<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<source>
  <publisher>Regeneron Pharmaceuticals Inc.</publisher>
  <publisherUrl>https://www.regeneron.com/</publisherUrl>
  <lastBuildDate>Sat, 16 May 2026 18:28:29 GMT</lastBuildDate>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41999]]></requisitionid>
    <referencenumber><![CDATA[R41999]]></referencenumber>
    <apijobid><![CDATA[r41999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41999/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team at our Menands campus with a Monday-Friday 8:00am-4:30pm shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p>As an HVAC Technician, a typical day might include the following:</p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li></ul><p>This role might be for you if you:</p><ul><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p>To be considered for the HVAC Technician you ideally should have an AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level. Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred.</p><ul><li>HVAC Technician II: AAS with 2+ years of relevant experience or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years of relevant experience or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Oncology]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45258]]></requisitionid>
    <referencenumber><![CDATA[R45258]]></referencenumber>
    <apijobid><![CDATA[r45258]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45258/associate-director-clinical-scientist-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><div><div><div><div><div><div><div><div><p><strong>As an Associate Director a typical day may include the following:</strong></p><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape as well as maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Possesses proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature.</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements.</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree, Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) is preferred. ≥ 10 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking proven leadership experience and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Strong cross-functional management, interpersonal and problem-solving skills. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Diagnostics]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45732]]></requisitionid>
    <referencenumber><![CDATA[R45732]]></referencenumber>
    <apijobid><![CDATA[r45732]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45732/associate-director-clinical-diagnostics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This role provides an exciting opportunity to lead projects across diverse therapeutic areas. As the Associate Director, Clinical Diagnostics (CDx), you will own the end-to-end strategy, development, and lifecycle management of companion diagnostic solutions that enable our therapeutics. This role drives cross-functional alignment across biomarker science, clinical development, regulatory, commercial, and external IVD partners to deliver fit-for-purpose assays that meet global regulatory requirements and support clinical decision-making. You will lead the CDx portfolio from early biomarker feasibility through clinical validation, registration, launch, and post-market sustainment, ensuring timely availability of high-quality diagnostics aligned with drug development milestones.</p><p><strong>A typical day might include</strong>:</p><ul><li><p>Set the global CDx strategy for assigned programs, aligning diagnostic milestones with clinical and regulatory timelines for the therapeutic.</p></li><li><p>Lead selection and oversight of IVD partners; negotiate scopes, timelines, budgets, and quality expectations; manage co-development and governance.</p></li><li><p>Define assay intent and target product profiles (TPP) for CDx platforms (e.g., NGS, PCR, IHC, Immunoassays), ensuring analytical and clinical performance meets intended use.</p></li><li><p>Partner with biomarker and clinical teams to integrate CDx into trial designs (screening, enrichment, stratification), including sample strategy and operational readiness.</p></li><li><p>Drive analytical validation plans (e.g., accuracy, precision, sensitivity/specificity, LoD, reproducibility) and clinical validation strategies linking assay results to drug safety and efficacy.</p></li><li><p>In collaboration with IVD Regulatory, support global regulatory strategy and submissions for CDx (e.g., FDA PMA/supplement, 510(k) where applicable, EU IVDR, PMDA), including pre-submission interactions and labeling alignment.</p></li><li><p>Ensure compliance with applicable standards and regulations (e.g., ISO 13485, ISO 14971, CLSI guidelines, IVDR, GCP alignment for diagnostic use in trials).</p></li><li><p>Coordinate cross-functional working groups, remove program obstacles, and provide transparent status reporting to governance bodies.</p></li><li><p>Oversee design transfer, manufacturing readiness, and supply planning with IVD partners to ensure clinical and commercial availability.</p></li><li><p>Drive risk management and mitigation plans across technical, regulatory, operational, and commercial domains.</p></li><li><p>Partner with commercial and medical affairs to shape CDx launch readiness (access, coverage, distribution, training, KOL engagement).</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>Proven track record delivering CDx aligned to drug approvals, including successful analytical/clinical validation and regulatory submissions.</p></li><li><p>Deep understanding of diagnostic platforms (NGS, PCR, IHC, Immunoassays) and associated validation standards and quality systems.</p></li><li><p>Experience managing external IVD partners and complex, cross-functional programs.</p></li><li><p>Strong knowledge of global regulations (FDA CDRH, EU IVDR, PMDA) and pathways for CDx approval and labeling.</p></li><li><p>Excellent communication, leadership, and stakeholder management skills.</p></li><li><p>Strategic thinking with the ability to translate scientific and clinical needs into executable diagnostic solutions.</p></li><li><p>Program leadership, planning, and risk management across multiple, fast-paced workstreams.</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><ul><li><p>Advanced degree in a relevant field (e.g., MS/PhD in molecular biology, pathology, biomedical engineering, or related) or equivalent experience.</p></li><li><p>8+ years of experience in diagnostics development, with 4+ years leading CDx or IVD programs in pharmaceutical or diagnostics settings</p></li></ul><p><strong>Travel:</strong></p><p>Travel up to 5–10% for partner meetings, clinical site visits, and regulatory interactions.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Cell Therapy)]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43023]]></requisitionid>
    <referencenumber><![CDATA[R43023]]></referencenumber>
    <apijobid><![CDATA[r43023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43023/senior-manager-clinical-study-lead-cell-therapy/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The <strong>Senior Clinical Study Lead</strong> (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives. </p></div><div><div><div><div><p><em>This role is not eligible fully remote. This role is required to be onsite in one of our locations. (Armonk, NY / Warren, NJ / Cambridge, MA / Dublin, Ireland / Uxbridge, London)</em></p><p><strong>A typical day in this role looks like: </strong> </p><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Provides operational input into protocol development</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Ensures compliance with the clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors </p></li><li><p>Provides input into baseline budget development and management</p></li><li><p>Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level</p></li><li><p>Leads the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Oversees/conducts site evaluation and selection</p></li><li><p>Leads investigator meeting preparation and execution</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</p></li><li><p>Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Ensures accurate budget management and scope changes for internal and external studies</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Oversees the execution of the clinical study against planned timelines, deliverables and budget</p></li><li><p>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</p></li><li><p>Ensure clinical project audit and inspection readiness through the study lifecycle</p></li><li><p>Supports internal audit and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>Contributes to clinical study report writing and review</p></li><li><p>Facilitates and contributes to study level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables</p></li><li><p>Recommends and participates in cross-functional and departmental process improvement initiatives</p></li><li><p>Responsible for identification of innovative approaches to clinical study execution including global considerations and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li><li><p>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require 25% travel</p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Exceptional interpersonal & leadership skills</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Advanced communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Strong budget management experience</p></li><li><p>An awareness of relevant industry trends</p></li><li><p>Ability to build, lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Advanced project management skills, cross-functional team leadership and organizational skills</p></li><li><p>Line management experience</p></li></ul><p><strong>In order to be considered qualified, </strong>a minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience.</p><p>A background in clinical trials within cell therapy and early phase clinical trials is preferred.</p></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$148,300.00 - $241,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Oncology]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45863]]></requisitionid>
    <referencenumber><![CDATA[R45863]]></referencenumber>
    <apijobid><![CDATA[r45863]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45863/associate-director-clinical-scientist-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>As an Associate Director a typical day may include the following:</strong></p><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape as well as maintaining compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Possesses proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature.</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements.</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree, Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) is preferred. ≥ 10 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking proven leadership experience and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Strong cross-functional management, interpersonal and problem-solving skills. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Trade & Distribution]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46153]]></requisitionid>
    <referencenumber><![CDATA[R46153]]></referencenumber>
    <apijobid><![CDATA[r46153]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46153/senior-manager-trade-distribution/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Trade & Distribution Operations is a key member of the team, responsible for end‑to‑end oversight of distribution and order fulfillment across Spain/France, Switzerland, and EU Rare Disease channels. Collaborating with internal teams, external vendors, customers, and logistics partners, you will be driving operational performance, vendor collaboration, regulatory/GDP compliance, budget stewardship, and continuous improvement to ensure reliable, efficient delivery.</p><p><strong>A Typical Day</strong></p><ul><li><p>Communicate proactively with internal and external collaborators to resolve distribution customer concerns and issues while maintaining high standards of order fulfillment.</p></li><li><p>Serve as the primary point of contact for vendors and partners; maintain collaboration and ensure adherence to contractual obligations and SLAs.</p></li><li><p>Be responsible for day‑to‑day distribution operations to ensure timely delivery, adherence to schedules, and operational efficiency.</p></li><li><p>Conduct regular vendor performance reviews and prepare quarterly reports for internal leadership and external collaborator presentations.</p></li><li><p>Provide oversight of 3PL activities with regulatory and contractual requirements, including GDP standards.</p></li><li><p>Handle and supervise distribution budgets, balancing cost efficiency with quality service delivery; track variances and drive corrective actions.</p></li><li><p>Track and report distribution metrics such as delivery timelines, inventory levels, and vendor performance; surface insights to guide decisions.</p></li><li><p>Rectify data anomalies using internal dashboards and systems; ensure accurate reporting, detailed data integration, and data integrity.</p></li><li><p>Support contract development, amendments, and compliance in collaboration with Legal and cross‑functional teams.</p></li><li><p>Resolve claims efficiently; establish standard operating procedures and conduct proactive reviews to optimize workflows and reduce recurrence.</p></li><li><p>Develop and maintain policies and procedures that strengthen distribution strategies and vendor relationships.</p></li><li><p>Ensure compliance with trade regulations, GDP standards, and other relevant distribution requirements across the broader EU operations.</p></li><li><p>Collaborate with cross‑functional teams (e.g., Quality, Finance, Customer Service, Supply Chain, Commercial) to implement process improvements aligned to organizational goals.</p></li><li><p>Produce reports and briefing materials for senior management on distribution performance, vendor adherence, and risk/mitigation status.</p></li><li><p>Identify and mitigate risks and dependencies early; recommend pragmatic solutions and secure cross‑functional alignment on course corrections.</p></li></ul><p><strong>This Role Might Be for You If You Have</strong></p><ul><li><p>Hands‑on experience leading distribution operations across Europe, especially ES/FR and Switzerland, with exposure to rare disease or specialty distribution.</p></li><li><p>Vendor and 3PL management expertise, including contract oversight, SLA governance and performance reviews.</p></li><li><p>Strong understanding of GDP, trade regulations, and compliance expectations for pharmaceutical/healthcare distribution in the EU and Switzerland.</p></li><li><p>Data fluency and analytical skills, including dashboarding and KPI reporting</p></li><li><p>Budget management experience with a focus on cost optimization and service quality.</p></li><li><p>Excellent communication and collaborator, adept at handling partner concerns and driving outcomes in a matrixed environment.</p></li><li><p>Process improvement demeanor with experience in standardizing procedures and implementing efficiencies</p></li><li><p>High attention to detail, organization, and follow‑through; ability to balance multiple priorities and deadlines.</p></li><li><p>Willingness to travel to vendor sites, 3PLs, and regional partners as needed.</p></li></ul><p><strong>To Be Considered</strong></p><p>Bachelor’s degree in supply chain or a related field. 6+ years of experience in distribution/trade operations, logistics, or vendor management, with a European focus</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 02:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Solutions Partner]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46276]]></requisitionid>
    <referencenumber><![CDATA[R46276]]></referencenumber>
    <apijobid><![CDATA[r46276]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46276/senior-director-solutions-partner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Business Solutions Partner - Research IT</strong></h3><p>We are looking for an experienced Business Solutions Partner to help shape how technology supports therapeutic pipeline development across our research organisation. In this role, you will serve as a strategic link between Research IT and scientific teams, translating complex research workflows into scalable digital solutions that accelerate discovery and development. You will guide high-impact programmes, influence technology investment decisions, and help build future-ready platforms, data practices, and delivery models that improve research outcomes.</p><h3><strong>A Typical Day:</strong></h3><ul><li>Partner with research leaders to align technology with pipeline priorities</li><li>Build business cases and resource proposals for strategic investments</li><li>Lead informatics programmes across biologics, genetic medicines, and screening</li><li>Translate scientific workflows into scalable systems and digital solutions</li><li>Guide projects from requirements through deployment and continuous improvement</li><li>Coordinate ELN, LIMS, registration, and BI platform initiatives</li><li>Champion data harmonisation, shareability, and semantic data practices</li><li>Mentor teams and strengthen delivery across internal and external partners</li></ul><h3><strong>This Role May Be For You If:</strong></h3><ul><li>You enjoy connecting scientific priorities with practical technology solutions</li><li>You are comfortable leading several complex programmes at the same time</li><li>You work well across scientists, informatics, operations, and technical teams</li><li>You can move easily between strategic planning and delivery oversight</li><li>You are drawn to improving research workflows through systems and data</li><li>You like shaping future-state solutions rather than maintaining the status quo</li><li>You are confident communicating recommendations and progress to senior leaders</li><li>You enjoy developing teams in a collaborative, matrixed environment</li></ul><p>To be considered, you should have a master’s degree in a life sciences discipline such as Biology, Biochemistry, Molecular Biology, or a related field, along with at least 10 years of progressive experience in a pharmaceutical or biopharmaceutical R&D environment with significant exposure to research IT and scientific operations. You should also have experience managing cross-functional teams of 20+ resources, including internal staff, contractors, and vendor partners, and a deep understanding of therapeutic biologics development workflows across antibody, genetic medicine, or small molecule research. Experience with scientific software platforms such as ELN, LIMS, registration systems, and BI tools is required. A PhD, experience leading system modernisation or data migration programmes, familiarity with semantic data modelling and data architecture, prior hands-on scientific research experience, and experience scaling SaaS or vendor partnerships are preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Dermatology]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46330]]></requisitionid>
    <referencenumber><![CDATA[R46330]]></referencenumber>
    <apijobid><![CDATA[r46330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46330/medical-director-clinical-development-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Medical Director, Clinical Sciences is responsible for facilitating assigned dermatology studies, providing investigator support of Regeneron driven studies, and may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into an Executive Medical Director, Clinical Sciences and is expected to have proficient knowledge of the drug development process, good clinical practice, study design and research methodology as well as understand Regulatory and compliance landscape in the pharmaceutical industry. This role utilizes scientific and clinical expertise to initiate, propose, design and execute research and development programs for early and/or late stage assets. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. Some industry experience preferred.</div><div><div><div><div><div><div><div><div><div><p>A typical day in the life may include the following responsibilities:</p><ul><li><p>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program. Clinical deliverables may include individual protocols; clinical components of regulatory documents/registration dossier and brand related medical information, clinical communication and publications</p></li><li><p>Advanced analytical skills and ability to communicate concise and clear messages</p></li><li><p>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts</p></li><li><p>Ability to lead activities within a matrix environment</p></li><li><p>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally</p></li></ul><p>This role may be for you if:</p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p>In order to be considered for this role, a M.D. degree or equivalent is required. Specialized clinical fellowship training in Dermatology is strongly preferred. A minimum of 2-4 years of clinical development experience in industry is preferred, but academic research experience will be considered.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 21:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Associate Scientist, Drug Product Development and Technology (1 of 3)]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46695]]></requisitionid>
    <referencenumber><![CDATA[R46695]]></referencenumber>
    <apijobid><![CDATA[r46695]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46695/sr-associate-scientist-drug-product-development-and-technology-1-of-3/]]></url>
    <company><![CDATA[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 Drug Product Development & Technology is seeking a Senior Associate Scientist as we work to support all stages of pre-clinical, clinical, commercial formulation, and drug product development for various drug product modalities. In this role, you will apply biochemical and biophysical methods to carry out developability assessment and formulation development studies on monoclonal antibody-based therapeutics, to support drug substance and drug product development.</p><p><em><strong>Job Duties:</strong></em></p><ul><li><p>Design and independently execute phase-appropriate formulation development studies, such as formulation screening, stability and compatibility studies, to support drug product development for early and late-stage development programs.</p></li><li><p>Conduct pre-formulation studies for monoclonal antibodies, bioconjugates and peptides, using various biophysical and biochemical techniques to identify critical quality attributes for formulation and drug product development.</p></li><li><p>Develop analytical methods for drug products, with primary focus on peptides, and supporting focus on antibody–drug conjugates, siRNA, monoclonal antibodies, and bispecific antibodies </p></li><li><p>Develop and qualify analytical methods for critical quality attributes to support formulation development, DP process development, and stability testing for programs in preclinical and clinical stage. </p></li><li><p>Characterize drug product formulation to support the process development and manufacturing of clinical drug substances and drug products.</p></li><li><p>Document findings and lab records in electronic laboratory notebook by following the organizational best practices and policies.</p></li><li><p>Contribute to formulation development technical reports to provide insights into process development and manufacturing of clinical drug substances and drug products.</p></li><li><p>Participate in meetings and present study results in cross-functional team meetings or department meetings.</p></li><li><p>Author protocols, technical documents for internal use and support regulatory filings.</p></li><li><p>Take part in the general laboratory and instrument maintenance.</p></li></ul><h3><em><strong>Job Requirements:</strong></em></h3><ul><li><p>Take direction and guidance for data-driven decision making, priority setting and technical problem solving.</p></li><li><p>Generate and organize data figures and data tables in a clear and insightful way</p></li><li><p>Communicate critical data in timely manner to supervisor and team</p></li><li><p>Strong ability to prioritize and manage multiple tasks effectively.</p></li><li><p>Highly organized, detail-oriented, self-motivated, effective team player.</p></li><li><p>Excellent oral and written communication skills.</p></li></ul><p>This role requires a B.S or M.S degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Biophysics, Biomedical Engineering, Analytical Chemistry, Chemical Engineering, or a related discipline with at least 3 years of industrial experience. The ability to design and execute experiments, as well as interpret, document, and communicate results with minimal supervision is required. Strong technical knowledge base and relevant experience with protein/peptide chemistry, biophysical/biochemical characterization of proteins, bioanalytical method development and biomolecule product development is desirable. Hands-on experience with biochemical and biophysical techniques for protein characterization, including chromatography (SEC, IEX, RP), viscosity, gel electrophoresis (CE-SDS, MCE, cIEF, iCE), particle size (DLS, HIAC, MFI), spectroscopy (UV-Vis, CD, AUC, fluorescence), and thermostability characterization (DSC, DSF) is desirable.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Compliance]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44121]]></requisitionid>
