notification preparation and submission activities<br>• Represent Regulatory Affairs within clinical, commercial, medical, and patient safety teams<br>• Support local labeling, patient information, and promotional material review activities<br>• You build strong partnerships across a global matrix environment</p><br><p><strong>This role requires:</strong></p><p>• Bachelor's degree in a scientific discipline; Master's degree preferred<br>• 10+ years in the pharmaceutical industry and 5+ years of relevant regulatory experience<br>• Experience managing health authority interactions, major submissions, and approvals in Japan<br>• Deep knowledge of Japan submission requirements, local regulations, and regulatory standards<br>• Knowledge of clinical trial requirements and ability to resolve local procedural challenges<br>• Experience supporting business start-up activities<br>• Ability to ensure compliance with Japan regulatory requirements and local standards<br>• Strategic thinking, commercial awareness, and strong written and verbal communication skills<br>• Ability to thrive in and foster effective matrix teamwork in a global environment<br>• Fluent Japanese and English language skills</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director - Data Management, Analytics, AI & Architecture]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50015]]></requisitionid>
    <referencenumber><![CDATA[R50015]]></referencenumber>
    <apijobid><![CDATA[r50015]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50015/executive-director-data-management-analytics-ai-architecture/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Building Our Future:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director of Data Management, Analytics, and Architecture will lead the strategy for commercial and G&A data capabilities at Regeneron, transforming enterprise data into trusted insights that drive business performance and operational excellence. This role partners closely with Digital & Technology leaders and senior executives to establish scalable data architecture, analytics, and governance standards that serve as a model across the organization.</p><p>The position has significant influence over how data, AI, and analytics are structured, managed, and leveraged to support commercial and operational decision-making. The leader also serves as the primary executive spokesperson for data management, analytics, and architecture across Commercial and G&A functions, including Finance, HR, Procurement, Legal, Compliance, and other corporate departments.</p><p><strong>Where & When:</strong></p><p><em>This role will sit on-site in our Sleepy Hollow, NY offices 4 days per week.</em></p><p><strong>Discover Your Role:</strong></p><ul><li>Own and execute the multi-year data management, analytics, AI, and enterprise data architecture strategy for Commercial and G&A functions, aligning investments with corporate objectives.</li><li>Lead and develop a high-performing team of data management, analytics, and architecture professionals, building organizational capability and delivery excellence.</li><li>Deliver trusted data platforms, analytics products, and self-service capabilities that empower business leaders across Commercial, Finance, HR, and other G&A functions.</li><li>Establish enterprise-wide data governance, stewardship, quality, lifecycle management, and master data standards to improve trust, consistency, and interoperability.</li><li>Modernize and simplify the data ecosystem through scalable cloud platforms, integration strategies, architecture standards, and executive reporting capabilities.</li><li>Advance AI, machine learning, automation, and responsible AI practices by identifying high-value use cases, managing risk, and ensuring regulatory compliance.</li><li>Drive measurable business outcomes through improved data quality, analytics adoption, automation, operational efficiency, productivity, and process standardization across global teams.</li><li>Oversee vendor partnerships, data security, architecture governance, and value realization, ensuring strategic investments deliver measurable business impact and long-term organizational value.</li></ul><p><strong>This Role Requires:</strong></p><ul><li>BS/BA in Computer Science, Data Science, Information Systems, or a related field required; MS. PhD or MBA preferred.</li><li>17+ years of progressive leadership in data management, data architecture, analytics, or business intelligence, including enterprise-scale programs; experience in life sciences, biotechnology, or another regulated industry is a plus.</li><li>Deep command of modern data management, analytics, and enterprise architecture capabilities (platform-agnostic, e.g., BI, cloud data platforms, data governance, data modeling, master data management).</li><li>Experience establishing enterprise data governance frameworks and reference architecture standards that scale across multiple business domains.</li><li>Strong understanding of AI, machine learning, and agentic AI concepts, including model risk, responsible AI practices, and the operational discipline, such as monitoring, validation, and lifecycle management, needed to run AI systems safely at enterprise scale.</li><li>Familiarity with regulatory and risk frameworks relevant to AI and data in regulated industries (e.g., GxP considerations, NIST AI RMF, ISO 42001) is a plus.</li><li>Experience partnering with Legal, Compliance, Security, and Privacy functions to manage data and AI risk, vendor risk, and audit readiness.</li><li>Proven ability to influence senior leaders, translate data into business outcomes, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45872]]></requisitionid>
    <referencenumber><![CDATA[R45872]]></referencenumber>
    <apijobid><![CDATA[r45872]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45872/principal-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Principal Analytical Sciences Scientist to support Manufacturing, Process Sciences (PS), and Quality Control (QC) by developing, optimizing, troubleshooting, validating, transferring, and applying analytical procedures across multiple modalities, including iSRNA/siRNA oligonucleotides and peptide therapeutics. You will advance QC capabilities by creating robust, phase‑appropriate and lifecycle‑managed analytical methods, integrating new assays and technologies, and serving as a technical leader who resolves complex issues and elevates analytical strategy for novel modalities.</p><p><strong>When & Where:</strong></p><p><strong>Location: Rensselaer, NY</strong></p><p><strong>Work Model: Monday-Friday 8am-4:30pm</strong></p><p><strong>Discover Your Role:</strong></p><ul><li>Establish, develop, and optimize analytical methods for product and raw materials, with a focus on iSRNA/siRNA and peptide modalities.</li><li>Design and review protocols for assay qualification and validation (e.g., ICH Q2 principles), ensuring methods are stability‑indicating and suitable for GMP release and characterization.</li><li>Engage with collaborators and vendors to identify, assess, and implement new instrumentation and technology (e.g., LC‑MS, CE, ion‑pair RP‑HPLC, hybridization‑based assays, peptide mapping).</li><li>Transfer control test procedures to QC and other relevant departments, including drafting transfer plans, training materials, and acceptance criteria.</li><li>Lead troubleshooting and provide analytical support for established test methods, process, and formulation issues (e.g., nuclease sensitivity in iSRNA, peptide oxidation/deamidation).</li><li>Conduct investigations (OOS/OOT), support deviation root‑cause analysis, and lead customer complaint assessments with data‑driven conclusions.</li><li>Present findings and scientific arguments in meetings and technical reports; communicate risk, impact, and mitigation strategies clearly.</li><li>Train and mentor junior team members; author and revise SOPs, protocols, and method lifecycle documents.</li><li>Manage the lifecycle of analytical testing methods (development, validation, transfer, change control, periodic review, and retirement).</li><li>Design and execute experiments independently to assess and optimize technologies; apply DOE and statistical trending where appropriate.</li><li>Produce and maintain accurate, compliant records consistent with data integrity and cGMP expectations.</li><li>Represent Analytical Sciences on interdepartmental teams and in program meetings; align analytical strategy with CMC and regulatory milestones.</li><li>Demonstrated experience developing and validating analytical methods for iSRNA/siRNA oligonucleotides and peptide therapeutics.</li><li>Hands‑on proficiency with LC‑MS/MS, CE, ion‑pair RP‑HPLC, peptide mapping, and oligonucleotide characterization assays.</li><li>Proven track record of method transfer to QC, troubleshooting, OOS/OOT investigations, and cross‑functional collaboration.</li><li>Strong technical writing, data integrity practices, and presentation skills; ability to mentor and lead.</li></ul><p><strong>This Role Requires:</strong></p><p>A PhD in Chemistry, Biochemistry, Biology, or related field, with 3+ years of relevant industry experience in analytical development and QC method lifecycle.</p><ul><li>Level determined based on qualifications.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50213]]></requisitionid>
    <referencenumber><![CDATA[R50213]]></referencenumber>
    <apijobid><![CDATA[r50213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50213/reimbursement-business-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><h3>When & where:</h3><ul><li>Greater Dallas, TX area</li><li>In the field 4 days a week</li></ul><h3>Discover your role:</h3><ul><li>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</li><li>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</li><li>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li><li>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</li><li>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</li></ul><h3>This role requires:</h3><ul><li>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience.</li><li>Experience working with products delivered through a Specialty Pharmacy network is essential.</li><li>Collaboration and proactive communication skills required.</li><li>Background in leadership and effective cross functional partnership a plus.</li><li>Established ability to work within an Account Management based structure.</li><li>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</li><li>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Hearing Loss and Vestibular Disorders]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50090]]></requisitionid>
    <referencenumber><![CDATA[R50090]]></referencenumber>
    <apijobid><![CDATA[r50090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50090/principal-scientist-hearing-loss-and-vestibular-disorders/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Scientist to join our team developing therapies for hearing loss and vestibular disorders. In this role, you will independently lead research projects and drive the development of novel therapies for inner ear disorders, while collaborating with a cross-functional team to advance translationally relevant studies.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul></li></ul><p><strong>Discover your role:</strong></p><ul><li><ul><li><p>Lead the design of rigorous experiments to address core questions in hearing biology that drive drug discovery and preclinical programs</p></li><li><p>Develop and characterize novel animal models to understand mechanisms of hearing loss and evaluate novel therapeutics</p></li><li><p>Design and execute in vivo and in vitro functional assays to understand syndromic and non-syndromic hearing loss</p></li><li><p>Work cross-functionally with a team to develop translationally relevant studies</p></li><li><p>Analyze and evaluate data with rigor, presenting findings internally and externally</p></li><li><p>Draft and review protocols and articles for publication independently</p></li><li><p>Motivate, develop, and supervise junior scientists, research associates, and other trainees</p></li><li><p>Thrive in a dynamic, fast-paced environment, adapting readily to shifting priorities</p></li></ul></li></ul><p><strong>This role requires:</strong></p><ul><li><ul><li><p>Ph.D. with a strong record of innovation and publication, plus 5+ years of relevant experience</p></li><li><p>Proven expertise in drug development</p></li><li><p>Strong ability to work both independently and in a team, communicating effectively across all levels</p></li><li><p>Resilience in overcoming challenges and a rigorous approach to scientific work</p></li><li><p>Preferred: managerial experience</p></li><li><p>Preferred: in vivo experimental experience</p></li><li><p>Preferred: strong understanding of human and mouse genetics and/or auditory physiology</p></li></ul></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology-Seattle, WA]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49995]]></requisitionid>
    <referencenumber><![CDATA[R49995]]></referencenumber>
    <apijobid><![CDATA[r49995]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49995/medical-specialist-ii-ophthalmology-seattle-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p>The Medical Specialist will report to the Regional Director, and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Seattle, WA</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Experience in biologics and buy and bill products</p></li><li><p>Demonstrated history of high sales performance</p></li><li><p>Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p></li></ul><p><strong>This role requires:</strong></p><ul><li>A Bachelor's degree is required and a degree in science or business is preferred (master’s degree a plus)</li><li>A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Buy and Bill experience</li><li>Ophthalmology with relevant retina experience is preferred.</li><li>Must be based in or located in close proximity to the assigned territory (relocation will not be provided). Ability to travel (40-60%).</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison - Northeast/Great Lakes]]></title>
    <date><![CDATA[Sun, 30 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50340]]></requisitionid>
    <referencenumber><![CDATA[R50340]]></referencenumber>
    <apijobid><![CDATA[r50340]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50340/associate-director-thought-leader-liaison-northeastgreat-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Oncology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position on Regeneron’s Commercial Oncology Marketing team reporting into the Associate Director/Director, Scientific Marketing. The role is focused on enhancing and improving interactions with key external US Oncology thought leaders at academic centers and leading community practices for our Oncology Solid Tumor portfolio, particularly in the area of Non-Small Cell Lung Cancer (NSCLC).</p><p>You will work closely with cross-functional leaders from Marketing, Sales, Medical Affairs, Key Accounts Management, Market Access, and the Oncology/Hematology Leadership Team to ensure alignment with the overall strategy and tactical execution. You will strive for success through collaboration, communication, and the ability to implement key initiatives.</p><h3>When & where:</h3><ul><li>In the field with a traveling expectation of 60-80%</li><li>Territory consists: Michigan, New York, CT, Ohio, PA, Vermont, New Hampshire, MA, Rhode Island, Maine</li></ul><h3>Discover your role:</h3><ul><li>The Oncology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</li><li>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</li><li>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</li><li>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or during day-to-day business</li><li>Develop/maintain list of key thought leaders in the assigned geography</li><li>Build and maintain relationships with established and emerging thought leaders</li><li>Support speaker bureau buildout efforts, including identification of potential speakers, managing logistics related to speaker trainings, providing feedback to speakers to improve presentation effectiveness in enhancing educational impact</li><li>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders to inform brand strategy and marketing opportunities</li><li>Ability to translate national strategies into regional execution and coordinate with multiple internal teams</li><li>Support regional/national advisory board planning efforts, making strategic recommendations on potential thought leader participants and liaising with selected thought leaders in coordinating their participation</li><li>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certification is a plus.</li><li>Minimum of 10 years of work experience in the following – Thought Leader Liaison role (previous or current), field sales, inline or regional brand marketing, relevant medical/clinical experience,</li><li>Experience in hematology/oncology markets strongly preferred, experience in lung cancer disease state preferred but not mandatory.</li><li>You also have expertise in marketing strategies within the pharmaceutical industry.</li><li>Ideally, you would have launch experience.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Publications]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50363]]></requisitionid>
    <referencenumber><![CDATA[R50363]]></referencenumber>
    <apijobid><![CDATA[r50363]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50363/director-publications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Publications, to join our Medical Affairs team, supporting cross-functional and alliance-wide publication strategy for assigned therapeutic assets. In this role, you will lead the strategic direction and operational performance of publication plans while collaborating with authors, Medical Affairs partners, cross-functional collaborators, and external agency partners. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>Location: Sleepy Hollow, NY or Warren, NJ<br>Work model/flexibility: On-site 4 days/week. If based in Warren, NJ, travel to Sleepy Hollow will be expected. </p><p><strong>Discover your role</strong>:<br>• Lead and accountable for cross-functional and alliance-wide publications teams.<br>• Lead publications review of annual plans and projects with senior management <br>• Lead in defining and building consensus on terms for literature and gap analyses to support scientific communication platform development and publication strategy<br>• Pub plan and medical communication strategy development and evolution<br>• Partner with procurement for agency selection and agency performance management<br>• Budget accountability for agency external resource scope of work (SOW) development, budget tracking, and invoicing according to approved SOW/PO, reflecting work completed<br>• Manage writers/agencies for individual pubs projects to effectively complete execution within specified timelines<br>• Responsibility for alignment on scientific content/communication objectives, author invitations, collection of author agreements, securing medical/clinical lead materials for kick-off meeting discussions, author kick-off calls<br>• Review assigned publications ensuring quality, alignment with scientific communication platform, and compliance with standards for ethical reporting of study data<br>• Oversee efficient and compliant financial management<br>• Ensure adherence to established compliance, regulatory, and ethical standards across all publication activities, including disclosure requirements, TOV guidelines, billing practices, and review documentation<br>• Proactively identify and communicate operational risks, delays, or issues<br>• Working with Executive Director, Publications identify and lead meaningful process improvements and innovations initiatives, as appropriate based on business needs</p><p><strong>This role requires:</strong><br>• Doctorate scientific degree required (PhD, PharmD, or MD) along with 7+ years of experience in medical communications or publications management within the pharmaceutical or biotechnology industry<br>• Minimum 3 years of experience independently leading cross-functional, therapeutic area-specific publication plans<br>• Proven track record managing complex, multi-asset publication plans, ideally within Oncology, Ophthalmology, Hematology, or Rare Diseases<br>• Experience managing external agency partners and publication vendors, including budget oversight and SOW management</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Boston Central]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50333]]></requisitionid>
    <referencenumber><![CDATA[R50333]]></referencenumber>
    <apijobid><![CDATA[r50333]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50333/medical-specialist-i-dermatology-boston-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Boston]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role</p></li><li><p>Location: Boston Central</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role 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>This role requires:</strong></p><ul><li><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</p></li><li><p>Having a minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred</p></li><li><p>We need someone with shown success and consistent sales performance in complex markets across diverse customer segments</p></li><li><p>This role requires the ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Fill/Finish Associate (Internal Fill/Finish MFG)]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50612]]></requisitionid>
    <referencenumber><![CDATA[R50612]]></referencenumber>
    <apijobid><![CDATA[r50612]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50612/fillfinish-associate-internal-fillfinish-mfg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Fill/Finish Associate. The Fill/Finish Associate performs all duties related to the production and support of drug product manufacturing. Works individually, and as part of a team, to support and perform operations to maintain formulation, filling, assembly, labeling and cartoning/packing equipment for parenteral biological products. Seeks to understand and develops proficiency in processes or procedures of increasing complexity.<br> </p><p>When & where:</p><ul><li>We offer multiple shifts that are 4 working days (10 hours) to support 24/7 production</li><li>Location: Rensselaer, New York, United States</li><li>Occasional flexibility may be requested for on-call schedule/weekend work</li></ul><p>What you'll do:</p><ul><li>Operate highly automated aseptic filling equipment to load drug product into vials, syringes, and cartridges within isolators or other cleanroom environments; assemble filled product into syringes and autoinjectors; and run state-of-the-art packaging lines to label and configure product for distribution.</li><li>Monitor production operations using process controls and feedback systems (pneumatics, robotics, manual checks, and PLCs) to ensure throughput, quality, and compliance.</li><li>Perform equipment changeovers, cleaning, handling, and installation of interchangeable parts; maintain clean, safe, and inspection-ready workspaces and equipment.</li><li>Maintain gowning qualification, adhere to aseptic/cleanroom behaviors, and perform environmental monitoring and sampling as required.</li><li>Create, follow, and improve SOPs and operating procedures aligned with cGMP and regulatory expectations; ensure compliance during execution and promptly escalate nonconformities.</li><li>Record and review GMP data with ALCOA principles (accurate, legible, attributable, contemporaneous); reconcile product and controlled materials; and ensure complete training documentation.</li><li>Utilize electronic systems (e.g., MES/eBR, LIMS, training systems, and Microsoft Office) to support manufacturing operations and documentation.</li><li>Travel domestically and internationally as needed to support production or technology transfer activities.</li></ul><p>The environment and physical rhythms of the role:</p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p>Let's find out if we're a fit:</p><ul><li>HS diploma/ GED</li><li>Or AS, BS or BA in Life Sciences or related field</li><li><em>Level is determined on qualifications relevant to the role. </em></li></ul><p>Thrive today. Grow Tomorrow.</p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$16.44 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 12:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Safety Scientist Lead - Rare Disease]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50469]]></requisitionid>
    <referencenumber><![CDATA[R50469]]></referencenumber>
    <apijobid><![CDATA[r50469]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50469/director-safety-scientist-lead-rare-disease/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global Patient Safety Sciences Delivery </strong>team.</p><p>The Director, Global Patient Safety Sciences Delivery, Rare Disease, serves as the first point of contact for all Rare Disease operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness. This role is responsible for high quality, compliant execution of safety surveillance, signal management, and aggregate reporting activities across the portfolio. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Uxbridge, UK</p></li><li><p>3 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>The Director is responsible for the development of their team, which is comprised of Safety Scientists. The Director will also be expected to work closely with other Directors on driving standardization and consistency in execution of signal detection activities in partnership. This role will report to the ED, Global Patient Safety Sciences Delivery. </p></li><li><p>Develop common practices, processes and templates to drive standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs </p></li><li><p>Ensure compliance and quality management of Safety Sciences Delivery activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Lead all aspects of signal detection coordination and signal management process across Rare Disease, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies,</p></li><li><p>Analyze aggregate safety data to identify emerging safety issues and patterns, in partnership with Safety Sciences Strategy </p></li><li><p>Support cross-functional coordination to support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Drive development and implementation of relevant training programs for GPS staff, including maintenance of a standardized Safety Sciences training curriculum, proficiency matrix, and knowledge management repository across both Strategy and Delivery </p></li><li><p>Serve as main point of contact to liaise with Safety Sciences Strategy Rare Disease GPS Leads </p></li><li><p>Collaborate with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Implement talent strategy and leadership development initiatives that raise capabilities across the organization </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced Degree required in life sciences or healthcare with 12+ years of PV experience, preferably with a focus on Safety Sciences and Rare Disease experience</p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Preferred experience leading a matrixed role working across multiple areas of an organization and people management experience </p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer, CMO Support]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49601]]></requisitionid>
    <referencenumber><![CDATA[R49601]]></referencenumber>
    <apijobid><![CDATA[r49601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49601/senior-project-engineer-cmo-support/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an experienced Project Engineer to join our growing Engineering team, supporting our Contract Manufacturing Organization (CMO) network. In this role, you will design, specify, and commission new biopharmaceutical process and clean utility equipment, renovate existing systems, and provide engineering support for equipment installed at contract manufacturing facilities. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Troy, New York, United States</p></li><li><p>Work model: On-site Monday-Friday 8:00am-4:30pm</p></li><li><p>Travel percentage: up to 25%, domestic and international</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Design and specify cGMP process equipment, piping, and/or controls, including development and review of engineering documentation</p></li><li><p>Manage small-to-mid sized projects related to process equipment and clean utilities, including start-up and commissioning</p></li><li><p>Assist in and lead the design review, site acceptance, and installation of equipment</p></li><li><p>Prepare piping and instrumentation diagrams and other related drawings, and develop Process Flow Diagrams for manufacturing processes</p></li><li><p>Support QA/Validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Investigate process equipment, utility system, and control system anomalies, as well as safety incidents, implementing corrective and preventive actions</p></li><li><p>Prepare and execute change controls, including engineering evaluation and test plan documentation</p></li><li><p>Supervise mechanical, electrical, and automation contractors</p></li><li><p>Procure equipment and equipment-related services, including negotiating with suppliers</p></li><li><p>Provide engineering support for equipment installed at contract manufacturing facilities</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree in Chemical Engineering, Biochemical Engineering, or another relevant Engineering discipline</p></li><li><p>5+ years of experience in project/process engineering, or an equivalent combination of education and experience</p></li><li><p>Direct experience with biopharmaceutical process equipment is preferred</p></li><li><p>Solid understanding of process control systems and automation</p></li><li><p>Thorough knowledge of engineering documentation for cGMP process equipment and sanitary equipment design requirements</p></li><li><p>Experience planning and tracking project activities and schedules</p></li><li><p>Strong interpersonal and cross-cultural communication skills, with the ability to lead without direct authority</p></li><li><p><strong>Gowning and Physical Requirements:</strong></p></li><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>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 10 Sep 2026 10:26:36 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement- Advanced Therapies]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46026]]></requisitionid>
    <referencenumber><![CDATA[R46026]]></referencenumber>
    <apijobid><![CDATA[r46026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46026/senior-manager-global-procurement-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Global Procurement – Advanced Therapies to join our Global Procurement organization, supporting our Contract Development and Manufacturing Organization (CDMO) category on an on-site basis. In this role, you will lead end-to-end procurement strategies and drive global category execution across Contract Development and Manufacturing Operations, while collaborating with Procurement management, business partners, and the Law department to align category priorities and deliver cost savings and efficiency gains.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, NY</p></li><li><p>Work model/flexibility: On-site</p></li><li><p>Schedule: Mon-Fri 8:00am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Defines and implements the global CMO Category strategy to serve global and regional business needs</p></li><li><p>Aligns category priorities with Procurement management and business partners through close cross-functional collaboration</p></li><li><p>Manages negotiations, supplier management, and partner engagement activities for the Packaging Category</p></li><li><p>Drives cost savings, cash flow improvement, and other efficiency gains through category management activities</p></li><li><p>Participates in organizational decisions within CMO categories that carry critical short- and long-term impact on category performance</p></li><li><p>Leads category activities to ensure compliance with GxPs and other applicable regulations</p></li><li><p>Negotiates contract terms and conditions in consultation with the Law department, aligned with Regeneron's priorities</p></li><li><p>Uses data and market knowledge to drive decision-making and continuous improvement across category projects</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Sr Manager Level: Bachelor's degree in a relevant field and 8+ years of progressive experience in procurement, including experience in Pharma/BioPharma or science in general, demonstrating growth in experience, scale, and development throughout</p></li><li><p>Experience managing teams of professional-level employees responsible for category management tasks (if applicable)</p></li><li><p>Preferred/nice-to-have: Working knowledge of sourcing and contracting tools, ERPs, and eRFx systems (e.g., Oracle, Zycus, Ariba)</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 10 Sep 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology-Winston-Salem, NC]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50631]]></requisitionid>
    <referencenumber><![CDATA[R50631]]></referencenumber>
    <apijobid><![CDATA[r50631]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50631/medical-specialist-i-pulmonology-winston-salem-nc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Winston-Salem]]></city>
    <state><![CDATA[North Carolina]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where:</strong></p><ul><li><p>Field role</p></li><li><p>Location: Winston Salem, NC</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Market Access Lead - Rare Diseases (Europe Region)]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50435]]></requisitionid>
    <referencenumber><![CDATA[R50435]]></referencenumber>
    <apijobid><![CDATA[r50435]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50435/director-market-access-lead-rare-diseases-europe-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Regional Market Access, Rare Diseases, Europe to join our market access function, supporting our Europe region in a hybrid work mode. In this role, you will shape pricing, reimbursement, and patient access strategies while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead rare disease access strategies aligned with global objectives and country needs.</p></li><li><p>Differentiate approaches across cost-effectiveness and list-price or free-pricing markets.</p></li><li><p>Monitor European policies, payer trends, and reimbursement frameworks.</p></li><li><p>Adapt global access tools and value propositions for regional stakeholders.</p></li><li><p>Manage health technology assessment dossiers, pricing negotiations, and reimbursement submissions.</p></li><li><p>Partner with medical affairs and access teams on evidence and health economics outcomes research plans.</p></li><li><p>Engage payers, policymakers, advocacy groups, and public affairs teams to advance access.</p></li><li><p>You build collaboration through advisory boards, market research, and landscape assessments.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>European rare disease pricing, reimbursement, launches, and approval experience.</p></li><li><p>Expertise in payer systems, economic models, and health technology assessment submissions.</p></li><li><p>Knowledge of NICE, ZIN, TLV, QALY frameworks, and free-pricing markets.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>English fluency; additional European languages are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix leadership, agility, and collaboration.</p></li><li><p>Healthcare policy shaping and multi-stakeholder engagement experience preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€119,900.00 - €200,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - GA]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48661]]></requisitionid>
    <referencenumber><![CDATA[R48661]]></referencenumber>
    <apijobid><![CDATA[r48661]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48661/field-reimbursement-manager-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>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><h3>A typical day may include the following:</h3><ul><li>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</li><li>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</li><li>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li><li>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</li><li>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</li></ul><br><h3>This role may be for you if:</h3><ul><li>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</li><li>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.</li><li>You possess excellent organizational, project management, and communication skills.</li></ul><p>To be considered for this opportunity, you will possess the following:</p><ul><li>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience.</li><li>Experience working with products delivered through a Specialty Pharmacy network is essential.</li><li>Collaboration and proactive communication skills required.</li><li>Background in leadership and effective cross functional partnership a plus.</li><li>Established ability to work within an Account Management based structure.</li><li>Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors.</li><li>Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 13:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Asturias Leon y Cantabria (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50496]]></requisitionid>
    <referencenumber><![CDATA[R50496]]></referencenumber>
    <apijobid><![CDATA[r50496]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50496/sales-representative-asturias-leon-y-cantabria-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Asturias Leon</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Patient Safety Standards & Training]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50969]]></requisitionid>
    <referencenumber><![CDATA[R50969]]></referencenumber>
    <apijobid><![CDATA[r50969]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50969/associate-director-global-patient-safety-standards-training/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Global Patient Safety Standards & Training</strong> team.</p><br><p>Reporting to the Head of Global Patient Safety (GPS) Standards & Training, this position is responsible for establishing and maintaining procedures and policies consistent with Pharmacovigilance regulatory requirements and industry standards. A key part of the role is close collaboration with the Process and Procedures (P&P) team and support of the Process Owner Network (PONs). The responsibilities of this job are foundational in the creation and maintenance of the Pharmacovigilance (PV) System that is essential in enabling the department, and therefore the company, to comply with regulatory PV requirements in all relevant territories worldwide, and to operate efficiently and effectively in alignment with established industry practices. The role supports GPS activities and ensures procedures remain compliant with applicable global regulations as they evolve.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Dublin, IRE</li><li>3 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Ensure that PV Intelligence updates are systematically assessed and reflected in GPS procedures, so that documented processes remain aligned with current regulatory expectations and the procedural framework is maintained in a state of audit and inspection readiness at all times.</li><li>Act as a key liaison to Process & Procedures (P&P) and the Learning Centre of Excellence (LCoE) for procedural updates, so that procedural changes are accurately captured, appropriately sequenced, and correctly reflected in the associated training curriculum.</li><li>As an SME, partner with the Head of GPS Safety Operations to validate that procedures are fit for purpose against safety practices, closing gaps between documented process and operational execution, including the mapping of procedural documents to regulations and to the training curriculum.</li><li>Apply deep PV process design expertise to develop, implement, and maintain GPS procedures in alignment with regulations, Regeneron Standards, and industry best practices — in partnership with Process & Procedures (P&P), Process Owners, and SMEs — and lead the assessment of evolving global PV regulations.</li><li>As a primary liaison to P&P, partner to set risk-based prioritization and sequencing in managing procedural updates across the GPS framework, in partnership with PONs and GPS Functional Leads.</li><li>Assist in ensuring the correct procedural documents are assigned to the relevant training curriculum.</li><li>Maintain oversight of and support for GPS Planned Process Deviations (PPDs), including guiding SMEs on meeting Global Development Quality (GDQ) approval criteria.</li><li>Coordinate with P&P to align PPD expiration dates with queued procedure projects, adjusting prioritization as needed.</li><li>Serve as GPS's escalation point for internal process and quality-event alignment challenges related to procedural updates, working in alignment with senior management and key stakeholders to investigate and resolve non-compliance.</li><li>Manage, alongside the Process Owners, the content of procedures for GPS, escalating material gaps to senior management, including the maintenance and accuracy of PSMF Annex E in relation to GPS procedures.</li><li>Maintain an overview of CAPAs associated with procedures, including those arising from both audits and inspections, and work closely with SMEs, PONs and the P&P team to ensure timely CAPA closure, including allowing appropriate time for associated training.</li><li>Provide regular metrics on CAPAs, process deviations, and training compliance to GPS department leadership.</li><li>Lead initiatives to enhance GPS process effectiveness and efficiency, including the analytical framework for performance metrics, and present findings and recommendations to leadership.</li><li>Liaise regularly with other functional teams e.g. Corporate and Clinical QA on potential impacts to GPS Processes or GXP-related activities.</li><li>Represent Standards & Training in audits and inspections.</li><li>Serve as the back-up GPS Standards & Training liaison to LCoE.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Minimum Bachelor's degree is required. Education in the life sciences is a strong plus.</li><li>7+ years' experience of Pharmacovigilance/Drug Safety, Regulatory Affairs or Quality Assurance in the pharmaceutical/biotech industry.</li><li>Thorough understanding of Pharmacovigilance/Drug Safety regulations and PV Quality Management Systems.</li><li>Extensive experience managing procedural updates.</li><li>Experience in PV process design and optimization.</li><li>Track record of successful project management relevant to document management.</li><li>Strong organizational skills.</li><li>Ability to write procedural documents to accepted standards of quality.</li><li>Experience presenting in audits and inspections.</li><li>Ability to work collaboratively across functions with SMEs, process owners and cross-functional partners.</li><li>Experience with Data Privacy is a plus</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€101,500.00 - €165,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 13:26:18 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Quality, Internal Audit]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48400]]></requisitionid>
    <referencenumber><![CDATA[R48400]]></referencenumber>
    <apijobid><![CDATA[r48400]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48400/senior-manager-quality-internal-audit/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager to join our Quality Assurance internal auditing team. They are responsible for providing professional expertise, leadership, oversight and assisting with strategic planning for the Regeneron Industrial Operations and Product Supply (IOPS) Quality Auditing function. Quality (GMP) Auditing is responsible for managing the internal audit programs and performing internal audits for Regeneron IOPS, with primary emphasis on GMP, IT and Quality audits that may impact GMP operations and/or products. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li><li>Travel percentage: 25-30% domestic & occasionally international</li></ul><p><strong>Discover your role:</strong></p><ul><li>Maintain up-to-date expertise in global GxP regulations and standards (Chapter 21 of the Code of Federal Regulations, Eudralex Volume 4 and associated Annexes, ISO Standards, and ICH, WHO and IPEC Guidelines, etc ) and internal policies; track and communicate industry trends, agency expectations, and warning letters</li><li>Lead enterprise audit programs (internal and external) across GMP, IT, and quality: set strategy, build schedules, plan, assign, and personally lead/participate in audits; ensure inspection readiness</li><li>Manage cross-functional and supplier relationships (procurement, manufacturing, quality, external manufacturing, quality assurance, operations, audit clients) to meet audit schedules, quality deliverables, and organizational goals</li><li>Provide leadership and subject-matter guidance to auditors; recruit, select, train, and assess external proxy auditors; coach, mentor, and develop internal GMP auditing staff; maintain robust training and qualification programs</li><li>Ensure auditing processes meet regulatory and industry requirements; carry out adherence to procedures; document and assess deviations and changes per IOPS processes; uphold safety and operational standards</li><li>Develop, maintain, and present metrics and targets (including RTO) to senior leadership to measure strategy execution and the health of quality auditing systems</li><li>Drive continuous improvement by periodically reassessing auditing processes; translate ambiguity into actionable plans; proactively solve problems to prevent deviations and operational issues</li><li>Accountable for team performance and outcomes of internal/external audit programs, including managing leaders where applicable; support inspections as needed</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Life Sciences; or equivalent combination of education and 8+ years of relevant experience</li><li>Experience with quality systems and auditing</li><li>Previous leadership/supervisory experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Upstream Bioprocessing & Cell Culture Development (IOPS)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50961]]></requisitionid>
    <referencenumber><![CDATA[R50961]]></referencenumber>
    <apijobid><![CDATA[r50961]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50961/2027-co-op-upstream-bioprocessing-cell-culture-development-iops/]]></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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Upstream Bioprocessing & Cell Culture Development (IOPS) to join Regeneron Industrial Operations and Product Supply (IOPS) <strong>Process Sciences</strong> department. This group develops and runs the manufacturing-scale processes used to grow and purify Regeneron's commercial biologic products.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Rensselaer, NY (Temple Lane / East Greenbush)</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$25.50 per hour.</p><p><strong>What you'll do:</strong></p><ul><li>Support upstream and manufacturing-support teams that grow and optimize Chinese Hamster Ovary (CHO) cell cultures used to produce medicines at commercial scale</li></ul><ul><li>Run lab-scale bioreactor experiments studying how process parameters affect cell culture performance</li></ul><ul><li>Conduct media and feed optimization studies</li></ul><ul><li>Investigate cell biology under stress conditions using multiomics methods</li></ul><ul><li>Support development of a biomarker panel that predicts and monitors cell line performance risk</li></ul><ul><li>Perform mammalian cell culture using aseptic technique</li></ul><ul><li>Conduct quantitative polymerase chain reaction (qPCR) assay development and data interpretation</li></ul><ul><li>Document experimental procedures and results</li></ul><p><strong> </strong></p><p><strong>Relevant majors: </strong>Chemical Engineering, Biotechnology, Biochemistry, Biological/Biomedical Engineering, Biology</p><p><strong>Let's find out if we're a fit:</strong></p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li></ul><ul><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li></ul><ul><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li></ul><ul><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Infectious Diseases]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50801]]></requisitionid>
    <referencenumber><![CDATA[R50801]]></referencenumber>
    <apijobid><![CDATA[r50801]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50801/senior-director-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director to lead our Infectious Diseases research team, setting strategic direction and identifying novel technological approaches to advance therapies for infectious diseases. In this role, you will guide drug targets from early discovery through clinical development, while representing Regeneron's Infectious Diseases research vision within the broader scientific community, cross-functional forums, and to senior leadership. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY </li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Build, develop, and directly supervise the Infectious Diseases research team, providing strategy, vision, and both short-term and long-term goals</li><li>Communicate and align on priorities, policies, and goals between senior leadership and the broader Infectious Disease group</li><li>Identify new strategies or technologies, including antibody engineering, vaccine platforms, and genetic medicines, for pursuing novel infectious disease targets</li><li>Set priorities and drive go/no-go decisions for targets and projects as they move through the development pipeline</li><li>Represent the group's goals and vision in departmental, cross-functional, senior leadership, and external meetings</li><li>Collaborate broadly across therapeutic focus areas and technology groups, forging relationships that advance infectious disease research as a systems-level endeavor</li><li>Mentor the Infectious Diseases group, providing opportunities and challenge to develop team members to their full potential</li><li>Oversee review of infectious diseases-related documents, including regulatory submissions, manuscripts, and contracts</li></ul><br><p><strong>This role requires:</strong></p><ul><li>BS/BA degree in a related field required; MS and/or Ph.D./M.D.</li><li>15+ years of progressive industry/relevant professional experience</li><li>Deep and broad expertise in infectious disease research (e.g., virology, immunology, microbiology, or a related field)</li><li>Familiarity with cutting-edge technologies, including antibody engineering, vaccine platforms, and genetic medicines, with proven experience applying them to infectious disease questions</li><li>Strong leadership, managerial, and mentorship experience, along with experience administratively directing a group (e.g., managing budget and organization)</li><li>Strong written and oral communication skills, with the ability to communicate both science and vision</li><li>Preferred: exposure to drug development or similar regulated activities</li><li>Preferred: broad network of colleagues and collaborators, strong publication record, and national/international reputation</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist: Bispecifics and Antibody Engineering]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47480]]></requisitionid>
    <referencenumber><![CDATA[R47480]]></referencenumber>
    <apijobid><![CDATA[r47480]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47480/senior-scientist-bispecifics-and-antibody-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a results-driven Senior Scientist to join our Antibody Engineering team within the Bispecifics and Antibody Engineering Department, designing, producing, and characterizing next-generation antibody and protein therapeutics across multiple therapeutic areas with a focus on myeloid cell biology. In this role, your work will directly contribute to the pipeline and help build new platform capabilities at a pivotal time for antibody engineering.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Tarrytown, N</p><p>Work model/flexibility: Onsite</p><br><p><strong>Discover your role:</strong></p><ul><li>Apply molecular and structural biology expertise to independently design innovative multi-specific antibodies with desired potency, selectivity, and developability</li><li>Perform molecular and structural-guided design, high-throughput construct generation, and vector engineering using modern software and tools</li><li>Produce and purify novel and logic-gated alternative format antibodies using mammalian expression systems and chromatographic techniques (e.g., AKTA systems)</li><li>Characterize binding affinities, binding kinetics, and stability</li><li>Design and implement high-throughput biochemical and cell-based assays (e.g., ELISA, AlphaLISA, flow cytometry binding, phagocytic assays, cell activation, and cytolytic assays)</li><li>Troubleshoot bioanalytical and cell-based assay data to inform subsequent iterations</li><li>Communicate biologic designs and data updates to program stakeholders to meet program objectives</li><li>Maintain timely, accurate records using Benchling and research ELN, and clearly convey results during cross-departmental meetings</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Ph.D. in molecular biology, cell biology, biochemistry, immunology, or a related field, with at least 1 year of relevant experience in academia or industry</li><li>Expertise in myeloid, molecular, and protein biology</li><li>Strong organizational, communication, and presentation skills</li><li>Ability to quickly learn new skills and troubleshoot antibody production and functional assays effectively</li><li>Preferred: hands-on experience with cloning, antibody expression in mammalian cell lines, antibody purification (e.g., using AKTA systems), and comprehensive protein characterization</li><li>Preferred: familiarity with cell-free expression and structural AI/ML-based design</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Genetics & Genomics (Regeneron Genetics Center)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51036]]></requisitionid>
    <referencenumber><![CDATA[R51036]]></referencenumber>
    <apijobid><![CDATA[r51036]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51036/2027-co-op-genetics-genomics-regeneron-genetics-center/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in to join our Regeneron Genetics Center (RGC), one of the world's most active human genetics programs.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer) and May/June-December (Summer-Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Analyze large-scale genetic and genomic data to study, for example: cardiovascular disease, proteomics and cardiac imaging; germline genetic vs pharmacological drug effects</li><li>Conduct genome-wide association studies (GWAS) and risk-prediction analyses that combine genetics, molecular biomarkers, and conventional risk factors</li><li>Analyze clinical outcomes data alongside genomic datasets</li><li>Write and test code to support large-scale genetic and multi-omics analyses</li><li>Collaborate with scientists across the Genetics Center to interpret findings</li><li>Document analytical methods and results, and present findings to the broader genomics research team</li><li>Contribute to research drawing on genomic data from millions of patients</li></ul><br><p><strong>Relevant majors: </strong>Bioinformatics, Statistics/Mathematics/Data Science, Computer Science/Information Technology, Genetics, Epidemiology/Public Health</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Upstream Bioprocessing & Cell Culture Development]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50944]]></requisitionid>
    <referencenumber><![CDATA[R50944]]></referencenumber>
    <apijobid><![CDATA[r50944]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50944/2027-co-op-upstream-bioprocessing-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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Upstream Bioprocessing & Cell Culture Development to join our Preclinical Manufacturing and Process Development (PMPD) team, which develops the manufacturing processes used to scale up and produce Regeneron's medicines.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support the development and optimization of cell culture and bioreactor processes used to grow the cells that produce Regeneron's medicines</li></ul><ul><li>Design and test new feed and media strategies to improve cell growth and productivity</li></ul><ul><li>Run bench-scale and pilot-scale bioreactor experiments and analyze the resulting data</li></ul><ul><li>Support reagent and cell bank production activities</li></ul><ul><li>Collaborate with scientists and engineers to troubleshoot process challenges</li></ul><ul><li>Document experimental procedures and results to support ongoing process development</li></ul><ul><li>Gain hands-on exposure to mammalian cell culture and general laboratory technique</li></ul><ul><li>Present findings and progress updates to the broader team</li></ul><br><p><strong>Relevant majors: </strong>Chemical Engineering, Biological/Biomedical Engineering</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[District Manger - Pulmonology - Smokey Mountain]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50697]]></requisitionid>
    <referencenumber><![CDATA[R50697]]></referencenumber>
    <apijobid><![CDATA[r50697]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50697/district-manger-pulmonology-smokey-mountain/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>The District Manager (DM), Pulmonology will report to the Regional Director, Pulmonology and be responsible for hiring, leading, developing and retaining Pulmonology Medical Specialists (sales representatives) in their assigned district. 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 District. The DM will work closely with their Alliance partner counterpart(s) to ensure 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>When & where:</strong></p><ul><li>Remote role</li><li>Location: <strong>Smokey Mountains (TN/KY/Greenville, SC/Winston-Salem, NC, Cincinnati, OH)</strong></li></ul><p><strong>Discover your role:</strong></p><br><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>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.</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>Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</li><li>Ability to partner and collaborate with other internal field teams and alliance partners.</li></ul><p><br><br></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required, Master’s degree or other advanced education/certifications a plus (Focused degree in science or clinical experience is a plus).</li><li>Minimum of 7 years of pharmaceutical/biopharmaceutical experience with 3 years of sales leadership/management in sub-cutaneous self-injectable biologic markets required. Experience in the Pulmonology market strongly preferred.</li><li>Ability to travel extensively with local and regional influence.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$195,500.00 - $264,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Sevilla Badajoz (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50491]]></requisitionid>
    <referencenumber><![CDATA[R50491]]></referencenumber>
    <apijobid><![CDATA[r50491]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50491/sales-representative-sevilla-badajoz-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Sevilla Badajoz</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Development Program Management]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51099]]></requisitionid>
    <referencenumber><![CDATA[R51099]]></referencenumber>
    <apijobid><![CDATA[r51099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51099/director-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>This role (Director, Development Program Management) uses extensive program management knowledge and experience in the drug development industry to provide operational leadership, direction, and support to assigned development program(s) and/or portfolio(s). This individual is expected to drive the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and monitor the execution of these plans from preclinical through commercialization/lifecycle management. Responsibilities may also include coaching and mentorship of junior colleagues, managing direct reports, working with collaborators, and contributing to departmental initiatives. This is a leadership role within the department and organization thus this individual is expected to independently execute responsibilities, interact effectively with senior leadership, and influence the direction and outcomes of assignments. </p><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY</li><li>Additional Locations: Warren, NJ or Cambridge, MA</li></ul><p><strong>Discover your role:</strong></p><ul><li><strong>Development Teams: </strong>Partners with the Global Program Head to drive strategic program teams (SPT) and sub teams by leading key governance meetings. Uses broad knowledge of drug development and project/program management coupled with leadership and problem-solving skills to align development teams around an integrated project/program plans, timelines and budgets based on program vision. Ensures efficient delivery of plans. Proposes and aligns annual program goals with program strategy and Regeneron’s corporate goals. Monitors progress against program goals and ensures accurate and timely reporting of program progress to management. Anticipates issues and program risks and drives timely development of risk management plans and issue resolution.</li><li><strong>Business Acumen: </strong>Utilizes knowledge of industry trends to identify risks/threats/opportunities and translates these to actionable activities for the development teams. Able to leverage political savvy and awareness of team dynamics to effectively drive decision making and achieve desired outcomes. Is proficient in project management planning systems (MS Project, SharePoint) and tools/techniques. Understands how systems and tools can be leveraged to move the program and business forward.</li><li><strong>Communication:</strong> Effective and trusted communicator that will develop a proven track record across the organization. Works effectively with different styles and adapts approaches in a cross-functional matrix environment to drive results. Establishes a culture which promotes and encourages open communication, transparency, accountability and learning from mistakes.</li><li><strong>Problem Solving: </strong>Is proficient at proactively identifying and critically analyzing potential problems that may affect the project, processes, or the team. Uses extensive industry and professional experience and knowledge to develop viable, long-term solutions to cross-functional, project, process, or team issues, driving alignment with impacted stakeholders. Proactively implements lessons learned/best practices across programs/TA and department to help other teams preempt or mitigate problems.</li><li><strong>Leadership</strong>: Strengthens teams and continuously works to drive teams to be high performing and efficient. Ability to align team members towards a common goal through expertise with conflict management, self/social awareness, and diverse team dynamics.</li></ul><p><strong>This role requires:</strong></p><ul><li>Minimal educational requirements: Bachelor’s Degree </li><li>12+ years of relevant broad project / program management experience required, preferably in the pharmaceutical or related industry </li><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels both internal and external to the company in order to establish credibility with professionals on the project teams. </li><li>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 entrepreneurial organizations; expert in dealing with ambiguity and uncertainty </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Clinical Supply Operations Specialist]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51007]]></requisitionid>
    <referencenumber><![CDATA[R51007]]></referencenumber>
    <apijobid><![CDATA[r51007]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51007/senior-clinical-supply-operations-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. The Sr. Clinical Supply Operations Specialist provides support to the Clinical Drug Supply & Logistics group in the Investigational Product (IP) distribution process, ancillary supplies process and comparator procurement process, for one or more molecules across multiple Therapeutic areas supporting highly complex studies as well as long-term departmental and cross-functional projects and on-going continuous improvement initiatives. May lead short-term projects. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron Standard Operating Procedures (SOPs) / Work Practice Documents (WPDs). This role applies to internally sourced studies and/or CRO/Partnered studies. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Warren, NJ or Armonk, NY</p><p>Travel percentage: Up to 25%</p><br><p><strong>Discover your role</strong><br>Solve complex problems, and initiate completion of the following items within broadly defined practices and policies including selecting methods, techniques, and evaluation criteria for obtaining results related to:</p><p> • IP Supply & Inventory Planning</p><p> o Accountability, Reconciliation, Returns & Destruction (ARRD)</p><p> o Internal System Management including lot creation, batch status, and inventory maintenance</p><p> o Assessment and Oversight activities (risks, stocking levels, trends)</p><p>• IP Shipments</p><p> o System and Non-system generated Shipments</p><p> o Depot transfers</p><p> o Temperature Excursion Management</p><p>• IP Supply Monitoring & Activity Documentation (Electronic Trial Master File - eTMF)</p><p> o Expected Document List (EDL) creation</p><p> o eTMF Document Management per regulatory requirements</p><p> o QA/QP Release Management</p><p> o Pack-and-label kit and sequence reconciliation o Inspection Readiness activities</p><p> o IRT management activities including IRT Alert management and UAT activities</p><p> o Suspected Serious Non-Compliance support</p><p>• Ancillary Supply & Inventory Planning/Management</p><p> o Procurement support (Includes Work Order Management)</p><p> o Vendor RFI support o Supply Planning & Inventory Management</p><p> o Ancillary Supply Plan creation</p><p> o Shipping & Logistics (Includes International Logistics requirements for Ancillaries)</p><p> o Shipping & logistics activities</p><p> o Temperature Excursions</p><p> o Lot management o eTMF activities</p><p> o ARRD activities</p><p>• Comparator Planning & Management</p><p> o Market Intelligence Reports o Quote/PO/Requisition Process Support</p><p> o IMN Creation</p><p> o Document Storage</p><p> o Temperature Excursions</p><p>• Financial Forecasting, Budgeting & Planning</p><p> o Forecast Submissions</p><p> o Order Ticket Entry</p><p> o Demand Updates</p><p>Work is performed under general direction and reviewed upon completion for adequacy in meeting objectives. Candidate is expected to participate in determining objectives of assignment and be able to plan schedules and arrange own activities in accomplishing objectives. Candidate will represent CDSL as a prime contact on contracts or projects. He/She will interact with senior internal and external personnel on significant matters often requiring coordination between organizations.</p><br><p><strong>JOB REQUIREMENTS:<br></strong>Fundamental knowledge of the clinical drug development process and clinical trial methodology including the inner-workings of cross-functional partners.<br></p><p>Fundamental knowledge of International Council of Harmonization (ICH) / Good Clinical Practices (GCP) & regulatory guidelines/directives</p><p> · Proficient in MS Word & Excel</p><p> · Efficient Problem Solving</p><p> · Excellent Time Management</p><p> · Thrives in Ambiguity</p><p> · Action Oriented</p><p> · Adaptability</p><p> · Collaborates Effectively</p><p> · Well Organized</p><p> · Communicates Effectively</p><p> · Detail Oriented</p><br><p><strong>MINIMAL EDUCATION REQUIRMENTS</strong></p><p>BS/BA degree in a related field. Minimum of 3+ years of experience in the following fields:</p><p>• Clinical Supplies</p><p>• QA/Regulatory</p><p>• Precision Medicine</p><p>• Supply Chain</p><p>• Manufacturing</p><p>• Or equivalent research/commercial biopharma experience<br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Ocular Immunology]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51108]]></requisitionid>
    <referencenumber><![CDATA[R51108]]></referencenumber>
    <apijobid><![CDATA[r51108]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51108/associate-scientist-ocular-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Scientist to join our Ophthalmology group, supporting the development of therapies for ocular immune and inflammatory diseases. In this role, you will engage in hands-on research across cell biology, immune-focused assays, and disease-relevant experimental models while collaborating with a team working across multiple preclinical programs.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where</strong></p><ul><li><strong>Location:</strong> Tarrytown, NY</li><li><strong>Work model/flexibility:</strong> Onsite</li></ul><br><p><strong>Discover your role</strong></p><ul><li>Handle and care for mice, including procedures such as injections, colony management, and blood/tissue sample collection.</li><li>Perform tissue dissection and cell isolation from ocular and other tissues for downstream analysis.</li><li>Maintain, expand, and/or treat cells in vitro, using established cell lines and primary human and mouse cells.</li><li>Perform immunoassays and molecular biology assays such as ELISA, Western blot, DNA/RNA extraction, and multiplex platforms such as MSD and Luminex/CBA.</li><li>Evaluate cell phenotype and function using ex vivo or in vitro assays, including flow cytometry.</li><li>Analyze data using biological and statistical software such as FlowJo, Excel, and Prism.</li><li>Document experimental procedures and results with care and accuracy.</li><li>Contribute to day-to-day lab operations, including equipment maintenance and ordering supplies/reagents.</li><li>Thrive in an innovative, team-driven environment, adapting readily to new techniques and shifting tasks.</li></ul><br><p><strong>This role requires</strong></p><ul><li>B.S. degree in a relevant field with 0–2 years of experience in a life-sciences discipline; practical, hands-on laboratory experience is valued over an advanced degree.</li><li>Strong organizational skills, attention to detail, and a creative approach to problem-solving.</li><li>Open and frequent communication with manager and team members.</li><li>A positive, proactive attitude and a track record of reliable, broad execution across multiple techniques rather than deep specialization in a single area.</li></ul><br><p><strong>Preferred qualifications</strong></p><ul><li>Hands-on experience with mouse handling and basic techniques, including injections, colony management, and blood collection.</li><li>Experience with mammalian cell culture, including cell lines and primary cells.</li><li>Experience with immunoassays such as ELISA, MSD, or Luminex; Western blot; or DNA/RNA extraction.</li><li>Experience with tissue dissection, cell isolation, or flow cytometry.</li><li>Prior experience as a research technician in an academic lab or associate scientist in industry.</li><li>Proficiency in basic computer applications and biological data collection/analysis.</li><li>Experience in ocular procedures is a plus but not essential.</li></ul><p><strong> </strong></p><p><strong>Does this sound like you?</strong> Apply now to take your first step toward living the Regeneron Way.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Postdoctoral Fellow]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51053]]></requisitionid>
    <referencenumber><![CDATA[R51053]]></referencenumber>
    <apijobid><![CDATA[r51053]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51053/postdoctoral-fellow/]]></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 postdoctoral fellow position is for early career scientist trainees who have finished graduate school and received their PhDs (or MDs, DVMs, etc.) to receive rigorous scientific postdoctoral training at Regeneron under the auspices of a scientist mentor. The program spans up to four years. We are looking for Fellows who are dedicated to seeing their research project and manuscript to completion. Fellows will be expected to conduct creative mechanistic exploratory research that results in publication. The program is academic in nature - the goal is to ask fundamental questions - not to work on Regeneron therapeutic agents.</p><br><p>Applications Accepted: October 1, 2026 - November 23, 2026.</p><br><p><strong>When & where:</strong></p><ul><li><strong>Work Location: </strong>Tarrytown, NY</li></ul><ul><li><strong>Flexibility & travel: </strong>Onsite with limited travel</li></ul><br><p><strong>What you’ll do: </strong></p><p>• Conduct forward-looking and innovative research to address a novel scientific question of your choice with the guidance of a mentor. </p><p>• Receive exposure to the biotechnology industry's most successful and innovative scientists.</p><p>• Explore opportunities to pursue groundbreaking, creative biomedical research in a prestigious, well-resourced, and dynamic industry environment. </p><p>• Publish and disseminate data via external conferences and peer-reviewed publications.</p><p>• Have the opportunity to assist with mentoring and guiding interns and other junior trainees.</p><p>• Participate in postdoctoral program activities such as weekly meetings, the annual research conference, and the Postdoc Retreat. </p><p>• Present data internally at lab meetings, trainee meetings, and company-wide seminars.</p><p>• Provide reports of research progress to supervisors and program staff. </p><p>• Travel to attend or present at conferences outside Regeneron one to two times year. </p><br><p>L<strong>et’s find out if we’re a fit: </strong></p><p>• Are pursuing a doctoral degree in a relevant subject area with an expected graduation date in 2026 or 2027, or have already received a doctoral degree in a relevant subject area.</p><p>• Are a scientist looking for your first postdoctoral training (or you have less than one year of postdoctoral training).</p><p>• Have outstanding scientific skills, including critical and analytical thinking. </p><p>• Demonstrated publication success as evidenced by peer-reviewed publications.</p><p>• Have good written and oral communication skills.</p><p>• Have the ability to interact dynamically and constructively with peers and cross-functionally when applicable.</p><br><p><strong>Required Documents:</strong></p><p>• A full academic CV</p><p>• At least two letters of recommendation</p><p>• Responses to two essay questions</p><br><p><strong>Important Information about our Process:</strong></p><p>• Within one business day of applying, you will receive an email with instructions on completing your essay questions and uploading documents.</p><p>• All documents must be submitted no later than November 23, 2026; Applications received after November 23, 2026 may not be considered.</p><p>• Following the close date, please allow 2-3 months for review and interviews.</p><p>• Initial interviews will take place virtually in January 2027.</p><p>• Final round interviews will take place in person in Tarrytown in February 2027.</p><p>• Targeted Start Date: Summer 2027, but the start date is flexible – depending on when you finish defending your graduate thesis or finish up prior manuscripts. Must start by November 1, 2027.</p><br><p>If you have an issue submitting your application or have questions, please email postdoctoral@regeneron.com.</p><br><p>Please note that the starting salary for this role is $95,000. </p><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$73,700.00 - $120,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Imaging Science Lead Sr. Principal Scientist]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51016]]></requisitionid>
    <referencenumber><![CDATA[R51016]]></referencenumber>
    <apijobid><![CDATA[r51016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51016/imaging-science-lead-sr-principal-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>Oncology Imaging Scientific Lead</strong></p><p><em>Clinical Imaging</em></p><br><p><strong>Build our future together:</strong></p><p>The successful candidate will lead the strategy and execution of complex early and late phase oncology imaging in clinical trials where imaging plays a critical role. Imaging includes all modalities with a special focus on PET and CT. In this role, you will lead the development of imaging biomarkers, support the scientific imaging aspects and tumor response assessment of oncology clinical studies. You will be a member of cross-functional program teams including Regeneron clinical and preclinical colleagues as well as external academic and industry partners.</p><p>This position offers excellent opportunities to develop innovative imaging biomarkers in support of clinical development and to bring treatment options to patients.</p><br><p><strong>When & where: </strong></p><p><strong>Locations: </strong>Willing to work from <strong>one </strong>of the following sites:</p><ul><li>Tarrytown, NY</li></ul><ul><li>Warren, NJ</li></ul><ul><li>Cambridge, MA</li></ul><ul><li>Boston, MA</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Work closely with imaging, therapeutic area and development leads to formulate appropriate imaging biomarker strategies to inform and advance the Regeneron clinical pipeline.</li></ul><ul><li>Lead, design and implement multimodality imaging measures as endpoints for oncology therapeutic clinical studies.</li></ul><ul><li>Collaborate closely with Regeneron clinical teams as imaging subject matter expert to ensure optimal design and execution of imaging strategy including development of protocols, imaging manuals, imaging charters and statistical analysis plan.</li></ul><ul><li>Work closely with Clinical Imaging Operations and imaging CROs to ensure the flawless conduct and data integrity of study's imaging components and endpoints.</li></ul><ul><li>Serve as Imaging Scientific Lead in clinical trials focused on qualification and utilization of novel imaging biomarkers.</li></ul><ul><li>Lead the interaction with regulatory agencies and site ethic committees for approval of clinical imaging biomarker development studies.</li></ul><ul><li>Design and implement novel PET, immuno-PET and other novel imaging agents/biomarkers in clinical trials.</li></ul><ul><li>Oversee image analysis and interpretation of results, work closely with colleagues to oversee the development of study reports and publications as appropriate.</li></ul><ul><li>Design and implement innovative imaging translational strategies in collaboration with preclinical/clinical research teams and external partners.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Experience in the implementation of central efficacy assessment using tumor response criteria such as RECIST 1.1, PCWG3, Lugano and IMWG in oncology clinical trials.</li></ul><ul><li>Leadership experience in the application of imaging as a quantitative endpoint in clinical and preclinical studies with an oncology focus.</li></ul><ul><li>A Doctorate degree in a relevant field, with 5+ years of industry and academic clinical oncology imaging experience.</li></ul><ul><li>Proven excellent written/verbal communication and organization skills.</li></ul><ul><li>Ability to champion imaging innovations and lead projects effectively.</li></ul><ul><li>Preferred: Minimum 5+ years of imaging experience in oncology drug development and clinical PET tracer development in a pharmaceutical/biotechnology setting. Level commensurate with years of experience.</li></ul><ul><li>Preferred: Experience in the application of imaging as a quantitative endpoint in clinical and preclinical studies.</li></ul><ul><li>Preferred: Experience with regulatory agencies and inspections.</li></ul><ul><li>Preferred: Direct experience with preclinical oncology imaging models using PET and immuno-PET imaging biomarkers.</li></ul><ul><li>Preferred: Strong background in oncology, biology, molecular imaging and familiar with precision medicine approaches.</li></ul><ul><li>Preferred: Imaging CRO oversight and implementation of quality control procedures.</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Supply Operations]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51121]]></requisitionid>
    <referencenumber><![CDATA[R51121]]></referencenumber>
    <apijobid><![CDATA[r51121]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51121/senior-manager-clinical-supply-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Senior Manager of Clinical Supply Operations is a key member of the Clinical Supply Operations Team, whose primary responsibility is leading Clinical Supply activities that support the development and operation of Clinical Supply Logistics processes. This position plays a key role in the operational oversight of Clinical Logistics Vendors and Clinical Supply processes, identifying areas of improvement, and driving continuous improvements, while leveraging data driven insights. The Senior Manager is responsible for managing CSO staff members.</p><br><p><strong>When & where:</strong></p><ul><li>Primary Location: Warren, NJ</li></ul><br><p><strong>Discover your role:</strong></p><p>Vendor Oversight and Operational Support:</p><ul><li>Manage and/or support distribution vendor oversight activities by acting as point of escalation for CDSL and monitor their performance against expectations and according to established policies and procedures. Leverages logistics performance metrics, identifies risks and implements remediation steps in partnership with our Vendors to ensure CDSL’s concerns are addressed.</li></ul><p>Departmental Leadership:</p><ul><li>Collaborate with cross functional partners to develop and enhance Clinical Supply Operational processes to ensure delivery of Clinical Trail Supply</li><li>Represent the needs of Clinical Supply Operations at cross functional discussions/initiatives and be a champion of change management.</li><li>Act as advisor to Clinical Supply Operations team members on operational tasks, process issues, projects, and initiatives. Mentors and trains others to obtain quality results.</li></ul><p>Supervising:</p><ul><li>Leads, coaches, and mentors CSO Specialists in the execution of IP activities (i.e. release, shipment, temperature excursion management, returns, reconciliation, and destruction) and maintenance of TMF documentation to support clinical studies.</li></ul><p>Continuous Improvement:</p><ul><li>Lead cross functional improvement initiatives to optimize operational efficiencies and support strategic decision-making/problem-solving.</li><li>Manages and leads strategic and operational standardization, analytics and continuous improvement.</li><li>Create and manage performance metrics to provide visibility to operational performance, insights, trends, and identify areas of opportunity.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Strong Leadership Skills</li><li>Ability to effectively communicate across an organization.</li><li>Experience working with external vendors.</li></ul><ul><li>Experience leading cross functional projects/initiatives.</li><li>Effective stakeholder management, influence and negotiation skills.</li><li>Ability to effectively multi-task and adapt to changing priorities.</li><li>Experiencing coaching and mentoring others.</li><li>Working knowledge of clinical trial methodology.</li></ul><ul><li>Working knowledge of GCP and ICH Guidelines.<br></li></ul><p><strong>Minimum: </strong></p><p>BS/BA degree in a related field. 8+ years of industry/relevant professional experience.</p><p><strong>Preferred:</strong></p><p>Masters/MBA/PharmD preferred with 8+ years of industry/relevant professional experience in the following fields:</p><ul><li>Clinical Supplies</li><li>QA/Regulatory</li><li>Precision Medicine</li><li>Supply Chain</li><li>Manufacturing</li></ul><p>Or equivalent research/commercial biopharma experience</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Strategy Planning & Operations]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50994]]></requisitionid>
    <referencenumber><![CDATA[R50994]]></referencenumber>
    <apijobid><![CDATA[r50994]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50994/senior-manager-strategy-planning-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>The Senior Manager, Strategy Planning & Operations is responsible for coordinating and executing key operational activities that support leadership effectiveness, organizational planning, and business execution across Development Operations, Portfolio Management & Biostatistics Data Management (DO, PM & BDM). Working closely with the Department Head and Senior Leadership Team, this role supports leadership forums, strategic initiatives, departmental programs, knowledge management, and operational processes critical to departmental success. The role requires sound judgment, discretion, and the ability to operate with significant autonomy while partnering closely with leadership to drive priorities, improve operational effectiveness, and support organizational objectives.</p><br><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY</li><li>Additional Locations: Armonk</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Lead the planning and execution of leadership and departmental meetings, including agenda development, meeting materials, communications, minutes, action tracking, and follow-through to drive accountability and timely completion of deliverables.</li><li>Coordinate and manage departmental operational processes and business rhythms, including annual planning activities, leadership team logistics, organizational communications, and key departmental milestones.</li><li>Manage and continuously improve departmental knowledge management and collaboration platforms (e.g., SharePoint, Microsoft Teams, intranet sites), ensuring content quality, accessibility, governance, and alignment with business needs.</li><li>Oversee departmental programs and initiatives, including workforce development, employee engagement, internship, mentorship, and other organizational programs, ensuring effective execution and stakeholder coordination.</li><li>Maintain organizational information, reporting materials, and operational documentation to support workforce planning, leadership decision-making, inspection readiness, and departmental governance activities.</li><li>Partner with department leadership to support strategic initiatives, organizational planning efforts, leadership priorities, special projects, and cross-functional business objectives.</li><li>Drive operational excellence through the identification, implementation, and continuous improvement of processes, tools, templates, and ways of working that enhance efficiency, consistency, communication, and organizational effectiveness.</li><li>Support the planning and execution of non-drug project activities and other departmental operational priorities through stakeholder coordination, project tracking, and management of ad hoc business needs.</li></ul><br><h3>This role requires:</h3><ul><li>Minimum of a Bachelors degree and 8+ years in operational or enterprise planning, including experience facilitating cross-functional alignment on processes and initiatives. Biopharma / drug development experience preferred.</li><li>Experience supporting enterprise planning, portfolio management, project management, resource management, or collaboration platforms in a biopharma, R&D, or regulated business environment.</li><li>Experience developing or maintaining business-rule documentation, knowledge articles, UAT materials, operational SOPs, decision records, or governance documentation.</li><li>Experience tracking adoption, user engagement, operational metrics, support trends, and service performance indicators.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Patent Attorney]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50548]]></requisitionid>
    <referencenumber><![CDATA[R50548]]></referencenumber>
    <apijobid><![CDATA[r50548]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50548/director-patent-attorney/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><br><p>The Director, Patent Attorney will act as legal counsel on matters related to the development, protection, and management of Regeneron’s valuable intellectual property pertaining to its manufacturing. The role will be responsible for patent activities relating to manufacturing and bioprocessing at all stages of the development pipeline including cell line technologies, purification, formulations, assay and media development. This position will partner closely with our world-class scientists and manufacturing development leaders around key strategies for our rapidly growing patent portfolio, patent filings, trade secret protection, and patent actions.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY</li><li>Work model/flexibility: 4 days per week on site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>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;</li><li>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;</li><li>Leading US and foreign administrative patent actions (e.g., oppositions, third party observations, inter partes reviews, etc.);</li><li>Supporting due diligence projects, agreements and other transactional work, administrative initiatives, and policy questions.</li><li>Advising on emerging legal issues, including monitoring and reviewing case law and legislative developments.</li><li>Possess strong interpersonal skills and the ability run multiple projects against competing priorities.</li><li>Excel at handling a large and sophisticated docket with minimal direction.</li><li>Have exceptional communication skills, including presentation, interpersonal, writing and conflict resolution.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Ph.D. in the life sciences (e.g., biochemistry, molecular biology, cell biology, or related fields)</li><li>Juris Doctorate from an accredited law school</li><li>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)</li><li>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.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Financial Analyst]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51097]]></requisitionid>
    <referencenumber><![CDATA[R51097]]></referencenumber>