    <referencenumber><![CDATA[R44121]]></referencenumber>
    <apijobid><![CDATA[r44121]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44121/manager-compliance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced Manager, Corporate Compliance to join our dynamic team in Japan. Reporting to the Japan Compliance Lead, you will play a pivotal role in supporting Regeneron’s compliance operations, ensuring the highest standards of ethical conduct and regulatory adherence. This is an exciting opportunity to contribute to the development and implementation of compliance programs that support our mission of advancing science and delivering life-changing medicines. If you are passionate about compliance and working in a collaborative, innovative environment, we invite you to explore this opportunity. </p><p><strong>A Typical Day: </strong></p><p>As the Manager, Corporate Compliance, you will: </p><p>- Collaborate with the Japan Compliance Lead and Global Compliance teams on healthcare compliance (HCC) matters. </p><p>- Implement and operationalize Regeneron’s compliance program and policies in Japan in alignment with headquarters. </p><p>- Develop and refine compliance policies, work instructions, and guidance to ensure adherence to local and international regulations, including JPMA and FTC codes. </p><p>- Deliver engaging compliance training programs for employees and third parties to promote understanding of applicable laws and industry codes. </p><p>- Provide compliance oversight and guidance to ensure interactions with healthcare professionals (HCPs) and organizations (HCOs) are conducted ethically and in accordance with established policies. </p><p>- Conduct internal reviews, risk assessments, and monitoring activities to identify and mitigate compliance risks effectively. </p><p>- Partner with cross-functional teams to provide creative solutions to compliance challenges. </p><p>- Support additional compliance projects and strategies as needed to enhance operations in Japan and the broader APAC region. </p><p><strong>This Role May Be For You If: </strong></p><p>- You have a strong knowledge of the pharmaceutical industry and its self-regulatory framework in Japan, including the JPMA and FTC codes. </p><p>- You thrive in collaborative environments and excel at building cross-functional relationships to achieve compliance goals. </p><p>- You are a problem solver with a creative approach to addressing compliance challenges and implementing practical solutions. </p><p>- You are proactive in identifying risks and opportunities to enhance compliance programs. </p><p>- You have exceptional communication skills in both Japanese and English, with the ability to deliver clear, concise, and impactful messages. </p><p>- You are detail-oriented and committed to maintaining the highest ethical standards in all aspects of your work. </p><p>- You are adaptable and willing to travel to meet the needs of the role. </p><p><strong>To Be Considered: </strong></p><p>We are looking for candidates with a minimum of a BA/BS degree (advanced degrees such as MBA or JD are preferred but not required) and at least 5 years of experience in healthcare compliance-related activities within the pharmaceutical industry in Japan. A strong working knowledge of Japan’s healthcare compliance laws, including the JPMA and FTC codes, is essential. Proficiency in both English and Japanese (written and verbal) is required, along with the ability to draft professional documents and guidance materials. </p><p>If you are ready to take the next step in your compliance career and contribute to a culture of integrity and innovation, we encourage you to apply today.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 02:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Operations Manager, Process & Procedures]]></title>
    <date><![CDATA[Sun, 19 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45064]]></requisitionid>
    <referencenumber><![CDATA[R45064]]></referencenumber>
    <apijobid><![CDATA[r45064]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45064/operations-manager-process-procedures/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Are you passionate about streamlining processes and creating impactful procedural documents? Join our Global Development team as an Operations Manager, Process & Procedures, where you’ll drive the development and management of our controlled procedural document portfolio. This role offers the opportunity to contribute to process innovation and collaborate with cross-functional teams in a dynamic, regulated environment. Based in Tokyo, this position is your chance to make a meaningful impact while advancing your career.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Lead the revision and creation of procedural documents through their lifecycle, including updates for process improvements and administrative changes.</p></li><li><p>Facilitate process mapping and content updates in collaboration with authors and subject matter experts (SMEs).</p></li><li><p>Support procedural document projects by partnering with functional owners and cross-functional SMEs to improve existing processes.</p></li><li><p>Coordinate review cycles and approval workflows for assigned procedural documents.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You thrive in a collaborative environment and enjoy working with cross-functional teams to achieve shared goals.</p></li><li><p>You are detail-oriented and excel at identifying gaps in processes and proposing innovative solutions.</p></li><li><p>You have strong organizational and project management skills, balancing multiple priorities with ease.</p></li><li><p>You possess expertise in controlled procedural document principles and process design.</p></li><li><p>You are proficient in tools like Microsoft Visio for process mapping and have experience with electronic document management systems.</p></li><li><p>You value integrity and trust, and you’re skilled at negotiating and influencing at all organizational levels.</p></li><li><p>You enjoy strategic thinking and problem-solving in a regulated environment.</p></li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor’s degree and at least 5 years of experience in a global regulated organization, with 3 years in a quality role focusing on procedural documents. Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements, as well as experience in controlled document principles, is essential. Preferred qualifications include expertise in Microsoft Visio or similar tools and familiarity with electronic document management systems.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Government Pricing]]></title>
    <date><![CDATA[Tue, 14 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46609]]></requisitionid>
    <referencenumber><![CDATA[R46609]]></referencenumber>
    <apijobid><![CDATA[r46609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46609/associate-director-government-pricing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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><p><strong>A typical day may include the following:</strong></p><ul><li><p>Ability to calculate, validate and report accurate monthly, quarterly, and annual government pricing.</p></li><li><p>Submit and monitor State Price Transparency regulations.</p></li><li><p>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.</p></li><li><p>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.</p></li><li><p>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.</p></li><li><p>Responsible for maintaining and updating SOP’s and reasonable assumptions, on a quarterly basis, as related to Government Programs/Pricing.</p></li><li><p>Monitor policies, procedures and processes supporting Government Pricing submissions and related areas to ensure ongoing compliance with external and internal requirements and guidance.</p></li><li><p>Understand and estimate impact of pricing and policy changes regarding government pricing.</p></li><li><p>Perform pricing research and analysis on special projects as assigned.</p></li><li><p>Ability to review and understand commercial contract language as pertaining to Best Price (BP), Average Sales Price (ASP) and FSS Tracking Customers.</p></li><li><p>Investigate Government pricing trends and cross channel impact. Also provide Government price inputs to the Gross to Net (GTN) team.</p></li><li><p>Monitor for Tracking customer violations, Bona Fide Service Fee treatments & Customer COT assignment.</p></li><li><p>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.</p></li><li><p>Serve as a liaison with Commercial Leadership, Pricing, Trade, Brand and Accounting/Finance teams regarding a variety of issues impacting government pricing.</p></li><li><p>Familiar with Fair Market Value methodology while determining bona fide service fees paid to Wholesaler, Pharmacy Benefit Manager (PBM) and Group Purchasing Organizations (GPOs).</p></li></ul><p><strong>The role may be for you if:</strong></p><ul><li><p>Understanding of current government pricing rules, regulations, and calculations</p></li><li><p>Must be able to identify potential problems, conduct analysis and use judgment to determine if problem exists as well as offer up potential solutions.</p></li><li><p>Highly analytical, able to analyze, interpret, and convey data and its commercial impact</p></li><li><p>Ability to decipher calculations to determine key causes of variances.</p></li><li><p>Strong communication skills and ability to communicate effectively to all levels of the organization.</p></li><li><p>Process oriented</p></li><li><p>Proven ability to successfully manage competing priorities, meet challenging deadlines, and work independently and across organizations</p></li><li><p>Demonstrated track record of strong attention to detail; accountability and ownership of results; flexibility and adaptability in a rapidly changing environment</p></li></ul><p>To be consider for this role, we expect you to have a bachelors degree and 7+ years prior experience in Government Pricing OR a related field such as finance, accounting, Medicare/Medicaid (with strong analytical skills). We also will need you to be open to traveling at times.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 15 Apr 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Product Biochemistry (siRNA Therapeutics, Lipid Nanoparticles)]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46533]]></requisitionid>
    <referencenumber><![CDATA[R46533]]></referencenumber>
    <apijobid><![CDATA[r46533]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46533/associate-scientist-product-biochemistry-sirna-therapeutics-lipid-nanoparticles/]]></url>
    <company><![CDATA[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 Product Biochemistry group, located in Tarrytown NY, is seeking an Associate Scientistwho will be responsible for providing in-depth characterization of nucleic acid therapeutics and Lipid Nanoparticles (LNP). In this exciting role, you will be expected to participate in technology innovation efforts aimed at enhancing our understanding of oligonucleotides and LNPs in solution and address both pre-clinical and late-stage program needs.</p><p><strong>A Typical Day in the Role of Associate Scientist Might Look Like:</strong></p><ul><li><p>Develop analytical methods and conduct biochemical and biophysical characterization experiments to elucidate quality attributes of gene therapy candidates. Help solve problems in real time.</p></li><li><p>Provide support for basic research efforts. Ability to adapt and/or optimize methods described in the literature.</p></li><li><p>Conduct time-sensitive biochemical and extended characterization of siRNAs to meet regulatory timelines.</p></li><li><p>Provide input on experimental design and suggest method adaptations to address specific needs of a program or attributes of colloidal systems.</p></li><li><p>Additional responsibilities will include method development of advanced technologies that evaluate the purity and/or thermodynamic and hydrodynamic interactions of siRNAs, mRNAs, CRISPR gRNA and LNP-nucleic acid complexes.</p></li><li><p>Support forced degradation studies evaluating environmental stressors and their impact on the stability of siRNA, LNPs and their cargos.</p></li><li><p>Document experiments, results, and findings in electronic laboratory notebook; presents work at group and departmental meetings, contributes to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed publications.</p></li><li><p>Maintain instruments, troubleshoots instrumental/experimental problems, and order/maintain supplies.</p></li></ul><p><strong>This Role Might Be For You If You Have:</strong></p><ul><li><p>Excellent oral and written communication skills</p></li><li><p>Strong initiative and drive to complete challenging tasks with a sense of urgency</p></li><li><p>Ability and desire to learn new technologies</p></li><li><p>A desire to work both independently and within a collegial and collaborative environment</p></li></ul><p>BS or MS in Biophysics, Biochemistry, Chemistry, Chemical Engineering, or related field with a minimum of 0-2 years or BS with 2+ years of relevant experience.</p><p>A fundamental understanding of practical biophysical chemistry of macromolecules in solution is essential. Basic knowledge of oligonucleotide properties, lipid biochemistry and gene editing therapeutics is important.</p><p>Good laboratory practice skills preparing samples, calculating concentrations, documenting, and maintaining cleanliness are critical. Basic practical experience in automated chromatography (FPLC, H/UPLC), spectroscopy (UV-Vis, fluorescence, FTIR and CD) and/or multi-angle/dynamic light scattering (MALS/DLS) of macromolecules is important. Experience with mass spectrometry (MS), NMR, ELSD/CAD, charge-based methods, and/or advanced imaging skills are a bonus. The position is primarily on-site with partially remote (hybrid) schedule.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, R&D Internal Communications]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45878]]></requisitionid>
    <referencenumber><![CDATA[R45878]]></referencenumber>
    <apijobid><![CDATA[r45878]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45878/associate-director-rd-internal-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[<div><div><p>As Associate Director, R&D Internal Communications, you will lead the strategy and execution of internal communications that connect, inform, and align employees across Research & Development (R&D). You will ensure R&D teams understand priorities, progress, and strategic direction, while fostering a strong, inclusive culture and clear line-of-sight to the company’s mission and impact on patients. </p><div><p>You will translate complex science and operations into clear, compelling narratives that mobilize action—from the bench to the clinic. You will be a trusted advisor to R&D leaders and help shape how they communicate, how teams engage with change, and how the organization celebrates scientific excellence and collaboration. </p></div><div></div><div><p>This role reports to the Senior Director and Head of R&D Communications and is a member of the Corporate Communications team in Corporate Affairs. You will partner closely with Enterprise Internal Communications, Human Resources, and R&D leadership teams. </p></div></div><div></div><div><p><strong><em>This role is based at our Sleepy Hollow, NY location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</em> </strong></p></div><div></div><div></div><div><p><strong>A typical day might include:</strong> </p></div><div></div><div><ul><li><p>Serving as a strategic communications advisor and trusted partner to R&D senior leaders. </p></li></ul></div><div><ul><li><p>Developing and implementing a comprehensive internal communications strategy aligned to R&D and enterprise goals with clear established governance, channel mix, and editorial standards. </p></li></ul></div><div><ul><li><p>Designing and delivering communications for change and transformation initiatives, including clear case-for-change narratives, leader toolkits, and cascade materials for managers. </p></li></ul></div><div><ul><li><p>Leading the planning and content for R&D forums and channels (e.g., town halls, newsletters), continuously measuring effectiveness and optimizing for reach, clarity and engagement. </p></li></ul></div></div><div><div><ul><li><p>Crafting executive messaging, talking points, and presentations for high visibility internal events. </p></li></ul></div><div><ul><li><p>Translating complex scientific topics into engaging content tailored to diverse audiences (research scientists, physician-scientists, and regulatory, medical affairs, and operational teams). </p></li></ul></div><div><ul><li><p>Overseeing R&D content strategy for the company intranet to ensure timely, accurate, and accessible information. </p></li></ul></div><div><ul><li><p>Supporting initiatives that reinforce R&D culture, scientific excellence, collaboration, inclusion and employee recognition in close partnership with Human Resources and other cross-functional stakeholders. </p></li></ul></div><div><ul><li><p>Managing agency partners and/or consultants, ensuring high standards of quality, consistency, and timelines. </p></li></ul></div><div></div><div><p><strong>This role might be for you if:</strong> </p></div><div><ul><li><p>You think strategically and execute tactically to deliver measurable business impact. </p></li></ul></div><div><ul><li><p>You have a proven ability to translate complex scientific concepts into clear, resonant narratives and visuals tailored to diverse internal audiences. </p></li></ul></div><div><ul><li><p>You demonstrate strong executive presence and sound judgement, confidently advising senior leaders and navigating sensitive or ambiguous situations. </p></li></ul></div><div><ul><li><p>You have deep experience in designing and delivering communications for change and transformation initiatives. </p></li></ul></div><div><ul><li><p>You are an excellent writer and editor, with strong storytelling skills and a keen eye for accuracy, clarity and tone. </p></li></ul></div><div><ul><li><p>You are results-oriented and collaborative, skilled at influencing, building consensus, and fostering trusted relationships across levels and functions. </p></li></ul></div><div><ul><li><p>You thrive in a fast-growing, ambiguous environment and can manage multiple priorities simultaneously with focus and agility. </p></li></ul></div><div><ul><li><p>You manage agencies and/or vendors effectively, integrating workstreams to deliver cohesive, high-quality outcomes. </p></li></ul></div><div></div><div><p> <br><strong>To be consider for this role you have:</strong> </p></div><div><p>A Bachelor’s degree in a related field is required. You bring 10+ years of proven excellence in strategic internal communications, with extensive change and transformation experience. Experience within the biopharma or life sciences industries will be looked at favorably. </p></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, IT Product Management - Financials]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45506]]></requisitionid>
    <referencenumber><![CDATA[R45506]]></referencenumber>
    <apijobid><![CDATA[r45506]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45506/associate-director-it-product-management-financials/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, IT Product Management –Financials you will lead the IT execution, delivery and operational ownership of Regeneron’s Record to Report (RTR) capabilities within a modern global ecosystem. This role is accountable for translating product strategy and roadmap direction into high-quality, scalable, and compliant solutions that support Global Finance, including Record‑to‑Report, Tax, Treasury, and integrated financial workstreams.</p><p>Success in this role requires not only deep Oracle EBS and Fusion RTR expertise, but also deep Financials, Tax and Treasury industry knowledge.</p><p>A typical day in this role might look like:</p><ul><li>Act as a strategic and trusted partner to Finance stakeholders and help with Business Roadmap and Strategy, and delivering on Business outcomes and value framework.</li><li>Serve as the IT Product owner for not only Oracle ERP Financials but also associated boundary systems and processes like, VAT, Sales Tax, Reval Treasury Management systems, AGIS, Concur, Intercompany, Lease Accounting, Project Accounting, Accounting Hub, and Collaboration Billing.</li><li>Drive execution across multiple concurrent workstreams while balancing strategic transformation and day‑to‑day operational needs, focused on supporting Global growth.</li><li>Lead a portfolio of ERP Financials initiatives in partnership with the PMO, including demand intake, prioritization, planning, execution, vendor management, and financial oversight.</li><li>Partnering strategically with business for Vendor Selections, RFPs, Total Cost of ownership and Cost benefit analysis, Application rationalization on an ongoing basis.</li><li>Provide oversight of system integrators and vendors, ensuring delivery aligns with enterprise standards, Oracle best practices, and future‑state architecture.</li><li>Lead ongoing improvements, configuration changes, and enhancements including but not limited to Oracle ERP and key boundary systems to improve efficiency and support evolving business needs.</li><li>Ensure application, integration, and data architecture standards are defined, maintained, and aligned across the ERP Financials ecosystem.</li><li>Oversee data migration and conversion activities related to ERP Financials, ensuring accuracy, reconciliation, and audit readiness.</li><li>Drive integrated and automated financial processes across upstream and downstream systems.</li><li>Maintain strong Identity and Access Management controls (RBAC / ABAC) across sensitive financial systems.</li><li>Partner with Infosec and other technology teams to ensure alignment with Regeneron security standards and ensure compliance on ERP platforms, SaaS, and third-party applications for patching, data security, privacy, security, risk, and regulatory standards.</li><li>Promote a data‑driven mindset, leveraging Oracle reporting and analytics tools (OTBI, BI Publisher, FDI, FRS, Smart View).</li><li>Apply emerging technologies, automation, and AI‑enabled capabilities to modernize financial operations and improve insight.</li><li>Ensure ERP Financials capabilities support global reporting, close, decision‑making needs.</li></ul><p>This role might be for you if you have:</p><ul><li>Strong understanding of ERP Financials processes including Record‑to‑Report, Intercompany, and Project Accounting, Tax, Treasury, Forex.</li><li>Strong understanding of enterprise Chart of Accounts (COA) design and governance, including structure, harmonization, mapping rules.</li><li>Strong understanding of SOX, ITGC, and regulated environments.</li><li>Strong problem analysis and resolution skills for both functional and end-to-end solution.</li><li>Ownership mindset, resilience, willingness to roll up sleeves to ensure delivery success.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in a related field (Accounting, Finance, Information Systems, Computer Science, or similar) and 10+ years of increasing responsibility delivering Oracle ERP Financials solutions plus a minimum of 4+ years partnering closely with Global Finance across multi‑functional workstreams and Oracle Fusion experience. Knowledge of EPM (ARCS,FCCS, EPBCS, PCMCS), Planning and Consolidation would be a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison - North Central]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46775]]></requisitionid>
    <referencenumber><![CDATA[R46775]]></referencenumber>
    <apijobid><![CDATA[r46775]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46775/associate-director-thought-leader-liaison-north-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Illinois]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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 Senior 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, 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>The typical day may include the following:</h3><ul><li><p>The Oncology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</p></li><li><p>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</p></li><li><p>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</p></li><li><p>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or during day-to-day business</p></li><li><p>Develop/maintain list of key thought leaders in the assigned geography</p></li><li><p>Assist with thought leader development</p></li><li><p>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</p></li><li><p>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</p></li><li><p>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</p></li><li><p>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</p></li></ul><h3>This role may be for you if:</h3><ul><li><p>You possess a strong science background with deep knowledge of Oncology</p></li><li><p>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</p></li><li><p>You can successfully collaborate with and provide input/feedback to all functions within the project team</p></li><li><p>You can balance/lead multiple projects simultaneously</p></li><li><p>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</p></li></ul><p>To be considered for this opportunity, we expect you to have a bachelor’s degree required; Master’s degree or other advanced education/certification is a plus. Along with specialty pharmaceutical/biopharmaceutical experience, with a minimum of 8 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. You also have expertise in marketing strategies within the pharmaceutical industry. Ideally, you would have launch experience. You must be able to travel 60%-80% of time </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Device Development & Secondary Packaging]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45549]]></requisitionid>
    <referencenumber><![CDATA[R45549]]></referencenumber>
    <apijobid><![CDATA[r45549]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45549/manager-device-development-secondary-packaging/]]></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 Manager, Combination Product Development, to join our Process Sciences—Drug Product Engineering team. In this role, you will lead the device product development group with a focus on secondary packaging, driving the development and advancement of drug delivery devices that address emerging needs across Regeneron’s product pipeline. </p><p>As a Manager, Combination Product Development a typical day might include the following: </p><ul><li>Own technical performance for a team delivering off the shelf and custom secondary packaging solutions for regulatory and commercial needs. </li></ul><ul><li>Ensure technically robust packaging via engineering analyses, reliability, and performance assessments. </li></ul><ul><li>Define design inputs and rationales; translate requirements into clear technical specifications. </li></ul><ul><li>Collaborate with suppliers to develop and qualify packaging design outputs. </li></ul><ul><li>Oversee product characterization and Design Verification testing connected to packaging. </li></ul><ul><li>Author protocols and technical reports to support development milestones. </li></ul><ul><li>Define essential performance requirements and traceability to design outputs. </li></ul><ul><li>Establish development control strategies, including statistically based, risk driven sampling plans. </li></ul><ul><li>Support regulatory filings (IND, BLA, MAA) for drug products. </li></ul><ul><li>Lead and develop a cross functional engineering team; recruit, coach, and grow talent. </li></ul><ul><li>Manage multiple projects to deliver on time, in scope, and within budget. </li></ul><ul><li>Partner with peer managers to ensure program success; escalate and resolve technical risks quickly. </li></ul><ul><li>Build strong interfaces with internal design, QA, external manufacturing, and broader engineering teams. </li></ul><ul><li>Champion design controls and technical excellence across IOPS. </li></ul><ul><li>Build organizational standards and systems to scale development for a growing product portfolio. </li></ul><ul><li>Define and integrate standard design and development procedures with Regeneron business and quality systems. </li></ul><ul><li>Identify and implement improvements to streamline device product development and cross team interfaces. </li></ul><ul><li>Represent the combination product device development group at industry forums. </li></ul><ul><li>Monitor evolving regulations, standards, and best practices. </li></ul><ul><li>Develop and maintain relationships with vendors, partners, and key opinion leaders. </li></ul><p>This role might be for you if you: </p><ul><li>Possess strong technical writing and oral communication skills. </li></ul><ul><li>Have experience with secondary packaging product design including cartons, carton inserts, blister trays and Tyvek lids, product and package labeling. </li></ul><ul><li>Enjoy developing, mentoring and coaching a team. </li></ul><ul><li>Have experience with different common secondary manufacturing technologies for secondary packaging and labeling. </li></ul><ul><li>Have experience with tolerance and mechanical stack analysis and other engineering analysis tasks. </li></ul><ul><li>Have knowledge and experience utilizing design of experiments or other problem-solving methodologies during product development. </li></ul><p>To be considered for the Manager, Combination Product Development you must be willing and able to work Monday- Friday, 8am-4:30pm and travel occasionally. You must have a B.S in Biomedical Engineering, Mechanical Engineering, Chemical Engineering or related field. For various levels you must have the following: </p><ul><li>Associate Manager Combination Product Development: 6+ years of relevant experience </li></ul><ul><li>Manager Combination Product Development: 7+ years of relevant experience </li></ul><p>Previous experience within packaging & combination product development is preferred. Previous people leadership/ supervisory experience is required. Level is determined based on qualifications relevant to the role. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 13:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Digital Lab Orchestration]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45569]]></requisitionid>
    <referencenumber><![CDATA[R45569]]></referencenumber>
    <apijobid><![CDATA[r45569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45569/associate-director-digital-lab-orchestration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Associate Director of Digital Lab Orchestration you will be responsible for leading designing, integrating, and deploying the orchestration layer that connects QC laboratory systems into a cohesive, compliant, and automated ecosystem. This role bridges QC operations, IT/OT, automation, and data governance to enable end-to-end digital QC workflows.</p></div><div><div><div><div><p>As an Associate Director, a typical day might include the following:</p><ul><li>Lead the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Enable automated sample lifecycle management, test execution, result capture, review, and release.</li><li>Support real-time and near-real-time data flow from lab instruments to enterprise systems.</li><li>Assist in annual IT budgeting, vendor negotiations, and resource allocation.</li><li>Ensure integrations comply with GxP, ALCOA+, 21 CFR Part 11, Annex 11 and data integrity requirements.</li><li>Partner with Quality and CSV teams to support validation strategies (risk-based, CSA where applicable).</li><li>Ensure auditability, traceability, and controlled change management.</li><li>Act as the primary integration point between QC, IT, automation, and external vendors.</li><li>Evaluate vendor platforms and integration tools for orchestration capabilities.</li><li>Lead technical discussions with system integrators and software suppliers.</li><li>Support incident resolution, root cause analysis, and continuous improvement.</li><li>Make decisions on integration patterns and drive a connected lab progression in 2026 and beyond</li><li>Ensure resiliency is incorporated into our architecture- as we move into a connected lab platform.</li></ul><p>This role may be for you if you have:</p><ul><li>Knowledge of integration technologies: REST APIs, middleware/iPaaS, message brokers, ETL.</li><li>Familiarity with orchestration/workflow engines.</li><li>Understanding of lab instrument connectivity and data flows.</li><li>Experience with cloud and/or hybrid architectures (AWS, Azure, or similar).</li><li>Industry experience implementing Lab orchestration including Scitara, Tetra Science, or any other emerging tools.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and </p><ul><li>Senior Manager: 8+ years industry experience in Information Systems and Technology or equivalent combination of education and experience. 6 of those years should be in managing employees and budgets, with 5+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment.</li><li>Associate Director: 10+ years industry experience in Information Systems and Technology or equivalent combination of education and experience. 8 of those years should be in managing employees and budgets, with 7+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment. </li><li>Experience with IT Compliance guidelines including PICS, CFR21 Part 11, Annex 11 and GAMP preferred.</li></ul></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor, Integrated Product Development Laboratories]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46489]]></requisitionid>
    <referencenumber><![CDATA[R46489]]></referencenumber>
    <apijobid><![CDATA[r46489]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46489/supervisor-integrated-product-development-laboratories/]]></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 seeking a Supervisor for the Integrated Product Development Laboratories to join our Process Sciences Drug Product Engineering department. They will oversee the packaging and labeling development laboratory spaces and equipment, drive commissioning and qualification efforts, and coordinate equipment activities to achieve organizational and regulatory objectives while leading a team of Engineering Technicians.</p><p>As a Supervisor, Integrated Product Development Laboratories, a typical day might include the following:</p><ul><li>Lead, coach, and develop a team of technicians supporting laboratory operations</li><li>Ensure laboratory compliance with Regeneron training requirements and GxP standards</li><li>Maintain laboratory infrastructure (facilities, utilities) and operational assets (equipment, instruments, software, documentation)</li><li>Drive continuous process improvement to enhance performance, reliability, and throughput</li><li>Manage relationships with internal stakeholders and external vendors/service providers</li><li>Help shape strategy and establish KPIs/metrics to measure effectiveness and compliance</li><li>Provide day-to-day leadership, direction, and performance management to direct reports</li><li>Develop equipment commissioning related documentation </li></ul><p>This role might be for you if you :</p><ul><li>Have experience with packaging equipment (vibration tables, drop testers, shakers etc.)</li><li>Excel at technical writing and clear, concise verbal communication</li><li>Manage projects and timelines, including coordination with external vendors</li><li>Demonstrate unwavering integrity, honesty, and transparency</li><li>Lead teams and take accountability for performance and results</li><li>Navigate ambiguity and translate it into clear, actionable plans</li></ul><p>To be considered for the Supervisor Integrated Product Development you must have willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS in Life Sciences, packaging science/engineering is preferred and 5+ years of relevant experience; or equivalent combination of education and experience. Previous people leadership/supervisory experience is required. Experience in combination products or medical devices is preferred. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 11:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Associate, PAPD Operations]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47143]]></requisitionid>
    <referencenumber><![CDATA[R47143]]></referencenumber>
    <apijobid><![CDATA[r47143]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47143/process-development-associate-papd-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>Regeneron, located in Tarrytown, NY, is seeking a Process Development Associate to support project management, technology transfer, and business operations for Regeneron Advanced Therapy Programs. This representative will work in the Advanced Therapy Project Management (AT-PM) group within Product, Analytical, and Process Development Operations (PAPD Ops) to help drive successful development and tech transfer of advanced therapies (e.g., AAV, bioconjugates, and synthetic chemistry programs) by enabling clear cross-functional ways of working, disciplined planning, and operational excellence with our internal partners and Contract Development & Manufacturing Organizations (CDMOs).</p><h3><strong>A Typical Day in This Role Might Look Like:</strong></h3><ul><li><p>Lead cross-functional teams to complete process transfer and establish production processes at Contract Development & Manufacturing Organizations (CDMOs). Help ensure successful start-up and execution of manufacturing campaigns by driving team alignment, tracking deliverables, and escalating risks/issues as needed.</p></li><li><p>Own effective, accurate, and timely communication across functional areas within project/program teams. Serve as a primary point of contact for project status, decisions, and next steps, ensuring stakeholders have clear visibility to scope, timelines, and key risks.</p></li><li><p>Build and maintain integrated timelines for development and transfer activities, including assumptions, dependencies, and critical path.</p></li><li><p>Anticipate and address risks to manufacturing readiness related to process, documentation, training, and supply/logistics.</p></li><li><p>Lead recurring and ad-hoc technical forums to troubleshoot issues, drive decision-making, and capture lessons learned to improve future development and tech transfers across modalities.</p></li><li><p>Contribute to continuous improvement efforts to streamline and standardize AT-PM ways of working (templates, trackers, dashboards, and reference guides).</p></li><li><p>Partner with procurement and internal stakeholders to support CDMO engagement activities (e.g., RFPs, contracting coordination, and invoices) and help maintain a healthy vendor network to meet pipeline capacity/capability needs.</p></li></ul><h3><strong>This Role Might Be For You If:</strong></h3><ul><li><p>You take initiative, follow through on commitments, and enjoy working in a fast-moving environment with evolving priorities.</p></li><li><p>You enjoy coordinating across functions (technical and non-technical) and can balance independent work with team-based execution across multiple projects.</p></li><li><p>You have strong planning and organizational skills and are comfortable leading meetings, aligning on next steps, and driving closure on open actions.</p></li><li><p>You proactively identify risks/roadblocks, communicate tradeoffs, and know when and how to escalate to keep programs on track while maintaining strong partner relationships.</p></li></ul><p>This role requires a BS in Chemical Engineering, Biochemical Engineering, Bioengineering, Biotechnology, Biochemistry, Biology, or Chemistry with an interest in Operations, Project Management, and Business, and 0–2 years of relevant experience in the biotechnology or pharmaceutical industry (internship/co-op experience may be considered). A strong customer-service mindset is essential. The ideal candidate can facilitate team collaboration, build and maintain clear project plans, and help design and improve repeatable business processes. Familiarity with cross-functional CMC concepts (e.g., process development, analytics, documentation readiness, and tech transfer to CDMOs) is preferred. Prior experience or knowledge of bioconjugation, gene therapy/AAV, or related advanced therapy process development is a plus.</p><p>If applicable, candidates may include GPA on their resume.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 13:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Corporate Finance]]></title>
    <date><![CDATA[Fri, 01 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45950]]></requisitionid>
    <referencenumber><![CDATA[R45950]]></referencenumber>
    <apijobid><![CDATA[r45950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45950/associate-manager-corporate-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Corporate Finance is seeking an Associate Manager to join the team and support enterprise-level financial planning, forecasting, and reporting. This role operates at the center of FP&A and requires strong financial judgment, ownership of complex analyses, and the ability to partner effectively across Finance and with senior stakeholders.</p><p><br> </p><p>The Associate Manager will independently own key corporate finance deliverables and models, support cross-functional partners, and contribute to leadership and Board-level materials. This position is well-suited for a high-performing individual contributor who is comfortable operating with limited direction while exercising sound financial judgment.</p><div></div><p><strong>A Typical Day in This Role Might Look Like</strong></p><ul><li><p>Execute key corporate finance deliverables, including Board presentations, the annual budget, monthly finance package, quarterly earnings support materials, and quarterly financial guidance packages</p></li><li><p>Serve as an owner of core corporate financial models, ensuring accuracy, consistency, and appropriate controls across budgeting, forecasting, and reporting cycles</p></li><li><p>Lead forecasting of key corporate inputs, including people expense, stock-based compensation, royalty income, amortization related to transactions, fully diluted share count, and free cash flow</p></li><li><p>Partner with functional finance teams to review forecast-to-forecast and actual-to-forecast variances, identify key drivers, and communicate implications to leadership</p></li><li><p>Work closely with Accounting to incorporate quarterly actuals, align on Non-GAAP adjustments, and ensure appropriate accounting treatment of transactions and collaborations is reflected in corporate forecasts</p></li><li><p>Collaborate with Tax to prepare quarterly legal-entity financials used in forecasting the effective tax rate</p></li><li><p>Partner with Treasury to prepare cash flow statements and forecast equity-related activity, including stock options, restricted stock, and share repurchases</p></li><li><p>Prepare ad hoc financial analyses and executive-ready presentation materials for the Leadership Team and Board of Directors</p></li><li><p>Identify and implement opportunities to improve forecasting processes, models, and standard deliverables, contributing to efficiency, consistency, and clarity across Corporate Finance</p></li><li></li></ul><div></div><p><strong>This Role May Be for You If You</strong></p><ul><li><p>Demonstrate strong decision quality and are comfortable making, explaining, and defending assumptions in situations involving ambiguity</p></li><li><p>Can independently own complex analyses and operate effectively with limited direction</p></li><li><p>Are comfortable interacting with and presenting to senior management</p></li><li><p>Balance speed and precision while managing competing priorities and tight deadlines</p></li><li><p>Communicate complex financial information clearly and concisely, both in writing and in presentations</p></li><li><p>Produce accurate, well-structured, executive‑-ready‑ analyses and presentation materials</p></li><li><p>Act as a finance advisor to cross-functional stakeholders, providing clear analysis and recommendations</p></li></ul><div></div><p>This role requires a BS in Finance, Accounting, Economics, or a related field; MBA, CPA, or CFA preferred. 5–7+ years of progressive, relevant experience in corporate finance, FP&A, investment banking, equity research, or a related analytical role is preferred. Advanced Excel‑based financial modeling capabilities required. Demonstrated experience owning integrated financial models supporting budgeting, forecasting, and strategic analysis preferred. Strong analytical, critical thinking and problem-solving skills and experience with financial systems; Hyperion experience strongly preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 01 May 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager - IT Applications Lab Systems]]></title>
    <date><![CDATA[Sun, 26 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47002]]></requisitionid>
    <referencenumber><![CDATA[R47002]]></referencenumber>
    <apijobid><![CDATA[r47002]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47002/manager-it-applications-lab-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Manager - IT Applications Lab Systems position leads the Laboratory Systems team within the Information Technology function and is responsible for managing the system lifecycle development, maintenance and compliance activities for Laboratory software systems in our QC, Chemistry, Micro and Virology labs. These systems include but are not limited to bench top computer systems and instrument software such as Endoscan V, SoftMax Pro and DataPro2.</p></div><div><div><div><div><div><div><div><div><div><p>As a Manager, a typical day might include the following,</p><ul><li>Manages team responsible for local operations, system administration and enhancements of bench top computer systems and instrument software such as Endoscan V, SoftMax Pro and DataPro2.across the Rensselaer site.</li><li>Supervises the Lab Systems team including performance management and people development activities.</li><li>Work with business teams and IT leadership to help develop strategy for a growing organization and team.</li><li>Technical coach and mentor for resources in their direct organization.</li><li>Coordinates the needs of functional departments and establishes priorities for Laboratory Systems requirements gathering, system design and implementation.</li><li>Develops and revises methods, record keeping, policies and procedures for Laboratory Systems in compliance with regulations and guidance.</li><li>Investigates and resolves computer software and IT hardware issues with QC instrumentation.</li><li>Collaborates with relevant QA organizations to ensure validated QC computers and software are maintained in a validated state.</li><li>Implements change control following established procedures.</li><li>Supports validation of Laboratory following SDLC design methodology.</li><li>Performs related duties as assigned.</li><li>Supports and prepare the teams for regulatory and internal audits.</li></ul><p>This role may be for you if you:</p><ul><li>Recognize the importance of ALCOA+ principles and Data Integrity in Bio-pharmaceutical production, should display a high level of integrity in the performance of his/her work.</li><li>Passionate about quality / right first time.</li><li>Organized and good documentation skills.</li><li>Proven ability to support Applications in a highly regulated environment.</li><li>Knowledge of cGMP, GAMP, 21 CFR Part 11, Annex 11.</li><li>Knowledge of helpdesk ticketing systems such as Service Now advantageous.</li><li>Knowledge of Regulatory Asset Manager Systems advantageous.</li><li>Excellent written and oral communication skills.</li><li>Good IT skills and knowledge of standard software packages (e.g., Microsoft Word, Excel, Teams etc.,).</li><li>Possess excellent customer facing skills allowing comfortable traversing of cross departmental levels.</li><li>Ability to think analytically and learn quickly.</li><li>Manage Operational budgets.</li><li>ITIL certified.</li><li>Project Management trained.</li></ul><p>In order to be considered for this position, you must hold a Bachelor's degree in Information Technology, Science/Engineering, Computer Science or related field and</p><ul><li>Associate Manager: 6+ years of experience, 2+ years of managing teams.</li><li>Manager: 7+ years of experience, 3+ years of managing teams.</li><li>GMP Laboratory/IT setting preferred.</li><li>May consider experience in lieu of education. Level is determined based on qualifications relevant to the role.</li></ul></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>$92,200.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 27 Apr 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Operations (FTC) – Toronto]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47104]]></requisitionid>
    <referencenumber><![CDATA[R47104]]></referencenumber>
    <apijobid><![CDATA[r47104]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/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>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 16:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Product MSAT Engineer]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46803]]></requisitionid>
    <referencenumber><![CDATA[R46803]]></referencenumber>