    <apijobid><![CDATA[r51097]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51097/sr-financial-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Program Finance Senior Analyst to join our Program Finance team, supporting our Global Development organization in a hybrid work model. In this role, you will provide financial planning, forecasting, budgeting, and analysis support for development programs while collaborating with Program Management, Development teams, Clinical Project Managers, Strategic Alliance Management, Accounting, and external collaborators. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Own financial support for assigned development programs and collaborations, including quarterly forecasts, monthly actuals reporting, and variance analysis.</li><li>Build detailed clinical trial budgets and monitor study financials through completion.</li><li>Translate development plan activities into detailed forecasts for internal and external clinical costs and maintain forecasts within Hyperion.</li><li>Partner with cross-functional teams, subject matter experts, Accounting, and external collaborators to communicate program financial performance and P&L implications.</li><li>Produce Global Development cost center reporting, monthly spend tracking, and variance analyses while maintaining governance-aligned budget controls.</li><li>Lead initiatives that streamline processes, standardize financial templates, and implement standard processes across therapeutic areas.</li><li>Perform ad hoc financial analyses and present actionable recommendations that support informed business decisions.</li><li>You thrive in a fast-paced environment, balancing multiple priorities while maintaining high-quality deliverables.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in finance, business, scientific, or quantitative field.</li><li>3-5 years minimum relevant experience, with demonstrated ability in forecasting, budgeting, and/or business partnering ideally within a science or research-driven environment.</li><li>Experience developing financial forecasts, budgets, actuals reporting, variance analysis, and business performance insights.</li><li>Ability to translate operational plans into detailed financial forecasts and manage financial data within Hyperion.</li><li>Excellent analytical skills with the ability to convert findings into actionable business solutions.</li><li>Experience identifying, communicating, and implementing operational improvements that enhance efficiency and accuracy.</li><li>Strong verbal and written communication, presentation, and stakeholder management skills.</li><li>Proven ability to manage several priorities in a fast-paced environment while maintaining a high standard of work.</li><li>Experience in pharmaceutical clinical development and knowledge of the drug development continuum, including critical path activities and functional interdependencies, is a plus.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist - Precision Medicine]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51096]]></requisitionid>
    <referencenumber><![CDATA[R51096]]></referencenumber>
    <apijobid><![CDATA[r51096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51096/principal-scientist-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Principal Scientist, Precision Medicine (Biomarker) Strategy Lead</strong></p><p><em>Precision Medicine</em></p><br><p><strong>Build our future together:</strong></p><p>The Precision Medicine department at Regeneron is responsible for designing and executing the overarching translational and clinical biomarker strategies for therapeutic candidates during clinical development. We are seeking to hire a Precision Medicine Strategy Lead at the Principal Scientist level focusing on solid tumor oncology, heme malignancies, and immune oncology.</p><p>In this highly matrixed role, the Principal Scientist will be responsible for defining the key scientific questions relating to the drug target mechanism of action, disease biology and prognostic biomarkers associated with disease heterogeneity and severity, as well as informing potential patient stratification or selection. This information will guide development of a robust Precision Medicine strategy.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY United States</p><br><p><strong>Discover your role:</strong></p><ul><li>Leading focused assay development and implementation of assays and associated sample collections throughout a clinical trial.</li></ul><ul><li>Coordinating data analysis through collaboration with computational scientists involved in integrating multi-omic data: genomics, transcriptomics, and proteomics.</li></ul><ul><li>Interpreting results and leading communication of the key impact of the data to guide decision making to inform the clinical development strategy.</li></ul><ul><li>Enabling advances in target identification, indication selection, early indication of biological activity and patient stratification/selection.</li></ul><ul><li>Partnering cross-functionally across Research, Clinical Development, Clinical Pharmacology, Companion Diagnostics, Biostatistics, and Clinical Operations to ensure seamless scientific alignment.</li></ul><ul><li>Managing internal and external research collaborations to enable development of clinical fit for purpose assays and translational research.</li></ul><ul><li>Contributing to technical reports, study memos, clinical study reports, and scientific publications.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>The ability to drive, manage, execute and deliver timely results for complex scientific projects.</li></ul><ul><li>Strong communication and presentation skills.</li></ul><ul><li>A strategic understanding of the application of biomarker technologies to basic, translational or clinical research.</li></ul><ul><li>Demonstrated ability to effectively collaborate and work in cross-functional teams.</li></ul><ul><li>A Ph.D., M.D., or MS and 4-7 years' experience participating effectively on cross-disciplinary teams in pharmaceutical or biotech.</li></ul><br><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Pharmacovigilance Systems & Enablement]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50326]]></requisitionid>
    <referencenumber><![CDATA[R50326]]></referencenumber>
    <apijobid><![CDATA[r50326]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50326/executive-director-pharmacovigilance-systems-enablement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Global Patient Safety </strong>team.</p><br><p>The Executive Director, PV Systems & Enablement serves as GPS’ forward-looking pharmacovigilance (PV) domain expert for PV systems and ways of working. This role owns the domain requirements of PV systems, data architecture, PV processes, and AI-enabled capabilities across all of GPS, proactively identifying and proposing modern, innovative, defensible ways of working in a GxP environment. Responsibilities span PV systems forward looking strategy, first-pass prioritization and domain assessment of AI use cases in partnership with the enterprise AI Center of Excellence (CoE), and partnership with GD-IT and other technology teams to execute the resulting roadmap, while maintaining GxP compliance and day-to-day operational reliability of existing systems.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA</li><li>4 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Serve as a domain pharmacovigilance (PV) expert on safety data, process and regulations across all of Global Patient Safety (GPS), proactively identifying and proposing modern, innovative, defensible ways of working in a GxP environment.</li><li>Define and own the PV systems forward looking strategy for GPS, including PV technology systems, data architecture, and AI-enabled capabilities (e.g., agentic AI, Claude, Copilot), partnering with GD-IT and other technology teams on execution</li><li>Define and communicate the function’s vision and strategy in alignment with enterprise goals and business priorities.</li><li>Collaborate with GPS functional leads to align priorities, identify enabling capabilities and develop a single, integrated roadmap that meets patient safety requirements.</li><li>Engage, partner with GD-IT and other technology teams across Regeneron as the PV domain owner, defining requirements, priorities, and dependencies for the GPS roadmap while GD-IT owns technical execution.</li><li>Own and maintain the GPS PV systems roadmap, balancing modernization initiatives with operational sustainability and regulatory compliance.</li><li>Identify opportunities to leverage AI and advanced analytics within PV processes and guide the teams in the appropriate solution design, validation and implementation of those solutions.</li><li>Conduct first-pass domain review and prioritization of AI use cases for GPS, partnering with the enterprise AI Center of Excellence (CoE), which owns formal AI governance.</li><li>Oversee implementation and drive user adoption of AI across GPS, including ongoing compliance and responsible use of AI.</li><li>Ensure new PV systems and ways of working are compliant with all GxP, validation, and data integrity requirements, and are defensible under regulatory inspection.</li><li>Translate business requirements into clear PV systems specifications in partnership with GPS functional leaders, GD IT, and other stakeholders.</li><li>Provide strategic oversight of PV systems (e.g., safety databases, signal detection tools, analytics platforms) to ensure alignment with GPS strategy and operational needs</li><li>Serve as primary GPS liaison with enterprise technology partners (e.g., GD IT, Cloud, Dev Ops, AI CoE, Compliance), representing PV systems and domain requirements.</li><li>Oversee system vendor performance, contract management, and PV systems modernization project delivery</li><li>Build, coach, and scale a high-performing team.</li><li>Lead talent strategy and leadership development initiatives that raise capabilities across the organization.</li><li>Influence cross-functional leaders to align PV priorities and drive enterprise results that benefit GPS and the broader Regeneron organization.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Minimum Bachelors Degree (MS preferred) with 17+ years of experience in pharmacovigilance, safety systems, PV systems modernization, data science, or AI-enabled capabilities within the life sciences industry</li><li>Deep understanding of PV processes and systems, including safety databases, signal detection tools, and reporting platforms.</li><li>Strong knowledge of AI and advanced analytic applications within PV regulated environments.</li><li>Ability to assess, prioritize, and design PV systems and AI-enabled solutions in compliance with global regulatory and quality expectations, in partnership with the enterprise AI CoE and other cross-functional partners.</li><li>Demonstrated experience modernizing PV systems and safety operations, including implementation of AI-enabled or other new PV capabilities in regulated environments.</li><li>Experience leading cross-functional initiatives involving Safety, IT, and data/AI teams.</li><li>Familiarity with AI governance frameworks (partnering with an enterprise AI CoE), validation, and compliance considerations for PV systems in regulated environments.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, GMP AI Engineering]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50615]]></requisitionid>
    <referencenumber><![CDATA[R50615]]></referencenumber>
    <apijobid><![CDATA[r50615]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50615/director-gmp-ai-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, AI Engineering to lead the AI function for our Industrial Operations and Product Supply (IOPS) organization — spanning governance and compliant operation of AI in a regulated environment, delivery of IOPS-specific AI use cases, and the education and enablement programs that drive adoption across the business. In this role, you will translate AI capability into adopted, measurable value — partnering with Quality, enterprise AI, and senior leaders across IOPS — while leading and developing a high-performing multidisciplinary team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York</li><li>Work model/flexibility: 8am - 4:30pm</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Own and execute the IOPS AI roadmap in alignment with business goals, including use-case intake, prioritization, and value measurement across a mature and growing project portfolio</li><li>Operate and evolve AI governance within a GMP environment — maintaining the IOPS AI policy and governance framework, computer system classification, validation procedures, qualified access, and data integrity — in close partnership with Quality and functional stakeholders</li><li>Sustain audit and inspection readiness for AI systems and governance processes; represent IOPS AI practices to internal and external assessors</li><li>Deliver IOPS-specific AI use cases end to end with an established multidisciplinary team, from business-need translation through deployment, adoption, and measured value</li><li>Lead AI education and enablement across IOPS — including fluency curricula for audiences from operators to executives, an embedded advocate network, and engagement channels that convert demand into adoption</li><li>Partner with Regeneron’s enterprise AI organization to adopt corporate platforms, tools, and standards, adapting them for GMP use rather than building parallel capability</li><li>Translate between technology and leadership, communicating AI strategy, risk, and value clearly to senior leaders across the organization</li><li>Lead, develop, and mentor an established high-performing team, fostering a culture of innovation and continuous learning</li></ul><br><p><strong>This role requires:</strong></p><ul><li>BS/BA in Engineering, Science, or a related technical discipline</li><li>Associate Director: 10+ years of industry experience required</li><li>Director: 12+ years of industry experience required</li><li>Equivalent combination of education and experience considered; level determined based on qualifications</li><li>Proven experience leading applied AI programs across governance, delivery, and education or adoption in a regulated environment</li><li>Direct experience operating AI or computerized systems in a GMP/GxP environment, including computer system validation, system classification, data integrity, and inspection readiness; pharmaceutical manufacturing or similarly regulated environment strongly preferred</li><li>Track record of delivering AI and intelligent automation use cases with measurable business value in manufacturing or operations settings</li><li>Experience building education, fluency, or enablement programs and champion or advocate networks that scale adoption without proportional headcount growth</li><li>Working fluency with the modern AI landscape including language models, machine learning, and intelligent automation, with sufficient technical depth to lead engineers, evaluate solutions, and govern systems credibly</li><li>Familiarity with Responsible AI principles; experience with model risk, model credibility, or AI validation and assurance frameworks a plus</li><li>Demonstrated ability to lead through influence across organizational lines and advocate effectively for AI initiatives with executive audiences</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$147,800.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer - Internal Medicine]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46213]]></requisitionid>
    <referencenumber><![CDATA[R46213]]></referencenumber>
    <apijobid><![CDATA[r46213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46213/principal-statistical-programmer-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Support or lead programming and quality control of analysis datasets, tables, listings, and graphs</li><li>Coordinate activities and communicate shifting timelines and milestones to the study team</li><li>Create and maintain programming specifications for analysis datasets across studies</li><li>Support creation and validation of submission requirements, including annotated CRFs and define documents</li><li>Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch</li><li>Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed</li><li>Participate in department working groups, contributing to tool development and process improvement</li><li>Design and test program logic independently, maintaining documentation in a regulated environment</li><li>Enjoy working independently while staying closely connected to a broader study team</li><li>Communicate clearly and proactively, especially around shifting timelines</li><li>Take pride in accuracy and consistency when documenting and maintaining code</li><li>Think analytically and enjoy solving programming and data challenges</li><li>Stay curious about process improvement and enjoy contributing ideas to working groups</li><li>Adapt comfortably to ad hoc requests and evolving priorities from senior leadership</li><li>Bring attention to detail and a quality mindset to regulated work</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 3+ years of relevant experience</li><li>Proven programming experience supporting clinical study data and analysis deliverables</li><li>Strong documentation and quality control skills within a regulated environment</li><li>Experience collaborating within a multidisciplinary study team</li></ul><br><p>#statprogregn</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Consumer Media & Advanced Analytics]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51050]]></requisitionid>
    <referencenumber><![CDATA[R51050]]></referencenumber>
    <apijobid><![CDATA[r51050]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51050/manager-consumer-media-advanced-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health</p><br><p>At Regeneron, we are seeking a Manager, Consumer Media & Advanced Analytics to join our Commercial Insights & Analytics organization in Hyderabad. As a founding member of Regeneron’s first Global Capability Center (GCC), this role will help establish the operating norms, analytics workflows, and measurement frameworks that will support consumer media, advanced analytics, and brand analytics capabilities for U.S. Immunology brands. The role will lead a team responsible for media measurement, attribution validation, advanced analytics, marketing mix modeling, and brand analytics, while partnering closely with U.S.-based stakeholders to drive data-driven commercial decision-making.</p><br><p><strong>When & where:</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li>Lead delivery across key workstreams including U.S. consumer media measurement and QA, marketing mix modeling (MMM), advanced analytics support, and brand analytics.</li><li>Manage and develop a team by providing day-to-day direction, reviewing outputs for quality and accuracy, and supporting employee growth in a matrixed environment.</li><li>Build scalable team capabilities through standardized methodologies, documentation, training, and operational standards.</li><li>Establish operating norms, analytics documentation standards, and measurement workflows for the Consumer Media & Advanced Analytics function within the Hyderabad GCC.</li><li>Collaborate with U.S.-based Commercial Insights & Analytics leaders to drive innovation, standards, and cross-functional alignment.</li><li>Partner with marketing, brand, sales, media, analytics, agency, and alliance stakeholders to align on measurement priorities, reporting requirements, and analytical support needs.</li><li>Lead knowledge-transfer and capability-building activities with U.S.-based counterparts to support successful transition of analytics work into the GCC.</li><li>Oversee media measurement, attribution modeling, dashboarding, audience quality assurance, MMM validation, and advanced analytics execution.</li><li>Review analytical findings, measurement outputs, and business insights to ensure accuracy, consistency, and relevance.</li><li>Drive continuous improvement initiatives that enhance reporting efficiency, measurement quality, and scalability of analytics capabilities.</li><li>Support resolution of complex data quality, measurement, and reporting challenges across multiple analytics workstreams.</li><li>Leverage AI, machine learning, and automation technologies to improve workflow efficiency and accelerate actionable insight generation.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in Marketing, Analytics, Communications, Life Sciences, or a related field. MBA from a Tier 1 institution or PMP certification preferred.</li><li>7+ years of experience in media measurement, marketing analytics, digital analytics, or related commercial analytics functions.</li><li>Minimum 2 years of people management experience leading analytics teams.</li><li>Strong understanding of media measurement, attribution modeling, audience segmentation, A/B testing, experimental design, and performance measurement.</li><li>Experience conducting advanced secondary data analytics across HCP, patient, customer journey, market dynamics, and commercial performance analyses.</li><li>Knowledge of pharmaceutical data sources such as IQVIA, claims, and audience-level data, along with analytical tools including SAS, SQL, and Python.</li><li>Understanding of advanced analytics methodologies including marketing mix modeling, promotional response analytics, targeting, and predictive modeling.</li><li>Experience with business intelligence and visualization platforms such as Tableau and Power BI.</li><li>Proven ability to manage multiple priorities, ensure quality control, and deliver results in a fast-paced environment.</li><li>Strong coaching and team development capabilities within a global matrix organization.</li><li>Excellent stakeholder management, communication, and cross-functional collaboration skills.</li><li>Ability to work effectively across time zones and contribute to building new processes and capabilities within a growing GCC environment.</li><li>Strategic thinking, problem-solving attitude, and passion for using data and analytics to drive commercial outcomes</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs]]></title>
    <date><![CDATA[Mon, 13 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47243]]></requisitionid>
    <referencenumber><![CDATA[R47243]]></referencenumber>
    <apijobid><![CDATA[r47243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47243/senior-manager-field-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Field Medical Affairs – Oncology, Japan to join our Medical Affairs team, supporting our oncology portfolio in a field-based role. In this role, you will engage in scientific exchange and collaborate with therapeutic area experts to provide disease and product information, as well as support research initiatives. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Field-based.</p><br><p><strong>Discover your role:</strong></p><ul><li>Identify and maintain relationships with medical and therapeutic area experts, investigator targets, and develop associated action plans.</li><li>Respond to requests for information on study indications, disease states, and therapeutic areas, presenting scientific and clinical data to diverse audiences in a compliant manner.</li><li>Educate practitioners, payers, and researchers on disease management and therapeutic areas.</li><li>Attend medical conferences to gather and share scientific, clinical, and competitive intelligence with internal stakeholders.</li><li>Support the investigator-initiated study program by building scientific relationships with investigators and identifying research opportunities.</li><li>Collaborate with Clinical Development, Clinical Operation, and trial staff to support site initiation, enrollment, and execution of Medical Affairs strategies.</li><li>Develop and implement rules and procedures for Field Medical activities to ensure compliance with relevant laws, regulations, guidelines, policies, and industry standards.</li><li>You excel in working collaboratively within a matrix organization and cultivating relationships in academic and clinical practice settings.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>A healthcare or scientific professional (PhD, MD, PharmD) with oncology experience and/or clinical trial experience. A Master’s Degree with extensive oncology expertise may be considered.</li><li>Deep knowledge and significant experience in lung cancer/solid tumors or hematology oncology; immuno-oncology experience is preferred.</li><li>At least 3 years of relevant experience in the pharmaceutical industry or clinical settings such as drug information, disease management programs, or clinical pharmacy/medicine.</li><li>Strong communication skills and fluency in Japanese and English.</li><li>Ability to travel 30–50%.</li><li>Experience working in a matrix organization and collaborating with academic and clinical practice settings.</li><li>A commitment to adhering to compliance culture and standards.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Change Control Specialist]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49439]]></requisitionid>
    <referencenumber><![CDATA[R49439]]></referencenumber>
    <apijobid><![CDATA[r49439]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49439/change-control-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking to fill multiple Change Control Specialist positions. These positions develop strategic plans related to change control and the implementation of robust corrective actions to support manufacturing operations by applying function expertise.</p><p><strong>Current Departments with Openings:</strong></p><ul><li><p>Bulk Drug Substance Manufacturing</p></li><li><p>Technical Operations</p></li><li><p>Fill/Finish Manufacturing</p></li></ul><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Craft business plans to independently advance change control initiatives to implement Corrective and Preventative Actions (CAPA’s) and process improvements in support of manufacturing operations</p></li><li><p>Assess sophisticated proposed change controls to evaluate if proposal satisfies company standards</p></li><li><p>Coordinate and prepare change control documentation that assesses and defines the scope, impact, risk, and regulatory impact associated with the change</p></li><li><p>Review, edit, and revise controlled documentation in accordance with cGMP standards</p></li><li><p>Coordinate and/or lead cross-functional meetings with multiple departments to drive change control implementation</p></li><li><p>Provide advice and mentorship to cross-functional teams to enable successful and GMP compliant change controls</p></li><li><p>Independently monitor and progress multiple projects concurrently – identifying, addressing, and/or raising potential obstacles in a timely manner</p></li><li><p>Present business critical and regulatory impactful change controls to senior leadership</p></li><li><p>Document all training</p></li><li><p>Assist with the training of new employees</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in Life Sciences, Engineering, or related field; or equivalent combination of education and experience, and the following amount of experience for each level:</p><ul><li><p>Associate Change Control Specialist: 0-2+ years of relevant experience</p></li><li><p>Change Control Specialist: 2+ years of relevant experience</p></li><li><p>Senior Change Control Specialist: 5+ years of relevant experience</p></li><li><p>Level will be determined based on experience</p></li></ul></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quality Assurance Validation Specialist]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49489]]></requisitionid>
    <referencenumber><![CDATA[R49489]]></referencenumber>
    <apijobid><![CDATA[r49489]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49489/senior-quality-assurance-validation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. QA Validation Specialist to join our Quality Assurance team. As the Senior QA Validation Specialist, you will validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Monday-Friday, 8am-4:30pm</li></ul><p><strong>What you’ll do: </strong></p><ul><li>Generates, executes and/or reviews master and completed qualification and validation protocols, summary reports and associated data for conformance to regulations, SOPs, specifications and other applicable acceptance criteria</li><li>Analyzes the results of testing and determines the acceptability of results against pre-determined criteria</li><li>Investigates and troubleshoots problems which occur and determines solutions or recommendations for changes and/or improvements</li><li>Reviews, edits and approves deviation notifications, deviation investigations, and corrective actions</li><li>Reviews, edits and approves change controls, SOPs, reports and other documentation</li><li>Coordinates with other departments or outside contractors/vendors to complete validation tasks Executed real-world and simulated transport studies, including gross-damage visual inspections, pallet configuration assessments, and qualification of secondary and tertiary packaging materials</li><li>Conducts temperature mapping for controlled environments and distribution lanes</li><li>Programs and deploys instrumentation to capture vibration and shock profiles; analyzed data to inform packaging design and handling recommendations</li><li>Programs humidity and pressure sensors and interpreted datasets to support test plans and root-cause analysis</li><li>Applies ASTM and/or ISTA standards to cold-chain shipping design, testing, and qualification</li><li>Performs small-parcel and palletized-load qualifications, including test planning, execution, and reporting</li></ul><p><strong>Gowning and Environment: </strong></p><ul><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>Requires B.S in life sciences or related field; may substitute proven experience for education requirement<ul><li>QA Validation Specialist: 4 + years of experience</li><li>Sr. QA Validation Specialist: 6+ years of experience</li></ul></li><li>Level will be determined based on experience</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li>Student loan paydown program & tuition reimbursement</li><li>Family care benefits</li><li>Relocation assistance</li><li>Inclusion, culture and well-being programs (including physical & mental health)</li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Assistant General Counsel – Market Access Legal]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48766]]></requisitionid>
    <referencenumber><![CDATA[R48766]]></referencenumber>
    <apijobid><![CDATA[r48766]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48766/senior-director-assistant-general-counsel-market-access-legal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build Our Future Together</strong></p></div><p>The Senior Director, Assistant General Counsel – Market Access Legal will provide proactive, efficient, strategic, and collaborative legal support to Regeneron’s Market Access Commercial Business Unit. More specifically, this person will advise a wide range of internal Market Access and other clients, including Market Access Strategy; National and Regional Payer Account Teams; the Government Pricing, Contract Strategy, Pricing, and Operation Team; as well as Commercial; Marketing; Sales; Public Policy and Government Affairs; Regulatory; and Corporate Compliance. The level of counseling requires a deep understanding of market access principles, market access strategy, payers, pharmacy benefit managers (“PBM”), payer and PBM contracts, pharmaceutical distribution channels, contract operations, government pricing, regulatory and compliance issues, the False Claims Act, the Anti-Kickback Statute, and OIG guidance, and other applicable state and federal healthcare laws. </p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>Work model/flexibility: 4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Providing proactive, efficient, strategic, and collaborative legal advice and support on market access, market access strategy, payer and PBM contracts, payer and PBM strategies, government pricing, and other Commercial-related matters in a fast-paced environment</p></li><li><p>Providing legal guidance on various issues, tactics, and activities, including market access strategy development, creation of market access materials, contract drafting and negotiation, government pricing reporting, and interactions with healthcare providers, distributors, pharmacies, payers, PBMs, and GPOs</p></li><li><p>Drafting and negotiating a wide variety of commercial contracts including payer and PBM agreements, GPO agreements, distribution agreements, pharmacy agreements, rebate agreements, service agreements, and other corporate agreements</p></li><li><p>Provide support to various Commercial teams and Product Attorneys on product-specific Market Access issues</p></li><li><p>Provide support to Corporate Compliance on Market Access issues</p></li><li><p>Maintain an independent and objective perspective while developing and maintaining a strong partnership with the client organizations</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Juris Doctor degree with 10+ years relevant legal experience</p></li><li><p>Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel</p></li><li><p>Prior in-house healthcare/pharmaceutical and/or biotech experience required</p></li><li><p>Significant knowledge of life sciences regulatory enforcement trends, market access, market access strategy, payer and PBM-related issues, payer and PBM contracts, other market access contracts, contract operations, government pricing requirements (ideally for both medical and pharmacy benefit products), regulatory and compliance issues, the FDCA, the False Claims Act, federal and state fraud and abuse laws, and antitrust laws</p></li><li><p>Excellent interpersonal and conflict resolution skills, and ability to work in highly collaborative, team-oriented environment</p></li><li><p>Excellent understanding of healthcare laws and proven experience in applying them to complex business situations</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Consumer Marketing (Ophthalmology)]]></title>
    <date><![CDATA[Thu, 30 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46178]]></requisitionid>
    <referencenumber><![CDATA[R46178]]></referencenumber>
    <apijobid><![CDATA[r46178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46178/associate-director-consumer-marketing-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director, Marketing will contribute to the financial success of the Ophthalmology franchise. Main area of responsibility will be to implement and manage key elements of the U.S. Consumer Marketing plan, ultimately to drive demand for the product.</p><p>Specifically, this will include omnichannel campaign implementation including, Television, Print/Mail, digital and social media marketing execution, patient engagement tool/material development, patient education plan development and implementation, strategic content creation, Agency collaboration, materials and inventory management, budget management, management of review materials schedule and process.</p><h3>When & where:</h3><ul><li>Office Based in Sleepy Hollow, NY for 4 days a week with ~10% travel expected</li></ul><br><h3>Discover your role:</h3><ul><li><p>Contributing to, and implementing consumer strategy, communications planning and tactical plans</p></li><li><p>Implementation of consumer initiatives and tactical plans</p></li><li><p>Delivering against omnichannel strategy and optimizing performance media programs against business goals and priorities</p></li><li><p>Manage & provide strategic input to Agency-led media planning that delivers against the goals of the business</p><ul><li><p>Evaluate, and provide feedback to, performance of media buys in an ongoing way ensure alignment with brand objectives</p></li><li><p>Work with internal Insights & Analytics Teams to expand our approach to measurement of campaigns and other omnichannel initiatives</p></li></ul></li><li><p>Developing innovative digital and social media programs that accelerate brand awareness and drive consumer action</p></li><li><p>Extend omnichannel strategies through an understanding of technical, data, and media system integration points and underlying platforms in a way that delivers incremental value to our customers, patients, and prospects</p><ul><li><p>Expand on compliant first-party data strategy that enriches our customer experience and drives value for our brand</p></li><li><p>Continue to refine our view of our customer, personas, segmentation, and related – business-critical user journeys</p><ul><li><p>Mature our approach to customer journeys in a way that delivers data, insights, and an evolution of our marketing activities</p></li></ul></li><li><p>Develop SEO-inspired content planning that delivers on the needs of our customers in a way that ladders up to critical success factors for our brand</p><ul><li><p>Content development in various formats including: long form, short form, video, social channel specific (Reddit vs Facebook vs LinkedIn), and email</p></li></ul></li><li><p>Develop a seamless holistic digital experience that fulfills on tactical goals including key site actions, engagement, and customer registrations for CRM programs</p></li><li><p>Enrich existing CRM strategy to be more inclusive of additional user needs, journeys, and conversion stages</p></li></ul></li><li><p>Driving selection of patient ambassadors and developing patient testimonials and videos</p></li><li><p>Implementing targeted communication programs</p></li><li><p>Representing promotional tactics for medical, legal, and regulatory team reviews and ensuring final deliverables are accurate and compliant.</p></li><li><p>Working closely with the cross functional marketing team</p></li><li><p>Managing budgets and closely monitoring performance, ensuring cost effective delivery of all programs while tracking and monitoring KPIs</p></li><li><p>Developing and managing patient education and engagement tools and materials- and related promotion through personal and digital distribution channels</p></li></ul><h3>This role requires:</h3><ul><li>Bachelor's Degree, MBA a plus.</li><li>Demonstrated experience in marketing of biologics preferred.</li><li>You have 10+ years of progressive marketing experience including at least 5 years in the Consumer space in pharmaceutical marketing.</li><li>Demonstrated omnichannel digital marketing experience.</li><li>Demonstrated Consumer marketing competencies in the pharmaceutical/biotech areas. Prior U.S. launch experience a plus.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, HCP Marketing - Dermatology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49593]]></requisitionid>
    <referencenumber><![CDATA[R49593]]></referencenumber>
    <apijobid><![CDATA[r49593]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49593/director-hcp-marketing-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director of HCP Marketing will lead healthcare professional marketing strategy and execution for Dermatology indications in the U.S. This highly visible role requires a forward-looking leader with deep marketing expertise and the ability to navigate complex alliance partnerships. The Director will partner closely with cross-functional and alliance teams to advance product growth, contribute to the financial success of the brand, and strengthen its leadership position in dermatology. This position reports to the Senior Director, Dermatology Marketing.</p><h3>When & where:</h3><ul><li>In the office located in Sleepy Hollow, NY for 4 days a week</li></ul><h3>Discover your role:</h3><ul><li>Leading the HCP marketing strategy for atopic dermatitis, ensuring full integration with the broader brand strategy.</li><li>Acting as a key advocate for the Dermatology strategy, clearly articulating priorities and ensuring alignment across Regeneron, Sanofi, and other critical stakeholders.</li><li>Overseeing the development of HCP promotion strategies, messages, and tactical campaigns tailored to Dermatologists and Advanced Practice Providers.</li><li>Building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</li><li>Driving strong cross-functional and alliance collaboration, partnering with Sales, Medical Affairs, TLLs, Market Research, Market Access, Regulatory, Legal, Clinical, and HEOR to deliver cohesive, compliant, and impactful initiatives.</li><li>Ensuring all marketing programs comply with corporate policies, regulatory/ethical frameworks, and alliance standards.</li><li>Managing marketing budgets, timelines, and deliverables to meet scope and performance expectations.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; MBA strongly preferred.</li><li>12+ years of progressive experience in the pharmaceutical/biotech industry or related field.</li><li>8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas.</li><li>Dermatology and/or Immunology marketing and sales experience strongly preferred.</li><li>Demonstrated success in navigating complex alliance or co-promotion partnerships.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Nord (Ematologia)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49791]]></requisitionid>
    <referencenumber><![CDATA[R49791]]></referencenumber>
    <apijobid><![CDATA[r49791]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49791/key-account-manager-nord-ematologia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Costruiamo insieme il nostro futuro:</strong></p><p>In Regeneron utilizziamo la scienza e l’innovazione per sviluppare farmaci che cambiano la vita delle persone con malattie gravi. Cerchiamo un Senior Sales Specialist, Ematologia Commerciale, Italia da inserire nel nostro team vendite di ematologia. La posizione supporterà il business italiano con un modello di lavoro sul territorio. In questo ruolo, promuoverai la crescita del territorio e relazioni di valore con i professionisti sanitari. Collaborerai con i colleghi dell’area medica e con altre funzioni. Questa posizione offre l’opportunità di contribuire a un’organizzazione in rapida crescita, guidata dalla scienza e orientata ai pazienti.</p><p><strong>Quando e dove:</strong></p><p>Italia Nord<br>Posizione sul territorio, con trasferte frequenti.</p><p><strong>Scopri il tuo ruolo:</strong></p><ul><li><p>Costruire relazioni di qualità con i professionisti sanitari utilizzando conoscenze scientifiche aggiornate e messaggi di vendita approvati.</p></li><li><p>Attuare i piani commerciali e di marketing per raggiungere gli obiettivi di vendita e gli indicatori di performance.</p></li><li><p>Gestire gli account strategici attraverso pianificazione, targeting e segmentazione, in linea con le indicazioni regionali.</p></li><li><p>Sviluppare piani locali per gli account utilizzando dati di mercato e aggiornarli in base alle dinamiche del mercato.</p></li><li><p>Collaborare con i colleghi dell’area medica su programmi regionali a supporto delle esigenze dei professionisti sanitari.</p></li><li><p>Rappresentare Regeneron Ematologia in congressi e incontri regionali, nazionali e internazionali.</p></li><li><p>Utilizzerai canali diretti e digitali per ottimizzare il coinvolgimento e contribuire al miglioramento della pratica clinica.</p></li></ul><p><strong>Questo ruolo richiede:</strong></p><ul><li><p>Laurea o qualifica equivalente riconosciuta per i professionisti delle vendite.</p></li><li><p>Almeno cinque anni di esperienza nelle vendite farmaceutiche, inclusa un’esperienza essenziale in ematologia.</p></li><li><p>Conoscenza del Codice della Federazione Europea delle Industrie e Associazioni Farmaceutiche e delle normative locali applicabili.</p></li><li><p>Ottima conoscenza dell’italiano; la conoscenza dell’inglese costituisce un vantaggio.</p></li><li><p>Attitudine tecnica alla vendita basata sulla patologia e sui concetti scientifici.</p></li><li><p>Capacità di utilizzare dati, sistemi multipli e piattaforme di Customer Relationship Management.</p></li><li><p>Eccellenti capacità di coinvolgimento del cliente, presentazione, pianificazione e definizione delle priorità.</p></li><li><p>Capacità di lavorare autonomamente entro scadenze ristrette, dimostrando integrità e una comunicazione etica.</p></li><li><p>L’esperienza nel lancio di prodotti costituisce un vantaggio.</p></li></ul></div><p>Ti riconosci in questa descrizione? Candidati ora per compiere il tuo primo passo verso il Regeneron Way! Ci impegniamo a costruire un ambiente di lavoro con una cultura inclusiva. Regeneron è un datore di lavoro che garantisce pari opportunità e tutti i candidati qualificati saranno presi in considerazione per l’assunzione senza distinzione di razza, colore della pelle, religione o credo (o loro assenza), sesso, orientamento sessuale, identità o espressione di genere, riassegnazione di genere, stato civile o di unione civile, gravidanza o stato genitoriale, età, disabilità, nazionalità, stato di cittadinanza, origine etnica o nazionale, appartenenza alla comunità dei Viaggiatori, stato familiare, informazioni genetiche, stato militare o di veterano, o qualsiasi altra caratteristica protetta dalla legge applicabile. Ove richiesto, forniremo adeguati accomodamenti ai candidati con disabilità o malattie croniche note durante il processo di selezione, salvo che tali accomodamenti comportino un onere eccessivo.</p><p>Dove necessario, divulghiamo le fasce salariali per i ruoli in tutti i Paesi in cui operiamo. L’offerta finale sarà determinata all’interno della fascia pertinente in base al Paese di impiego, allo specifico livello del ruolo e alle competenze ed esperienze del candidato. In alcuni Paesi possono essere applicati contratti collettivi di lavoro (CCNL), che possono influenzare determinati elementi della retribuzione o dei benefit. Regeneron offre un pacchetto di total rewards competitivo e completo che può includere, a seconda del Paese e del ruolo: bonus annuali o altri piani di incentivazione, assegnazioni azionarie, benefici pensionistici o di previdenza, contributo aziendale al piano 401(k), programmi per la salute e il benessere, centri fitness, coperture assicurative (ad es. sanitaria, odontoiatrica, oculistica, vita e invalidità), ferie e permessi retribuiti e benefit per il supporto alla famiglia. Per ulteriori informazioni sui benefit Regeneron negli Stati Uniti, visita <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. Per le altre sedi, ulteriori informazioni verranno fornite durante il processo di selezione. Per qualsiasi domanda, rivolgiti al tuo recruiter.</p><p>Ti informiamo che in Regeneron crediamo di dare il meglio di noi quando lavoriamo insieme. Per questo motivo, molti ruoli richiedono la presenza in sede. Per maggiori informazioni sulle aspettative di lavoro in presenza per il tuo ruolo e la tua sede, parla con il tuo recruiter e con il responsabile delle assunzioni.</p><p>Nell’ambito del processo di selezione, potranno essere effettuati determinati controlli di background in conformità con le leggi del Paese in cui è basata la posizione. Lo scopo di tali controlli è verificare alcune informazioni prima dell’inizio del rapporto di lavoro, come l’identità, il diritto al lavoro e le qualifiche formative.</p><p>Per le posizioni in Canada: questo annuncio si riferisce a una posizione già esistente.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing – Eosinophilic Esophagitis (EoE)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49763]]></requisitionid>
    <referencenumber><![CDATA[R49763]]></referencenumber>
    <apijobid><![CDATA[r49763]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49763/associate-director-hcp-marketing-eosinophilic-esophagitis-eoe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director of HCP Marketing will lead healthcare professional omnichannel/non-personal promotions marketing strategy and execution as well as support execution of personal promotions marketing strategy for EoE in the US. This highly visible role requires a forward-looking individual with deep marketing expertise and the ability to navigate across cross-functional partners and complex alliance partnerships in a growing competitive market. The Associate Director will partner closely with cross-functional and alliance teams to advance product growth, contribute to the brand's financial success, and strengthen its leadership position in Gastroenterology and Allergy/Immunology. This position reports to the Director, EoE HCP Marketing.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY office 4 days a week</li><li>Must be willing to travel 25-30% (including weekend travel as needed)</li></ul><h3>Discover your role:</h3><ul><li>Lead HCP non-personal promotions/omnichannel marketing strategy, planning, and execution, ensuring full integration with the broader brand strategy.</li><li>Understand customer segmentation and strategies to build and implement metrics driven multi-channel plans for focused non-personal HCP engagements and optimal channel distribution.</li><li>Support execution of HCP personal promotions marketing strategy developing resources used by field sales team in HCP engagements.</li><li>Contribute to building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</li><li>Ensure all marketing programs align with corporate policies, regulatory/ethical frameworks, and alliance standards.</li><li>Drive strong cross-functional and alliance collaboration, alignment, and decision-making, partnering with Sales, Medical Affairs, TLLs, Market Research, Analytics, Market Access, Training, Regulatory, and Legal to deliver cohesive, compliant, and impactful initiatives.</li><li>Have a proven track record of leadership and influence across organizational levels.</li><li>Combine strategic and scientific competence with ability to translate insights into actionable marketing strategies.</li><li>Excel in execution and project management within a fast-paced dynamic environment, managing multiple projects simultaneously and working through ambiguity.</li><li>Bring exceptional communication and presentation skills, with the ability to simplify and convey complex strategies to diverse audiences—both technical and non-technical, including senior executives.</li><li>Demonstrate organizational agility, adapting priorities and strategies to external market shifts or internal dynamics.</li><li>Possess strong experience in managing agencies and external partners, ensuring creative excellence and accountability.</li><li>Disciplined in managing budgets and resources aligned to strategic objectives.</li></ul><h3>This role requires:</h3><ul><li>Bachelor’s degree required; MBA strongly preferred.</li><li>10+ years of progressive experience in the pharmaceutical/biotech industry or related field.</li><li>8+ years of US commercial experience in pharmaceutical/biotech marketing, product management, or related areas.</li><li>Gastroenterology/Allergy/Immunology biologics experience strongly preferred.</li><li>Demonstrated success in navigating complex alliance or co-promotion partnerships.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Manager Benelux (Oncology)]]></title>
    <date><![CDATA[Wed, 12 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49979]]></requisitionid>
    <referencenumber><![CDATA[R49979]]></referencenumber>
    <apijobid><![CDATA[r49979]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49979/sales-manager-benelux-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regional Sales Manager, Oncology to join our international oncology organisation, supporting our HUB Markets in a remote role. In this role, you will lead sales teams and deliver business goals across multiple markets while collaborating with Marketing, Medical, Commercial Operations, and local partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Netherlands (Field)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead field sales and key account teams across multiple markets.</p></li><li><p>Coach and develop talent to achieve consistent sales performance.</p></li><li><p>Deliver national, regional, and local account plans against business goals.</p></li><li><p>Run cycle meetings and training using approved messages and materials.</p></li><li><p>Manage analytics, key performance indicators, incentives, and Veeva CRM processes.</p></li><li><p>Build trusted partnerships with customers, local partners, and cross-functional teams.</p></li><li><p>You adapt quickly, prioritise solutions, and remain steady across changing markets.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Extensive biopharma experience in international oncology sales management.</p></li><li><p>Proven leadership of field teams meeting or exceeding sales targets.</p></li><li><p>Field management experience and operational knowledge of sales technology.</p></li><li><p>Experience with CRM platforms and digital promotion activities.</p></li><li><p>Fluent English with strong leadership, planning, communication, and presentation skills.</p></li><li><p>A record of ethical, compliant sales performance and trusted stakeholder relationships.</p></li><li><p>Immuno-oncology experience and established oncology opinion-leader relationships are preferred.</p></li><li><p>Willingness to travel approximately 40%, including some weekends.</p></li><li><p>Proximity to an international airport is advantageous.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€93,000.00 - €155,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs Hematology Austria]]></title>
    <date><![CDATA[Tue, 18 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49862]]></requisitionid>
    <referencenumber><![CDATA[R49862]]></referencenumber>
    <apijobid><![CDATA[r49862]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49862/senior-manager-field-medical-affairs-hematology-austria/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Field Medical Affairs Hematology Austria to join our Medical Affairs team, supporting our hematology business area in a field-based work mode. In this role, you will drive scientific exchange, generate field insights, and support research initiatives while collaborating with key opinion leaders, healthcare professionals, investigators, and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Austria - Field-based</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Build and maintain engagement plans with medical experts and investigators.</li><li>Establish scientific relationships with key opinion leaders in hematologic malignancies.</li><li>Act as a clinical and scientific resource on disease state information.</li><li>Support company-sponsored studies through investigator selection, site initiation, and enrolment activities.</li><li>Advance investigator-initiated study concepts with investigators and Medical Affairs partners.</li><li>Identify medical insights, research gaps, and collaboration opportunities.</li><li>Present scientific and clinical data compliantly to healthcare professionals and researchers.</li><li>You bring external insights that help shape medical strategy and priorities.</li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>PhD, PharmD, MD, or Doctor of Veterinary Medicine (DVM).</li><li>4+ years of relevant experience, including 2+ years as a Medical Science Liaison in hematology.</li><li>Knowledge of hematology; lymphoma and/or multiple myeloma experience preferred.</li><li>Understanding of treatment guidelines, clinical research processes, EU regulations, and compliant practices.</li><li>Ability to communicate complex scientific data and engage as a scientific peer.</li><li>Established relationships with hematology key opinion leaders and relevant institutions preferred.</li><li>Experience supporting cross-functional collaboration within a matrix pharmaceutical environment.</li><li>Ability to identify opportunities, tackle problems, manage priorities, and work independently.</li><li>Strong written and verbal communication skills with audience-focused communication.</li><li>Experience balancing field activities and project participation.</li><li>Proficiency with word processing, presentations, and spreadsheet applications.</li><li>Valid driver’s license, clean driving record, and ability to travel approximately 80%, including overnight travel.</li><li>Fluency in German and English.</li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€103,425.00 - €172,375.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Medical Affairs Hematology  - Austria]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49861]]></requisitionid>
    <referencenumber><![CDATA[R49861]]></referencenumber>
    <apijobid><![CDATA[r49861]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49861/director-medical-affairs-hematology-austria/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Vienna]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Austria]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director Hematology Medical Affairs Austria to join our Medical Affairs team, supporting our hematology business area in a hybrid work mode. In this role, you will provide scientific and medical leadership, shape medical strategy, and advance clinical and medical initiatives while collaborating with Medical Affairs, Clinical Sciences, Regulatory, Commercial, Market Access, and external experts. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When</strong> <strong>&</strong> <strong>where:</strong></h3><p>Austria & Fieldbased</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Serve as the in-country medical lead for hematology programs and scientific initiatives.</li><li>Represent Medical Affairs in cross-functional planning with regional, international, and headquarters teams.</li><li>Lead and develop the hematology medical team through mentoring, hiring, training, and performance management.</li><li>Support clinical development through investigator engagement, site identification, and research activities.</li><li>Deliver scientific presentations to physicians, pharmacists, and other healthcare partners.</li><li>Partner with field medical teams on congresses, symposia, advisory boards, and medical content.</li><li>Provide medical input to commercialization, market access, launch readiness, and lifecycle strategies.</li><li>You build positive relationships and bring actionable insights that strengthen patient-focused decision making.</li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>MD or PhD with hematology expertise and significant pharmaceutical or biotechnology Medical Affairs experience.</li><li>Recent multiple myeloma experience and a well-established network of clinical experts.</li><li>Solid understanding of Medical Affairs practices and applicable country codes of conduct.</li><li>Experience supporting clinical research and clinical development, preferably in hematology.</li><li>Understanding of the local healthcare environment and product lifecycle development.</li><li>Ability to identify strategic Medical Affairs opportunities and optimize planning.</li><li>Proven success working across matrix and cross-functional organizations.</li><li>Ability to build credibility with internal stakeholders, key opinion leaders, and external experts.</li><li>Strong leadership, mentor, and people management capabilities.</li><li>Excellent scientific communication skills with the ability to deliver strategic, actionable insights.</li><li>Ability to manage multiple projects independently while maintaining compliance standards.</li><li>Fluency in English and German.</li><li>Ability and willingness to travel 30-50%.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€121,800.00 - €203,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (f/m/d) - Nürnberg - Erlangen - Würzburg - Aschaffenburg]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49972]]></requisitionid>
    <referencenumber><![CDATA[R49972]]></referencenumber>
    <apijobid><![CDATA[r49972]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49972/sales-specialist-oncology-fmd-nuernberg-erlangen-wuerzburg-aschaffenburg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist Oncology (f/m/d) to represent our Oncology division across the Nürnberg - Erlangen - Würzburg - Aschaffenburg territory. In this role, you will build strong relationships with Healthcare Professionals (HCPs), identify key opinion leaders, and tailor your approach to individual and account needs, all in service of bringing our Oncology portfolio to the patients who need it. This is an opportunity to bring a "patient first" mindset to a fast-growing, science-driven organisation making a meaningful difference to patients worldwide.</p><br><p><strong>Where:</strong></p><p>Field-based in Nürnberg - Erlangen - Würzburg - Aschaffenburg territory</p><br><p><strong>Discover your role:</strong></p><ul><li>Establish and lead high-quality HCP interactions by keeping your scientific knowledge of the product, indication, and brand sales messaging current, and reliably implementing sales & marketing plans</li><li>Consistently deliver on the brand's value proposition, ensuring objectives are met through clear key message communication to HCPs</li><li>Manage your territory with professional account planning, applying a targeting & segmentation approach aligned with regional and country-level guidance</li><li>Develop and implement a local account plan grounded in key data sources and local market insights, in line with the Germany Brand Plan</li><li>Collaborate closely with medical colleagues to implement regional programmes and activities that support HCP needs</li><li>Leverage all communication channels, including digital, in collaboration with other functions, to achieve the best possible share of voice in the market</li><li>Report results and developments proactively and clearly to the Germany leadership team</li></ul><p><br> </p><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree or equivalent experience, plus a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</li><li>5+ years of sales experience within the biotech / pharmaceutical sector, including experience in Oncology</li><li>Proficiency in German, plus conversational English</li><li>A deep understanding of the local healthcare economy, with the ability to identify key players in Oncology</li><li>A "patient first" value system</li><li>Readiness for very frequent travel and a Class 3/B driver's licence</li></ul><br><p><br>Salary range (annually)</p><p>73,125 -121,875 €</p><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Houston West]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50038]]></requisitionid>
    <referencenumber><![CDATA[R50038]]></referencenumber>
    <apijobid><![CDATA[r50038]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50038/medical-specialist-i-allergyent-houston-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Houston]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Houston West Medical Specialist (Sales Representative), Allergy/ENT (MS)<strong> </strong>will report to the District Manager, Allergy/ENT and be responsible for engaging Allergists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US</p><p>The MS is responsible for developing strategy and executing tactics within key allergists in the Dermatology and Respiratory therapeutic areas to generate product utilization. The MS will develop strong working relationships with experts and all Allergists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: Houston West</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</p></li><li><p>Specialty pharmaceutical/biopharmaceutical experience with minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Dermatology or Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market</p></li><li><p>Ability to travel and cover large geographic territories</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Oracle Fusion ERP Deployment Lead]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50016]]></requisitionid>
    <referencenumber><![CDATA[R50016]]></referencenumber>
    <apijobid><![CDATA[r50016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50016/executive-director-global-oracle-fusion-erp-deployment-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Building Our Future:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is making the largest technology investment in its history through a global Oracle Fusion Cloud deployment that will serve as the enterprise platform for finance, planning, manufacturing, and operations worldwide. The Executive Director, Oracle Fusion Global Lead will be accountable for the end-to-end technology delivery of this transformation, from strategy and design through implementation, stabilization, and ongoing optimization. This leader will drive the modernization of Regeneron's operating model, including evaluating the insourcing of key capabilities and integrating support from the company's Global Capability Center in India. As the technology owner of the program, they will shape platform strategy, oversee enterprise-wide execution, and serve as the primary Digital & Technology representative to senior stakeholders, vendors, and delivery partners.</p><p><strong>When & Where:</strong></p><p>This role will sit in our Sleepy Hollow, NY office 4 days per week.</p><p><strong>Discover Your Role:</strong></p><ul><li>Own the global Oracle Fusion Cloud strategy, roadmap, and investment priorities, ensuring alignment with corporate objectives and enterprise performance goals.</li><li>Lead end-to-end technology delivery of the Oracle Fusion transformation, accountable for the ERP business case, budget, governance, milestones, stakeholder alignment, ERP-AI strategy, and deployment execution through stabilization.</li><li>Direct a global organization of employees and contractors, driving talent development, resource planning, organizational effectiveness, and a culture of accountability and execution excellence.</li><li>Establish enterprise standards for application integration, data management, analytics, AI, and platform governance, creating a scalable foundation for future Regeneron technology platforms.</li><li>Partner with Finance, Manufacturing, Procurement, HR, and other business leaders to align Oracle Fusion capabilities with operational priorities and measurable business outcomes.</li><li>Modernize and standardize global business and technology operations by simplifying workflows, improving data quality, enhancing reporting and analytics, advancing AI-enabled automation, and aligning global operating models across regions, shared services, and the GCC.</li><li>Evaluate and execute opportunities to internalize strategic capabilities, while managing strategic vendors, implementation partners, managed services, contracts, and technology spend to ensure delivery quality and financial discipline.</li><li>Ensure long-term platform success through SOX-compliant operations, financial systems support (ERP/EPM), release governance, data and integration standards, and ownership of value realization against the approved ERP business case.</li></ul><p><strong>This Role Requires:</strong></p><ul><li>BS/BA in Computer Science, Information Systems, or a related field required; MS or MBA preferred.</li><li>17+ years of progressive enterprise applications leadership, including large-scale Oracle Fusion Cloud (ERP/EPM/HCM) programs at global scale; experience leading a program of similar magnitude to Regeneron's largest-ever technology investment is strongly preferred.</li><li>Proven experience leading global, multi-year ERP transformation programs, including program governance, business case development, value realization, and cross-functional delivery.</li><li>Experience designing and integrating global operating models that incorporate a Global Capability Center (GCC) or similar offshore/nearshore delivery model spanning both business and technology operations.</li><li>Track record evaluating build-vs-buy and insourcing/outsourcing decisions for strategic technology and business process capabilities.</li><li>Preferred to have deep expertise in Oracle Fusion architecture, release strategy, and integrations. Outstanding leaders with a strong history of success with SAP implementations may be considered.</li><li>Hands-on, current knowledge of Oracle Fusion Cloud technologies, including recent platform releases, embedded AI/ML capabilities, and evolving analytics and integration tooling, is a plus.</li><li>Proven ability to lead global teams, negotiate complex matters, set standards across functional areas, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Consumer Marketing - EOE]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50325]]></requisitionid>
    <referencenumber><![CDATA[R50325]]></referencenumber>
    <apijobid><![CDATA[r50325]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50325/associate-director-consumer-marketing-eoe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director of Gastroenterology Consumer Marketing will have a passion for advancing patient education for people living with eosinophilic esophagitis (EoE). This individual translates EoE brand strategy into best-in-class execution – with primary ownership of the day-to-day development of the digital ecosystem, non-personal promotion, and patient engagement programs. Success in this role requires exceptional attention to detail, the ability to navigate a highly matrixed organization within an alliance brand, and a self-directed drive to turn strategy into flawless execution. This position reports to the Director, GI Consumer Marketing.</p><h3>When & where:</h3><p>Four days on-site in Sleepy Hollow, NY, and to travel up to 15% (including occasional weekend travel as needed)</p><h3>Discover your role:</h3><ul><li>Translating EoE brand strategy into flawless tactical execution the consumer non-personal promotion ecosystem — social, display, online video, audio, programmatic, and patient-facing materials — driving each asset from brief through medical/legal/regulatory approval and in-market launch.</li><li>Owning the EoE consumer CRM program email content, cadence, segmentation, and personalization across the patient and caregiver journey to drive enrollment, engagement, and education.</li><li>Owning the EoE website and content experience – keeping it discoverable across evolving search (SEO/SEM) and AI-driven environments and adopting new data and audience capabilities (including alliance-delivered precision-marketing platforms) to sharpen targeting.</li><li>Managing the materials life cycle for consumer materials, ensuring 100% accuracy and compliance and anticipating the downstream implications of every change before anything is disseminated to patients. This includes Veeva/asset management.</li><li>Managing multiple external agencies (creative, digital, media, production) across briefs, timelines, SOWs, and budgets – holding partners accountable to cost-efficient, strategically sound, and compliant deliverables.</li><li>Supporting media planning and buying across digital and offline channels (TV/online video, programmatic and endemic display, social, and search) in partnership with the media AOR; contributing to channel, flighting, spending, and measurement decisions.</li><li>Translating data from marketing mix models, campaign analytics, market research, and the EoE patient journey and consumer behavior into actionable optimizations and maintaining concise KPI dashboards and performance reporting for senior leadership.</li><li>Serving as the day-to-day Regeneron consumer lead within the alliance – partnering closely with alliance counterparts, driving brand alignment and building consensus.</li><li>Leading patient engagement and education programs, such as the patient/caregiver ambassador program, webinars, and signature initiatives from concept through measurement and learning.</li><li>Partnering cross-functionally with Medical, Regulatory, Legal, Patient Support Services, Advocacy, Communications, HCP marketing, Sales, and Global partners to ensure a unified message across the consumer journey.</li><li>Ensuring all marketing processes, programs, and materials are developed and administered consistently with corporate guidance and all regulatory, legal, and ethical guidelines.</li></ul><h3>This role requires:</h3><ul><li>A bachelor’s degree (required); an MBA is a plus.</li><li>10+ years of progressive industry or relevant professional experience, including 3+ years of pharmaceutical/biotech marketing, product management, or DTC/consumer experience.</li><li>Experience in Gastroenterology and/or Immunology preferred.</li><li>Alliance / co-promote experience preferred.</li><li>Demonstrated ability to manage multiple external agencies and navigate MLR/JRC review processes.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology (NYC and NJ)]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50182]]></requisitionid>
    <referencenumber><![CDATA[R50182]]></referencenumber>
    <apijobid><![CDATA[r50182]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50182/associate-director-field-medical-affairs-hematology-nyc-and-nj/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where: </strong>Territory: NYC (all boroughs) and NJ<br>Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><p><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally</p><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. <br> </p><p>#medicalscienceliaison #msl #HFM #AD</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Programmer/Associate Manager - Statistical Programming, Central Services]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50211]]></requisitionid>
    <referencenumber><![CDATA[R50211]]></referencenumber>
    <apijobid><![CDATA[r50211]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50211/principal-programmerassociate-manager-statistical-programming-central-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager Statistical Programming Central Services to join our Statistical Programming team, supporting integrated analysis, regulatory submissions, and clinical trial disclosure activities in a hybrid work model. In this role, you will deliver high-quality programming solutions, support global regulatory submissions, and advance programming processes while collaborating with project programmers, biostatisticians, clinical transparency teams, and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Hyderabad, India (Hybrid).</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Create integrated datasets, pooled analysis datasets, reports, and programming documentation in line with established standards and processes.</p></li><li><p>Support the preparation and review of electronic data packages for regulatory submissions while ensuring compliance with global regulatory and industry standards.</p></li><li><p>Coordinate with Clinical Transparency and Trial Disclosure teams, biostatisticians, and cross-functional partners to deliver datasets and outputs required for disclosure activities.</p></li><li><p>Provide technical expertise in developing tools, standard processes, and programming solutions that improve efficiency and compliance.</p></li><li><p>Troubleshoot programming, validation, and submission-related issues and support the implementation of procedures across assigned areas.</p></li><li><p>Support inspection readiness activities and respond to programming-related inquiries during regulatory inspections.</p></li><li><p>Collaborate effectively across project programming teams and broader functions to achieve reporting and submission objectives.</p></li><li><p>You bring a diligent, problem-solving attitude and thrive in a fast-paced environment with multiple priorities.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>MS (or BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline.</p></li><li><p>5+ years of programming experience with an MS degree or 6+ years with a BS degree, preferably processing clinical trial data within the biotechnology, pharmaceutical, or health-related industry.</p></li><li><p>Project and people management experience.</p></li><li><p>Proven experience supporting regulatory submissions and compliance with global standards, including CDISC, FDA, EMA, and PMDA requirements.</p></li><li><p>Proficient SAS programming skills in a clinical data environment, including Base SAS, SAS/STAT, Macro, and Graph.</p></li><li><p>Strong expertise in CDISC standards, including SDTM, ADaM, and Define-XML.</p></li><li><p>Proficiency with Pinnacle 21 (P21), including reviewing and troubleshooting validation reports and issues.</p></li><li><p>Familiarity with electronic Common Technical Document (eCTD) submission formats.</p></li><li><p>Knowledge of open-source programming languages such as R and Python is highly desirable.</p></li><li><p>SAS certification is a plus.</p></li><li><p>Excellent communication, interpersonal, collaboration, problem-solving, and organizational skills, with strong attention to detail and the ability to manage multiple priorities.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, IT Operations for Labs]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45565]]></requisitionid>
    <referencenumber><![CDATA[R45565]]></referencenumber>
    <apijobid><![CDATA[r45565]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45565/senior-manager-it-operations-for-labs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Applications Manager (Manager or Senior Manager) to join our IOPS IT team, overseeing the day-to-day maintenance, support, and development of Regeneron's IT Applications portfolio — including Empower CDS, SDMS, and other business-critical systems. In this role, you will lead a team of analysts, drive audit readiness and compliance, and ensure applications are maintained in a validated and compliant state — while collaborating closely with peer managers, QA, IT leadership, and global counterparts. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead and develop a team of IT Applications analysts through performance management, coaching, mentoring, and goal setting; conduct monthly performance reviews and annual evaluations</li><li>Drive audit readiness across the application portfolio; serve as a key point of contact during FDA inspections and internal audits, ensuring systems, audit trails, and documentation are inspection-ready at all times</li><li>Ensure all supported applications are maintained in a compliant and validated state; proactively identify and resolve data integrity and compliance issues in accordance with 21 CFR Part 11, ALCOA+ principles, applicable SOPs, and policies</li><li>Maintain accuracy of system documentation including User Requirement Specifications, Design Specifications, Configuration Specifications, and Test Plans for validated systems</li><li>Collaborate closely with peer managers overseeing complementary application portfolios to ensure alignment, shared best practices, and coordinated delivery across the broader IOPS IT Applications function</li><li>Partner with global counterparts to support and maintain globally deployed QC systems in a consistent and compliant manner</li><li>Manage vendor relationships including performance, contract adherence, and delivery of services in line with business and regulatory compliance requirements</li><li>Develop and implement operational metrics and controls; drive continuous improvement initiatives that enhance workflows, system reliability, and team efficiency; contribute to the strategic vision of the IOPS IT Applications function</li><li>Strong knowledge of cGMP, GAMP, 21 CFR Part 11, and Annex 11; experience supporting applications in a highly regulated GMP laboratory or IT environment preferred</li><li>Demonstrated understanding of ALCOA+ principles and data integrity requirements in biopharmaceutical production</li><li>Proven ability to lead teams through FDA inspections and internal audits with confidence and thoroughness</li><li>Knowledge of Regulatory Asset Manager systems advantageous</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Information Technology, Science, Engineering, Computer Science, or a related field</li><li>Manager: 7+ years of relevant experience with 3+ years managing teams</li><li>Senior Manager: 8+ years of relevant experience with 4+ years managing teams</li><li>May consider experience in lieu of education. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Biostatistics - Genetic Medicine]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46282]]></requisitionid>
    <referencenumber><![CDATA[R46282]]></referencenumber>
    <apijobid><![CDATA[r46282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46282/associate-director-biostatistics-genetic-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Biostatistics </strong>team.</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>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>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>This role requires:</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>#Regnbiostats</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, Neurology]]></title>
    <date><![CDATA[Sun, 23 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50235]]></requisitionid>
    <referencenumber><![CDATA[R50235]]></referencenumber>
    <apijobid><![CDATA[r50235]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50235/senior-medical-director-medical-affairs-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Neurology/Myasthenia Gravis Medical Affairs Team. The Senior Medical Director is responsible for the co-development of medical strategy and planning & execution of medical affairs activities at Regeneron. This hire will provide medical leadership and serve as a key scientific/medical resource. The Senior Medical Director will report to Head of Medical Affairs, Neurology and work in a cross-functional, matrix organization. He/she will also collaborate with external stakeholders such as healthcare practitioners, key opinion leaders and payers.</p><p><strong>When & Where:</strong></p><p>Location: Sleepy Hollow, New York; Warren, New Jersey; or Cambridge, Massachusetts</p><p><em>*If hired in Warren, NJ or Cambridge, MA frequent travel to Sleepy Hollow, MA may be required*</em></p><p><strong>Discover your role:</strong></p><ul><li><p>You maintain deep scientific and medical knowledge of Neurology / Myasthenia Gravis, treatment landscape and clinical decision making</p></li><li><p>undefined</p></li><li><p>You function as an integral member of the cross-functional Medical Team</p></li><li><p>You are responsible for data generation, data analyses and interpretation as it relates to Phase 4 studies, including interventional and observational research</p></li><li><p>undefined</p></li><li><p>You are responsible for the medical content of post-marketing study reports, analyses of clinical data, safety monitoring, and activities that ensure patient safety</p></li><li><p>You provide scientific and medical support for development of strategic medical, publications, communications and integrated evidence generation plans</p></li></ul><ul><li><p>You participate in developing and presenting medical content at congresses, symposia and advisory boards</p></li><li><p>undefined</p></li><li><p>You proactively bring patients' & physicians' voice on cross-functional teams, to enable effective and impactful decision making</p></li><li><p>You provide medical training for internal staff on investigational and/or approved products, disease state and unmet needs</p></li></ul><p><strong> </strong></p><p><strong>This role requires:</strong></p><ul><li><p>MD or equivalent with board eligibility/board certification in Neurology with a minimum of 10 years of relevant experience and 5+ years of Medical Affairs experience in Pharma/Biotech</p></li><li><p>PhD or PharmD with a minimum of 12 years of relevant experience and 8+ years of Medical Affairs experience in Pharma/Biotech</p></li><li><p>Direct experience in Myasthenia Gravis or Neurology Rare Disease, and prior launch experience is strongly preferred</p></li><li><p>Experience and ability in working in a dynamic, matrix environment; excellent collaboration and communication skills</p></li><li><p>undefined</p></li><li><p>Ability to demonstrate deep understanding of all medical affairs accountabilities</p></li><li><p>undefined</p></li><li><p>Thorough understanding of Neurology and Myasthenia Gravis healthcare environment and key stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Quality Assurance, Drug Product (Filling)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46662]]></requisitionid>
    <referencenumber><![CDATA[R46662]]></referencenumber>
    <apijobid><![CDATA[r46662]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46662/senior-manager-quality-assurance-drug-product-filling/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>Regeneron is currently seeking a Senior Manager Quality Assurance (QA) to join our internal QA Drug Product Manufacturing team. This role is responsible for quality floor oversight of the filling (i.e. equipment prep, formulation, and filling) operations for SA12.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Provide leadership to multiple teams under your supervision</li><li>Oversee quality of all equipment prep, formulation, and filling (multiple lines)</li><li>Own programs that support the department, such as area walkthroughs</li><li>Support the development and growth of your team, including your people leaders</li><li>Serve as the leadership point of contact for escalation of events and process updates</li><li>Demonstrate leadership in cGMP environments, including speaking to and preparing for regulatory inspections and audits</li><li>Collaborate and communicate effectively cross-functionally</li><li>Think critically and drive continuous process improvement</li><li>Lead a GMP department through a fast-paced, dynamic environment</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Life Sciences or related field; or equivalent combination of education and experience and 8+ years of relevant experience</li><li>Previous people leadership/supervisory experience</li><li>Experience with drug product manufacturing and/or fill finish is preferred</li></ul><p>#REGNQA</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs - Hematology (OH, MI, KY, IN)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50512]]></requisitionid>
    <referencenumber><![CDATA[R50512]]></referencenumber>
    <apijobid><![CDATA[r50512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50512/associate-director-field-medical-affairs-hematology-oh-mi-ky-in/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where: </strong>Territory: OH, MI, IN, KY<br>Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><br><p><strong>Discover your role:</strong><br>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.<br>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies.<br>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.<br>• Participates in the development and management of company sponsored clinical trials including.<br>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy.<br>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.<br>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><br><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. <br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. <br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.<br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. <br> </p><p>#medicalscienceliaison #msl #HFM #AD</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Thoracic Oncology and Pan-Tumor (northern CA, NV, WA, OR, AK)]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50437]]></requisitionid>
    <referencenumber><![CDATA[R50437]]></referencenumber>
    <apijobid><![CDATA[r50437]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50437/associate-director-field-medical-affairs-thoracic-oncology-and-pan-tumor-northern-ca-nv-wa-or-ak/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs responsible for engaging in the exchange of scientific data and other medical and/or scientific information with key opinion leaders (KOLs), health care providers (HCPs), researchers, pharmacists and population-based decision makers. We demonstrate a thorough understanding of solid tumors, including thoracic malignancies, and other tumors of interest within clinical development and aligned with our strategic medical plans. <br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Field-northern, CA, Nevada, Idaho, Oregon, Alaska</p><p>• Travel: approximately 50% of the time, including air travel, overnight and occasionally on weekends</p><p><strong>Discover your role:</strong><br>• Establish, foster, cultivate and maintain peer relationships with KOLs. <br>• Act as the primary clinical/scientific resource to HCPs for information pertaining to disease state and our product(s) to ensure awareness and understanding.<br>• Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans.<br>• Support evidence generation (company sponsored trials and investigator initiated studies (IIS)) research initiatives<br>• Identify and report medical insights.<br>• Identifies gaps in research and educational needs to inform medical strategy.<br>• Responds to requests for information and presents/discusses scientific and clinical data to appropriate audience in a compliant manner.<br>• Performs disease management and therapeutic area education with identified practitioners, payers and researchers.<br>• Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence with the purpose of informing internal partners.<br>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><p><strong>This role requires</strong><br>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.<br>• 8+ years of experience with a minimum of 4 years’ experience as an Oncology Medical Science Liaison function is required.<br>• Knowledge or experience in the Oncology therapeutic area is required, and experience in thoracic malignancies preferred.<br>• Established relationships with KOLs in thoracic malignancies and knowledge of institutions focused on Solid Tumor Malignancies preferred.<br>• Drug launch experience is strongly preferred.<br>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines.<br>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.</p><p>#ofm #msl #medicalscienceliaison<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager CMC Regulatory Affairs]]></title>
    <date><![CDATA[Sat, 12 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49131]]></requisitionid>
    <referencenumber><![CDATA[R49131]]></referencenumber>
    <apijobid><![CDATA[r49131]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49131/manager-cmc-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager CMC Regulatory Affairs to join our CMC Regulatory Affairs team. In this role, you will interpret the current, approved, and planned clinical regulatory landscape by contributing to the management of the regulatory submission form process — supporting the review of documentation submitted to global health authorities to enable the release of lots to clinical trials. You will collaborate across cross-functional teams while managing a team of your own, ensuring submissions appropriately support the release of investigational product. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Hyderabad, India (hybrid)</p><p><strong>Discover your role:</strong></p><p>Contribute to the management of the regulatory submission form process, which involves reviewing documentation submitted to global health authorities to support the release of lots to clinical trials.</p><p>Support cross-functional departments in understanding the current, approved regulatory landscape for all global CTAs.</p><p>Participate in cross-functional meetings to help identify CMC regulatory issues related to submission documentation for clinical trials, ensuring timely communication between IOPS and global development.</p><p>Participate in the development of procedures and systems for enhanced tracking of global regulatory submission packages and approval status.</p><p>Lead meetings and presentations on more complex regulatory issues and participate in creating regulatory justifications.</p><p>Keep management and all stakeholders informed of assessments, overall strategy, and project status.</p><p>Contribute to training programs, metrics, and invoice approvals.</p><p>Act as a submission compliance liaison with other areas of Regulatory Affairs, Regulatory Submission Management, Clinical Drug Supply and Logistics, and Quality to ensure submissions appropriately support the release of IP.</p><p>Manage and lead a team.</p><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in Chemistry, Biology, or a related field (advanced degree preferred).</p></li><li><p>Minimum of 7–9 years of experience working in the biopharmaceutical manufacturing or related industry, including experience in regulatory or compliance related activities.</p></li><li><p>Minimum of 2 years of leadership and/or managerial experience.</p></li><li><p>Strong compliance background preferred.</p></li><li><p>Experience in program management a plus.</p></li><li><p>Ability to build collaboration and teamwork across cross-functional teams.</p></li><li><p>Ability to work in an ambiguous environment and produce maximum results with minimum direction and guidance.</p></li><li><p>Demonstrated history of building and maintaining positive relationships both internally and externally.</p></li><li><p>Strong communication and negotiation skills.</p></li><li><p>Open and receptive to change, while continually looking for opportunities to improve processes.</p></li><li><p>Strong understanding of quality principles in a regulated manufacturing environment is helpful.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 13 Sep 2026 11:56:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Tax Operations]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50515]]></requisitionid>
    <referencenumber><![CDATA[R50515]]></referencenumber>