    <apijobid><![CDATA[r46803]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46803/drug-product-msat-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role The Drug Product (DP) Manufacturing Science and Technology (MSAT) Engineer supports equipment selection, CMO selection strategy, management of equipment qualification and 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 off-site manufacturing, reviews process data to ensure operational consistency after the processes are successfully transferred and provides support for investigations.</p><p><strong>As a Drug Product MSAT Engineer, a typical day might include the following:</strong></p><ul><li>Providing drug product manufacturing process knowledge for new product introduction, technology transfer, process troubleshooting and issue resolution</li><li>Acting as the technical lead, with the support of cross-functional teams, for technology transfer of the drug product manufacturing processes to manufacturing facilities</li><li>Tracking and reporting project milestones related to raw material/component procurement, equipment readiness, analytical process transfer, manufacturing document creation, etc</li><li>Reviewing and approving cGMP batch documentation (e.g. master batch records, component specifications, validation protocols, material specifications, etc.) required to support cGMP production at manufacturing facilities</li><li>Assisting with investigation and root cause determination and identifies/implements CAPA for manufacturing deviations</li><li>Trending process performance and collaborates with internal and external teams to establish/improve process capability to ensure process is operating within intended process control strategy and within cGMP operations</li><li>Authoring policies, technical reports/protocols, change controls, etc. in support of cGMP activities</li><li>Supporting development of sampling plans for GMP batches related to lot release, stability and characterization</li><li>Assisting in equipment selection, qualification and start up activities.</li><li>Working with manufacturing to ensure robust procedures are utilized for operation of equipment</li><li>Partnering with Strategic Sourcing/Procurement to specify technical requirements associated with raw materials, components, equipment and services to ensure external vendor on time delivery</li><li>Maintaining required training status on Regeneron specific work instructions and SOPs</li></ul><p>To be considered for this role you should have a BS/BA in engineering and 2 years of experience in a pharmaceutical / biologics cGMP environment or equivalent combination of education and experience. Travel to contract manufacturers or business partners, as required, up to 25-50%.</p><p><strong>Education and Experience:</strong></p><ul><li>Associate Engineer: Minimum 0–2 years of experience</li><li>Engineer: Minimum 2 years of experience</li></ul><p>#LI-Onsite #JOBSIEST #IRELIM #REGNIEEC </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Site Office Manager]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46900]]></requisitionid>
    <referencenumber><![CDATA[R46900]]></referencenumber>
    <apijobid><![CDATA[r46900]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46900/site-office-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for an Office Manager who will play a central role in keeping our office running smoothly and supporting a positive, well-organised workplace. In this role, you’ll coordinate day‑to‑day office operations, working closely with teams such as HR, IT, Facilities, and Communications to ensure employees have everything they need to work safely and effectively. You’ll help create an environment where people can focus on what they do best, while contributing to a collaborative and efficient workplace.</p><h3>A Typical Day:</h3><ul><li><p>Coordinating office operations to ensure a safe, functional workplace</p></li><li><p>Liaising with HR, IT, Facilities, and other internal teams</p></li><li><p>Managing vendors, purchase orders, and supplier relationships</p></li><li><p>Overseeing office supplies, inventory, and general facilities needs</p></li><li><p>Supporting health, safety, and emergency preparedness activities</p></li><li><p>Organising repairs, maintenance, and workplace improvements</p></li><li><p>Assisting with onboarding logistics and equipment coordination</p></li><li><p>Preparing meeting notes and supporting site communications</p></li></ul><h3>This Role May Be For You:</h3><ul><li><p>Enjoy creating organised, efficient workplace environments</p></li><li><p>Like working across teams and coordinating multiple stakeholders</p></li><li><p>Are comfortable managing vendors and external service providers</p></li><li><p>Take ownership of practical tasks that support a whole office</p></li><li><p>Stay calm when handling multiple requests and shifting priorities</p></li><li><p>Enjoy improving spaces and finding better ways to work</p></li></ul><p>To be considered, you should have a minimum of 2–3 years’ experience in a similar role and a secondary education qualification (or equivalent), with further education preferred; relevant experience may be considered in place of formal education. A good level of English alongside the local language is required. You should also have solid technical proficiency with tools such as Microsoft Office (Outlook, Word, Excel, PowerPoint, Teams, SharePoint) and familiarity with office systems; experience with purchase order systems (e.g. Oracle) is an advantage</p><p><br></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 05:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist, Antibody Engineering - Oligonucleotide Delivery]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46985]]></requisitionid>
    <referencenumber><![CDATA[R46985]]></referencenumber>
    <apijobid><![CDATA[r46985]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46985/senior-scientist-antibody-engineering-oligonucleotide-delivery/]]></url>
    <company><![CDATA[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 skilled and motivated Senior Scientist to join our research team focused on innovative oligonucleotide therapeutics strategies. The Senior Scientist will lead projects to develop novel oligonucleotide delivery methods and optimize approaches for oligonucleotide therapeutics quantification across diverse biological matrices; will collaborate across multidisciplinary teams and participate in strategic planning. Responsibilities include mentoring junior scientists, managing laboratory resources, and preparing scientific reports and presentations.</p><p>The ideal candidate will have a solid base in molecular biology, nucleic acid technologies, and antibody engineering, with a consistent track record to drive innovation in oligonucleotide-related fields. This role offers the chance to create impactful discoveries in oligonucleotide-based therapeutics.</p><p><strong>In this role, a typical day might include the following:</strong></p><p>· Developing and applying in vitro and in vivo strategies to improve oligonucleotide delivery efficiency; evaluating and optimizing delivery modalities (e.g., conjugates, nanoparticles); assessing uptake and target gene knockdown in relevant cellular and animal models; troubleshooting delivery barriers; and integrating pharmacokinetic and bio-distribution data with chemistry and in vivo teams to refine approaches.</p><p>· Designing and implementing in vitro and in vivo oligonucleotide tracing for advanced detection and analysis; collaborating on labeling techniques (e.g., fluorescent, radioactive, enzymatic tags); establishing sensitive detection protocols; analyzing tissue and cellular distribution; applying quantitative assays to monitor oligonucleotide fate and function; and interpreting complex data to inform therapeutic development.</p><p>· Exploring new directions in oligonucleotide technology development, including novel chemical modifications, targeting strategies, and combination therapies; staying current with advancements; proposing innovative project ideas; conducting proof-of-concept experiments; and collaborating with cross-functional teams to translate findings into next generation platforms.</p><p><strong>This job might be for you if you:</strong></p><p>· Have validated ability to lead research projects, mentor junior scientists, and work effectively within multidisciplinary teams.</p><p>· Are skilled in preparing scientific reports, presentations, and publications, with strong written and verbal communication abilities.</p><p>· Are a creative problem solver with a track record of proposing and implementing novel solutions in oligonucleotide therapeutics and related fields.</p><p>· Have hands-on experience with mammalian cell culture and working with preclinical animal models for evaluating oligonucleotide delivery and efficacy.</p><p><strong>In order to be considered for this role, you must have:</strong></p><p>- A PhD - Molecular biology, biochemistry, or related field.</p><p>- Research experience in genetics medicine.</p><p>- Validated experience and strong proficiency in molecular biology methods, including PCR, qPCR, cloning, and nucleic acid purification; as well as experience in troubleshooting and optimizing protocols.</p><p>- Consistent record of strong analytical and quantitative skills, with expertise in quantitative assays (e.g., ELISA, digital PCR, fluorescence-based detection) for analyzing oligonucleotides and proteins in biological samples.</p><p>Good understanding in RNAi technologies, experience with optimizing delivery of RNAi molecules to target cells, evaluating knockdown efficiency; familiarity with in vitro and in vivo models to study RNAi-mediated gene regulation, quantitative assays to measure gene expression changes; and experience/skills in protein engineering, particularly in designing and modifying antibodies for improved specificity and affinity are highly preferred.</p><p>Experience with antibody-drug conjugates (ADCs), bispecific antibodies, and other formats used for targeted delivery of therapeutics, and understanding of strategies to link antibodies to oligonucleotides or nanoparticles for enhanced cellular uptake and tissue targeting are a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager R&D Finance]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47472]]></requisitionid>
    <referencenumber><![CDATA[R47472]]></referencenumber>
    <apijobid><![CDATA[r47472]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47472/associate-manager-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>Regeneron's Program Finance group is looking for an energetic <strong>Associate Manager R&D Finance</strong> to become an integral part of the Program Finance team. Program Finance is responsible for development programs within assigned 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 clinical trial and regulatory budget planning and forecasting and maintain a solid command of all aspects of programs.</p><p><strong>This role is based at Regeneron's offices in Sleepy Hollow, NY or Warren, NJ (4 days a week onsite.) We do offer shuttle services from NYC as well as the train station.</strong></p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Own and lead the Financial Reporting and Analysis 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</p></li><li><p>Support clinical teams with building detailed budges for clinical trials, and track and monitor clinical trial financials through study completion.</p></li><li><p>Translate operational components of development plans to detailed forecasts for internal and external clinical costs and load into Hyperion</p></li><li><p>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</p></li><li><p>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</p></li><li><p>Perform ad hoc projects and financial analyses to solve business problems and effectively communicate findings and recommendations to senior management and other stakeholders</p></li></ul><p><strong>This Role May Be For You If You:</strong></p><ul><li><p>Implement best practices to drive efficient management across areas of focus</p></li><li><p>Develop detailed and accurate financial forecasts and deliver other financial reviews as required</p></li><li><p>Can readily identify and update assumptions incorporated in forecasts/budgets to reflect the latest information and works closely subject matter experts to test all assumptions</p></li><li><p>Use a repertoire of financial analyses to support decision making and to validate that budgets are based on realistic assumptions</p></li></ul><p><strong>To be considered for this role</strong>, you must have a BS in a business or quantitative field with 6-8+ years’ experience with forecasting, budgeting and/or business partnering ideally in a science or research-driven environment. MBA/CPA/CFA a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 19:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Finance]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45804]]></requisitionid>
    <referencenumber><![CDATA[R45804]]></referencenumber>
    <apijobid><![CDATA[r45804]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45804/director-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p><strong>About Regeneron</strong> </p></div><div><p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. </p></div><div></div><div><p>As a Finance Director you will serve as the Finance Partner for India and act as a key interface with global CFO functions. You will lead critical planning and forecasting, drive performance insights, ensure governance, and support strategic decisions that enable our business outside the US to scale.</p></div><div><p><strong>This position is office-based and will be on site at Regeneron’s Hyderabad office.</strong> </p></div><div></div><div><p><strong>A typical day may include the following: </strong> </p></div><div><ul><li><p>Serve as the Finance Partner for India, contributing to leadership discussions and business planning </p></li></ul></div><div><ul><li><p>Provide forward-looking insights that influence decisions on cost, growth, resourcing, and profitability </p></li></ul></div><div><ul><li><p>Act as the local steward for governance and compliance related to CFO policies and controls </p></li></ul></div><div><ul><li><p>Lead country-level budgeting and forecasting, including system submission and management presentations </p></li></ul></div><div><ul><li><p>Drive Actuals vs Forecast variance analysis with actionable recommendations </p></li></ul></div><div><ul><li><p>Implement tools and handle resource planning/FTE utilization across programs and cost centers </p></li></ul></div><div><ul><li><p>Partner with Accounting to review legal entity financial data and financial documents, ensuring accuracy and clarity </p></li></ul></div><div><ul><li><p>Liaise with Treasury to ensure local operations are adequately funded; provide cash forecasts </p></li></ul></div><div><ul><li><p>Coordinate with Tax on annual filings, ensuring accurate inputs for calculations and forecasts </p></li></ul></div><div><ul><li><p>Support broader ex-US consolidation and above-country finance planning and analysis as required </p></li></ul></div><div><p><strong>This job may be for you if you have:</strong> </p></div><div><ul><li><p>Strong expertise in forecasting, budgeting, governance, and business partnering </p></li></ul></div></div><div><div><ul><li><p>A proven ability to operate in ambiguity, influence stakeholders, and drive outcomes proactively </p></li></ul></div><div><ul><li><p>Executive communication skills — able to translate numbers into decisions </p></li></ul></div><div></div><div><p>To be considered for this role you must have 12+ years post-qualification experience in Finance leadership, ideally within the biotech/pharma industry, or Shared Service/Global Capability environment. You will have a relevant undergraduate degree; with MBA/CA/CMA/CPA or equivalent preferred. You will be proficient in English & local language. </p></div><div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Manager QA (Visual Inspection, Packaging& Labeling)]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46659]]></requisitionid>
    <referencenumber><![CDATA[R46659]]></referencenumber>
    <apijobid><![CDATA[r46659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46659/sr-manager-qa-visual-inspection-packaging-labeling/]]></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 seeking a Sr Manager Quality Assurance to join our internal QA Drug Product Manufacturing team. This role is responsible for the quality floor oversight of the finish (i.e. visual inspection, assembly, labeling, and packaging) operations and visual inspection qualification program for SA13.</p><p>As a Sr. Manager QA, a typical day might include the following:</p><ul><li><p>Provide leadership to multiple teams under your supervision, including being responsible for:</p><ul><li><p>AQL of inspection, assembly, and packaging activities</p></li><li><p>Quality Oversight of all finish operations</p></li><li><p>Qualification of all visual inspection operators (including manufacturing, quality, and QC)</p></li></ul></li><li><p>Responsible for programs that support the department, for example: in-process reject management</p></li><li><p>Support development and growth of team, including your people leaders</p></li><li><p>Leadership point of contact for escalation of events, process updates, etc.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven leadership in cGMP environments, including experience speaking and preparing for regulatory inspections and audits</p></li><li><p>Strong collaboration and communication cross-functionally</p></li><li><p>Ability to think critically, and continuously improve processes</p></li><li><p>Ability to lead a department through a fast-paced and dynamic environment</p></li></ul><p>Gowning and Environment </p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </p></li></ul><p>To be considered for the Sr. Manager Quality Assurance you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Life Sciences or related field and 8+ years of experience. Experience in fill/finish manufacturing is preferred. Previous supervisory/ people leadership experience is required. May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Pulmonology, Marketing (HCP)]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47356]]></requisitionid>
    <referencenumber><![CDATA[R47356]]></referencenumber>
    <apijobid><![CDATA[r47356]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47356/associate-director-pulmonology-marketing-hcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of HCP Marketing will lead healthcare professional marketing strategy and execution for Asthma indications in the U.S. This highly visible role requires a forward-looking individual with deep marketing expertise and the ability to navigate complex alliance partnerships. The Associate Director will partner closely with cross-functional and alliance teams to advance the products growth, contribute to the brand's financial success, and strengthen its leadership position in Pulmonology. This position reports to the Director, Pulmonology HCP Marketing.</p><p><strong>A Typical Day Might Look Like:</strong></p><ul><li><p>Leading the HCP marketing strategy for the Asthma indication, ensuring full integration with the broader brand strategy.</p></li><li><p>Acting as a key advocate for the brand strategy, clearly articulating priorities and ensuring alignment across Regeneron, Sanofi, and other critical stakeholders.</p></li><li><p>Overseeing the development of HCP engagement strategies, messages, and tactical campaigns tailored to Pulmonologists and Advanced Practice Providers.</p></li><li><p>Building and deploying a competitive market strategy that proactively addresses evolving competitors and market dynamics.</p></li><li><p>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.</p></li><li><p>Ensuring all marketing programs comply with corporate policies, regulatory/ethical frameworks, and alliance standards.</p></li><li><p>Tracking and managing marketing spend, timelines, and deliverables to meet budget, scope, and performance expectations.</p></li></ul><p><strong> </strong></p><p><strong>This Role Might Be For You If You:</strong></p><ul><li><p>Combine strategic and scientific acumen with an ability to translate insights into actionable marketing strategies.</p></li><li><p>Have a proven track record of leadership and influence across organizational levels.</p></li><li><p>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.</p></li><li><p>Excel in execution and project management within a fast-paced, dynamic, and competitive marketplace.</p></li><li><p>Demonstrate organizational agility, adapting priorities and strategies to external market shifts or internal dynamics.</p></li><li><p>Thrive in cross-functional and alliance settings, effectively shaping collaboration, alignment, and decision-making.</p></li><li><p>Possess strong experience in managing agencies and external partners, ensuring creative excellence and accountability.</p></li><li><p>Are disciplined in managing budgets and resources aligned to strategic objectives.</p></li></ul><p><strong> </strong></p><p>To be considered for the role, we expect you to have a Bachelor’s degree required; MBA strongly preferred. We are also seeking 10+ years of progressive experience in the pharmaceutical/biotech industry or related field and 8+ years of U.S. commercial experience in pharmaceutical/biotech marketing, product management, or related areas. It is preferred to have Respiratory and/or Immunology experience strongly preferred. Lastly, we expect you to be onsite in Sleepy Hollow, NY 4 days a week and willing to travel 30% of the time.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Biostatistician - General Medicine]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46406]]></requisitionid>
    <referencenumber><![CDATA[R46406]]></referencenumber>
    <apijobid><![CDATA[r46406]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46406/principal-biostatistician-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[<div><p>This position is for a qualified Statistician/Biostatistician to support Clinical Biostatistics within Global Development.</p><p><strong>A typical day might include:</strong></p><p>The incumbent will work with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. The incumbent will co-author clinical study protocols, statistical analysis plans, and perform statistical analyses for interim and final reports. The incumbent will also develop and deliver training to non-statistical colleagues, collaborate on development of new infrastructure and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and publications.</p><p><strong>This role might be for you if you can:</strong></p><ul><li><p>Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.</p></li><li><p>Develop individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis.</p></li><li><p>Collaborate with Statistical Programming on the programming of tables, figures and listings to support decision making and for regulatory reporting. </p></li><li><p>Evaluate appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</p></li><li><p>Analyze data and interprets results from clinical trials and of data from non-trial sources to facilitate program-level decision making. </p></li><li><p>Prepare presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management. </p></li><li><p>Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD or equivalent degree in statistics/biostatistics or related disciplines with internship experience, or MS degree in statistics/biostatistics with >5 years’ experience in the pharmaceutical industry as a statistician. </p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Expertise in statistical software such as R or SAS is required</p></li></ul></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>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Protein Expression Science]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47298]]></requisitionid>
    <referencenumber><![CDATA[R47298]]></referencenumber>
    <apijobid><![CDATA[r47298]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47298/associate-scientist-protein-expression-science/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an <strong>Associate Scientist</strong> to join the B cell Isolation Group in the Protein Expression Sciences department. You will be primarily responsible for the preparation and immunofluorescence staining of mouse splenocytes for the isolation of antibody expressing cells through <strong>fluorescence activated cell sorting</strong> (FACS). You will be working in the B Cell Isolation group, which is key to the Regeneron therapeutic pipeline. Through this platform, you will get exposure to different targets, giving you the opportunity to see a wide range of therapeutic focus areas. This is a lab-based role, with great opportunity to perform cutting-edge research, and great potential for growth.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li>Laboratory animal handling (mice) – splenectomy, lymphadenectomy, hind limb removal, post-mortem bleed collection</li><li>Single cell suspension preparation from organs (mouse spleen, lymph nodes, bone marrow)</li><li>Immunofluorescence cell staining</li><li>Analyzing flow cytometry data from stained samples</li><li>Isolating target cells through fluorescence activated cell sorting (FACS)</li><li>Immunofluorescence beads based binding affinity assay</li><li>Documentation of experimental procedures and results</li><li>Recording and organizing data in electronic notebook/database, Powerpoint and LIMS</li><li>Analyze data using tools such as <strong>FlowJo, Omiq, Microsoft Office, MacOS, and GraphPad Prism</strong></li><li>Periodic data presentation</li><li>Lab preparation, organization and resource acquisition</li><li>Collaborating and coordinating workflow intra and interdepartmentally to keep antibody discovery pipeline on track</li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li>Enjoy working in a collaborative and fast paced environment</li><li>Have a strong desire to develop your skills</li><li>Excel at maintaining experimental documentation, exhibit meticulous attention to detail</li><li>Have great oral and written communication skills, organizational skills, as well as good interpersonal skills</li><li>Are comfortable working in a dynamic environment where priorities can change from day to day</li><li>Self-starter with an ability to follow protocols, ask scientific questions, and adapt to evolving methods</li><li>Have an eye for detail and pride yourself on the quality of your work</li><li>Work on current problems while thinking of future solutions</li></ul><p>To be considered for this role, you must have a minimum of B.S. in Molecular Biology, Cellular Biology or related field with 2+ years of laboratory experience. We would like someone with cellular biology lab experience, and <strong>basic laboratory animal handling experiences (mice</strong>). Experiences with immunofluorescence-based techniques, immunofluorescence cell staining, and knowledge of immunology are preferred. Experience with flow cytometry is a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Pharmacy Support Services]]></title>
    <date><![CDATA[Thu, 14 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44682]]></requisitionid>
    <referencenumber><![CDATA[R44682]]></referencenumber>
    <apijobid><![CDATA[r44682]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44682/senior-manager-pharmacy-support-services/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Manager, Pharmacy Support Services</strong> (PSS) serves as a high‑impact subject matter expert in investigational product (IP) management and pharmacy operations across our clinical portfolio. In this role, you will guide best practices for IP handling, preparation, and administration; develop high‑quality pharmacy documentation and training; and support global clinical sites to ensure safe, compliant, and streamlined trial execution.</p><p>You will partner closely with Formulation Development Group (FDG), Clinical Operations, and CDSL leadership to shape strategy, improve processes, and directly influence the success of our trials. This is an opportunity to elevate your clinical and scientific expertise in a role that blends technical depth, operational leadership, and cross‑functional collaboration.</p><p><strong>A typical day in this role looks like: </strong></p><p><strong>Lead Pharmacy & Clinical Trial Support</strong></p><ul><li>Act as the primary SME on investigational product preparation, administration, blinding, and pharmacy‑related ancillary supplies.</li><li>Shape the development of pharmacy manuals, clinical study documents, and training materials supporting biologics and gene therapy programs.</li><li>Partner with Clinical Operations, CROs, and site pharmacy teams to ensure IP readiness, compliance with regulatory requirements, and optimal preparation workflows.</li></ul><p><strong>Drive Study Execution Excellence</strong></p><ul><li>Lead or contribute to Kick‑Off Meetings, Site Initiation Visits, Investigator Meetings, and IP‑focused training for global clinical teams.</li><li>Support the review and resolution of IP‑related deviations and practice‑based issues to maintain protocol integrity and patient safety.</li><li>Manage ancillary supply compatibility assessments in collaboration with FDG.</li></ul><p><strong>Uphold Quality, Compliance & Continuous Improvement</strong></p><ul><li>Provide guidance on IP‑related quality assurance issues and support risk mitigation strategies.</li><li>Ensure adherence to GCP, ICH guidelines, and federal/international regulatory standards.</li><li>Identify opportunities to enhance processes and elevate site experience through data‑driven improvements and feedback mechanisms.</li></ul><p><strong>Develop & Mentor Talent</strong></p><ul><li>Create engaging training modules for internal teams, monitors, and research sites.</li><li>Play a key role in onboarding new colleagues and fostering a culture of scientific excellence, collaboration, and shared knowledge.</li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Expertise in sterile product preparation and infusion‑based drug administration</li><li>Experience with biologics; cell and gene therapy exposure preferred</li><li>Strong understanding of clinical supply chains and clinical trial execution</li><li>Exceptional communication, documentation, and presentation skills</li><li>Ability to manage complex projects and influence cross‑functional teams</li><li>Adaptability, critical thinking, and a continuous‑improvement mindset</li><li>Familiarity with PCAB, FDA, USP <795>/<797>, NABP/VPP, and EU CTR guidelines</li><li>Strong analytical, decision‑making, and problem‑solving capabilities</li></ul><p><strong>In order to be considered qualified</strong>, a minimum of a bachelor’s degree in pharmacy or nursing with 8+ years of experience in hospital pharmacy, clinical research, or pharma/biotech. Or a PharmD with 6+ years of experience in hospital pharmacy, clinical research, or pharma/biotech.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Pharmacovigilance Hub]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47624]]></requisitionid>
    <referencenumber><![CDATA[R47624]]></referencenumber>
    <apijobid><![CDATA[r47624]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47624/director-pharmacovigilance-hub/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director, PV Hub to join our Patient Safety organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>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><strong>This role might be for you if can: ​</strong></p><ul><li><p>Maintain a comprehensive understanding of local legislation and Health Authority requirements and keep Worldwide Operations Office (WWOO) leadership informed of updates or changes to local requirements or processes (e.g., SOP addenda, safety communications, labeling updates, and local submission requirements) in alignment with country-specific regulatory requirements </p></li><li><p>Track local process status, changes, and risks to drive consistency and continuous improvement for hub’s geographic markets, including maintaining and monitoring via common tool (e.g., tracker, dashboard) </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Ensure country compliance with the global PV quality system, supporting inspections, audits, CAPAs, and timely resolution of deviations or non-compliance </p></li><li><p>Serve as local safety PoC to coordinate with global GPS (e.g., PV Enablement, CER, SS) and non-GPS (e.g., Med Affairs, Regulatory) teams to: </p></li><li><p>Guide and inform global teams on local requirements and ensure compliance with local legislations </p></li><li><p>Coordinate with other PV hub(s) as needed for contributions to activities and/or local documentation </p></li><li><p>Shape compliant programs that provide high quality adverse event reports </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum Bachelor’s Degree (Advanced Degree preferred) with 12+ years of PV experience and demonstrated achievements in patient safety</p></li><li><p>Experience supporting regulatory inspections, audits, and quality issue management at the country or regional level </p></li><li><p>Preferred experience with AI technologies </p></li><li><p>Ability to coordinate across functions and cultures, operating effectively as an execution and escalation lead rather than a policy owner </p></li><li><p>Strong organizational and communication skills, with the ability to surface local risks early and drive resolution through global governance channels </p></li></ul><p>#GDPSJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as 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[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44637]]></requisitionid>
    <referencenumber><![CDATA[R44637]]></referencenumber>
    <apijobid><![CDATA[r44637]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44637/associate-director-clinical-scientist-internal-medicine-cardio-metabolic-renal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Associate Director leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the Director Clinical Sciences, and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3><strong>As an Associate Director, a typical day may include the following: </strong></h3><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies proficient scientific expertise to propose, design, and complete clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal stakeholders</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Applies proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><h3>This role may be for you if:</h3><ul><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs.</p></li><li><p>Strong cross-functional management, interpersonal and problem-solving skills with a proven track in clinical trial process improvements.</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have ≥ 10 years of pharmaceutical clinical drug development experience. We are seeking experience in managing clinical trials in one or more of the following therapeutic areas – cardiovascular, renal, metabolic disease. Demonstrate proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills. Other levels considered depending on experience. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><p>(1 of 2)</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Market Access DACH (f/m/d)]]></title>
    <date><![CDATA[Sat, 14 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45066]]></requisitionid>
    <referencenumber><![CDATA[R45066]]></referencenumber>
    <apijobid><![CDATA[r45066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/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>This role has been created to provide end-to-end management of the HTA submissions and price negotiation in Germany, Switzerland & Austria for specific products and their indications, ensuring timely alignment on strategy with affiliate and global teams. As a Senior Manager Market Access, you will manage cross-functional input into the submission and negotiation strategy by working in conjunction with the medical and brand teams at an affiliate level and with market access and pricing at a global level. The role will manage cross-functional input into the submission and negotiation strategy by working in conjunction with the medical and brand teams at an affiliate level and with market access and pricing at a global level. </p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Working with Global and affiliate Market Access leads to ensure robust and timely submissions to HTA bodies in Germany, Switzerland & Austria Leading data analysis in areas of G-BA benefit assessment, access, pricing and contracting, and brand performance </p></li><li><p>Develop and align on a market access and pricing strategy for the medicine with the Affiliate Commercial Teams </p></li><li><p>Identifying and communicating payer needs effectively to local Market Access (for real-world evidence), HEOR and/or Medical Affairs to inform evidence-generation prioritization and content in order to develop Value Dossiers for the effective communication of the value of products, and submit critical Market Access requirements to the Affiliate Head of Market Access/Govt. Affairs </p></li><li><p>Inputting into strategic price-setting at a global level, supporting the local price negotiation process and identifying innovative solutions for market access, including innovative pricing / contracting arrangements with national payers </p></li><li><p>Supporting country to ensure each brand has appropriate market access plans in place to execute global strategy, in the context of local payer environment </p></li><li><p>Supporting and providing input to new indication or new product launches, assessing potential and payer value story, regulatory and label considerations </p></li><li><p>Preparing and developing KPIs and analytics, supporting country-level pricing review </p></li></ul><p><strong>This may be for you if you are: </strong></p><ul><li><p>Experienced in a Market Access role in the Pharma sector in multi-disciplinary, matrix and global context </p></li><li><p>Experienced in delivering HTA submissions </p></li><li><p>Have strong experience designing and implementing market access strategies and achieving exceptional results for product </p></li><li><p>Have a proven track record in developing and delivering compelling value propositions and access strategies </p></li><li><p>Able to demonstrate success in driving price execution to deliver optimal commercial return </p></li><li><p>Experienced in developing KPIs and dashboards, to support sustainable growth and performance </p></li></ul><p><strong>To be considered for this position</strong>, you are required to have: At least 5 years of experience in a Market Access role within the pharmaceutical industry. Strong knowledge of the German, Austrian & Swiss healthcare system and experience negotiating with Health Authorities. Expertise in Oncology is highly desirable, and you have to be comfortable in working in an international environment. A post-graduate qualification such as an MBA, MSc, or equivalent is preferred. Fluency in German & English is required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 14 Feb 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Procurement - Direct (Chemicals Category)]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41123]]></requisitionid>
    <referencenumber><![CDATA[R41123]]></referencenumber>
    <apijobid><![CDATA[r41123]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41123/director-global-procurement-direct-chemicals-category/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director, Global Procurement - Direct / Chemicals, with experience in end-to-end procurement strategies/processes and with proven successful global category execution in Raw Materials and Manufacturing Operations. Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led for 36 years by physician-scientists, Regeneron's unique ability to translate science repeatedly and consistently into medicine has led to numerous FDA-approved treatments and products in development, almost all of which were homegrown in Regeneron's laboratories.</p><p><strong>As the Director, Global Procurement - Chemicals a typical day may include:</strong></p><ul><li>Leading, defining, and implementing the global Raw Material / Chemicals Category strategy to serve global and regional business needs. Category may include Chemicals and/or other Raw Materials.</li><li>Manage a team of professional level employees responsible for performing category management tasks. Provide coaching and guidance on job performance and career development to direct reports.</li><li>Working closely with internal & external partners to lead discussions related to the Raw Material Categories and aligning the category priorities.</li><li>Leading negotiations, supplier management activities, and stakeholder engagement activities.</li><li>Driving value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</li><li>Representing Global Procurement by participating in organizational decisions in the Raw Material categories with critical short and long-term impact on the success, efficiency, growth, and results of the organization and company.</li><li>Leads category activities to ensure compliance with appropriate GxPs and other applicable regulations and proficiency on procurement technical skills among global procurement team.</li></ul><p><strong>This role might be right for you if you have:</strong></p><ul><li>Demonstrated knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support growth and evolution of programs as well as the knowledge to drive improvement across the category</li><li>Experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</li><li>Expertise in developing influential relationships with stakeholders and suppliers.</li><li>Led cross-functional teams to drive results in Raw Material categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</li><li>Expert insights and knowledge regarding rates, unit costs, and costing structures to enable optimal negotiations.</li><li>Ability to leverage external data sources, market information, and supplier engagement to constantly improve the intelligence / analytics of supply market dynamics.</li><li>Operate with integrity, focus, and clarity in an environment of ambiguity to drive change and improvement.</li></ul><p><strong>To be considered for this role you must possess </strong><strong>a bachelor's degree in a relevant field of study plus 15+ years of progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma. </strong><strong>Experience leading manager level professionals in a multi-national firm including writing performance reviews, setting annual objectives, coaching, and developing direct reports. Working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other) Ability to leverage standard business applications for communicating, presenting and analyzing (i.e. Word, Excel, PowerPoint)</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$169,600.00 - $282,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 06:56:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Production / Manufacturing Operations]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45601]]></requisitionid>
    <referencenumber><![CDATA[R45601]]></referencenumber>
    <apijobid><![CDATA[r45601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45601/production-manufacturing-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div>Within this role you will be working as part of the Manufacturing Team you will be performing tasks to support the manufacturing operations of both clinical and commercial manufacturing programs at Regeneron Ireland.</div></div></div><div><div><div><div><p><strong>Working a shift pattern in a fully gowned, cleanroom environment, a typical shift might include, but is not limited to, the following:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as advised by Team Leads and Supervisors</p></li><li><p>Ensuring all associated documentation such as manufacturing batch records & logbooks are completed, accurate and verified in accordance with SOPs and cGMP Standards</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Maintaining housekeeping in designated area and adhering to the hygiene standards of the facility</p></li><li><p>Ensuring all required training is up to date and completed in a timely manner</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You enjoy working in a team that brings out the best in each other</p></li><li><p>You like tackling problems that need solving, using your verbal and written communication skills to ask questions and adapt quickly</p></li><li><p>You can adhere to the letter and spirit of policies and regulations</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p>To be considered for this opportunity you must have a Leaving Certificate qualification to include math's and a science or engineering subject as a minimum or equivalent qualification. Experience working shift in a GMP (Good Manufacturing Practice) environment/industry is preferred</p><p>Our site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyle</p><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber / Car Valet</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p>#IREADV #JOBSIEST #LI-Onsite #REGNIEEC #REGNIELSM</p></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Sustaining Engineering]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44518]]></requisitionid>
    <referencenumber><![CDATA[R44518]]></referencenumber>
    <apijobid><![CDATA[r44518]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44518/manager-sustaining-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an experienced and strategic Combination Products Sustaining Engineer to manage a team in addition to monitor, investigate, maintain and/or improve the quality and performance of commercial combination products. They will provide comprehensive leadership in engineering product management, regulatory compliance (design controls), and cross-functional collaboration with internal and external stakeholders, for the maintenance of commercial products.</p><p>A typical day for a Manager Sustaining Engineering might include:</p><ul><li><p>Implementing design changes to improve the quality of existing products and/or the customer experience.</p></li><li><p>Assisting with customer complaint investigations to identify root cause.</p></li><li><p>Performing design change assessments for changes to existing products.</p></li><li><p>Maintaining Risk Management Files for existing products based on post marketing surveillance and manufacturing events.</p></li><li><p>Facilitating design transfer of existing products to new manufacturing sites.</p></li><li><p>Performing technical evaluations related to supplier and manufacturing changes.</p></li><li><p>Integrating identified product performance enhancements to new product development.</p></li><li><p>Providing technical guidance to sustaining engineers.</p></li><li><p>Participating in cross-functional design teams to address design issues.</p></li><li><p>Developing and maintaining key business partner relationships throughout Regeneron.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Understand relevant FDA regulations, particularly 21 CFR Part 3 and 21 CFR 820.30.</p></li><li><p>Have experience with design history file management (21 CFR 820.30).</p></li><li><p>Possess strong project management and interpersonal skills and strong analytical and problem-solving capabilities.</p></li><li><p>Can balance business objectives with technical constraints.</p></li><li><p>Can work effectively across multiple functional teams.</p></li><li><p>Seek out continuous improvements and collaborative opportunities to improve internal processes and stakeholder relationships.</p></li><li><p>Have strong technical writing and oral communication skills.</p></li><li><p>Targeted to have direct reports within the Sustaining Engineering organization, to support multiple combination products in commercial distribution.</p></li></ul><p>To be considered for the Manager Sustaining Engineering you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a B.S in Engineering; Biomedical Engineering, Mechanical Engineering, Industrial Engineering is preferred.. For various levels you must have the following:</p><ul><li><p>Associate Manager Sustaining Engineering: 6+years of relevant experience </p></li><li><p>Manager Sustaining Engineering: 7+ years of relevant experience</p></li></ul><p>Previous experience in manufacturing of medical devices and/or combination products is preferred. Previous supervisory/ people leadership experience is required. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$103,300.00 - $197,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor, Vivarium Operations - Cage Wash]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45952]]></requisitionid>
    <referencenumber><![CDATA[R45952]]></referencenumber>
    <apijobid><![CDATA[r45952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45952/supervisor-vivarium-operations-cage-wash/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Velocigene team is seeking a <strong>Cage Wash Supervisor </strong>to join their innovative and collaborative group. This position reports directly to the Cage Wash Manager. As Cage Wash Supervisor you will assist management in the daily operation of the Regeneron Vivarium’s cage wash and loading dock operations. Ensuring all caging and equipment are sanitized and processed according to regulatory standards and internal SOPs. This position is also responsible for the basic oversight and support of waste streams, supply receipt, inventory maintenance and multiple areas associate with dirty-side operations.</p><p>You will act as a liaison with animal care staff, management, EHS and Facilities to provide support and ensure all areas of the cage wash and loading dock are properly maintained and running smoothly.</p><p><strong>A Typical Day in the Role Might Look Like: </strong></p><ul><li>Oversee daily operations, including the processing of caging materials, autoclaving supplies, routine maintenance of machines and staff oversight.</li><li>Schedule, train, mentor, and evaluate cage wash personnel.</li><li>Perform daily quality assurance checks and document results. Able to address or report all deviations in a timely manner.</li><li>Assist management in creating weekly schedules and filling service requests. </li><li>Ensure adequate staffing and coverage for all shifts and assist when needed.</li><li>Understand and follow all policies and procedures to ensure compliance with state, local and federal agencies, including adherence to the “Guide for the Care and Use of Laboratory Animals”. </li><li>Working with internal Facilities Operations group to maintain facility, equipment and troubleshoot equipment malfunctions and alarms. </li><li>Monitor and maintain rack washers, robotic cage washing systems, bulk autoclaves, tabletop autoclaves, dump stations, water flush systems, chemical dispensing systems and other associated operational equipment.</li><li>Adherence to internal EHS guidelines and ability to readjust operations as guidelines evolve. </li><li>Order, receive and maintain inventory of supplies such as bedding, chemicals, PPE, caging, caging components, feed and enrichment.</li><li>Manage daily workflow of reusable PPE stocking, collection and laundry pickup. </li><li>Coordinate equipment repairs, including coordination with vendors. </li><li>Maintain areas as “inspection ready” at all times.</li><li>Operate under and enforces strict adherence to safety protocols, biosecurity measures, proper use of PPE and institutional SOPs to ensure safe a working environment at all times.</li><li>Maintain support areas such as, feed rooms, necropsy rooms, animal receiving rooms, chemical storage and supply storage rooms.</li></ul><p><strong>This Job Might Be for You If You: </strong></p><ul><li>Have an interest in science and enjoy hands-on work.</li><li>Thrive in a team environment, can collaborate effectively, and work independently when needed. </li><li>Have excellent verbal, written, time management, organizational and communication skills. </li><li>Have a strong attention to detail and can follow procedures accurately. </li><li>Are comfortable asking questions, providing feedback, and taking initiative. </li></ul><p>A High School Diploma or equivalent technical certification is required. Two or more years of experience operating in a lead role in a cage wash environment. AALAS certification at the ALAT level, or equivalent years of working experience. Strong understand of sanitation procedures and the use of traditional cleaning chemicals typically used in a cage wash setting. Strong leadership, communication and problem-solving abilities. Basic ability to use Outlook, email, PowerPoint, Excel, Microsoft Word, and internal IT applications. The ability to stand for long periods of time, perform repetitive motions, work around chemicals and operate in an environment that may get wet, have elevated temperature and mechanical noise. Perform physical duties such as breaking down pallets, disassembling caging and equipment, processing bulk supplies and moving large drums of chemicals. Operation of a forklift, electric pallet jack, bulk bedding hoist and other associated equipment necessary to maintain operations.</p><p><strong>Work Environment: </strong></p><p>This position involves physical demands, including but not limited to:</p><ul><li>Lifting up to 50 lbs., bending, pushing, pulling, and moving supplies and equipment.</li><li>Extended periods of walking and standing.</li><li>Use of Personal Protective Equipment (PPE).</li><li>Working in environments with potential noise, increased temperature, wet surfaces and allergens.</li></ul><p>Reasonable accommodations will be made for individuals with disabilities to perform essential job functions.</p><p><strong>Weekend and Holiday Requirements:</strong></p><p>This role is classified as essential personnel, meaning weekend and holiday work may be required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Biostatistics - Immunology & Inflammation]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46192]]></requisitionid>