    <apijobid><![CDATA[r50515]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50515/director-tax-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director of Tax Operations to own the day-to-day management of the company's global tax reporting and compliance functions for the US. Reporting to the Head of Tax Operations, the Director runs the operational execution of tax accounting (ASC 740), U.S. compliance, indirect taxes, SOX controls, audits, and the systems and data that support them. In this role you will modernize the tax operating model — embedding artificial intelligence (AI), automation, and analytics into everyday tax work while maintaining rigorous controls and human review. The Director coordinates with Tax Strategy counterparts on planning, technical positions, and shared or cross-functional work, and manages the U.S. and Ireland operations as a single, well-run team.</p><p><strong>When & Where:</strong></p><p>This position is full-time and will sit in our Sleepy Hollow, NY office four days per week.</p><p><strong>Discovery Your Role:</strong></p><ul><li>Manage ASC 740 tax accounting including provisions, reconciliations, financial statement disclosures, and external audit coordination</li><li>Ensure SOX-compliant internal controls over tax reporting processes, including AI and automation-enabled workflows</li><li>Oversee all U.S. federal, state, and international tax compliance, filings, payments, and audit-ready documentation</li><li>Manage tax credits (R&D, orphan drug), indirect taxes (sales/use, property, excise), and tax audits/examinations</li><li>Monitor and implement regulatory changes including OECD Pillar Two, U.S. CAMT, and international statutory requirements</li><li>Lead tax operations AI strategy by identifying use cases, piloting solutions, and establishing responsible-use guardrails</li><li>Own tax technology platforms, analytics tools, and data initiatives while driving process transformation and team upskilling</li><li>Partner with Tax Strategy and cross-functional stakeholders while leading and developing the Tax Operations team</li></ul><p><strong>This Role Requires:</strong></p><ul><li>Bachelor's Degree in Tax, Accounting, Finance, or a related field plus at least 10 years of progressive corporate tax experience (or equivalent combination of education and professional experience) working for or with publicly traded, multinational companies; a combination of Big 4 and in-house experience is strongly preferred.</li><li>Deep expertise in ASC 740, including provisions, uncertain tax positions, financial statement disclosures, and strong U.S. federal and state income tax experience, with exposure to indirect taxes.</li><li>Life sciences or biopharmaceutical industry experience nice to have.</li><li>International and statutory reporting experience (FRS 102, IFRS); Ireland experience a plus nice to have.</li><li>Familiarity with the OECD global minimum tax (Pillar Two) and the U.S. corporate alternative minimum tax (CAMT) nice to have.</li><li>Experience leading tax technology, automation, or data-analytics initiatives nice to have.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regional Market Access Lead - Europe]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50654]]></requisitionid>
    <referencenumber><![CDATA[R50654]]></referencenumber>
    <apijobid><![CDATA[r50654]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50654/director-regional-market-access-lead-europe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Milan]]></city>
    <state><![CDATA[Milano]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regional Access Lead to join our Market Access function, supporting our European region in a hybrid work mode. In this role, you will drive market access, pricing, and reimbursement strategies for our neurology portfolio while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead European market access strategies aligned with global objectives and country needs.</p></li><li><p>Monitor payer trends, healthcare policies, and reimbursement frameworks across Europe.</p></li><li><p>Represent Europe in global access strategy discussions and shape future approaches.</p></li><li><p>Adapt access tools, payer value propositions, and objection handlers for regional use.</p></li><li><p>Support Health Technology Assessment dossiers, mock negotiations, and payer engagements.</p></li><li><p>Build relationships with payers, policymakers, and patient advocacy groups.</p></li><li><p>Align evidence generation and health economics outcomes research with payer requirements.</p></li><li><p>You bring an agile, collaborative mindset when influencing cross-functional teams.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>Regional market access launch experience across competitive therapeutic areas.</p></li><li><p>Proven European pricing, reimbursement, Health Technology Assessment, and negotiation success.</p></li><li><p>Experience developing and adapting economic models for regional and national submissions.</p></li><li><p>In-depth knowledge of European payer systems and reimbursement challenges.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>Fluent English; another European language and neurology experience are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix working, and stakeholder engagement skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€93,825.00 - €156,375.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[National Sales Director - Immunology]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50430]]></requisitionid>
    <referencenumber><![CDATA[R50430]]></referencenumber>
    <apijobid><![CDATA[r50430]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50430/national-sales-director-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a National Sales Director Immunology Commercial Leadership Spain to join our Commercial Immunology Leadership Team. In this role, you will lead the field organization to deliver business results, support patient access, and drive successful execution of commercial objectives while collaborating with Sales Managers, Commercial Operations, alliance partners, customers, and international colleagues.</p><h3><strong>When & where:</strong></h3><p>Madrid, Spain (strongly preferred)</p><p>Hybrid work model</p><p><strong>Discover your role:</strong></p><ul><li><p>Drive business results aligned with company objectives across the Spanish market.</p></li><li><p>Lead the Field Team through Sales Managers to ensure seamless execution of commercial strategies and objectives.</p></li><li><p>Manage, coach, motivate, and inspire a senior team of sales professionals to achieve high performance.</p></li><li><p>Build and maintain strong relationships with key customers to support business success and patient access.</p></li><li><p>Partner with the Commercial Operations Team to provide performance, forecasting, and market insights for discussion with senior leadership.</p></li><li><p>Enforce company policies and procedures to ensure quality and compliant ways of working.</p></li><li><p>Collaborate with international sales leaders, sharing best practices and contributing as an active member of the International Sales Head community.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor’s degree in business, marketing, or a related field; with 10+ years of pharmaceutical industry and/or relevant sales experience; marketing experience preferred and 5+ years of people management experience leading teams.</p></li><li><p>Proven track record of success in pharmaceutical or biotechnology sales roles.</p></li><li><p>Deep understanding of the Spanish healthcare ecosystem, including market access.</p></li><li><p>Strong analytical skills and business acumen with the ability to drive team performance.</p></li><li><p>Relevant leadership experience with the ability to lead a senior team.</p></li><li><p>Previous experience within a co-promotion or alliance environment preferred.</p></li></ul><p><strong>Salary Range (annually)</strong></p><p>€89,775.00 - €149,625.00</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 15 Sep 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[VP Digital & Technology Solutions Partner - Finance, Accounting & Oracle ERP]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50017]]></requisitionid>
    <referencenumber><![CDATA[R50017]]></referencenumber>
    <apijobid><![CDATA[r50017]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50017/vp-digital-technology-solutions-partner-finance-accounting-oracle-erp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is a leading biotechnology company built on a simple but powerful mission: to use the power of science to bring new medicines to patients, over and over again. Founded and led by physician-scientists, we've turned that mission into one of the industry's most productive pipelines, nearly all of it homegrown in our own laboratories, powered by proprietary technologies like our VelociSuite® platform. From Dupixent and EYLEA to a rapidly expanding portfolio across oncology, cardiovascular and metabolic disease, neuroscience, and rare disease, our science is reaching millions of patients worldwide, and we're just getting started.</p><br><p>As we invest billions in new manufacturing capacity, expand our global footprint, and build the next generation of digital and technology capabilities to match the scale of our ambition, Regeneron offers a rare combination: the resources and reach of an industry leader, paired with the energy, curiosity, and relentless focus on invention of a company still writing its next chapter. This is a place where technology doesn't just support the business, it accelerates the science that changes patients' lives.</p><br><p><strong>Role Description</strong></p><p>Regeneron is seeking a Vice President to lead the digital and technology portfolio for Finance, Investor Relations, Facilities Management, Audit, Tax, Treasury and software delivery compliance across G&A. This role will also have accountability for the largest single application environment at Regeneron, our Oracle E-Business Suite (EBS) and Fusion platforms. This executive owns the technology backbone for how a leading global biotechnology company manages its finances, engages investors, runs its workplaces, and governs how software is built and released worldwide.</p><br><p><strong>Scope & Impact</strong></p><p>This executive sets enterprise technology strategy across multiple corporate functions and leads through a team of directors and managers. Decisions carry enterprise-level impact on company performance; this individual influences executive stakeholders on the most significant matters and represents technology with external partners.</p><br><p><strong>What You'll Lead</strong></p><ul><li>Set enterprise technology strategy across Finance, Investor Relations, Facilities Management, Audit, Tax, and Treasury, partnering with senior business leaders to align the Oracle E-Business Suite (EBS), Fusion, and related platform roadmaps with corporate strategy, operational priorities, and company-wide performance goals.</li></ul><ul><li>Lead a multi-team technology organization through directors, managers, and a large network of external professionals.</li></ul><ul><li>Drive measurable business outcomes by improving key performance indicators such as financial close cycle time, forecast accuracy, working capital visibility, reporting timeliness, controls effectiveness, automation adoption, system reliability, and user productivity across Finance and adjacent corporate functions.</li></ul><ul><li>Lead the Oracle EBS and Fusion platform strategies, including modernization and integration decisions.</li></ul><ul><li>Own the multi-year transformation roadmap across Finance and G&A systems, prioritizing investments, sequencing modernization initiatives, simplifying legacy complexity, and driving adoption of new digital capabilities.</li></ul><ul><li>Establish and govern the Finance data, analytics, and decision intelligence strategy, including data quality, master data alignment, trusted executive reporting, and analytics capabilities that enable faster and more confident business decisions.</li></ul><ul><li>Drive global operating model and process standardization across regions, legal entities, shared services, and business units, with emphasis on close, planning, procure-to-pay, treasury, tax, audit, and reporting workflows.</li></ul><ul><li>Manage strategic vendors, managed services, implementation partners, and technology spend with accountability for partner performance, contract outcomes, portfolio prioritization, and financial discipline across the supported systems landscape.</li></ul><ul><li>Strengthen resilience and operational risk management for mission-critical finance platforms, partnering across cybersecurity, access governance, disaster recovery, incident response, and business continuity to protect critical business operations.</li></ul><ul><li>Define and advance the AI strategy and AI agent roadmap for Regeneron’s financial operations, identifying high-value opportunities to automate work, improve decision support, strengthen controls, and responsibly scale AI-enabled capabilities across Finance and related corporate functions.</li></ul><ul><li>Direct more than 1,000 integration points between Regeneron’s financial applications and boundary systems.</li></ul><ul><li>Support the systems strategy and delivery capabilities for global financial consolidations, statutory reporting, and operational performance reporting.</li></ul><ul><li>Own the technology systems and controls supporting Audit, Tax, and Treasury, and establish enterprise software development lifecycle (SDLC) standards and governance across the Commercial and G&A technology organization.</li></ul><ul><li>Ensure SOX-compliant technology operations across in-scope financial systems, with accountability for effective controls execution, audit readiness, remediation of control gaps, and consistently strong internal and external audit results.</li></ul><br><p><strong>What You Bring</strong></p><ul><li>BS/BA in Computer Science, Information Systems, Finance, or a related field required; MBA preferred.</li></ul><ul><li>18+ years of progressive technology leadership, including finance systems and enterprise platforms such as Oracle E-Business Suite (EBS) and/or Oracle Fusion. Candidates with extensive SAP FI/CO leadership experience may be considered.</li></ul><ul><li>A history of successful executive command of finance technology, investor relations, facilities/real estate systems, and audit, tax, or treasury platforms; familiarity with SDLC governance frameworks is a plus.</li></ul><ul><li>Proven ability to lead at enterprise scale, influence executive stakeholders, negotiate the most complex matters, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II - Oncology - Fresno, CA]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50630]]></requisitionid>
    <referencenumber><![CDATA[R50630]]></referencenumber>
    <apijobid><![CDATA[r50630]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50630/medical-account-specialist-ii-oncology-fresno-ca/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><br><h3>When & where:</h3><ul><li>Reside in the greater Fresno, CA region</li></ul><br><h3>Discover your role:</h3><ul><li>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</li><li>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</li><li>Develop strong working relationships with aligned designated accounts and specialists</li><li>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</li><li>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</li><li>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</li><li>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</li></ul><br><br><h3>This role requires:</h3><ul><li>Bachelors degree; Master’s degree or additional advanced education/certifications a plus and</li><li>Minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred).</li><li>Buy and bill experience with biologics required.</li><li>Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions.</li><li>Current account management experience in calling on large Oncology group practices and/or integrated delivery networks.</li><li>You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization.</li><li>We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</li><li>Must have ability to travel and cover large geography territories.<br></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 <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 10:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[AI/MLOps SRE Lead Engineer]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50759]]></requisitionid>
    <referencenumber><![CDATA[R50759]]></referencenumber>
    <apijobid><![CDATA[r50759]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50759/aimlops-sre-lead-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><br><p>At Regeneron Digital & Technology, we are expanding our AI and Platform Engineering capabilities to support next-generation intelligent systems, machine learning platforms, and cloud-native technologies. We are seeking an AI/MLOps SRE Lead Engineer to drive reliability, scalability, observability, and operational excellence across our AI, ML, and cloud ecosystem. This role will lead the design and operation of resilient platforms supporting machine learning workloads, LLMs, AI Agents, and enterprise-scale automation while enabling engineering teams to innovate with speed and confidence.</p><br><p><strong>When & Where</strong></p><p>Hyderabad (Hybrid)</p><br><p><strong>Discover your role</strong></p><ul><li>Drive service reliability, availability, and performance across multi-cloud environments by establishing SLOs, SLIs, error budgets, and reliability standard methodologies.</li><li>Design, build, and operate enterprise ML platform infrastructure using technologies such as Dataiku, Amazon SageMaker AI, Databricks, and Google Vertex AI.</li><li>Develop AI-powered observability capabilities using anomaly detection, predictive analytics, and automated remediation to proactively identify and resolve operational issues.</li><li>Lead the implementation, monitoring, and optimization of LLM, SLM, RAG, and AI Agent platforms, ensuring performance, governance, scalability, and operational excellence.</li><li>Design and implement Infrastructure as Code, CI/CD pipelines, self-healing systems, and platform automation solutions to improve engineering productivity and platform resilience.</li><li>Architect enterprise ChatOps solutions integrating operational events, observability platforms, AI workflows, and automated remediation capabilities.</li><li>Partner closely with Data Science, AI Engineering, and Platform teams to deliver secure, scalable, and production-ready AI/ML solutions.</li><li>Evaluate emerging AI-native operational technologies and integrate innovative solutions that enhance platform reliability, engineering efficiency, and business value.</li><li>Conduct technical debt assessments, identify architectural risks, and provide strategic recommendations to improve enterprise platform maturity.</li><li>Serve as a technical leader and trusted advisor, mentoring engineers and influencing reliability engineering, MLOps, cloud platform strategy, and AI-enabled operations across the organization.</li></ul><br><p><strong>This role requires</strong></p><ul><li>Bachelor's degree in Computer Science, Information Technology, Engineering, Data Science, Artificial Intelligence, or a related field; Master's degree preferred.</li><li>6-8 years of experience in Site Reliability Engineering, Platform Engineering, DevOps, or related technology subject areas with enterprise-scale delivery experience.</li><li>Strong hands-on experience operating across two or more major cloud platforms, including AWS, GCP, and Azure.</li><li>Deep expertise with ML platform technologies including Databricks, Amazon SageMaker AI, Dataiku, and Google Vertex AI.</li><li>Proven experience implementing end-to-end ML workflows including model training, experiment tracking, deployment, monitoring, and pipeline orchestration.</li><li>Hands-on experience applying machine learning techniques such as anomaly detection, predictive analytics, time-series modelling, and operational intelligence within enterprise environments.</li><li>Advanced proficiency with Infrastructure as Code tools such as Terraform, Pulumi, AWS CDK, and modern CI/CD automation practices.</li><li>Strong programming and scripting skills in Python, Go, Bash, or similar languages.</li><li>Experience designing enterprise observability solutions using Prometheus, Grafana, Datadog, OpenTelemetry, distributed tracing, logging, and monitoring platforms.</li><li>Demonstrated expertise in anomaly detection, predictive analytics, automated remediation, and AI-assisted operational capabilities.</li><li>Proven experience designing and implementing enterprise ChatOps solutions, including operational workflow automation and AI-enabled integrations.</li><li>Strong ability to identify technical debt, assess platform risks, influence technical strategy, and drive modernization initiatives.</li><li>Experience using AI tools, AI Agents, and LLM-powered assistants to improve engineering operations, incident management, and developer productivity.</li><li>Experience with Kubernetes and container orchestration platforms such as EKS, GKE, or AKS preferred.</li><li>Familiarity with MLOps technologies including Kubeflow, Feast, MLflow, and model evaluation frameworks such as LangSmith, RAGAS, Evidently AI, or Weights & Biases preferred.</li><li>Knowledge of cloud cost optimization, policy-as-code, compliance automation, FinOps practices, and multi-cloud governance preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Integrated Data Review & Quality]]></title>
    <date><![CDATA[Tue, 15 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50031]]></requisitionid>
    <referencenumber><![CDATA[R50031]]></referencenumber>
    <apijobid><![CDATA[r50031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50031/director-integrated-data-review-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, Integrated Data Review provides strategic leadership for the development, implementation, and continuous improvement of integrated data review processes across clinical programs. In partnership with Biostatistics and cross-functional collaborators, this role establishes scalable frameworks, standards, and oversight models to enable proactive, risk-based identification of data issues and ensure high-quality, inspection-ready clinical data. The position drives consistent execution of Data Review Plans and promotes adoption of integrated data review practices across study teams.</p><br><h3>When & where:</h3><ul><li>Location: Warren NJ, Armonk NY, and TarryTown NY</li><li>Work model/flexibility: on site 4 days a week</li><li>Travel percentage: 10%</li></ul><br><h3>Discover your role:</h3><ul><li>Define and lead the Integrated Data Review (IDR) strategy, including the implementation of an appropriate operating model, and governance framework across the portfolio.</li><li>Accountable for consistent execution, oversight, and critical issue of Data Review Plans (DRPs), and proactive identification of data quality risks.</li><li>Define minimum requirements and develop standardized data review plans methodologies, templates, processes, and guidance to enable consistent and effective execution across study teams.</li><li>Provide oversight of data review plans execution through established governance processes, KPIs, and quality metrics to ensure consistency, effectiveness, adherence to standards, and continuous improvement across programs.</li><li>Partner with the Clinical Data Reporting group to develop, implement, and maintain standardized libraries of data review outputs, including visualizations, listings, dashboards, and patient profiles, that support scalable and consistent execution of integrated data review processes across programs.</li><li>Collaborate with Quantitative Innovation and Statistical Strategy (QISS) team to translate Risk-Based Data Management (RBDM) methodologies into practical data review approaches and study-level requirements.</li><li>Proactively identify potential risks to data quality, integrity, and delivery timelines and implement mitigation strategies to ensure continuity, compliance, and successful delivery of departmental objectives.</li><li>Drive continuous improvement and innovation in IDR methodologies and technologies through analysis of metrics, lessons learned, inspection observations, and evolving industry practices.</li><li>Develop and maintain SOPs, work instructions, templates, and training materials using quality-by-design principles to support integrated data review processes.</li><li>Lead implementation, change management, and training initiatives to ensure consistent adoption.</li><li>Drive adoption of IDR methodologies across clinical and external data domains to support proactive issue detection and improved data quality outcomes.</li><li>Liaise with internal and external collaborators to develop strong relationships and ensure effective cross-functional collaboration and communication with respect to deliverables and throughout drug development process.</li></ul><br><h3>This role requires:</h3><ul><li>12+ years in Clinical Data Management within within the biotechnology, pharmaceutical or health related industry. With 5+ years of people management, leadership, and mentoring</li><li>Expert knowledge of clinical data management principles, processes, technologies and industry best practices.</li><li>Expert knowledge of integrated data review principles, data quality management, and critical-to-quality concepts.</li><li>Deep understanding of regulatory requirements and industry standards, including ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, and global data privacy regulations, with the ability to apply these in an operational setting.</li><li>Working knowledge of RBDM principles and their application to Integrated Data Review, including centralized monitoring activities.</li><li>Understanding of Risked Based Quality Management (RBQM) principles and their relationship to integrated data review and centralized monitoring.</li><li>Demonstrated experience establishing, implementing, and evolving integrated data review frameworks, governance models, and methodologies across clinical programs.</li><li>Experience identifying critical data and defining risk-based data review strategies.</li><li>Experience interpreting and analyzing clinical, operational, and external data to identify data trends and potential quality issues.</li><li>Experience developing, implementing, and overseeing Data Review Plans and associated governance processes.</li><li>Demonstrated ability to partner with cross-functional collaborators to support risk-based and integrated data review approaches.</li><li>Understanding of KPIs and quality metrics used to assess effectiveness and impact of integrated data review activities.</li><li>Demonstrated success in solving complex business problems through strategic and critical thinking.</li><li>Proven ability to lead and influence within a matrix organization, driving alignment and outcomes across cross-functional stakeholders without direct authority.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 06:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[AI/MLOps SRE Lead Engineer]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50758]]></requisitionid>
    <referencenumber><![CDATA[R50758]]></referencenumber>
    <apijobid><![CDATA[r50758]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50758/aimlops-sre-lead-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases.</p><br><p>At Regeneron Digital & Technology, we are expanding our AI and Platform Engineering capabilities to support next-generation intelligent systems, machine learning platforms, and cloud-native technologies. We are seeking an AI-MLOps SRE Lead Engineer to drive reliability, scalability, observability, and operational excellence across our AI, ML, and cloud ecosystem. This role will lead the design and operation of resilient platforms supporting machine learning workloads, LLMs, AI Agents, and enterprise-scale automation while enabling engineering teams to innovate with speed and confidence.</p><br><p><strong>When & Where</strong></p><p>Hyderabad (Hybrid)</p><br><p><strong>Discover your role</strong></p><ul><li>Drive service reliability, availability, and performance across multi-cloud environments by establishing SLOs, SLIs, error budgets, and reliability standard methodologies.</li><li>Design, build, and scale enterprise ML platform infrastructure using technologies such as Dataiku, Amazon SageMaker AI, Databricks, and Google Vertex AI.</li><li>Develop AI-powered observability solutions using anomaly detection, predictive analytics, and automated remediation to proactively identify and resolve operational issues.</li><li>Lead the implementation, evaluation, and monitoring of LLMs, SLMs, RAG pipelines, and AI Agent platforms, ensuring performance, governance, scalability, and operational efficiency.</li><li>Design and implement Infrastructure as Code (IaC), CI/CD pipelines, self-healing systems, and automation capabilities that improve engineering productivity and platform resilience.</li><li>Architect enterprise ChatOps solutions integrating AI/ML operations, observability platforms, operational events, and automated remediation workflows.</li><li>Partner with Data Science, AI Engineering, and Platform teams to deliver secure, scalable, and production-ready AI/ML platforms and services.</li><li>Evaluate emerging AI-native operational technologies and AI-assisted engineering solutions to improve platform reliability and operational excellence.</li><li>Conduct technical debt assessments, identify architectural risks, and provide strategic recommendations to modernize enterprise platforms.</li><li>Serve as a technical leader and trusted advisor, mentoring engineers and influencing SRE, MLOps, cloud platform, and AI operations strategy across the organization.</li></ul><br><p><strong>This role requires</strong></p><ul><li>Bachelor's degree in Computer Science, Information Technology, Engineering, Data Science, Artificial Intelligence, or a related field; Master's degree preferred.</li><li>6-8 years of experience in Site Reliability Engineering, Platform Engineering, DevOps, or related technology subject areas within enterprise-scale environments.</li><li>Strong hands-on experience working across two or more cloud platforms, including AWS, GCP, and Azure.</li><li>Deep expertise with ML platform technologies such as Databricks, Amazon SageMaker AI, Dataiku, and Google Vertex AI.</li><li>Proven experience implementing end-to-end ML workflows, including model training, deployment, experiment tracking, monitoring, and pipeline orchestration.</li><li>Hands-on experience applying ML techniques such as anomaly detection, predictive analytics, time-series modeling, and operational intelligence within enterprise platforms.</li><li>Advanced proficiency with Infrastructure as Code tools, including Terraform, Pulumi, AWS CDK, and modern CI/CD automation practices.</li><li>Strong programming and scripting capabilities in Python, Go, Bash, or similar languages.</li><li>Experience building enterprise observability platforms using Prometheus, Grafana, Datadog, OpenTelemetry, distributed tracing, metrics, and logging solutions.</li><li>Proven expertise designing and implementing enterprise ChatOps architectures, operational workflows, and AI-enabled automation solutions.</li><li>Strong ability to assess technical debt, influence technical strategy, and drive platform modernization initiatives.</li><li>Experience using AI tools, LLM-powered assistants, and AI Agents to enhance engineering productivity and platform operations.</li><li>Experience with Kubernetes and container orchestration technologies such as EKS, GKE, or AKS preferred.</li><li>Familiarity with MLOps and LLM evaluation technologies including Kubeflow, Feast, LangSmith, RAGAS, Evidently AI, MLflow, and Weights & Biases preferred.</li><li>Knowledge of cloud cost optimization, FinOps, policy-as-code, compliance automation, and multi-cloud governance practices preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 04:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Quantitative Biomarker Scientist]]></title>
    <date><![CDATA[Tue, 22 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50738]]></requisitionid>
    <referencenumber><![CDATA[R50738]]></referencenumber>
    <apijobid><![CDATA[r50738]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50738/senior-quantitative-biomarker-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 is advancing its pipeline portfolio using a data-driven human translational approach. As part of this initiative, the Precision Medicine team is integrated with Discovery Research and Clinical Development teams to promote early adoption of biomarker strategy to guide clinical translation. The team collaborates with Clinical Sciences colleagues to develop the clinical experimental sciences (CES) studies for generating clinically testable, mechanistic hypotheses for each molecule, including developing scientific rationale for initial and new indications for PoC. Precision Medicine leads the biomarker strategy and execution, to achieve proof of mechanism/concept in early clinical trials. The team also implements Precision Medicine strategies, including patient stratification and selection, to support late-stage clinical programs and companion diagnostics.</p><br><p>This is a statistical computational role that falls within Precision Medicine Quantitative Translational Sciences (PMQTS), the analytical arm of Precision Medicine. We are looking for a motivated individual who can conduct clinical trial data management and data analysis in an open and collaborative working environment. This role will encompass exploratory analyses and visualization of omics, EHR, wearable sensor, imaging, and other biomarker data. This position is also involved in the development of tools and dashboards for processing, analyzing, querying, visualizing, and cleaning data. </p><br><p><strong>When & where:</strong></p><ul><li>Work Location:<strong> </strong>Tarrytown, NY or Armonk, NY</li><li>Work model/flexibility: : 4 days per week on site<br></li></ul><p><strong>Discover your role:</strong></p><ul><li>Liaise with Precision Medicine Quantitative Translational Sciences to analyze biomarker data types across a range of Precision Medicine and biomarker studies.</li><li>Provide computational and technical expertise on data cleaning and data visualization.</li><li>Integrate complex datasets to perform statistical analysis on exploratory biomarker data and clinical endpoints. Use technical tools, language, or custom coding and systems analysis to clean data and select or create datasets for analysis.</li><li>Understand and follow data quality concepts and best practices and tools. Identify data anomalies and work with data stewards in other units to perform root cause analysis on data quality issues.</li><li>Assist in the preparation of scientific presentations, manuscripts, and reports, including the preparation of quality checked tables and graphs depicting research results.</li><li>Effectively communicate analytical plans and timelines for multiple concurrent projects with study team members.</li><li>Develop, benchmark, and implement new computational workflows as necessary</li><li>Maintain best coding and data cataloguing practices for business consistency and scientific reproducibility.</li></ul><p><strong>This role requires:</strong></p><ul><li>PhD, or Masters with minimum 2 years of relevant work experience in one of the following or otherwise related quantitative fields: Computer Science, Computational Biology, Systems Biology, Quantitative Biology, Bioinformatics, Data Analytics, Statistics, Biostatistics, Mathematics, Applied Mathematics, Physics, Chemistry.</li><li>You have experience with statistical modeling/regression, machine learning, and other relevant data blending abilities.</li><li>You have experience in at least one of the following scripting languages: R, Python, MATLAB. Other languages such as SQL, Spark, and C++ are a bonus. </li><li>You have experience working in a Linux and/or cloud, shell scripting, and notebook environment.</li><li>You have knowledge of structured data, with the ability to perform data mapping for systems integration, data provisioning, and data consumption (strongly preferred).</li><li>You have a working knowledge of clinical trials (strongly preferred.)</li></ul><br><p>#PMQBS</p><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 23 Sep 2026 18:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff GMP Statistician]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49064]]></requisitionid>
    <referencenumber><![CDATA[R49064]]></referencenumber>
    <apijobid><![CDATA[r49064]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49064/staff-gmp-statistician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal or Staff Statistician to join our team, supporting advanced statistical leadership across a cross-functional, science-driven environment. In this role, you will drive root cause analysis, process improvement, and strategic deployment initiatives with a high degree of autonomy, while collaborating with manufacturing, quality, and executive stakeholders across Regeneron's manufacturing facility. This position offers the opportunity to apply cutting-edge statistical and modeling techniques that directly accelerate drug development and approval at a global scale.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30p</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead identification and implementation of strategic deployment initiatives, operating autonomously within a collaborative team environment</li><li>Apply advanced statistical modeling methods — including Bayesian and kinetic modeling — to historical data to accelerate process knowledge and inform earlier go/no-go decisions</li><li>Build, validate, and maintain automation frameworks within a GxP environment for routine statistical analyses and report generation</li><li>Use predictive models, process simulations, and forecasting techniques to enable early signal detection, proactive risk management, and optimized resource allocation</li><li>Drive root cause analysis and develop proactive metrics using data and statistical techniques to support continuous process improvement</li><li>Translate complex statistical findings into clear, actionable narratives through business analytics and data storytelling for executive audiences</li><li>Mentor colleagues within and outside the department on leading-edge statistical methodologies to deliver impactful, organization-wide results</li><li>May manage direct reports at this level</li><li>High-level proficiency in statistical software such as JMP, Minitab, R, or SAS</li><li>Experience with business analytics platforms such as Power BI or Tableau preferred</li><li>Deep expertise in diverse statistical methods including multivariate regression, design of experiments, difference and equivalency testing, and control charts</li><li>Proficiency in coding and automation of statistical analyses and dashboard reporting workflows</li><li>Experience building and maintaining automation frameworks in a GxP environment preferred</li><li>Strong written and oral communication skills, with demonstrated ability to present to executive audiences</li></ul><p><strong>This role requires:</strong></p><ul><li>Master’s degree in Statistics, Mathematics, or a related field</li><li>Principal: 7+ years of relevant experience</li><li>Staff: 9+ years of relevant experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$103,300.00 - $197,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Pharmacokineticist, PPK/PD]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50660]]></requisitionid>
    <referencenumber><![CDATA[R50660]]></referencenumber>
    <apijobid><![CDATA[r50660]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50660/pharmacokineticist-ppkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Pharmacokineticist for PPK/PD to serve as a senior independent contributor in the Translational Pharmacokinetics and Pharmacodynamics (TPK/PD) Group, taking ownership of PK/PD analyses end-to-end and serving as a pharmacokinetics point of contact across assigned studies. This person will independently plan and execute non-compartmental and compartmental PK/PD analyses in support of nonclinical and (potentially) clinical studies using Phoenix WinNonlin and other analysis software, and will prepare and quality-control standardized datasets from CRO and internal bioanalytical data for regulatory submission. This person will lead PK/TK protocol design/input, support CRO studies, produce Pharmacometrics deliverables and regulatory tables/figures/listings, contribute to standard-setting and best practices for the group, and mentor and provide technical guidance to junior analysts, following all SOPs to ensure GxP/GLP compliance.</p><br><p><strong>When & Where:</strong></p><br><p>This role will sit at our Tarrytown, NY office and is expected to be on-site 4 days per week.</p><br><p><strong>Discover Your Role:</strong></p><br><ul><li>Independently leads, performs, and takes ownership of non-compartmental PK and compartmental PK/PD analyses in support of nonclinical and (potentially) clinical studies, according to GxP as appropriate, and serves as the pharmacokinetics point of contact and lead analyst for assigned studies.</li><li>Conducts compliance-related activities (SOPs, etc.); ensures regulatory-submission conformance, data integrity, and GxP compliance; adheres to controlled SOPs; helps set group standards by authoring/revising SOPs and providing senior compliance review of others' deliverables; and meets mandatory-training and data-confidentiality requirements.</li><li>Owns the preparation, quality control, and senior review of standardized CDISC SEND datasets (e.g., PC/PP domains and associated SUPPQUAL) from CRO and internal bioanalytical data, with auditable, source-traceable derivations that conform to controlled terminology and regulatory-submission standards, and sets and maintains the dataset standards and conventions the group follows.</li><li>Owns and leads CRO study support; tracks study requirements, project priorities, status, and milestones; serves as the primary PK point of contact and liaison to CROs and functional groups; and drives coordination across the study lifecycle.</li><li>Independently owns and executes a broad array of work supporting department priorities in routine and non-routine Pharmacometrics deliverables on study design, analysis, and reporting, and sets methodology and best-practice standards for the group.</li><li>Produces and formats tables and listings (TFLs), including PK concentration and parameter summaries, for regulatory documents using validated tools (e.g., Phoenix WinNonlin, R), and owns, sets, and reviews against the group's consistent, submission-ready presentation standard.</li><li>Produces and reviews figures and graphical outputs (e.g., concentration-time profiles) for study reports and regulatory submissions using validated tools, and owns and sets the group's graphical presentation standard.</li></ul><br><p><strong>This Role Requires:</strong></p><br><ul><li>Bachelors degree with 5-7 years of professional experience, or a Masters degree with 3-5 years of professional experience</li><li>Strong, in-depth understanding of pharmacokinetics concepts and techniques</li><li>Proficient in relevant software, including Phoenix WinNonlin; knowledge of NLME/population PK a plus</li><li>Experience in animal PK/TK studies, including protocol design & study conduct</li><li>Able to clearly describe and perform advanced pharmacometric techniques, interpret results independently, and mentor and provide technical guidance to junior staff</li><li>Ability to help set group standards and best practices, with experience working in a GLP environment and following SOPs</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Strategic Finance (US)]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50689]]></requisitionid>
    <referencenumber><![CDATA[R50689]]></referencenumber>
    <apijobid><![CDATA[r50689]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50689/senior-manager-strategic-finance-us/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Strategic Finance to be a key business partner to Commercial Finance, Program Finance, R&D Finance, Strategic Alliances, and Alliance counterparts. The Senior Manager will manage multiple alliances in the Commercial and R&D stages to ensure adherence to contractual agreements and partner with alliance counterparts & internal stakeholders. This position is responsible for managing milestones and royalty obligations to and from Regeneron across all collaborations. This position will be responsible for consolidation of various alliance budgets including leading and executing the core processes for forecasting, budgeting, and analysis for decision support of Regeneron’s current and future alliance commercial products. This includes working closely with collaboration partner counterparts to analyze budget and actual information and working with Commercial Finance to consolidate Regeneron budgets, forecasts and management reporting. </p><br><p><strong>When & Where:</strong></p><p>This role will sit in our Sleepy Hollow, NY office and is expected to be on-site 4 days per week.</p><br><p><strong>Discover Your Role:</strong></p><ul><li>Oversee collaborations arrangements and work with functional finance teams and Strategic Alliances to manage deliverables and milestones</li><li>Lead, participate in and coordinate Joint Finance Committees for multiple collaborators and manage meeting materials (presentations, agendas, meeting minutes, etc.)</li><li>Proactively identify potential issues and work collaboratively with internal and external stakeholders to problem solve</li><li>Prepare financial analysis in support of ad hoc requests and various special projects for senior management</li><li>Work closely with internal Finance colleagues for corporate needs and deliverables associated with Alliance data including Quarterly Reforecasts</li><li>Manage overall milestone and royalty obligations to and from Regeneron across collaborations</li><li>Assist in analyzing quarterly budget to actual variance reports</li><li>Compile, develop and analyze commercial-related forecasts for partnered products in conjunction with internal Commercial/Medical Affairs Finance colleagues</li><li>Works with Accounting to reconcile quarterly actuals for purposes of settlement with collaborators</li></ul><br><p><strong>This Role Requires:</strong></p><br><ul><li>Bachelors degree and 8 years of relevant professional experience, or equivalent. Masters degree/MBA is preferred.</li><li>Experience in the pharmaceutical industry is highly preferred.</li><li>Ability to analyze commercial financial data and prepare clear, actionable management reports</li><li>Strong financial modeling skills</li><li>Strong presentation skills and executive presence</li><li>Experience with ERP financial applications (Oracle or Hyperion is a plus)</li><li>Basic understanding of Commercialization of products in Biotech/Pharma industry is a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Instrument Engineer]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49609]]></requisitionid>
    <referencenumber><![CDATA[R49609]]></referencenumber>
    <apijobid><![CDATA[r49609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49609/senior-instrument-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are looking for an experienced Instrument Engineer to join our team! Our Instrument Engineers support projects for new and/or replacement instruments and assure they are fit-for-purpose. We support investigations where measurement issues may be a contributing root cause, and we develop specifications and standards for instruments. In this role, you will support authoring and maintain configuration specifications for manufacturing equipment for the production of our life-changing products. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Onsite Monday-Friday, 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Operate as a project manager; plan, execute, and close projects within scope, time, and budget constraints</li><li>Specify cGMP process instrumentation, components, and spare parts</li><li>Set priorities for and complete Calibration Range and Tolerance Justifications forms for new instruments</li><li>Evaluate new instruments for Functional Equivalence to existing instrumentation that has become obsolete</li><li>Review and approve input/output lists for automated systems</li><li>Conduct troubleshooting and root cause analysis for complex instrumentation and associated systems</li><li>Create and maintain configuration specifications for cGMP manufacturing equipment</li><li>Assist in the design review of equipment, and approved supplier lists for instrumentation</li><li>Write and execute test plans to demonstrate instrument suitability</li><li>Implement corrective/preventative actions for existing equipment</li><li>Prepare engineering evaluations and test plans for change control documentation</li><li>Possibly supervise engineering contractors</li></ul><br><h3>This role requires:</h3><ul><li>BS/BA in Engineering; Electrical Engineering preferred and the following minimum years of relevant experience engineering experience for each level:<ul><li>Senior Instrument Engineer: 5+ years</li><li>Principal Instrument Engineer: 8+ years</li></ul></li><li>Understanding of common process instrumentation, including load cells, pressure transmitters/gauges, pH sensors, dissolved oxygen sensors, temperature sensors, mass flow meters, UV analyzers, conductivity sensors, TOC analyzers, and level sensors</li><li>Demonstrated ability to guide the prioritization, coordination, and completion of multiple projects within tight timeframes, while maintaining a high level of attention to detail</li><li>Ability to think independently to make quality decisions based on analyzing available and potentially limited information</li><li>Experience utilizing advanced problem-solving methods and leadership for investigations</li><li>Direct experience with biopharmaceutical process equipment is highly desirable</li><li>Understanding of process control systems and automation is preferred</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Visual Inspection Associate Program Manager]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50662]]></requisitionid>
    <referencenumber><![CDATA[R50662]]></referencenumber>
    <apijobid><![CDATA[r50662]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50662/visual-inspection-associate-program-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Visual Inspection Associate Program Manager to join our technical team, supporting our clinical and commercial fill/finish operations. In this role, you will lead the site’s visual inspection program — from inspection standards and regulatory compliance to equipment performance and technology innovation — while collaborating with Manufacturing Operations, Quality Assurance, Regulatory, and Process Development to ensure every dose meets the highest quality standards.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, NY</li></ul><ul><li>Work model: On-site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Leads the Visual Inspection Technical Services team and Defect Creation Lab, building a culture of quality and continuous improvement</li></ul><ul><li>Owns the site’s visual inspection program strategy, standards, and defect classification/acceptance criteria for liquid and lyophilized injectable products</li></ul><ul><li>Ensures inspection processes and documentation meet USP <1790>, EU Annex 1, 21 CFR Part 211, and applicable ICH/PDA guidance</li></ul><ul><li>Drives development of KNAPP/test sets and defect libraries used for operator and equipment qualification</li></ul><ul><li>Monitors and trends program KPIs, such as defect detection and false reject rates, to guide data-driven continuous improvement</li></ul><ul><li>Partners cross-functionally with Manufacturing, QA, Regulatory, Process Development, and EHS on inspection processes, equipment, and product quality</li></ul><ul><li>Evaluates emerging inspection technologies, including automated and AI/ML-based detection, to drive program innovation</li></ul><ul><li>Manages, coaches, and develops team members while maintaining cGMP and GDP compliance across the program</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Associate Manager Level: Bachelor’s degree in scientific or engineering discipline or related field and 6+ years of manufacturing experience, including prior supervisory experience or equivalent combination of education and experience</li></ul><ul><li>Experience in a cGMP fill/finish environment with exposure to visual inspection program elements</li></ul><ul><li>Demonstrated leadership experience managing technical teams within a regulated manufacturing environment</li></ul><br><p><strong>Preferred qualifications:</strong></p><ul><li>undefined</li></ul><ul><li>Demonstrated ownership of visual inspection program elements and applicable regulatory requirements</li></ul><ul><li>Experience evaluating or implementing automated and AI/ML-based inspection technologies</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 08:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Pathologist]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50767]]></requisitionid>
    <referencenumber><![CDATA[R50767]]></referencenumber>
    <apijobid><![CDATA[r50767]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50767/principal-pathologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together:</strong></p><br><p>The Pathology group within Regeneron’s Drug Safety and Pharmacometrics organization is looking for a Principal Pathologist who is excited to help advance innovative medicines from discovery through development. In this highly collaborative role, you will provide critical pathology expertise across the drug development continuum, including pathology peer review of Regeneron toxicology studies and close partnership with research scientists to support the discovery, characterization, and preclinical development of diverse therapeutic modalities, including large-molecule therapeutics, gene therapies, and oligonucleotide-based drugs targeting a broad range of diseases.</p><br><p><strong>When & Where:</strong></p><p>This position will be based on-site in our Tarrytown, NY offices four days per week.</p><br><p><strong>Discover Your Role:</strong></p><ul><li>Apply your expertise in toxicologic pathology to help shape research programs that support the discovery and development of transformative medicines.</li><li>Serve as the study pathologist for in-house discovery studies and produce high-quality pathology reports that inform scientific decision-making and support regulatory submissions.</li><li>Provide digital or glass-slide pathology peer review for Regeneron toxicology studies conducted at contract research organizations.</li><li>Leverage digital image analysis, when appropriate, to strengthen study interpretation and scientific insight.</li><li>Contribute to the continued development of a forward-looking, in-house digital pathology program.</li><li>Present your scientific contributions through internal and external forums that support regulatory and discovery programs.</li><li>Contribute to scientific publications, including manuscripts, abstracts, posters, and oral presentations.</li><li>Stay connected with the toxicologic pathology community through seminars, workshops, and conferences.</li></ul><p><strong> </strong></p><p><strong>This Role Requires:</strong></p><ul><li>DVM or PhD in Pathology</li><li>2 years of professional experience relevant to the position</li><li>Board certification in veterinary anatomic pathology (DACVP or DECVP). </li><li>Experience at a contract research organization is preferred. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Commercialisation Manager]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50428]]></requisitionid>
    <referencenumber><![CDATA[R50428]]></referencenumber>
    <apijobid><![CDATA[r50428]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50428/commercialisation-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Commercialization Manager Immunology Respiratory Spain to join our Commercial Immunology team, supporting Spain in a hybrid work model. In this role, you will create and complete local commercialization activities across respiratory indications, drive market development and commercial performance, and represent Regeneron in alliance partnerships while collaborating with sales, marketing, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Madrid, Spain</p><p>Hybrid work model</p><br><p><strong>Discover your role:</strong></p><ul><li>Cooperate with alliance partners to implement local immunology commercialization strategies across respiratory indications.</li><li>Partner with the Sales team to provide training and direction that supports execution of strategic priorities.</li><li>Support implementation of local tactical plans and develop sales support materials that enable effective field execution.</li><li>Track agreed key performance indicators (KPIs) to identify opportunities for early course correction and optimize execution of key tactics.</li><li>Collaborate with regional and global marketing teams to provide local market insights, advise strategy, and support brand planning activities.</li><li>Support commercial training efforts for our local Salesforce team</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required; MBA preferred and 5+ years of experience in marketing and/or alliance management in the pharmaceutical industry.</li><li>Proficiency in Spanish and English.</li><li>Established track record of success in pharmaceutical marketing roles.</li><li>Outstanding knowledge of specialty care commercialization in Spain.</li><li>Strong business acumen and analytical capabilities.</li><li>Experience in immunology and/or respiratory therapeutic areas preferred.</li><li>Product launch experience preferred.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€58,200.00 - €97,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 05:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Madrid Toledo (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50494]]></requisitionid>
    <referencenumber><![CDATA[R50494]]></referencenumber>
    <apijobid><![CDATA[r50494]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50494/sales-representative-madrid-toledo-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Madrid Toledo</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Representative - Alicante (Inmunología Respiratorio)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50490]]></requisitionid>
    <referencenumber><![CDATA[R50490]]></referencenumber>
    <apijobid><![CDATA[r50490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50490/sales-representative-alicante-inmunologia-respiratorio/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Representative to join our Immunology team, supporting our Spanish Respiratory business in a field-based work model. In this role, you will drive commercial performance across your territory through strategic account management, customer engagement, and implementation of sales and marketing plans while collaborating with medical colleagues and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Spain, Alicante</p><p>Work model: Field-based</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop positive relationships with key healthcare professionals, effectively communicating the value of our portfolio.</p></li><li><p>Execute the brand strategy within the territory through high-quality scientific and commercial interactions.</p></li><li><p>Design and implement territory plans aligned with the national strategy, leveraging data and market insights.</p></li><li><p>Identify, segment, and prioritize key accounts and stakeholders to maximize impact and patient access.</p></li><li><p>Collaborate with medical and cross-functional teams to implement regional initiatives and programs.</p></li><li><p>Utilize both in-person and digital channels to optimize customer engagement and brand presence.</p></li><li><p>Monitor market trends and competitor activity, sharing relevant insights with the broader organization.</p></li><li><p>Thrive in a newly established, high-performance environment while fostering collaboration both within and outside the company.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Bachelor's degree or equivalent, preferably in Life Sciences, Pharmacy, Chemistry, or Biology and 5+ years of sales experience within the biotechnology or pharmaceutical industry.</p></li><li><p>Proven track record to manage territories, key accounts, account planning, targeting, and segmentation activities.</p></li><li><p>Experience communicating scientific and commercial messages to healthcare professionals.</p></li><li><p>Strong capability to utilize multiple customer engagement channels, including face-to-face interactions, remote calls, approved emails, and digital platforms.</p></li><li><p>Experience working as part of an alliance is highly desirable.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Global Site Start Up Lead]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50818]]></requisitionid>
    <referencenumber><![CDATA[R50818]]></referencenumber>
    <apijobid><![CDATA[r50818]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50818/temp-global-site-start-up-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Manager, Global Site Start-Up Lead (SSU Lead) is responsible for driving the global execution of site activation for clinical trials, performing the role with moderate oversight 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.</p><br><p><strong>When & where:</strong></p><p>Location: Armonk, or Warren</p><p>Work model/flexibility: in office 3-4 days per week</p><p>May require up to 25% travel<br><br></p><p><strong>Discover your role:</strong></p><br><p>Site Start-up Strategy</p><ul><li>Develop the site start up strategy for each study, outlining all dependencies impacting site activation and actively mitigating and escalating risks. Oversee the tracking and analysis of study metrics, including risks and mitigation strategies and to evaluate CRO performance and implement corrective actions.<ul><li>Advocate for optimized site selection strategies, leveraging data-driven insights to guide cross-functional teams toward effective decision-making.</li></ul></li><li>Lead the development, assessment, and alignment of site activation projections, ensuring cross-functional and CRO collaboration to meet strategic objectives.<ul><li>Ensure comprehensive and compliant documentation of site start-up materials in the Trial Master File (TMF) to maintain inspection readiness.</li></ul></li></ul><p>Country Start-up</p><ul><li>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. <ul><li>Monitor and maintain country intelligence data to support informed decision-making and develop accurate startup projections and strategic plans.</li><li>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.</li></ul></li><li>Ensure timely country submission deliverables (ensure task completion; all roles clarity, identification of critical path items, effective communication pathway). </li></ul><p>Site Start up Management</p><ul><li>Lead and oversee all aspects of site start-up activities, including fast-track site initiation, site calls, document collection, and milestone tracking, ensuring timely and efficient completion of processes.</li><li>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.</li><li>Oversee CRO site start up management or in house site facing regional SSU team, where applicable<ul><li>Lead the collection and analysis of site intelligence to support strategic site selection and site start-up.</li><li>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.</li></ul></li></ul><p>Team Interactions</p><ul><li>Represent SSU on cross-functional teams, providing updates, escalating challenges, and proposing mitigation strategies for site start-up issues.</li><li>Act as the escalation point for CRO and internal team to ensure timely SSU issue resolution </li></ul><p>Process Improvement</p><ul><li>Recommends and participates in cross functional and department process improvements.<br></li></ul><p><strong>Minimum Years of Experience: </strong></p><p>At least 7 years of relevant experience in the biotechnology/pharmaceutical industry.</p><br><p>Masters/MBA/PharmD with 5+ years of relevant industry experience.<br></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Muscle Biology & Energy Metabolism]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50757]]></requisitionid>
    <referencenumber><![CDATA[R50757]]></referencenumber>
    <apijobid><![CDATA[r50757]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50757/senior-scientist-muscle-biology-energy-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Scientist to join the Obesity, Metabolism and Muscle Diseases Group to support the identification and validation of novel drug targets for metabolic disorders. This is a lab-based role for a scientist with a strong foundation in skeletal muscle physiology and energy metabolism. The ideal candidate can independently design and conduct in vitro and in vivo studies while collaborating and communicating efficiently across the group and other teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where</strong></p><ul><li>Location: Tarrytown, NY</li></ul><ul><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role</strong></p><ul><li>Identify and implement novel areas, technologies and approaches for validating muscle-related targets and target modalities in metabolic disease drug discovery</li></ul><ul><li>Design and conduct in vitro (e.g. primary and/or iPSC-derived myotube/myofiber models) and ex vivo (e.g. biomarker testing via ELISA) assays to support target validation</li></ul><ul><li>Design and perform in vivo studies in animal models to characterize muscle and/or metabolic phenotypes, and provide mechanistic insights into the underlying biology</li></ul><ul><li>Apply muscle histological approaches (e.g. IHC/IF, fiber-typing, in situ activity assays, in situ hybridization) to complement molecular and functional readouts</li></ul><ul><li>Analyze data, draw scientifically sound conclusions and identify knowledge gaps</li></ul><ul><li>Provide timely updates on scientific progress, communicating efficiently across teams and functions</li></ul><ul><li>Thrive in a fast-paced, multi-project environment, staying detail-oriented and well-organized</li></ul><ul><li>Work well both independently and as part of a team</li></ul><ul><li>Bring curiosity and a desire to expand your areas of expertise as new questions arise</li></ul><br><p><strong>This role requires</strong></p><ul><li>Ph.D. with a minimum of 3 years of post-doctoral research experience</li></ul><ul><li>Broad expertise in skeletal muscle biology and energy metabolism (e.g., muscle bioenergetics, substrate utilization, mitochondrial function, muscle-organ crosstalk), with clear relevance to obesity, diabetes, lipid metabolism or endocrinology</li></ul><ul><li>Ability to independently design and perform complex in vitro and in vivo studies, interpret data, and summarize results</li></ul><ul><li>Passion and creativity to generate and pursue independent research ideas to advance drug discovery and development</li></ul><ul><li>Excellent communication and presentation skills, with a strong record of scientific publications</li></ul><ul><li>Preferred: experience with muscle histological techniques</li></ul><ul><li>Preferred: strong understanding of human and mouse genetics</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 11:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Strategic Partnerships & Business Operations]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50748]]></requisitionid>
    <referencenumber><![CDATA[R50748]]></referencenumber>
    <apijobid><![CDATA[r50748]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50748/director-strategic-partnerships-business-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<br><p><strong> Build our future together</strong></p><br><p>The Director, Strategic Partnerships and Business Operations is responsible for overseeing and ensuring compliance across a large portfolio of global investment and data licensing collaborations involving genetic and associated health data. This leader will be responsible for tracking and monitoring the research, business and finance deliverables of each collaboration, maintaining compliance and reporting out to leadership on the status of the active portfolio. The Director will be responsible for overseeing data governance, collaboration finance, strategic vendor contracting and Confidential Disclosure Agreement (CDA) processing, working in collaboration with senior leaders in research program management, business, legal and finance. The Director will oversee several headcount, both directly and indirectly in the management of this portfolio. </p><br><p><strong>When & where: </strong></p><ul><li>Location: Tarrytown, NY or Cambridge, MA</li><li>Work model/flexibility: 4 days onsite</li></ul><br><p><strong>Discover your role: </strong></p><br><ul><li>Track and manage compliance across a portfolio of 155+ global data licensing collaborations involving genetic and associated health data, including ongoing monitoring, risk assessment, and remediation.</li><li>Oversee the development and operationalization of RGC data governance policies, procedures, consent frameworks, data use agreements, specific to genetic and health data; collaborate with the Privacy Office on privacy impact assessments and other regulatory requirements</li><li>Lead, mentor, and develop a team of data governance and compliance professionals; foster a culture of accountability, transparency, and continuous learning.</li><li>Collaborate cross-functionally with Legal (including the Privacy Office), IT Security, Research, and Business Development to embed privacy-by-design into data collaboration workflows and new initiatives.</li></ul><br><p><strong>This role requires: </strong></p><br><ul><li>Master's degree in Genetics, Business, Legal, Bioethics, Life Sciences, or a related field; OR relevant degree with experience in contract compliance and sponsored research. </li><li>An equivalent combination of advanced education and 15+ years of directly relevant experience may be considered.</li></ul><ul><li>Minimum 10 years of progressive experience in contracting, alliance/portfolio management or compliance, with at least 5 years focused on genetic or health data in a research, biopharmaceutical, or biotech setting.</li><li>Strong knowledge of genomic data governance frameworks, international privacy laws, including the NIH Genomic Data Sharing Policy and GA4GH standards.</li><li>Exceptional written and verbal communication skills, with the ability to translate complex regulatory requirements for scientific, and executive audiences.</li><li>Proven leadership ability with experience building and managing high-performing compliance teams.</li></ul><p>#RGC</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 08:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Translational PK/PD Modeling]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47275]]></requisitionid>
    <referencenumber><![CDATA[R47275]]></referencenumber>
    <apijobid><![CDATA[r47275]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47275/associate-director-translational-pkpd-modeling/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of Translational/Preclinical Modeling develops and implements quantitative and mechanistic PK/PD models to aid in the understanding of target biology, therapeutic modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic direction of modeling and simulation sciences.</p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Independently develops and implements quantitative and mechanistic mathematical PK/PD models that inform preclinical-to-early clinical translation, including human efficacious dose predictions and first-in-human dose selection.</p></li><li><p>Actively contributes to the advancement and strategic direction of modeling and simulation sciences</p></li><li><p>Provides expert support to pre-clinical PK/PD project representatives and R&D project teams to design, execute and interpret in vitro and in vivo quantitative pharmacology studies. This included working with the Research PK group to optimize use of mouse PK data to inform translation to nonhuman primate and human PK.</p></li><li><p>Effectively integrates and summarizes modeling and simulation analyses into useable information for multidisciplinary project teams.</p></li><li><p>Remains apprised of emerging science and literature, and effectively collaborates with subject matter experts in Clinical Pharmacology, Quantitative Pharmacology and R&D to advance modeling and simulation sciences.</p></li><li><p>Presents work at internal/external scientific meetings and publishes work in scientific journals</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>Experience using one or more modeling and simulation platforms (e.g., Phoenix NLME, NONMEN, Monolix, ADAPT, MATLAB, SimBiology, etc.)</p></li><li><p>Strong theoretical and practical foundation in pharmacokinetics, including non-compartmental, compartmental, PK/PD and PBPK.</p></li><li><p> Effectively work in a fast-paced, highly-matrixed team-based environment and leverages scientific reasoning to influence key stakeholders.</p></li><li><p>Ability to learn new areas of biological sciences to develop quantitative and mechanistic PK/PD models for emerging therapeutic modalities.</p></li><li><p>Familiarity with biotherapeutic modalities, including monoclonal and bispecific antibodies, gene therapy, CAR-T, siRNAs and other targeting agents preferred</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><p>Ph.D. or M.S. in pharmacokinetics, pharmaceutical sciences, engineering, applied mathematics or related disciplines with a track record of applying quantitative and mechanism-based PK/PD modeling and simulation approaches to advance the discovery and development of therapeutics. Greater than 6 years of pharmaceutical industry or related experience in developing and applying mechanism-based PK/PD models to guide R&D teams from early discovery to IND-stage clinical development.</p><p><strong> </strong></p><p><strong> </strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Downstream Purification, Analytics, & Bioconjugate Process Development]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51018]]></requisitionid>
    <referencenumber><![CDATA[R51018]]></referencenumber>
    <apijobid><![CDATA[r51018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51018/2027-co-op-downstream-purification-analytics-bioconjugate-process-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Downstream Purification & Bioconjugate Process Development to join our Preclinical Manufacturing and Process Development (PMPD) team, which develops the manufacturing processes used to scale up and produce Regeneron's medicines.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support the purification of medicines using chromatography, filtration, and resin-development techniques</li></ul><ul><li>Develop and qualify new analytical resins and liquid chromatography methods used to evaluate process impurities</li></ul><ul><li>Contribute to chemistry work used to attach drug payloads to antibodies and characterize resulting impurities</li></ul><ul><li>Run small-scale lab experiments to evaluate purification process performance</li></ul><ul><li>Analyze historical process data to identify trends and improvement opportunities</li></ul><ul><li>Collaborate with process scientists and engineers to solve purification challenges</li></ul><ul><li>Document experimental results and contribute to technical reports</li></ul><ul><li>Present findings to the broader development team</li></ul><br><p><strong>Relevant majors: </strong>Chemical/Biochemical Engineering, Biochemistry, Biological Sciences</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Drug Product Development and Technology]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51033]]></requisitionid>
    <referencenumber><![CDATA[R51033]]></referencenumber>
    <apijobid><![CDATA[r51033]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51033/2027-co-op-drug-product-development-and-technology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Drug Product Development and Technology, including formulation development, analytical development, drug product process development and new Technology for drug delivery, to join our team, which determines how molecules are turned into stable, patient-ready medicines.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support studies that determine what goes into a medicine beyond the active ingredient, including stabilizers, buffers, and delivery vehicles</li><li>Conduct stability and degradation studies on drug formulations</li><li>Perform analytical characterization using techniques such as high-performance liquid chromatography (HPLC), mass spectrometry, and capillary electrophoresis</li><li>Support high-throughput formulation screening experiments</li><li>Contribute to building artificial intelligence and machine learning (AI/ML) models that predict formulation behavior</li><li>Analyze data from formulation experiments to guide next steps</li><li>Document experimental results and contribute to technical reports</li><li>Collaborate with formulation scientists across lab- and data-focused projects</li></ul><br><p><strong>Relevant majors: </strong>Chemistry, Biochemistry, Analytical Chemistry, Organic Chemistry, Biophysics, Pharmacy/Pharmaceutical Sciences, Chemical/Biomedical Engineering</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Medical Affairs Operations, France]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49885]]></requisitionid>
    <referencenumber><![CDATA[R49885]]></referencenumber>
    <apijobid><![CDATA[r49885]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49885/manager-medical-affairs-operations-france/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Manager, Medical Affairs Operations, France</h3><p><strong>Build</strong> <strong>our</strong> <strong>future</strong> <strong>together:</strong> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Manager, Medical Affairs Operations, France</strong> to join our Medical Affairs team in France, supporting our country organisation in a hybrid work mode. In this role, you will deliver compliant country Medical Affairs activities while collaborating with local Medical Affairs colleagues and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When</strong> <strong>&</strong> <strong>where:</strong> Paris, office-based - Hybrid</p><h3><strong>Discover</strong> <strong>your</strong> <strong>role:</strong></h3><ul><li>Maintain audit readiness through documentation, tracking, and records management.</li><li>Optimise transparency reporting, Anti-Bribery and Anti-Corruption documentation, and compliance processes.</li><li>Complete assigned medical activities in local systems through regulatory and GxP completion.</li><li>Localize global, regional, and local standard operating procedures and work instructions.</li><li>Handle vendor onboarding, contracts, purchase orders, budgets, and expense reconciliation.</li><li>Coordinate medical meetings, congress logistics, agenda flow, actions, and follow-up.</li><li>You bring structure and service focus to cross-functional Medical Affairs operations.</li></ul><h3><strong>This</strong> <strong>role</strong> <strong>requires:</strong></h3><ul><li>Bachelor’s degree in life sciences, business, or a related field, or equivalent experience.</li><li>7+ years in Medical Affairs operations, coordination, project support, or administration.</li><li>Pharmaceutical or biotech environment experience.</li><li>Experience in a country organization or local operating company.</li><li>Solid understanding of compliance, transparency, and regulated country-level processes.</li><li>Fluency in French, with business-proficient English preferred.</li><li>Microsoft Office and relevant systems experience, including Veeva CRM, Vault Medical, PromoMats, and procurement tools.</li><li>Occasional business travel as required.</li><li>Country Medical Affairs operations experience, including event and congress planning.</li><li>Contract and procurement systems knowledge, such as iCertis or SAP.</li><li>Experience partnering with Finance and Procurement teams.</li><li>Commercial operations experience desirable.</li><li>Strong organization, communication, stakeholder management, and cross-functional collaboration skills.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€60,750.00 - €101,250.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Development Program Management]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51217]]></requisitionid>
    <referencenumber><![CDATA[R51217]]></referencenumber>
    <apijobid><![CDATA[r51217]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51217/director-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>This role (Director, Development Program Management) uses extensive program management knowledge and experience in the drug development industry to provide operational leadership, direction, and support to assigned development program(s) and/or portfolio(s). This individual is expected to drive the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and monitor the execution of these plans from preclinical through commercialization/lifecycle management. Responsibilities may also include coaching and mentorship of junior colleagues, managing direct reports, working with collaborators, and contributing to departmental initiatives. This is a leadership role within the department and organization thus this individual is expected to independently execute responsibilities, interact effectively with senior leadership, and influence the direction and outcomes of assignments. </p><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY</li><li>Additional Locations: Warren, NJ or Cambridge, MA</li></ul><p><strong>Discover your role:</strong></p><ul><li><strong>Development Teams: </strong>Partners with the Global Program Head to drive strategic program teams (SPT) and sub teams by leading key governance meetings. Uses broad knowledge of drug development and project/program management coupled with leadership and problem-solving skills to align development teams around an integrated project/program plans, timelines and budgets based on program vision. Ensures efficient delivery of plans. Proposes and aligns annual program goals with program strategy and Regeneron’s corporate goals. Monitors progress against program goals and ensures accurate and timely reporting of program progress to management. Anticipates issues and program risks and drives timely development of risk management plans and issue resolution.</li><li><strong>Business Acumen: </strong>Utilizes knowledge of industry trends to identify risks/threats/opportunities and translates these to actionable activities for the development teams. Able to leverage political savvy and awareness of team dynamics to effectively drive decision making and achieve desired outcomes. Is proficient in project management planning systems (MS Project, SharePoint) and tools/techniques. Understands how systems and tools can be leveraged to move the program and business forward.</li><li><strong>Communication:</strong> Effective and trusted communicator that will develop a proven track record across the organization. Works effectively with different styles and adapts approaches in a cross-functional matrix environment to drive results. Establishes a culture which promotes and encourages open communication, transparency, accountability and learning from mistakes.</li><li><strong>Problem Solving: </strong>Is proficient at proactively identifying and critically analyzing potential problems that may affect the project, processes, or the team. Uses extensive industry and professional experience and knowledge to develop viable, long-term solutions to cross-functional, project, process, or team issues, driving alignment with impacted stakeholders. Proactively implements lessons learned/best practices across programs/TA and department to help other teams preempt or mitigate problems.</li><li><strong>Leadership</strong>: Strengthens teams and continuously works to drive teams to be high performing and efficient. Ability to align team members towards a common goal through expertise with conflict management, self/social awareness, and diverse team dynamics.</li></ul><p><strong>This role requires:</strong></p><ul><li>Minimal educational requirements: Bachelor’s Degree </li><li>12+ years of relevant broad project / program management experience required, preferably in the pharmaceutical or related industry </li><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels both internal and external to the company in order to establish credibility with professionals on the project teams. </li><li>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 entrepreneurial organizations; expert in dealing with ambiguity and uncertainty </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Biologics Drug Product Development (DPDT)]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49363]]></requisitionid>
    <referencenumber><![CDATA[R49363]]></referencenumber>
    <apijobid><![CDATA[r49363]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49363/principal-scientist-biologics-drug-product-development-dpdt/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Principal Scientist</strong> to join our Drug Product Development & Technology (DPDT) team. You'll lead drug product development activities from candidate selection and pre-clinical development through clinical development and commercialization for a variety of drug modalities, which may include protein (antibody), siRNA, peptides, bioconjugates (antibody-oligo or antibody-drug), and AAV, across a variety of drug and delivery presentations including liquid and lyophilized DP and novel drug delivery technologies. You'll work independently to lead your project/program(s), applying biochemical, biophysical, and/or microbiology principles to execute both simple and complex experiments and processes.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Shift Requirements: Full-time, standard business hours, with flexibility to support before- and after-hours executive meetings, town halls, and corporate events</li><li>Location: On-site in Tarrytown, NY</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Works independently and applies technical knowledge to design rigorous experiments that may include formulation, analytical, and process development and technology transfer</li><li>Acts as a resource and is recognized as a subject matter expert (SME) within their field; applies QbD approaches to drug product development and stays knowledgeable about current regulatory guidelines</li><li>Applies scientific and statistical knowledge of software packages (JMP or equivalent) to support study design and data analysis</li><li>Independently makes decisions of moderate complexity in a timely manner, including with limited information, understanding how decisions impact target priorities and cross-functional teams; uses a risk-based approach to make complex decisions and demonstrates judgment on when feedback from management is needed</li><li>Receives information and direction from leadership, and is responsible for planning and leading complex, long-term projects</li><li>Collaborates effectively as an SME and within cross-functional teams to support timely execution of deliverables</li><li>Proactively researches and implements new approaches toward problem-solving and/or process optimization for product development and new technology evaluations; capable of diving into novel fields and developing expertise needed in new areas or technologies</li><li>Brings managerial experience with demonstrated success developing direct reports; trains junior scientists in technical skills and mentors junior colleagues</li><li>Communicates effectively with varied audiences internally and externally, clearly explaining technical data that support recommendations or strategic direction</li><li>Participates in team meetings and prepares data presentations and documents, including publications and patents</li><li>Generates internal reports and authors external documents, which may include protocols, technical reports, risk assessments, regulatory documents, and patents</li><li>Maintains complete and accurate laboratory record documentation and complies with all data integrity procedures and system requirements, including ELN, SDMS, LIMS, and EDMS</li><li>Engages in lab and instrument maintenance activities, acting as instrument SME or team lead, and may champion implementation of new instrumentation and analytical techniques</li><li>Complies with environmental, health, and safety requirements</li></ul><h3><strong>This role requires:</strong></h3><ul><li>A PhD in Pharmaceutical Sciences, Biochemistry, Chemistry, Biophysics, Biomedical or Chemical Engineering, or a related field with 4+ years of relevant industry experience in the biopharma space; or a BS/MS with a minimum of 10 years, of relevant industry experience</li><li>Industry experience with bioconjugates, particularly antibody-oligonucleotide formulation development, is preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer I - Purification Data Analysis]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48653]]></requisitionid>
    <referencenumber><![CDATA[R48653]]></referencenumber>
    <apijobid><![CDATA[r48653]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48653/process-development-engineer-i-purification-data-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[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Process Development Engineer I</strong> to join our Purification Development team within Preclinical Manufacturing and Process Development (PMPD) in an on-site capacity. In this role, you will develop, build, and deploy analyses, visualizations, and data solutions that support purification process development, working at the intersection of software engineering, data science, and bioprocess domain expertise, while collaborating with scientists and process engineers across Purification's varied subgroups.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li>Location: On-site in Tarrytown, NY</li><li>Work model/flexibility: Onsite, full-time</li></ul><br><h3><strong>What you'll do:</strong></h3><ul><li>Partner closely with scientists, engineers, and analysts to understand purification development workflows and identify high-impact opportunities to improve data flows</li><li>Aggregate, clean, and structure complex datasets to enable scalable, repeatable analyses and visualizations</li><li>Design, develop, and apply statistical and modeling techniques to drive data-informed decision-making and accelerate daily operations</li><li>Deploy data pipelining and aggregation tools that help engineers easily find the data they need and derive insights</li><li>Maintain communication with Purification and IT stakeholders to evaluate solutions</li><li>Collaborate with data scientists and engineers across PMPD to improve best practices and teach citizen developers</li><li>Enhance, maintain, and extend existing analytics tools and platforms to support new use cases and evolving business needs</li><li>Contribute as an active member of Agile teams within a Scaled Agile Framework (SAFe), supporting planning, delivery, and continuous improvement</li></ul><h3><strong>This role might be for you if you have:</strong></h3><ul><li>Analytical rigor and creative problem-solving skills</li><li>The ability to drive projects autonomously while thriving in cross-functional teams</li><li>Excellent written and verbal communication skills</li><li>A passion for innovation and continuous learning</li></ul><br><h3><strong>Let's find out if we're a fit:</strong></h3><br><h3><strong>Must-haves:</strong></h3><ul><li>Master's degree in Chemical Engineering, Biomedical Engineering, Computer Science, or a related discipline with 0-3 years of experience, or a Bachelor's degree with 3+ years of experience in bioprocess development, pharmaceutical manufacturing, or a closely related domain</li><li>Demonstrated ability to design and develop data tools to solve complex, real-world problems</li><li>Programming skills in Python and SQL, with an understanding of data modeling and database design</li><li>Experience working in Linux/Unix environments and using Git for version control and collaboration</li></ul><br><h3><strong>Preferred / nice-to-haves:</strong></h3><ul><li>Excellent communication skills and a collaborative mindset, with the ability to partner effectively with scientists, engineers, and analysts while mentoring citizen data scientists</li></ul><br><h3><strong>Thrive today. Grow tomorrow.</strong></h3><ul><li>Student Loan Paydown program & Tuition Reimbursement</li><li>Family Care Benefits</li><li>Relocation Assistance</li><li>Inclusion, Culture and Well-Being programs (including physical & mental health)</li></ul><p><strong>#pmpd</strong></p><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 09:26:17 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist, Medical Coding]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50665]]></requisitionid>