    <referencenumber><![CDATA[R46192]]></referencenumber>
    <apijobid><![CDATA[r46192]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46192/senior-director-biostatistics-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron is seeking a Senior Director, Biostatistics to drive our Immunology and Inflammation therapeutic area.</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><p>The incumbent will have responsibility for strategic and operational activities and for assisting the Head, Biostatistics in the development and implementation of departmental scientific policies, operational guidelines, and administrative structure. The incumbent could also serve as senior research expert, with demonstrated ability to be a leader within Global Development and within the field for specific statistical methodology or application. The successful candidate should have a track record in leading teams and the ability to effectively structure a function to manage the anticipated growth in the product pipeline. They must also possess excellent communication skills to interface with senior leadership on behalf of the department and work closely with medical study directors to provide and receive direction on clinical programs and have the ability to influence the medical and clinical teams.</p><p><strong>This role might be for you if have proven experience:</strong></p><ul><li><p>Determining Department goals and resource allocation in conjunction with the Department Executive Director.</p></li><li><p>Ensure project teams have high quality statistical support for creation of clinical development plans, study design, and operational aspects.</p></li><li><p>Work with senior management to ensure statistical representation in key project decisions and regulatory meetings. Serve as departmental representative on corporate‐wise teams.</p></li><li><p>Oversee process for statistical reporting. Review critical documents, such as SAP, analysis results presentations, CSR, and integrated summaries. Ensure compliance with data submission guidelines.</p></li><li><p>Plan and track project activities, timelines, and resource use. Provide justification for planned resource needs. Seek to optimize resource utilization across projects or areas. Effect long‐range planning.</p></li><li><p>Ensure technical direction and mentoring for staff. Encourage personal development in the context of project work. Learn and apply techniques to promote teamwork, quality, and motivation. Recruit, develop, and retain high quality staff.</p></li><li><p>Maintain awareness of industry standards and regulatory requirements. Alert staff to new or changing standards. Within area of control, harmonize policies with departmental guidelines SOPs and with industry standards. Develop polices promoting application of corporate values in work practices.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Ph.D. in statistics or related discipline with 10+ years of experience (or MS in statistics or related discipline with 15+ years) in the biotechnology, pharmaceutical or health related industry, including significant interaction with both FDA and EMEA, history of successful project and people management (6+ years), and expertise in multiple therapeutic areas.</p></li><li><p>Active research interests in area related to clinical trial.</p></li><li><p>Demonstrated ability to work in a changing and busy environment and to exercise judgment in interpreting, modifying, and adapting procedures, practices, methods, etc. in accordance with existing policies and standards for application to specific problems or tasks.</p></li><li><p>Ability to work independently – self‐directed, high energy and strong work ethic. High degree of creativity, latitude and attention to detail required.</p></li><li><p>Demonstrated strong leadership, project management, teamwork and interpersonal skills.</p></li><li><p>Excellent presentation skills.</p></li><li><p>Experience and proven ability leading and managing major process and technology initiatives with utilization and impact across multiple functional groups.</p></li><li><p>Broad knowledge and superior understanding of advanced statistical concepts and techniques.</p></li><li><p>Outstanding ability and skills to effectively represent Biostatistics and Data Management in interactions with senior management or cross‐functional committees.</p></li><li><p>Thorough knowledge of pharmaceutical clinical development and life cycle management; ability to innovatively apply technical principles, theories and concepts to clinical drug development leading to regulatory approvals.</p></li><li><p>Thorough working knowledge of regulatory guidelines on drug development, regulatory submissions, and statistical practice.</p></li><li><p>Understanding of the drug discovery and development process, regionally and globally.</p></li><li><p>Strong administrative skills.</p></li><li><p>Ability to influence others to achieve results.</p></li></ul><p>#GDBDMJobs</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 16:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Proces Development Engineer III, Bioconjugation Development]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45915]]></requisitionid>
    <referencenumber><![CDATA[R45915]]></referencenumber>
    <apijobid><![CDATA[r45915]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45915/proces-development-engineer-iii-bioconjugation-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking and dynamic Process Development Engineer III for its new Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will develop conjugation and purification processes for bioconjugation of proteins to a diverse range of smaller-molecules. You would work in close collaboration with cross-functional teams for process development and optimization using the principles of Quality by Design (QbD) to make the processes suitable for GMP production. This role also involves process scale-up and technology transfer of manufacturing related workflows to Contract Development and Manufacturing Organizations (CDMOs) or Regeneron based manufacturing suites to ensure timely and reliable entrance to the clinic through product commercialization.</p><h3><strong>A Typical Day in the role of Process Development Engineer III might include:</strong></h3><ul><li><p>Working at the bench to design and develop scalable, robust and controlled GMP-ready bioconjugation and purification processes.</p></li><li><p>Collaborating with analytical groups within or outside the organization to establish supportive analytical characterization techniques.</p></li><li><p>Discussing plans and data in cross functional teams to evaluate processes and determine developmental goals and ensure integrated program success.</p></li><li><p>Proactively complying to lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</p></li><li><p>Using statistical design of experiments (DOE) to optimize bioconjugation processes including conjugation reactions, purification operations, and analytical characterization.</p></li><li><p>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to provide technical assessment of CDMO’s intended for GMP production and successfully transferring processes with immediate, first-time success.</p></li><li><p>Researching, identifying, and developing new technologies to improve processes, generate predictive process models, and pioneer novel at-line/in-line process analytical technologies (PAT) to ensure robust and controllable bioconjugation and purification processes.</p></li><li><p>Authoring robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</p></li><li><p>Analyzing and presenting data in a clear and cohesive manner to a broad audience facilitating data-driven decision making.</p></li><li><p>Authoring, reviewing, or providing domain expertise for publications, reports, tech transfer documents, regulatory support documents and patents.</p></li><li><p>Being a responsible lab citizen by ensuring timely maintenance of lab equipment, keeping the lab tidy and organized and proactively planning for lab resources.</p></li><li><p>Coaching and mentorship of junior team members of the organization as needed.</p></li></ul><h3><strong>This Role May Be For You If You:</strong></h3><ul><li><p>Enjoy working in the lab to advance exciting new drug modalities to patients.</p></li><li><p>Have strong initiative and aim to complete challenging tasks and learn new technologies.</p></li><li><p>Have a strong fundamental understanding of various protein purification and technology transfer principles</p></li><li><p>Are capable of multi-tasking and working both independently and in a collaborative environment involving cross-functional teams.</p></li><li><p>Have excellent interpersonal, verbal and written communication skills.</p></li><li><p>Can think critically and demonstrate problem-solving skills.</p></li></ul><p>This role requires a Bachelor’s + 10+ years relevant experience or Master’s+ 8+ years relevant experience or a PhD + 0-3 years experience in chemical/biochemical engineering or a related field. Experience with antibodies in the bioconjugates space is highly preferable. Hands on experience with bioconjugation processes (lysine-based, cysteine-based, site-specific etc.) with practical knowledge of downstream purification techniques such as chromatography, ultrafiltration/diafiltration, membrane technologies etc. is preferred. Experience with a variety of analytical characterization tools such as high-performance liquid chromatography (HPLC), UV spectroscopy, etc. is preferred.</p><p>Note: title will be commensurate with experience</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Therapeutic Area Genetics (Immunology)]]></title>
    <date><![CDATA[Thu, 26 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46254]]></requisitionid>
    <referencenumber><![CDATA[R46254]]></referencenumber>
    <apijobid><![CDATA[r46254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46254/associate-director-therapeutic-area-genetics-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an extremely talented Scientist to join our Immunology Therapeutic Area Genetics (TAG) team. Within the RGC, the Immunology TAG team is using large-scale human exome sequencing for discovery and validation of new therapeutic targets in autoimmune and other immune-mediated disease. You will be responsible for designing and executing studies integrating large scale human genetics and multidimensional omics datasets derived from RGC and public resources in the immunology space to identify new targets for inflammatory and auto-immune diseases and accelerate target transition to novel therapeutics. You will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to catalyze therapeutic development for genetically-validated targets in immunologic diseases.</p><p><em><strong>This role will require 4 days per week onsite at our campus in Tarrytown, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Understand and leverage RGC and Regeneron datasets, external resources, and the scientific/medical literature to generate research questions and then generate relevant phenotypes from longitiudinal clinical data, design and execute genetic association studies, and perform integrative omics analyses to address these research questions</p></li><li><p>Deploy computational methods to integrate genetic data with multiple omics data to more effectively identify/prioritize drug targets illuminated by genetic association data.</p></li><li><p>Work closely with other members of the Immunology and other TAG teams, Analytic Genetics, Sequencing, and GIDE in cross-functional initiatives within the RGC and Regeneron.</p></li><li><p>Collaboratively summarize insights of investigations into a variety of formats (e.g. documents, presentations, patent applications, publications, etc.) for audiences with broad bacgrounds.</p></li><li><p>Partner with Clinical Development to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations.</p></li></ul><p><strong>This job might be for you if you can/have</strong></p><ul><li><p>Bring innovative thinking to human genetics and epidemiological studies</p></li><li><p>Experience leading complex human genetics research incorporating different analytic methods, phenotypes, and study designs.</p></li><li><p>Ability to use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions.</p></li><li><p>Worked with multidisciplinary teams to characterize the functional consequences of discovered disease gene variants</p></li><li><p>Understanding of drug development and clinical trial design and execution. Experience in the clinical management or medical research relating to autoimmune and immune-mediated disease is a plus.</p></li><li></li></ul><p><strong>To be considered for this opportunity, you must have </strong>a PhD , MD preferred with 8+ years of experience in the use of WES/GWAS datasets, RNA-Seq, proteomics and other large-scale platforms for genomic/proteomics. Demonstrated expertise in immunobiology, genetics, and mechanisms; familiarity with large genetic studies that deliver novel genetic findings and medically relevant gene discoveries; and demonstrated ability to manage and collaborate in a multi-disciplinary team, to discover and evolve immunology-related drug discovery pipelines. Individuals with proficiency in computational immunology research are particularly encouraged to apply.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 27 Mar 2026 19:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Information]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46258]]></requisitionid>
    <referencenumber><![CDATA[R46258]]></referencenumber>
    <apijobid><![CDATA[r46258]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46258/associate-director-medical-information/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As Associate Director, Medical Information, you will lead scientific communication and medical information strategy for assigned therapeutic areas, enabling high-quality, compliant scientific exchange with healthcare professionals, patients, and internal team members. You will manage the tactical execution of Global and US Medical Affairs medical information plans, convert insights into strategic recommendations, and serve as a trusted partner. We ensure excellence in delivery while maintaining full adherence to company policies, procedures, and all regulations and industry standards.</p><p><strong>Where & When</strong><br>• On-site 4 days/week in Sleepy Hollow, NY or Warren, NJ<br>• If based in Warren, NJ, occasional travel to Sleepy Hollow, NY is expected<br>• Travel (up to 10% is expected) </p><p><strong>A typical day may include the following: </strong><br>• Develop and deliver high-quality, balanced, and scientifically accurate responses to medical inquiries; resolve complex and brought up inquiries.<br>• Lead the creation and maintenance of deliverables, including literature reviews, Standard Response Documents (SRDs), verbal FAQs, Q&As, AMCP dossiers, and compendium.<br>• Medical reviewer on Promotional and Medical Review Committees, ensuring medical accuracy, clarity, and compliance. <br>• Own department reporting processes and dashboards, including metrics, insights generation, digital analytics, and trend reporting for internal partners.<br>• Evaluate, pilot, and implement AI-enabled tools and technologies to streamline medical information processes and improve efficiency and quality.<br>• Collaborate with global and regional Medical Affairs partners to ensure alignment and share best practices.<br>• Provide scientific support for congress planning, booth activities, and real-time scientific exchange.<br>• Mentor and train new hires and less experienced colleagues; may directly supervise Senior Managers, Specialists, and contractors.</p><p>To be considered a minimum of 5 years of Medical Information experience within the pharmaceutical industry along with a PharmD or PhD is required. Strong scientific knowledge and expertise in a therapeutic area including evaluating and communicating clinical trial and disease state information to a wide range of audiences. Neurology is preferred. Demonstrated experience in conducting scientific literature review, and management of medical inquiries, including the development and review of deliverables (e.g., standard response documents, FAQs, dossier, compendium submissions, etc.). Practical experience and knowledge of FDA guidance’s. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 14:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology - Cincinnati, OH]]></title>
    <date><![CDATA[Mon, 06 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46417]]></requisitionid>
    <referencenumber><![CDATA[R46417]]></referencenumber>
    <apijobid><![CDATA[r46417]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46417/medical-specialist-i-pulmonology-cincinnati-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cincinnati]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Cincinnati, OH (Hillsboro, Chillicothe, Jackson)</strong></p><p>The Medical Specialist (MS) will report to the District Manager and be responsible for engaging customers in the Pulmonary therapeutic area within an assigned geographical universe, presenting clinically focused selling messages to create and drive growth, and consistently delivering product goals.<br><br><strong>A Typical Day Might Look Like This</strong></p><ul><li><p>Demonstrate strong and consistent sales performance related to product goals in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p></li><li><p>Develop strategy and execute tactics within key accounts in the Pulmonary therapeutic area to generate product utilization.</p></li><li><p>Develop strong working relationships with Pulmonologists and Midlevel experts in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p></li><li><p>Collaborate with their regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography.</p></li><li><p>Participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).<br> </p></li></ul><p><strong>This Position Might Be For You If</strong><br> </p><ul><li><p>Demonstrate advanced clinically based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers<br> </p></li></ul><p>To be considered for this role you must have a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Pulmonary market or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Apr 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Administrative Coordinator – Global Market Access]]></title>
    <date><![CDATA[Sun, 19 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46432]]></requisitionid>
    <referencenumber><![CDATA[R46432]]></referencenumber>
    <apijobid><![CDATA[r46432]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46432/senior-administrative-coordinator-global-market-access/]]></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 Sr. Administrative Coordinator is primarily responsible for managing and providing administrative support to the Market Access Customer Engagement Vice President, and their direct support team.</p><p>Responsibilities include, but are not limited to, calendar management, coordination of in-house and offsite meetings (sourcing, planning, execution), expense reconciliation, and arranging US and international travel. The coordinator should exercise considerable judgment and initiative with the ability to influence stakeholders and understand key relationships, while ensuring sensitive data is held in strict confidence.</p><p><strong>A Typical Day Might Look Like This:</strong></p><ul><li><p>Proactively manage calendar for the Customer Engagement VP using a thorough understanding of department and leadership priorities. Ability to anticipate the needs of leadership and their teams to manage and problem solve when scheduling conflicts occur.</p></li><li><p>Arrange and coordinate travel logistics for the Customer Engagement VP which may include conference registrations, travel and meeting itineraries, air, hotel and ground transportation, along with reconciling corresponding expense reports.</p></li><li><p>Occasional domestic travel in support of the annual National Meeting, brand planning meetings, and various department team builders may be required.</p></li><li><p>Responsible for on and offsite meeting planning, including catering, rooming lists, audio visual requests, and team builders, while ensuring adherence to budgetary guidelines.</p></li><li><p>Maintain department SharePoint site including archives of documents and maintaining user access to confidential materials. Organize, create, maintain, and upload documents. Ensure sensitive data is maintained. Manipulating picture files, electronic filing, scanning hardcopy documents, creating folder structures, and creating and maintaining databases.</p></li><li><p>Work closely with our external collaborators to coordinate meetings and events.</p></li><li><p>Demonstrates a working knowledge of company policies, procedures, resources and where to find them.</p></li><li><p>Implements a highly organized and efficient administrative workflow. Identifies, develops, and/or supports administrative process improvements.</p></li><li><p>Work closely with the other Market Access administrative coordinators, including bi-weekly touchpoints to review priorities and important activities.</p></li><li><p>Process and submit purchase requisitions and enter SOW, CDA, MSA information into the contract management system including onboarding new vendors. Track requisitions approval status and assignment of purchase orders and ensure alignment with department budget.</p></li><li><p>Manage the ABAC Risk Assessment Platform for due diligence of new vendors - InfoSec, SSP New Supplier Intake.</p></li><li><p>Responsible for collaborating with Strategic Sourcing and Procurement to manage and negotiate contracts, entering and adhering to budgetary guidelines for off-site meetings, team builders and events.</p></li><li><p>Reconcile expenses for the Customer Engagement VP as well as expenses incurred for offsite meetings and department purchasing card.</p></li><li><p>Actively manage customized email distribution lists.</p></li><li><p>Complete visitor pre-registration and provide internet access for attendees. Meet, greet, and escort guests to conference rooms.</p></li><li><p>Onboard new, in-house employees (includes ordering preferred laptop and peripherals, seat assignment, supplies).</p></li><li><p>Any other ad hoc administrative assignments such as ordering birth/bereavement gifts, holiday field and inhouse gifts.</p></li></ul><p><strong>This role may be a fit for you if you:</strong></p><p><strong> </strong></p><ul><li><p>You are a collaborative teammate with proficient written and verbal communication skills, actively listens and builds relationships, demonstrates effective customer service, exhibits high attention to detail, has ability to interact with all levels of employees and maintain confidentiality.</p></li><li><p>You demonstrate strong initiative and drive to complete tasks, enjoy working independently and within teams on multiple tasks or projects simultaneously.</p></li><li><p>You anticipate and proactively adjust for challenges and roadblocks, understanding how/when to provide feedback and when to escalate to the right people.</p></li></ul><ul><li><p>Demonstrates strong organizational skills and ability to understand Commercial Business Unit priorities.</p></li><li><p>Adaptive learner who can shift gears with ease and make good decisions during change or ambiguity.</p></li><li><p>Exercises good judgement and be willing to go above and beyond; takes initiative.</p></li><li><p>Proficiency in MS Office is necessary. Knowledge in SharePoint, Concur, Oracle, iCertis and MS Teams are preferred but not required.</p></li></ul><p>This role requires an Associate or BA/BS, with BA strongly preferred. Minimum of 2 -4 years of relevant administrative experience in a fast-paced environment. Collaborative team player with excellent oral and written communication skills. Excellent organizational skills with demonstrated attention to detail. Ability to learn new technologies and systems quickly and easily. Proficient is all MS Office applications.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$33.80 - $52.93]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, ERP Product Management (Cloud Fusion)]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45912]]></requisitionid>