    <referencenumber><![CDATA[R50665]]></referencenumber>
    <apijobid><![CDATA[r50665]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50665/specialist-medical-coding/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. </p><br><p>We are seeking a Specialist, Medical Coding to join our Clinical Data Management team. In this role, you will support the accurate, consistent, and timely coding of clinical trial data using MedDRA and WHODrug dictionaries. You will work with study teams and cross-functional partners to review and reconcile coded data, support study milestones, and help deliver high-quality, inspection-ready clinical data.</p><p><strong>When & where: </strong></p><p>Hyderabad (hybrid) </p><br><p><strong>Discover your role: </strong></p><ul><li>Perform medical coding for assigned studies using MedDRA and WHODrug dictionaries in line with company conventions, study requirements, and established procedures. </li></ul><ul><li>Review auto-coded and manually coded terms to support coding accuracy, consistency, and quality. </li></ul><ul><li>Contribute to Medical Coding Plans and support coding-related study setup activities within medical coding systems. </li></ul><ul><li>Work with EDC Programmers and study teams to implement coding requirements in clinical systems. </li></ul><ul><li>Assist with testing and validating coding configurations and reports. </li></ul><ul><li>Maintain study-specific coding documentation and apply relevant coding conventions and guidelines. </li></ul><ul><li>Support coding reconciliation between Clinical Data Management and Drug Safety. </li></ul><ul><li>Collaborate with Clinical Data Managers, Medical Monitors, Clinical Scientists, Drug Safety, Biostatistics, CROs, and other partners to resolve coding issues and queries. </li></ul><ul><li>Identify coding issues, data quality concerns, and study risks, and escalate them when needed. </li></ul><ul><li>Support database lock activities and ensure coding documentation and milestone deliverables are inspection-ready. </li></ul><ul><li>Participate in the evaluation and improvement of medical coding systems, automation tools, and AI-assisted coding solutions. </li></ul><ul><li>Contribute to process improvements, training, and knowledge-sharing activities.</li></ul><br><p><strong>This role requires: </strong></p><ul><li>A bachelor's degree in Pharmacy, Life Sciences, Nursing, or a related healthcare field. </li></ul><ul><li>At least 2 years of medical coding experience within biotechnology, pharmaceutical, CRO, or a health-related industry. </li></ul><ul><li>Experience performing clinical data management medical coding using MedDRA and WHODrug dictionaries. </li></ul><ul><li>Working knowledge of MedDRA and WHODrug conventions, hierarchy structures, and coding practices. </li></ul><ul><li>Working knowledge of medical coding systems such as Medidata Rave Coder. </li></ul><ul><li>Strong knowledge of medical and medication terminology within clinical development. </li></ul><ul><li>Experience supporting study setup, coding documentation, coding queries, and coding quality reviews. </li></ul><ul><li>Familiarity with coding reconciliation between Clinical Data Management and Drug Safety. </li></ul><ul><li>An understanding of clinical development processes and cross-functional interactions. </li></ul><ul><li>Basic knowledge of 21 CFR Part 11, ICH-GCP, GxP, GDPR, and applicable regulatory requirements. </li></ul><ul><li>Strong analytical, organizational, problem-solving, communication, and attention-to-detail skills. </li></ul><ul><li>The ability to manage assigned deliverables, meet study timelines, and collaborate with cross-functional teams and external partners. </li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro) -Dayton, Ohio]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50965]]></requisitionid>
    <referencenumber><![CDATA[R50965]]></referencenumber>
    <apijobid><![CDATA[r50965]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50965/medical-specialist-i-gastro-dayton-ohio/]]></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><br>Job Description</p><br><p><strong>Build our future together:</strong></p><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p><strong>When & where:</strong></p><ul><li>Remote role</li><li>Location: Dayton, Ohio </li></ul><p><strong>Discover your role:</strong></p><ul><li>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</li><li>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)</li><li>Demonstrate advanced clinically-based selling skills</li><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</li><li>Results oriented with a proven track record of success with product launches</li><li>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>Experience with in-servicing and training office staff, nurses and office managers</li><li>Ability to partner and collaborate with other internal field teams and alliance partners</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</li><li>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</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Data Validation Strategy]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51019]]></requisitionid>
    <referencenumber><![CDATA[R51019]]></referencenumber>
    <apijobid><![CDATA[r51019]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51019/associate-director-data-validation-strategy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Data Validation Strategy join our Clinical Data Management organization, leading the strategy and execution of integrated data review, helping ensure our clinical data is high-quality and inspection-ready. You will collaborate with Biostatistics, Clinical Data Reporting, Quantitative Innovation and Statistical Strategy (QISS), and study teams. </p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & wher</strong>e</p><p>• Location: Warren, NJ, Armonk or Tarrytown, NY</p><p>• Work model: Primarily on-site with hybrid flexibility</p><p>• Travel percentage: Up to 25%</p><br><p><strong>Discover your role</strong></p><p>• Lead the implementation and execution of the Integrated Data Review (IDR) strategy, operating model, standards, and governance</p><p>• Oversee the development, execution, and quality of Data Review Plans (DRPs), including issue tracking, escalation, and resolution</p><p>• Partner with Biostatistics, QISS, Clinical Data Reporting, and study teams delivering risk-based data review aligned with critical-to-quality factors</p><p>• Monitor performance through KPIs and quality metrics to identify trends and drive continuous improvement</p><p>• Support the development of SOPs, work instructions, templates, and training materials for IDR activities</p><p>• Lead training, coaching, and change management to drive adoption of IDR across clinical and external data domains</p><p>• Drive innovation, automation, and AI-enabled analytics initiatives </p><p>• Manage, mentor, and develop the Integrated Data Review and Quality team</p><br><p><strong>This role require</strong>s</p><p>• Bachelor's degree in Life Sciences, Statistics, Computer Science, or a related field</p><p>• 10+ years of Clinical Data Management experience within the biotechnology, pharmaceutical, or healthcare industry and 5+ years of people, team, and project leadership experience</p><p>• Experience implementing integrated data review, quality management, risk-based data management, or centralized review processes</p><p>• Strong working knowledge of ICH E6 (R3), ICH E8 (R1), GxP, 21 CFR Part 11, and RBDM/RBQM principles</p><p>• Experience supporting inspection readiness activities</p><p>• Experience with data review tools, visualization, and analytics for proactive issue detection</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[International Payroll Analyst]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51386]]></requisitionid>
    <referencenumber><![CDATA[R51386]]></referencenumber>
    <apijobid><![CDATA[r51386]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51386/international-payroll-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an International Payroll Analyst to join our payroll function, supporting our international countries in a hybrid setting. In this role, you will deliver accurate, compliant, timely payroll while collaborating with in-country vendors, Human Resources and Finance. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Dublin (Hybrid)</p><br><h3><strong>Disc</strong>over yo<strong>ur role:</strong></h3><ul><li>Prepare, validate and reconcile Irish and international payroll inputs and outputs.</li><li>Manage end-to-end vendor cycles: submission, variance review, approval and funding.</li><li>Ensure statutory compliance, including Irish Pay As You Earn, Pay Related Social Insurance, Universal Social Charge and Revenue reporting.</li><li>Process starters, leavers, benefits, allowances, bonuses and equity events.</li><li>Reconcile payroll to the general ledger monthly, supporting audits and year-end filings.</li><li>Support mobile employees through tax equalisation and shadow payroll.</li><li>Assess legislative impacts, resolve employee queries and document processes for automation and efficiency.</li><li>You bring a service-minded approach.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree or equivalent.</li><li>Three-plus years’ payroll experience, including one to two years in international payroll.</li><li>Strong Irish legislation and statutory-reporting knowledge, including PAYE Modernisation.</li><li>Vendor/bureau and Human Resources Information System experience, such as Workday, ADP, SAP SuccessFactors or Papaya.</li><li>Advanced Excel: VLOOKUP/XLOOKUP, pivot tables and reconciliations.</li><li>Attention to detail, confidential-data handling and clear written/verbal communication across time zones.</li><li>Payroll qualification preferred, such as Chartered Institute of Payroll Professionals or Payroll Ireland Certificate/Diploma.</li><li>Shadow payroll, expatriate-tax or equity/share-plan experience preferred.</li><li>Sarbanes-Oxley or internal-controls exposure and additional European languages preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€46,200.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 03:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientific Writer]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51103]]></requisitionid>
    <referencenumber><![CDATA[R51103]]></referencenumber>
    <apijobid><![CDATA[r51103]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51103/scientific-writer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Scientific Writer to join our Scientific Writing team, translating complex nonclinical PK/PD and pharmacology data into clear regulatory narratives that support critical drug development and regulatory decisions. In this role, you will serve as the primary Scientific Writing partner to Translational Pharmacokinetics & Pharmacodynamics and Nonclinical Pharmacology, helping teams communicate exposure-response relationships, dose selection rationale, and mechanistic insights across development programs.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: [Insert location]</li><li>Work model/flexibility: [Insert work model]</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Independently author nonclinical PK/PD study reports, eCTD summaries, and Investigator's Brochure content</li><li>Lead development of integrated regulatory narratives that synthesize PK, PD, and mechanistic data</li><li>Collaborate with scientists and cross-functional teams to interpret data and ensure consistent PK/PD messaging across programs</li><li>Coordinate data inputs, reviews, timelines, and stakeholder communications to support high-quality, on-time deliverables</li><li>Drive process improvements through authoring guidance, workflow optimization, and AI-enabled writing and quality-control solutions</li><li>Serve as the scientific writing lead for assigned programs, providing strategic document planning and cross-functional coordination</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in a life sciences discipline; advanced degree (MS or PhD) preferred</li><li>Relevant combination of scientific and regulatory writing experience supporting nonclinical development programs</li><li>Experience working with laboratory-generated pharmacology, PK, and/or PD data on a nonclinical drug development team</li><li>Knowledge of drug development, eCTD guidelines, and ICH, FDA, and EMA/CHMP nonclinical requirements, including eCTD Modules 2.4, 2.6, and 4</li><li>Experience using document authoring, review, and collaboration tools in a regulated environment</li></ul><br><p>Submitting a cover letter is strongly encouraged.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Market Access Insights & Analytics Lead]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51049]]></requisitionid>
    <referencenumber><![CDATA[R51049]]></referencenumber>
    <apijobid><![CDATA[r51049]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51049/manager-market-access-insights-analytics-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. Through science and innovation, we are redefining what is possible in healthcare while building a culture focused on collaboration, excellence, and impact.</p><br><p>We are seeking a Manager, Market Access Insights & Analytics Lead to join Regeneron's Global Capability Center (GCC) in Hyderabad. This role will lead the Market Access Insights & Analytics function, coordinating a team of franchise-aligned analysts and serving as the primary point of coordination between the GCC and US-based Market Access and Field Reimbursement (FRM) stakeholders. The position plays a critical role in driving patient access analytics, reimbursement insights, reporting excellence, and operational scalability while helping establish foundational processes and ways of working for Regeneron's growing GCC.</p><br><p><strong>When & Where</strong></p><p>Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role</strong></p><ul><li>Lead the Market Access Insights & Analytics function within the GCC and supervise a team of franchise analysts supporting Oncology, Ophthalmology, Cardiovascular/Rare Disease, Neuroscience, and Enterprise business areas.</li><li>Drive workforce planning, performance management, employee development, and business continuity activities for the team.</li><li>Manage workload allocation, quality standards, and delivery timelines across analytical workstreams.</li><li>Serve as the primary escalation point for analytical requests and stakeholder concerns</li><li>Lead knowledge-transfer activities and support the transition of outsourced analytics processes into the GCC environment.</li><li>Contribute to the development of GCC operating models, governance practices, workflows, and standards.</li><li>Partner closely with US-based Market Access, Brand, and Field Reimbursement teams to support business priorities and patient access strategies.</li><li>Build strong relationships with cross-functional stakeholders and ensure alignment on deliverables, priorities, and reporting needs.</li><li>Collaborate with Data Management and business teams to establish reporting systems, governance processes, and delivery calendar.</li><li>Support documentation of business rules, analytical methodologies, and reporting standards.</li><li>Provide strategic recommendations and actionable insights to support access, reimbursement, and patient support program decisions.</li><li>Direct development and optimization of reporting processes supporting patient access, reimbursement, copay assistance, PAP tracking, and program performance monitoring.</li><li>Supervise monthly reporting cycles and ensure delivery of high-quality analytics and insights to business leaders.</li><li>Monitor reporting accuracy, data quality, and compliance with established standards.</li><li>Translate complex business questions into actionable analytical approaches and recommendations.</li><li>Drive continuous improvement initiatives to enhance reporting efficiency, scalability, and stakeholder experience.</li></ul><br><p><strong>This role requires</strong></p><ul><li>Bachelor's degree in Life Sciences, Pharmacy, Business, Statistics, Economics, Data Analytics, Engineering, or a related field.</li><li>8+ years of experience in Pharmaceutical, Biotechnology, Healthcare Analytics, Market Access Analytics, Commercial Analytics, Consulting, or a related environment.</li><li>Strong understanding of Market Access, Field Reimbursement, Patient Support Programs, Access Services, and Reimbursement processes.</li><li>Experience working with patient access, copay assistance, PAP, reimbursement, and benefit verification analytics.</li><li>Demonstrated experience leading teams and handling multiple priorities in a matrix environment.</li><li>Strong stakeholder management skills with the ability to influence senior leaders and cross-functional partners.</li><li>Excellent verbal, written, presentation, and executive communication skills.</li><li>Strong analytical, problem-solving, and project management capabilities.</li><li>Experience working across global teams and time zones.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48463]]></requisitionid>
    <referencenumber><![CDATA[R48463]]></referencenumber>
    <apijobid><![CDATA[r48463]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48463/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Dublin, Ireland</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€172,500.00 - €288,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Accounting Operations]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47280]]></requisitionid>
    <referencenumber><![CDATA[R47280]]></referencenumber>
    <apijobid><![CDATA[r47280]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47280/manager-accounting-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This role leads Accounting Operations systems and process optimization for biopharmaceutical manufacturing, ensuring a single source of truth across modules, plants, and functions. In addition to core responsibilities, the Manager drives standardization and automation across accounting and ERP workflows. The Manager sets cadence, standards, and systems discipline to deliver accurate, timely, and data-driven outputs that support monthly close, compliance, and operational decision-making.</p><p><strong>A day in the life may look like:</strong></p><ul><li><p>Own end-to-end configuration, maintenance, and governance of accounting’s Oracle applications across OPM, Order Management, Inventory, and Financials</p></li><li><p>Govern close calendars, achievements, templates, and submission protocols to drive accountability and timely, accurate financial results</p></li><li><p>Liaise with Accounting and IT to diagnose and resolve functional setup issues and sophisticated system problems impacting close and financial reporting</p></li><li><p>Engage with process owners to identify automation opportunities, assess feasibility, prioritize implementation, and measure realized efficiency gains</p></li><li><p>Translate business requirements into clear deliverables: functional design specifications, use cases, and workflow/process diagrams</p></li><li><p>Conduct end-to-end testing cycles for application improvements, ERP upgrades, and project implementations, with rigorous impact analysis and UAT sign-off</p></li><li><p>Partner with Manufacturing, Supply Chain, and Corporate Finance to align master data, mappings, and policies across modules for smooth close and reporting</p></li><li><p>Deliver executive-ready outputs: reconciliations, variance analyses, issue logs with root-cause and corrective actions, KPI dashboards, and control health check</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Drive automation of recurring close reporting, reconciliations, exception dashboards, and data quality checks</p></li><li><p>Partner with IT on improvements and UAT</p></li><li><p>Define model structures, hierarchies, and master data standards that enable efficient consolidation, consistent mappings, and flexible scenario analysis.</p></li><li><p>Standardize accounting definitions and cross-module controls for GL, AR, AP, FA, Inventory, and Order Management to reduce manual work and errors</p></li><li><p>Identify and implement improvements that shorten cycle time, strengthen controls, and improve insights for stakeholders across Finance and Operations</p></li><li><p>Translate ambiguous asks into structured solution options with assumptions, risks, effort estimates, and recommendations</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><p>BS/BA in Accounting, Information Systems, or a related field; 7+ years experience</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, External Manufacturing]]></title>
    <date><![CDATA[Wed, 15 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49012]]></requisitionid>
    <referencenumber><![CDATA[R49012]]></referencenumber>
    <apijobid><![CDATA[r49012]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49012/senior-manager-external-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, External Manufacturing (Operations Lead) to drive day-to-day execution, operational readiness, and world-class performance across our Contract Manufacturing Organization (CMO) network while leading a team focused on continuous improvement and technical excellence.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, NY</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li><li><p>Travel requirement: 25-50%</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Ensures product manufacture occurs in compliance with cGMP and applicable regulations.</p></li><li><p>Facilitates all External Manufacturing activities at CMO/partner sites: batch scheduling, supply of materials, direct shipment, cycle time tracking, reports and technical expertise.</p></li><li><p>Ensures, in collaboration with EM Project Management, timely routing/review of technical transfer activities, validation plans, MRs, SOPs, and other documentation.</p></li><li><p>Implements site initiatives in production operation as directed by site management.</p></li><li><p>Leads continuous improvements, system implementations and/or strategy development to reduce cycle times and improve efficiency for area.</p></li><li><p>Ensures off-site inspections, testing and shipping/packaging is done according to guidelines and specifications.</p></li><li><p>Ensures product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers.</p></li><li><p>Supports investigations which concern External Manufacturing or associated shipping operations, as required.</p></li><li><p>Manages direct reports and/or lead a sub-team in continuous process improvements, system/equipment implementation and/or strategy development.</p></li><li><p>Assists in developing metrics to analyze department activities, workload and performance.</p></li><li><p>Maintains required training status on Regeneron specific work instructions and SOPs.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in business or scientific discipline and 8 years of related experience, including a minimum of 5 years of direct cGMP manufacturing operations experience (clinical and/or commercial); remaining years may be satisfied through supplier management experience or equivalent combination of education and experience. MBA preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, New Products]]></title>
    <date><![CDATA[Sun, 19 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49405]]></requisitionid>
    <referencenumber><![CDATA[R49405]]></referencenumber>
    <apijobid><![CDATA[r49405]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49405/director-new-products/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Director, New Products and Commercial Development leads commercial strategy and value maximization for key pipeline assets within Regeneron's portfolio. Partnering closely with Clinical Development and other key functions, the role shapes strategic vision, informs development decisions, and advances early launch planning for high-priority programs spanning various stages of development.</p><h3>When & where:</h3><ul><li>Sleepy Hollow, NY for 4 days a week in office</li></ul><h3>Discover your role:</h3><ul><li>Provide commercial leadership to shape the strategic vision, program strategy, value proposition, and development plan of early and pre-launch development programs</li><li>Communicate a clear, well-reasoned commercial perspective to development leadership as a core member of cross-functional Strategic Program Teams</li><li>Lead key commercial deliverables as needed for each stage of development, including target product profile (TPP) development, positioning/key claims, brand naming, launch readiness and lifecycle optimization</li><li>Collaborate with marketing research, analytics, strategic analysis and competitive intelligence to develop strategic insights and ensure fact-based decision making and forecasting</li><li>Contribute commercial insights to program related decision points on device, formulation, dosing frequency, packaging, distribution channel and other critical product attributes</li><li>Provide commercial input to clinical trial design, endpoint selection and prioritization, to ensure programs may deliver competitive claims</li><li>Partner with Market Access and HEOR teams to build differentiated value propositions and indications prioritizations to support optimal access in US and International markets</li><li>Develop commercialization plans in partnership with key functions, including Marketing, Access, Insights, Medical, Communications, Legal, Regulatory, and Sales</li><li>Present to commercial and development leadership as needed</li><li>Support business development activities in aligned therapeutic areas, including diligence and commercial case development</li></ul><h3>This role requires:</h3><ul><li>12+ years of pharmaceutical or biotech industry experience, including at least 10 years of pharmaceutical marketing and/or related commercial experience</li><li>Experience in new product commercialization and/or launching new pharmaceutical or biotech products is strongly preferred</li><li>Strong scientific acumen with knowledge of immunology/inflammation and/or obesity disease areas</li><li>Working knowledge of the legal and regulatory environment governing pharmaceutical and biotech commercialization</li><li>Background in industry-relevant consulting, investment analysis, health economics and outcomes research, or related fields is a plus</li><li>Proven ability to lead and influence cross-functionally, building strong relationships across internal teams, alliance partners, and health care providers, with strong learning agility</li><li>Ability to combine strategic thinking with business and scientific acumen, translating complex data and clinical information into clear, actionable recommendations</li><li>Ability to thrive in a fast-paced, ambiguous environment, independently managing multiple projects against tight deadlines</li><li>Need to be entrepreneurial and innovative, with strong written and verbal communication skills</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Neurology Account Director - Northeast]]></title>
    <date><![CDATA[Thu, 23 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48149]]></requisitionid>
    <referencenumber><![CDATA[R48149]]></referencenumber>
    <apijobid><![CDATA[r48149]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48149/neurology-account-director-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Massachusetts]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Neurology Account Director (NAD) is a field-based institutional key account role responsible for driving the launch and ongoing commercial performance of Regeneron's C5 inhibitor for generalized myasthenia gravis (gMG) within approximately 10 - 12 assigned academic medical centers (AMCs) infusion centers, and neuromuscular specialty centers. The account director serves as a Regeneron commercial point of contact within targeted institutions, responsible for formulary access, infusion suite education and pull-through, and long-term institutional partnership development. The AD combines deep MG clinical acumen, institutional navigation skills, financial acumen, and cross-functional coordination to maximize patient access and revenue within their assigned territory.</p><p><strong>When & where: </strong></p><ul><li><p>Remote role </p></li><li><p>Location: Northeast (New York, Pennsylvania, Massachusetts, Vermont, New Hampshire, Maine)</p></li><li><p>Travel: Up to 60–70%, including overnight travel within assigned territory</p></li></ul><p><strong>Discover your role: </strong></p><p><em>Institutional Account Management</em></p><ul><li><p>Own and manage a portfolio of approximately 10 -12 AMCs and neuromuscular specialty centers within an assigned U.S. region, serving as the institutional commercial lead.</p></li><li><p>Develop and execute comprehensive account plans for each institution, including formulary strategy, stakeholder mapping, competitive positioning, and patient access pathways.</p></li><li><p>Navigate complex institutional buying environments including P&T committees, pharmacy contracting, hospital administration, and infusion center operations.</p></li><li><p>Build and maintain deep, trust-based relationships with neurology department heads, treating neurologists, clinical pharmacists, infusion nurses, and medical directors.</p></li></ul><p><em>Formulary & Market Access Pull-Through</em></p><ul><li><p>Lead formulary and pathway submissions and P&T committee presentations at targeted institutions, positioning the C5 inhibitor for preferred or unrestricted formulary status.</p></li><li><p>Partner with Market Access National and Payer Account Directors to align institutional contracting with broader payer strategy and resolve prior authorization barriers.</p></li><li><p>Coordinate with specialty pharmacy partners and Patient Services hub to ensure seamless reimbursement workflows for buy-and-bill infusion products.</p></li><li><p>Track formulary status, pull-through metrics, and access barriers across all assigned accounts; escalate systemic issues with data-driven recommendations.</p></li></ul><p><em>Stakeholder & KOL Engagement</em></p><ul><li><p>Identify, develop, and maintain relationships with key opinion leaders (KOLs) in neuromuscular medicine within assigned territory, in coordination with Medical Affairs.</p></li><li><p>Represent Regeneron at national and regional neurology congresses (AAN, MGFA), medical education events, and institutional grand rounds as appropriate.</p></li></ul><p><em>Analytics, Planning & Reporting</em></p><ul><li><p>Maintain detailed CRM records and account intelligence; leverage IQVIA/Symphony Health data for prescriber-level targeting and performance measurement.</p></li><li><p>Track and report on KPIs including accounts engaged, formulary inclusions achieved, patient switches, revenue per account, and competitive share of voice.</p></li><li><p>Prepare and present quarterly business reviews to the Executive Director, highlighting account progress, barriers, competitive dynamics, and resource needs.</p></li><li><p>Contribute to territory realignment recommendations and Year 2 expansion planning based on field-level market intelligence.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree required; PharmD, RN, or advanced degree in life sciences strongly preferred.</p></li><li><p>Minimum 10-12+ years institutional sales, market access, or account management experience in pharmaceutical/biotech.</p></li><li><p>Demonstrated experience with hospital/AMC formulary processes, P&T committee engagement, and institutional buy-and-bill contracting.</p></li><li><p>Track record of success in rare disease, neurology, or specialty biologic sales/account management, ideally including launch experience.</p></li><li><p>Strong clinical acumen with the ability to engage physicians, pharmacists, and medical directors in scientifically rigorous conversations.</p></li><li><p>Experience executing competitive switch or conversion strategies in institutional settings.</p></li><li><p>Proficiency with CRM systems and commercial analytics platforms (IQVIA, Symphony Health, specialty pharmacy data).</p></li><li><p>Ability to manage complex, multi-stakeholder account relationships independently with minimal supervision.</p></li><li><p>Willingness to travel 60–70% within assigned territory, including overnight travel.</p></li><li><p>Candidates must reside within the assigned territory.</p></li></ul><p><em>Preferred:</em></p><ul><li><p>Experience in complement biology, neuromuscular disease, or C5/FcRn inhibitor markets.</p></li><li><p>Existing relationships with neurology KOLs or MGFA-recognized center-of-excellence leadership.</p></li><li><p>Prior experience with infusion biologic launches in hospital/outpatient infusion settings.</p></li><li><p>Knowledge of specialty pharmacy hub operations, patient assistance programs, and prior authorization workflows.</p></li><li><p>Understanding of medical benefit (Part B) reimbursement, ASP pricing dynamics, and buy-and-bill economics.</p></li></ul><p><em>Core Competencies:</em></p><ul><li><p>Clinical Credibility – Translates C5 mechanism of action, dosing differentiation, and clinical evidence into compelling value propositions that resonate with treating physicians and institutional decision-makers.</p></li><li><p>Institutional Account Navigation – Expertly engages across all levels of AMC hierarchies, from neurology fellows to C-suite administrators, pharmacy directors to infusion center leadership.</p></li><li><p>Strategic Account Planning – Builds data-driven, multi-quarter account strategies that address formulary access, competitive positioning, and patient journey barriers.</p></li><li><p>Patient Journey Management – Coordinates cross-functionally with Patient Services, specialty pharmacy, and market access to remove barriers and ensure seamless treatment initiation and continuation.</p></li><li><p>Relationship Building – Develops deep, trust-based institutional partnerships that create long-term competitive advantages in rare neuromuscular disease.</p></li><li><p>Results Orientation – Drives measurable outcomes through disciplined account planning, KPI tracking, and relentless follow-through on formulary wins.</p></li></ul><div><div><div><div><div><div><div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations, GMP IT/OT]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43879]]></requisitionid>
    <referencenumber><![CDATA[R43879]]></referencenumber>
    <apijobid><![CDATA[r43879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r43879/associate-director-of-it-operations-gmp-itot/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an IT Operations Leader (Senior Manager or Associate Director) to join our IOPS IT team, ensuring the reliable operation and management of IT and Operational Technology infrastructure and services across our GxP manufacturing environment. In this role, you will provide strategic direction and operational oversight for IT/OT infrastructure, service delivery, and compliance — while collaborating with corporate IT, automation teams, service providers, and cross-functional partners to maintain robust, secure, and scalable operations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Ensure reliable operation of IT/OT infrastructure including servers, hardware, communications, desktop support, and wireless networks; provide operational oversight for data centre operations, network services, telecom, and asset management</li><li>Define, implement, and lead IT/OT infrastructure architecture with a focus on hyper-converged systems, advanced networking, and wireless technologies to ensure robust connectivity and security across industrial and enterprise environments</li><li>Maintain compliance with GxP, FDA, and global regulatory requirements; ensure data integrity, disaster recovery planning, and robust security measures are in place across IT/OT infrastructure</li><li>Maintain compliance with automation system standards including DeltaV/Emerson and Rockwell/Allen-Bradley; ensure systems and procedures support effective monitoring and reporting</li><li>Manage service providers to ensure high-quality delivery aligned to SLAs; act as escalation point for major incidents and provide regular management reporting on service performance and IT operations</li><li>Collaborate with corporate IT and OT partners to ensure seamless system integration and alignment across the enterprise</li><li>Lead, mentor, and develop a diverse technical team spanning Helpdesk, Desktop, Server, and Network functions; oversee recruitment, training, performance evaluations, and goal setting for the IT Operations team</li><li>Drive implementation and continuous improvement of ITIL practices, SLAs, metrics, and operational best practices across the IT Operations function</li><li>Demonstrated experience managing diverse technical teams including Helpdesk, Desktop, Server, and Network staff; experience managing vendors and managed service providers required</li><li>Experience developing and deploying SLAs, metrics, and operational best practices; proven track record implementing ITIL practices within an organization</li><li>Strong background in Microsoft OS including Server and GPO elements; strong understanding of data integrity and associated tools</li><li>Experience with Business Continuity and Disaster Recovery planning required</li><li>Knowledge of IT compliance guidelines including PIC/S, 21 CFR Part 11, Annex 11, and GAMP preferred</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology or a related field</li><li>Senior Manager: 8+ years of progressively more responsible experience, including 8+ years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment</li><li>Associate Director: 10 years of progressively more responsible experience, including 10 years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Market Access Hematology Japan]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49826]]></requisitionid>
    <referencenumber><![CDATA[R49826]]></referencenumber>
    <apijobid><![CDATA[r49826]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49826/senior-manager-market-access-hematology-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Market Access Hematology Japan to join our market access team, supporting our Japan hematology business in a hybrid work model. In this role, you will drive launch, pricing, and reimbursement strategy while collaborating with commercial, medical affairs, HEOR, regulatory affairs, clinical, and global market access teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><p>Tokyo, Japan</p><p>Work model: Hybrid</p><br><h3>Discover your role:</h3><ul><li>Lead market access strategy for the hematology portfolio across Japan</li><li>Serve as the interface between global market access and the Japan affiliate</li><li>Drive NHI pricing and reimbursement submissions, including HTA dossiers</li><li>Execute price and HTA negotiations aligned to product strategy</li><li>Monitor reimbursement policy changes and assess business impact</li><li>Provide Japan-specific insights to shape value strategy and evidence plans</li><li>Represent Japan in global access forums and launch readiness reviews</li><li>You thrive in a collaborative, evolving environment with diverse stakeholders</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree required</li><li>8+ years of in-country market access experience</li><li>Strong knowledge of reimbursement systems, payer environments, cost comparator pricing methodology, and policy trends in Japan</li><li>Experience developing pricing strategy and reimbursement approaches</li><li>Excellent verbal and written communication skills</li><li>Business-level English and native-level Japanese</li><li>Strong project and process management skills with the ability to prioritize multiple tasks</li><li>Demonstrated initiative, critical thinking, and effectiveness in complex environments</li><li>Hematology launch or inline experience preferred</li><li>Proven negotiation experience with authorities in Japan preferred</li><li>Health Technology Assessment (HTA) experience and negotiation experience in Japan preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Responsible AI & Enterprise Governance]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49699]]></requisitionid>
    <referencenumber><![CDATA[R49699]]></referencenumber>
    <apijobid><![CDATA[r49699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49699/executive-director-responsible-ai-enterprise-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We're looking for an Executive Director, Responsible AI & Enterprise Governance to join our fast-moving Enterprise Data & AI organization. You'll build and run our enterprise AI governance framework, setting the policies, standards, and controls that let Regeneron move fast with confidence, auditability, and trust. You'll partner closely with Legal, Compliance, and the CISO to keep AI use safe, compliant, and aligned with our values. This role reports to the SVP, Chief AI Officer, and offers the chance to shape governance as an accelerant for AI adoption, not a barrier to it.</p><br><h3><strong>When & where:</strong></h3><ul><li><strong>Location:</strong> This role is open to any of our Tri-State locations: Sleepy Hollow, NY, Tarrytown, NY, Armonk, NY, Warren, NJ or Cambridge, MA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Drive the enterprise AI governance program with senior business stakeholders across all Regeneron functions - AI governance forums, use case intake, and enterprise wide accountability</li><li>Lead the citizen development governance program - safe, auditable, enterprise-approved boundaries for non-technical builders</li><li>Define and own Regeneron's enterprise AI governance strategy across all model types, risk tiers, and deployment contexts</li><li>Build and lead a team of specialists across model validation, guardrails engineering, regulatory compliance, and citizen development governance</li><li>Establish the enterprise AI risk framework - taxonomy, classification standards, and control requirements across classical ML, foundation models, LLMs, fine-tuned models, and agentic systems</li><li>Set the technical assurance that includes validation frameworks, red-teaming, production monitoring, and pre-production sign-off gates</li><li>Own the end-end AI model lifecycle governance standard from ideation to deployment and monitoring</li><li>Drive LLM and agentic AI governance - grounding standards, retrieval integrity, tool use controls, autonomous action limits, and human-in-the-loop enforcement</li><li>Own GxP AI validation strategy and audit readiness across all regulated environments</li><li>Lead AI regulatory intelligence e.g. FDA, EMA, EU AI Act and emerging global frameworks, coordinated with Legal and business units to get ahead of compliance obligations</li><li>Partner at the executive level with Legal, Compliance, Regulatory Affairs, and CISO on regulatory interpretation, risk posture, and technical standards</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Have led AI governance or technical risk functions in a complex, regulated industry and built the teams that execute them</li><li>Bring technical depth to set strategy and leadership range to hire and hold accountable the experts who implement it</li><li>Understand the distinct risk profiles of predictive, generative, and agentic systems and have governed them in production</li><li>Have driven GxP AI validation strategy in a life sciences or biopharma setting</li><li>Stay ahead of FDA AI/ML guidance, EU AI Act, and emerging frameworks — and convert them into enterprise action</li><li>Operate with credibility at the engineering level and the board level</li><li>See AI governance as a strategic capability that accelerates the business — and build it that way</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>A Bachelor's degree in a related field (advanced degree required for certain scientific or clinical positions)</li><li>17+ years of experience in AI governance, risk management, regulatory affairs, or compliance</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49975]]></requisitionid>
    <referencenumber><![CDATA[R49975]]></referencenumber>
    <apijobid><![CDATA[r49975]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49975/director-international-commercialization-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Madrid]]></city>
    <state><![CDATA[Madrid]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Madrid, Spain - multiple locations are being considered for this role</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>96.000,00 € - 160.000,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Development Program Management- Oncology]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49992]]></requisitionid>
    <referencenumber><![CDATA[R49992]]></referencenumber>
    <apijobid><![CDATA[r49992]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49992/senior-director-development-program-management-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Development Program Management to join our Portfolio and Program Management team, supporting our Oncology in a hybrid capacity. In this role, you will lead program strategy while collaborating with cross-functional teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY or Warren, NJ</li><li>Hybrid</li><li>Travel percentage: 25%</li></ul><h3>Discover your role:</h3><p>We are seeking a highly experienced and dynamic Senior Director Development Project Manager to join our team. The successful candidate will primarily be responsible for identifying and developing a team of manager through associate director ready program managers. Additionally, the successful candidate will provide operational leadership, direction, and support to assigned small and/or low to medium complexity development program(s).</p><h3><strong>Team</strong> <strong>Leadership</strong> <strong>and Management</strong> <strong>(Primary responsibility)</strong>:</h3><ul><li>Recruit, hire, build and lead a team of high performing, early-career program managers.</li><li>Lead & advance talent-- from manager to associate-director ready talent-- with emphasis on developing, improving, or enhancing PM capabilities, processes & initiatives.</li><li>Identify and assess development needs of direct reports; Ensure direct reports have actionable development plans and receive ongoing coaching and feedback to enable growth and future leadership</li><li>Establish and maintain comprehensive training and development curriculum for program managers that aligns with department goals and career ladder.</li><li>Build project allocation model and process to support the pipeline and development of direct reports.</li><li>Collaborate with portfolio management to understand longer range resourcing needs and develop plan to address.</li></ul><h3><strong>Project Leadership and Management: </strong></h3><ul><li>Partner with the Global Program Head on small and/or low to medium complexity program(s) to drive Strategic Program Teams, leading the management and execution from preclinical through late development and life cycle management.</li><li>Develop and ensure delivery of comprehensive integrated plans, including timelines and budgets, and ensure alignment with company goals.</li></ul><h3><strong>Continuous Improvement</strong>:</h3><ul><li>Identify opportunities for process improvements and implement best practices in project management. Proactively share lessons learned within the team and across the organization.</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree required. Master's preferred. Minimum of 15+ years' experience relevant broad project / program management experience required, preferably in the pharmaceutical or related industry</li><li>Have extensive experience in Pharma R&D project management, a deep understanding of the end-to-end drug development process and a proven ability to deliver results</li><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels both internal and external to the company in order to establish credibility with professionals on the project teams.</li><li>Have strong presentation and critical thinking skills.</li><li>Actively promote constructive interactions among team members to address difficult situations.</li><li>Resolve and negotiate conflicts or problems with tact, diplomacy and composure.</li><li>Handle multiple projects and priorities with exceptional organizational and time management skills</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Digital & Technology - HR, Corporate Affairs, Business Development, Corporate Strategy, Investor Relations]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50014]]></requisitionid>
    <referencenumber><![CDATA[R50014]]></referencenumber>
    <apijobid><![CDATA[r50014]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50014/executive-director-digital-technology-hr-corporate-affairs-business-development-corporate-strategy-investor-relations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Building Our Future:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Director to lead the technology strategy and roadmap supporting HR, Corporate Affairs, Business Development, Corporate Strategy, Investor Relations, and Strategic Alliances at Regeneron, including ownership of the Workday platform and related enterprise solutions. Partnering closely with senior executives, this leader aligns technology investments with talent, partnership, and strategic business objectives. The role has significant influence over how the company manages its workforce, external relationships, and strategic initiatives through technology. Additionally, the individual serves as the primary technology advisor and executive spokesperson for these functions.</p><p><strong>When & Where:</strong></p><p>This role will sit in our Sleepy Hollow, NY office 4 days per week.</p><p><strong>What You'll Lead</strong></p><ul><li>Lead the technology strategy and multi-year roadmap for HR, Corporate Affairs, Business Development, Corporate Strategy, Investor Relations and Strategic Alliances, aligning investments with enterprise priorities.</li><li>Own and optimize the HR technology portfolio, including Workday and related platforms supporting talent acquisition, employee experience, learning, workforce planning, and people analytics.</li><li>Deliver technology solutions for business development, strategic planning, alliance management, partner collaboration, and AI-enabled opportunity intelligence.</li><li>Build and lead a high-performing global technology organization, developing talent and driving execution across complex business functions.</li><li>Drive measurable business outcomes through improved hiring, onboarding, HR service delivery, deal execution, alliance effectiveness, automation, system reliability, and productivity.</li><li>Modernize and standardize technology platforms, processes, operating models, and data capabilities across supported functions.</li><li>Advance AI, automation, workforce analytics, and decision intelligence strategies to improve business performance and user experience.</li><li>Oversee vendor management, technology investments, Workday governance, cybersecurity, data privacy, and platform resilience to ensure secure, scalable, and high-value solutions.</li></ul><p><strong>What You Bring</strong></p><ul><li>BS/BA in Computer Science, Information Systems, Human Resources, or a related field required; MS or MBA preferred.</li><li>17+ years of progressive HR technology leadership, including large-scale Workday (HCM) programs.</li><li>Deep expertise in Workday architecture, release strategy, and integrations.</li><li>Familiarity with technology needs of business development, corporate strategy, or alliance management functions is a plus.</li><li>Proven ability to influence senior leaders, set standards across functional areas, and attract top talent.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Partnership and Trial Optimization]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49872]]></requisitionid>
    <referencenumber><![CDATA[R49872]]></referencenumber>
    <apijobid><![CDATA[r49872]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49872/director-global-partnership-and-trial-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a Director, Global Development Strategic Partnerships to identify, establish, and manage strategic relationships with external organisations and institutions. You will coordinate across a matrix of teams to create partnership opportunities that strengthen clinical development, clinical research, and Regeneron’s broader R&D objectives. You will support partnership agreements from identification and evaluation through contract drafting, execution, and ongoing relationship management, working closely with internal leaders to maintain collaboration, continuity, and alignment.</p><p><strong>When & where</strong></p><p>Uxbridge (hybrid).</p><p><strong>Discover your role</strong></p><ul><li><p>Develop a long-term, company-wide strategy for working with external organisations to support clinical trials and translational and basic research.</p></li><li><p>Identify and evaluate external partners based on agreed organisational needs, opportunities, and capability gaps.</p></li><li><p>Drive the evaluation and coordination of partnership opportunities, engaging internal experts when additional support is required.</p></li><li><p>Coordinate new opportunities with existing and prospective partner organisations.</p></li><li><p>Support contract drafting and execution while remaining connected to strategic relationships throughout the agreement lifecycle.</p></li><li><p>Manage and track external partnership opportunities in collaboration with project management and other external-facing colleagues.</p></li><li><p>Build consistent communication channels with internal and external partners to maintain continuity, alignment, and productive relationships.</p></li><li><p>You work collaboratively across functions to prioritise strategic partnerships and identify opportunities for innovation and efficiency.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Previous experience and a deep understanding of the drug development process.</p></li><li><p>A proven track record of developing and maintaining partner relationships at all organisational levels.</p></li><li><p>Strong existing relationships and a positive reputation within the life sciences industry, particularly with academic medical centres and large health systems.</p></li><li><p>Strong business and financial management acumen, with experience in strategic planning and tactical execution.</p></li><li><p>The ability to manage and prioritise multiple tasks and projects with urgency while working within a matrix organisation.</p></li><li><p>Outstanding written, verbal, presentation, and consensus-building skills, with the ability to communicate accurately and concisely.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, GPS Quality & Compliance]]></title>
    <date><![CDATA[Wed, 26 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50204]]></requisitionid>
    <referencenumber><![CDATA[R50204]]></referencenumber>
    <apijobid><![CDATA[r50204]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50204/director-gps-quality-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Our Global Patient Safety (GPS) organization is seeking a Director, GPS Quality & Compliance to support our quality event management and inspection readiness programs. This role partners closely with the Senior Director, GPS leadership, Global Development Quality, and the QPPV Office, and operates as a functional leader who coordinates and delegates work across the team to ensure consistent, high-quality program delivery. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Warren, NJ (preferred), Armonk or Tarrytown, NY, or Cambridge, MA<br>• Work model: 4 days/week on-site<br>• Travel percentage: 20% with some fluctuation expected based on onsite audit/inspection support needs.</p><p><strong>Discover your role:</strong><br>• Lead functional workstreams across quality event management and inspection programs, coordinating and delegating work across a team<br>• Serve as a trusted point of contact during GCP and GVP audits and inspections, guiding teams through preparation and real-time response<br>• Bring order to complexity by maintaining inspection readiness materials and translating regulatory frameworks into practical action<br>• Champion a culture of accountability and continuous improvement, acting as an escalation point when issues arise<br>• Turn data into direction, reviewing quality metrics and trend analyses to shape clear, actionable recommendations for senior leadership<br>• Communicate with confidence and clarity, presenting governance topics and quality insights to senior team members<br>• Lead through influence, coordinating across teams and functions regardless of formal reporting lines</p><p><strong>This role requires:</strong><br>• A Bachelor's degree required; advanced degree preferred with a minimum of 12 years of pharmaceutical industry experience; Healthcare Professional background preferred<br>• Deep knowledge of global PV regulations, quality management systems, and inspection readiness frameworks (FDA CFR, GVP Modules)<br>• Demonstrated experience facilitating FDA and EMA/MHRA inspections (GCP and GVP), including direct experience as an inspection point of contact<br>• Proven track record overseeing QMP governance, metrics programs, and cross-functional quality oversight<br>• Experience managing relationships across GDQ, QPPV Office, Regulatory Affairs, and vendors<br>• People management experience preferred<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Precision Medicine (Clinical Diagnostics)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49909]]></requisitionid>
    <referencenumber><![CDATA[R49909]]></referencenumber>
    <apijobid><![CDATA[r49909]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49909/associate-director-precision-medicine-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with diagnostic execution. This role owns CDx programs from early biomarker feasibility through clinical validation, regulatory submission, and launch — translating biological insights and clinical hypotheses into validated, fit-for-purpose assays that support drug development decisions. You'll work at the interface of biomarker science, clinical development, regulatory, and external IVD partners to ensure diagnostics keep pace with therapeutic milestones. </p><p><strong>When & where: </strong></p><ul><li><p>Location: Uxbridge, United Kingdom (multiple locations are being considered for this role.)</p></li><li><p>Work model/flexibility: 3 days onsite</p></li></ul><p><strong>Discover your role: </strong></p><ul><li><p>Translate emerging biomarker and mechanism-of-action data into diagnostic target product profiles (TPPs), defining assay intent across platforms (Next Generation Sequencing, polymerase chain reaction, immunohistochemistry, immunoassays). </p></li><li><p>Partner with translational and clinical teams to design biomarker strategies for patient selection, stratification, and enrichment, including sample strategy and specimen logistics.</p></li><li><p>Lead analytical and clinical validation planning (accuracy, precision, sensitivity/specificity, limit of detection, reproducibility), linking assay performance to clinical safety and efficacy endpoints. </p></li><li><p>Set global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines. </p></li><li><p>Select and oversee In Vitro Diagnostic (IVD) development partners; manage co-development scope, timelines, and quality expectations. </p></li><li><p>Support global regulatory strategy and submissions (Food and Drug Administration PMA/supplement, EU IVDR, PMDA) in collaboration with IVD Regulatory, including labeling alignment. </p></li><li><p>Ensure compliance with relevant standards (ISO 13485, ISO 14971, CLSI, IVDR, GCP alignment). </p></li><li><p>Lead cross-functional working groups, translating scientific rationale into program plans and clear governance reporting. </p></li><li><p>Support design transfer, manufacturing readiness, and launch preparation with commercial and medical affairs. </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>PhD or advanced degree in molecular biology, pathology, biomedical engineering, or related translational/biomedical science field. </p></li><li><p>8+ years in diagnostics or translational research, with 4+ years leading biomarker-driven CDx or IVD programs bridging bench discovery and clinical application. </p></li><li><p>Track record translating biomarker science into validated assays supporting drug approvals. </p></li><li><p>Working knowledge of global CDx regulatory pathways (FDA CDRH, EU IVDR, PMDA). </p></li><li><p>Ability to translate complex scientific and clinical data for cross-functional and executive audiences. </p></li><li><p>Experience managing external partners and multi-workstream programs under QMS/GxP-adjacent conditions. </p></li></ul><p>#PrecisionMedicineCDX</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Data Management (CDM), Study Lead]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50130]]></requisitionid>
    <referencenumber><![CDATA[R50130]]></referencenumber>
    <apijobid><![CDATA[r50130]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50130/manager-clinical-data-management-cdm-study-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><strong>Manager, Clinical Data Management (CDM), Study Lead </strong><strong>(Tarrytown, NY)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks a Manager Clinical Data Management (CDM), Study Lead (Tarrytown, NY) to serve as the primary DM supporting clinical study teams and external partners on small or noncomplex studies or supporting larger studies within a given therapeutic area. Coordinate all DM activities from study start-up to archiving. Provide expertise in data management, support eCRF and database design, and ensure data quality. Perform data quality review procedures, data acceptance, and coordinate data transfers with CROs. Document and support CRO data management activities, ensuring adherence to SOPs and identifying data quality issues. Review and approve study documentation, including DMP, CRF, and validation specifications. Maintain eTMF documentation and perform quality reviews to ensure inspection readiness. Responsible for data management deliverables, ensuring timelines align with business needs and objectives. Monitor data quality, assess data issue progress, and propose risk mitigations. May act as a Subject Matter Expert (SME) for specific topics and provide training. Represent DM in study-level forums and meetings. Telecommuting permitted.</p><p>SALARY RANGE: $172,994.00 - $187,400.00 per year</p><p><strong>Job Requirements:</strong></p><p>Requires a Bachelor’s degree in Mathematics, Pharmaceutical Science, Pharmaceutics or related field and 6 years of clinical data management experience in biotechnology, pharmaceutical, or health-related industry. Must have experience with: Applying applicable regulations, including 21 CFR Part 11, ICH GCP Guidelines, and CDISC standards, to clinical data collection and management activities; Supporting and coordinating clinical studies and study teams within a regulated data processing environment; Applying data management processes and industry best practices across the clinical data lifecycle, including data collection, validation, and delivery; Evaluating existing data management workflows and recommending process improvements to meet study and organizational objectives; Resolving complex data related issues by analyzing requirements, identifying root causes, and implementing compliant solutions; Preparing and delivering written documentation and verbal communications for crossfunctional clinical study teams; and Collaborating with crossfunctional, geographically distributed study teams in a matrixed environment.</p><p>Apply at https://careers.regeneron.com; Reference code: R50130</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Dir Field Medical Affairs (Neurology)]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50581]]></requisitionid>
    <referencenumber><![CDATA[R50581]]></referencenumber>
    <apijobid><![CDATA[r50581]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50581/sr-dir-field-medical-affairs-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><strong>Build our future together:</strong></p><p><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Neurology Field Medical Affairs, to lead our US-based Field Medical team, supporting our Neurology therapeutic area. In this role, you will shape and implement Field Medical strategy, build and develop a high-performing MSL organization, and drive scientific exchange with thought leaders. Responsible for providing oversight of all activities in accordance with current regulatory and health care compliance guidelines in the US. Participates in the coordination of investigator sponsored clinical trials as applicable.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: US <br>• Work model/flexibility: Field<br>• Travel percentage: 50%</p><p><strong>Discover your role:</strong><br>• Lead and develop a national field medical team with credibility, compliance, and a customer-first mindset<br>• Build strong relationships with thought leaders and healthcare professionals in Neurology and Myasthenia Gravis<br>• Translate Medical Affairs strategy into clear field activity goals and metrics<br>• Partner cross-functionally with Clinical Development, Medical Information, and commercial teams to align on shared goals<br>• Guide your team through complex scientific discussions, congress planning, and evidence communication<br>• Identify gaps in research and education, then create opportunities to close them through investigator collaboration<br>• Bring an analytical, evidence-based approach to problem-solving and decision-making<br>• Communicate complex scientific information clearly to diverse audiences</p><p><strong>This role requires:</strong><br>• Advanced medical or scientific degree (e.g., MD/DO, PhD, PharmD, NP, DVM) with 15+ years of experience in Medical Affairs<br>• Demonstrated experience building, leading, and managing US field-based teams (MSLs), including direct people management<br>• Strong interpersonal, verbal, and written communication skills with the ability to build internal and external relationships<br>• Experience in Neurology, with knowledge of Myasthenia Gravis highly desirable<br>• Prior US product launch experience<br>• Experience developing MSL-facing materials such as slide decks and FAQs<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Virology]]></title>
    <date><![CDATA[Tue, 15 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49250]]></requisitionid>
    <referencenumber><![CDATA[R49250]]></referencenumber>
    <apijobid><![CDATA[r49250]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49250/associate-director-virology/]]></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 looking for an Associate Director of Virology This is primarily a technical role responsible for ownership and disposition of an effective viral safety program for a bulk biopharmaceutical manufacturing facility. The individual will assess the current status, develop a robust program and enact improvements based on industry best practices and regulatory concerns. Additionally, this person will act as a senior management advisor for all virology related matters.</p><p><strong>When & Where:</strong></p><ul><li>Monday–Friday, 8:00am–4:30pm</li><li>Location: Rensselaer, New York, United States</li></ul><p><strong>Discover your role:</strong></p><ul><li>Responsible for evaluating and establishing viral control strategy and implementing remediation efforts where necessary.</li><li>Responsible for reviewing procedures and protocols for viral detection, containment and decontamination.</li><li>Interface with Regulatory Authorities and maintain an up-to-date awareness of regulatory issues related to viral control.</li><li>Own scientific oversight for virology program and report management.</li><li>Develop a broad understanding of virological subtleties with respect to the biotechnological processes and stay current with technical and professional literature.</li><li>Develop and approve test protocols.</li><li>Approve & perform investigations and remediation plans.</li><li>Play an integral part in investigating and troubleshooting equipment, testing and process abnormalities related to virology.</li><li>Lead investigations related to virological abnormalities.</li><li>Participate in laboratory investigations to ensure effective root-cause analysis and corrective action plans determination.</li></ul><p><strong>This role requires:</strong></p><ul><li>PhD in virology or related field preferred; will consider substituting relevant experience in biopharmaceutical virology in lieu of advanced degree.</li><li>Minimum 10 years in GMP biopharmaceutical/pharmaceutical environment.</li><li>Experience participating in regulatory inspections, presenting/defending positions in audits or regulatory inspections.</li><li>Level will be determined based on experience and qualifications.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$147,800.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 16 Sep 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Enterprise Architect]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50607]]></requisitionid>
    <referencenumber><![CDATA[R50607]]></referencenumber>
    <apijobid><![CDATA[r50607]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50607/executive-director-enterprise-architect/]]></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 role leads Enterprise Architecture for the organization, setting the technology vision, standards, and governance that align business strategy with scalable, secure, and future-ready technology platforms. The Executive Director partners with senior IT and business leadership to shape the enterprise technology roadmap, drive architecture decision-making across data, cloud and infrastructure, application, and integration domains, and ensure technology investments deliver measurable business value.</p><p>This is both a strategic and hands-on leadership role, requiring the ability to influence at the executive level while maintaining the technical depth to guide complex, enterprise-wide architecture decisions, and to build and mentor a high-performing architecture organization. Security and AI architecture are delivered through close collaboration with the CISO and CAIO organizations, which maintain their own dedicated architecture teams; business architecture is owned by a separate business strategy function outside Digital and Technology.</p><p>Where and When</p><p>This is an on-site position 4 days/week, primarily based at our Sleepy Hollow, NY or Warren, NJ office. If eligible, we can offer relocation benefits; we cannot offer a fully remote option.</p><p>Enterprise Architecture Strategy & Vision </p><ul><li>Define and own the enterprise architecture strategy, principles, and target-state blueprints across the data, cloud and infrastructure, application, and integration domains, incorporating security and AI architecture standards set in partnership with the CISO and CAIO organizations. </li></ul><ul><li>Translate business strategy and digital transformation priorities into a coherent, multi-year enterprise technology roadmap. </li></ul><ul><li>Establish and evolve the enterprise's architecture operating model, ensuring architecture decisions scale with business growth and complexity. </li></ul><ul><li>Assess emerging technology trends (AI/ML, cloud-native platforms, automation) and determine their strategic fit and adoption path for the enterprise. </li></ul><ul><li>Champion a “business capability first” architecture approach, ensuring technology investments map directly to business outcomes.</li></ul><p> Architecture Governance & Standards </p><ul><li>Establish and lead the enterprise architecture governance framework, including review boards, design authority processes, and exception management. </li></ul><ul><li>Define and enforce enterprise architecture standards, patterns, and reference architectures across build, buy, and integrate decisions. </li></ul><ul><li>Own the architecture review process for major programs and capital investments, ensuring alignment with enterprise standards, security, and regulatory requirements. </li></ul><ul><li>Maintain the enterprise architecture repository (current-state and future-state models, technology inventories, and roadmaps) as an authoritative source of truth. </li></ul><ul><li>Partner with Security, Risk, and Compliance to ensure architecture decisions meet enterprise risk tolerance and regulatory obligations (e.g., GxP, data privacy). </li></ul><p>Technology Roadmap & Investment Planning </p><ul><li>Lead enterprise-wide technology rationalization efforts, identifying opportunities to consolidate, retire, or modernize legacy platforms. </li></ul><ul><li>Partner with Finance and business unit leaders to build the business case for architecture-driven investments, balancing innovation with cost discipline. </li></ul><ul><li>Guide platform and vendor selection decisions for enterprise-critical systems, ensuring architectural fit, scalability, and total cost of ownership are fully evaluated. </li></ul><ul><li>Own the enterprise's cloud and infrastructure strategy, ensuring architecture decisions support performance, resilience, and cost efficiency at scale. </li></ul><ul><li>Drive the integration architecture strategy across the enterprise, enabling seamless data flow and interoperability between core business systems. </li></ul><p>Business & Digital Transformation Partnership </p><ul><li>Serve as a trusted architecture advisor to business unit leaders, translating business problems into technology-enabled solutions. </li></ul><ul><li>Partner with product, engineering, and program leadership to embed architecture thinking early in the delivery lifecycle, reducing rework and technical debt. </li></ul><ul><li>Lead architecture input into major digital transformation and modernization initiatives, ensuring solutions are designed for scale, security, and long-term maintainability. </li></ul><ul><li>Evaluate and guide the adoption of AI, automation, and data platforms to accelerate business capabilities and competitive differentiation. </li></ul><ul><li>Act as an escalation point for cross-functional architecture conflicts, driving resolution through data-driven, business-aligned decision-making. </li></ul><p>Solution & Platform Architecture Oversight </p><ul><li>Provide senior oversight and quality assurance for solution architectures developed by domain and solution architects across the enterprise. </li></ul><ul><li>Ensure architectural consistency and reuse across programs, preventing siloed or duplicative technology investments. </li></ul><ul><li>Guide the design of resilient, secure, and scalable platform architectures for enterprise applications, data platforms, and integration layers. </li></ul><ul><li>Champion architecture practices that support DevOps, CI/CD, and infrastructure-as-code adoption across delivery teams. </li></ul><ul><li>Oversee technical due diligence for mergers, acquisitions, and strategic partnerships, assessing architectural risk and integration complexity. </li></ul><p>Executive Stakeholder Engagement & Communication </p><ul><li>Present enterprise architecture strategy, roadmaps, and investment recommendations to executive leadership, technology governance forums, as needed. </li></ul><ul><li>Build strong, trusted relationships with the Digital and Technology Leadership, and business unit executives to ensure architecture remains a strategic partner, not a bottleneck. </li></ul><ul><li>Communicate complex technical concepts and trade-offs in clear, business-relevant terms to non-technical executive audiences. </li></ul><ul><li>Represent the enterprise architecture function in vendor, industry, and partner forums, staying current on best practices and market direction. </li></ul><ul><li>Establish and sustain the operating model for collaboration with the CISO and CAIO organizations' own architecture teams — defining clear decision rights, escalation paths, and shared standards so security and AI architecture decisions remain aligned to enterprise architecture without duplicated ownership. </li></ul><ul><li>Partner with the business strategy function that owns business architecture, ensuring enterprise technology roadmaps remain traceable to business capability models maintained outside Digital and Technology. </li></ul><p>People Leadership, Mentoring & Team Culture </p><ul><li>Build, lead, and develop a high-performing architecture team, directly leading the Data & AI, Cloud & Infrastructure, Application, and Integration Domain Architects, and fostering a culture of technical excellence and collaboration. </li></ul><ul><li>Mentor and coach architects and senior technical leaders, investing in career growth, technical depth, and succession planning. </li></ul><ul><li>Establish architecture communities of practice and knowledge-sharing forums that elevate architecture maturity across the broader technology organization. </li></ul><ul><li>Champion diversity, equity, and inclusion in hiring, development, and team culture within the architecture function. </li></ul><ul><li>Model and reinforce a culture of intellectual curiosity, pragmatism, and accountability across the architecture team. </li></ul><p>Technical Competencies </p><ul><li>Deep expertise in enterprise architecture frameworks and methodologies (TOGAF, Zachman, or equivalent) and their practical application in a large, complex organization. </li></ul><ul><li>Strong technical grounding across cloud platforms (AWS, Azure, GCP), enterprise integration, data architecture, and application architecture patterns. </li></ul><ul><li>Strong grounding in enterprise integration architecture — API management, event-driven patterns, and integration platform strategy. </li></ul><ul><li>Working knowledge of AI/ML platforms, data and analytics architecture, and emerging technology evaluation. </li></ul><ul><li>Experience with enterprise security architecture, identity and access management, and regulatory/compliance frameworks relevant to the industry (e.g., GxP, data privacy). </li></ul><ul><li>Familiarity with modern software delivery practices — DevOps, CI/CD, microservices, and infrastructure-as-code. </li></ul><p>Leadership & People Skills </p><ul><li>Proven ability to build, scale, and lead high-performing architecture teams, including hiring, developing, and retaining top technical talent. </li></ul><ul><li>Experience leading architecture functions within a global, matrixed organization, including geographically distributed teams. </li></ul><ul><li>Ability to mentor and grow architects and technical leaders, building bench strength and succession depth. </li></ul><ul><li>Experience establishing and sustaining a collaborative operating model with peer architecture functions (e.g., the CISO's and CAIO's own architecture teams), ensuring clear accountability without duplicated ownership. </li></ul><p>Strategic & Business Skills </p><ul><li>Strong business acumen and the ability to translate business strategy into a coherent, executable technology roadmap. </li></ul><ul><li>Sound judgment in balancing innovation, risk, cost, and speed to market in architecture decision-making. </li></ul><ul><li>Ability to lead through ambiguity, structuring clear technology direction from complex or evolving business requirements. </li></ul><p>Communication & Stakeholder Abilities </p><ul><li>Executive presence and the ability to influence and communicate effectively with senior business and technology leaders, including at the EVP and possibly the board level. </li></ul><ul><li>Ability to translate complex technical topics into clear, business-relevant narratives for non-technical audiences. </li></ul><ul><li>Strong collaboration skills across global, cross-functional, and cross-cultural stakeholder groups. </li></ul><p>Requirements</p><ul><li>Bachelor’s degree in Computer Science, Information Technology, Engineering, or a related field is required. </li></ul><ul><li>A Master’s degree or MBA is strongly preferred. </li></ul><ul><li>17+ years of progressive experience in enterprise architecture, IT strategy, or technology leadership roles. </li></ul><ul><li>10+ years in senior leadership roles guiding architecture, engineering, or technology strategy teams within a large, complex, global organization. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 08:56:46 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Dir Product Management]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49123]]></requisitionid>
    <referencenumber><![CDATA[R49123]]></referencenumber>
    <apijobid><![CDATA[r49123]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49123/assoc-dir-product-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Job Description</div></div><div><div><div><div><div><div><div><div><div><p><strong>Build our future together:</strong></p></div></div></div></div></div></div></div></div></div><p>The Global Development IT (GD IT) Associate Director, Product Lead is a leader within the GD IT Delivery & Operations organization, accountable for the strategy, delivery, and continuous improvement of a portfolio of technology products spanning standards-led protocol digitization (USDM/ICH M11), Digital Data Flow (DDF), and human sample lifecycle management. This role may provide line management to a team of Product Leads and Product Analysts, set the domain vision and roadmap, and partner with senior business stakeholders, Business Solution Partners (BSPs), Business Process Owners, SMEs, Corporate IT, and vendor partners to translate enterprise priorities into capabilities that enable standard-led protocol digitization, biospecimen and sample management, and AI/agentic orchestration across Global Development. The Associate Director assumes domain-level product ownership, including end-to-end implementation, governance, compliance, and support for all products that fall within the domain.</p><p><strong>Where: </strong>Based at our Warren, NJ location</p><p><strong>When: </strong>4 days onsite per week required</p><p><strong>Discover your role:</strong></p><ul><li>Lead, coach, and develop a team of Product Leads and Product Analysts across protocol digitization, biospecimen/sample management, and AI/agentic orchestration</li><li>Set objectives, build domain capabilities, and instill a process-improvement culture.</li></ul><ul><li>Own the multi-product domain strategy, vision, and roadmap for standards-led protocol digitization (USDM/ICH M11), Digital Data Flow (DDF), and the human sample lifecycle, prioritizing and making trade-offs across product lines.</li><li>Build and manage senior stakeholder relationships across BSPs, Business Process Owners, SMEs, Corporate IT, and vendors</li><li>Chair domain steering committees and governance forums and drive alignment, consistency, and reuse across Product Leads</li><li>Take end-to-end ownership of the domain product portfolio—implementation, performance, and continuous improvement—overseeing requirements, testing/UAT, risk-based CSV, and ITIL-aligned release, change, and incident processes to meet business expectations, audit readiness, and compliance</li><li>Intake, assess, prioritize, and validate domain requirements in partnership with BSPs, managing scope, dependencies, and trade-offs to align technology roadmaps with product priorities.</li><li>Set direction for human-in-the-loop, multi-agent orchestration and regulated-AI governance (prompt/version control, evaluation, audit trails, risk-based CSV) aligned to 21 CFR Part 11/Annex 11 and GxP.</li><li>Drive build-vs-buy assessments, RFPs, software/services contracting, and vendor performance management; identify resourcing needs and oversee internal, vendor, and managed-service delivery.</li><li>Direct establishment of the digital protocol and structured Schedule of Activities as system of record, ensuring traceable continuity from protocol intent through CRF/EDC to SDTM, ADaM, and analysis outputs.</li><li>Provide direction over biospecimen/sample standards, metadata, and the integration ecosystem (MDR, EDC, IRT, LIMS/LIS, CTMS, analytics), ensuring lineage and reconciliation aligned to central and specialty lab operating models.</li><li>Provide subject matter expertise to manage business expectations, timelines, and domain budget; present innovative solutions and represent the organization in industry and standards forums (e.g., TransCelerate DDF, CDISC 360).</li><li>Collaborate with GD IT, Corporate IT, and other functions on enterprise systems, standards, and governance, serving as senior point of contact and escalation for the domain across Global Development.</li></ul><p><strong>This role requires: </strong></p><ul><li>Strong command of ICH M11/USDM, CDISC SDTM/ADaM, controlled terminology, and standards governance, with demonstrated delivery of structured protocol authoring and protocol-to-data automations with traceable lineage into SDTM/ADaM; experience with USDM-aligned tools (e.g., Nurocor) or equivalent MDRs</li><li>Excellent communication skills and the ability to influence senior leaders and stakeholders, including executive-ready communications</li><li>Practical understanding of human sample workflows in clinical trials (kit management, barcoding, collection/processing, shipping/receipt, chain of custody, reconciliation), central/specialty lab operating models, and biospecimen/lab and SAP/EDC integrations</li><li>Experience managing technology capability identification, selection, implementation, and operations, including LIMS/LIS integrations with EDC, IRT, CTMS, and analytics, and vendor governance across global teams</li><li>Experience applying AI and multi-agent/agentic systems (tool/function calling, RAG, prompt management, evaluation, monitoring) with human-in-the-loop controls, plus technical fluency in integration patterns (REST/GraphQL APIs, events) and data pipelines (ETL/ELT) on modern cloud platforms</li><li>Knowledge of pharmaceutical Global Development business capabilities, processes, and systems and of SDLC and ITSM/ITIL frameworks, with strong project, budget, and stakeholder management skills and demonstrated success interacting with senior leadership</li><li>Preferred: familiarity with SQL/Python or R for prototyping/validation and MLOps in regulated environments (model/package registries, approval workflows); exposure to TransCelerate DDF and CDISC 360 initiatives</li><li>Experience applying risk-based CSV and regulated-AI governance (audit trails, evaluation, prompt/version control) aligned to 21 CFR Part 11/Annex 11, GxP, and data protection (HIPAA/GDPR, RBAC)</li><li>Experience hiring, supervising, motivating, and coaching a team of direct reports—including leading or mentoring Product Leads/Product Managers—instilling a process-improvement culture and championing agile ways of working across cross-functional partners</li><li>Experience leading an end-to-end product launch or shutdown across multiple teams.</li></ul><ul><li>Ability to act tactically and think strategically, switching leadership styles to influence, guide, and coach, and to manage multiple priorities and a portfolio of products amid ambiguity and changing priorities</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Payroll Service Delivery Analyst (US)]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50454]]></requisitionid>
    <referencenumber><![CDATA[R50454]]></referencenumber>
    <apijobid><![CDATA[r50454]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50454/payroll-service-delivery-analyst-us/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, our Global Business Services organization plays a critical role in delivering efficient, compliant, and employee-focused operations that support our global workforce. We are seeking a <strong>Payroll Service Delivery Analyst</strong> to join our Global Capability Center (GCC). In this role, you will support the accurate, timely, and compliant delivery of payroll services, with a main focus on United States payroll operations while also contributing to global payroll initiatives. You will partner closely with Payroll, HR, Finance, Tax, and business collaborators to ensure payroll accuracy, compliance, operational excellence, and a positive employee experience. This role offers an opportunity to build expertise in payroll operations, contribute to process improvements, and support service delivery within a dynamic global organization.</p><p><strong>When & Where</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role</strong></p><ul><li><p>Support the preparation and processing of US payroll, ensuring accurate, timely, and compliant payroll delivery.</p></li><li><p>Validate payroll data, review transactions, and perform audit checks and reconciliations to maintain payroll accuracy and adherence to internal controls.</p></li><li><p>Process garnishments, child support orders, tax levies, and other statutory deductions in accordance with regulatory requirements.</p></li><li><p>Collaborate with HR, Finance, Global Payroll, and business partners to ensure employee data integrity and timely resolution of payroll-related inquiries.</p></li><li><p>Support payroll tax administration, including multi-state tax considerations, employee tax updates, and compliance with federal, state, and local regulations.</p></li><li><p>Assist with payroll reporting, month-end and quarter-end activities, reconciliations, and ad hoc requests from internal and external team members.</p></li><li><p>Participate in payroll system testing, upgrades, enhancements, and projects involving Workday, Oracle Time & Labor (OTL), and related payroll applications.</p></li><li><p>Contribute to continuous improvement initiatives, process standardization efforts, and operational excellence programs within the GCC.</p></li><li><p>Maintain the highest standards of confidentiality, compliance, data integrity, and control adherence across all payroll activities.</p></li><li><p>Provide cross-functional support and backup coverage to ensure continuity of payroll operations and service delivery.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Bachelor’s degree in Accounting, Finance, Human Resources, Business Administration, or a related subject area; equivalent experience considered.</p></li><li><p>4+ years of payroll experience, with proven knowledge of payroll operations and payroll tax compliance.</p></li><li><p>Understanding of federal, state, and local payroll tax regulations, multi-state payroll requirements, and applicable statutory compliance obligations.</p></li><li><p>Experience processing payroll transactions, performing reconciliations, analyzing payroll data, and resolving payroll discrepancies.</p></li><li><p>Proficiency with Microsoft Excel, including data analysis, reporting, and reconciliation activities.</p></li><li><p>Familiarity with payroll and HRIS platforms such as Workday, Oracle, ADP, CloudPay, or similar systems.</p></li><li><p>Strong analytical, problem-solving, and organizational skills with exceptional attention to detail.</p></li><li><p>Effective communication and stakeholder management skills with the ability to collaborate across teams and functions.</p></li><li><p>Experience supporting audits, compliance reviews, and internal control activities within payroll operations.</p></li><li><p>Ability to manage multiple priorities in a fast-paced shared services or global operations environment.</p></li><li><p>Payroll certifications such as CPP, FPC, or equivalent credentials preferred.</p></li><li><p>Experience supporting US payroll operations within a Shared Services Center or Global Capability Center preferred.</p></li><li><p>Ability to work a hybrid schedule and periodically align with US business hours to support payroll processing and team member requirements.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manufacturing Specialist, Drug Production]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50602]]></requisitionid>
    <referencenumber><![CDATA[R50602]]></referencenumber>
    <apijobid><![CDATA[r50602]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50602/associate-manufacturing-specialist-drug-production/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Biotech Production Specialist to join our Global Manufacturing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.</p><p>When & where:</p><ul><li><p>We offer multiple shifts that are 4 working days (10 hours) to support 24/7 production</p></li><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Occasional flexibility may be requested for on-call schedule/weekend work</p></li></ul><p>What you'll do:</p><ul><li><p>Covering all facets 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><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>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><br><p>The environment and physical rhythms of the role:</p><ul><li><p>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><br><p>Let's find out if we're a fit:</p><ul><li><p>HS diploma + 4 years of relevant work experience is required</p></li><li><p>Or AS, BS or BA in Life Sciences or related field</p></li><li><p>Level will be determined based on experience</p></li></ul><p>Thrive today. Grow Tomorrow.</p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family care benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$21.78 - $46.59]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Specialist - Data Quality & Governance]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50557]]></requisitionid>
    <referencenumber><![CDATA[R50557]]></referencenumber>
    <apijobid><![CDATA[r50557]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50557/specialist-data-quality-governance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Data Quality & Governance Specialist – Snowflake Data Operations to join our Data Governance team, supporting our Data Analytics Data Science organization in a hybrid work model. In this role, you will implement data quality, data catalogue, lineage, and access governance activities on the Snowflake platform while collaborating with data owners, data stewards, Analytics, Data Science, and Data Governance teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Profile assigned data assets within Snowflake to assess completeness, consistency, accuracy, uniqueness, and timeliness, producing reports that support data quality rule prioritization.</li><li>Implement and monitor data quality rules using Snowflake Data Metric Functions, Dynamic Data Masking, and Row Access Policies, following agreed rule logic and coding standards.</li><li>Generate exception reports and dashboards, track remediation activities, and raise issues or ambiguities to senior team members when needed.</li><li>Maintain the Data Quality Rule Register, ensuring rule logic, thresholds, rationale, and change history documentation remain accurate and current.</li><li>Manage catalogue entries within Horizon and support the documentation and validation of data lineage, classifications, ownership assignments, and provenance records.</li><li>Support Snowflake role-based access control (RBAC) governance activities, access certification reviews, audit evidence preparation, and Data Marketplace catalogue management.</li><li>You actively develop expertise in Snowflake governance and data quality practices while seeking feedback and continuous learning opportunities.</li><li>You collaborate effectively with technical and business partners, sharing progress, supporting team objectives, and helping maintain high governance standards.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree and 3+ years of relevant experience; advanced degree may be considered with 2+ years of relevant experience.</li><li>Foundational hands-on experience with Snowflake, or a strong demonstrated ability and eagerness to rapidly develop Snowflake expertise, including SQL, Data Metric Functions, and Row Access Policies.</li><li>Proficiency in SQL with the ability to write and review data quality rule logic and perform basic data transformations.</li><li>Understanding of data quality concepts, including profiling techniques and quality dimensions such as completeness, consistency, accuracy, uniqueness, and timeliness.</li><li>Knowledge of data governance principles, including metadata management, data ownership, and data catalogue practices.</li><li>Ability to create clear, structured documentation, reports, dashboards, and governance records for technical and business audiences.</li><li>Familiarity with Snowflake Horizon catalogue management, lineage documentation, classifications, and ownership assignment processes.</li><li>Understanding of access governance concepts, including role-based access control (RBAC) and access certification activities.</li><li>Exposure to a regulated industry, preferably pharmaceutical, or awareness of data integrity principles in a compliance-focused environment.</li><li>Snowflake SnowPro Core certification or active progress toward certification.</li><li>Familiarity with data catalogue platforms.</li><li>Basic Python or dbt experience supporting data transformation activities.</li><li>Exposure to data lineage concepts or related tooling.</li><li>Familiarity with enterprise data governance tools and practices.</li><li>Strong organizational skills with the ability to manage assigned tasks, meet deadlines, and raise blockers appropriately.</li><li>Effective interpersonal and communication skills, with the ability to engage data owners and business partners on routine governance matters.</li><li>Conscientious, diligent, collaborative, reliable, and committed to accuracy in governance and documentation activities.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - QA Specialist]]></title>
    <date><![CDATA[Sun, 27 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50728]]></requisitionid>
    <referencenumber><![CDATA[R50728]]></referencenumber>
    <apijobid><![CDATA[r50728]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50728/temp-qa-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temp QA Specialist </strong>to join our <strong>QA Operations Batch Review </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick</li></ul><p><strong>What you’ll do:</strong></p><ul><li>Providing QA oversight and support for manufacturing operations, serving as the primary quality representative within production areas</li><li>Partnering with cross-functional teams to facilitate issue resolution, including troubleshooting equipment, process, and schedule disruptions, while ensuring appropriate documentation and quality oversight</li><li>Assessing and triaging potential non-conformances in real time, ensuring required information and documentation are secured to support investigations</li><li>Reviewing and approving documentation associated with routine and non-routine manufacturing activities, including area clearances, incursions, changeovers, and other operational events</li><li>Participating in shift meetings and operational discussions, providing quality mentorship, observations, and recommendations related to ongoing activities and containment actions</li><li>Providing quality consultation and guidance in alignment with QA policies, procedures, and regulatory expectations</li><li>Representing Quality Assurance in the management of complex deviations, change controls, CAPAs, and other quality systems, including active participation in investigations, root cause analysis, and corrective action implementation</li><li>Supporting employee development through training, coaching, and mentoring on QA processes, procedures, and standards</li><li>Performing activities related to product disposition and release, including review of manufacturing records and supporting documentation</li><li>Reviewing and approving investigations associated with product, process, and manufacturing events</li><li>Identifying opportunities for continuous improvement and support initiatives that improve product quality, compliance, and operational efficiency</li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>Excellent organisational skills and attention to detail</li><li>You have the ability to learn and utilise computerised systems for daily performance of tasks</li><li>Strong written, verbal and interpersonal communication skills and can optimally interact cross functionally</li><li>You have the ability to prioritise, manage multiple tasks, and meet deadlines</li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><strong>Assoc Specialist </strong>- BS/BA in scientific discipline or related field or equivalent combination of education and experience</li><li><strong>Specialist </strong>- BS/BA in scientific discipline or related field with min 3 years of relevant work experience in pharmaceutical or related industry or equivalent combination of education and experience</li><li><strong>Sr Specialist </strong>- BS/BA in scientific discipline or related field with 5+ years or MS 4+ years of relevant work experience in pharmaceutical or related industry or equivalent combination of education and experience</li></ul><p>Thrive today. Grow tomorrow.</p><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLQA #REGNQA</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 28 Sep 2026 05:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op QC Analytical & Bioassay Sciences (IOPS)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50984]]></requisitionid>
    <referencenumber><![CDATA[R50984]]></referencenumber>
    <apijobid><![CDATA[r50984]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50984/2027-co-op-qc-analytical-bioassay-sciences-iops/]]></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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in QC Analytical & Bioassay Sciences (IOPS) to join Regeneron Industrial Operations and Product Supply (IOPS) <strong>Quality Control (QC) Analytical Sciences</strong> team which tests the identity, strength, purity, potency, and stability of Regeneron's commercial products.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><p><strong>Location: </strong>Rensselaer, NY (Temple Lane / Tech Valley)</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><em>This role typically runs from January through August, January through May, or May through December.</em></p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$25.50 per hour.</p><p><strong> </strong></p><p><strong>What you’ll do:</strong></p><ul><li>Support analytical method development and validation for monoclonal antibody, cell therapy, and gene therapy quality control</li></ul><ul><li>Perform chromatography, mass spectrometry, quantitative polymerase chain reaction (qPCR), enzyme-linked immunosorbent assay (ELISA), and droplet digital PCR (ddPCR) techniques</li></ul><ul><li>Contribute to assay automation and new-technology onboarding, including next-generation sequencing (NGS)-based assays and liquid-handling robotics</li></ul><ul><li>Support cell banking process scale-up activities</li></ul><ul><li>Contribute to potency assay development for cell and gene therapy products</li></ul><ul><li>Perform statistical analysis supporting method comparability studies</li></ul><ul><li>Develop automated methods comparable to existing manual methods</li></ul><ul><li>Document experimental procedures and results</li></ul><p><strong> </strong></p><p><strong>Relevant majors: </strong>Chemistry, Biochemistry, Biology, Analytical Chemistry, Biotechnology, Computer Science (for automation-focused projects)</p><p><strong> </strong></p><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li></ul><ul><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li></ul><ul><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li></ul><ul><li>Cumulative GPA of 3.0 or higher preferred</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Genome Engineering & Transgenic Model Development]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51076]]></requisitionid>
    <referencenumber><![CDATA[R51076]]></referencenumber>
    <apijobid><![CDATA[r51076]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51076/2027-co-op-genome-engineering-transgenic-model-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a 2027 Co-op in Genome Engineering & Transgenic Model Development to join our VelociGene team, which develops next-generation gene-editing tools to improve the precision and safety of genome engineering for cell lines, mouse models, and future therapeutics.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Contribute to the development of a proprietary gene-editing enhancement platform designed for both in vitro and in vivo use</li><li>Screen engineered protein variants using a fluorescence-based reporter assay to identify compact, enhanced versions that retain function</li><li>Apply computational structure-prediction tools to help design engineered protein variants</li><li>Evaluate a modified, DNA-nicking version of Cas9 to assess whether it reduces unwanted genomic effects while preserving editing efficiency</li><li>Perform basic molecular biology techniques such as polymerase chain reaction (PCR), cloning and subcloning, and western blotting</li><li>Perform mammalian cell culture techniques, including sterile technique, passaging, and transfection or electroporation</li><li>Work with viral vectors and flow cytometry methods</li><li>Document experimental procedures and results using tools such as Excel and Prism, and collaborate with scientists across the VelociGene team</li></ul><br><p><strong>Relevant majors: </strong>Biology, Biomedical Engineering, Molecular Biology, Genetics, Chemistry</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Fire Systems Specialist]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50851]]></requisitionid>
    <referencenumber><![CDATA[R50851]]></referencenumber>
    <apijobid><![CDATA[r50851]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50851/senior-fire-systems-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[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Fire Systems & Life Safety Specialist to monitor, maintain, and improve fire protection systems and life safety protocols across our US IOPS organization. In this role, you will oversee fire protection projects and programs, conduct fire system assessments, respond to life safety incidents, ensure NFPA regulatory compliance, and collaborate with cross-functional teams to implement and enhance fire protection and life safety measures. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Onsite Monday-Friday, 8:00am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Implement new fire protection technologies and evolving industry standards for fire and life-safety detection and response, partnering with Security Operations, Facilities Maintenance, and Facilities Engineering to integrate them into operations</li><li>Oversee third-party fire protection contractors and consultants, and manage procurement cycles for fire systems equipment, including budget oversight, purchase orders, and invoice approvals</li><li>Conduct fire system audits and life safety risk assessments to identify vulnerabilities and recommend improvements</li><li>Ensure regulatory and compliance alignment for pharma/manufacturing environments, including Class 1, Division 1 hazardous area and GMP requirements</li><li>Coordinate with local fire code officials, the Authority Having Jurisdiction (AHJ), and other third parties on plan reviews, inspections, and permit processes</li><li>Provide recommendations on critical initiatives such as long-term fire system upgrades, NFPA compliance audits, and life safety infrastructure improvements</li><li>Support crisis management and emergency response programs, including fire emergency preparedness, incident response workflows, mass notification, evacuation procedures, and business continuity readiness</li><li>Interpret and apply NFPA and local fire codes to ensure systems meet regulatory and operational requirements in hazardous and explosive environments</li><li>Review, approve, and maintain fire system commissioning reports, configuration baselines, inspection records, and compliance documentation</li></ul><br><h3>This role requires:</h3><ul><li>Bachelors degree in fire protection, mechanical, or electrical engineering, or a related technical field, and 5+ years of relevant fire systems experience, or an equivalent combination of education and experience</li><li>Experience in pharmaceutical or manufacturing/GMP environments, including hazardous area classifications (Class 1, Division 1)</li><li>Demonstrated experience with addressable fire alarm systems, clean agent suppression technologies, and Honeywell fire protection platforms, as well as wet and dry suppression systems</li><li>Proven experience working with the AHJ on plan reviews, inspections, and permitting, and managing fire protection equipment procurement and vendor trade-off analyses</li><li>Ability to manage multiple concurrent projects from system design through commissioning and maintenance, with knowledge of fire system integration with Building Management Systems (BMS)</li><li>Excellent communication and interpersonal skills, including training delivery and executive-level reporting on life safety compliance</li><li>Certifications such as NICET Fire Alarm Systems, NFPA, or similar recognized industry fire protection certifications preferred; PMP/PgMP or equivalent project experience preferred</li><li><strong>Gowning and Physical Requirements:</strong></li><li>Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, makeup and nail adornments when wearing cleanroom attire</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, R&D Chemistry, Peptidomimetics]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48138]]></requisitionid>
    <referencenumber><![CDATA[R48138]]></referencenumber>
    <apijobid><![CDATA[r48138]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48138/associate-director-rd-chemistry-peptidomimetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hawthorne]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director (Peptidomimetics), R&D Chemistry to play a pivotal role in expanding Regeneron’s peptidomimetic antibody-conjugate drug discovery capabilities, driving the development of innovative therapeutics across diverse research areas while leveraging the company’s expertise in biologics and genetic medicines. The role requires deep expertise in peptidomimetic, medicinal, and synthetic organic chemistry, including SAR optimization, linker-payload synthesis, and advanced bioconjugation strategies. Success depends on applying both chemical and biological approaches to overcome drug discovery challenges and advance development candidates. The individual will also provide strong leadership, collaboration, and communication to guide cross-functional teams in a highly innovative research environment.</p><p><strong> </strong></p><p><strong>Discover Your Role</strong></p><ul><li>Directly supervise and manage the day-to-day activities of the R&D Chemistry Peptidomimetic group, providing vision, inspiration, and both short-term and long-term goals. Communicate priorities, policies, and goals of Regeneron Senior Leaders to the group.</li><li>Perform medicinal chemistry inspired and SAR-driven generation of novel peptidomimetic drug modalities, using synthetically feasible and simplistically designed linkers to provide overall optimal <em>in vitro</em> and <em>in vivo</em> properties of antibody-conjugated therapeutics</li><li>Troubleshoot and optimize peptide potency and stability using standard peptide-based principles (e.g., Ala scans), non-natural amino acid incorporation, alpha-Me/N-Me peptide backbone modifications, and other medicinal chemistry strategies that are guided by <em>in vitro</em> assays, plasma/serum stability, and met ID data.</li><li>Champion and lead the R&D Chemistry Peptidomimetic efforts on internal/external project teams, and demonstrate the ability to multi-task and parallel process to add to our continuous pipeline of Regeneron development candidates</li><li>Identify new strategies and technologies (e.g., linker and payload design) to improve on existing Regeneron platforms for pursuing novel synthesis and bioconjugation of peptidomimetic drug modalities</li><li>Actively participate in departmental, cross-functional, leadership, and external meetings to contribute expertise and to represent the vision of the R&D Chemistry Peptidomimetic group.</li><li>Interact broadly and collaboratively with other Regeneron groups, forging relationships and active collaborations.</li></ul><p><strong> </strong></p><p><strong>When & Where</strong></p><ul><li>This is an on-site position located in our Hawthorne, NY facility</li><li>Occasional travel to our nearby Tarrytown facility may be required</li></ul><br><p><strong>This Role Requires</strong></p><ul><li>Ph.D. in peptide and/or synthetic organic chemistry or a related field.</li><li>Minimum of 10 years of professional industry experience.</li><li>Extensive drug discovery experience with antibody-targeted peptidomimetic drug modalities, experience with the synthesis and manufacturing of peptidomimetic payloads and linkers, expertise in modern methods in medicinal chemistry structure-activity relationships, and a deep understanding of biological MOAs (extracellular/intracellular target evaluation, ADME/PK, PD/efficacy, toxicological evaluation). </li><li>A track record of success in the field of either peptidomimetics, small molecules or antibody targeted therapeutics (i.e., advancement of molecules into the clinic) with experience building and leading teams is required.<em> </em></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Business Intelligence Architect]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50835]]></requisitionid>
    <referencenumber><![CDATA[R50835]]></referencenumber>
    <apijobid><![CDATA[r50835]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50835/associate-manager-business-intelligence-architect/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager Business Intelligence Architecture Analytics to join our Data, Tech, and Innovation function, supporting our Global Development analytics initiatives in a hybrid work mode. In this role, you will lead the execution of analytical datasets, data models, and data products while collaborating with the Senior Manager, Business Intelligence Architect, Specialist Business Intelligence Architect, Director of BI Architecture, and downstream analytics teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Coordinate work with the Senior Manager and Specialist Business Intelligence Architects to align deliverables with project requirements and development standards.</li><li>Escalate architectural decisions and delivery blockers appropriately to support timely project execution.</li><li>Build, refine, and maintain data pipelines and transformation workflows in Databricks and Snowflake using SQL and PySpark.</li><li>Develop and unit test analytical data models and curated datasets, including migration of existing workflows to Databricks.</li><li>Implement reusable, well-structured code aligned with established development standards, naming conventions, and architecture patterns.</li><li>Own end-to-end delivery of assigned data products and support analytics, dashboarding, and artificial intelligence/machine learning use cases.</li><li>Ensure dataset accuracy and completeness through validation, data quality checks, discrepancy investigation, and root cause analysis while maintaining structured documentation for downstream teams.</li><li>You bring a collaborative approach and focus on delivering high-quality outcomes in a fast-paced environment.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree with 6 years of relevant experience, or Master’s degree in Data Science, Analytics, Computer Science, or a related field with 4+ years of relevant experience.</li><li>Experience in data analytics, data engineering, business intelligence, or a related field.</li><li>Managerial experience.</li><li>Hands-on experience with Snowflake for data engineering and analytics workflows.</li><li>Experience with programming languages such as Python and SQL.</li><li>Familiarity with cloud-based data platforms and tools.</li><li>Strong analytical and problem-solving skills with the ability to understand and interpret complex datasets.</li><li>Excellent communication skills with the ability to translate technical insights into business value.</li><li>Proficiency in Tableau for data visualization and dashboard creation preferred.</li><li>Experience working with Databricks in addition to Snowflake preferred.</li><li>Experience developing data products for artificial intelligence use cases and integrating artificial intelligence into business reporting tools preferred.</li><li>Knowledge of advanced analytics techniques, including machine learning, statistical modeling, and data mining preferred.</li><li>Familiarity with clinical trial operational data preferred.</li><li>Collaborative and team-oriented attitude with the ability to work effectively in a fast-paced environment.</li><li>Strong attention to detail and commitment to delivering high-quality work.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Translational PK/PD Modeling]]></title>
    <date><![CDATA[Thu, 01 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50725]]></requisitionid>
    <referencenumber><![CDATA[R50725]]></referencenumber>
    <apijobid><![CDATA[r50725]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50725/principal-scientist-translational-pkpd-modeling/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Prinicpal Scientist of Translational PK/PD Modeling to develop and implement quantitative and mechanistic PK/PD models to aid in the understanding of target biology, therapeutic modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic direction of modeling and simulation sciences. </p><br><p><strong>When & Where:</strong></p><p>This role will be based in our Tarrytown, NY office and is expected to be on-site four days per week.</p><br><p><strong>Discover Your Role:</strong></p><ul><li>Independently develops and implements quantitative and mechanistic mathematical PK/PD models that inform preclinical-to-early clinical translation, including human efficacious dose predictions and first-in-human dose selection.</li><li>Actively contributes to the advancement and strategic direction of modeling and simulation sciences</li><li>Provides expert support to pre-clinical PK/PD project representatives and R&D project teams to design, execute and interpret in vitro and in vivo quantitative pharmacology studies. This included working with the Research PK group to optimize use of mouse PK data to inform translation to nonhuman primate and human PK.</li><li>Effectively integrates and summarizes modeling and simulation analyses into useable information for multidisciplinary project teams.</li><li>Remains apprised of emerging science and literature, and effectively collaborates with subject matter experts in Clinical Pharmacology, Quantitative Pharmacology and R&D to advance modeling and simulation sciences.</li><li>Shares learnings and develops best practices across disease areas and therapeutic approaches.</li><li>Committed to sharing technical expertise and the development / mentoring of others.</li><li>Presents work at internal/external scientific meetings and publishes work in scientific journals</li></ul><br><p><strong>This Role Requires</strong></p><ul><li>Ph.D. and 4+ years of experience, or M.S. and 6+ years of experience in pharmacokinetics, pharmaceutical sciences, engineering, applied mathematics or related disciplines with a track record of applying quantitative and mechanism-based PK/PD modeling and simulation approaches to advance the discovery and development of therapeutics.</li><li>Pharmaceutical industry experience required</li><li>Experience using one or more modeling and simulation platforms (e.g., Monolix, Phoenix NLME, NONMEN, ADAPT, MATLAB, SimBiology, etc.)</li><li>Strong theoretical and practical foundation in pharmacokinetics, including non-compartmental, compartmental, PK/PD and PBPK.</li><li>Ability to learn new areas of biological sciences to develop quantitative and mechanistic PK/PD models for emerging therapeutic modalities.</li><li>Familiarity with biotherapeutic modalities, including monoclonal and bispecific antibodies, gene therapy, CAR-T, siRNAs and other targeting agents preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 01 Oct 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Clinical Imaging Operations]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50766]]></requisitionid>
    <referencenumber><![CDATA[R50766]]></referencenumber>
    <apijobid><![CDATA[r50766]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50766/associate-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><strong>Build Our Future Together:</strong></p><p>As an Associate Manager, Clinical Imaging Operations, you will have a central role in the execution of key operational aspects of complex early and late phase clinical trials that will be focused on supporting our diverse general medicine portfolio. General medicine includes a wide variety of Imaging modalities such as US, MRI, DXA, CT and photography. 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 imaging 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>When & Where:</strong></p><p>This role can sit on-site in our Tarrytown, NY, Warren, NJ or Cambridge, MA office four days per week.</p><p><br><strong>Discover Your Role:</strong></p><ul><li>Collaborate with clinical study leads and cross-functional teams to manage imaging start-up activities, including vendor selection, requests for proposals, and timeline management.</li><li>Oversee external imaging vendors at the study level to support successful delivery of study data and milestones.</li><li>Author, review, and 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).</li><li>Provide technical support and training to clinical site personnel, including site initiation visits or teleconferences when needed. Review and approve training materials for imaging facilities and clinical site personnel.</li><li>Track imaging progress during clinical studies and resolve issues in collaboration with clinical study teams, sites, and imaging CROs. Provide day-to-day functional oversight by monitoring key imaging performance indicators, supporting query resolution, and troubleshooting timeliness and quality concerns.</li></ul><p><strong>This Role Requires:</strong></p><ul><li>Qualified candidates will possess a basic knowledge of clinical imaging alongside familiarity with imaging vendor processes.</li><li>BA/BS degree and 3+ years of clinical trial experience. A focus on imaging is preferred.</li><li>Preference for experience in implementation of complex site start-up logistics like site training and camera qualification.</li><li>Regulatory inspection experience is not required but would be preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Protein Expression Sciences]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50168]]></requisitionid>
    <referencenumber><![CDATA[R50168]]></referencenumber>
    <apijobid><![CDATA[r50168]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50168/senior-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[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a highly motivated Senior Scientist to join our Protein Expression Sciences Department. In this role, you will create antibody production cell lines using state-of-the-art mammalian expression technologies and develop new technologies to further advance our expression platform, while collaborating with cross-functional scientific teams.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model: On-site</li></ul><h3>Discover your role:</h3><ul><li>Apply innovative mammalian expression technologies to generate regulatory-compliant stable cell lines</li><li>Perform aseptic cell culture, handling, and transfection of cell lines</li><li>Conduct flow cytometry assays and operate liquid handler platforms (Hamilton) to analyze stable cell lines</li><li>Perform molecular biology and protein biochemistry techniques, including PCR, RT-PCR, plasmid sub-cloning, isolation of genomic DNA and RNA from CHO cells, SDS-PAGE, and western blotting</li><li>Independently design, conduct, and analyze multicolor flow cytometry experiments</li><li>Analyze and present data at smaller team and broader department meetings</li><li>Maintain complete, accurate, and timely records of experiments and data analysis</li></ul><br><h3>This role requires:</h3><ul><li>PhD with 0-3 years of postdoctoral experience, or BS/MS with 4-8 years of experience, in Immunology, Cell Biology, or Molecular Biology</li><li>Hands-on technical experience in cell culture, flow cytometry, and antibody staining</li><li>Experience with molecular biology techniques such as PCR and cloning</li><li>Passion for innovation and a desire to lead new scientific directions</li><li>Working independently, demonstrating strong problem-solving skills and the ability to manage multiple tasks efficiently without direct supervision</li><li>Strong desire to develop your skills and work with a cross-functional team and the ability to thrive in a collaborative, fast-paced environment</li><li>Experience with gene editing, lentivirus infections, CRISPR library workflows, and NGS is a plus</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Logistics Associate]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51109]]></requisitionid>
    <referencenumber><![CDATA[R51109]]></referencenumber>
    <apijobid><![CDATA[r51109]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51109/logistics-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>Build our future together:</p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Logistics Associate to join our Workplace Services team, supporting our Tarrytown campus in an on-site role. In this role, you will receive, track, and deliver incoming and outgoing materials and mail, helping colleagues get what they need on time, while collaborating with end-users, Accounting, and Environmental Health and Safety.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3>When & where:</h3><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: On-site</li></ul><h3> </h3><h3>Discover your role:</h3><ul><li>Receive, scan, and record incoming packages and packing slips to keep deliveries accurate and traceable</li><li>Deliver packages and mail to end-users across campus in a timely way</li><li>Load and unload delivery trucks and relocate materials between the main campus and associated sites</li><li>Ship returns and research samples, both domestic and international</li><li>Complete and close out work order requests from end-users</li><li>Support Accounting's 3-way match by capturing PO numbers on incoming material</li><li>Notify Environmental Health and Safety of incoming radioactive material</li><li>Collect confidential material from nearby sites for shredding, manage dry ice replenishment, and step in on mailroom duties or daily truck logs as needed</li></ul><h3> </h3><h3> </h3><h3>This role requires:</h3><ul><li>1-2 years of experience in a logistics associate role, including prior delivery experience</li><li>Valid driver's license recognized by New York State and a clear driving record, maintained throughout employment in line with Regeneron's Fleet Safety Policy</li><li>Ability to operate a forklift and power jack</li></ul><ul><li>Comfortable in a hands-on, physical, fast-moving environment, and willing to work overtime when needed</li></ul><ul><li>Pay close attention to detail and keep accurate records, clear communication and organization</li><li>Proficiency with Microsoft Office and shipping systems (UPS, FedEx)</li><li>DOT and IATA certification within one year of hire</li><li>Willingness to complete the Defensive Driving Course, sign off on the Fleet Safety Policy, and promptly report any license-related incidents to your Supervisor and EHS</li></ul><p><strong> </strong></p><p><strong> </strong><br></p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$19.86 - $31.11]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Director Rare Disease Commercial - EU4+UK Region]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49844]]></requisitionid>
    <referencenumber><![CDATA[R49844]]></referencenumber>
    <apijobid><![CDATA[r49844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49844/sales-director-rare-disease-commercial-eu4plusuk-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Sales Director Rare Disease Commercial EU4+UK Region</h3><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sales Director Rare Disease</strong> to join our International Rare Disease team, supporting our EU4+UK region. In this role, you will lead a high-performing field organization and drive commercial execution across our rare disease portfolio while collaborating with cross-functional teams and regional leadership. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Location: Paris, France - Office based, Hybrid.</p><h3><strong>Discover your role:</strong></h3><ul><li>Lead a sales team across EU4+UK to deliver company objectives.</li><li>Drive account targeting, segmentation, and multichannel customer engagement.</li><li>Set performance objectives and lead coaching, development, and succession planning.</li><li>Align incentive compensation plans with brand strategies and targets.</li><li>Partner with Commercial Operations on training, analytics, KPIs, Veeva CRM, and territory alignment.</li><li>Provide field insights on customer feedback, patient journey barriers, and competitive intelligence.</li><li>Partner with cross-functional team members to address market trends and dynamics.</li><li>You champion excellence, accountability, and patient-centricity across the organization.</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Bachelor’s degree required.</li><li>Advanced degree in life sciences, pharmacy, medicine, or business strongly preferred.</li><li>Minimum 10 years’ experience in the pharmaceutical or biotechnology industry.</li><li>Minimum 3 years in a first-line field sales management role.</li><li>Proven success hiring, mentoring, developing, and retaining high-performing teams.</li><li>Experience in rare disease, specialized medicines, or gene therapy/ATMP commercialization preferred.</li><li>Ability to operate within sophisticated multi-stakeholder account environments.</li><li>Knowledge of market access and reimbursement frameworks across EU4+UK markets.</li><li>Ability to mentor teams on value-based and access-oriented payer engagement.</li><li>Experience with Veeva CRM, Salesforce effectiveness tools, data analytics, and digital promotion.</li><li>Proficiency in English and one additional European language highly desirable (French, German, Italian, or Spanish)</li><li>Knowledge of EFPIA and applicable national pharmaceutical industry codes.</li><li>Ability to travel 50% or more across EU4+UK and hold a valid driving licence.</li><li>Established KOL relationships in rare metabolic, musculoskeletal, or hearing loss areas are desirable.</li><li>Strong leadership, communication, and interpersonal skills in multicultural environments.</li></ul><div></div><p><strong>Salary range (annually):</strong> 86,550€ - 144,250€ </p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director International Commercialization Immunology]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49976]]></requisitionid>
    <referencenumber><![CDATA[R49976]]></referencenumber>
    <apijobid><![CDATA[r49976]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49976/director-international-commercialization-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director International Commercialization Immunology to join our International Immunology team, supporting our international markets business. In this role, you will lead commercialization strategy, geographic expansion, and launch readiness across international markets while collaborating with alliance partners, Global Marketing, Pricing, Market Access, and cross-functional stakeholders. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Paris, France - multiple locations are being considered for this role</p><p>Hybrid - 3 days / week on site</p><p><strong>Discover your role:</strong></p><ul><li><p>Develop international commercialization strategies and execution plans across major and mid-sized markets.</p></li><li><p>Lead geographic expansion activities and establish commercial presence in new markets.</p></li><li><p>Coordinate launch readiness and commercialization activities with Global Marketing teams.</p></li><li><p>Guide a matrix network of commercialization leads across international markets.</p></li><li><p>Act as the regional lead for commercial alliance activities and partner engagement.</p></li><li><p>Review pricing approaches and commercial business cases with Global Pricing and Market Access.</p></li><li><p>Represent Regeneron in international meetings, conferences, and public affairs activities.</p></li><li><p>Build strong partnerships across cultures and functions to drive shared goals.</p></li></ul><div><p><strong>This role requires:</strong></p><ul><li><p>Bachelor's degree or equivalent; MBA or equivalent preferred.</p></li><li><p>12+ years of pharmaceutical industry experience in regional or international commercialization.</p></li><li><p>Experience establishing affiliate teams or commercial operations in new international markets.</p></li><li><p>Knowledge of international legal, regulatory, reimbursement, payer, and pricing environments.</p></li><li><p>Experience leading cross-functional matrix teams to deliver commercialization outcomes.</p></li><li><p>Commercial leadership or significant involvement in product and indication launches.</p></li><li><p>Experience working in strategic partnerships or alliance environments.</p></li><li><p>Experience with biologics and international forecasting, budgeting, or business case development.</p></li><li><p>Project management experience and willingness to travel as needed.</p></li><li><p>Immunology experience preferred, including dermatology, respiratory, or gastroenterology.</p></li><li><p>Cross-cultural experience, international exposure, or multilingual capabilities preferred.</p></li><li><p>Strong collaboration, stakeholder management, and communication skills.</p></li></ul></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>100.275,00 € - 167.125,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 14:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regional Market Access Lead - Europe]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50655]]></requisitionid>
    <referencenumber><![CDATA[R50655]]></referencenumber>
    <apijobid><![CDATA[r50655]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50655/director-regional-market-access-lead-europe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Paris]]></city>
    <state><![CDATA[Paris]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Regional Access Lead to join our Market Access function, supporting our European region in a hybrid work mode. In this role, you will drive market access, pricing, and reimbursement strategies for our neurology portfolio while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead European market access strategies aligned with global objectives and country needs.</p></li><li><p>Monitor payer trends, healthcare policies, and reimbursement frameworks across Europe.</p></li><li><p>Represent Europe in global access strategy discussions and shape future approaches.</p></li><li><p>Adapt access tools, payer value propositions, and objection handlers for regional use.</p></li><li><p>Support Health Technology Assessment dossiers, mock negotiations, and payer engagements.</p></li><li><p>Build relationships with payers, policymakers, and patient advocacy groups.</p></li><li><p>Align evidence generation and health economics outcomes research with payer requirements.</p></li><li><p>You bring an agile, collaborative mindset when influencing cross-functional teams.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>Regional market access launch experience across competitive therapeutic areas.</p></li><li><p>Proven European pricing, reimbursement, Health Technology Assessment, and negotiation success.</p></li><li><p>Experience developing and adapting economic models for regional and national submissions.</p></li><li><p>In-depth knowledge of European payer systems and reimbursement challenges.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>Fluent English; another European language and neurology experience are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix working, and stakeholder engagement skills.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€100,275.00 - €167,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, External Data Acquisition and Delivery]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51126]]></requisitionid>
    <referencenumber><![CDATA[R51126]]></referencenumber>
    <apijobid><![CDATA[r51126]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51126/manager-external-data-acquisition-and-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><br><p>We are seeking a Manager, External Data Acquisition and Delivery to join our Clinical Data Management team in a hybrid role. In this role, you will lead external data acquisition, delivery, and reconciliation activities across assigned Clinical Development Units, ensuring high-quality and compliant external data management practices. You will be responsible for the development of medium to high complexity Data Transfer Specifications (DTS), handle vendor oversight activities, support inspection readiness, and partner with CROs, external data providers, and cross-functional stakeholders to ensure timely and accurate delivery of external clinical data. This position offers the opportunity to drive data integrity, enhance operational perfection, and support successful study execution in a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Hyderabad (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead the development, maintenance, and governance of Data Transfer Specifications (DTS) for assigned studies and Clinical Development Units.</li><li>Author DTS documents in alignment with CDISC standards and Regeneron processes while collaborating with internal and external partners.</li><li>Act as a key liaison between Clinical Data Management, CROs, external vendors, and study teams to ensure successful external data delivery.</li><li>Provide oversight for external data vendors, including onboarding, performance monitoring, issue resolution, and escalation management.</li><li>Track DTS milestones, results, and timelines across multiple programs and data domains.</li><li>Support protocol reviews, vendor specifications, operational data flows, and data structure requirements.</li><li>Perform and supervise reconciliation between EDC and vendor data systems to ensure data integrity, completeness, and consistency.</li><li>Collaborate with Database Development, Biostatistics, Data Managers, and external partners to investigate and resolve data discrepancies.</li><li>Monitor data trends, identify risks, and support continuous improvement initiatives across External Data Services.</li><li>Support inspection readiness activities, reconciliation documentation, audit trails, eTMF maintenance, data locking, and archival activities.</li><li>Mentor and coach junior associates while serving as a Subject Matter Expert across external data domains.</li><li>Contribute to SOPs, work instructions, guidance documents, training programs, and other External Data Services tools and templates.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree in Science, Health, Mathematics, Engineering, Computational Sciences, or a related field.</li><li>7+ years of experience in External Clinical Data Acquisition or Clinical Data Management within biotechnology, pharmaceutical, or healthcare industries.</li><li>Experience handling multiple clinical data types including biomarker, eCOA, imaging, ECG, PK, genomics, and laboratory data.</li><li>Solid understanding of CDISC standards, database structures, and clinical data management procedures.</li><li>Knowledge of regulatory requirements, including 21 CFR Part 11 and ICH-GCP guidelines.</li><li>Sophisticated experience extracting and handling data in SAS, CSV, and XML formats.</li><li>Experience with EDC platforms such as Medidata Rave, Veeva, Oracle Inform, and external data reconciliation processes.</li><li>Strong project management, analytical, problem-solving, and strategic thinking skills.</li><li>Ability to influence and collaborate effectively across global, cross-functional, and matrixed teams.</li><li>Excellent interpersonal, verbal, and written communication skills.</li><li>Ability to thrive in a fast-paced environment while handling multiple priorities and timelines.</li><li>Society of Clinical Data Management (SCDM) certification is preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Principal Scientist - Neurology and Ophthalmology Imaging]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51014]]></requisitionid>
    <referencenumber><![CDATA[R51014]]></referencenumber>
    <apijobid><![CDATA[r51014]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51014/senior-principal-scientist-neurology-and-ophthalmology-imaging/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Senior Principal Scientist, Ophthalmology & Neurology</strong></p><p><em>Clinical Imaging</em></p><br><p><strong>Build our future together:</strong></p><p>We are seeking a Senior Principal Scientist with a focus in Ophthalmology and Neurology to join our Clinical Imaging team. You will conceptualize, support, execute, and optimize complex imaging measures and biomarkers in early- to late-phase clinical trials. You will work closely with Regeneron clinical, preclinical and external partners, with emphasis on delivery of high-quality imaging data and development of innovative imaging-based biomarkers across imaging modalities and indications.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY United States</p><br><p><strong>Discover your role:</strong></p><ul><li>Guide Regeneron clinical teams as imaging subject matter expert to ensure optimal design and execution of imaging biomarker strategy related to study endpoints, including development of protocols, imaging manuals, imaging charters and statistical analysis plans, and be the main clinical team collaborate with imaging Clinical Research Organizations, ensuring flawless conduct and data integrity of study's imaging components.</li></ul><ul><li>Collaborate closely with Research colleagues to develop and qualify imaging biomarkers with a view toward clinical translation.</li></ul><ul><li>Lead the development and execution of innovative joint image analyses projects, including novel imaging biomarker development, while collaborating closely with different departments and functions such as Regeneron Genetics Center, Imaging Sciences, Translational Medicine, Biostatistics and Data Management, etc.</li></ul><ul><li>Collaborate closely with external vendors, investigators and site personnel and Clinical operations teams to ensure the appropriate selection of Imaging equipment and parameters for image acquisition and pre- and on-study QC/calibration and standardization.</li></ul><ul><li>Oversee image analysis and interpretation of results and work closely with colleagues to oversee the development of study reports and publications as appropriate.</li></ul><ul><li>Support regulatory submission packages with the appropriate original content and documentation.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Demonstrated outstanding oral and written communication skills.</li></ul><ul><li>Work efficiently within a fast-paced, collaborative environment.</li></ul><ul><li>Come up with new and outstanding ideas that move solutions forward.</li></ul><ul><li>Possess a broad knowledge and perspective and are future oriented.</li></ul><ul><li>Desire to make a broader impact on developing medicines for patients with serious diseases.</li></ul><ul><li>A PhD in a relevant field, with 6+ years of demonstrated ability in Ophthalmology and Neurology Clinical Imaging.</li></ul><ul><li>Extensive familiarity with ocular and neuro imaging modalities such as OCT, FA, CFP, MRI, PET etc.</li></ul><ul><li>A strong understanding of imaging file formats and analysis methods.</li></ul><ul><li>Demonstrated ability in the development and validation of imaging biomarkers.</li></ul><ul><li>Industry experience in creating and managing imaging protocols, manuals, and charters, and proficiency in statistical analysis plans related to imaging endpoints.</li></ul><p><br><br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Medical Affairs Operations, Canada]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51069]]></requisitionid>
    <referencenumber><![CDATA[R51069]]></referencenumber>
    <apijobid><![CDATA[r51069]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51069/manager-medical-affairs-operations-canada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build</strong><strong> our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Medical Affairs Operations, Canada to join our Medical Affairs team, supporting our Canadian organization in a hybrid work mode. In this role, you will deliver compliant, high-quality medical operations while collaborating with local colleagues, cross-functional stakeholders, and global teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Mississauga, Canada</p><p>Office based, Hybrid</p><p>Occasional business travel is required.</p><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Drive timely, compliant execution of country Medical Affairs priorities across therapeutic areas.</li><li>Maintain audit readiness, legally required documentation, transparency reporting, and anti-bribery and anti-corruption records.</li><li>Execute regulatory and Good Practice processes end-to-end through local systems.</li><li>Localize procedures, maintain process guides, and identify operational improvement opportunities.</li><li>Manage vendor lifecycles, contracts, purchasing, budgets, expenses, and spend reporting.</li><li>Lead medical meetings, congress logistics, agendas, communications, action tracking, and follow-up.</li><li>You build collaboration through onboarding, operational communications, standardized processes, and team coordination.</li></ul><br><h3><strong>This role requires:</strong></h3><br><ul><li>Bachelor’s degree in life sciences, business, a related field, or equivalent experience.</li><li>Seven to nine years’ pharmaceutical or biotechnology experience in medical operations, project support, coordination, or administration.</li><li>Country organization experience and knowledge of compliance, transparency, Medical Governance, and regulated processes.</li><li>Microsoft Office proficiency and experience with Veeva CRM, Vault Medical, PromoMats, and procurement tools.</li><li>Fluency in the local language, with business-proficient English preferred.</li><li>Strong organization, communication, prioritization, and stakeholder management with limited supervision.</li><li>A proactive, collaborative, detail-oriented approach to cross-functional operational and project work.</li><li>Event and congress expertise plus contract or procurement knowledge, including iCertis or SAP, are preferred.</li><li>Finance, Procurement, or commercial operations experience is desirable.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Chicago Central-Triad]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51335]]></requisitionid>
    <referencenumber><![CDATA[R51335]]></referencenumber>
    <apijobid><![CDATA[r51335]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51335/medical-specialist-i-dermatology-chicago-central-triad/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Chicago]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><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.<br></p><p><strong>When & where:</strong></p><ul><li>Remote role</li><li>Location: Chicago, IL</li></ul><br><p><strong>Discover your role:</strong></p><br><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><li>demonstrate strong and consistent sales performance that exceeds expectations related to product goals</li></ul><br><br><p><strong>This role requires:</strong></p><br><ul><li>A Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus</li><li>We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience</li><li>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</li><li>This role requires the ability to travel and cover large geographic territories</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 17:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QC Microbiology Scientist]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49155]]></requisitionid>
    <referencenumber><![CDATA[R49155]]></referencenumber>
    <apijobid><![CDATA[r49155]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49155/qc-microbiology-scientist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> QC Microbiology Associate Scientist / Scientist</strong> to join our <strong>QC Tech Resources </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li><p>Location: Raheen, Limerick</p></li></ul><h3><strong>What you’ll do:</strong></h3><ul><li><p>Validating methods and equipment related to sterility, bioburden, endotoxin testing, and microbial identifications.</p></li><li><p>Writing technical documentation, including position papers, validation reports, and microbiological investigations.</p></li><li><p>Culturing organisms, conducting research, and characterizing them for use in investigations and cleaning development.</p></li><li><p>Reviewing new test procedures and assays for accuracy and compliance.</p></li><li><p>Evaluating and acquiring new methodologies, techniques, and equipment as needed.</p></li><li><p>Overseeing contract laboratory testing to ensure quality and compliance.</p></li><li><p>Setting product specifications and alert/action levels for microbiological standards.</p></li><li><p>Leading technical troubleshooting and problem investigations.</p></li><li><p>Reviewing assay, process, and equipment validation reports, as well as other technical documents for correctness and regulatory compliance.</p></li><li><p>Coaching junior team members on good microbiology lab practices and modern aseptic techniques.</p></li><li><p>Supporting and participating in regulatory inspections to ensure compliance.</p></li><li><p>Demonstrating investigational skills and working knowledge of microbiology assay development and validation.</p></li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li><p>You have a proven record to work independently or as part of a team.</p></li><li><p>Possessing a strong background in pharmaceutical microbiology, GMP working experience in QC labs, and aseptic techniques.</p></li><li><p>You possess strong trouble-shooting and problem solving skills.</p></li><li><p>You have strong attention to detail & excellent written and oral skills.</p></li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li><p>Assoc QC Microbiology Scientist: Minimum 0-2 years of Experience</p></li><li><p>QC Microbiology Scientist: Minimum 2 years of Experience</p></li><li><p>To be considered for this opportunity you should have a BS/BA or equivalent experience in Microbiology or related field and 2+ years of validated experience, or equivalent combination of education and experience.</p></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><p><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIEQC</strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 03:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Translational Medicine Program Manager]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51189]]></requisitionid>
    <referencenumber><![CDATA[R51189]]></referencenumber>
    <apijobid><![CDATA[r51189]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51189/senior-manager-translational-medicine-program-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>The Senior Manager, Translational Medicine Program Management, provides program management support to cross-functional Translational Working Groups (spanning multiple development programs) and will also lead program agnostic initiatives. This role manages translational activities from preclinical research through post-marketing by driving the development and implementation of integrated Translational Medicine strategies, goals, timelines, and key deliverables.</p><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY</li></ul><br><h3><strong>Discover your role: </strong> </h3><ul><li>Provides scientific and/or operational direction to R&D functions for assigned Translational Medicine portfolio.</li><li>Drives Translational Working Groups by integrating key partners from Research, Preclinical, Translational Medicine (Precision Medicine, Clinical Imaging, Digital Biomarkers), Drug Safety and Pharmacometrics, Bioanalytical Sciences, Clinical Development, Program Operations, and other Global Development functions.</li><li>Develops and maintains integrated Translational Medicine program plans and timelines for strategy development and key program/study milestones, assay/platform/technology deliverables, interim/final data deliverables, and related decision points.</li><li>Supports development and execution of the Translational Medicine Strategy and its incorporation into clinical strategy, Integrated Development Plans, program/study plans in systems/tools, relevant governance discussions, and ensures cross-functional alignment and smooth transitions across pipeline stages. Manages relationships and communications across Translational Medicine, Research, Clinical Development, Program Management, and other cross-functional partners to improve alignment, execution, and visibility of deliverables.</li><li>May support cross-functional program-agnostic Translational Medicine initiatives, including process and technology development, and systems/tools enablement.</li><li>Interacts with senior leaders and may support executive-level communications, Translational Medicine Leadership reviews, and portfolio-level discussions.</li><li>Independently executes responsibilities. Contributes to program strategy goals and objectives. Influences the direction of the team.</li></ul><p><strong> </strong></p><h3><strong>This role requires:</strong></h3><ul><li>Have knowledge of Translational Medicine, Precision Medicine/translational sciences, biomarker and clinical outcome assessment strategies, biomarker/assay development, imaging, digital biomarkers, and sample management planning/logistics.</li><li>Have a high-level knowledge of drug discovery and development.</li><li>Proven track record in life sciences program management, including drug discovery and/or development programs.</li><li>Have excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company to establish credibility with Subject Matter Experts on the project teams.</li><li>Have strong presentation, critical thinking, planning, problem-solving, and executive communication skills.</li><li>Actively promote constructive interactions among team members to address difficult situations.</li><li>Resolve and negotiate conflicts or problems with tact, diplomacy and composure.</li><li>Handle multiple projects and priorities with exceptional organizational and time management skills (both project and self).</li></ul><ul><li>Bachelor’s and/or master’s degree with 8+ years, or a PhD with 7+ years, plus progressive project or program management experience in the pharmaceutical, biotechnology, life sciences, or a related industry. Experience supporting translational medicine and biomarker strategy, clinical development and/or Cross-functional portfolio/program planning and program management certification is preferred.<br></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Site Budgets]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51290]]></requisitionid>
    <referencenumber><![CDATA[R51290]]></referencenumber>
    <apijobid><![CDATA[r51290]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51290/manager-site-budgets/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><br><p>For assigned studies: responsible for (1) developing accurate and timely total investigator grants and per subject cost estimates, based on the study design and schedule of events (using a fair market value tool), (2) reviewing CROs’ and/or sites’ proposed changes to the study-specific budget parameters (in partnership with other business lines internally), (3) ensuring the delivery of high quality, compliant, effective, and timely deliverables, (4) maintaining productive relationships with internal client groups, (5) leading ongoing process improvements and training sessions (including participating on strategic initiatives), (6) onboarding, training, and mentoring peers, and (7) potentially having direct reports.</p><br><h3><strong>Discover your role:</strong></h3><p><strong>Core Responsibilities</strong></p><ul><li>Provide subject matter expertise for assigned therapeutic areas</li><li>Accountable for ensuring performance and efficiency standards are met for assignments</li><li>Perform in a manner consistent with Regeneron’s values</li></ul><p><strong>Budgeting & Financial Analysis</strong></p><ul><li>Provide ongoing guidance to peers on site budgeting</li><li>Utilize a fair market value tool and other relevant data to develop total investigator grants, per-subject cost estimates, and budget scenarios</li><li>Utilize per-subject cost output, along with protocol design, historical information, and operational approach, to determine overall investigator grant cost</li><li>Develop and present budget scenarios to study teams for OPRB and related meetings</li><li>Understand the nuances between early and final budget estimates</li><li>Manage changes to study scope, ensuring timely budget amendment and implementation</li><li>Serve as single point of contact for non-standard budget line items requiring internal approval</li></ul><p><strong>Stakeholder Engagement</strong></p><ul><li>Engage with relevant stakeholders from early planning throughout the end-to-end budgeting lifecycle</li><li>Work closely with stakeholders and communicate effectively to ensure business objectives are met</li><li>Develop and enhance relationships with stakeholders</li><li>Handle site budgeting–related escalations effectively and efficiently; resolve issues of moderate to high complexity</li></ul><p><strong>Process Improvement & Systems</strong></p><ul><li>Help develop and enhance site budgeting processes</li><li>Stay current on industry standards and help identify new best practices to drive continuous improvement</li><li>Lead ongoing process improvements and training sessions, including participation in strategic initiatives</li><li>Develop guidance documents</li><li>Ensure internal systems are updated in a timely, accurate, and complete manner</li><li>Effectively and efficiently prioritize assignments</li><li>Responsible for making timely decisions and directing outcomes</li></ul><p><strong>People Development</strong></p><ul><li>Help train others on site budgeting and industry practices</li><li>Onboard, train, and mentor peers</li><li>Potentially manage direct reports</li></ul><p><strong>Travel</strong></p><ul><li>May require up to 25% travel</li></ul><h3><strong>This role requires:</strong></h3><ul><li>Ability to mitigate and drive solutions regarding site budgeting challenges</li><li>Ability to identify and implement best practices and contribute to continuous improvement for site budgeting</li><li>Ability to influence vendors and internal stakeholders</li><li>Strong knowledge of site budgeting practices</li><li>Comfortable participating on and occasionally leading cross functional teams of peers</li><li>Ability to lead, manage, coach, and train peers or direct reports</li><li>Ability to effectively onboard, train, and mentor peers</li><li>Ability to lead ongoing, process improvements (including participating on strategic initiatives)</li><li>Functional subject matter expert</li></ul><p><strong> </strong></p><p><strong>Minimum Years of Experience:</strong></p><ul><li>Bachelor’s degree plus 7 years of relevant experience</li><li>Required minimum of 3-5 years of direct experience with clinical site budgeting at a biopharmaceutical company, CRO, or site</li><li>Required minimum of 6 months of applicable mentoring and training and/or matrix-level people management experience</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 14:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ophthalmology Medical Specialist II LA, MS, AR]]></title>
    <date><![CDATA[Thu, 08 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51213]]></requisitionid>
    <referencenumber><![CDATA[R51213]]></referencenumber>
    <apijobid><![CDATA[r51213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51213/ophthalmology-medical-specialist-ii-la-ms-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Louisiana]]></city>
    <state><![CDATA[Louisiana]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together: </h3><br><p>At Regeneron, we are committed to transforming the lives of patients through science and innovation. As a leading biotechnology company, we discover, develop, manufacture, and commercialize medicines for serious diseases. We are seeking a <strong>Medical Specialist, Ophthalmology</strong> to join our Retina team, supporting the Louisiana, Mississippi, and Arkansas territory in a field-based role. In this position, you will help bring innovative retinal therapies to healthcare providers, build trusted partnerships with retina specialists and ophthalmology practices, and drive business results that improve patient outcomes. Working closely with customers and cross-functional partners, you will play a critical role in expanding access to life-changing treatments while contributing to a purpose-driven organization dedicated to advancing science and patient care.</p><br><h3>When & where:</h3><ul><li><strong>Location:</strong> Louisiana, Mississippi, Arkansas territory</li><li><strong>Work model/flexibility:</strong> Field-based</li><li><strong>Travel percentage:</strong> Approximately 40-60%</li></ul><br><h3>Discover your role:</h3><ul><li>Develop and grow strategic relationships with retina specialists, ophthalmologists, and key customer accounts throughout the territory.</li><li>Execute territory business plans to achieve sales objectives and support the growth of Regeneron’s ophthalmology portfolio.</li><li>Educate healthcare providers on clinical data, product benefits, patient identification, and treatment pathways.</li><li>Partner with customers to identify opportunities that enhance patient access and improve treatment outcomes.</li><li>Navigate complex account environments using strong business acumen and strategic account management skills.</li><li>Collaborate cross-functionally to address customer needs and deliver valuable solutions that support practice success.</li><li>Analyze market trends, customer insights, and territory dynamics to inform business planning and prioritization.</li><li>Manage a geographically dispersed territory while balancing customer engagement, business objectives, and travel requirements.</li><li>Maintain expertise in the ophthalmology and retina landscape, including competitive, reimbursement, and market developments.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor’s degree and a minimum of 5 years of specialty sales experience within the pharmaceutical or biotechnology industry.</li><li>Demonstrated history of high sales performance and consistent achievement of territory goals and business objectives.</li><li>Experience selling biologics and buy-and-bill products within specialty healthcare settings.</li><li>Strong understanding of reimbursement programs, government programs, managed care, formulary processes, and contract negotiations.</li><li>Ophthalmology sales experience preferred, with retina-focused experience strongly preferred.</li><li>Proven ability to develop strategic relationships with physicians, retina specialists, and other key customer stakeholders.</li><li>Strong business acumen, account management capabilities, and the ability to navigate complex customer and market dynamics.</li><li>Excellent communication, customer engagement, and cross-functional collaboration skills.</li><li>Must reside within or near the assigned Louisiana, Mississippi, and Arkansas territory; relocation assistance is not provided.</li><li>Ability and willingness to travel approximately 40-60% of the time in support of customer and business needs.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$162,000.00 - $220,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Oct 2026 22:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Supply Systems]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51368]]></requisitionid>
    <referencenumber><![CDATA[R51368]]></referencenumber>
    <apijobid><![CDATA[r51368]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51368/manager-clinical-supply-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Supply Systems Manager to join our Clinical Supply Systems Group, supporting our clinical trials in a hybrid setting. In this role, you will support Interactive Response Technology (IRT) systems while collaborating with clinical trial management, data management, biostatistics and clinical supply leads. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Mulitiple locations are being considered for this role (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead IRT study-team support from protocol-aligned requirements through conduct and closeout.</li><li>Oversee vendor functionality, processes and performance through routine issue-resolution and risk-management meetings.</li><li>Manage deployment timelines and application launches with internal teams and vendors.</li><li>Maintain requirements, user guides, training materials and communication plans.</li><li>Coordinate user acceptance testing.</li><li>Coordinate randomisation and kit-list uploads with Clinical Logistics and biostatistics.</li><li>Develop vendor-supported clinical-team and site training, presenting functionality and requirements at investigator meetings or clinical research associate training when required.</li><li>You bring a collaborative, solution-focused mindset.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree or eight years’ equivalent experience.</li><li>Four years’ biotechnology/pharmaceutical experience, including two directly with IRT systems.</li><li>Clinical-trial IRT development experience, protocol interpretation and IRT/programming terminology knowledge.</li><li>International Council for Harmonisation/Good Clinical Practice and regulatory guideline/directive knowledge.</li><li>Microsoft Office Suite competency.</li><li>Understanding of current and future business trends.</li><li>Leadership, negotiation, mentoring and coaching skills.</li><li>Multitasking, prioritisation, problem-solving, project management and organisational skills.</li><li>Written, verbal and small/large-group presentation skills.</li><li>Cross-functional/cross-cultural awareness and matrix-working ability.</li><li>Disease/therapeutic-area knowledge is a plus.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 05:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Toxicologist]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47420]]></requisitionid>
    <referencenumber><![CDATA[R47420]]></referencenumber>
    <apijobid><![CDATA[r47420]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47420/senior-toxicologist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Toxicologist utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with guidance from her/his direct supervisor working effectively within cross-functional project teams. The Sr. Toxicologist will demonstrate a thorough understanding of GLP regulations and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the design, conduct, interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/toxicology studies in rodent and non-rodent safety models. The Sr. Toxicologist will provide primary authorship of all regulatory documentation required for submission packages, demonstrating excellent problem solving and communication skills (written and verbal).</p><p>Experience with multiple therapeutic modalities preferred, including antibody, oligonucleotide, and genetherapy products.</p><p><strong>JOB RESPONSIBILITIES:</strong></p><ul><li><p>Represent toxicology on global research and development project teams communicating non-clinical safety assessment strategy.</p></li><li><p>Coordinate cross-department execution of the experimental plan including program budgets, and timing of toxicology studies in relation to regulatory and clinical milestones.</p></li><li><p>Work with study monitoring group to coordinate, design, monitor, and report toxicology and safety pharmacology studies at contract research organizations.</p></li><li><p>Communicate toxicology study findings, including relevant interpretation, to project teams and management.</p></li><li><p>Contributing to non-clinical sections of regulatory documents including IND and NDA submissions.</p></li><li><p>Maintain currency with GLP regulations and ICH, FDA and EMEA non-clinical safety guidelines.</p></li><li><p>Keep up with the latest scientific developments by reading the current literature and attending conferences.</p></li></ul><p><strong>JOB REQUIREMENTS:</strong></p><ul><li>Advanced degree (e.g. PhD, DVM) in pharmacology, toxicology or closely related biological science along with 3-5 years relevant pharmaceutical industry experience, or Master’s Degree + ≥ 10 years relevant pharmaceutical industry</li><li>Experience in designing, monitoring and interpreting non-clinical safety studies.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Validation Specialist, Fill Finish]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46783]]></requisitionid>
    <referencenumber><![CDATA[R46783]]></referencenumber>
    <apijobid><![CDATA[r46783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46783/principal-qa-validation-specialist-fill-finish/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Quality Assurance (QA) Validation Specialist to join our QA Validation team. They will lead the utilities and EMPQ team for our internal fill finish facility, overseeing qualification of utilities, cleanrooms, and filling lines critical to commercial production; ensure regulatory compliance, strengthen the contamination control strategy, and drive key licensure activities.</p><p><strong>When & where:</strong></p><ul><li>Location: Rensselaer, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead validation and serve as SME for utilities and environmental qualification; assess change controls, review CAPAs/NOEs, approve documents, and lead audits</li><li>Plan and execute cleanroom qualifications and requalification; oversee EMPQ for filling line clean air equipment</li><li>Drive QRM deliverables including HACCP assessments and continuous trending/reporting</li><li>Lead investigations of contamination events associated with environmental monitoring in cleanrooms and clean air equipment</li><li>Qualify critical utilities: Water for Injection (WFI) , pharmaceutical air, AHUs, clean steam generators, and nitrogen distribution systems</li><li>Manage and develop a specialist and a team of consultants to meet project milestones and deliver qualification/documentation deliverables</li><li>Establish processes that ensure compliance with regulatory requirements, including participation in Annex 1 gap assessments</li><li>Influence the creation and revision of local/global policies, standards, procedures, and business processes to align with industry best practices</li><li>Demonstrated experience in a cGMP-regulated environment, including validation, inspection and audit readiness</li><li>Possesses strong cross-functional collaboration and communication skills</li></ul><p><strong>The environment and physical rhythms of the role:</strong></p><ul><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Engineering, Chemistry, or Life Sciences and 8+ years of relevant experience</li><li>Experience in utility and facility qualification/validation</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Health Economics & Outcomes Research, Solid Tumors]]></title>
    <date><![CDATA[Mon, 27 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45357]]></requisitionid>
    <referencenumber><![CDATA[R45357]]></referencenumber>
    <apijobid><![CDATA[r45357]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45357/associate-director-health-economics-outcomes-research-solid-tumors/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong><br> At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. As an Associate Director you will develop HEOR strategies and plans, conduct HEOR and RWE studies and develop publications and deliverables. We work closely with Market Access, Medical Affairs, Clinical Development, Commercial, Regulatory and other groups to ensure evidence needs are identified and addressed to demonstrate the value with a focus on solid tumors<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Sleepy Hollow, NY</p><p><strong>Discover your role:</strong><br>• Develop and implement HEOR strategies and programs throughout the product’s lifecycle, to inform and support clinical development and regulatory needs during early pipeline phase and ensuring optimal market access.<br>• Collaborate with business partners to develop and support compelling product value propositions with aim to optimize patient access.<br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation.<br>• Leverage RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams generating insights to inform development programs and key business questions.<br>• Co-lead conduct of regulatory-grade real world evidence studies and provide education on emerging opportunities for employing RWE across the solid tumor portfolio.<br>• Collaborate on conduct and communication of epidemiology and pharmacoepidemiology analyses and studies.<br>• Provide relevant input into selection of patient population, comparators and endpoints within clinical trials to enable demonstration of robust incremental value over standard of care that can facilitate optimal patient access.<br>• Develop and implement Clinical Outcomes Assessment (COA) measurement strategies and plans in support of product labeling, patient access and product differentiation.<br>• Develop and validate COA endpoints for integration in clinical studies. Produce COA evidence dossiers for regulatory submissions.<br>• Evaluate relevant payer and health technology assessment (HTA) decisions, collect feedback in advisory meetings and apply key takeaways. <br>• Maintain an up-to-date awareness of regulatory and payer/HTA considerations that may impact planning for and implementation of HEOR programs.<br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.</p><p><strong>This role requires:</strong><br>• An Advanced degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field and 4+ years with PhD or 6+ years with MS in HEOR; at least 3 years of life science company or healthcare consulting experience is a plus. <br>• Strong technical expertise required in design and conduct of HEOR studies and models. <br>• Solid understanding of regulatory (e.g. FDA, EMA) and HTA considerations. <br>• Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data. <br>• Experience with Oncology is preferred<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Product & Pipeline Communications - Oncology & Hematology]]></title>
    <date><![CDATA[Tue, 28 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47986]]></requisitionid>
    <referencenumber><![CDATA[R47986]]></referencenumber>
    <apijobid><![CDATA[r47986]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47986/senior-manager-product-pipeline-communications-oncology-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>BUILD OUR FUTURE TOGETHER:</strong><br>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Corporate Communication to join our Product and Pipeline Communications team within Corporate Affairs, supporting our U.S. and international oncology business in a hybrid role. In this role, you will lead communications for our blood cancer portfolio and pipeline and support solid tumour programmes while collaborating with Commercial, Clinical, Medical Affairs, Legal, Regulatory, and in-country Corporate Affairs teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>WHEN & WHERE: </strong>Sleepy Hollow, NY. Hybrid, minimum four days on-site per week.</p><p><br><strong>DISCOVER YOUR ROLE:</strong><br>- Lead U.S. and Global communications for our blood cancer portfolio and pipeline</p><p>- Partner with Commercial, Clinical, Legal, and Regulatory teams as a trusted strategist and media coach</p><p>- Manage media relations, congress support, regulatory milestones, and stakeholder engagement</p><p>- You translate complex science into compelling narratives for diverse external audiences</p><p>- Identify and assess communications risks, recommending response strategies</p><p>- Collaborate with in-country Corporate Affairs teams to extend global strategies locally</p><p>- Oversee agency partners, resources, and budget to deliver cohesive outcomes</p><p>- You build consensus and foster trusted relationships across functions and levels</p><p><br><strong>THIS ROLE REQUIRES:</strong><br>- Bachelor's degree with 8–10+ years of relevant experience, including 5+ years in product or pipeline communications (in-house or agency)</p><p>- Strong writing, editing, and content design skills with ability to translate complex clinical data for external audiences</p><p>- Knowledge of the regulatory, commercial, and legal landscape governing pre-approval and post-approval pharmaceutical communications</p><p>- Proven experience with social media and digital communications strategies</p><p>- Experience managing agency partners and vendor workstreams</p><p>- Background in biotechnology or pharmaceutical communications in oncology (preferred)</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Key Account Manager Sud (Ematologia)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49793]]></requisitionid>
    <referencenumber><![CDATA[R49793]]></referencenumber>
    <apijobid><![CDATA[r49793]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49793/key-account-manager-sud-ematologia/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Italy]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Costruiamo insieme il nostro futuro:</strong></p><p>In Regeneron utilizziamo la scienza e l’innovazione per sviluppare farmaci che cambiano la vita delle persone con malattie gravi. Cerchiamo un Senior Sales Specialist, Ematologia Commerciale, Italia da inserire nel nostro team vendite di ematologia. La posizione supporterà il business italiano con un modello di lavoro sul territorio. In questo ruolo, promuoverai la crescita del territorio e relazioni di valore con i professionisti sanitari. Collaborerai con i colleghi dell’area medica e con altre funzioni. Questa posizione offre l’opportunità di contribuire a un’organizzazione in rapida crescita, guidata dalla scienza e orientata ai pazienti.</p><p><strong>Quando e dove:</strong></p><p>Italia Sud<br>Posizione sul territorio, con trasferte frequenti.</p><p><strong>Scopri il tuo ruolo:</strong></p><ul><li><p>Costruire relazioni di qualità con i professionisti sanitari utilizzando conoscenze scientifiche aggiornate e messaggi di vendita approvati.</p></li><li><p>Attuare i piani commerciali e di marketing per raggiungere gli obiettivi di vendita e gli indicatori di performance.</p></li><li><p>Gestire gli account strategici attraverso pianificazione, targeting e segmentazione, in linea con le indicazioni regionali.</p></li><li><p>Sviluppare piani locali per gli account utilizzando dati di mercato e aggiornarli in base alle dinamiche del mercato.</p></li><li><p>Collaborare con i colleghi dell’area medica su programmi regionali a supporto delle esigenze dei professionisti sanitari.</p></li><li><p>Rappresentare Regeneron Ematologia in congressi e incontri regionali, nazionali e internazionali.</p></li><li><p>Utilizzerai canali diretti e digitali per ottimizzare il coinvolgimento e contribuire al miglioramento della pratica clinica.</p></li></ul><p><strong>Questo ruolo richiede:</strong></p><ul><li><p>Laurea o qualifica equivalente riconosciuta per i professionisti delle vendite.</p></li><li><p>Almeno cinque anni di esperienza nelle vendite farmaceutiche, inclusa un’esperienza essenziale in ematologia.</p></li><li><p>Conoscenza del Codice della Federazione Europea delle Industrie e Associazioni Farmaceutiche e delle normative locali applicabili.</p></li><li><p>Ottima conoscenza dell’italiano; la conoscenza dell’inglese costituisce un vantaggio.</p></li><li><p>Attitudine tecnica alla vendita basata sulla patologia e sui concetti scientifici.</p></li><li><p>Capacità di utilizzare dati, sistemi multipli e piattaforme di Customer Relationship Management.</p></li><li><p>Eccellenti capacità di coinvolgimento del cliente, presentazione, pianificazione e definizione delle priorità.</p></li><li><p>Capacità di lavorare autonomamente entro scadenze ristrette, dimostrando integrità e una comunicazione etica.</p></li><li><p>L’esperienza nel lancio di prodotti costituisce un vantaggio. </p></li></ul><p>Ti riconosci in questa descrizione? Candidati ora per compiere il tuo primo passo verso il Regeneron Way! Ci impegniamo a costruire un ambiente di lavoro con una cultura inclusiva. Regeneron è un datore di lavoro che garantisce pari opportunità e tutti i candidati qualificati saranno presi in considerazione per l’assunzione senza distinzione di razza, colore della pelle, religione o credo (o loro assenza), sesso, orientamento sessuale, identità o espressione di genere, riassegnazione di genere, stato civile o di unione civile, gravidanza o stato genitoriale, età, disabilità, nazionalità, stato di cittadinanza, origine etnica o nazionale, appartenenza alla comunità dei Viaggiatori, stato familiare, informazioni genetiche, stato militare o di veterano, o qualsiasi altra caratteristica protetta dalla legge applicabile. Ove richiesto, forniremo adeguati accomodamenti ai candidati con disabilità o malattie croniche note durante il processo di selezione, salvo che tali accomodamenti comportino un onere eccessivo.</p><p>Dove necessario, divulghiamo le fasce salariali per i ruoli in tutti i Paesi in cui operiamo. L’offerta finale sarà determinata all’interno della fascia pertinente in base al Paese di impiego, allo specifico livello del ruolo e alle competenze ed esperienze del candidato. In alcuni Paesi possono essere applicati contratti collettivi di lavoro (CCNL), che possono influenzare determinati elementi della retribuzione o dei benefit. Regeneron offre un pacchetto di total rewards competitivo e completo che può includere, a seconda del Paese e del ruolo: bonus annuali o altri piani di incentivazione, assegnazioni azionarie, benefici pensionistici o di previdenza, contributo aziendale al piano 401(k), programmi per la salute e il benessere, centri fitness, coperture assicurative (ad es. sanitaria, odontoiatrica, oculistica, vita e invalidità), ferie e permessi retribuiti e benefit per il supporto alla famiglia. Per ulteriori informazioni sui benefit Regeneron negli Stati Uniti, visita <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. Per le altre sedi, ulteriori informazioni verranno fornite durante il processo di selezione. Per qualsiasi domanda, rivolgiti al tuo recruiter.</p><p>Ti informiamo che in Regeneron crediamo di dare il meglio di noi quando lavoriamo insieme. Per questo motivo, molti ruoli richiedono la presenza in sede. Per maggiori informazioni sulle aspettative di lavoro in presenza per il tuo ruolo e la tua sede, parla con il tuo recruiter e con il responsabile delle assunzioni.</p><p>Nell’ambito del processo di selezione, potranno essere effettuati determinati controlli di background in conformità con le leggi del Paese in cui è basata la posizione. Lo scopo di tali controlli è verificare alcune informazioni prima dell’inizio del rapporto di lavoro, come l’identità, il diritto al lavoro e le qualifiche formative.</p><p>Per le posizioni in Canada: questo annuncio si riferisce a una posizione già esistente.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Respiratory *Tokyo, Chiba Area]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49804]]></requisitionid>
    <referencenumber><![CDATA[R49804]]></referencenumber>