    <referencenumber><![CDATA[R45912]]></referencenumber>
    <apijobid><![CDATA[r45912]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45912/senior-director-erp-product-management-cloud-fusion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Director, ERP Product Management, leads the strategy, architecture, and delivery of Regeneron’s enterprise ERP capabilities and the broader Finance, Procurement, Tax, Treasury, Accounting, and Supply Chain ecosystem. Working with BRMs, IT leaders, and functional business executives, this leader shapes a cross‑functional, capabilities‑based roadmap aligned to medium‑ and long‑term business goals. The Sr. Director oversees cross‑functionally aligned product managers and partners with program leadership to ensure seamless delivery during the Oracle EBS → Oracle Fusion transition and beyond.</p><p><em><strong>The role will be based onsite at our office in Sleepy Hollow, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><strong>A typical day: </strong></p><ul><li><p>Shape the cross‑functional ERP technology strategy with BRMs, IT leaders, and functional executives, building a cohesive, capabilities‑based framework aligned to 3–5+ year business goals.</p></li><li><p>Lead teams of cross‑functionally aligned product managers overseeing solution design, architecture, and delivery in line with product strategy, standards, and enterprise architecture.</p></li><li><p>Align product delivery and technology plans to strategic goals and multi‑function roadmaps; ensure product managers supporting each function meet their strategic objectives.</p></li><li><p>Manage prioritization and alignment using industry standards, best practices, and ERP/cloud trends; regularly update the ERP roadmap to reflect market and business changes.</p></li><li><p>Advise senior leaders on the optimal mix of ERP capabilities and products that balance functional outcomes and technology strategy over a multi‑year horizon.</p></li><li><p>Own the ERP product organization budget; coordinate with product managers and portfolio management to manage demand, forecasting, and the project portfolio; drive strategic product decisions in line with business objectives and budgets.</p></li><li><p>Serve as executive IT owner for Oracle EBS and adjacent platforms; partner across Finance, Procurement, Tax, Treasury, Accounting, HR, Legal, and Supply Chain to deliver capabilities that support enterprise objectives.</p></li><li><p>Partner closely with the Senior Director, ERP Program Management IT Lead (Oracle Fusion) to stay informed of Fusion program milestones, upcoming go-lives, and wave planning — ensuring the operational ERP team is ready to receive and support each new Fusion capability as it is delivered.</p></li><li><p>Drive execution and optimization: configuration, extensions, integrations, data migration, reporting enablement, identity & access governance (RBAC/ABAC), testing (UAT/SIT), deployment, and hypercare.</p></li><li><p>Own the ERP enhancement backlog: triage requests, determine EBS vs. native Fusion design, and prevent capability gaps during the transition and cutover waves.</p></li><li><p>Manage the EBS-to-Fusion cutover period from an operations perspective: maintain EBS stability during parallel run periods, coordinate data freeze windows with business partners, and ensure hyper care support is in place post-go-live.</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Proven success leading global, multi‑entity ERP implementations, upgrades, or modernization programs (EBS → Fusion experience strongly preferred).</p></li><li><p>Deep knowledge of finance and adjacent business processes (Order to Cash, Procure to Pay, Record to Report, Acquire to Retire), and experience with EPM/reporting.</p></li><li><p>Expertise in ERP architecture, integrations (APIs, middleware), data migration, security, identity/access management, and cloud operations.</p></li><li><p>Demonstrated experience establishing governance, change control, and audit readiness (SOX, ITGC; GxP as applicable).</p></li><li><p>Strong portfolio, budget, and vendor/SI management; able to align investment decisions to multi‑year product and technology strategy.</p></li><li><p>Track record of developing product managers and cross‑functional teams; excellent executive communication and stakeholder influence.</p></li></ul><p><br><strong>To be considered:</strong></p><ul><li><p>15+ years of progressive leadership across ERP and enterprise applications, including significant experience with Oracle Fusion Cloud ERP and Oracle EBS.</p></li><li><p>Experience managing ERP operations during parallel EBS and Fusion waves, including cutover planning and hypercare.</p></li><li><p>Hands‑on familiarity with Oracle Tax (EBTax), Treasury (Cash Management/bank connectivity), and/or EPM (planning/forecasting).</p></li><li><p>Background in global ERP rollouts, M&A integrations, and multi‑entity consolidation on Oracle platforms.</p></li><li><p>Oracle Cloud/EBS certifications; MBA or advanced degree.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal External Manufacturing Specialist]]></title>
    <date><![CDATA[Tue, 14 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46638]]></requisitionid>
    <referencenumber><![CDATA[R46638]]></referencenumber>
    <apijobid><![CDATA[r46638]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46638/principal-external-manufacturing-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>We are currently looking to fill a Principal External Manufacturing Specialist. The Principal External Manufacturing Specialist oversees all aspects of external manufacturing contract manufacturing operations (filling, assembly, packaging) including day-to-day operations, ensuring timely completion of associated operations/documentation and assisting in the monitoring of cGMP compliance. Additionally, the Principal Specialist provides guidance to other specialists as well as consults with management on all contract manufacturing operations and GMP compliance issues.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Serves as a Regeneron operational contact for contract manufacturing and/or business partner sites concerning day-to-day activities.</p></li><li><p>Coordinates 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 bulk or finished product, 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>Coordinates/oversees multiple external manufacturing activities at multiple sites, as required.</p></li><li><p>Coordinates/oversees DS and FDS manufacturing at CMO as dictated by project.</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><li><p>Leads sub-teams in continuous process improvements, system/equipment implementation and/or strategy development.</p></li><li><p>Leads or supports all investigations which concern external manufacturing and associated shipping operations.</p></li><li><p>Ensures product integrity and company reputation monitoring of cGMP compliance at external manufacturing contract manufacturers and business partners.</p></li><li><p>Performs reviews of pre-production master batch records and executed batch records.</p></li><li><p>Authors documents and procedures.</p></li><li><p>Supports audit operations, both internal and external.</p></li><li><p>Analyzes data for trends and potential issues.</p></li><li><p>Travels 25% (target) or more (domestic and international), as required.</p></li></ul><p>This role might be for you if:</p><ul><li><p>Knowledge of external manufacturing from formulation through the final package.</p></li><li><p>Knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.</p></li><li><p>Proficient in Excel, PowerPoint, Visio, Word, Oracle etc. in addition to experience working within shared work environments.</p></li><li><p>Strong interpersonal, written and oral communication skills.</p></li><li><p>Exhibits confidence, has a high emotional IQ, and has strong interpersonal, written and oral communication skills for providing team updates.</p></li><li><p>Ability to impart understanding of provided instructions, develop instructions and sets and works towards goals with minimal supervision.</p></li><li><p>Exhibits a degree of ingenuity, creativity and resourcefulness in evolving and ambiguous environments.</p></li><li><p>Shows resiliency and flexibility in the face of challenges and adversarial situations.</p></li><li><p>Understands and listens to team members and stakeholders needs while supporting productive team environments toward a common objective.</p></li><li><p>Competent in German and/or French (oral and written) is a plus.</p></li></ul><p>To be considered for the Principal External Manufacturing Specialist, you must have a BS/BA in a scientific discipline and 8 years of related experience in cGMP manufacturing operations (clinical and/or commercial external manufacturing), including experience collaborating with CMOs/CROs, or equivalent combination of education and experience.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 15 Apr 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Distribution Operations – Japan]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46261]]></requisitionid>
    <referencenumber><![CDATA[R46261]]></referencenumber>
    <apijobid><![CDATA[r46261]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46261/director-distribution-operations-japan/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a dynamic and strategic leader to join our team as the Director of Distribution Operations in Japan. This pivotal role offers the opportunity to shape the distribution network, optimize cost-to-serve, and contribute to delivering best-in-class service in the pharmaceutical sector. If you are passionate about driving operational excellence and fostering collaboration, this is your chance to make a meaningful impact.</p><p><strong>A Typical Day:</strong></p><ul><li>Set the strategic direction and governance model for Japan’s distribution network, including wholesalers and 3PLs.</li><li>Define and manage vendor SLAs/KPIs, conduct quarterly business reviews, and negotiate contracts in collaboration with Legal.</li><li>Oversee distribution budgets, pricing guidance, and rebate programs to support revenue maximization and sustainability.</li><li>Direct implementation and governance of in-market sales data systems, ensuring data quality and delivering actionable analytics.</li><li>Establish standardized processes for claims, returns, and multi-brand Return/Replacement Programs, reducing friction and costs.</li><li>Drive risk management and business continuity planning for distribution operations, including contingency plans and operational risk monitoring.</li><li>Build and lead a high-performing team, fostering a culture of accountability, transparency, and continuous improvement.</li><li>Serve as the senior liaison with wholesalers and key market stakeholders, addressing complaints and supporting sales promotion programs.</li></ul><p><strong>This Role May Be For You, if you:</strong></p><ul><li>Thrive in strategic and analytical roles, translating insights into operational and commercial outcomes.</li><li>Have deep knowledge of GDP, MHLW requirements, trade compliance, contract law basics, and sustainability standards.</li><li>Are skilled in project and program management, capable of handling multiple initiatives, timelines, and stakeholders concurrently.</li><li>Excel in executive communication and negotiation, influencing senior leaders, external partners, and cross-functional teams.</li><li>Are proficient in tools like SAP/S4, WMS/TMS, Power BI/Tableau, SharePoint, and Microsoft Excel/PowerPoint.</li><li>Are passionate about fostering collaboration and developing talent within your team.</li><li>Bring demonstrated success in leading distribution/trade operations in the Japan pharmaceutical market.</li></ul><p><strong>To Be Considered:</strong></p><ul><li>12–15+ years of experience in international biopharmaceutical distribution/trade operations, including cross-functional leadership.</li><li>5+ years of direct people leadership and vendor governance experience.</li><li>Proven expertise in Japan distribution models and wholesaler management; EU/US market exposure is a plus.</li><li>Native level proficiency in Japanese and fluent English; familiarity with Japan-specific cultural business practices.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 04:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs, East]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46697]]></requisitionid>
    <referencenumber><![CDATA[R46697]]></referencenumber>
    <apijobid><![CDATA[r46697]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46697/senior-manager-field-medical-affairs-east/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced Field Medical Affairs professional specializing in Hematology to join our team in Spain. In this pivotal role, you will serve as a scientific and clinical resource, engaging with key opinion leaders, healthcare professionals, and internal stakeholders to advance disease awareness and support innovative research initiatives. By collaborating across Medical Affairs, Clinical Development, Market Access and Commercial, you’ll help drive impactful strategies that shape the future of hematological care. This is your chance to create a meaningful difference in patient outcomes while growing your expertise in a dynamic, matrix-driven environment.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Building and nurturing peer relationships with leading experts in Hematological Malignancies.</p></li></ul><ul><li><p>Presenting scientific and clinical data to healthcare professionals and investigators.</p></li><li><p>Supporting and managing clinical trials by identifying investigators and trial sites.</p></li></ul><ul><li><p>Collaborating with internal teams and cross-functional partners to align strategies.</p></li></ul><ul><li><p>Responding to requests for information about disease states and Regeneron’s products.</p></li></ul><ul><li><p>Ensuring compliance with company policies and regulatory guidelines.</p></li></ul><ul><li><p>Assisting with the development of abstracts, posters, and manuscripts for scientific communication.</p></li></ul><ul><li><p>Providing support to the commercial team.</p></li></ul><p><strong>This Role May Be For You, if you:</strong></p><ul><li><p>Thrive in a collaborative, matrix environment and enjoy cross-functional teamwork.</p></li></ul><ul><li><p>Value building and maintaining positive relationships with healthcare professionals and investigators.</p></li></ul><ul><li><p>Are committed to scientific integrity and professional communication at all times.</p></li></ul><ul><li><p>Excel at organizing, planning, and balancing multiple priorities, both independently and as part of a team.</p></li></ul><ul><li><p>Are passionate about advancing hematological research and supporting innovative clinical initiatives.</p></li></ul><p><strong>To Be Considered</strong></p><p>Applicants must hold a Bachelors degree, with preferably 5+ proven experience, including at least 3 years in a Field Medical or Medical Manager role within the biotech or pharmaceutical industry, focusing on Oncology or Hematology. Expertise in the Hematology therapeutic area is required, with experience in lymphoma and/or multiple myeloma strongly preferred. Established relationships with key opinion leaders in malignant hematology and familiarity with institutions specializing in Hematologic Malignancies are advantageous. Drug launch experience, knowledge of treatment guidelines, clinical research processes, EU and pharma regulations, and strong communication skills are essential. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MEDICAL REPRESENTATIVE (MR) – DERMATOLOGY AICHI AREA]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46729]]></requisitionid>
    <referencenumber><![CDATA[R46729]]></referencenumber>
    <apijobid><![CDATA[r46729]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46729/medical-representative-mr-dermatology-aichi-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong></p><p>You will primarily work in the Aichi area.</p><p>Your residence is expected to be in Aichi(Gifu or Northern Mie also available for consultation)</p><p>Are you ready to make a meaningful impact in the pharmaceutical industry? At Regeneron, we’re committed to putting patients first, and we’re looking for a passionate Sales Representative to join our Dupixent ROW Commercial Team in Japan. This role is your opportunity to drive dermatology sales objectives while working with a team dedicated to innovation and excellence. With a focus on delivering value to healthcare professionals and patients alike, this position offers the chance to grow your career while making a difference in people’s lives.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Achieve sales objectives by effectively managing territory budgets and resources.</p></li><li><p>Develop and implement an annual territory business plan that incorporates market insights and aligns with marketing strategies.</p></li><li><p>Regularly update business plans to adapt to changing market dynamics.</p></li><li><p>Utilize key data sources to create strategic action plans for the territory.</p></li><li><p>Conduct disease and concept selling to engage healthcare professionals and deliver tailored solutions.</p></li><li><p>Perform administrative tasks, including expense reporting, marketing feedback, and call reporting.</p></li><li><p>Collaborate with alliance partners to meet overall objectives and ensure compliance with regulatory guidelines.</p></li><li><p>Attend local, regional, and national meetings as required, and complete all training programs provided by Regeneron.</p></li><li><p>Maintain company property in good order and adhere to safe driving practices.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You excel at building strong relationships with customers and delivering value-driven solutions.</p></li><li><p>You have a knack for strategic thinking and can manage your time effectively to achieve goals.</p></li><li><p>You thrive in independent work environments and can execute plans under tight timelines.</p></li><li><p>You’re organized, detail-oriented, and comfortable with administrative responsibilities.</p></li><li><p>You enjoy collaborating with others to achieve shared objectives.</p></li><li><p>You’re adaptable and willing to travel, including evenings and weekends, as needed.</p></li></ul><p><strong>To Be Considered:</strong></p><p>Candidates must have a Bachelor’s degree (or equivalent) and at least five years of sales representative experience in the pharmaceutical industry. A valid driver’s license and MR certification are required. While fluency in English is a plus, it is not essential for this role. Preferred qualifications include therapy area knowledge in dermatology, sales experience in biologics, and established relationships with key opinion leaders in dermatology.</p><p>Join us at Regeneron, where your expertise and dedication can make a real difference. Apply today to become a part of a team that’s revolutionizing healthcare and improving lives worldwide.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 04:26:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Quality Control (Microbiology)]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46658]]></requisitionid>
    <referencenumber><![CDATA[R46658]]></referencenumber>
    <apijobid><![CDATA[r46658]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46658/associate-manager-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>Within this role you will manage the QC Microbiology team and provide critical microbiology support to manufacturing and facilities.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li>Managing a team of laboratory analysts within the QC microbiology department involved in the analysis of raw materials, intermediates (in process) and bulk drug substance in a cGMP regulatory environment</li><li>Implementing and managing the environmental monitoring programme, including surface, settling and viable and non-viable particulate air monitoring of aseptic operations and controlled areas</li><li>Managing QC microbiological operations to ensure compliance with cGMP standards and accurate sample analysis</li><li>Designing and overseeing microbiological validations as needed for drug substance, in-process controls and buffers</li><li>Managing the design, validation and execution of the clean utilities qualification and re-qualification program</li><li>Supporting manufacturing personnel in the identification of microbiological root cause analysis and provide technical advice on QC related topics as needed</li><li>Participating in the investigation and review of alert and action limit investigations as needed and implements corrective action as appropriate</li><li>Ensuring that all work carried out is in compliance with the required regulatory standards, conforms to company policies and standard operating procedures (SOPs)</li><li>Reviewing and approving method protocols, reports and SOPs</li><li>Assisting in the preparation for internal/customer/regulatory inspections</li><li>Ensuring a safe working environment within the laboratory</li><li>Overseeing or conducting laboratory investigations and generates reports in response to invalid assays, Deviations, OOS/OOT</li><li>Ensuring that CAPAs and Change Controls are initiated and completed on time and in accordance with site procedures</li><li>Presenting analytical data reports clearly and concisely to senior management, including QC performance metrics and trend</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have the ability to train, develop and mentor direct reports and effectively manage the performance of individuals</li><li>You can proactively identify and implement lab process improvements, lean initiatives</li></ul><p>To be considered for this opportunity you should have a BS/BA in Microbiology or closely related field with 6+ years’ experience in microbiology lab, preferably in the pharmaceutical or biotech industry with 3+ years’ experience in a leadership role in microbiology laboratory management.</p><p>#REGNIRLTO #IREADV #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Manager Quality Control]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46583]]></requisitionid>
    <referencenumber><![CDATA[R46583]]></referencenumber>
    <apijobid><![CDATA[r46583]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46583/sr-manager-quality-control/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>Within this role you will oversee a team involved in laboratory quality control testing, and has technical responsibility for all aspects of QC testing.</p><p><br><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li>Coordinating with members of Manufacturing, Stability, and Business Ops to provide analytical support</li><li>Managing QC Analysts, distributes work load, and monitors progress</li><li>Managing product testing to ensure efficient and compliant operations</li><li>Ensuring QC Analysts receive proper training</li><li>Attending meetings to keep informed of manufacturing priorities</li><li>Ensuring that safety standards are maintained</li><li>Ensuring compliance with applicable cGMP regulations and SOPs</li><li>Investigating a typical and OOS test results as necessary</li><li>Managing transfers internally from R&D to the QC laboratory or from PAS to the QC Laboratory</li><li>Managing transfers externally from QC laboratory to contract labs, includes audits if needed</li><li>Managing QC projects including analytical commitments for Regulatory filing, follow-up actions for general GMP inspections and its readiness</li><li>Tracking and monitoring the timeline of analytical validation projects</li><li>Monitoring the team performance for Compliance events, track, assist and organize continuous improvement events</li><li>Interacting with Regulatory Agencies as needed to ensure cGMP compliance</li><li>Performing personnel management functions including time sheet submissions, scheduling of vacations, personnel development/feedback, and performance evaluations</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Contribute to special projects as assigned</li><li>Demonstrate strong coordination during major analytical investigations</li><li>Review and approve test reports for accuracy and compliance</li></ul><p>To be considered for this role, you should have a Bachelor’s degree (BS/BA) in Chemistry or Biology, along with relevant experience in a pharmaceutical or biotechnology environment, particularly in laboratory management and analytical sciences. Relevant experience may be accepted in lieu of formal qualifications.</p><p><br><strong>Education and Experience:</strong></p><ul><li>Manager : Minimum 7+ years of experience</li><li>Sr Manager: Minimum 8+ years of experience</li></ul><p>#IRELIM #JOBSIEST #LI-Onsite</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist,  CRISPR Screening & Target Identification]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46074]]></requisitionid>