    <apijobid><![CDATA[r49804]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49804/medical-representative-mr-respiratory-startokyo-chiba-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Sales Representative Immunology Dermatology Japan to join our Immunology Commercial Team, supporting our Japan business in a field-based work mode. In this role, you will achieve dermatology sales objectives through strategic territory management while collaborating with alliance partners and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Japan</p><p>Work model: Field-based</p><br><p><strong>Discover your role:</strong></p><ul><li>Achieve respiratory sales objectives through effective territory and budget management.</li><li>Develop annual territory business plans using market insights and brand strategies.</li><li>Create territory action plans using key data sources.</li><li>Deliver customer value through disease and concept-focused selling.</li><li>Complete expense, call, marketing, and field insight reporting.</li><li>Ensure compliance with Regeneron legal and regulatory requirements.</li><li>Collaborate with alliance partners to achieve shared business objectives.</li><li>You build trusted customer relationships and adapt to changing market needs.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree or equivalent.</li><li>Minimum five years of pharmaceutical sales representative experience.</li><li>Valid driver license and MR Certification.</li><li>Strong customer engagement skills with a focus on value delivery.</li><li>Ability to conduct disease and concept selling.</li><li>Excellent written, verbal, and presentation skills.</li><li>Strong planning, organization, and territory management capabilities.</li><li>Ability to present effectively to diverse audiences.</li><li>Ability to work independently against strategic and tactical plans.</li><li>Computer proficiency with word processing, spreadsheets, databases, and email software.</li><li>Alliance partnership experience.</li><li>Therapy area knowledge in respiratory or ENT and biologics sales experience preferred.</li><li>Current clinical knowledge of relevant therapy areas and competitor products preferred.</li><li>Established Key Opinion Leader relationships within respiratory or ENT preferred.</li><li>English fluency is a plus.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Clinical Data Management]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45840]]></requisitionid>
    <referencenumber><![CDATA[R45840]]></referencenumber>
    <apijobid><![CDATA[r45840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45840/senior-director-clinical-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><h3>Build our future together</h3><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Director, Clinical Data Management, India to join our Clinical Data Management Leadership Team, supporting our clinical pipeline in an on-site role. You will shape the global operational vision and strategy for Data Management, build a high-performing regional organisation, and support the recruitment of top talent across other R&D functions. You will also act as the local R&D Lead for the Global Capability Centre, working across Clinical Data Operations, Central Services, External Data Acquisition, and external partners.</p><br><h3>When & where</h3><p>Hyderabad (on-site).</p><br><h3>Discover your role</h3><ul><li><p>Build and lead a regional Clinical Data Management organisation spanning reporting, review, coding, laboratory data processing, and database operations.</p></li><li><p>Serve as the R&D Lead for the Regeneron Global Capability Centre and the local point of contact for all R&D functions.</p></li><li><p>Provide local leadership and guidance while supporting culture and engagement across R&D teams.</p></li><li><p>Define functional metrics and quality indicators to drive compliance, quality, and timely portfolio delivery.</p></li><li><p>Oversee functional service providers and external data vendors, managing performance and risk.</p></li><li><p>Lead cross-functional initiatives that strengthen operations, improve efficiency, and support inspection readiness.</p></li><li><p>Advance automation and AI solutions that reduce manual effort and accelerate data access.</p></li><li><p>Shape organisation design, evaluate resource needs, and hire and develop talent across the team.</p></li></ul><h3>This role requires</h3><ul><li><p>15+ years of clinical data management experience in pharmaceutical or biotech, including 10+ years of functional leadership and 8+ years of people management.</p></li><li><p>Experience leading teams of 50–150 supporting global data management functions.</p></li><li><p>Strong knowledge of clinical data management regulations and standards, including 21 CFR Part 11, ICH-GCP, GxP, and GDPR.</p></li><li><p>Expertise in clinical data management systems such as EDC, eSource, eCOA, IRT, and medical coding platforms.</p></li><li><p>Willingness to travel up to 25%.</p></li></ul></div><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49635]]></requisitionid>
    <referencenumber><![CDATA[R49635]]></referencenumber>
    <apijobid><![CDATA[r49635]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49635/associate-medical-director-clinical-development-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Medical Director, Clinical Development to join our Clinical Development Program (CDP) team, supporting our Ophthalmology therapeutics portfolio. In this role, you will serve as Medical Lead for clinical trials, designing clinical study concepts and leading the Global Clinical Study Team, while collaborating with discovery teams, the Therapeutic Head, and Strategic Program Teams to deliver high-quality, scientifically sound program milestones. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p><strong>Location:</strong> Tarrytown, NY or Cambridge, MA</p></li><li><p><strong>Travel: </strong>10% to relevant conferences</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Act as medical expert and leader in interactions with external stakeholders</p></li><li><p>Define clinical trial-related Clinical Development Program goals and objectives</p></li><li><p>Partner with discovery teams to shape the next generation of targets in the field</p></li><li><p>Ensure the scientific accuracy of clinical study concepts through rigorous review and consultation with internal and external experts</p></li><li><p>Present clinical study concepts to the Therapeutic Head, Strategic Program Teams, and internal governance meetings</p></li><li><p>Lead the Global Clinical Study Team to deliver high-quality program milestones on schedule</p></li><li><p>Oversee the medical content of clinical study reports and the analysis of clinical data, including safety monitoring, to ensure patient safety</p></li></ul><br><h3>This role requires:</h3><ul><li><p>MD or equivalent, with board eligibility or certification in Ophthalmology</p></li><li><p>0-2 years of academic clinical or translational research experience</p></li><li><p>Experience in Ophthalmic drug development strongly preferred</p></li></ul><p>#MDJobs, #MDJobsCD, #Ophthalmology, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$243,600.00 - $329,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Insights & Analytics - Ophthalmology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48440]]></requisitionid>
    <referencenumber><![CDATA[R48440]]></referencenumber>
    <apijobid><![CDATA[r48440]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48440/executive-director-commercial-insights-analytics-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director </strong>to lead our <strong>Commercial</strong><strong> Insights and Analytics Ophthalmology</strong> team. The Executive Director, Commercial Insights and Analytics (I&A), Ophthalmology, will report directly into the Vice President, Commercial Strategy and Insights & Analytics (CSI&A) within the CSI&A department. This role will lead the I&A team responsible for the Ophthalmology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions across some of Regeneron’s leading brands. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong> </strong></p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY or Warren, NJ</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Ophthalmology team in providing business analytics, customer insights and competitive intelligence to deliver rich insights to solve key business problems</p><p>2) Set the strategic I&A direction that aligns with CBU priorities and helps drive launch excellence</p><p>3) Serve as a member of the Ophthalmology CBU Leadership Team, providing I&A expertise</p><p>4) Serve as a member of the CSI&A leadership team to drive cross-commercial innovation and best-in-class delivery</p><p><em>Develop</em></p><p>5) Translate complex analyses into compelling insights and recommendations that will be used to inform business decision-making for senior Regeneron teams, including the CBU, Chief Commercial Officer, Chief Executive Officer and Board of Directors</p><p>6) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent</p><p>7) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform brand differentiation, market growth and business impact; and <strong>b)</strong> consider business potential for pipeline products</p><p><em>Partnership and collaboration</em></p><p>8) Collaborate with the Ophthalmology CBU and other members of senior leadership to contribute to ongoing brand strategies and decisions, including long-term data, analytics and insights roadmap</p><p>9) Develop and maintain a mutually beneficial partnership with CBU stakeholders; ensure insight generation and feedback are embraced; strike a balance between project rigor, timelines and ability to influence decisions</p><p>10) Lead efforts to identify and crystalize insights that inform strategic plans for the Ophthalmology CBU </p><p>11) Work with other CSI&A leads to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analyses, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>12) Proactively communicate with the Ophthalmology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>13) Construct and deliver integrated business reviews, I&A summary overviews with the Ophthalmology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>This role requires:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with buy-and-bill brands in highly competitive markets is required</p></li><li><p>Minimum Bachelor’s degree in data science, public health, statistics, engineering, or a related field (MBA, MPH, MS preferred)</p></li><li><p>Functional expertise in business analytics, customer insights, analog forecast development, market access, and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, customer insights, market access analytics, and competitive intelligence</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution with hands on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li><li><p>Ophthalmology disease category experience is strongly desired</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Supply Analyst, Kinaxis Maestro]]></title>
    <date><![CDATA[Mon, 10 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43446]]></requisitionid>
    <referencenumber><![CDATA[R43446]]></referencenumber>
    <apijobid><![CDATA[r43446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r43446/principal-supply-analyst-kinaxis-maestro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Kinaxis Maestro Solution Author to join our IOPS Supply Chain team, supporting planning and execution across our life sciences operations. In this role, you will design, implement, and optimize solutions on the Kinaxis Maestro platform, enabling smarter campaign management, inventory optimization, and lifecycle planning, while collaborating with operations, logistics, manufacturing, finance, and planning teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide, with room to grow into broader solution architecture responsibility as our platform footprint expands.</p><br><h3>When & where:</h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday-Friday, 8am-4:30pm</li></ul><br><h3>Discover your role:</h3><ul><li>Design and configure Kinaxis Maestro solutions for campaign management, lifecycle planning, and inventory optimization in a complex, regulated supply chain environment</li><li>Translate business requirements into technical specifications; build custom worksheets, dashboards, templates, algorithms, and scripts to enhance platform functionality</li><li>Integrate Maestro with ERP systems (Oracle preferred) and adjacent supply chain platforms; familiarity with GMP frameworks a plus</li><li>Monitor system performance, resolve data integrity issues, and identify opportunities for continuous improvement</li><li>Maintain documentation for workflows, configurations, and validation activities to support deployment and audit readiness</li><li>Partner cross-functionally with operations, logistics, planning, manufacturing, and finance stakeholders to align solutions with evolving supply chain needs</li><li>Train end-users on Maestro functionality and best practices; provide ongoing support and troubleshooting</li><li>Stay current on Kinaxis Maestro advancements and emerging supply chain trends, proposing solutions to enhance resilience and agility</li></ul><h3>This role requires:</h3><ul><li>Bachelor's degree in Supply Chain Management, Industrial Engineering, or a related field</li><li>Senior Supply Analyst: 5+ years experience in supply chain planning solutions, including 3+ years hands-on configuration experience with an advanced planning platform (e.g., Kinaxis RapidResponse/Maestro, o9, Blue Yonder, SAP IBP, OMP, Anaplan)</li><li>Principal Supply Analyst: 8+ years experience in supply chain planning solutions, including 3+ years hands-on configuration experience with an advanced planning platform (e.g., Kinaxis RapidResponse/Maestro, o9, Blue Yonder, SAP IBP, OMP, Anaplan)</li><li>Experience in life sciences, pharma, or another regulated/complex manufacturing environment (medical device, aerospace, specialty chemicals) preferred</li><li>Kinaxis Maestro Author certification, Level 1 or higher, preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Mechanical Engineer]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49590]]></requisitionid>
    <referencenumber><![CDATA[R49590]]></referencenumber>
    <apijobid><![CDATA[r49590]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49590/senior-mechanical-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior Mechanical Engineer </strong>to join our <strong>Site Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Acting as the primary Mechanical Engineering representative within multidisciplinary project teams from concept development through design, construction, commissioning, qualification, and handover</li><li>Coordinating with Process, I&C, Electrical, Maintenance, Operations and Quality groups</li><li>Establishing, maintaining and continuously improving site mechanical specifications, design guidelines, equipment datasheets, piping layouts, P&IDs, utility designs, calculations, equipment evaluations, and vendor submissions</li><li>Supporting contractor management, construction activities, commissioning plans, startup activities, qualification support, and system turnover documentation</li><li>Leading mechanical engineering activities supporting manufacturing, laboratories, clean utilities, process utilities, HVAC systems, building services, and site infrastructure projects</li><li>Providing technical oversight and reviewing of engineering consultants, contractors, and vendor designs</li><li>Participating in and leading design reviews, constructability reviews, risk assessments, HAZOPs, and engineering evaluations</li><li>Evaluating new technologies, equipment upgrades, system expansions, and obsolescence replacement projects</li><li>Supporting the development of project scopes, business cases, budgets, schedules, resource plans, and technical justifications</li><li>Collaborating with Operations, Maintenance, Manufacturing Sciences, Process Engineering, Quality Assurance, Validation, EHS, and Facilities groups</li><li>Mentoring junior engineers and providing technical coaching across the Site Engineering organization</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have excellent technical and analytical skills.</li><li>You are skilled at problem-solving and continuous improvement.</li><li>You possess strong communication and collaboration skills.</li><li>You are adaptable and can work in a fast-paced, regulated environment</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Bachelor’s degree in Mechanical Engineering or related discipline.</li><li>Minimum 8 years of engineering experience with increasing responsibility in mechanical systems, utilities, facilities, or project engineering.</li><li>Demonstrated experience leading mechanical engineering activities for projects within pharmaceutical, biotechnology or other highly regulated industries.</li><li>Strong knowledge of mechanical systems including HVAC, utilities distribution, piping systems, pumps, pressure vessels, clean utilities, and facility infrastructure.</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#LI-Onsite #JOBSIEPR #IRELIM #REGNIRLTO</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €103,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Solutions Partner (Scientific Data Product Owner)]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49399]]></requisitionid>
    <referencenumber><![CDATA[R49399]]></referencenumber>
    <apijobid><![CDATA[r49399]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49399/associate-director-solutions-partner-scientific-data-product-owner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>We are seeking an <strong>Associate Director Solutions Partner </strong>to be a Scientific Data Product Owner and to lead the holistic data strategy for modelling, connecting, and managing Research and preclinical development scientific data in our enterprise data lake. This data originates from our transactional lab informatics systems (e.g., ELN, LIMS, instrument and analytical platforms, registration systems), and our goal is to transform it from siloed transactional records into well-modelled, connected, and reusable data products.</p><p>Sitting at the intersection of science, data engineering, and product management, you will own the vision and roadmap for how scientific data from Research and preclinical development is structured and surfaced within the data lake. You will partner closely with Digital & Technology teams that need connected data products to analyze and report on scientific outcomes, and with data scientists who require curated, connected scientific datasets to power analytics, modelling, and AI initiatives. You will also work hand in hand with data engineering teams to build these connected data products in the lake.</p><p>This is a strategic, cross-functional role for someone who understands both the underlying science and the data architecture required to make that science discoverable and actionable at scale, and who is able to productively partner with multiple stakeholders at multiple levels throughout the organization.</p><p><strong>When: </strong>Based at our Tarrytown, NY location</p><p><strong>Where: </strong>4 days onsite per week required</p><p> <strong>Discover your role:</strong></p><ul><li>Define and drive the holistic data strategy for modelling and managing connected scientific data in the data lake, ensuring data flowing in from transactional lab informatics systems is harmonized, contextualized, and connected.</li><li>Partner with data engineering to define and shape the ingestion, transformation, and integration pipelines (ETL/ELT) that move data from transactional lab informatics systems into the data lake and turn it into connected, production-grade data products.</li><li>Own the product vision, roadmap, and backlog for scientific data products, prioritizing based on scientific value, downstream demand, and organizational impact.</li><li>Design and govern data models that capture the relationships across scientific entities (e.g., compounds, biologics, samples, assays, experiments, results, instruments, and study metadata) so that data is connected rather than isolated.</li><li>Translate the needs of scientific, Digital & Technology, and analytics stakeholders into clear data product requirements, acceptance criteria, and delivery plans, and drive outcomes that are aligned with all stakeholders, as well as with the corporate Digital and Transformation strategy.</li><li>Partner with Digital & Technology teams that consume connected data products from the data lake for analysis and reporting, ensuring data products meet their integration, quality, and access requirements.</li><li>Partner with data scientists seeking connected scientific datasets, ensuring datasets are analytics-ready, well-documented, and fit for modelling and AI/ML use cases.</li><li>Establish and uphold data quality, governance, lineage, metadata, and FAIR (Findable, Accessible, Interoperable, Reusable) principles across scientific data products.</li><li>Conceive, elicit, and champion the use of AI-driven approaches for searching and discovering structured scientific data, improving how users find and connect relevant datasets.</li><li>Act as the primary point of contact and advocate for scientific data products, gathering feedback and continuously improving usability, coverage, and value.</li></ul><p><strong>This role requires:</strong> </p><ul><li>BS/BA degree and/or MS degree in a related field required.</li><li>10+ years of progressive experience managing scientific laboratory data, ideally within the biopharmaceutical or life sciences industry.</li><li>Strong scientific background (e.g., chemistry, biology, molecular biology, biochemistry, immunology, pharmacology, or a related discipline), with the ability to understand the meaning and context of the data being modelled.</li><li>Hands-on experience with data modelling and an understanding of how to connect data across multiple source systems.</li><li>Ability to drive diverse stakeholders to alignment on desired outcomes, and to influence others at multiple levels without direct authority.</li><li>Working knowledge of data engineering concepts — data pipelines, ETL/ELT, and data transformation — sufficient to define requirements for and collaborate effectively with data engineers.</li><li>Strong SQL skills, plus proficiency in a primary Databricks language (e.g., SQL, Python/PySpark).</li><li>Familiarity with transactional lab informatics systems such as ELN, LIMS, and instrument or analytical data platforms.</li><li>Product ownership or product management experience, including roadmap definition, backlog prioritization, and stakeholder management.</li><li>Strong communication skills and the ability to bridge scientific, technical, and analytics audiences.</li><li>Advanced degree in a biology discipline required; PhD in molecular biology, biochemistry, genetics, or immunology preferred.</li></ul><p><strong>Strongly Desired</strong></p><ul><li>Hands-on experience with Databricks (or a comparable lakehouse platform) for managing and delivering data products.</li><li>Experience leveraging AI to search, discover, and interrogate structured data.</li><li>Experience with knowledge graphs, ontologies, controlled vocabularies, or semantic data models for connecting scientific entities.</li><li>Understanding of data lake / lakehouse architectures and modern data engineering practices.</li><li>Experience working with data scientists and analytics teams to deliver analytics-ready datasets.</li></ul><p><strong>Nice to Have</strong></p><ul><li>Familiarity with data governance frameworks and FAIR data principles in regulated and unregulated environments.</li><li>Experience with metadata management, data cataloging, and data lineage tooling.</li><li>Experience with AI/ML workflows and the data requirements that support them.</li><li>Awareness of regulatory and compliance considerations relevant to pharmaceutical R&D data.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Assurance Specialist, On the floor (Overnights)]]></title>
    <date><![CDATA[Wed, 19 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49582]]></requisitionid>
    <referencenumber><![CDATA[R49582]]></referencenumber>
    <apijobid><![CDATA[r49582]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49582/quality-assurance-specialist-on-the-floor-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Quality Assurance (QA) Specialist to join our QA Drug Product team. This position will support QA initiatives for a broad range of topics relative to the start-up and operations of a drug product facility. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: East Greenbush, New York, United States</p></li><li><p>Work model, available shifts:</p><ul><li><p>3rd shift, Friday-Tuesday, 10pm-8:30am</p></li><li><p>3rd shift, Monday-Friday, 10pm-8:30am</p></li></ul></li></ul><p><strong>What you’ll do:</strong></p><ul><li><p>Work on and potentially lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team</p></li><li><p>Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures</p></li><li><p>Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.</p></li><li><p>Maintain project timelines to support the evolving business</p></li><li><p>Perform on-the-floor quality review of documents, such as: equipment logs, training records, testing results, batch records and supporting documents</p></li><li><p>Review and approval of documents (electronic and paper-based)</p></li><li><p>Provide mentorship during on-the-floor manufacturing</p></li><li><p>Support audits, inspections and investigations</p></li><li><p>Perform quarantine, segregation of material and line clearances</p></li><li><p>Contribute to the continuous improvement initiatives</p></li><li><p>Adjust schedule based on facility start up, filling, and manufacturing needs</p></li><li><p>Collaborate with cross-functional internal teams</p></li></ul><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li><p>Gowning: full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li><p>Requires B.S in life sciences or related field; may substitute proven experience for education requirement</p><ul><li><p>Assoc QA Specialist : 2+ years of experience</p></li><li><p>QA Specialist : 4 + years of experience</p></li></ul></li></ul><p>Level will be determined based on experience</p><p><strong>Thrive today. Grow tomorrow.</strong></p><ul><li><p>Student loan paydown program & tuition reimbursement</p></li><li><p>Family Care Benefits</p></li><li><p>Relocation assistance</p></li><li><p>Inclusion, culture and well-being programs (including physical & mental health)</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$62,355.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Instrumentation & Controls Engineer]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49591]]></requisitionid>
    <referencenumber><![CDATA[R49591]]></referencenumber>
    <apijobid><![CDATA[r49591]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49591/senior-instrumentation-controls-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Senior Instrumentation & Controls (I&C) Engineer </strong>to join our <strong>Site Engineering </strong>team.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>Where:</strong></h3><ul><li>Location: Raheen, Limerick.</li></ul><h3><strong>What you’ll do:</strong></h3><ul><li>Acting as the primary I&C representative within multidisciplinary project teams for projects from concept development through design, construction, commissioning, qualification and handover</li><li>Coordinating with Process, Mechanical, Electrical, Maintenance, Operations and Quality groups</li><li>Providing technical leadership for instrumentation and control systems across manufacturing, utility and facility infrastructure projects</li><li>Supporting troubleshooting and root cause investigations associated with instrumentation and control system performance issues</li><li>Specifying and evaluating field instrumentation including pressure, temperature, flow, level, load cells, pH, conductivity, TOC, UV and analytical instrumentation</li><li>Leading design reviews and approving instrumentation philosophies, P&IDs, instrument indexes, I/O lists, control narratives, loop drawings and vendor packages</li><li>Participating in HAZOPs, risk assessments, constructability reviews and design verification activities</li><li>Reviewing and approving instrumentation wiring diagrams, panel designs and control architecture</li><li>Establishing, maintaining and continuously improving site instrumentation and controls engineering standards and specifications</li><li>Providing technical direction to engineering consultants, system integrators and construction contractors</li><li>Leading technical assessments for equipment obsolescence, instrument upgrades and functional equivalency evaluations</li><li>Supporting FAT, SAT, commissioning, qualification and startup activities for new systems and modifications</li></ul><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>You have excellent technical and analytical skills</li><li>Problem-solving and continuous improvement skills</li><li>You possess strong communication and collaboration skills</li><li>You are adaptable and can work in a fast-paced, regulated environment</li></ul><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>Bachelor’s degree in Instrumentation Engineering, Electrical Engineering, Automation Engineering or related discipline.</li><li>Minimum 8 years of engineering experience with increasing responsibility in instrumentation, controls and automation systems.</li><li>Demonstrated experience leading I&C engineering activities for projects within pharmaceutical, biotechnology or other highly regulated industries.</li><li>Strong knowledge of process instrumentation, industrial control systems and GMP regulated manufacturing environments.</li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><h3><strong>#IRELIM #JOBSIEST #LI-Onsite #REGNIETO</strong></h3><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€54,200.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, CMC Regulatory Affairs]]></title>
    <date><![CDATA[Thu, 20 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50070]]></requisitionid>
    <referencenumber><![CDATA[R50070]]></referencenumber>
    <apijobid><![CDATA[r50070]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50070/associate-manager-cmc-regulatory-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, CMC Regulatory Affairs to join our Regulatory Affairs team, supporting our Japan organization in a hybrid work mode. In this role, you will support regulatory CMC strategy and submissions across therapeutic areas while collaborating with Global Regulatory CMC, CMC Regulatory Science, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Location: Tokyo, Japan</p><p>Working model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Support planning, scientific writing, and critical review of CTN, J-NDA, and eCTD supplement submissions.</li><li>Prepare Japanese application forms and regulatory dossiers for high-quality submissions.</li><li>Support regulatory decision-making with cross-functional teams based on local requirements.</li><li>Act as a local liaison with PMDA for CMC submissions and information requests.</li><li>Assess CMC change controls against regulatory filings to maintain compliance.</li><li>Review manufacturing processes and specifications for investigational product release requests.</li><li>Monitor project timelines to support on-time regulatory submissions.</li><li>You thrive in a collaborative environment and communicate effectively across global teams.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree in a scientific discipline; Master's degree preferred.</li><li>Strong biopharmaceutical and regulatory Chemistry, Manufacturing and Controls (CMC) background.</li><li>10+ years of regulatory CMC experience, including health authority interactions, major submissions, and approvals in Japan.</li><li>Experience supporting CTN, J-NDA, eCTD submissions, PCA, MCN, and PMDA responses.</li><li>Knowledge of Japanese regulatory requirements, guidance documents, and regulatory resources.</li><li>Experience participating in agency meetings and supporting regulatory communications.</li><li>Ability to obtain and maintain Foreign Manufacturing Accreditation or Foreign Manufacture Registration.</li><li>High fluency in Japanese and English.</li><li>Ability to interpret regulations, communicate effectively, and contribute strategically.</li><li>Strong work ethic with the ability to collaborate across teams and apply lessons learned.</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[VP Enterprise Data & Information Management]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49704]]></requisitionid>
    <referencenumber><![CDATA[R49704]]></referencenumber>
    <apijobid><![CDATA[r49704]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49704/vp-enterprise-data-information-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>Regeneron's Enterprise Data & AI organization is newly established and moving fast, built to drive AI transformation and adoption at scale across every part of the enterprise. This is a high-visibility, high-velocity position where the work is directly tied to business and scientific impact.</p><p>The VP of Enterprise Data & Information Management is the guardian of Regeneron's most differentiated AI asset: our data. This role ensures Regeneron's data advantage, anchored by Regeneron's proprietary scientific and clinical assets and external data partnerships, is structured, governed, and AI-ready at enterprise scale. This leader will ensure the integrity, accessibility, and governance of Regeneron's enterprise data assets and enterprise data products.</p><p>The VP of Enterprise Data & Information Management will build Regeneron's enterprise data program from the ground up and establish foundational data capabilities and governance structures. This leader will set and enforce enterprise data quality standards, policies, and compliance requirements; manage the enterprise data catalog, metadata infrastructure, and semantic layer; partner with business units to mature data as a foundational and differentiating capability for AI at scale; ensure compliant, GxP-ready data pipelines; and build the federated multimodal infrastructure that makes production-grade AI possible. Data must be not just available, but trustworthy, traceable, and ready for enterprise AI use.</p><p>This position reports to the SVP Chief AI Officer.</p><p>This leader owns the multi-year enterprise data strategy and holds executive accountability for it, including hiring and directing the Executive Director, Enterprise Data, who leads day-to-day governance and engineering execution against that strategy.</p><p><strong>Core Responsibilities</strong></p><p><strong>Data Governance, Cataloging, MDM & Quality</strong></p><ul><li>Sets the enterprise data quality standard and governance policy for Regeneron's data estate, and decides where the organization invests in master data management and cataloging capability to meet it.</li></ul><ul><li>Holds executive accountability for data governance outcomes across the enterprise, arbitrating trade-offs when data quality priorities compete with delivery timelines across business units.</li></ul><p><strong>Enterprise Semantic Layer</strong></p><ul><li>Sets the strategic direction and investment priority for the enterprise semantic layer, deciding which domains and data models are standardized centrally versus federated to business units.</li></ul><ul><li>Holds enterprise accountability for semantic consistency as new AI capabilities and data products are introduced, resolving definitional conflicts that cross functional lines.</li></ul><p><strong>Business Glossary & Taxonomy</strong></p><ul><li>Sets the enterprise standard and investment priority for Regeneron's business glossary and taxonomy program, determining which domains require centrally governed vocabulary.</li></ul><p><strong>Knowledge Graphs</strong></p><ul><li>Sets the enterprise strategy and investment case for knowledge graph infrastructure, prioritizing which domains and use cases justify the build.</li></ul><p><strong>Federated Data Ecosystem</strong></p><ul><li>Owns the enterprise architecture strategy for a federated, AI-ready data ecosystem, setting the standards that balance domain-owned data products against centralized governance and a graph-enabled semantic layer.</li></ul><p><strong>GxP-Compliant Data Standards</strong></p><ul><li>Sets enterprise policy for GxP-compliant data standards and holds executive accountability for regulated data pipeline compliance across the data layer.</li></ul><ul><li>Owns the executive relationship with Regulatory Affairs, Quality, and Legal leadership on GxP and data privacy requirements, escalating emerging regulatory risk to the SVP, Chief AI Officer.</li></ul><p><strong>Data Privacy & Security</strong></p><ul><li>Sets enterprise policy and risk tolerance for data privacy and security across the data estate and holds executive accountability for Regeneron's data protection posture.</li></ul><ul><li>Owns the executive relationship with the CISO organization and Legal on privacy-by-design strategy for data architecture and access patterns.</li></ul><p><strong>People & Organizational Leadership</strong></p><ul><li>Builds, develops, and leads a multidisciplinary data organization spanning data governance, data engineering, metadata management, and data architecture, including hiring and directing the Executive Director, Enterprise Data, and setting the multi-year strategy the organization executes against.</li></ul><ul><li>Sets the standard for how data infrastructure must be buildable, scalable, and maintainable at platform level, and owns the handoff model between data strategy and data engineering execution.</li></ul><ul><li>Represents the enterprise data strategy and roadmap to executive leadership, holding ultimate accountability for the data foundation across Enterprise Data & AI. Partners with peers across Enterprise Data & AI to ensure the data foundation is integrated with AI delivery, governance, and enablement functions.</li></ul><p><strong>Qualifications</strong></p><ul><li>BS/BA degree in a related field required. </li></ul><ul><li>20+ years leading enterprise data management, data governance, or data architecture organizations, with a demonstrated track record of building data foundations that enable AI and analytics at scale.</li></ul><ul><li>Deep expertise in data governance frameworks, master data management, metadata management, and enterprise data quality, including experience establishing these disciplines from scratch in a complex enterprise.</li></ul><ul><li>Hands-on architectural depth in federated data architecture, semantic layers, and multimodal data infrastructure. Able to operate as both strategist and technical leader.</li></ul><ul><li>Experience with GxP data compliance in a regulated life sciences or biopharma environment strongly preferred. Understanding how data governance intersects with regulatory, clinical, and commercial data requirements.</li></ul><ul><li>Deep familiarity with the current AI data landscape: vector databases, knowledge graphs, retrieval-augmented generation, and modern data platforms that support enterprise AI workloads.</li></ul><ul><li>Experience partnering with distributed engineering organizations. Successful experience governing data standards and architecture with a team in India or similar global delivery model is strongly preferred.</li></ul><ul><li>Ability to communicate and influence effectively across Digital & Technology, business units, scientific functions, Legal, and Regulatory Affairs.</li></ul><ul><li>Strong people leadership. Experience building and developing senior data engineering and governance talent in a competitive market.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Delegado de Ventas, Islas Canarias, España]]></title>
    <date><![CDATA[Sun, 30 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50158]]></requisitionid>
    <referencenumber><![CDATA[R50158]]></referencenumber>
    <apijobid><![CDATA[r50158]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50158/delegado-de-ventas-islas-canarias-espana/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>En Regeneron utilizamos la ciencia y la innovación para desarrollar medicamentos que cambian la vida de personas con enfermedades graves. Buscamos un <strong>Delegado de Ventas Spain para unirse a nuestro equipo de Inmunología (área respiratoria),</strong> apoyando nuestra actividad en España en un modelo de trabajo de campo. En este puesto, impulsarás el crecimiento y la interacción con clientes dentro del área terapéutica de inmunología respiratoria, colaborando con profesionales sanitarios, compañeros regionales y socios comerciales. Esta posición ofrece la oportunidad de contribuir a una organización dinámica, impulsada por la ciencia y comprometida con mejorar la vida de los pacientes en todo el mundo.</p><p><strong>When & where:</strong></p><p>Ubicación: Islas Canarias, España</p><p>Modalidad de trabajo: Trabajo de campo</p><p><strong>Discover your role:</strong></p><ul><li><p>Establecer y mantener relaciones de calidad con profesionales sanitarios.</p></li><li><p>Comunicar mensajes clave alineados con los planes médico-comerciales aprobados.</p></li><li><p>Gestionar el crecimiento del territorio mediante planificación y segmentación de cuentas clave.</p></li><li><p>Desarrollar planes territoriales basados en datos de mercado y oportunidades locales.</p></li><li><p>Colaborar con equipos regionales y socios comerciales para responder a las necesidades de los clientes.</p></li><li><p>Representar al negocio de inmunología en reuniones y congresos científicos.</p></li><li><p>Reportar resultados comerciales y desarrollos relevantes al equipo directivo de España.</p></li><li><p>Te caracterizas por construir relaciones colaborativas y mantener una fuerte orientación al cliente.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Mínimo cinco años de experiencia como Delegado de Ventas especializado en productos de diagnóstico hospitalario.</p></li><li><p>Se valorará experiencia previa trabajando dentro de una alianza comercial.</p></li><li><p>Capacidad para comunicar eficazmente información científica y de producto a profesionales sanitarios.</p></li><li><p>Experiencia en gestión de cuentas clave y planificación territorial.</p></li><li><p>Capacidad para interactuar con clientes a través de canales presenciales, remotos, correo electrónico y plataformas digitales.</p></li><li><p>Capacidad para alcanzar objetivos de ventas, crecimiento y gestión de cuentas.</p></li><li><p>Sólidas habilidades de planificación, organización y elaboración de informes.</p></li><li><p>Compromiso con las normativas del sector, los procedimientos de la compañía y las prácticas promocionales éticas.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50178]]></requisitionid>
    <referencenumber><![CDATA[R50178]]></referencenumber>
    <apijobid><![CDATA[r50178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50178/senior-manager-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager Global Procurement International Markets UK France to join our Global Procurement team, supporting our international markets organization in a hybrid work model. In this role, you will drive indirect and commercial procurement activities across the UK and France while collaborating with country stakeholders, international market leads, and global category teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Uxbridge, United Kingdom</p><p>Work model: Hybrid</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead procurement activities across the UK and France markets.</p></li><li><p>Implement global category strategies within local markets.</p></li><li><p>Provide country input to strengthen global category strategies.</p></li><li><p>Execute sourcing, negotiation, contracting, and supplier management activities.</p></li><li><p>Partner with stakeholders on budgets, spend planning, and future business needs.</p></li><li><p>Review local contracts and analyze spend trends and patterns.</p></li><li><p>Drive procurement process consistency and best practices across international markets.</p></li><li><p>You build strong relationships and influence stakeholders to deliver results.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Experience in Indirect Procurement and/or Commercial Procurement.</p></li><li><p>Bachelor’s degree in a relevant field and progressive procurement experience.</p></li><li><p>Experience in procurement within the pharmaceutical or biopharmaceutical industry preferred.</p></li><li><p>Experience leading or supporting global category teams, suppliers, and procurement processes.</p></li><li><p>Expertise in sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Knowledge of local market requirements and supply markets.</p></li><li><p>Experience using market intelligence, risk, compliance, and financial assessment tools.</p></li><li><p>Ability to deliver cost savings, cash flow improvements, and category value.</p></li><li><p>Strong data analysis and data-driven decision-making skills.</p></li><li><p>Experience coaching procurement professionals and leading teams preferred.</p></li><li><p>Working knowledge of sourcing, contracting, ERP, and eRFx systems, including Oracle, Zycus, GEP, Ariba, or similar tools.</p></li><li><p>Proficiency with Word, Excel, and PowerPoint.</p></li><li><p>Strong stakeholder management skills and ability to operate effectively in ambiguous environments.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Submission Project Management]]></title>
    <date><![CDATA[Mon, 24 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44752]]></requisitionid>
    <referencenumber><![CDATA[R44752]]></referencenumber>
    <apijobid><![CDATA[r44752]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44752/manager-regulatory-submission-project-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager Regulatory Submission Project Management Japan to join our Regulatory Operations team, supporting our Japan regulatory business area in a hybrid work model. In this role, you will drive timely, compliant regulatory submissions while collaborating with Regulatory Publishing, vendors, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><p><strong>Discover your role:</strong></p><p>• Ensure consistency and standardization across regulatory submissions.<br>• Support PMDA consultations, Clinical Trial Notifications, PCAs, MCNs, and NDAs.<br>• Track submission deliverables in Veeva Vault RIM through submission objects and metadata.<br>• Manage submission readiness with Regulatory Publishing and external vendors.<br>• Support eCTD preparation within defined business timelines.<br>• Review submission content plans for compliance with health authority and ICH guidelines.<br>• Guide teams on document uploads and submission-related issue resolution.<br>• You thrive in a fast-paced environment with changing priorities.</p><p><strong>This role requires:</strong></p><p>• Bachelor’s degree or equivalent experience.<br>• 6+ years of pharmaceutical industry or related experience.<br>• Fluency in Japanese and proficiency in English.<br>• Strong knowledge of PMDA, MHLW, ICH, and applicable regulatory requirements.<br>• Experience with submission processes and systems, including Veeva Vault RIM and docuBridge.<br>• Strong eCTD knowledge and experience.<br>• Experience with Microsoft Office applications and Adobe Acrobat.<br>• Ability to manage firm deadlines and adapt quickly to changing priorities.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Market Access Strategy (Ophthalmology)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50432]]></requisitionid>
    <referencenumber><![CDATA[R50432]]></referencenumber>
    <apijobid><![CDATA[r50432]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50432/associate-director-market-access-strategy-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Associate Director of Market Access Strategy is a critical role on a fast-paced, energetic Market Access team. This team member will be responsible for leading and assisting in development/implementation of market access strategies across key segments of our business including: the Payer account team, Field Reimbursement Managers (FRM) and Ophthalmology Account Directors (OAD). Primary responsibilities consist of leading and/or assisting in the development of market access initiatives and tactics and ensuring effective implementation and execution across field teams. Additionally, this individual must maintain a high-level of collaboration and integration with all field teams (FRM, OAD and Payer ) Contract Strategy, Brand Marketing, Training, Pricing, Trade, Market Research and others.</p><h3>When & where:</h3><ul><li>Location: In the Sleepy Hollow, NY Office 4 days a week</li></ul><h3>Discover your role:</h3><ul><li>Leads and ensures strategic effectiveness across all core market access segments and supports the development of certain HCP reimbursement strategies and tactical execution</li><li>Works directly with all MA field teams to evaluate the effectiveness of strategies and initiatives launched by the MA Strategy team and makes strategic recommendations stemming from customer insights</li><li>Serves as a key MA strategy point of contact for access field teams (Payer, OAD, FRM) with regard to account engagement planning, live customer engagements, account specific content creation, and matrix collaboration across various functional areas</li><li>Manages core business review assets and account collaboration initiatives for market access field teams including the OAD custom account content, FRM Payer Business Reviews and other select initiatives</li><li>Leads market access strategy engagement activities at major congresses and in key customer meetings with HCPs, Practice Administrators, Payers, and GPO/SDs</li><li>Develops promotional materials for HCP congresses including booth materials, digital ads/banners, displays, floor signage, etc.</li><li>Leads the HCP Market Access Advisory Committee including development of the annual advisory board meeting plan across HCP and practice administrator steering committees</li><li>Ensures effective execution of pull through strategies and initiatives (pull through playbook, regional planning, Payer coverage report, etc.) and strategy implementation guides for all access field teams</li><li>Manages key relationships with professional Retina/Ophthalmology societies including monthly joint meetings</li><li>Participates in all MA Core teams</li><li>Supports POA strategy development across all MA teams (content development as needed)</li><li>Sets and measures critical metrics for tactical initiatives and collaborates with the I&A team as needed</li><li>Regularly engages and maintains relationship with KOLs, HCP advisors, Retina CEOs/CFOs, Administrators and other key partners</li></ul><h3>This role requires:</h3><ul><li>Bachelor's Degree, MBA preferred</li><li>The ideal candidate must have a minimum of 7 years progressive experience in biologics marketing and brand strategy development and execution in the life sciences</li><li>10+ years of "progressive" industry/relevant professional experience</li><li>Biotechnology or small specialty pharmaceutical marketing experience preferred</li><li>Pharmaceutical Sales experience preferred</li><li>Ophthalmology (Retina) experience preferred</li><li>Demonstrated background of strong planning and tactical development skills</li><li>Excellent project management skills, proven abilities to manage multiple collaborators, meet tight timelines and produce consistent, outstanding work products</li><li>Ability to manage multiple projects and tasks ensuring timing delivery while maintaining a high level of quality and on budget</li><li>Strong Teamwork, cross-functional collaboration, and leadership skills, including the ability to build team member trust, gain alignment and navigate ambiguity</li><li>Excellent understanding of the US market access landscape and the legal/regulatory environment for pharmaceuticals/biopharmaceuticals</li><li>Experience in the buy and bill space</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Field Medical Affairs-(Gastroenterology-TX, OK, AR, LA, MS, NM)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50464]]></requisitionid>
    <referencenumber><![CDATA[R50464]]></referencenumber>
    <apijobid><![CDATA[r50464]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50464/associate-director-field-medical-affairs-gastroenterology-tx-ok-ar-la-ms-nm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs, to join our Gastroenterology team, supporting healthcare providers and payers in a field-based role. In this role, you will establish and maintain scientific exchange with medical specialists and decision-makers, ensuring accurate and timely dissemination of clinical data on in-line and pipeline products, while collaborating with Global Medical Affairs leadership and clinical research investigators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>Where & when: </strong></p><p>• Location: TX, OK, AR, LA, MS, NM<br>• Travel: Capable of engaging in frequent business travel (approximately 40-50% of the time), including air travel, overnight and occasionally on weekends. </p><p><strong>Discover your role:</strong><br>• Engage in scientific discussions with Healthcare Professionals and payers, aligned with Medical Affairs objectives.<br>• Demonstrate deep scientific expertise in assigned molecules/products and therapeutic area.<br>• Build and nurture relationships with key external scientific and medical specialists across the region.<br>• Stay ahead of evolving healthcare trends within the Dermatology therapeutic landscape.<br>• Shape and implement local medical strategy in line with Global Medical Affairs direction and timelines.<br>• Support clinical research sites and investigators.<br>• Deliver clinical and health economic information that enhances the appropriate use of our products.<br>• Communicate scientific and clinical information ethically, accurately, and in a customer-focused manner.</p><p><strong>This role requires:</strong><br>• A Doctorate level clinical/science degree (e.g., MD, PharmD, PhD) with a minimum of 5 years of related work experience (clinical, managed care, or industry)<br>• Experience as a Medical Science Liaison within Immunology. Gastroenterology is preferred.<br>• Strong ability to communicate and disseminate scientific and clinical data.<br>• Residency within the territory</p><p>#msl #medicalscienceliaison #ifm<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Payroll Service Delivery Analyst - Tax & Mobility (US)]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50456]]></requisitionid>
    <referencenumber><![CDATA[R50456]]></referencenumber>
    <apijobid><![CDATA[r50456]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50456/sr-payroll-service-delivery-analyst-tax-mobility-us/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>At Regeneron, our Global Business Services organization delivers critical services that support our global workforce and business operations. We are seeking a <strong>Senior Payroll Service Delivery Analyst, Tax & Mobility (US)</strong> to join our Global Capability Center (GCC). In this role, you will support the accurate, timely, and compliant delivery of US payroll services, with a primary focus on payroll tax compliance, employee mobility, multi-jurisdictional taxation, and payroll operations. You will collaborate with Payroll, Global Mobility, HR, Finance, and external service providers to ensure operational excellence, regulatory compliance, and a seamless employee experience.</p><p><strong>When & Where</strong></p><p>Hyderabad (Hybrid)</p><p><strong>Discover your role</strong></p><ul><li><p>Support end-to-end payroll operations with a focus on US payroll tax compliance, employee mobility, and multi-state payroll processing.</p></li><li><p>Review and process garnishments, child support orders, tax levies, and other payroll deductions in compliance with applicable regulations.</p></li><li><p>Ensure accurate tax withholding and reporting for employees working across multiple jurisdictions, including employees on domestic and international assignments.</p></li><li><p>Partner with Global Mobility, HR, Payroll, Finance, and external vendors to support mobility programs, shadow payroll, tax equalization, and assignment-related payroll activities.</p></li><li><p>Perform payroll audits, reconciliations, and compliance reviews to ensure data integrity and adherence to company policies and regulatory requirements.</p></li><li><p>Support payroll reporting, month-end and quarter-end activities, tax reporting requirements, and collaborator data requests.</p></li><li><p>Participate in payroll system enhancements, testing activities, process optimization initiatives, and automation projects.</p></li><li><p>Maintain payroll documentation, process maps, operational controls, and standard operating procedures to drive consistency and compliance.</p></li><li><p>Contribute to continuous improvement and GCC standardization initiatives focused on payroll tax and mobility operations.</p></li><li><p>Provide operational support across payroll functions to ensure seamless service delivery and achievement of payroll deadlines.</p></li></ul><p><strong>This role requires</strong></p><ul><li><p>Bachelor’s degree in Business, Human Resources, Accounting, Finance, or a related field; equivalent experience considered.</p></li><li><p>5+ years of payroll experience with proven knowledge of US payroll tax regulations and compliance requirements.</p></li><li><p>Knowledge of federal, state, and local payroll tax laws, including multi-state taxation and employee mobility considerations.</p></li><li><p>Experience supporting payroll operations, payroll tax reporting, reconciliations, and compliance activities.</p></li><li><p>Strong analytical, problem-solving, and organizational skills with exceptional attention to detail.</p></li><li><p>Advanced proficiency in Microsoft Excel and experience working with payroll and HRIS platforms such as Workday, Oracle, ADP, or similar systems.</p></li><li><p>Ability to manage multiple priorities and deliver results in a fast-paced, deadline-driven environment.</p></li><li><p>Effective communication and stakeholder management skills with the ability to collaborate across global teams.</p></li><li><p>Experience working in Shared Services, Global Business Services, or Global Capability Center environments preferred.</p></li><li><p>Professional certifications such as CPP, FPC, or other payroll-related credentials preferred.</p></li><li><p>Experience supporting US payroll operations and employee mobility programs preferred.</p></li><li><p>Flexibility to support critical US payroll cycles and collaborate across multiple global time zones.</p></li><li><p>Proven knowledge of payroll tax regulations, employee mobility programs, and multi-jurisdictional payroll compliance.</p></li><li><p>Commitment to operational excellence, process improvement, and service delivery.</p></li><li><p>Ability to build solid relationships across Payroll, HR, Mobility, Finance, and external partners.</p></li><li><p>Demonstrated ability to thrive in a global, collaborative, and continuously evolving environment.</p></li><li><p>Focus on accuracy, confidentiality, and delivering a high-quality employee experience.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 10 Sep 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Market Access Lead - Rare Diseases (Europe Region)]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50646]]></requisitionid>
    <referencenumber><![CDATA[R50646]]></referencenumber>
    <apijobid><![CDATA[r50646]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50646/director-market-access-lead-rare-diseases-europe-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Regional Market Access, Rare Diseases, Europe to join our market access function, supporting our Europe region in a hybrid work mode. In this role, you will shape pricing, reimbursement, and patient access strategies while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead rare disease access strategies aligned with global objectives and country needs.</p></li><li><p>Differentiate approaches across cost-effectiveness and list-price or free-pricing markets.</p></li><li><p>Monitor European policies, payer trends, and reimbursement frameworks.</p></li><li><p>Adapt global access tools and value propositions for regional stakeholders.</p></li><li><p>Manage health technology assessment dossiers, pricing negotiations, and reimbursement submissions.</p></li><li><p>Partner with medical affairs and access teams on evidence and health economics outcomes research plans.</p></li><li><p>Engage payers, policymakers, advocacy groups, and public affairs teams to advance access.</p></li><li><p>You build collaboration through advisory boards, market research, and landscape assessments.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>European rare disease pricing, reimbursement, launches, and approval experience.</p></li><li><p>Expertise in payer systems, economic models, and health technology assessment submissions.</p></li><li><p>Knowledge of NICE, ZIN, TLV, QALY frameworks, and free-pricing markets.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>English fluency; additional European languages are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix leadership, agility, and collaboration.</p></li><li><p>Healthcare policy shaping and multi-stakeholder engagement experience preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€111,675.00 - €186,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Représentant Pharmaceutique]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50952]]></requisitionid>
    <referencenumber><![CDATA[R50952]]></referencenumber>
    <apijobid><![CDATA[r50952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50952/representant-pharmaceutique/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Construisons notre avenir ensemble :</strong></p><p>Chez Regeneron, nous utilisons la science et l’innovation pour développer des médicaments qui changent la vie des personnes atteintes de maladies graves. Nous recherchons un(e) représentant(e) pharmaceutique pour rejoindre notre équipe commerciale et soutenir nos activités en immunologie au Canada dans un rôle basé sur le terrain. Dans ce poste, vous contribuerez à l’atteinte des objectifs commerciaux sur votre territoire tout en collaborant avec des collègues du domaine médical et des partenaires interfonctionnels. Cette opportunité vous permettra de rejoindre une organisation en forte croissance, guidée par la science et engagée à faire une réelle différence pour les patients à travers le monde.</p><br><p><strong>Où et quand :</strong></p><ul><li>Québec</li><li>Mode de travail : Basé sur le terrain</li></ul><br><p><strong>Découvrez votre rôle :</strong></p><br><ul><li>Mener des échanges de qualité avec les professionnels de santé en vous appuyant sur des connaissances scientifiques actualisées.</li><li>Communiquer efficacement les messages clés afin de démontrer la valeur de notre portefeuille.</li><li>Élaborer et mettre en œuvre des plans de comptes locaux fondés sur les données et les connaissances du marché.</li><li>Collaborer avec les équipes médicales pour soutenir les programmes régionaux et répondre aux besoins des professionnels de santé.</li><li>Utiliser des canaux numériques et traditionnels pour renforcer l’engagement des clients.</li><li>Communiquer les résultats du territoire et les évolutions du marché à la direction de l’immunologie.</li><li>Vous vous épanouissez dans un environnement collaboratif et performant et vous vous adaptez facilement au changement.</li></ul><br><p><strong>Ce poste requiert :</strong></p><br><ul><li>Un diplôme universitaire (baccalauréat).</li><li>Au moins 5 ans d’expérience en vente pharmaceutique.</li><li>De 1 à 2 ans d’expérience avec des produits biologiques spécialisés.</li><li>Une expérience en immunologie; une expertise en gastroentérologie, ORL et/ou allergologie constitue un atout.</li><li>Une expérience en planification de territoire, gestion de comptes, ciblage et segmentation.</li><li>Une expérience dans l’engagement des professionnels de santé par l’intermédiaire de multiples canaux de communication.</li><li>La capacité de voyager régulièrement ainsi qu’un permis de conduire valide.</li><li>La maîtrise du français et de l’anglais.</li><li>De solides compétences en collaboration et la capacité à établir des partenariats internes et externes.</li><li>Une expérience de travail dans un environnement d’alliance constitue un atout.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 05:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Statistical Programming, Pharmacometrics]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50700]]></requisitionid>
    <referencenumber><![CDATA[R50700]]></referencenumber>
    <apijobid><![CDATA[r50700]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50700/manager-statistical-programming-pharmacometrics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together</h3><p>At Regeneron, we use data, science, and innovation to accelerate the development of transformative medicines. As a Manager, Pharmacometrics Programming, you will provide programming leadership supporting clinical development programs and pharmacometric analyses that inform critical development decisions. This role offers the opportunity to work across multidisciplinary teams, contribute to regulatory submissions, and drive the delivery of high-quality analyses that support clinical pharmacology and development objectives. You will also help advance departmental standards, improve processes, and strengthen programming capabilities that enable efficient and compliant drug development.<br></p><h3>When & where</h3><ul><li><strong>Location:</strong> <strong>Tarrytown, NY</strong></li><li><strong>Work Model:</strong> <strong>Four days per week on-site</strong></li></ul><br><h3>Discover your role</h3><ul><li>Lead programming and quality control activities for analysis datasets, tables, figures, and listings across multiple projects.</li><li>Coordinate pharmacometrics programming activities and deliverables with cross-functional teams and study stakeholders.</li><li>Create, maintain, and validate programming specifications that support standardized analyses and reporting.</li><li>Integrate data across studies to support exposure-response, population PK, and population PK/PD analyses.</li><li>Support regulatory requests, data-driven analyses, scientific publications, and conference presentations.</li><li>Lead creation and validation of electronic submission deliverables and supporting documentation.</li><li>Partner with multidisciplinary study teams to deliver high-quality clinical trial analyses and reports.</li><li>Drive process improvements, standards development, and departmental initiatives that enhance efficiency and compliance.</li></ul><br><h3>This role requires</h3><ul><li>Bachelor's degree required; Master's degree preferred</li><li>Must have 7-9+ years of progressive experience in statistical programming. Experience in pharma regulated environment preferred.</li><li>Advanced SAS programming experience within a clinical research or pharmaceutical environment.</li><li>Strong understanding of pharmacometrics analyses, including pharmacokinetics, immunogenicity, exposure-response, and population PK methodologies.</li><li>Experience supporting clinical study reporting, regulatory deliverables, and CDISC data standards.</li><li>Strong project management, communication, problem-solving, and cross-functional collaboration skills.</li><li>Ability to manage multiple priorities while delivering high-quality work in a regulated environment.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Statistical Programming, Pharmacometrics]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50699]]></requisitionid>
    <referencenumber><![CDATA[R50699]]></referencenumber>
    <apijobid><![CDATA[r50699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50699/director-statistical-programming-pharmacometrics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together</h3><p>At Regeneron, our mission is to use science and innovation to deliver life-changing medicines for patients worldwide. As a Director, Pharmacometrics Programming, you will lead strategic programming initiatives supporting clinical development programs across therapeutic areas. This position combines technical leadership, organizational influence, and people management to ensure high-quality pharmacometric analyses and regulatory deliverables. You will help shape departmental strategy, drive standardization and innovation, develop programming talent, and collaborate with stakeholders across the organization to advance critical development programs from clinical studies through regulatory submissions and beyond.<br></p><h3>When & where</h3><ul><li><strong>Location:</strong> <strong>Tarrytown, NY</strong></li><li><strong>Work Model:</strong> <strong>Four days per week on-site</strong></li></ul><br><h3>Discover your role</h3><ul><li>Lead programming strategy and execution across multiple therapeutic areas and clinical development programs.</li><li>Drive implementation of standardized tools, technologies, and methodologies that support analysis and reporting.</li><li>Coordinate pharmacometrics programming activities, timelines, and deliverables with cross-functional partners.</li><li>Guide the integration of data across studies to support exposure-response, population PK, and population PK/PD analyses.</li><li>Lead planning and validation of electronic submission deliverables and supporting documentation.</li><li>Develop talent through hiring, coaching, performance management, and career development activities.</li><li>Champion process improvements, operational excellence, and adoption of departmental standards.</li><li>Represent the pharmacometrics programming function in strategic, operational, and organizational discussions.</li></ul><br><h3>This role requires</h3><ul><li>Master's degree in Statistics, Computer Science, Mathematics, Engineering, Life Sciences, or a related discipline.</li><li>12+ years of programming experience supporting clinical trial data within the biotechnology, pharmaceutical, healthcare, or related industry.</li><li>SAS Certification desirable.</li><li>Expert SAS programming experience in a clinical development environment.</li><li>Experience leading teams of 4 or more direct reports.</li><li>Demonstrated success leading complex clinical development projects and managing people and resources.</li><li>Strong understanding of pharmacometrics, biostatistics, clinical trial reporting, and regulatory submission requirements.</li><li>Experience implementing CDISC standards and programming standardization methodologies.</li><li>Strong leadership, strategic thinking, communication, and stakeholder management skills.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Payroll Service Delivery Analyst (US)]]></title>
    <date><![CDATA[Mon, 14 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50453]]></requisitionid>
    <referencenumber><![CDATA[R50453]]></referencenumber>
    <apijobid><![CDATA[r50453]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50453/payroll-service-delivery-analyst-us/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together</strong></p><p>Regeneron is built on the belief that the right idea, coupled with the right team, can transform lives. Our mission is to invent, develop, and commercialize life-transforming medicines for people with serious diseases. Through scientific innovation, operational excellence, and a commitment to patients, we continue to redefine what is possible.</p><p>The Global Payroll team plays a vital role in supporting Regeneron's global workforce by ensuring accurate, timely, and compliant payroll operations. We are seeking a <strong>Payroll Service Delivery Analyst</strong> to join our Global Capability Center (GCC) in Hyderabad. In this role, you will support U.S. payroll operations, collaborate with global collaborators, and contribute to delivering an exceptional employee experience while maintaining the highest standards of compliance, accuracy, and service excellence.</p><p><strong>When & Where</strong></p><p>Hyderabad, India (Hybrid)</p><p><strong>Discover your role</strong></p><p>As a Payroll Service Delivery Analyst, you will:</p><ul><li><p>Support the accurate and timely processing of U.S. payroll by validating, reviewing, and maintaining employee payroll data.</p></li><li><p>Process garnishments, child support orders, tax levies, and other payroll transactions in accordance with federal, state, and local regulations.</p></li><li><p>Review payroll results, perform reconciliations, and implement audit controls to ensure payroll accuracy and compliance.</p></li><li><p>Partner with Payroll, HR, Finance, and business collaborators to resolve payroll inquiries and maintain employee data integrity.</p></li><li><p>Support payroll tax administration and multi-state payroll requirements while ensuring regulatory compliance.</p></li><li><p>Generate payroll reports and assist with month-end, quarter-end, and year-end payroll activities.</p></li><li><p>Participate in payroll system testing, enhancements, and projects involving Workday, Oracle Time & Labor, and related payroll applications.</p></li><li><p>Contribute to process improvement initiatives, standardization efforts, and operational excellence across payroll services.</p></li><li><p>Maintain strict confidentiality and adherence to internal controls, audit requirements, and company policies.</p></li><li><p>Provide cross-functional backup support to ensure continuity of payroll operations and service delivery.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Hold a Bachelor's degree in Business, Human Resources, Accounting, Finance, or a related subject area.</p></li><li><p>Have 4+ years of payroll experience with proven knowledge of payroll operations and payroll tax regulations.</p></li><li><p>Possess knowledge of federal, state, and local payroll tax laws, including multi-state payroll requirements.</p></li><li><p>Have experience performing payroll reconciliations, audits, and resolving payroll discrepancies.</p></li><li><p>Demonstrate strong analytical, organizational, and problem-solving skills with high attention to detail.</p></li><li><p>Have excellent verbal and written communication skills and the ability to collaborate across functions and geographies.</p></li><li><p>Are proficient in Microsoft Excel and comfortable working with payroll and HR systems.</p></li><li><p>Have experience or exposure to Workday, Oracle, ADP, CloudPay, or similar payroll platforms.</p></li><li><p>Thrive in a fast-paced, service-oriented shared services environment while managing multiple priorities.</p></li><li><p>Bring a continuous improvement approach focused on enhancing payroll processes and employee experience.</p></li><li><p>Experience supporting U.S. payroll operations within a Shared Services Center or Global Capability Center environment.</p></li><li><p>Professional payroll certifications such as CPP, FPC, or equivalent credentials.</p></li><li><p>Experience supporting payroll system implementations, enhancements, or transformation initiatives.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro)-Portland, OR]]></title>
    <date><![CDATA[Wed, 23 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50771]]></requisitionid>
    <referencenumber><![CDATA[R50771]]></referencenumber>
    <apijobid><![CDATA[r50771]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50771/medical-specialist-i-gastro-portland-or/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Portland]]></city>
    <state><![CDATA[Oregon]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><br><p><strong>When & where:</strong></p><ul><li>Hybrid role</li><li>Location: Portland, OR<br></li></ul><p><strong>Discover your role:</strong></p><br><ul><li>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</li><li>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</li><li>Results oriented with a proven track record of success with product launches</li><li>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>Experience with in-servicing and training office staff, nurses and office managers</li><li>Ability to partner and collaborate with other internal field teams and alliance partners</li></ul><br><p><strong>This role requires:</strong></p><br><ul><li>Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus</li><li>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</li><li>Demonstrate advanced clinically-based selling skills</li><li>Ability to travel and cover large geographic territories</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 24 Sep 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Mon, 21 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49617]]></requisitionid>
    <referencenumber><![CDATA[R49617]]></referencenumber>
    <apijobid><![CDATA[r49617]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49617/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Project Engineer to join our growing Project Engineering team. In this role, you will design, specify, and commission new and renovated process and clean utility equipment. You will lead deviation investigations and provide engineering support across manufacturing processes. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Troy, New York, United States</li><li>Work model: Onsite Monday-Friday 8:00am-4:30pm</li><li>Travel: up to 10%, domestic and international</li></ul><br><h3>Discover your role:</h3><ul><li>Design and specify cGMP process equipment, piping, and controls, including engineering documentation</li><li>Manage mid-to-large projects for process equipment and clean utilities, including start-up, commissioning, and site acceptance</li><li>Lead design review and installation of equipment</li><li>Prepare piping and instrumentation diagrams and develop Process Flow Diagrams</li><li>Support QA/Validation with design documents and protocol execution</li><li>Investigate process equipment, utility, and control system anomalies, implementing corrective and preventive actions</li><li>Supervise mechanical, electrical, and automation contractors</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree in Chemical Engineering, Biochemical Engineering, or another relevant Engineering discipline</li><li>5+ years of project/process engineering experience for Senior Project Engineer, 8+ years for Principal Project Engineer</li><li>Direct experience with biopharmaceutical process equipment is preferred</li><li>Solid understanding of process control systems and automation.</li><li>Thorough knowledge of engineering documentation for cGMP process equipment and sanitary equipment design requirements</li><li>Experience planning and tracking project activities and schedules</li><li>Strong interpersonal and cross-cultural communication skills, with the ability to lead without direct authority</li><li><strong>Gowning and Physical Requirements:</strong></li><li>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) -Oncology *Saitama Area]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50987]]></requisitionid>
    <referencenumber><![CDATA[R50987]]></referencenumber>
    <apijobid><![CDATA[r50987]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50987/medical-representative-mr-oncology-starsaitama-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sales Specialist, Oncology to join our Oncology Sales team, supporting our oncology business area in a field-based role. In this role, you will drive the adoption of our oncology product portfolio while collaborating with healthcare professionals and cross-functional partners. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><br></p><p><strong>When & where:</strong></p><p>You will be responsible for the Saitama area.</p><p>Your residence is expected to be in Saitama.</p><p><br></p><p><strong>Discover your role:</strong></p><ul><li>Drive sales and adoption of the oncology product portfolio within assigned territory</li><li>Develop and execute territory business plans to achieve sales targets</li><li>Build and maintain relationships with healthcare professionals and key accounts</li><li>Deliver approved scientific and clinical information to support customer decisions</li><li>Identify and engage new business opportunities in the oncology space</li><li>Collaborate with cross-functional teams to support customer needs</li><li>You adapt to evolving priorities and thrive in a results-driven environment</li><li>You demonstrate strong communication and relationship-building skills</li></ul><p><br></p><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree in life sciences, business, or related field</li><li>Proven sales experience in the pharmaceutical, biotech, or healthcare industry</li><li>Knowledge of oncology or related therapeutic area</li><li>Strong communication, presentation, and negotiation skills</li><li>Ability to travel within assigned territory as required</li><li>Driver license and MR certification</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Cell Medicines Research & Development]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51037]]></requisitionid>
    <referencenumber><![CDATA[R51037]]></referencenumber>
    <apijobid><![CDATA[r51037]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51037/2027-co-op-cell-medicines-research-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops to join our Regeneron Cell Medicines (RCM) team, Regeneron's cell therapy unit developing next-generation T-cell therapies for cancer.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Cambridge, MA / Seattle, WA</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer), May/June-December (Summer-Fall), and August-December (Fall).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support in vitro safety and efficacy testing of cell therapy candidates</li></ul><ul><li>Develop tumor antigen expression and flow cytometry methods</li></ul><ul><li>Contribute to viral-vector production and process development for cell engineering</li></ul><ul><li>Support high-throughput protein production activities</li></ul><ul><li>Contribute to analytical method development supporting Good Manufacturing Practice (GMP) manufacturing</li></ul><ul><li>Support digital-transformation initiatives for manufacturing operations</li></ul><ul><li>Document experimental procedures and results</li></ul><ul><li>Collaborate with scientists across the cell therapy team</li></ul><br><p><strong>Relevant majors: </strong>Biology, Biochemistry, Biomedical Engineering</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Data Science & Digital Innovation (Preclinical Manufacturing & Research IT)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51031]]></requisitionid>
    <referencenumber><![CDATA[R51031]]></referencenumber>
    <apijobid><![CDATA[r51031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51031/2027-co-op-data-science-digital-innovation-preclinical-manufacturing-research-it/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Data Science & Digital Innovation to join our Preclinical Manufacturing & Research Information Technology (IT) team, which builds the tools that make sense of Regeneron's manufacturing and research data.<br></p><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer).</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Build custom applications, dashboards, and automation workflows that support day-to-day lab and manufacturing operations</li></ul><ul><li>Develop artificial intelligence and machine learning (AI/ML) models that predict bioreactor performance (data science)</li></ul><ul><li>Computational Fluid Dynamics (CFD)</li></ul><ul><li>Support data-platform migrations for research teams</li></ul><ul><li>Contribute to scientific data solutions used across the organization</li></ul><ul><li>Write and test code to support ongoing development projects</li></ul><ul><li>Collaborate with scientists and engineers to understand data and business needs</li></ul><ul><li>Analyze data to uncover insights supporting manufacturing operations</li></ul><ul><li>Present progress and findings to the broader team</li></ul><br><p><strong>Relevant majors: </strong>Computer Science, Data Science, Bioinformatics, Information Systems, Chemical/Biomedical Engineering, Nuclear Engineering, Mechanical Engineering</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op Data Science & Computational Biology (Research)]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51032]]></requisitionid>
    <referencenumber><![CDATA[R51032]]></referencenumber>
    <apijobid><![CDATA[r51032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51032/2027-co-op-data-science-computational-biology-research/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking multiple 2027 Co-ops in Data Science & Computational Biology to join our Research team, which applies machine learning and data analysis to early-stage drug discovery problems.</p><br><p>These positions offer the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Tarrytown, NY</p><p><strong>Timeframe: </strong>Our Co-op positions are full-time and onsite from January-August (Spring-Summer). </p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Build models to predict how a genetic variant affects a protein</li></ul><ul><li>Develop computational tools for high-throughput image analysis</li></ul><ul><li>Harmonize metadata across large public and internal ribonucleic acid (RNA)-sequencing datasets</li></ul><ul><li>Apply machine learning and data analysis techniques to research questions</li></ul><ul><li>Work with large, complex datasets to identify meaningful patterns</li></ul><ul><li>Collaborate with researchers to translate data findings into actionable insights</li></ul><ul><li>Write and test code to support ongoing analyses</li></ul><ul><li>Present results to the broader research team</li></ul><br><p><strong>Relevant majors: </strong>Bioinformatics, Data Science, Computer Science, Statistics</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 40 hours per week from January-August, May/June-December, or August-December</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Quality Compliance Specialist]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51167]]></requisitionid>
    <referencenumber><![CDATA[R51167]]></referencenumber>
    <apijobid><![CDATA[r51167]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51167/temp-quality-compliance-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a<strong> Temporary Quality Compliance Specialist </strong>to join our <strong>Quality Assurance Raw Materials </strong>team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Raheen, Limerick</li></ul><br><p><strong>What you’ll do:</strong></p><ul><li>Ensuring compliance with all aspects of Quality for the Raheen site and administration and oversight of site quality systems including deviations, CAPA Change Control, Audits, Customer Complaints and Quality Risk Management</li><li>Reviewing and approving failure investigations, change control documents, corrective/preventative action documents and standard operating procedures</li><li>Maintaining electronic systems used for Change Control and Deviation Management</li><li>Reviewing procedures, policies and other instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements</li><li>Monitoring and trending metrics associated with site quality systems</li><li>Actively participating in continuous improvement initiatives</li><li>Participating in regulatory and customer audits and quality risk assessments</li><li>Collaborating with functional departments to resolve issues and maintain compliance</li></ul><br><p><strong>The environment and physical rhythms of this role:</strong></p><ul><li>You have a quality mindset and excellent attention to detail</li><li>You demonstrate strong interpersonal skills</li><li>You are comfortable working in a fast-paced setting</li></ul><br><p><strong>Let’s find out if we’re a fit:</strong></p><ul><li>Requires BSc/BEng in scientific discipline or related field with 3+ years of relevant work experience in pharmaceutical or related industry.<strong><br></strong></li></ul><p><strong>Thrive today. Grow tomorrow.</strong></p><br><p>#IRELIM #JOBSIEST #LI-Onsite #REGNIRLQA #REGNQA</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[District Manger - Pulmonology - Northwest]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50717]]></requisitionid>
    <referencenumber><![CDATA[R50717]]></referencenumber>
    <apijobid><![CDATA[r50717]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50717/district-manger-pulmonology-northwest/]]></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> </strong></p><p><strong>Build our future together:</strong></p><br><p>The District Manager (DM), Pulmonology will report to the Regional Director, Pulmonology and be responsible for hiring, leading, developing and retaining Pulmonology Medical Specialists (sales representatives) in their assigned district. 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 District. The DM will work closely with their Alliance partner counterpart(s) to ensure 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>When & where:</strong></p><ul><li>Remote role</li><li>Location: Pacific Northwest (MN, NE & UT)</li></ul><br><p><strong>Discover your role:</strong></p><br><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>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.</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>Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</li><li>Ability to partner and collaborate with other internal field teams and alliance partners.</li></ul><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required, Master’s degree or other advanced education/certifications a plus (Focused degree in science or clinical experience is a plus).</li><li>Minimum of 7 years of pharmaceutical/biopharmaceutical experience with 3 years of sales leadership/management in sub-cutaneous self-injectable biologic markets required. Experience in the Pulmonology market strongly preferred.</li><li>Ability to travel extensively with local and regional influence.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$195,500.00 - $264,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Talent Acquisition]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51156]]></requisitionid>
    <referencenumber><![CDATA[R51156]]></referencenumber>
    <apijobid><![CDATA[r51156]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51156/senior-manager-talent-acquisition/]]></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>Are you passionate about connecting top talent with impactful opportunities? Join our dynamic Global Recruiting Team as a Senior Manager, Talent Acquisition and contribute to the growth and innovation of one of the most exciting organizations in the Biotech/Pharma industry.</p><br><p>As a Senior Manager, Talent Acquisition, you will play a key role in crafting our recruiting strategies and delivering outstanding candidate and hiring manager experiences. This position partners closely with our <strong>Global Development Teams </strong>(Clinical Sciences, Medical Directors, Regulatory Affairs, Clinical Operations), driving full-cycle recruitment processes and ensuring we attract and hire the best talent for our thriving organization.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Sleepy Hollow, NY</li><li>4 Days on-site, 1 day from home</li><li>Travel percentage: 25%, must be able to travel to Tarrytown, NY, Armonk, NY, Warren, NJ for in-person candidate interviews and hiring manager meetings.</li><li></li></ul><h3>Discover your role:</h3><p><strong>As a Senior Manager a typical day might include the following:</strong></p><ul><li>Source, screen, and lead candidates through the full recruitment lifecycle, providing an outstanding candidate experience.</li><li>Build and sustain proactive pipelines for critical, hard to fill, and leadership roles through sophisticated search techniques, Talent Relationship Management tools (Beamery), and professional networks.</li><li>Be responsible for candidate experience initiatives, ensuring consistent and high-quality touchpoints across the recruitment lifecycle.</li><li>Advise and collaborate with hiring leaders on strategies to address current and future talent gaps.</li><li>Collaborate with hiring managers to define roles, responsibilities, and draft compelling job postings that reflect organizational objectives and attract top talent.</li><li>Partner with leaders across Global Development teams to build and implement tailored recruiting strategies that meet each function’s outstanding talent needs.</li><li>Outstanding partner management with the abilities to influence; you have a history of building trust and credibility with senior leaders</li><li>Stay current on industry trends, labor market conditions, and recruiting best practices to continuously improve strategies.</li><li>Handle candidate activity within the applicant tracking system (ATS) and TRM system (Beamery).</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>A self-motivated, proactive professional who thrives in a fast-paced, collaborative environment. You excel at building rapport, balancing multiple priorities, and getting results.</li><li>A Bachelor’s degree in Human Resources, Industrial-Organizational Psychology, or a related field (Master’s degree is a plus).</li><li>At least 10+ years of recruiting experience</li><li>Experience working in-house in a pharmaceutical or biotech company required</li><li>Must have experience recruiting in scientific development functions including clinical sciences, medical directors, regulatory affairs, medical affairs.</li><li>MD recruitment experience strongly preferred</li><li>Strong problem-solving skills and the ability to navigate ambiguity with confidence.</li><li>Excellent written and verbal communication skills, with a talent for providing clear and insightful updates to candidates, colleagues, and business partners.</li><li>Proficiency in Microsoft Word, Excel, and Outlook.</li><li>Strong communication skills, exceptional candidate experience, and relationship building skills</li></ul><br><p><strong>Why Join Us?</strong></p><p>At Regeneron, we believe our people are our greatest asset. We offer:</p><ul><li>A collaborative, high-performance culture</li><li>Comprehensive benefits, including health and wellness programs, fitness centers, and employee stock options.</li><li>Opportunities to grow and make a meaningful impact in a rapidly evolving industry.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 19:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Data Privacy Operations]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50442]]></requisitionid>
    <referencenumber><![CDATA[R50442]]></referencenumber>
    <apijobid><![CDATA[r50442]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50442/senior-manager-data-privacy-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together</strong></p><br><p>Regeneron is seeking an experienced and forward-thinking Senior Manager Legal Data Privacy Operations to lead privacy program operations within the Law Department / Privacy Office. As a key member of the Privacy Office within Regeneron’s Law Department, you will play an important role in advancing our data privacy program. This includes managing complex privacy projects, delivering tactical operational support, and supporting governance initiatives. By leading well-designed and executed privacy operations, this role plays a central part in building the organizational foundation that enables Regeneron to manage data responsibly, maintain trust, and support the company's overall mission.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Sleepy Hollow, NY, Warren, NJ and Cambridge, MA</li><li>Work model/flexibility: 4 days per week onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Managing and identifying opportunities to improve core privacy operations, including Privacy Impact Assessment, Record of Processing Activities, and Data Subject Access Request processes across multiple business units, geographies, and regulatory frameworks.</li><li>Leading complex privacy program initiatives that involve coordinating and aligning privacy processes with other business functions and leveraging technology and AI to automate, find efficiencies, and enhance how privacy operations are managed and executed.</li><li>Documenting advice and implementation of online privacy notices and controls, tracking technologies, and privacy-enhancing tools.</li><li>Developing and maintaining privacy program metrics and KPIs.</li><li>Maintaining and developing internal policies, procedures, guidance documents, training and awareness, including our Intranet site.</li><li>Coordinating Privacy Steward engagement to advance enterprise-wide privacy initiatives in 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><br><p><strong>This role requires:</strong></p><ul><li>A bachelor's degree, advanced degree in a related field preferred.</li><li>At least 8 years of experience in privacy, with a preference for at least 3 years managing privacy operations within a legal or compliance privacy function.</li><li>Certified Information Privacy Manager (CIPM) or Certified Information Privacy Technologist (CIPT) Project Management Professional (PMP) or equivalent certification.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I Pulmonology- Knoxville, TN]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50698]]></requisitionid>
    <referencenumber><![CDATA[R50698]]></referencenumber>
    <apijobid><![CDATA[r50698]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50698/medical-specialist-i-pulmonology-knoxville-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Knoxville]]></city>
    <state><![CDATA[Tennessee]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><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><br><p><strong>When & where:</strong></p><ul><li>Field role</li><li>Location: Knoxville, TN</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</li><li>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. </li><li>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</li></ul><p><strong>This role requires:</strong></p><ul><li>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.</li><li>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</li><li>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.</li><li>Ability to travel and cover large geographic territories.</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Lead Information Security Analyst (Insider Risk)]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49245]]></requisitionid>
    <referencenumber><![CDATA[R49245]]></referencenumber>
    <apijobid><![CDATA[r49245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49245/lead-information-security-analyst-insider-risk/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>The Lead Insider Risk Analyst supports Regeneron's insider risk capability within the Global Data Protection & AI Security pillar, working alongside the Insider Risk & IP Protection lead. The role focuses on insider data risk, intellectual property protection, and employee-risk procedures, applying detection, triage, and case-management skills with discretion and defensible casework. Reporting lines in the pillar stay flat to the Senior Director; the analyst partners closely with HR, Legal, and the Data Protection Monitoring function on insider signal. </p><br><p><strong>Where: </strong>Based at our Sleepy Hollow, NY location</p><p><strong>When: </strong>4 days onsite per week required</p><br><p><strong>Discover your role:</strong></p><ul><li>Operational lead for the insider risk program: detection, triage, and case management for insider data risk. </li></ul><ul><li>Contribute to IP-protection monitoring across sensitive data and research assets. </li></ul><ul><li>Standardize employee-risk procedures, including performance-plan-related monitoring, in partnership with HR and Legal. </li></ul><ul><li>Partner with the Data Protection Monitoring and Engineering functions on insider signal quality and tuning. </li></ul><ul><li>Maintain case documentation and chain-of-custody discipline. </li></ul><ul><li>Support investigations and escalations with appropriate confidentiality and legal coordination. </li></ul><ul><li>Apply insider-risk detection use cases and thresholds, escalating material findings to the Insider Risk & IP Protection lead. </li></ul><ul><li>Contribute to insider-risk reporting and metrics for pillar leadership.</li></ul><p><strong>This role requires: </strong></p><ul><li>Bachelor's degree in Information Technology, Computer Science, Cybersecurity, Criminal Justice, or related field required. </li><li>6+ years in security, insider risk, or investigations. </li><li>Experience supporting insider-risk or DLP investigations with HR/Legal partnerships.</li></ul><ul><li>Case management and documentation discipline, including chain of custody. </li></ul><ul><li>Familiarity with insider-risk detection signal and behavioral indicators. </li></ul><ul><li>Working knowledge of data protection concepts and how monitoring signal supports insider cases.</li></ul><br><p>Preferred</p><ul><li>Insider-risk tooling experience (e.g., DLP, UEBA, insider-risk platforms). </li></ul><ul><li>Investigations or e-discovery background. </li></ul><ul><li>Regulated industry experience. </li></ul><ul><li>Relevant certifications (e.g., Security+, CFE, or equivalent). </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 12:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Engineer]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51237]]></requisitionid>
    <referencenumber><![CDATA[R51237]]></referencenumber>
    <apijobid><![CDATA[r51237]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51237/automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking an<strong> Automation Engineer </strong>to join our <strong>Automation </strong>team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Limerick</li></ul><br><h3><strong>What you’ll do:</strong></h3><ul><li>Delivering end-user support for Small Manufacturing Equipment applications, troubleshooting issues and communicating clearly with management, business process owners and users</li><li>Developing and maintaining automation documentation, including SOPs, work instructions and configuration specifications.</li><li>Managing essential administrative tasks relating to functional support and user account administration</li><li>Serving as the trusted Subject Matter Expert (SME), working closely with functional departments on projects to develop, implement and enhance systems</li><li>Implementing software and hardware changes and upgrades, with a clear understanding of their impact on Manufacturing and Facilities</li><li>Providing support before, during and after Regulatory and Partner inspections</li><li>Participating in, or leading projects to introduce new Small Manufacturing Equipment or upgrading existing applications</li><li>Working with Validation and Quality to ensure automation applications for small manufacturing equipment are implemented in line with the development life cycle approach</li><li>Leading and supporting security access and periodic audit trail reviews</li></ul><br><h3><strong>The environment and physical rhythms of this role:</strong></h3><ul><li>Excellent verbal and written communication skills, with the ability to collaborate effectively across teams</li><li>Strong analytical and problem-solving skills</li><li>Project management experience would be an advantage</li></ul><br><h3><strong>Let’s find out if we’re a fit:</strong></h3><ul><li>BS/BA or higher in Science, Engineering, Instrumentation, Information Technology or a related field</li><li>Minimum of 2 years’ relevant experience preferred, relevant experience may be substituted for education</li></ul><br><h3>Thrive today. Grow tomorrow.</h3><p>#IRELIM #JOBSIEST #LI-Onsite</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €75,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49902]]></requisitionid>
    <referencenumber><![CDATA[R49902]]></referencenumber>
    <apijobid><![CDATA[r49902]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49902/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 - ECEP Program </strong></p><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking highly motivated Associate Scientists to join Regeneron's Early Career Exploration Program (ECEP). This program is a full-time opportunity for former Regeneron interns graduating with a BS in Biology, Biochemistry, Biophysics, Chemistry, or a related field to find a full-time home at Regeneron post-graduation. The ECEP provides participants with the chance to explore multiple positions across Regeneron's Research & Pre-Clinical Development (R&D) function, all while building strong foundational knowledge in biotechnology.</p><p>Participants will be placed in assignments 3–6 months in length, covering for colleagues on leave of absence, with opportunities to explore multiple R&D functions. The program runs for up to 2 years before participants are expected to find a permanent placement. This is intended to be a small cohort, aimed at building a strong entry-level talent pipeline for Regeneron R&D. Participants will have a centralized manager guiding them throughout their journey, providing advice, mentorship, and other developmental opportunities.</p><p>We hope you are excited by the opportunity to work with numerous functional groups to develop innovative approaches for tackling some of the most challenging therapeutic discovery projects being pursued at Regeneron.</p><p><strong>When & where:</strong></p><p>Location: Tarrytown, NY, On-site</p><p><strong>Discover your role:</strong></p><p>There is no "typical" day for our ECEP participants, but below are some examples of what you may do during your assignments:</p><ul><li><p>Conducting basic laboratory work including pipetting, culturing, and qPCR</p></li><li><p>Working with automated systems, including robotic liquid handlers</p></li><li><p>Maintaining cell cultures</p></li><li><p>Assisting with small and large-scale protein expression using bacteria, insect cells, and other systems</p></li><li><p>Participating in journal clubs and data presentations</p></li><li><p>Performing routine molecular biology techniques such as plasmid and bacmid purification and baculovirus production</p></li><li><p>Performing protein biochemical analysis</p></li><li><p>Conducting protein purification (affinity, ion exchange, and size exclusion) and biochemical/biophysical analysis</p></li><li><p>Analyzing experimental data and assessing quality</p></li><li><p>Writing standard operating procedures (SOPs)</p></li><li><p>Maintaining adequate inventory of laboratory supplies and reagents</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>A current undergraduate senior, graduating with (or having earned) a BS in Biology, Biochemistry, Biophysics, Chemistry, or a related field by Winter 2026 or Spring 2027</p></li><li><p>Hiring preference given to former Regeneron R&D interns</p></li><li><p>A passion for science and innovation, with a strong dedication to continual improvement</p></li><li><p>Enjoyment of working in a fast-paced, deadline-driven team environment to discover lifesaving medicines for people with serious medical conditions</p></li><li><p>The desire and ability to work on multiple projects in parallel</p></li><li><p>Ability to multi-task, prioritize work, and maintain confidentiality</p></li><li><p>A growth mindset, with willingness to be flexible and work in an ever-changing environment</p></li><li><p>Comfortability with ambiguity</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming - Internal Medicine]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43877]]></requisitionid>
    <referencenumber><![CDATA[R43877]]></referencenumber>
    <apijobid><![CDATA[r43877]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r43877/senior-manager-statistical-programming-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Statistical Programming to join our Statistical Programming team, supporting a therapeutic area across our clinical portfolio. In this role, you will provide programming leadership on project teams, overseeing deliverables from single studies through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and departmental colleagues to shape and implement programming standards.</p><br><h3>When & where:</h3><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: onsite</li></ul><br><h3>Discover your role:</h3><ul><li>Coordinate and oversee analysis programming within your therapeutic area, tracking progress and completion of deliverables</li><li>Manage and coordinate programming and quality control of analysis datasets and outputs in support of regulatory submissions</li><li>Mentor others on the use of standardization tools and therapeutic area standard analysis approaches</li><li>Serve as the programming representative on a multidisciplinary study team, ensuring timely, quality support through regulatory approval and launch</li><li>Develop data models, programming standards, and code, and train end users on project standards</li><li>Mentor junior staff, fostering a collaborative environment and modeling strong team behavior</li><li>Contribute to programming development and quality control using established tools and methodologies</li><li>Advise team members on procedures for data, records, and information retention</li><li>Enjoy leading programming work independently while staying closely connected to a broader project team</li><li>Think in terms of standards, consistency, and reusable processes across studies</li><li>Communicate clearly with cross-functional and multidisciplinary stakeholders</li><li>Take pride in mentoring and developing less experienced colleagues</li><li>Stay organized and detail-oriented when managing multiple deliverables and timelines</li><li>Approach quality control with rigor and a genuine sense of ownership</li><li>Adapt comfortably to shifting priorities, including ad hoc requests from senior leadership</li></ul><br><h3>This role requires:</h3><ul><li>Master's degree with 10+ (or BS 12+) years of relevant experience</li><li>Proven experience leading programming deliverables within a clinical or therapeutic area</li><li>Strong mentoring and team collaboration skills</li><li>Experience developing and applying programming standards and data models</li><li>Nice to haves: SAS Certification</li></ul><br><p>#statprogregn</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Statistical Programming - Internal Medicine]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51122]]></requisitionid>
    <referencenumber><![CDATA[R51122]]></referencenumber>
    <apijobid><![CDATA[r51122]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51122/manager-statistical-programming-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will lead programming deliverables from a single study through regulatory approval, product launch, and annual reports, while collaborating with study teams, CROs, and cross-functional colleagues to ensure timely, high-quality analysis and reporting.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Develop expertise within a therapeutic area or standard tool, working independently to coordinate and oversee project deliverables</li><li>Lead the development and quality control of tables, listings, and graphs in support of analysis requirements</li><li>Manage programming effort, tracking progress and completion of deliverables, including complex ad hoc requests</li><li>Serve as programming representative on a multidisciplinary study team, ensuring timely support through regulatory approval and launch</li><li>Partner with management to determine resource requirements for your therapeutic area or department</li><li>Contribute to hiring by reviewing resumes and screening candidates for contractor and permanent roles</li><li>Provide feedback to management on team members' contributions to support performance evaluations and goal-setting</li><li>Advise direct reports on procedures for data, records, and information retention</li><li>Enjoy working with minimal supervision and taking ownership of complex deliverables</li><li>Communicate clearly with cross-functional, multidisciplinary teams</li><li>Think analytically and stay organized when managing multiple priorities and timelines</li><li>Take initiative in developing deep expertise within a specialized area</li><li>Bring a collaborative mindset to hiring, feedback, and team development</li><li>Adapt easily to shifting priorities, including last-minute requests from senior leadership</li><li>Approach quality and documentation with rigor in a regulated environment</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 6+ years (or BS 7+) of relevant work experience </li><li>Proven experience leading programming deliverables within a clinical study team</li><li>Experience providing input on hiring, feedback, and performance evaluation</li><li>Strong organizational and documentation skills within a regulated environment</li><li>Nice to have: SAS Certification</li></ul><br><p>#statprogregn</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Insight & Analytics (US and Global)]]></title>
    <date><![CDATA[Sun, 11 Oct 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50942]]></requisitionid>
    <referencenumber><![CDATA[R50942]]></referencenumber>
    <apijobid><![CDATA[r50942]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50942/senior-manager-insight-analytics-us-and-global/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases.</p><br><p>As part of Regeneron's first Global Capability Center (GCC) in Hyderabad, we are seeking a Senior Manager, Insights & Analytics (US & Global Immunology) to lead a high-performing team supporting Commercial Insights & Analytics initiatives. This role will play a critical part in establishing analytics capabilities, operating models, and standards within the GCC while supporting key commercial decisions across Regeneron's Immunology portfolio.The role will lead teams across Direct-to-Consumer/Patient (DTC/P) Analytics, Customer & Market Insights, and Competitive Intelligence, partnering closely with U.S. and Global stakeholders to transform complex data into actionable business recommendations that influence commercial strategy for both in-line and pipeline products.</p><br><h3>When & Where:</h3><p><strong>Hyderabad, India (Hybrid)</strong></p><br><h3>Discover your role:</h3><ul><li>Serve as the primary point of contact for DTC/P Analytics, Customer & Market Insights, and Competitive Intelligence activities, partnering with U.S. and Global Insights & Analytics leadership.</li><li>Lead and oversee a team of 10+ professionals supporting media measurement, performance analytics, market research operations, and competitive intelligence activities.</li><li>Build and scale capabilities across DTC/P Analytics, Customer & Market Insights, and Competitive Intelligence within the Hyderabad GCC.</li><li>Provide day-to-day leadership, coaching, prioritization, and quality oversight while supporting team development in a matrixed environment.</li><li>Establish operating norms, workflows, governance practices, and analytics standards for the GCC.</li><li>Collaborate with Associate Directors and cross-functional stakeholders to drive innovation, standardization, and standards.</li><li>Lead knowledge-transfer initiatives with U.S.-based teams to localize and expand commercial analytics capabilities within the GCC.</li><li>Direct analytics projects supporting commercial strategy for key Immunology products.</li><li>Translate complex analytical findings into clear, actionable recommendations for senior leadership.</li><li>Develop continuous improvement and operational excellence across multiple analytics workstreams.</li><li>Partner effectively with stakeholders across geographies and functions to deliver high-quality insights and business impact.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor's degree in Business, Analytics, Life Sciences, or a related field; MBA or advanced degree preferred.</li><li>10+ years of experience in commercial analytics, market research, media/digital analytics, competitive intelligence, or related pharmaceutical/biotech functions.</li><li>Minimum 2 years of people management experience.</li><li>Strong understanding of media measurement and attribution methodologies, including data clean-room outputs.</li><li>Experience with survey-based market research operations, study methodologies, and vendor management.</li><li>Knowledge of competitive intelligence methodologies, secondary research, and insight synthesis.</li><li>Familiarity with business intelligence and visualization tools such as Power BI and Tableau.</li><li>Strong understanding of the pharmaceutical commercial ecosystem and Immunology market landscape.</li><li>Proven ability to lead teams across multiple specialized workstreams while ensuring quality and prioritization.</li><li>Strong stakeholder management skills with experience acting as a key liaison to senior leaders.</li><li>Demonstrated ability to drive innovation, standardization, and operational excellence.</li><li>Excellent problem-solving, communication, and presentation skills.</li><li>Strong written and verbal English communication skills.</li><li>Experience working effectively with global teams across multiple time zones.</li><li>Ability to thrive in a fast-paced, evolving GCC environment and help build new capabilities from the ground up.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 12 Oct 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Product Management - Delivery & Operations Product Lead - Medical Affairs Domain]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47701]]></requisitionid>
    <referencenumber><![CDATA[R47701]]></referencenumber>
    <apijobid><![CDATA[r47701]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47701/senior-manager-product-management-delivery-operations-product-lead-medical-affairs-domain/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Global Development IT (GDIT) is seeking an experienced and motivated Senior Manager with deep technical and functional expertise in Veeva CRM, Veeva Medical Vault, Medical Affairs systems and AI. This role is responsible for end-to-end implementation, support and continuous improvement of technology products and data within the Medical Affairs domain. This role will also work closely with their business counterparts, Business Process Owners, Subject Matter Experts, Training, Process and Procedures and Corporate Enterprise IT. </p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead detailed business and technical requirements' analysis for Veeva Medical CRM, Veeva Medical Vault and Medical Affairs systems, translating Medical processes into scalable, complaint system designs.</p></li><li><p>Configure and optimize Veeva CRM components, including but not limited to: Medical Inquiry, Call Reporting, Key Medical Insights, Events, Approved email, Consent Management, Page layout, Profiles, Permission sets and Sharing Rule.</p></li><li><p>Design and configure Veeva Vault Medical Vault objects, relationships, lifecycles, workflows, user roles, document types, and metadata to support scientific content management and medical review processes.</p></li><li><p>Define and support AI-driven Medical Affairs workflows including automated medical inquiry categorization, sentiment and topic analysis of MSL interactions, and proactive identification of emerging medical insights.</p></li><li><p>Collaborate with Global Development and IT team members to extract insights from CRM and other data sources using AI and digital tools.</p></li><li><p>Define and maintain Veeva data models and data quality standards to enable AI/ML readiness, ensuring alignment across CRM and Vault platforms, including reference data, picklists, field dependencies, and master data governance.</p></li><li><p>Partner with integration teams to design and validate integrations using Veeva APIs, Vault APIs, middleware platforms, and standard connectors with systems such as MDM, ERP, data lakes, and analytics tools.</p></li><li><p>Collaborate with global stakeholders in Medical Affairs, GDIT functions, Corporate IT and other relevant functions to support multi-country deployments, localization, and regulatory requirements across FDA, EMA, and other regional compliance frameworks.</p></li></ul><p><strong> This Job might Be for you if you have:</strong></p><ul><li><p>Knowledge of Medical Affairs business processes, systems and key trends in the Industry.</p></li><li><p>Experience on Jira, Agile product management, backlog management, Scrum and Kanban boards.</p></li><li><p>Technical Experience and ability to Partner with data science and integration teams to build, validate, and operationalize AI solutions using APIs, middleware, and AI/ML platforms (e.g., NLP, large language models, predictive analytics).</p></li><li><p>Proven track record of managing competing priorities across a multitude of stakeholders, and to lead teams to deliver value-oriented, prioritized solutions. </p></li><li><p>Excellent interpersonal skills, and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience </p></li><li><p>Experience managing technology capability identification, selection, implementation, and operations </p></li><li><p>Excellent problem-solving skills to address day-to-day challenges associated with business solutions </p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>A BS/BA Degree with 8+ years of relevant experience, or a MS Degree with 6+ years relevant experience</p></li></ul><ul><li><p>Experience partnering with technology teams and driving value in the Medical Affairs space with specific technologies like Veeva Medical CRM, Veeva Medical Vault, Salesforce</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Wed, 10 Jun 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48464]]></requisitionid>
    <referencenumber><![CDATA[R48464]]></referencenumber>
    <apijobid><![CDATA[r48464]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48464/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Uxbridge, UK</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Canada]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46239]]></requisitionid>
    <referencenumber><![CDATA[R46239]]></referencenumber>
    <apijobid><![CDATA[r46239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46239/associate-director-finance-administration-canada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are hiring an Associate Director, Finance & Administration to partner closely with country leadership and commercial teams, supporting high‑impact business decisions through financial insight, forecasting, and analysis. This role sits at the centre of the country organisation, working across Finance, Accounting, Tax, Treasury, and global CFO functions to shape commercial performance, governance, and long‑term planning.</p><p>If you enjoy combining critical thinking with hands‑on delivery—and value visible ownership at country level—this is a role where your expertise will genuinely influence outcomes.</p><h3>What You’ll Be Doing:</h3><ul><li><p>Partnering with country leadership on budgeting, forecasting, and financial planning</p></li><li><p>Preparing and presenting forecasts, including actuals versus forecast analysis</p></li><li><p>Managing resource planning, including FTE utilisation across cost centres</p></li><li><p>Supporting commercial teams with P&L ownership and profitability insights</p></li><li><p>Translating epidemiology and commercial data into financial forecasts</p></li><li><p>Coordinating with Accounting on revenue accuracy, accruals, and reporting</p></li><li><p>Acting as a local finance liaison across Tax, Treasury, and CFO functions</p></li><li><p>Ensuring compliance with internal policies and external regulations</p></li></ul><h3>This Role May Be For You If:</h3><ul><li><p>You enjoy working closely with senior collaborators to support sound decisions</p></li><li><p>You like roles that balance strategic perspective with practical execution</p></li><li><p>You are comfortable partnering across commercial, medical, and G&A teams</p></li><li><p>You value clear country ownership and accountability</p></li><li><p>You enjoy collaborating with global and local finance colleagues</p></li><li><p>You are motivated by improving processes and strengthening governance</p></li></ul><h3>To Be Considered:</h3><p>You will have a relevant undergraduate degree, along with a postgraduate qualification (such as an MBA) and/or a recognised professional finance qualification. You will bring at least five years of post‑qualification finance experience, primarily within the biotech or pharmaceutical industry, including experience supporting commercial P&Ls. Fluency in English and the local country language is required. International experience and additional language skills are an advantage.</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Marketing - Oncology]]></title>
    <date><![CDATA[Tue, 14 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49102]]></requisitionid>
    <referencenumber><![CDATA[R49102]]></referencenumber>
    <apijobid><![CDATA[r49102]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49102/manager-marketing-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Country Marketing, Oncology to join our Commercial Oncology team, supporting our Japan business in a hybrid work mode. In this role, you will lead local oncology brand marketing strategy and execution across commercialised indications and future launches, while collaborating with cross-functional and cross-regional collaborators including Medical Affairs and the Sales Team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Japan. Hybrid work model. Travel required 30–40%, including some weekends for conferences and meetings.</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Lead local oncology brand strategy and provide input to global brand plans.</li><li>Drive the brand planning process, analysing competition and identifying promotional opportunities.</li><li>Partner with Medical Affairs to create and agree an aligned brand strategy.</li><li>Deliver external collaborator engagement plans, including national congresses and HCP meetings.</li><li>Manage the local promotional budget and spend against approved limits.</li><li>You develop customer-focused, differentiated messages for key target audiences.</li><li>You collaborate with the Sales Team on Field Plans of Action and communications.</li><li>You uphold the highest ethical and compliance standards in every action.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>Bachelor's degree, with preference for a science background.</li><li>5+ years of biotech or pharmaceutical brand marketing experience.</li><li>Working knowledge of local healthcare compliance codes and promotional regulations.</li><li>Expertise managing advertising agencies and suppliers, and developing annual budgets.</li><li>Excellent planning, prioritization, communication and presentation skills.</li><li>Written and spoken English language skills.</li><li>Oncology marketing experience preferred; product launch experience a plus.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology (f/m/d) - Heidelberg - Mainz - Trier - Saarbrücken]]></title>
    <date><![CDATA[Sun, 26 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48524]]></requisitionid>
    <referencenumber><![CDATA[R48524]]></referencenumber>
    <apijobid><![CDATA[r48524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48524/sales-specialist-immunology-fmd-heidelberg-mainz-trier-saarbruecken/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>As a Sales Specialist Immunology (f/m/d), you will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Respiratory division at key meetings. You will identify the key people in Pneumology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our portfolio.</p><p><strong>Where:</strong></p><p>Field based in the territory: <strong>Heidelberg - Mainz - Trier - Saarbrücken</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Competent advice and support for relevant Healthcare Professionals (HCP) and, where applicable, customers in the hospital segment</p></li><li><p>Building and maintaining intensive and sustainable customer relationships - in person and using digital channels</p></li><li><p>Target-oriented, substantive dialogue focused on the benefits for customers and added value for patients</p></li><li><p>Independent regional management including account analyses, route planning and documentation of your activities in the CRM system</p></li><li><p>Participation in trade fairs and congresses as well as independent planning, coordination and realization of training events and specialist presentations</p></li><li><p>Regular reporting to the sales management</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Deep understanding of the local healthcare economy, with the ability to identify key players in Pneumology</p></li><li><p>“Patient first” value system</p></li><li><p>Bachelor’s degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification</p></li><li><p>5+ years of sales experience within the biotech/pharmaceutical sector</p></li><li><p>Respiratory experience is preferred</p></li><li><p>Proficiency in German as well as conversational English</p></li><li><p>Readiness for very frequent travel and a driver's license cl. 3/B.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>64.125,00 € - 106.875,00 €]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - Statistical Programming]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49715]]></requisitionid>
    <referencenumber><![CDATA[R49715]]></referencenumber>
    <apijobid><![CDATA[r49715]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49715/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Statistical Programming, Central Services to join our Statistical Programming team, supporting our Central Services function in a hybrid work model. In this role, you will lead statistical programming activities across integrated data and reporting, regulatory submissions, exploratory analyses, and clinical trial disclosure while collaborating with Statistical Programming, Biostatistics, Clinical Transparency and Trial Disclosure, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Location: Hyderabad, India (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead programming support for integrated datasets, pooled analyses, and reporting deliverables across assigned projects.</p></li><li><p>Create and maintain programming documentation, including integrated dataset specifications such as pooled ADaM datasets, following established standards and processes.</p></li><li><p>Support the creation and review of electronic data packages for regulatory submissions to ensure compliance with regulatory, industry, and internal standards.</p></li><li><p>Coordinate with Clinical Transparency and Trial Disclosure, Biostatistics, Statistical Programming, and cross-functional teams to deliver disclosure-ready datasets and outputs.</p></li><li><p>Provide technical expertise in developing tools, standard processes, and programming solutions that improve efficiency and compliance.</p></li><li><p>Troubleshoot and resolve complex programming and submission-related issues while supporting inspection readiness activities and regulatory inquiries.</p></li><li><p>Collaborate effectively across teams to achieve submission and reporting objectives in a highly regulated environment.</p></li><li><p>Guide and support team members in developing their technical skills and knowledge of submission programming.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related field.</p></li><li><p>7+ years of programming experience, preferably processing clinical trial data within the biotechnology, pharmaceutical, or health-related industry.</p></li><li><p>Proven experience in regulatory submissions and compliance with global standards, including FDA, European Medicines Agency (EMA), Pharmaceuticals and Medical Devices Agency (PMDA), and Clinical Data Interchange Standards Consortium (CDISC) requirements.</p></li><li><p>Proficient SAS programming skills in a clinical data environment with expertise in at least one, preferably multiple, therapeutic areas.</p></li><li><p>Strong understanding of CDISC standards, including Study Data Tabulation Model (SDTM), Analysis Data Model (ADaM), and Define-XML.</p></li><li><p>Proficiency with Pinnacle 21 (P21), including experience reviewing and troubleshooting P21 reports and issues.</p></li><li><p>Good knowledge of electronic Common Technical Document (eCTD) regulatory submission formats.</p></li><li><p>Experience with project and people management, including leading teams and managing deliverables.</p></li><li><p>Strong problem-solving skills with the ability to handle complex technical and programming challenges.</p></li><li><p>Proficiency with SAS Base, Stat, Macro, and Graph.</p></li><li><p>Excellent communication and interpersonal skills, with the ability to collaborate across functional areas.</p></li><li><p>Strong attention to detail and the ability to manage multiple priorities in a fast-paced environment.</p></li><li><p>SAS certification is a plus.</p></li><li><p>Knowledge of open-source programming languages such as R and/or Python is a plus.</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Obesity, Muscle & Metabolism]]></title>
    <date><![CDATA[Wed, 29 Jul 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47888]]></requisitionid>
    <referencenumber><![CDATA[R47888]]></referencenumber>
    <apijobid><![CDATA[r47888]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47888/senior-scientist-obesity-muscle-metabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Sr. Scientist to join our Obesity, Metabolism and Muscle Diseases Group, supporting the identification and validation of novel drug targets for metabolic disorders. In this role, you will design and conduct in vitro and in vivo studies to advance target validation and mechanistic understanding, while collaborating and communicating efficiently across the Obesity, Metabolism and Muscle Diseases Group and other teams and functions.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY</p></li><li><p>Work model/flexibility: Onsite</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Identify and implement novel areas, technologies, and approaches for validating targets and target modalities in metabolic disease drug discovery</p></li><li><p>Design and conduct in vitro assays to support target validation</p></li><li><p>Design and perform in vivo studies in animal models to support target validation and mechanistic understanding</p></li><li><p>Analyze data and draw scientifically sound conclusions</p></li><li><p>Provide timely updates on scientific progress, communicating efficiently across teams and functions</p></li><li><p>Thrive in a fast-paced, multi-project environment, staying detail-oriented and well-organized</p></li><li><p>Work well both independently and as part of a team</p></li><li><p>Bring curiosity and a desire to expand your areas of expertise as new questions arise</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Ph.D. with a minimum of 3 years of post-doctoral research experience</p></li><li><p>Broad expertise in biochemistry, molecular biology, in vitro assay development, and in vivo techniques</p></li><li><p>Ability to independently design and perform complex in vivo studies, interpret data, and summarize results</p></li><li><p>Expertise in at least one metabolism research area (e.g., diabetes, endocrinology, obesity, lipid and energy metabolism)</p></li><li><p>Excellent communication and presentation skills, with a documented strong scientific record</p></li><li><p>Preferred: strong understanding of human and mouse genetics</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49456]]></requisitionid>
    <referencenumber><![CDATA[R49456]]></referencenumber>
    <apijobid><![CDATA[r49456]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49456/executive-medical-director-clinical-program-lead-immunology-rheumatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Executive Medical Director to join our Hematology team, providing overall clinical scientific leadership for our non I/O BCMA program. You'll be responsible for our clinical development strategy and execution of clinical trials in this area, partnering closely with the Global Program Head to design the optimal development strategy for this portfolio. You'll serve as a clinical role model for the team, bringing outstanding clinical scientific knowledge to hematology clinical research and leading a team of MDs and clinical scientists. You'll report directly to the VP, Therapeutic Area Lead, Hematology.</p><p>This position offers the opportunity to provide clinical scientific leadership on a fast-growing, science-driven cell therapy program making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Travel: 10% to relevant conferences/congresses</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards</p></li><li><p>Uses excellent scientific standing among peers and the ability to address issues with scientific rigor and creative solutions; uses that creativity and knowledge to build and defend data-driven plans and decisions, both with internal scientific management and the Company's partners/collaborators</p></li><li><p>Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape; designs and develops smaller, yet robust and innovative FIH as well as Phase 2/3 programs</p></li><li><p>Drives strong consensus-building skills and the ability to lead multi-disciplinary teams towards sound decision-making; leads dynamic and matrixed clinical teams in a fast-paced and hands-on environment</p></li><li><p>Leads and develops a team of MDs and clinical scientists to meet business needs</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>An advanced degree in medicine (MD or equivalent) required; Specialized fellowship training in Immunology or Rheumatology preferred.</p></li><li><p>A minimum of 6-8 years of industry experience in related therapeutic area clinical development is preferred</p></li><li><p>Demonstrated consistent track record in a range of leadership roles, including working with senior clinical development staff and establishing credibility with external collaborators such as opinion leaders and regulators</p></li><li><p>Substantial experience in drug development, including experience with both IND and BLA/NDA submission</p></li><li><p>Experience leading study start-up, directing and guiding study team execution, data cleaning, medical review, database locks, and handling health authority responses</p></li><li><p>A strong commitment to impacting patients through drug development and the ability to work well within a team setting</p></li><li><p>People management experience is a plus</p></li></ul><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45330]]></requisitionid>
    <referencenumber><![CDATA[R45330]]></referencenumber>
    <apijobid><![CDATA[r45330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r45330/senior-manager-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Pharmacovigilance Safety Operations Japan to join our Global Patient Safety team, supporting our Japan business in a hybrid work mode. In this role, you will oversee Japan pharmacovigilance reporting and compliance activities while collaborating with cross-functional teams, external partners, and service providers. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><p>Japan</p><p>Work model: Hybrid</p><br><h3><strong>Discover your role:</strong></h3><ul><li>Serve as the primary contact for Japan ICSR, research report, and FSMT activities.</li><li>Review vendor-prepared safety evaluations and PMDA submissions for accuracy.</li><li>Oversee pharmacovigilance service providers and monitor contract compliance.</li><li>Drive process improvements that strengthen quality and compliance.</li><li>Author and update working instructions and deliver related training.</li><li>Contribute to J-RMP development and execution activities.</li><li>Partner with external departments and license partners on safety deliverables.</li><li>You build collaborative relationships to support effective safety outcomes.</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>More than 7 years of pharmacovigilance and post-marketing surveillance operations experience.</li><li>Strong knowledge of PMDA, MHLW, and International Council for Harmonisation guidelines and regulations.</li><li>Experience supporting Japan aggregate reporting and local pharmacovigilance activities.</li><li>Experience managing external service providers and vendor relationships.</li><li>Experience supporting J-NDA safety content and responding to PMDA inquiries.</li><li>Experience with regulatory inspections, including PMDA re-examination, MAH license renewal, or GCP reliability inspection.</li><li>Experience leading complex projects, including team improvement, safety database implementation, or safety data migration initiatives.</li><li>Experience collaborating with Medical Affairs, Regulatory Affairs, Sales and Marketing, and Clinical Development teams.</li><li>Prior global pharmacovigilance experience.</li><li>Strong project management and cross-functional collaboration skills.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Director, Hematology, Japan]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49676]]></requisitionid>
    <referencenumber><![CDATA[R49676]]></referencenumber>
    <apijobid><![CDATA[r49676]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49676/sales-director-hematology-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Sales Director, Hematology Japan</strong> to join our <strong>Commercial Oncology team</strong>, leading our <strong>Japan Hematology business</strong>. In this role, you will <strong>lead the hematology field sales organization, drive commercial execution, and deliver strong sales performance aligned with company goals</strong> while collaborating with <strong>cross-functional stakeholders, commercial operations, and marketing teams</strong>. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Tokyo, Japan</p><p>Work model: Hybrid</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead and develop a high-performing hematology sales team.</li><li>Drive sales performance that meets or exceeds brand objectives.</li><li>Coach, develop, and retain talent through feedback and development planning.</li><li>Create national, regional, and local account plans with measurable tactics.</li><li>Oversee CRM use, sales analytics, and business key performance indicators.</li><li>Build relationships with key healthcare professionals across oncology.</li><li>Partner with cross-functional teams to address market trends and opportunities.</li><li>You champion ethical conduct, accountability, and a winning team culture.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree required; advanced degree or certification preferred.</li><li>Minimum 5 years of sales leadership or management in oncology or hematology.</li><li>Proven success hiring, coaching, developing, promoting, and retaining top talent.</li><li>Strong record of sales performance with high integrity and accountability.</li><li>Experience developing account plans and implementing commercial strategies.</li><li>Proficiency with sales data, analytics, and customer relationship management systems.</li><li>Strong collaboration, leadership, interpersonal, communication, presentation, planning, and prioritization skills.</li><li>Ability to build deep customer relationships and organizational credibility.</li><li>Ability and willingness to travel 30-40%, including some weekends.</li><li>Fluent Japanese language skills.</li><li>Hematology or biologics experience preferred.</li><li>Intermediate English language skills preferred.</li><li>Highest personal values and ethical standards.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Process Specialist, Fill Finish Manufacturing]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47994]]></requisitionid>
    <referencenumber><![CDATA[R47994]]></referencenumber>
    <apijobid><![CDATA[r47994]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r47994/staff-process-specialist-fill-finish-manufacturing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Process Specialist — Manufacturing (Principal, Staff, or Senior Staff) to join our IOPS team, providing on-the-floor technical direction and leadership across our biopharmaceutical manufacturing process. In this role, you will resolve process challenges, coach manufacturing personnel, lead investigations, and drive continuous improvement — while collaborating with Process Science, Engineering, Quality, Regulatory, and Facilities teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: East Greenbush, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><h3><strong>Discover your role:</strong></h3><ul><li>Provide on-the-floor technical input to resolve process problems, coach manufacturing personnel on critical process steps, and support implementation of process and work system improvements in the production suites</li><li>Lead investigations into process variances, support CAPA implementation, and guide validation activities involving manufacturing equipment and processes</li><li>Support technology transfer of the manufacturing process, liaising with process science and technology transfer teams on transfer and startup activities</li><li>Track, trend, and present relevant technical and business process metrics; prepare reports by collecting and analyzing information for review with the Process Science Group</li><li>Write, review, and approve SOPs, specifications, regulatory filings, and other controlled documents; perform cGMP audits and represent Manufacturing during regulatory and client audits</li><li>Act as system owner for defined manufacturing equipment, coordinating all non-routine activities and ensuring policies and procedures comply with regulatory requirements</li><li>Lead and implement continuous improvement initiatives; support safety improvements requiring technical and engineering input</li><li>Interface cross-functionally with Facilities, Process Development, Engineering, Process Analytical Sciences, Regulatory, Quality Assurance, and Quality Control</li><li>Knowledge of cGMP manufacturing and familiarity with formulation, aseptic filling, visual inspection, assembly, labeling, and/or packaging of liquid and lyophilized injectable products</li><li>Technology transfer and equipment and process validation experience in aseptic parenteral fill/finish operations preferred</li><li>Experience with lyophilization a plus; experience operating and qualifying highly automated equipment a plus</li></ul><br><h3><strong>This role requires:</strong></h3><ul><li>BS in Life Sciences or a related field</li><li>Principal Process Specialist: 8+ years of relevant cGMP manufacturing, engineering, or scientific experience</li><li>Staff Process Specialist: 10+ years of relevant cGMP manufacturing, engineering, or scientific experience</li><li>Senior Staff Process Specialist: 12+ years of relevant cGMP manufacturing, engineering, or scientific experience</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role</li><li>Gowning: Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Market Access Analytics - Neurology]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46822]]></requisitionid>
    <referencenumber><![CDATA[R46822]]></referencenumber>
    <apijobid><![CDATA[r46822]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46822/associate-director-market-access-analytics-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director</strong> to join our <strong>Market Access Analytics, Neurology</strong> team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Sleepy Hollow, NY</p></li><li><p>4 days per week on site</p></li></ul><p><strong>Discover your role:</strong></p><p>This is a hands-on analytics role responsible for transforming complex data assets and advanced analytical tools into evidence-based market access decisions across Payer & Provider/GPO, Contracting, and Pricing. The Associate Director will lead the design, curation, and evaluation of market access data - translating it into strategic analytical solutions that sharpen payer and channel strategy, optimize provider and GPO contracting, and drive portfolio performance.</p><p><em>Lead </em></p><p>1) Shape payer and channel strategy by synthesizing market, payer, and account-level data to inform strategic positioning, coverage decisions, and channel optimization across the portfolio.</p><p>2) Drive payer segmentation and policy analytics across Commercial, Medicare Part B/D, Medicare Advantage, Managed Medicaid, FFS Medicaid, VA/DoD, and Exchange segments - integrating intelligence on Payer willingness and ability to manage drug utilization to surface actionable insight.</p><p><em>Partnership and Collaboration </em></p><p> 3) Build strong, productive relationships with cross-functional stakeholders across Market Access Strategy, Payer Account teams, GPO Account Directors, and Brand colleagues - balancing analytical rigor, timelines, and influence to drive aligned outcomes.</p><p>4) Serve as a strategic thought partner by sharpening business questions, structuring analyses, and translating complex findings into clear, compelling recommendations for senior leadership.</p><p><em>Develop </em></p><p>5) Proactively identify emerging analytics opportunities that address critical market access challenges and unlock growth across the portfolio.</p><p>6) Advance measurement frameworks to evaluate pre- and post-performance across Payer and GPO initiatives, enabling continuous strategic improvement.</p><p>7) Deliver provider and GPO analytics - including account- and segment-level opportunity assessments and pull-through analysis tied to recent payer coverage or brand-level developments.</p><p><em>Execute </em></p><p>8) Serve as the day-to-day analytics partner to Market Access Strategy, HEOR, Pricing, Trade, GPO, and Field Reimbursement teams - scoping questions, executing analyses, and delivering actionable insights on time.</p><p>9) Lead performance reporting tied to strategic imperatives and priority business questions, ensuring clarity, consistency, and alignment across stakeholders.</p><p>10) Triangulate across diverse datasets to surface and deliver actionable insights that uncover opportunities and portfolio-level strategies.</p><p>11) Manage analytics vendor workstreams from scoping through delivery - defining deliverables, maintaining rigor, and driving timely execution.</p><p>12) Apply Regeneron's proprietary Market Access semantic layer across key third-party data sources - including payer medical policy, patient-level claims, and reimbursement data - to ensure analytical consistency and depth.</p><p><strong>This role requires:</strong></p><ul><li><p>Minimum 10 years of pharmaceutical/biotech commercial experience (or 7+ years for MBA/MS), in roles of increasing accountability; prior experience with market-leading brands is desired.</p></li><li><p>BS/BA in STEM related field, e.g., Statistics, Econometrics, Mathematics, Business Analytics; Advanced degree preferred. </p></li><li><p>Proficiency across key market access data sources — MMIT, IQVIA LAAD/DDD/Xponent, Remittance, Model N, Integrichain 852/867, and Patient HUB — with working knowledge of Payer spine bridge files and account hierarchy.</p></li><li><p>Experience coding in Python, R and/or SQL. </p></li><li><p>Experience in data visualization and commercial business intelligence tools required (e.g., Dataiku, Databricks, PowerBI, Tableau, QlikView, Oracle BI, Microstrategy, Cognos, Spotfire or similar tools). </p></li><li><p>Expertise in data visualization and data storytelling of key findings. </p></li><li><p>Advanced proficiency in Excel, and PowerPoint required. </p></li><li><p>Experience in data mining, descriptive analytics, application of statistical methods, analyses and modeling, predictive modeling, opportunity assessment and quantification. </p></li><li><p>Proven track record of managing multiple external vendors and project teams concurrently against stringent deadlines in a fast-paced, timeline-driven atmosphere. </p></li><li><p>Communication and influencing skills with demonstrated ability to succinctly and effectively present compelling reviews of analyses that integrate analytics and patient journey implications/actions to be taken. </p></li><li><p>Strong analytical skills and strategic thinking ability. </p></li><li><p>Concise and impactful written and verbal communication skills with demonstrated experience in influencing and driving decision making. </p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Patient Safety Sciences Delivery]]></title>
    <date><![CDATA[Tue, 11 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48142]]></requisitionid>
    <referencenumber><![CDATA[R48142]]></referencenumber>
    <apijobid><![CDATA[r48142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48142/executive-director-global-patient-safety-sciences-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Executive Director</strong> to join our <strong>Patient Safety</strong> team.</p><p>The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk-related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. This role requires the ability to work cross-functionally, partnering with the Safety Sciences TAHs and other leaders. They will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director, Global Patient Safety Sciences Delivery is also responsible for the development and management of their team. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA</p></li><li><p>4 days per week onsite</p></li><li><p>Travel: As needed</p></li></ul><p><strong>Discover your role:</strong> ​</p><ul><li><p>Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes, templates </p></li><li><p>Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix, and knowledge management repository </p></li><li><p>Enable the Global Capability Center (GCC) to operate more efficiency and scale with the demands of the business </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li></ul><p><em>Operational Delivery Oversight </em></p><ul><li><p>Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Coordinate and support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery </p></li></ul><p><em>Cross-Functional Partnership </em></p><ul><li><p>Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads </p></li><li><p>Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li></ul><p><em>Talent Development & Organizational Leadership </em></p><ul><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization. </p></li></ul><p><strong>This role requires:</strong> ​</p><ul><li><p>Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.</p></li><li><p>17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required </p></li><li><p>6+ years of leading a team and people management experience </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li></ul><p>#GDPSJobs</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Systems & Collaboration Platforms Business Operations]]></title>
    <date><![CDATA[Mon, 17 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49917]]></requisitionid>
    <referencenumber><![CDATA[R49917]]></referencenumber>
    <apijobid><![CDATA[r49917]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49917/senior-manager-systems-collaboration-platforms-business-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>The Senior Manager, Systems & Collaboration Platforms Business Operations serves as the business-side operational owner for Enterprise Planning and Collaboration Platforms, including Planisware, Planview Advisor, Microsoft 365 collaboration platforms, and related enterprise systems. This role is responsible for supporting effective platform operations, governance, business administration, user support, and operational readiness across the enterprise.</p><p>Reporting to the Director, Enterprise Planning & Collaborations Platforms, this position partners closely with Regeneron Digital & Technology, Enterprise Stewardship & Standards, Data Stewardship & Quality, DADS, Business Process Owners, and Functional Area subject matter experts across the enterprise to ensure platforms operate efficiently, support business objectives, and remain aligned with governance standards and operational requirements. The role owns platform operations and business administration while working within established data governance frameworks and stewardship processes.</p><br><h3>When & where:</h3><ul><li>Location: Tarrytown, NY or Warren, NJ</li></ul><br><h3>Discover your role:</h3><ul><li>Execute operational priorities established by the Enterprise Planning & Collaborations Platforms Lead, ensuring day to day administration, platform performance & reliability, operational effectiveness, and user readiness across Enterprise Planning and Collaboration Platforms.</li><li>Serve as the business-side owner for platform operations, partnering with Regeneron-Digital & Technology to support system administration/product owner activities, user access management, incident resolution, system upgrades, releases, and operational support.</li><li>Manage business administration processes, including access approvals, user onboarding, operational support, issue intake, and request tracking.</li><li>Coordinate User Acceptance Testing (UAT) activities for system enhancements and releases, ensuring business readiness, stakeholder engagement, and effective issue resolution.</li><li>Establish and maintain operational standards, service processes, governance documentation, knowledge articles, and business-rule documentation to support compliance, audit readiness, and consistent platform use.</li><li>Prepare decision records, impact assessments, recommendations, and escalation packages to support governance forums and operational decision-making.</li><li>Partner with stakeholders across the enterprise, including Enterprise Stewardship & Standards, Data Stewardship & Quality, DADS, Regeneron-Digital & Technology, Business Process Owners, and Functional Area leaders, to ensure platform operations, governance processes, reporting readiness, and business requirements remain aligned with enterprise standards and strategic objectives.</li><li>Support governance and change-control processes by evaluating operational impacts, maintaining documentation, and facilitating implementation of approved changes.</li><li>Monitor and report key operational metrics, including user satisfaction, issue resolution performance, change success rates, platform adoption, and compliance with approved standards.</li><li>Identify and implement opportunities to improve user experience, platform effectiveness, operational efficiency, and governance maturity across the enterprise platform ecosystem.</li><li>Support functional SMEs, Change Agents, and business stakeholders by providing operational guidance, responding to platform-related inquiries, and ensuring user needs are represented in platform decisions.</li><li>Maintain operational records, documentation, and knowledge repositories to support compliance, transparency, and business continuity.</li></ul><br><h3>This role requires:</h3><ul><li>Minimum of a Bachelors degree and 8+ years in operational or enterprise planning, including experience facilitating cross-functional alignment on processes and initiatives. Biopharma / drug development experience preferred.</li><li>Experience supporting enterprise planning, portfolio management, project management, resource management, or collaboration platforms in a biopharma, R&D, or regulated business environment.</li><li>Experience with Planisware, Planview Advisor, Microsoft 365, SharePoint, Power Platform, Power BI, or similar business operations and workflow platforms.</li><li>Experience developing or maintaining business-rule documentation, knowledge articles, UAT materials, operational SOPs, decision records, or governance documentation.</li><li>Experience supporting platform governance, change control boards, release management, access governance, template governance, or operational support models.</li><li>Familiarity with data stewardship, data governance, analytics/reporting, and enterprise glossary concepts is preferred, particularly to support partnership with Enterprise Stewardship & Standards.</li><li>Experience tracking adoption, user engagement, operational metrics, support trends, and service performance indicators.</li></ul><br><h3>Preferred Qualifications:</h3><ul><li>PMI Project Management Professional (PMP) is preferred but not required.</li><li>Demonstrated success leading cross-functional initiatives and influencing stakeholders across a complex matrix organization</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Key Accounts Marketing]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50073]]></requisitionid>
    <referencenumber><![CDATA[R50073]]></referencenumber>
    <apijobid><![CDATA[r50073]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50073/director-key-accounts-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>This role of Director, Oncology Key Accounts Marketing will be responsible for supporting our vision for best-in-class capabilities and innovative solutions to support engaging Oncology and Hematology Key Strategic Provider Accounts.</p><p>This candidate facilitates development of, any updates to our Provider Key Account Strategy for our Commercial Business Unit. In this role, will develop Key Account Marketing sponsorships strategy aligned to annual brand plan plus content and executes rollout to the Oncology Key Account Leader (OKAL) team focused on building loyalty with customers and ensures our Oncology brand(s) resonate with stakeholders and C-Suite and D-Suite leaders in key oncology accounts in the US. This individual will report to the Global Core Brand Lead.</p><h3>When & where:</h3><ul><li>In the Sleepy Hollow, NY Office - 4 days a week</li><li>Travel up to 30% of the time</li></ul><h3>Discover your role:</h3><ul><li>Develop promotional strategy and tactical plan as well as develop all tactics for OKAL use with Key acct/VA targets aligned to the brand plan including approval through RC</li><li>Partner with brand marketing teams to develop deep understanding of indication and overall brand strategy and US tactical focus, as well as share data and insights Key Accts Performance to inform marketing plans across the brand.</li><li>Work closely with OKAL Leader and OKALs as a dotted line member of the OKAL Leadership Team, attending regular OKAL team calls and meetings, and attend professional association meetings to connect regularly with OKAL target customers/partners</li><li>Provide leadership support to the development of the overall Brand Plan and strategy focusing on key accounts.</li><li>Ensure innovative solutions and procedures are demonstrated for reaching OKAL Acct based partners, C-Suite and acct operational leadership, developing collaborative projects as agreed upon with OKAL Sr Director and Head of Marketing</li><li>Understand and leverage trends in the marketplace and competitive benchmarking to inform strategies for key acct engagement.</li><li>Actively collaborate and provide additional support to OKAL Sr Director and OKAL team operations work e.g. targeting, performance reporting, and business planning/presentations</li><li>Manage the Key Accounts Marketing budget, ensure cost effective delivery of all programs while tracking and monitoring effectiveness including KPI’s, ROI and actionable findings.</li></ul><h3>This role requires:</h3><ul><li>At least 12 years of progressive experience in the pharmaceutical or biotech industry, with significant leadership experience in marketing, sales, and sales management in oncology preferred. At least 5 years in a marketing role.</li><li>A bachelor’s degree Required, MBA preferred.</li><li>Demonstrated competency in marketing innovation including managing ad agencies/vendors, and marketing strategy and tactical effectiveness measures</li><li>Demonstrated ability to lead strategically, drive performance, build alignment, inform, negotiate, and collaborate.</li><li>Proven track record of market analysis and identifying growth opportunities.</li><li>Ability to synthesize inputs from external and internal collaborators such as HCPs, field teams, and market access colleagues.</li><li>Effective written and oral communication; experience delivering complex messages to diverse internal and external collaborators with a track record of influential presentations.</li><li>Ability to communicate and act promptly; demonstrated initiative and creativity; and the agility to work effectively in complex, rapidly changing environments.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Cell Therapy]]></title>
    <date><![CDATA[Thu, 13 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49309]]></requisitionid>
    <referencenumber><![CDATA[R49309]]></referencenumber>
    <apijobid><![CDATA[r49309]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49309/senior-medical-director-clinical-development-cell-therapy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together:</strong></h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Hematology team supporting Cell Therapy Clinical Development. In this role, you will provide clinical leadership and responsibility for all clinical deliverables within an assigned section of a clinical program in Hematology/Oncology, operating with minimal supervision from the Program Lead MD. Clinical deliverables may include individual protocols consistent with the Clinical Development Plan (CDP), clinical components of regulatory documents and registration dossiers, brand-related medical information, and clinical communications and publications. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a significant difference for patients worldwide.</p><h3><strong>When & where:</strong></h3><ul><li><p>Location: Tarrytown, NY or Warren, NJ</p></li><li><p>Travel: 10%, to relevant congresses and conferences</p></li></ul><h3><strong>Discover your role:</strong></h3><ul><li><p>Manage all operational aspects and drive execution of clinical programs, in partnership with global line functions, the assigned Clinical Scientist, and Clinical Operations associates, to ensure timely execution of assigned clinical deliverables within approved budget.</p></li><li><p>Lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups) and internal stakeholders (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, Health Economics & Outcomes Research [HE&OR]), as well as internal decision boards.</p></li><li><p>Ensure the overall safety of the compound in collaboration with the Safety Lead for the assigned program</p></li><li><p>Lead development of clinical sections of program-level regulatory documents, such as Investigators' Brochures, briefing books, safety updates, and IND/NDA (Investigational New Drug/New Drug Application) submission documents, and lead responses to Health Authority questions</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>A M.D. or equivalent medical degree (e.g., D.O., MBBS), preferably with clinical training in a relevant disease area such as Hematology or Oncology.</p></li><li><p>Significant demonstrated experience of 4+ years in clinical research within an industry environment, spanning clinical activities across Phases 1 through 4. Cell Therapy experience preferred.</p></li><li><p>Strong understanding of the global regulatory environment, including key regulatory agencies and approval processes.</p></li><li><p>Strong understanding of the operational aspects of all phases of clinical trial conduct (start-up, conduct, close-out).</p></li><li><p>People management experience preferred but not required.</p></li></ul><p>#MDJobs #MDJobsCD #GDTherapeuticJobs #Hematology #CellTherapy</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Quality Assurance Reviewer]]></title>
    <date><![CDATA[Sun, 16 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R48353]]></requisitionid>
    <referencenumber><![CDATA[R48353]]></referencenumber>
    <apijobid><![CDATA[r48353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r48353/principal-quality-assurance-reviewer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Quality Assurance (QA) Specialist/Reviewer to support our Fill Finish facility. In this role, you will perform all compliance related tasks necessary to review and approve investigations and provide quality oversight to the implementation of robust corrective actions for supporting manufacturing operations. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Location: Rensselaer, New York, United States</p></li><li><p>Work model: Monday-Friday, 8am-4:30pm</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Independently reviews and approves:</p><ul><li><p>Investigations into non-conformances and proposed actions to prevent reoccurrences in support of manufacturing operations</p></li><li><p>Laboratory investigations into out of specification (OOS) and out of trend ( OOT) results</p></li><li><p>Supplier corrective action requests and proposed vendor actions</p></li></ul></li><li><p>Coaches investigation team to enable preparation of investigation reports that include recommendations on investigation findings for medium/high severity non-conformances</p></li><li><p>Analyzes and evaluates information captured through investigations, summarizes information and trends in investigation reports</p></li><li><p>Presents quality considerations and recommendations at group meetings with multiple levels of management</p></li><li><p>Reviews primary data sources to assure the accuracy of investigative conclusions in accordance with cGMP standards in support of investigations</p></li><li><p>Provides quality reviews and oversight on a wide range of investigations of differing subject matter</p></li><li><p>Monitors production processes and quality systems data to acquire vital data in support of investigations and track efficiency of changes</p></li><li><p>Participates in and/or leads cross-functional study teams to get results</p></li><li><p>Captures, trends and analyzes process related data to drive consistency and timeliness</p></li><li><p>Trains employees on investigative processes and techniques</p></li><li><p>Coordinates and/or leads cross-functional meetings with multiple departments</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>BS/BA in Life Sciences, Engineering or related field; or equivalent combination of education and experience</p><ul><li><p>Principal QA Specialist: 8+ years of relevant experience</p></li><li><p>Staff QA Specialist: 10+ years of relevant experience</p></li><li><p>Level will be determined based on experience</p></li></ul></li><li><p>Experience with sterile drug product manufacturing, fill finish and/or quality control testing</p></li></ul><p>#REGNQA</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Medical Affairs - Rare Diseases]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50256]]></requisitionid>
    <referencenumber><![CDATA[R50256]]></referencenumber>
    <apijobid><![CDATA[r50256]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50256/director-medical-affairs-rare-diseases/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><div><div><div><div><div><div><div><div><div><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Medical Affairs, Rare Diseases - Europe to join our Medical Affairs team. In this hybrid role, you will lead medical strategy and scientific engagement across investigational and approved therapies in rare diseases. Working closely with Global Medical Affairs, Clinical Development, HEOR, Medical Operations, Publications and Statistics, you will drive evidence generation, build scientific partnerships and translate external insights into strategic recommendations supporting patient needs and medical excellence.</p><p><strong>When & where:</strong></p><p>Amsterdam (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead medical strategies and tactical plans across assigned rare disease assets and therapeutic areas.</p></li><li><p>Provide scientific and medical leadership throughout pre-launch, launch and post-launch phases.</p></li><li><p>Establish scientific partnerships with healthcare professionals, researchers, advocacy organisations, payers and other external stakeholders.</p></li><li><p>Drive evidence generation through Medical Affairs studies, data analysis, publications and scientific communication plans.</p></li><li><p>Translate clinical and country insights into recommendations supporting medical strategy, patient access and value demonstration.</p></li><li><p>Manage complex priorities, budgets and timelines while maintaining scientific integrity and compliance.</p></li><li><p>You bring a collaborative, patient-focused approach to scientific leadership and external engagement.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MD, DO, PharmD, PhD or an equivalent advanced scientific or clinical degree.</p></li><li><p>Minimum 8 years of Medical Affairs experience with increasing responsibility.</p></li><li><p>Expertise in rare diseases and/or genetic medicine.</p></li><li><p>Experience leading medical strategy, scientific communications and evidence generation.</p></li><li><p>Strong understanding of drug development and lifecycle management.</p></li><li><p>Fluency in English and willingness to travel nationally and internationally approximately 30–50%.</p></li><li><p>Experience in rare genetic diseases, gene therapy, regenerative medicine or rare bone, muscle or cardiovascular disorders preferred.</p></li><li><p>Product launch, clinical trial, publication or field Medical Affairs leadership experience preferred.</p></li><li><p>Multi-country experience and additional languages preferred.</p></li></ul></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€111,675.00 - €186,125.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Medical Affairs - Rare Diseases]]></title>
    <date><![CDATA[Thu, 27 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50255]]></requisitionid>
    <referencenumber><![CDATA[R50255]]></referencenumber>
    <apijobid><![CDATA[r50255]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50255/director-medical-affairs-rare-diseases/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Medical Affairs, Rare Diseases - Europe to join our Medical Affairs team. In this hybrid role, you will lead medical strategy and scientific engagement across investigational and approved therapies in rare diseases. Working closely with Global Medical Affairs, Clinical Development, HEOR, Medical Operations, Publications and Statistics, you will drive evidence generation, build scientific partnerships and translate external insights into strategic recommendations supporting patient needs and medical excellence.</p><p><strong>When & where:</strong></p><p>Munich (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead medical strategies and tactical plans across assigned rare disease assets and therapeutic areas.</p></li><li><p>Provide scientific and medical leadership throughout pre-launch, launch and post-launch phases.</p></li><li><p>Establish scientific partnerships with healthcare professionals, researchers, advocacy organisations, payers and other external stakeholders.</p></li><li><p>Drive evidence generation through Medical Affairs studies, data analysis, publications and scientific communication plans.</p></li><li><p>Translate clinical and country insights into recommendations supporting medical strategy, patient access and value demonstration.</p></li><li><p>Manage complex priorities, budgets and timelines while maintaining scientific integrity and compliance.</p></li><li><p>You bring a collaborative, patient-focused approach to scientific leadership and external engagement.</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>MD, DO, PharmD, PhD or an equivalent advanced scientific or clinical degree.</p></li><li><p>Minimum 8 years of Medical Affairs experience with increasing responsibility.</p></li><li><p>Expertise in rare diseases and/or genetic medicine.</p></li><li><p>Experience leading medical strategy, scientific communications and evidence generation.</p></li><li><p>Strong understanding of drug development and lifecycle management.</p></li><li><p>Fluency in English and willingness to travel nationally and internationally approximately 30–50%.</p></li><li><p>Experience in rare genetic diseases, gene therapy, regenerative medicine or rare bone, muscle or cardiovascular disorders preferred.</p></li><li><p>Product launch, clinical trial, publication or field Medical Affairs leadership experience preferred.</p></li><li><p>Multi-country experience and additional languages preferred.</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€125,250.00 - €208,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ultra-Pure Water Technician (Nights)]]></title>
    <date><![CDATA[Sun, 30 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49198]]></requisitionid>
    <referencenumber><![CDATA[R49198]]></referencenumber>
    <apijobid><![CDATA[r49198]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49198/ultra-pure-water-technician-nights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>Our Ultra-Pure Water (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. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Rensselaer, New York, United States</li><li>Working shift: Wednesday-Saturday 2:00pm-12:30am</li><li>Training shift: Monday-Friday 7:00am-3:30pm for up to 6 months</li></ul><br><h3>What you'll do:</h3><ul><li>Perform preventative and predictive maintenance on related clean utilities and systems that support manufacturing</li><li>Maintain water rooms and related equipment such as pumps, motors, Water for Injection (WFI) stills, Clean Steam Generators, and related piping</li><li>Perform activities such as troubleshooting, hands-on repairs on all related clean utility equipment and systems, and WFI point-of-use flushing</li><li>Maintain documents and records on all validated equipment and systems</li><li>Collaborate with other departments and contractors on scheduling repairs and maintenance of clean utility systems</li><li>Perform monitoring and control of systems using computer-driven Business Automation System (BAS) and PLC controls</li><li>Communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li></ul><br><h3>This role requires:</h3><ul><li>AAS degree, preferably in an Engineering or Construction Technologies related field and the following minimum years of relevant experience for each level<ul><li>Clean Utilities Technician II: 2+ years of related experience, or HSD/GED with 5+ years of related experience</li><li>Clean Utilities Technician III: 5+ years of related experience, or HSD/GED with 8+ years of related experience</li></ul></li><li>Ability to read and/or understand piping, electrical, and instrumentation drawings</li><li>Basic troubleshooting skills as they relate to the water room and mechanical proficiency</li><li>Understanding additional mechanical equipment and systems such as pharmaceutical compressed air, domestic water lines, plant steam, and high/low pressure condensate return systems</li><li>Participating in rotational on-call schedule</li><li>Prior experience in the maintenance and operation of a large-scale utilities plant is preferred</li></ul><p>Level will be determined based on qualifications relevant to the role</p><br><h3>The environment and physical rhythms of the role:</h3><ul><li>Gowning: Full cleanroom attire (examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</li><li>Ability to remove jewelry, makeup and nail adornments when wearing cleanroom attire</li><li>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</li><li>Some physical requirements can include but are not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Lab Integration Developer]]></title>
    <date><![CDATA[Tue, 25 Aug 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45570]]></requisitionid>
    <referencenumber><![CDATA[R45570]]></referencenumber>
    <apijobid><![CDATA[r45570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal IT Lab Integration Developer (Senior or Principal) to join our IOPS IT team, designing, developing, validating, and supporting integrations between laboratory systems, analytical instruments, enterprise platforms, and data systems within our regulated pharmaceutical environment. In this role, you will combine application development, system integration, data management, and regulatory compliance expertise — partnering with QC, QA, R&D, Manufacturing, and external vendors to enable end-to-end digital lab workflows. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Troy, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li></ul><p><strong>Discover your role:</strong></p><ul><li>Support the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across laboratory instruments and middleware; define integration patterns including APIs, event-driven architectures, message queues, and file-based approaches</li><li>Design and develop integrations between instruments and the Orchestration Layer; build and support API-based, file-based, and message-based integrations using REST, SOAP, SFTP, JSON, and XML</li><li>Translate QC business processes into orchestrated digital workflows; develop instrument data capture and automation workflows and configure and support middleware and integration platforms</li><li>Ensure all integrations comply with GxP, 21 CFR Part 11, and ALCOA+ data integrity requirements; participate in Computer System Validation activities including IQ/OQ/PQ documentation and perform impact assessments and change control documentation</li><li>Monitor and troubleshoot integration issues in production environments; provide Level 2/3 support for QC Lab Systems</li><li>Partner with QC Analysts, QA, IT infrastructure, and external vendors; collaborate with QC, R&D, Manufacturing, and QA teams to align integration solutions with business needs</li><li>Support audits and regulatory inspections; ensure scalability, resilience, and performance across all lab integrations</li></ul><p><strong>This role requires:</strong></p><ul><li>BS/BA in Information Technology, Mathematics, or a related field</li><li>Senior: 5+ years of relevant experience,</li><li>Principal: 8+ 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>Experience connecting laboratory instruments such as liquid handlers and analyzers to central platforms including 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 orchestration engines and disparate lab hardware</li><li>Proficiency in Python or VBA for customizing automated workflows and data parsing</li><li>Strong understanding of data formats, naming conventions, and data governance to ensure consistent and accurate data delivery across systems</li><li>Experience with GxP, 21 CFR Part 11, and CSV/CSA practices in a regulated pharmaceutical or biotech environment preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50249]]></requisitionid>
    <referencenumber><![CDATA[R50249]]></referencenumber>
    <apijobid><![CDATA[r50249]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50249/senior-manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Clinical Study Lead to join our Clinical Trial Management team, supporting our Inflammation & Immunology therapeutic area. The Senior Clinical Study Lead (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. You will be 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.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Armonk, NY, Warren, NJ</p></li><li><p>Work Model: Primarily on-site with hybrid flexibility</p></li><li><p>Travel: 25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</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>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; Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level; Leads the feasibility assessment to select relevant regions and countries for the study</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; Monitors data entry and query resolution and acts on any deviations from agreed metrics</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>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>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></ul><p><strong>This role requires:</strong></p><ul><li><p>A minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience</p></li><li><p>We are seeking experience with line management as well as exceptional interpersonal and leadership skills</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization; Ability to influence and negotiate across a wide range of stakeholders</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>We are seeking 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>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Compliance Counsel]]></title>
    <date><![CDATA[Wed, 09 Sep 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50268]]></requisitionid>
    <referencenumber><![CDATA[R50268]]></referencenumber>
    <apijobid><![CDATA[r50268]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50268/associate-director-compliance-counsel/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>In this role at Regeneron, the Associate Director, Compliance Counsel will work on investigations to ensure compliance with all laws, regulations, and company policies. This role will coordinate and conduct compliance investigations and provide guidance to internal stakeholders on addressing risks associated with conducting business in global markets. The successful attorney will be able to work across the organization, establish positive relationships, and provide a neutral and informed perspective.</p><div><p><strong>When & where: </strong></p><ul><li><p><strong>Location</strong>: Sleepy Hollow, NY</p></li><li><p><strong>Work model/flexibility</strong>: 4 days onsite</p></li></ul></div><div><p><strong>Discover your role:</strong> </p></div><ul><li><p>Responding to alleged violations of policies, procedures, and standards of Regeneron’s Code of Business Conduct and Ethics by evaluating or recommending the initiation of investigative procedures </p></li><li><p>Lead investigations of allegations of violations of law or policy, as may be needed, from various countries worldwide</p></li><li><p>Provide support to partners on risks emanating from laws, codes and regulations</p></li><li><p>Provide input into and develop policies, procedures and guidance documents</p></li><li><p>Stay on top of legislative and regulatory developments impacting Regeneron’s global operations </p></li><li><p>Liaise with other Compliance or Law Department functions both in the US and globally to ensure integrated support and timely updates.</p></li><li><p>Provide guidance to internal stakeholders on risks emanating from international laws, codes and regulations.</p></li><li><p>Monitor and assess legislative and regulatory developments impacting Regeneron’s global operations.</p></li></ul><h3><strong> </strong></h3><p><strong>This role requires: </strong></p><ul><li><p>You must have JD with 4+ years of validated experience, with at least 2 years working in or with pharmaceutical companies on healthcare compliance related activities.</p></li><li><p>You are licensed to practice law in New York or eligible for licensure as a registered in-house counsel.</p></li><li><p>You have experience conducting internal, compliance, and/or government investigations. </p></li><li><p>You possess high level of influencing skills and ability to inspire change as it relates to implementing remedial actions.</p></li><li><p>Knowledge of anti-kickback and anti-bribery prohibitions as they apply to pharmaceutical sales, off-label/inappropriate promotion issues, Open Payments Act reporting obligations, and other primary laws governing key pharmaceutical compliance areas is helpful.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 09 Sep 2026 18:42:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs, Respiratory (Southern California and Central Valley)]]></title>
    <date><![CDATA[Sun, 13 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50243]]></requisitionid>
    <referencenumber><![CDATA[R50243]]></referencenumber>
    <apijobid><![CDATA[r50243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50243/associate-director-field-medical-affairs-respiratory-southern-california-and-central-valley/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Field Medical Affairs, to join our Respiratory team, supporting healthcare providers and payers in a field-based role. In this role, you will establish and maintain scientific exchange with medical specialists and decision-makers, ensuring accurate and timely dissemination of clinical data on in-line and pipeline products, while collaborating with Global Medical Affairs leadership and clinical research investigators.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Southern California (including Los Angeles, Orange County, Ventura County, and the Central Valley)</p><p>• Travel: Capable of engaging in frequent business travel (approximately 40-50% of the time), including air travel, overnight and occasionally on weekends.</p><p><strong>Discover your role:</strong><br>• Engage in scientific discussions with Healthcare Professionals and payers, aligned with Medical Affairs objectives.<br>• Demonstrate deep scientific expertise in assigned molecules/products and therapeutic area.<br>• Build and nurture relationships with key external scientific and medical specialists across the region.<br>• Stay ahead of evolving healthcare trends within the Dermatology therapeutic landscape.<br>• Shape and implement local medical strategy in line with Global Medical Affairs direction and timelines.<br>• Support clinical research sites and investigators. <br>• Deliver clinical and health economic information that enhances the appropriate use of our products.<br>• Communicate scientific and clinical information ethically, accurately, and in a customer-focused manner.</p><p><strong>This role requires:</strong><br>• A Doctorate level clinical/science degree (e.g., MD, PharmD, PhD) with a minimum of 5 years of related work experience (clinical, managed care, or industry)<br>• Experience as a Medical Science Liaison within Immunology. Respiratory is preferred.<br>• Strong ability to communicate and disseminate scientific and clinical data.<br>• Residency within the territory</p><p>#ifm #msl #medicalscienceliaison</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 14 Sep 2026 20:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Real-World Data and Analytics (HEOR)]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49657]]></requisitionid>
    <referencenumber><![CDATA[R49657]]></referencenumber>
    <apijobid><![CDATA[r49657]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49657/senior-manager-real-world-data-and-analytics-heor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Real-World Data and Analytics (RWDnA) will support the generation of real-world evidence (RWE) in oncology by delivering data-driven insights through the analysis of real-world data (RWD). The individual will contribute to query/protocol/statistical analysis (SAP) development and execute analyses of RWD to support the generation of RWE to address research questions. The successful candidate will conduct hands-on programming on internal RWD assets, support publication activities, and participate in vendor management.<br>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong><br>• Location: Sleepy Hollow, NY</p><p><strong>Discover your role:</strong><br>• Contribute to the development of RWE queries, protocols, and statistical analysis plans (SAPs) within oncology<br>• Translate analytic findings into clear insights and communicate them directly to project teams<br>• Support end-to-end RWE query and study delivery, including hands-on programming and quality control of analytic code<br>• Evaluate and identify appropriate real-world data sources to address specific research questions<br>• Contribute to scientific communications, including abstracts, posters, manuscripts, and internal presentations<br>• Support senior team members in coordinating activities with external analytics vendors and research partners</p><p><strong>This role requires:</strong><br>• Doctoral degree in a quantitative field focused on the application of data science to healthcare data with 2+ years of hands-on programming experience; or a Master's degree in a related field with 4+ years of hands-on programming experience<br>• Hands-on experience with real-world data sources such as large-scale administrative claims data (e.g., Optum, Medicare, Komodo claims) and electronic health records (EHRs)<br>• Experience in oncology research and with oncology-specific real-world data (e.g., Flatiron, ConcertAI)<br>• Advanced programming capabilities using SAS and R<br>• Proficiency in statistical methodologies including survival analysis, propensity score methods, and generalized linear models.<br>• Experience with machine learning approaches applied to real-world data<br>• Excellent written and verbal communication skills<br> </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 11 Sep 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Pittsburgh, PA]]></title>
    <date><![CDATA[Tue, 15 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50475]]></requisitionid>
    <referencenumber><![CDATA[R50475]]></referencenumber>
    <apijobid><![CDATA[r50475]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50475/medical-specialist-i-pulmonology-pittsburgh-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Pittsburgh]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Pittsburgh, PA-representative must reside within or close to the territory.</strong></p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role requires:</strong></p><ul><li>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</li><li>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches </li><li>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</li><li>Ability to travel and cover large geographic territories</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 16 Sep 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Marketing - Rare Disease, Japan]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50681]]></requisitionid>
    <referencenumber><![CDATA[R50681]]></referencenumber>
    <apijobid><![CDATA[r50681]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50681/senior-manager-marketing-rare-disease-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Rare Disease Marketing Strategy, Japan to join our Rare Disease Commercial Business Unit, supporting our Japan business in a hybrid work model. In this role, you will lead brand strategy and execution across rare disease areas while collaborating with Medical Affairs, Sales, and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Location: Japan</p><p>Work model: Hybrid</p><br><p><strong>Discover your role:</strong></p><ul><li>Lead brand strategy and execution for designated rare disease areas in Japan.</li><li>Drive local brand planning through market analysis and customer-focused messaging.</li><li>Partner with Medical Affairs to develop aligned brand strategies.</li><li>Analyze brand performance drivers, risks, and opportunities to improve outcomes.</li><li>Develop and deliver disease area and product education to cross-functional teams.</li><li>Lead external stakeholder engagement, including congresses and healthcare professional meetings.</li><li>Create promotional materials and support field execution through sales communications.</li><li>You thrive in a fast-changing environment and build alignment across stakeholders.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor's degree required.</li><li>8+ years of biotech or pharmaceutical brand marketing experience.</li><li>Marketing launch experience.</li><li>Demonstrated ability to lead initiatives from strategy through execution independently.</li><li>Proven success delivering results in highly cross-functional environments with limited resources.</li><li>Expertise managing advertising agencies, suppliers, and annual budgets.</li><li>Knowledge of local healthcare compliance requirements and promotional regulations.</li><li>Experience developing brand strategies, promotional plans, and stakeholder engagement programs.</li><li>Strong leadership, ownership, initiative, creativity, and adaptability.</li><li>Excellent planning, prioritization, communication, and presentation skills.</li><li>Business-level English proficiency, written and spoken.</li><li>Ability and willingness to travel 10-20%, including occasional weekends.</li><li>Rare disease sales and marketing experience preferred.</li><li>Science background preferred.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 03:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Safety Scientist Lead - General Medicine]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50471]]></requisitionid>
    <referencenumber><![CDATA[R50471]]></referencenumber>
    <apijobid><![CDATA[r50471]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50471/director-safety-scientist-lead-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Director</strong> to join our <strong>Global Patient Safety Sciences Delivery </strong>team.</p><p>The Director, Global Patient Safety Sciences Delivery, General Medicine, serves as the first point of contact for all General Medicine operations including safety data processing, submission creation, and documentation to ensure completeness, accuracy, and timeliness. This role is responsible for high quality, compliant execution of safety surveillance, signal management, and aggregate reporting activities across the portfolio. </p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li><p>Work Location: Uxbridge, UK</p></li><li><p>3 days per week on site</p></li><li><p>25% Travel may be required</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>The Director is responsible for the development of their team, which is comprised of Safety Scientists. The Director will also be expected to work closely with other Directors on driving standardization and consistency in execution of signal detection activities in partnership. This role will report to the ED, Global Patient Safety Sciences Delivery. </p></li><li><p>Develop common practices, processes and templates to drive standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs </p></li><li><p>Ensure compliance and quality management of Safety Sciences Delivery activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools </p></li><li><p>Lead all aspects of signal detection coordination and signal management process across General Medicine, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies,</p></li><li><p>Analyze aggregate safety data to identify emerging safety issues and patterns, in partnership with Safety Sciences Strategy </p></li><li><p>Support cross-functional coordination to support high quality, timely, and compliant delivery of benefit-risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required </p></li><li><p>Drive development and implementation of relevant training programs for GPS staff, including maintenance of a standardized Safety Sciences training curriculum, proficiency matrix, and knowledge management repository across both Strategy and Delivery </p></li><li><p>Serve as main point of contact to liaise with Safety Sciences Strategy General Medicine GPS Leads </p></li><li><p>Collaborate with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management) </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li><li><p>Implement talent strategy and leadership development initiatives that raise capabilities across the organization </p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Advanced Degree required in life sciences or healthcare with 12+ years of PV experience, preferably with a focus on Safety Sciences and General Medicine experience</p></li><li><p>Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency, and ensure high-quality, compliant execution across activities </p></li><li><p>Strong leadership capabilities and presence, interpersonal, verbal and written communication skills organizational and workload planning skills along with the ability to manage multiple different projects simultaneously </p></li><li><p>Preferred experience with oversight of operations within a global patient safety organization </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Preferred experience leading a matrixed role working across multiple areas of an organization and people management experience </p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Lancaster, PA]]></title>
    <date><![CDATA[Thu, 10 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50393]]></requisitionid>
    <referencenumber><![CDATA[R50393]]></referencenumber>
    <apijobid><![CDATA[r50393]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50393/medical-specialist-i-pulmonology-lancaster-pa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Pennsylvania]]></city>
    <state><![CDATA[Pennsylvania]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong></p><ul><li><p>Field role</p></li><li><p>Location: <strong>Lancaster, PA - representative must reside within the territory (e.g. Lancaster, West Chester, Wyomissing, Wilmington, DE).</strong></p></li></ul><p><strong>​</strong></p><p><strong>Discover your role:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups.</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p>​<strong>This role requires:</strong></p><ul><li><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required.</p></li><li><p>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners.</p></li><li><p>Ability to travel and cover large geographic territories.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><p><strong>Salary Range (annually)</strong></p><p>$143,500.00 - $187,500.00</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$154,743.00 - $209,358.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager-Allergy/ENT-Fresno, CA]]></title>
    <date><![CDATA[Sun, 20 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50632]]></requisitionid>
    <referencenumber><![CDATA[R50632]]></referencenumber>
    <apijobid><![CDATA[r50632]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50632/field-reimbursement-manager-allergyent-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>Build our future together:</strong></p><p>The Field Access & Reimbursement environment for specialty biologics has proven to be highly challenging for HCPs and Patients. Payer Formularies and restrictive Utilization Management Criteria including Prior Authorization Processes, Step Edits, Appeals, detailed Clinical Documentation, Peer to Peer reviews etc. requires dedicated and focused customer facing support through the Reimbursement Management Team.</p><p>The Field Reimbursement Manager is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. The primary purpose of this role is to support Health Care Practitioner offices in obtaining appropriate access to Regeneron products for patients. Ensuring optimal access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron product portfolio. Support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate across multiple internal customers, sales teams, Payer teams, Alliance partners, HUBs, etc. The Field Reimbursement Management reports to the District Manager of Field Market Access.</p><br><p><strong>When & where:</strong></p><ul><li>Remote role</li><li>Location: Fresno, CA</li></ul><p><strong>Discover your role:</strong></p><ul><li>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment. Complete a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</li><li>Complete established performance parameters and monitor personal performance against these agreed parameters: Work closely with partners as assigned; District Sales Managers, Medical Specialists, other FRM, Reimbursement, Marketing and Access team members in assigned geographical areas to insure efficient coverage and customer knowledge of this process and all REGN patient services within defined accounts</li><li>Provide appropriate process, payer, and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products, in efforts to streamline the coverage and specialty pharmacy processes to acquire alliance products</li><li>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</li></ul><p><strong>This role requires:</strong></p><ul><li>A bachelor’s degree and at least 5 years of experience in the biopharma reimbursement, market access or field-based access roles working in a matrix environment – with at least 2 years direct Reimbursement experience supporting medical benefit therapies (buy & bill preferred)</li><li>We are also expecting you to have experience across specialty pharmacy distribution models, including white bagging and site of care management</li><li>Candidate must live in the territory</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 21 Sep 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Systems Automation]]></title>
    <date><![CDATA[Wed, 16 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R49612]]></requisitionid>
    <referencenumber><![CDATA[R49612]]></referencenumber>
    <apijobid><![CDATA[r49612]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r49612/senior-manager-systems-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Automation Manager (Manager or Senior Manager) to join our IOPS Automation team, leading a technical team responsible for automation systems support across our manufacturing and support areas. In this role, you will manage team performance, coordinate deviation investigations, deliver large-scale improvement projects, and ensure automation systems remain compliant and reliable — while collaborating with Manufacturing, Quality Assurance, Engineering, and IT infrastructure teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><ul><li>Location: Menands, New York, United States</li><li>Work model: Monday - Friday 8am - 4:30pm</li><li>Travel percentage: 5 - 10% to Ireland</li></ul><p><strong>Discover your role:</strong></p><ul><li>Lead and develop a technical automation team, managing performance, development, and results while empowering team members to deliver under demanding timelines and situations</li><li>Provide technical automation systems support to manufacturing and support areas; coordinate investigations of manufacturing deviations and anomalies related to automation systems, IT infrastructure, and software</li><li>Lead projects related to corrective action and systems performance improvement; deliver on large-scope projects requiring analysis of business metrics including production, performance, and operational data</li><li>Provide technical review of lifecycle documentation, software testing, and protocols; lead the team in supporting Quality Assurance with automated system test plan approval for change control and validation projects</li><li>Create, maintain, and approve SOPs and Software Lifecycle Documentation; develop and edit design documents, technical evaluations, and test plans in accordance with cGMP and GAMP 5 guidelines</li><li>Manage and maintain project portfolio and work metrics, departmental data, and technical reports; communicate effectively across engineering staff, cross-functional departments, and management</li><li>Design, configure, and troubleshoot networked systems; balance changing priorities and increasing workload through timely decision-making and effective delegation</li></ul><p><strong>This role requires:</strong></p><ul><li>BS in Engineering, Computer Science, or a related field</li><li>Manager: 7+ years of experience in the design, configuration, administration, and management of software, databases, and computerized systems</li><li>Senior Manager: 8+ years of relevant experience; level determined based on qualifications</li><li>Prior experience in a pharmaceutical or biopharmaceutical manufacturing facility preferred</li><li>Solid understanding of PI Historian and Rockwell applications; familiarity with PLC, HMI, historian, and product testing software strongly preferred</li><li>Highly skilled in developing and editing Software Lifecycle Documentation, design documents, technical evaluations, and test plans following cGMP and GAMP 5 guidelines also preferred</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$121,100.00 - $231,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 17 Sep 2026 06:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Digital Marketing Oncology - Germany]]></title>
    <date><![CDATA[Mon, 21 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50593]]></requisitionid>
    <referencenumber><![CDATA[R50593]]></referencenumber>
    <apijobid><![CDATA[r50593]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50593/associate-manager-digital-marketing-oncology-germany/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build</strong><strong> our future together:</strong></p><br><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, Digital Marketing to join our Commercial Oncology team, supporting our brand portfolio in a hybrid work mode. In this role, you will execute digital and omnichannel marketing activities while collaborating with brand teams, agencies, and the field force. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3><strong>When & where:</strong></h3><ul><li>Location: Munich, Germany</li><li>Office-based, Hybrid</li><li>Willingness to travel occasionally.</li></ul><br><h3><strong>Discover your role:</strong></h3><br><ul><li>Execute omnichannel campaigns within timelines, guidelines, and the local Omnichannel Framework.</li><li>Coordinate email, website, social media, and banner advertising deployment.</li><li>Localize approved content with brand teams and agencies across digital and non-digital channels.</li><li>Maintain KPI reports and identify practical performance improvements with senior colleagues.</li><li>Train the field force on digital tools and answer routine digital ecosystem questions.</li><li>Coordinate vendors, timelines, budgets, quality standards, project documentation, and deliverables.</li><li>Maintain Veeva and digital platforms, ensuring data accuracy and resolving issues with IT.</li><li>You foster compliant customer engagement across Medical, Sales, Marketing, and Excellence teams.</li></ul><br><h3><strong>This role requires:</strong></h3><br><ul><li>Bachelor’s degree in marketing, communications, business administration, or equivalent experience.</li><li>Five years’ relevant experience for Associate Manager</li><li>Digital marketing execution experience, ideally in regulated life sciences, healthcare, or pharmaceuticals.</li><li>Knowledge of email marketing, SEO/SEM, social media, and banner advertising.</li><li>Familiarity with Veeva, web technologies, data privacy, HWG, UWG, and EFPIA/VFA Pharmakodex.</li><li>Project management knowledge; agile/SCRUM, JIRA, or Confluence familiarity is beneficial.</li><li>Fluent German and English.</li><li>Strong organization, communication, collaboration, multitasking, attention to detail, and customer focus.</li></ul><br><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€68,250.00 - €113,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 22 Sep 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Market Access Lead - Rare Diseases (Europe Region)]]></title>
    <date><![CDATA[Thu, 17 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50648]]></requisitionid>
    <referencenumber><![CDATA[R50648]]></referencenumber>
    <apijobid><![CDATA[r50648]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50648/director-market-access-lead-rare-diseases-europe-region/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Director, Regional Market Access, Rare Diseases, Europe to join our market access function, supporting our Europe region in a hybrid work mode. In this role, you will shape pricing, reimbursement, and patient access strategies while collaborating with global, regional, and local teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><h3><strong>When & where:</strong></h3><p>Multiple locations are being considered for this role (Hybrid)</p><h3><strong>Discover your role:</strong></h3><ul><li><p>Lead rare disease access strategies aligned with global objectives and country needs.</p></li><li><p>Differentiate approaches across cost-effectiveness and list-price or free-pricing markets.</p></li><li><p>Monitor European policies, payer trends, and reimbursement frameworks.</p></li><li><p>Adapt global access tools and value propositions for regional stakeholders.</p></li><li><p>Manage health technology assessment dossiers, pricing negotiations, and reimbursement submissions.</p></li><li><p>Partner with medical affairs and access teams on evidence and health economics outcomes research plans.</p></li><li><p>Engage payers, policymakers, advocacy groups, and public affairs teams to advance access.</p></li><li><p>You build collaboration through advisory boards, market research, and landscape assessments.</p></li></ul><h3><strong>This role requires:</strong></h3><ul><li><p>Ten years’ pharmaceutical experience, including eight years in market access.</p></li><li><p>European rare disease pricing, reimbursement, launches, and approval experience.</p></li><li><p>Expertise in payer systems, economic models, and health technology assessment submissions.</p></li><li><p>Knowledge of NICE, ZIN, TLV, QALY frameworks, and free-pricing markets.</p></li><li><p>Advanced life sciences, health economics, or business degree preferred.</p></li><li><p>English fluency; additional European languages are advantageous.</p></li><li><p>Strong communication, data synthesis, matrix leadership, agility, and collaboration.</p></li><li><p>Healthcare policy shaping and multi-stakeholder engagement experience preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€125,250.00 - €208,750.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 18 Sep 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Affairs- Hematology (northern CA/Nevada)]]></title>
    <date><![CDATA[Tue, 29 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51003]]></requisitionid>
    <referencenumber><![CDATA[R51003]]></referencenumber>
    <apijobid><![CDATA[r51003]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51003/associate-director-medical-affairs-hematology-northern-canevada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><br><p>As an Associate Director, Field Medical Affairs (Medical Science Liaison) you will engage in the exchange of our scientific data and medical information with KOLs, HCPs, researchers, pharmacists and population-based decision makers. You will demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong> Territory: northern CA, Nevada</p><p><strong>Travel: </strong>Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.</p><br><p><strong>Discover your role</strong>:</p><br><p>• Identifying and maintaining a list of medical/therapeutic area experts, investigator targets and associated plans of action.</p><p>• Establishing, fostering, cultivating and maintaining relationships with KOLs in Hematological Malignancies.</p><p>• Act as the primary clinical/scientific resource for information pertaining to disease state and our products ensuring awareness and understanding.</p><p>• Participates in the development and management of company sponsored clinical trials including.</p><p>• Establishing scientific relationships with investigators and internal Medical Affairs, supporting investigator-initiated study (IIS) concept program.</p><p>• Identifying relevant insights on research developments, treatment landscape to shape medical strategy.</p><p>• Identifies gaps in research needs and creates opportunities by collaborating with potential and existing investigators and site personnel.</p><p>• Responds to requests for information related to study indications, disease state and therapeutic area, and presents/discusses scientific/clinical data.</p><p>• Attend medical conferences collecting and reporting relevant, scientific, clinical, & competitive intelligence.</p><p>• Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally.</p><br><p><strong>This role requires</strong></p><br><p>• A terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required.</p><p>• 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. </p><p>• Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. </p><p>• Residency in the assigned territory and possession and maintaining a valid driver’s license and clean driving record.</p><p>• Established relationships with KOLs and institutions focused on Hematologic Malignancies as is Drug launch experience is preferred. </p><br><p>#medicalscienceliaison #msl #HFM #AD</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 30 Sep 2026 19:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Business Analyst - Commercial Systems and Operations]]></title>
    <date><![CDATA[Mon, 28 Sep 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50727]]></requisitionid>
    <referencenumber><![CDATA[R50727]]></referencenumber>
    <apijobid><![CDATA[r50727]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50727/senior-business-analyst-commercial-systems-and-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong> </p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Business Analyst, CRM & Operations to join our Commercial Operations team, supporting International Business Operations. In this role, you will drive commercial projects, business analysis activities, CRM transformation initiatives, and operational planning while collaborating with Commercial Operations, Sales, Marketing, in-country teams, and IT partners. </p><br><p><strong>When & where:</strong> </p><p>Location: UK or Ireland </p><p>Work model: Hybrid (3 days in office) </p><p>12-month contract </p><p> 25%-30% travel involved </p><br><p><strong>Discover your role:</strong> </p><ul><li>Plan, coordinate, and deliver commercial operations projects, ensuring timelines, milestones, risks, and dependencies are effectively managed. </li></ul><ul><li>Lead project governance activities, including status reporting, RAID management, action tracking, meeting facilitation, and stakeholder communications. </li></ul><ul><li>Gather, analyze, and document business requirements, translating operational needs into functional requirements, user stories, and process improvements. </li></ul><ul><li>Support Veeva CRM and Veeva Events activities, including improvements, user support, data quality management, reporting, and system optimization. </li></ul><ul><li>Contribute to CRM transformation initiatives through current-state assessments, user acceptance testing, training coordination, and deployment support. </li></ul><ul><li>Coordinate meetings, events, and business planning activities, ensuring flawless execution and compliance with operational processes. </li></ul><ul><li>Partner with Commercial Operations, Sales, Marketing, IT, and in-country teams to improve business processes and drive operational efficiency. </li></ul><br><p><strong>This role requires:</strong> </p><ul><li>Bachelor's degree in business, Life Sciences, Information Technology, or a related discipline, or equivalent practical experience and 6+ years of experience in project coordination, project administration, business analysis, or commercial operations within pharmaceuticals, life sciences, or another regulated industry. </li></ul><ul><li>Experience gathering business requirements and creating functional specifications, user stories, process maps, and business documentation. </li></ul><ul><li>Solid understanding of Veeva CRM, Veeva Events, or similar CRM platforms, with experience supporting commercial business systems and process improvements. </li></ul><ul><li>Understanding of pharmaceutical commercial operations, including compliance requirements and healthcare professional engagement processes.</li></ul><ul><li>Experience supporting CRM migrations, business process transformation, user acceptance testing, and change management activities is advantageous.</li></ul><ul><li>Strong stakeholder management, communication, organizational, analytical, and problem-solving skills, with the ability to prioritise in a cross-functional environment.</li></ul><br><br><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 29 Sep 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I Pulmonology Los Angeles East]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51092]]></requisitionid>
    <referencenumber><![CDATA[R51092]]></referencenumber>
    <apijobid><![CDATA[r51092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51092/medical-specialist-i-pulmonology-los-angeles-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Build our future together: </strong></h3><br><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><br><br><p><strong>When & where: </strong></p><ul><li>Field role</li><li>Location: <strong>Los Angeles East (Rancho Cucamonga; Riverside; Corona; Loma Linda; Redlands; Orange; Anaheim; Fullerton; Upland and Ontario)</strong></li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</li><li>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.</li><li>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</li><li>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</li><li>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</li></ul><br><p>​<strong>This role requires:</strong></p><br><ul><li>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.</li><li>Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches.</li><li>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.</li><li>Ability to travel and cover large geographic territories.</li></ul><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$140,675.00 - $190,325.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager GCP Quality]]></title>
    <date><![CDATA[Mon, 05 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50181]]></requisitionid>
    <referencenumber><![CDATA[R50181]]></referencenumber>
    <apijobid><![CDATA[r50181]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50181/senior-manager-gcp-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, GCP Quality Management - Global Development to join our Global Development Quality team, supporting our global clinical development organisation in a hybrid work model. In this role, you will lead risk-based quality management across clinical trials while collaborating with study teams, clinical functions, contract research organisations, and quality colleagues. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><p><strong>When & where:</strong></p><p>Multiple locations are being considered for this role (Hybrid)</p><p><strong>Discover your role:</strong></p><ul><li><p>Lead risk-based quality management across assigned clinical trials</p></li><li><p>Drive protocol-stage Quality Risk Assessment and Control Tracker activities under ICH E6 R3</p></li><li><p>Manage quality issues, audit responses, corrective actions, preventive actions, and trend analysis</p></li><li><p>Partner with study leads, monitoring teams, and contract research organisations on site risks</p></li><li><p>Escalate significant quality events and trends to Executive Quality Leadership</p></li><li><p>Support inspection readiness, responses, and follow-up actions across relevant functions</p></li><li><p>Manage onboarding, development goals, coaching, performance discussions, and team administration</p></li><li><p>You champion quality, integrity, continuous learning, and trusted partnerships</p></li></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelor’s degree and eight years’ relevant healthcare or pharmaceutical industry experience</p></li><li><p>Quality, compliance, clinical development, Good Clinical Practice, or Good Pharmacovigilance Practice experience</p></li><li><p>Advanced risk-based quality management, risk assessment, and compliance knowledge</p></li><li><p>Experience managing complex issues, regulatory inspections, and inspection readiness</p></li><li><p>Subject matter expert, process owner, training, presentation, and staff management experience</p></li><li><p>Process improvement, project management, prioritisation, and time management skills</p></li><li><p>Advanced Microsoft Outlook, Word, Excel, and PowerPoint skills</p></li><li><p>Strong communication, collaboration</p></li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 05 Oct 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[2027 Co-op, Accounting]]></title>
    <date><![CDATA[Fri, 02 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51088]]></requisitionid>
    <referencenumber><![CDATA[R51088]]></referencenumber>
    <apijobid><![CDATA[r51088]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51088/2027-co-op-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>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a 2027 Co-op to join our Accounting team.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p><strong>Location: </strong>Sleepy Hollow, NY</p><p><strong>Timeframe: </strong>This Co-op position is part-time and <strong>onsite</strong> from January-May (Spring)</p><p><strong>Pay</strong>: Intern and Co-op pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for these locations is: $17.90-$50.90 per hour.</p><br><p><strong>What you’ll do:</strong></p><ul><li>Support accounting projects and initiatives that contribute to Regeneron's global business operations.</li></ul><ul><li>Gain exposure to accounting processes, financial reporting activities, and operational workflows.</li></ul><ul><li>Collaborate with accounting professionals and cross-functional business partners on ongoing projects.</li></ul><ul><li>Develop and maintain reports, presentations, and other tools that support business objectives.</li></ul><ul><li>Participate in meetings with team members and business stakeholders to better understand organizational operations.</li></ul><ul><li>Present project updates, findings, and recommendations to managers and leadership teams.</li></ul><ul><li>Contribute to meaningful project work that delivers value to the business while developing professional skills.</li></ul><br><p><strong>Relevant majors: </strong>Accounting or related majors</p><br><p><strong>Let’s find out if we’re a fit</strong>:</p><ul><li>Must be enrolled in, or accepted to, an academic program pursuing an Undergraduate or Graduate degree (and be returning to school the semester following the position or graduating after the position)</li><li>Must be able to commit to 16-24 hours per week from January-May</li><li>Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community preferred</li><li>Cumulative GPA of 3.0 or higher preferred</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 02 Oct 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Automation Technician (Overnights)]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51060]]></requisitionid>
    <referencenumber><![CDATA[R51060]]></referencenumber>
    <apijobid><![CDATA[r51060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51060/automation-technician-overnights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are currently looking for an experienced Automation Technician to join our growing team. Our Automation Technicians are responsible for supporting and troubleshooting biopharmaceutical manufacturing/filling/packaging equipment that utilize Human Machine Interfaces (HMIs) and Programmable Logic Controllers (PLCs) at Regeneron's Industrial Operation and Product Supply organization. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: East Greenbush, New York, United States</li><li>Working shift: Sunday-Thursday, 12:00am-8:30am</li><li>Training shift: Monday-Friday, 8:00am-4:30pm for approximately 6 months</li></ul><h3>Discover your role:</h3><ul><li>Provide automation technical support, troubleshooting, and assistance during routine operations, maintenance activities, equipment setups, and changeovers for manufacturing operations of GMP Bulk Biologics, Fill/Finish, and Clean Utilities systems</li><li>Identify and implement corrective or preventive maintenance, component replacements, or corrections on automated systems as needed</li><li>Communicate and coordinate Automation issue resolution for manufacturing and facilities groups</li><li>Full gowning when entering and working on production floor</li><li>Utilize specialized personal protective equipment as required, including arc flash, when working near energized equipment or when working in construction environments</li><li>Work independently and safely around all industrial equipment</li></ul><br><h3>This role requires:</h3><ul><li>Associate degree in Engineering or a related technical field and the following years of experience supporting process control and/or data acquisition systems; equivalent combination of education and experience may be considered:<ul><li>Automation Technician II: 2+ years of related experience</li><li>Automation Technician III: 5+ years of related experience</li><li>Automation Technician IV: 8+ years of related experience</li></ul></li><li>Experience troubleshooting PLCs, HMIs, and computerized systems, preferably in a regulated environment</li><li>Knowledge of ladder logic, PID control, electrical control systems, instrumentation, and current and voltage characteristics in DC and 120/240/480 VAC circuits</li><li>Ability to diagnose or troubleshoot electrical control circuits utilizing a digital multimeter and electrical schematics</li><li>Basic understanding of data integrity regulations</li><li>Special emphasis on machine controls preferred, with specific knowledge of Allen-Bradley and Siemens control system products strongly preferred; basic knowledge of B&R control system products is helpful</li><li>Experience with servers, virtualization, distributed control, and basic networking is preferred</li><li>Strong written and verbal communication skills</li></ul><br><p>Level will be determined based on qualifications relevant to the role</p><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Regulatory Affairs Strategy - Genetics Medicine]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51185]]></requisitionid>
    <referencenumber><![CDATA[R51185]]></referencenumber>
    <apijobid><![CDATA[r51185]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51185/associate-director-regulatory-affairs-strategy-genetics-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an <strong>Associate Director </strong>to join our <strong>Regulatory Affairs Strategy</strong> team.</p><br><p>This position in Regulatory Affairs involves the ability to integrate/apply knowledge of global regulations governing pharmaceutical drug development to all aspects of Regeneron's quality, preclinical and clinical drug development programs, policies, and procedures, so that Development teams are able to meet all objectives within specified timelines and so that the necessary state of compliance is maintained relative to all regulatory commitments/requirements.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Work Location: Tarrytown, NY or Warren, NJ</li><li>4 days per week on site</li><li>25% Travel may be required</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Develop regulatory strategies for assigned programs in collaboration with Regeneron's Regulatory senior management and by analysis of guidances and assessment of drug developed for similar indication to obtain approval of activities in support of Regeneron’s development and marketing objectives within specified timelines</li><li>Liaison responsible for communication with FDA and other health authorities for assigned programs</li><li>Management of all regulatory activities associated with Regeneron drug development programs.</li><li>Participate in multidisciplinary project teams to provide regulatory guidance and communicate regulatory goals.</li><li>Provide guidance to multidisciplinary teams on the regulatory requirements to support clinical development, include preparation and maintenance of IND or CTA filings.</li><li>Oversee development of all regulatory filings in support of program.</li><li>In collaboration with team, perform/manage critical analyses of data (clinical, preclinical and manufacturing), independently develop interpretations and conclusions. Perform reviews of clinical protocols and of clinical and preclinical study reports with respect to clarity, completeness, and regulatory requirements.</li><li>Lead multidisciplinary teams in the authoring of regulatory communications such as regulatory briefing packages.</li><li>Accountable for ensuring the completeness and accuracy of information provided in regulatory submissions.</li><li>Supervises regulatory staff with the planning, preparation and submission of all regulatory documentation.</li><li>Management of the planning, preparation and submission of licensing applications.</li><li>Provide guidance/instruction to multidisciplinary teams on the content, format, style architecture and timing of a Biologics Licensing Application (BLA) and MAA.</li><li>Assist with the scientific writing and review of application. Evaluate conformance with the regulatory requirements, clarity, and completeness.</li><li>Manage timelines/budgets with project management as appropriate and provide progress updates to senior management</li><li>Continually monitor newly published FDA guidelines and international guidance documents in the context of new and ongoing development programs. Provide training on applicable requirements for scientific staff as required.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>An MD, Ph.D., Pharm.D., or equivalent advanced degree; a relevant scientific discipline is strongly preferred.</li><li>A minimum of 10 years of pharmaceutical industry experience, at least 5 of which should include regulatory experience.</li><li>Research laboratory, process development or manufacturing experience with biotechnology products highly desirable.</li><li>Must possess excellent written and verbal communication skills.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Delegado(a) de ventas - Barcelona, Gerona y Lerida]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50498]]></requisitionid>
    <referencenumber><![CDATA[R50498]]></referencenumber>
    <apijobid><![CDATA[r50498]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50498/delegado-a-de-ventas-barcelona-gerona-y-lerida/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Construyendo nuestro futuro juntos:</strong></p><p>En Regeneron, utilizamos la ciencia y la innovación para desarrollar medicamentos que cambian la vida de las personas con enfermedades graves. Buscamos un Delegado de Ventas Biotecnología y Farmacéutica España para unirse a nuestro equipo comercial de Inmunología Gastroenterlogia, apoyando nuestra actividad en España bajo un modelo de trabajo de campo. En esta posición, impulsarás los objetivos de la marca, maximizarás el acceso de los pacientes y desarrollarás interacciones científicas y comerciales de alto valor en tu territorio, colaborando estrechamente con equipos médicos y multifuncionales. Tendrás la oportunidad de contribuir a una organización en crecimiento, impulsada por la ciencia y comprometida con generar un impacto significativo para los pacientes en todo el mundo.</p><br><p><strong>Cuando y Donde:</strong></p><p>España Barcelona - Gerona - Lerida</p><p>Modelo de trabajo: En campo</p><br><p><strong>Descubre tu rol:</strong></p><ul><li>Desarrollar relaciones de confianza con profesionales sanitarios clave, comunicando de forma efectiva el valor de nuestro portafolio.</li></ul><ul><li>Ejecutar la estrategia de marca en el territorio mediante interacciones científicas y comerciales de alta calidad.</li></ul><ul><li>Diseñar e implementar planes territoriales alineados con la estrategia nacional, aprovechando datos e información del mercado.</li></ul><ul><li>Identificar, segmentar y priorizar cuentas y stakeholders clave para maximizar el impacto y el acceso de los pacientes.</li></ul><ul><li>Colaborar con equipos médicos y multifuncionales para implementar iniciativas y programas regionales.</li></ul><ul><li>Utilizar canales presenciales y digitales para optimizar el engagement con clientes y la presencia de la marca.</li></ul><ul><li>Monitorizar tendencias de mercado y actividad de la competencia, compartiendo información relevante con la organización.</li></ul><ul><li>Desenvolverte con éxito en un entorno de nueva creación y alto rendimiento, fomentando la colaboración dentro y fuera de la compañía.</li></ul><br><p><strong>Este rol requiere:</strong></p><ul><li>Titulación universitaria o equivalente, preferiblemente en Ciencias de la Vida, Farmacia, Química o Biología y 5 años de experiencia en ventas dentro de la industria biotecnológica y/o farmacéutica.</li></ul><ul><li>Experiencia en gestión de territorios, cuentas clave y ejecución de estrategias de marca con profesionales sanitarios.</li></ul><ul><li>Conocimiento de los estándares regulatorios, éticos y de compliance del sector farmacéutico.</li></ul><ul><li>Capacidad para utilizar eficazmente canales presenciales y digitales para la interacción con clientes.</li></ul><ul><li>Sólidas habilidades de comunicación, colaboración y gestión de múltiples prioridades; la experiencia previa en alianzas será valorada. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€49,800.00 - €83,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Lab Project Management]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50797]]></requisitionid>
    <referencenumber><![CDATA[R50797]]></referencenumber>
    <apijobid><![CDATA[r50797]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50797/manager-clinical-lab-project-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build Our Future Together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Manager, Precision Medicine Clinical Laboratory Operations will be responsible for Clinical Laboratory Project & Program management for various therapeutic areas working closely with Director, Precision Medicine Clinical Laboratory Operations and key cross-functional collaborators. The primary role will be to keep laboratory deliverables across the portfolio on track, ensuring that study start timelines are met, provide risk management. This will be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory Operations Management, Global Development colleagues and central and specialty testing laboratories to support early and late-stage programs within our pipeline. </p><br><p><strong>When & Where:</strong></p><p>This role can be based remotely (within the US), or sit on-site in our Warren, NJ or Armonk, NY office. If on-site, the role would be expected to be on-site four days per week.</p><br><p><strong>Discover Your Role:</strong></p><ul><li>Perform clinical laboratory portfolio management for complex Regeneron clinical trials and review clinical laboratory operations timelines and risks. Manage and communicate those risks to ensure study starts and data delivery are aligned with expectations </li></ul><ul><li>Active knowledge on central and specialty laboratory processes; leverage this experience to be a trusted collaborator and ensure clinical laboratory deliverables </li></ul><ul><li>Track biomarker strategy delivery schedules for clinical development programs/studies on track, identifying and tracking risks and decisions, creating mitigation plans </li></ul><ul><li>Oversee clinical laboratory operations goals, including progress, schedules of testing/data generation across the portfolio with clear objectives and deadlines </li></ul><ul><li>Liaise with internal and cross functional partners, including Precision Medicine Clinical Lab Study Management, Precision Medicine Strategy Leads and others within Global Development to manage and implement program level clinical laboratory management </li></ul><ul><li>Demonstrate understanding of complex non-oncology clinical laboratory trial requirements on the program and implement operational decisions and harmony.</li></ul><ul><li>Communicate with clinical study teams on laboratory program direction. Demonstrate knowledge for the studies related to the program.</li></ul><br><p><strong>This Role Requires:</strong></p><ul><li>Bachelors degree required, Masters degree preferred.</li><li>Minimum of 8 years experience preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. </li><li>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. </li><li>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. </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ex Dir Regulatory, Medical, & CDU Solutions Partner]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51005]]></requisitionid>
    <referencenumber><![CDATA[R51005]]></referencenumber>
    <apijobid><![CDATA[r51005]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51005/ex-dir-regulatory-medical-cdu-solutions-partner/]]></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 Executive Director, Reg, Medical & CDU Business Solution Lead will serve as the key interface between business leadership and Digital & Technology for Regeneron's Regulatory Affairs, Medical Affairs, and Clinical Data functions, orchestrating D&T capabilities to deliver on business objectives and priorities across platforms including Veeva RIM, Mediverse, iEnvision, and the platforms supporting Precision Medicine, Clinical Imaging, and Digital Medicine. This role owns the technology roadmap and strategy for the domain, prioritizing investment in partnership with the business and will lead a team of Directors delivering platform strategy, delivery governance, and compliant operations across the regulatory, medical affairs, and clinical data technology portfolio. The Business Solution Lead will partner closely with Regulatory Affairs, Medical Affairs, and Clinical Development business leadership, Enterprise IT, and Information Security to ensure these systems support Regeneron's regulatory submission, medical information, and clinical data obligations.</p><p>This role reports to the Executive Director, Global Development IT and will collaborate closely with Regulatory Affairs, Medical Affairs, and Clinical Development leadership to shape the technology roadmap and ensure delivery excellence across the platform portfolio.</p><p><strong>Key Responsibilities</strong></p><p>In this role, you will own platform strategy and delivery for Regeneron's Regulatory Affairs, Medical Affairs, and Clinical Data technology portfolio, leading a team of Directors across the domain. Your day-to-day responsibilities will include:</p><p><strong>Reg, Medical & CDU Strategy & Ownership</strong></p><ul><li>Partner with senior Regulatory Affairs, Medical Affairs, and Clinical Development leadership to align technology and capabilities to deliver on enterprise objectives and priorities.</li></ul><ul><li>Own and prioritize, in partnership with the business, the multi-year platform strategy and roadmap, translating regulatory, medical affairs, and clinical data priorities into a funded, prioritized delivery plan.</li></ul><ul><li>Own the organizational design of the Reg, Medical & CDU Business Solution function, including structure, role allocation, and resourcing across Directors and Managers assigned to the domain.</li></ul><ul><li>Establish governance frameworks, standards, and validation practices for platform delivery, ensuring consistency across teams and vendor engagements.</li></ul><ul><li>Own budget, forecast, and vendor contract accountability for the domain's platform portfolio, including software licensing and services agreements.</li></ul><p><strong>Delivery Oversight & Team Leadership</strong></p><ul><li>Serve as the escalation and quality-assurance point for planning, prioritization, and execution of platform initiatives led by reporting Directors.</li></ul><ul><li>Oversee product backlog, incident management, and release governance across the domain's platform portfolio, ensuring consistent reporting of value delivered against plan.</li></ul><ul><li>Coach and develop Directors and Managers, ensuring delivery commitments are met and domain capabilities continue to mature.</li></ul><ul><li>Manage steering committee meetings, working groups, and issue/release management for upgrades to existing platforms.</li></ul><p><strong>Regulatory & Medical Compliance</strong></p><ul><li>Partner with Regulatory Affairs, Medical Affairs, and Quality organizations to ensure platforms meet validation, data integrity, and audit-readiness standards for regulatory submissions and medical information.</li></ul><ul><li>Own data classification, access, and quality standards for regulatory, medical affairs, and clinical data, ensuring compliance with global submission and reporting obligations (e.g., FDA, EMA).</li></ul><ul><li>Maintain oversight of regulatory information management, medical inquiry, and clinical data workflows to ensure platforms support timely and accurate business outcomes.</li></ul><p><strong>Cross-Functional & Vendor Partnership</strong></p><ul><li>Partner with Enterprise IT, Enterprise Architecture, and Information Security to align platform investments with enterprise standards and security requirements.</li></ul><ul><li>Build and maintain relationships with key platform vendors to clarify demands, resolve conflicts, and align technology roadmaps to business needs.</li></ul><ul><li>Represent Reg, Medical & CDU technology priorities in enterprise architecture and governance forums, ensuring alignment with enterprise-wide standards.</li></ul><p><strong>Executive & Stakeholder Engagement</strong></p><ul><li>Serve as the primary point of contact for senior Regulatory Affairs, Medical Affairs, and Clinical Development leadership on matters requiring negotiation of complex or ambiguous issues.</li></ul><ul><li>Build relationships with key business leaders to clarify demands, resolve conflicts, and align technology roadmaps with regulatory and medical affairs priorities.</li></ul><ul><li>Monitor industry trends in regulatory information management, medical affairs technology, and clinical data platforms, bringing forward innovative approaches to senior leadership.</li></ul><ul><li>Prepare and deliver executive-level materials on the health and roadmap of the platform portfolio for governance forums and senior leadership.</li></ul><p><strong>Qualifications and Requirements</strong></p><p><strong>Education & Experience</strong></p><ul><li>Bachelor’s degree in Computer Science, Information Systems, Business Administration, or a related field (Master’s degree preferred).</li></ul><ul><li>15+ years of progressive industry/relevant professional experience, including significant experience managing enterprise-scale regulatory, medical affairs, or clinical data technology platforms.</li></ul><ul><li>Experience in the biotech, pharma, or life sciences industry strongly preferred.</li></ul><ul><li>Proven experience leading a multi-disciplinary team of Directors and Managers, including budget and vendor contract accountability for a major function.</li></ul><p><strong>Technical Expertise</strong></p><ul><li>Deep expertise in regulatory information management and medical affairs systems (e.g., Veeva RIM, Veeva Vault, medical inquiry/response platforms).</li></ul><ul><li>Experience with clinical data and precision medicine technology (e.g., clinical imaging and digital medicine platforms).</li></ul><ul><li>Strong knowledge of GxP validation practices and solution delivery life cycle management.</li></ul><ul><li>Experience managing technology capability identification, selection, and implementation across multiple simultaneous platform initiatives.</li></ul><p><strong>Skills & Competencies</strong></p><ul><li>Proven track record of budget and vendor management for a department or major function.</li></ul><ul><li>Strong stakeholder management and negotiation skills, with experience influencing senior management internally and externally.</li></ul><ul><li>Demonstrated ability to grow, motivate, and develop teams, coaching Directors and Managers through career milestones and progression.</li></ul><ul><li>Strategic mindset with the ability to define organizational structure and set long-term goals and objectives for a major function.</li></ul><ul><li>Exceptional executive communication skills, with experience engaging senior/executive leadership on sensitive or ambiguous matters.</li></ul><p><strong>Certifications (Preferred)</strong></p><ul><li>PMP or equivalent project/program management certification.</li></ul><ul><li>ITIL or SAFe Agile certification.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Benefits]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50250]]></requisitionid>
    <referencenumber><![CDATA[R50250]]></referencenumber>
    <apijobid><![CDATA[r50250]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50250/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[<h3>Build our future together:</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an experienced 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.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Sleepy Hollow, New York or Rensselaer, New York, United States</li><li>Work model: Onsite 4 days a week</li><li>Travel percentage: Travel to other New York offices approximately once a month</li></ul><br><h3>Discover your role:</h3><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><strong>Benefits Administration</strong> – Oversee day-to-day operations of employee benefits programs (health plans and additional benefits), ensuring timely enrollment, compliance, and accurate processing of transactions; serve as the point of escalation for complex benefits issues and inquiries.</li><li><strong>Team Leadership</strong> – Lead, mentor, and manage a team of benefits specialists, providing coaching, training, and professional development opportunities while fostering a positive, inclusive team environment that encourages collaboration, innovation, and continuous improvement.</li><li><strong>Compliance and Reporting</strong> – Ensure compliance with all federal, state, and local regulations (ACA, ERISA, COBRA, HIPAA), overseeing preparation and submission of required reports to regulatory agencies; stay current on changing laws, advising leadership and updating policies and procedures as needed in partnership with appropriate stakeholders.</li><li><strong>Vendor Management</strong> – Manage relationships with benefits vendors and third-party administrators, negotiating contracts, monitoring service levels, and evaluating performance through regular meetings that surface issues and opportunities to improve the employee and administrator experience.</li><li><strong>Strategic Planning</strong> – Collaborate with HR leadership to design and implement benefits strategies aligned with organizational goals, analyzing data and trends to identify cost-saving and program-enhancement opportunities while championing initiatives that promote employee well-being and engagement.</li><li><strong>Communication and Education</strong> – Develop clear communication materials and organize informational sessions, workshops, and open enrollment events to educate employees on their benefits options and ensure a positive experience; address employee inquiries directly.</li><li><strong>Cross-Functional Partnership</strong> – Collaborate with the Law Department and partner with the HR service center.</li></ul><br><h3>This role requires:</h3><ul><li>Bachelor’s degree in Human Resources, Business Administration, or a related field and a minimum of 10 years of experience in employee benefits management with hands-on experience, including leading a team</li><li>Experience administering a self-insured health plan including plan design and budgeting</li><li>Strong 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><li>Certified Employee Benefits Specialist (CEBS) or similar credentials preferred</li><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 and proficiency in Excel and Microsoft suite</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Funzioni aziendali]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Clinical Laboratory Study Management]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50977]]></requisitionid>
    <referencenumber><![CDATA[R50977]]></referencenumber>
    <apijobid><![CDATA[r50977]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50977/associate-manager-clinical-laboratory-study-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together</h3><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. As an Associate Manager, Precision Medicine Clinical Laboratory Study Management, you will play a critical role in advancing precision medicine capabilities across multiple therapeutic areas, including Non-Immuno-Oncology. Partnering with cross-functional teams across clinical development, precision medicine, data management, and laboratory operations, you will help ensure the successful delivery of high-quality biospecimens and laboratory data that inform clinical decision-making. Through operational excellence, leadership, and collaboration, you will support the execution of biomarker and non-biomarker strategies that accelerate the development of innovative therapies for patients worldwide.</p><br><h3>When & where</h3><ul><li>Location: Remote within the United States or office-based in Tarrytown, NY; Armonk, NY; or Warren, NJ</li><li>Work model: Remote or hybrid</li><li>On-site expectation: 4 days per week for office-based employees</li></ul><br><h3>Discover your role</h3><ul><li>Lead and support Clinical Laboratory Study Managers (CLSMs) and external functional service provider resources across assigned therapeutic programs and studies.</li><li>Partner with clinical study teams, precision medicine leaders, laboratory vendors, CROs, and internal stakeholders to execute sample collection, testing, and data delivery strategies.</li><li>Oversee operational planning and lifecycle activities for central and specialty laboratory services, including study start-up, execution, and close-out.</li><li>Monitor clinical sample acquisition and handling activities, ensuring compliance with informed consent requirements and protocol-defined procedures.</li><li>Provide subject matter expertise on laboratory operations, biospecimen management, and sample-related clinical trial processes within assigned therapeutic areas.</li><li>Support vendor selection activities by contributing to RFP development, bid evaluations, and scope of work assessments related to sample testing and laboratory services.</li><li>Collaborate with data management and sample logistics teams to establish processes for laboratory data capture, transfer, blinding, and reporting.</li><li>Identify operational risks, resolve sample-related issues, and help ensure critical study milestones and laboratory deliverables are achieved on schedule.</li></ul><br><h3>This role requires</h3><ul><li>Bachelor's degree required.</li><li>Minimum 6-8 years of pharmaceutical, biotechnology, academic, or governmental cross-functional experience required.</li><li>Minimum 5 years of clinical trial experience with a focus on clinical sample collection.</li><li>Extensive experience in clinical laboratory operations, biospecimen logistics, and/or clinical study management.</li><li>Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery.</li><li>Demonstrated knowledge of clinical research, scientific principles, and emerging technologies supporting clinical studies.</li><li>Proven ability to manage stakeholders, lead internal and external meetings, and develop practical solutions to complex operational challenges.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Ricerca e sviluppo preclinico]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager - Reporting Analytics]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R50651]]></requisitionid>
    <referencenumber><![CDATA[R50651]]></referencenumber>
    <apijobid><![CDATA[r50651]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r50651/associate-manager-reporting-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Associate Manager Reporting Analytics & Business Intelligence to join our Reporting team, supporting Global Development analytics initiatives in a hybrid work model. In this role, you will build, test, maintain, and optimize dashboards and analytics solutions that enable data-driven decision making while collaborating with reporting specialists, senior leadership, and onshore teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><p>Hyderabad, India (Hybrid)</p><br><p><strong>Discover your role:</strong></p><ul><li>Design, develop, and implement advanced Tableau and Power BI dashboards, visualizations, reports, metrics, and analytics.</li><li>Build, test, maintain, and refine reporting workbooks and dashboards to support Global Development analytics initiatives.</li><li>Provide day-to-day technical guidance and task direction to the Reporting Specialist while reviewing deliverables for quality and standards adherence.</li><li>Collaborate with onshore teams to identify and implement predictive and prescriptive analytics solutions.</li><li>Drive optimization of reporting platforms and tools to improve performance, scalability, and usability.</li><li>Ensure data quality, integrity, security, relevance, and accuracy across visualization outputs.</li><li>Lead identified opportunities to integrate artificial intelligence and Large Language Models into business intelligence reporting solutions.</li><li>Communicate technical concepts in business terms and business needs in technical language while fostering collaborative partnerships.</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Bachelor’s degree with 6 years of relevant experience, or Master’s degree in Data Science, Analytics, Computer Science, or a related field with 4+ years of relevant experience.</li><li>Experience in data analytics, business intelligence, or a related field.</li><li>Hands-on experience with Tableau and Power BI.</li><li>Strong proficiency in Tableau for data visualization and dashboard creation.</li><li>Experience integrating Large Language Models within a reporting landscape for advanced reporting capabilities.</li><li>Experience designing, developing, and maintaining dashboards, visualizations, reports, metrics, and analytics solutions.</li><li>Familiarity with clinical trial operational data.</li><li>Hands-on experience with Qlik preferred.</li><li>Strong analytical and problem-solving skills with the ability to understand and interpret complex datasets.</li><li>Excellent communication skills with the ability to translate technical insights into business value.</li><li>Collaborative, team-oriented approach with the ability to work effectively in a fast-paced environment.</li><li>Strong attention to detail and commitment to delivering high-quality work.</li></ul><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 02:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Administrative Coordinator]]></title>
    <date><![CDATA[Tue, 06 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51183]]></requisitionid>
    <referencenumber><![CDATA[R51183]]></referencenumber>
    <apijobid><![CDATA[r51183]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51183/senior-administrative-coordinator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Administrative Coordinator to join our team, supporting the VP Biostatistics within the Biostatistics and Data Management team based on-site in Tarrytown, NY. In this role, you will proactively manage calendars, coordinate travel and meeting logistics, and help teams execute day-to-day objectives, while collaborating with leaders, administrative peers, and cross-functional partners like IT, Facilities, and Procurement.</p><br><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location: Tarrytown, NY</li><li>Work model/flexibility: 4 days a week on-site</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Anticipate the needs of leaders and teams, solving logistics before they become problems</li><li>Own coordination of internal and external meetings, seminars, and events from start to finish</li><li>Bring organization to team town halls, offsites, and agendas that keep people aligned</li><li>Navigate ambiguity and shifting priorities with composure and good judgment</li><li>Build trusted relationships across all levels, while keeping sensitive information confidential</li><li>Step in as backup support for fellow coordinators when the team needs it</li><li>Stay curious and pick up new tools and systems quickly, for yourself and those you support</li><li>Bring a collaborative, solutions-first mindset to daily administrative workflows</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Associate's or Bachelor's degree preferred; 5+ years of administrative experience (years of relevant experience may be considered in lieu of degree)</li><li>2+ years of industry experience in a relevant business function, desirable</li><li>Strong written and verbal communication skills, with the ability to interact confidently across all levels of the organization</li><li>Demonstrated independence, sound judgment, and problem-solving ability</li><li>A track record of building effective relationships up, down, and across teams</li></ul><br><p><br>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (hourly)</strong></p>$33.80 - $52.93]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 06 Oct 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Tech Training Specialist (Assoc - Sr.)]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51231]]></requisitionid>
    <referencenumber><![CDATA[R51231]]></referencenumber>
    <apijobid><![CDATA[r51231]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51231/tech-training-specialist-assoc-sr/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases.</p><br><p>Regeneron is currently seeking a <strong>Training Specialist</strong> to join our <strong>Industrial Operations & Product Supply (IOPS)</strong> organization. This role offers the opportunity to make a meaningful impact by supporting employee development, operational excellence, and the successful onboarding of new hires across the business.</p><br><p><strong>When & Where:</strong></p><br><ul><li><strong>Location:</strong> Raheen, Limerick, Ireland.</li><li>This is a full-time onsite position.</li><li>This role supports employees across multiple IOPS functions.</li></ul><br><p><strong>What You'll Do:</strong></p><br><ul><li>Deliver instructor-led, on-the-job, and administrative training across a variety of IOPS roles.</li><li>Assess employee readiness and support qualification for core job responsibilities.</li><li>Develop and maintain onboarding and training materials that support employee growth and development.</li><li>Partner with subject matter experts and cross-functional teams to identify and address training needs.</li><li>Coordinate onboarding schedules, training plans, and cross-training opportunities.</li><li>Maintain accurate training records and support compliance with training requirements.</li><li>Utilize learning management systems to monitor training progress and support site metrics.</li><li>Participate in training-related projects, audits, inspections, investigations, and continuous improvement initiatives.</li></ul><br><p><strong>The Environment and Physical Rhythms of This Role:</strong></p><br><ul><li>Thrive in a fast-paced manufacturing and operations environment.</li><li>Build strong partnerships with colleagues across multiple functions and levels of the organization.</li><li>Balance multiple priorities while maintaining accuracy and attention to detail.</li><li>Communicate effectively with a variety of audiences and learning styles.</li><li>Support a culture of continuous learning, collaboration, and operational excellence.</li></ul><br><p><strong>Let's Find Out if We're a Fit:</strong></p><br><ul><li>Requires a BS/BA in Life Sciences, Education, Training & Development, or a related field, or an equivalent combination of education and experience.</li><li>For <strong>Associate Training Specialist</strong>: 0-2 years of relevant experience.</li><li>For <strong>Training Specialist</strong>: 2+ years of relevant experience in biotechnology, pharmaceuticals, manufacturing, education, training, or a related industry.</li><li>For <strong>Senior Training Specialist</strong>: 5+ years of relevant experience in biotechnology, pharmaceuticals, manufacturing, education, training, or a related industry.</li><li>Strong communication, collaboration, facilitation, and organizational skills with the ability to work effectively in a regulated environment.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>€37,000.00 - €88,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Operazioni industriali e fornitura di prodotti]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 06:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing - Rare Disease]]></title>
    <date><![CDATA[Wed, 07 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51149]]></requisitionid>
    <referencenumber><![CDATA[R51149]]></referencenumber>
    <apijobid><![CDATA[r51149]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51149/associate-director-hcp-marketing-rare-disease/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3>Build our future together:</h3><br><p>The Associate Director, U.S. HCP Marketing, is a critical role within the Global Rare Disease Commercial Business Unit. By leading, planning, and implementing multiple HCP marketing efforts for both in-line and pipeline products in our rare disease portfolio, this role will ensure the integration of diverse marketing elements to deliver exceptional customer experience. We believe you will support strategic and operational analysis as well as takes a lead role in driving large projects within the business, allowing for deep insight and access to business strategy and marketing direction. Key core responsibilities will include digital marketing, speaker programs, conventions/congresses, and launch readiness/go-to-market planning for pipeline products. This position will contribute to the success of and growth of the Global Rare Disease portfolio and will report to the Senior Director, US Marketing Lead.</p><br><h3>When & where:</h3><br><ul><li>Office Based for 4 days a week in Sleepy Hollow, NY</li></ul><br><h3>Discover your role:</h3><br><ul><li>Partners with brand leadership, sales leadership, marketing and market access to set marketing strategy, find opportunities, gaps and solutions to drive commercial success</li><li>Assists in operational analysis, analyzing existing business strategy and derive recommendations to drive ad-hoc projects within the business, allowing for improved understanding in support of marketing execution</li><li>Lead the implementation of innovative HCP digital marketing strategies and programs in the US market.</li><li>Lead KOL engagement and HCP Speaker program strategy and tactical execution</li><li>Drive and manage Patient Diagnosis efforts such as sponsored genetic testing programs across the rare disease portfolio</li><li>Contribute to HCP brand planning across two brands and execute programs within allocated budgets, tracking KPIs and balancing priorities between in-line growth and pipeline launch preparation (including Congress planning and execution</li><li>Develop compliant unbranded disease education and pre-launch HCP strategies for pipeline products, in partnership with Medical Affairs</li><li>Drive HCP segmentation, targeting, and customer insights, including identification of treaters and centers of excellence in a rare disease setting</li><li>Lead field enablement, including sales training, POA (plan of action) content, and HCP-facing resources, in partnership with sales leadership</li><li>Manage agency partners and lead promotional materials through Medical, Legal, and Regulatory review</li></ul><br><h3>This role requires:</h3><br><ul><li>Bachelor’s degree required; MBA strongly preferred</li><li>10+ years of progressive experience in the pharmaceutical/biotech industry or related field</li><li>8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas.</li><li>Preferred to have Rare Disease experience.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commerciale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 07 Oct 2026 06:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming - Hematology]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46205]]></requisitionid>
    <referencenumber><![CDATA[R46205]]></referencenumber>
    <apijobid><![CDATA[r46205]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r46205/senior-manager-statistical-programming-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><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a <strong>Senior Manager, Statistical Programming</strong> to join our Statistical Programming function, providing technical leadership across project teams within one or more therapeutic areas. In this role, you will drive high-quality programming deliverables from single studies through regulatory approval, product launch, and beyond, while collaborating with partnering functions, external service providers, and study teams. </p><br><p>This position offers the opportunity to shape department strategy and mentor talent within a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><p><strong>When & where:</strong></p><ul><li>Location<strong>: </strong>Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: Onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Lead programming support across multiple studies, ensuring timely, high-quality deliverables</li><li>Coordinate programming documentation and specifications, following established standards</li><li>Champion company values through excellence, collaboration, and accountability</li><li>Communicate proactively with study and project teams to clarify requirements and guide programmers</li><li>Lead submission-ready programming deliverables for global regulatory authority filings</li><li>Drive department goals and serve as a subject matter expert on key topics</li><li>Guide the development of direct reports through goal-setting, coaching, and mentoring</li><li>Contribute to hiring by screening and interviewing programming candidates</li><li>You bring advanced SAS skills honed in a clinical data environment, ideally across multiple therapeutic areas</li><li>You understand pharmaceutical clinical development, statistical concepts, and regulatory submission requirements</li><li>You collaborate naturally across global, interdisciplinary teams</li><li>You juggle multiple projects and priorities without losing sight of quality</li><li>You solve problems with initiative, creativity, and a self-starter mindset</li><li>You enjoy influencing, mentoring, and coaching others toward strong results</li><li>You lead with accountability and hold yourself to a high bar</li><li>You're energized by both hands-on programming work and people leadership</li></ul><br><p><strong>This role requires:</strong></p><ul><li>MS or BS in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline, with 10+ years (12+ for BS) of programming experience — preferably in clinical trial data within biotechnology, pharmaceutical, or health-related industries, including some project and people management experience</li><li>Advanced SAS programming expertise in a clinical data environment</li><li>Strong understanding of clinical trial principles and regulatory submission requirements</li><li>Proven ability to lead global, cross-functional teams</li><li>Experience managing multiple concurrent projects and priorities</li><li>Demonstrated mentoring or coaching experience with junior programmers</li><li>Preferred/nice to haves:<strong> </strong>Knowledge of additional programming languages such as R or Python</li></ul><br><p>#statprogregn</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer - Internal Medicine]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44896]]></requisitionid>
    <referencenumber><![CDATA[R44896]]></referencenumber>
    <apijobid><![CDATA[r44896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r44896/principal-statistical-programmer-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Principal Statistical Programmer to join our Statistical Programming team, supporting a study team across our clinical portfolio. In this role, you will provide programming leadership and support for processing clinical trial data, designing and testing program logic while ensuring consistent, high-quality documentation, all while collaborating with a multidisciplinary study team to support analysis and reporting through regulatory approval and beyond.</p><p>This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.</p><br><h3>When & where:</h3><ul><li>Location: Warren, NJ or Cambridge, MA</li><li>Work model/flexibility: onsite</li></ul><br><p><strong>Discover your role:</strong></p><ul><li>Support or lead programming and quality control of analysis datasets, tables, listings, and graphs</li><li>Coordinate activities and communicate shifting timelines and milestones to the study team</li><li>Create and maintain programming specifications for analysis datasets across studies</li><li>Support creation and validation of submission requirements, including annotated CRFs and define documents</li><li>Work within a multidisciplinary study team to provide timely, quality support through regulatory approval and launch</li><li>Provide programming support for presentations and statistical ad hoc requests, assisting with more complex data as needed</li><li>Participate in department working groups, contributing to tool development and process improvement</li><li>Design and test program logic independently, maintaining documentation in a regulated environment</li></ul><br><p><strong>This role might be for you if you:</strong></p><ul><li>Enjoy working independently while staying closely connected to a broader study team</li><li>Communicate clearly and proactively, especially around shifting timelines</li><li>Take pride in accuracy and consistency when documenting and maintaining code</li><li>Think analytically and enjoy solving programming and data challenges</li><li>Stay curious about process improvement and enjoy contributing ideas to working groups</li><li>Adapt comfortably to ad hoc requests and evolving priorities from senior leadership</li><li>Bring attention to detail and a quality mindset to regulated work</li></ul><br><p><strong>This role requires:</strong></p><ul><li>Master's degree with 3+ years of relevant experience</li><li>Proven programming experience supporting clinical study data and analysis deliverables</li><li>Strong documentation and quality control skills within a regulated environment</li><li>Experience collaborating within a multidisciplinary study team</li></ul><br><p>#statprogregn</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Development Program Management (Hematology)]]></title>
    <date><![CDATA[Fri, 09 Oct 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R51061]]></requisitionid>
    <referencenumber><![CDATA[R51061]]></referencenumber>
    <apijobid><![CDATA[r51061]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/it/opportunita-di-lavoro/r51061/director-development-program-management-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together:</strong></p><p>This role (Director, Development Program Management) uses extensive program management knowledge and experience in the drug development industry to provide operational leadership, direction, and support to assigned development program(s) and/or portfolio(s). This individual is expected to drive the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and monitor the execution of these plans from preclinical through commercialization/lifecycle management. Responsibilities may also include coaching and mentorship of junior colleagues, managing direct reports, working with collaborators, and contributing to departmental initiatives. This is a leadership role within the department and organization thus this individual is expected to independently execute responsibilities, interact effectively with senior leadership, and influence the direction and outcomes of assignments. </p><p><strong>When & where:</strong></p><ul><li>Primary Location: Tarrytown, NY or Cambridge, MA</li><li>Additional Locations: Warren, NJ</li></ul><p><strong>Discover your role:</strong></p><ul><li><strong>Development Teams: </strong>Partners with the Global Program Head to drive strategic program teams (SPT) and sub teams by leading key governance meetings. Uses broad knowledge of drug development and project/program management coupled with leadership and problem-solving skills to align development teams around an integrated project/program plans, timelines and budgets based on program vision. Ensures efficient delivery of plans. Proposes and aligns annual program goals with program strategy and Regeneron’s corporate goals. Monitors progress against program goals and ensures accurate and timely reporting of program progress to management. Anticipates issues and program risks and drives timely development of risk management plans and issue resolution.</li><li><strong>Business Acumen: </strong>Utilizes knowledge of industry trends to identify risks/threats/opportunities and translates these to actionable activities for the development teams. Able to leverage political savvy and awareness of team dynamics to effectively drive decision making and achieve desired outcomes. Is proficient in project management planning systems (MS Project, SharePoint) and tools/techniques. Understands how systems and tools can be leveraged to move the program and business forward.</li><li><strong>Communication:</strong> Effective and trusted communicator that will develop a proven track record across the organization. Works effectively with different styles and adapts approaches in a cross-functional matrix environment to drive results. Establishes a culture which promotes and encourages open communication, transparency, accountability and learning from mistakes.</li><li><strong>Problem Solving: </strong>Is proficient at proactively identifying and critically analyzing potential problems that may affect the project, processes, or the team. Uses extensive industry and professional experience and knowledge to develop viable, long-term solutions to cross-functional, project, process, or team issues, driving alignment with impacted stakeholders. Proactively implements lessons learned/best practices across programs/TA and department to help other teams preempt or mitigate problems.</li><li><strong>Leadership</strong>: Strengthens teams and continuously works to drive teams to be high performing and efficient. Ability to align team members towards a common goal through expertise with conflict management, self/social awareness, and diverse team dynamics.</li></ul><p><strong>This role requires:</strong></p><ul><li>Minimal educational requirements: Bachelor’s Degree </li><li>12+ years of relevant broad project / program management experience required, preferably in the pharmaceutical or related industry </li><li>Have excellent written, verbal, and interpersonal communication skills and the ability to effectively interact with all levels both internal and external to the company in order to establish credibility with professionals on the project teams. </li><li>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 entrepreneurial organizations; expert in dealing with ambiguity and uncertainty </li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.</p><p>Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a>. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter. </p><br><p>Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.</p><br><p>As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.</p><br><p>For jobs in Canada: this posting is for an existing position.</p><br><p><strong>Salary Range (annually)</strong></p>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Sviluppo globale]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 09 Oct 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
</source>