    <referencenumber><![CDATA[R46074]]></referencenumber>
    <apijobid><![CDATA[r46074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46074/scientist-crispr-screening-target-identification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly qualified scientist to join the Oncology & Immuno‑Oncology group. The successful candidate will support the identification and validation of novel tumor drug targets using in vitro and in vivo approaches. The ideal applicant is motivated, organized, detail‑oriented, and effective in a fast‑paced, team‑driven environment. Strong communication skills are essential. Experience with murine tumor models, mammalian cell culture, and molecular or cell‑based assays is highly desirable. Familiarity with CRISPR screening is a plus.</p><h3>As a Scientist, CRISPR, a typical day may include:</h3><ul><li><p>Perform vivo tumor experiments in mice, including injection, blood and tissue collection</p></li><li><p>Perform vitro cell culture and molecular biology experiments</p></li><li><p>Analyze and document data, and communicate results clearly and concisely to supervisor and peers</p></li><li><p>Organize and compile results into a finished format for presentation</p></li><li><p>Maintain precise lab notebooks</p></li><li><p>Daily lab maintenance (e.g., ordering reagents and supplies)</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li><li></li></ul><p><strong>To be considered for this role, you must meet the following:</strong></p><ul><li><p>BS or MS with at least 3 years work experience.</p></li><li><p>Experience with mouse tumor models (e.g., subcutaneous implantation, drug dosing, measuring tumors and tumor harvest)</p></li><li><p>Experience with mammalian cell culture</p></li><li><p>Experience with basic molecular biology and biochemistry techniques (e.g., preparation of cell/tissue lysates for DNA/RNA protein analysis, western blots, transfection, PCR, and cloning)</p></li><li><p>Experience designing FACS panels, performing multi-color FACS analysis preferred but not required</p></li><li><p>Experience with CRISPR screens preferred but not required</p></li><li><p>Strong organization and communication skills</p></li><li><p>Strong ability to learn new techniques</p></li><li><p>Ability to work well in a team</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Oligonucleotides]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45260]]></requisitionid>
    <referencenumber><![CDATA[R45260]]></referencenumber>
    <apijobid><![CDATA[r45260]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45260/senior-associate-scientist-oligonucleotides/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly skilled and motivated Associate Scientist/Senior Associate Scientist to join Nucleic Acid Therapeutics group devoted to the drug discovery and technology development specifically in the field of oligonucleotide therapeutics such as siRNAs and antisense oligonucleotide. </p><p><strong>As a Senior Associate Scientist, a typical day may include:</strong></p><p>The responsibilities of this position include assay development to enable high throughput oligonucleotide library screenings and the execution of high throughput screening involve hundreds to Thousands of candidate molecules. Assays including but not limited to: cell culture optimization, bDNA, RT-qPCR, cell line generation, transfecting optimization, probe design and compatibility tests, western blot, etc. </p><p><strong>This role may be for you if: </strong></p><ul><li><p> You enjoy working in a fast-paced environment</p></li><li><p>You are a fast learner and have desire to expand your skill set and learn new techniques</p></li><li><p>You are detail oriented, well-organized and can multi-task</p></li><li><p>You are a team player</p></li><li><p>You have strong communication skills</p></li></ul><p><strong>To be considered for this role, you must meet the following: </strong></p><ul><li>Work with automated or semi-automated processes, previous experiences with liquid handlers, KindFisher, QuantStudio are desired. Knowledge on oligonucleotide chemistry, RNA biology, is a plus.</li><li>Independently executes and refines techniques and/or technologies, with general guidance. Multi-tasks and shifts priorities based on communicated department needs. </li><li>Bachelor's degree is required + 3-4 Year Master's degree is preferred, +2 years of industrial experience in relevant field is highly appreciated.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Utilities Maintenance, Monday-Friday 2nd Shift]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46968]]></requisitionid>
    <referencenumber><![CDATA[R46968]]></referencenumber>
    <apijobid><![CDATA[r46968]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46968/supervisor-utilities-maintenance-monday-friday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking to add a Supervisor Utilities Maintenance with a Monday- Friday 2pm-10:30pm schedule to our team. Our Supervisor Utilities Maintenance is primarily responsible for the direction, organization and supervision of utilities maintenance operations. This position is responsible for operations and maintenance of High Purity Water/Steam systems and Plant Utility systems that support Process Manufacturing and overall facility buildings. </p><p>As a Supervisor Utilities Maintenance, a typical day might include the following:</p><div><div><ul><li><p>Planning and scheduling of maintenance, repairs and modifications to Plant Boilers, WFI equipment, distribution systems, compressed gas systems, and plant steam</p></li></ul></div><div><ul><li><p>Planning, scheduling and assigning work tasks utilizing the Blue Mountain Work Request System</p></li></ul></div><div><ul><li><p>Directing supervision of Regeneron facilities maintenance technicians to high performance goals in a cGMP - FDA regulated environment</p></li></ul></div><div><ul><li><p>Administration of contract maintenance personnel responsible for repairs and facility modernization to remain compliant with regulatory codes</p></li></ul></div><div><ul><li><p>Maintaining the physical condition and environment of owned areas</p></li></ul></div><div><ul><li><p>Troubleshooting equipment and developing maintenance plans</p></li></ul></div><div><ul><li><p>Leading teams in continuous improvement, 5S, Lean initiatives</p></li></ul></div><div><ul><li><p>Coaching, counselling and managing performance of direct reports</p></li></ul></div><div><ul><li><p>Followig current good manufacturing practices (cGMPs) and good business practices (G)</p></li></ul></div></div><div><div><ul><li><p>Complying with site safety policies and striving to maintain an accident free environment</p></li></ul></div><div><ul><li><p>Reviewing departmental operations and recommending changes to management</p></li></ul></div><div><ul><li><p>Forecasting resource requirements and submitting budget recommendations to management</p></li></ul></div><div><ul><li><p>Preparing reports for management review</p></li></ul></div><div><ul><li><p>Supervising, coordinating and assuring compliance with contractors and Regeneron employees on all applicable codes and standards</p></li></ul></div><div><ul><li><p>Supporting Deviation Management process including NOE, EOE and DNF investigations and reviews</p></li></ul></div><div><ul><li><p>Other duties and responsibilities as assigned</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Develop and implement ideas and suggestions for improving efficiency</p></li><li><p>Possess good demonstrated supervisory skills</p></li><li><p>Have strong interpersonal, oral and written communication skills</p></li><li><p>Proficient understanding of word processing, spreadsheet and database management software</p></li><li><p>Ensure work conduct is completed with a “Safety First” mindset</p></li><li><p>Demonstrate acute organizational skills to direct personnel during a building crisis or emergency</p></li></ul><p>To be considered for this position you must have an AAS in construction or related technologies and 5+ years of experience, including experience in planning, organizing and supervising a diverse workforce involved in the building maintenance of a large multi-building manufacturing complex. You should also have supervisory experience including training, assigning work, setting expectations and performance evaluations. Equivalent combination of education and experience may be considered. You must be willing and able to work a Monday - Friday 2pm-10:30pm schedule.</p><p>#REGENTOSK</p></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 04:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Rheumatology]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45255]]></requisitionid>
    <referencenumber><![CDATA[R45255]]></referencenumber>
    <apijobid><![CDATA[r45255]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45255/senior-medical-director-clinical-development-rheumatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Medical Director, Clinical Sciences is responsible for facilitating assigned studies, providing investigator support of Regeneron driven studies, and may serve as a resource to anticipate and/or resolve study clinical and conduct issues. This role reports into the Clinical Program Lead, Clinical Sciences and is expected to have proficient knowledge of the drug development process, good clinical practice, study design and research methodology as well as understand Regulatory and compliance landscape in the pharmaceutical industry. This role utilizes scientific and clinical expertise to initiate, propose, design and execute research and development programs for early and/or late stage assets for rheumatology/autoimmunity indications. This role may be suitable for an Rheumatologist, Allergist, Immunologist, Pulmonologist, or Dermatologist with industry experience. Clinical research experience in the academic/clinical setting may be considered at the Medical Director level.</div><div></div><div><div><div><div><p>A typical day in the life may include the following responsibilities:</p><ul><li>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program. Clinical deliverables may include individual protocols; clinical components of regulatory documents/registration dossier and brand related medical information, clinical communication and publications</li><li>Demonstrated ability to influence team and may influence across function</li><li>Ability to lead activities within a matrix environment</li><li>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally</li><li>Advanced analytical and influencing skills</li><li>Ability to communicate concise and clear messages</li><li>Seeks to understand different perspectives and cultures and values differing points of view</li><li>Can identify critical risks and mitigation</li><li>Proficient medical writing skills and advanced presentation skills</li></ul><p>This role may be for you if:</p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p>In order to be considered for this role, a M.D. degree or equivalent is required. Specialized clinical fellowship training in Rheumatology, Allergy, Immunology, Pulmonology, or Dermatology is strongly preferred. 1-4 years of industry experience in clinical development is preferred. Clinical Research experience in the academic/clinical setting may be considered at the Medical Director level.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 14:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Pulmonology - Grand Rapids, MI]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46983]]></requisitionid>
    <referencenumber><![CDATA[R46983]]></referencenumber>
    <apijobid><![CDATA[r46983]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46983/medical-specialist-i-pulmonology-grand-rapids-mi/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Grand Rapids, MI</strong></p><p>The Medical Specialist (MS) will report to the District Manager and be responsible for engaging customers in the Pulmonary therapeutic area within an assigned geographical universe, presenting clinically focused selling messages to create and drive growth, and consistently delivering product goals.<br><br><strong>A Typical Day Might Look Like This</strong></p><ul><li><p>Demonstrate strong and consistent sales performance related to product goals in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p></li><li><p>Develop strategy and execute tactics within key accounts in the Pulmonary therapeutic area to generate product utilization.</p></li><li><p>Develop strong working relationships with Pulmonologists and Midlevel experts in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p></li><li><p>Collaborate with their regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography.</p></li><li><p>Participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).<br> </p></li></ul><p><strong>This Position Might Be For You If</strong><br> </p><ul><li><p>Demonstrate advanced clinically based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>Experience with in-servicing and training office staff, nurses and office managers<br> </p></li></ul><p>To be considered for this role you must have a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Pulmonary market or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Control Room Supervisor]]></title>
    <date><![CDATA[Sat, 02 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46906]]></requisitionid>
    <referencenumber><![CDATA[R46906]]></referencenumber>
    <apijobid><![CDATA[r46906]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46906/control-room-supervisor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking to add a Control Room Supervisor to our growing team, working a Sunday-Wednesday 6am-4:30pm shift. In this role you will oversee our Facilities Control Room team responsible for Building Automation Systems and Pi Historian.</p><p>As a Control Room Supervisor, a typical day might include the following:</p><ul><li>Performing supervisory responsibilities including timesheet review and approval, employee development, performance feedback, and selection.</li><li>Ensuring the team is reviewing, monitoring, responding and reacting as necessary to alarm notifications from the Building Automation Systems and Pi Historian.</li><li>Providing guidance to facilities consultants.</li><li>Ensuring accurate and contemporaneous documentation of all alarms in Facilities CMMS system.</li><li>Monitoring employees’ training to ensure that all requirements are met, including OJT and that all the proper SOPs are followed.</li><li>Scheduling, assigning, completing and reviewing work specifically to control room activities.</li><li>Ensuring employees make positive contact and coordinate with asset owners and Facilities Management when alarms for unplanned events occur.</li><li>Participating in compliance and related investigations and providing historical data trends when necessary.</li><li>Collaborating with other departments, contractors and disciplines for alarm response.</li><li>Communicating and setting expectations of IOPS and facilities department initiatives.</li><li>Following current good manufacturing practices (cGMPs) including proper communication of compliance related events to facilities compliance team.</li></ul><p>This position might be for you if you:</p><ul><li>Are adept at collaborating with cross-functional teams and communicating effectively with partners.</li><li>Have a strong attention to detail.</li><li>Are able to see the “Big Picture” and demonstrate the ability to respond accordingly.</li><li>Ensure the highest level of customer service.</li><li>Are skilled in the use of Microsoft office applications.</li></ul><p>To be considered for this role you must be willing and able to work Sunday-Wednesday 6:00am-4:30pm. Candidates ideally should have a technical certificate or AAS in Engineering or Construction Technologies along with 5 years of relevant experience. 3+ years of leadership experience is required. Equivalent combination of education and experience may be considered.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 02 May 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director GPO & Account Management - Ophthalmology]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47287]]></requisitionid>
    <referencenumber><![CDATA[R47287]]></referencenumber>
    <apijobid><![CDATA[r47287]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47287/senior-director-gpo-account-management-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Area Director (ADO), Ophthalmology will report to the Executive Director – GPO and Key Accounts Ophthalmology and will be responsible for recruiting, leading, developing and retaining the Ophthalmology Account Director team in the Region. The ADO handles ensuring strong and consistent performance that meets and exceeds brand goals, GPO program and driving accountabilities for all results throughout the Region. Developing OAD team and Showing Regeneron’s presence in the Ophthalmology market. ADO will work closely with their internal cross functional stakeholders for collaboration and success across all accounts in the region. The ADO will work closely with internal teams including Executive Leadership, Sales, MA, Legal, Trade and Training and Development within the region designed to continue to meet and exceed brand goals. The ADO will carry out 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><h3><strong>The typical day may include the following:</strong></h3><ul><li>Build and develop a high performance, high integrity, high quality OAD team and provide overall leadership to the team.</li><li>Responsible for meeting and/or exceeding brand objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</li><li>Lead regional activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</li><li>Ensure each employee is trained and effectively implements all resources to support customer and account goals.</li><li>Communicate most current knowledge of the industry and competitor products to teams.</li><li>Ensure participation in industry related trade shows, meetings, conferences, etc.</li><li>Analyze data to ensure proper resources are deployed in the region.</li><li>Allocate and manage the region's budget and use of resources.</li><li>Ensure strong, consistent performance that consistently meets or exceeds brand objectives while demonstrating accountability for all results.</li><li>Building the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, GPO) in the field of Ophthalmology.</li><li>Ensure the Ophthalmology Account Directors are viewed by their customers as experts in the field of GPO and Ophthalmology account management.</li><li>Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support account and brand and objectives.</li><li>Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including government programs, managed health care and evolving health care systems.</li><li>Oversee key aspects of strategic account management activities for specific key accounts within region in and ensure plans, resources, and performance objectives for the accounts are maximized.</li></ul><h3><strong>To be considered for this opportunity,</strong></h3><ul><li>Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</li><li>Minimum of 15 years of pharmaceutical/biopharmaceutical experience with 7 years of sales leadership/management of which 5 years must be at the Regional Director/District Manager level or higher with focus in Retina or Oncology</li><li>Experience in Biologics and buy and bill products or strong relevant experience in the Ophthalmology required.</li><li>Proven success and track record of performance with a high degree of integrity as a Team Leader in complex markets required.</li><li>Successful record of hiring, coaching, developing, promoting, and keeping top talent within span of control.</li><li>Strong understanding of Group Purchasing Organizations, payer environment, reimbursement and challenges within National/Regional market including GPO relationships, government programs, managed health care and evolving landscape of Retina.</li><li>Proven ability and success in developing business experts in a regional scope required.</li><li>Excellent leadership and interpersonal skills; should be an effective team player who can empower credibility and confidence.</li><li>Strong ability to partner and collaborate with other internal field teams and partners.</li><li>70% travel with local and regional geography.</li><li>Ability to manage and drive a region's objectives and goals.</li><li>Strong analytic, presentation, organization, administration and communication skills.</li><li>Product launch experience.</li><li>Experience with selling to diverse customer segments.</li><li>Ability to analyze market data and provide clear direction resulting in execution and meeting/exceeding brand goals.</li><li>Strategic thinker who will challenge status quo to improve performance.</li><li>Leadership skills include motivation, mentoring and the ability to provide professional development to his/her team.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Development Program Management]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44512]]></requisitionid>
    <referencenumber><![CDATA[R44512]]></referencenumber>
    <apijobid><![CDATA[r44512]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44512/manager-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>With guidance, this role M<strong>anager, Development Program Management </strong>uses program management knowledge and experience in the drug development industry to provide operational leadership and manage components of development program(s). This individual contributes to the cross functional development team (Strategic Program Team) to develop strategic plans including goals, budgets, timelines and track the execution of these plans from preclinical through commercialization/lifecycle management. </p><p><em>***Note this role is expected to be onsite 4 days per week with 1 day from home either to be based in Warren, NJ or Tarrytown, NY and is not eligible remote. </em></p><p><strong>As a Manager, a typical day may include: </strong></p><ul><li><strong>Development Teams: </strong>Under the direction of their manager or DPM Lead, supports select subteam and/or functional area meetings. May lead functional area and/or working group meetings. Participates in development of risk management plans. Tracks deliverables, risks, and issues.</li><li><strong>Business Acumen: </strong> Under direction of their manager or DPM Lead, Identifies stakeholders across organization to facilitate cross functional reviews/alignments of key documents. Manages project management planning systems (MS Project, SharePoint) for assigned programs/projects. Uses systems and tools to move the program and business forward. </li><li><strong>Communication: </strong>Facilitates collaboration on selected assignments between functional areas to ensure effective, accurate, and timely scientific/technical and program-related communication. Keeps manager and other stakeholders informed to ensure alignment of key decisions/actions items of the assigned projects. Escalates issues/risks to appropriate stakeholders in a timely manner. </li><li><strong>Problem Solving: </strong>Supports the team and lead DPM in gathering information relevant to issues and formulating solutions to issues encountered during project implementation. With direction, supports development of processes and tools to document issues and their resolution. Escalates complex problems or issues to lead DPM in a timely and appropriate manner </li><li><strong>Leadership:</strong> Influences within workstream and/or sub-sets of project team. Builds relationships and effectively collaborates with department and cross-functional colleagues. Seeks out support for resolution of conflicts.</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Are action oriented and organized</li><li>Intellectually curious</li><li>Comfortable dealing with ambiguity</li><li>Demonstrate good judgement</li><li>Think critically</li><li>Communicate and collaborate well</li><li>Are a team player </li><li>Regularly demonstrate professional maturity, and take setbacks and constructive criticism well.</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree is required and 5+ years of relevant project management experience, preferably in the drug development/pharmaceutical industry.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Strategic Partnerships & Business Operations]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41651]]></requisitionid>
    <referencenumber><![CDATA[R41651]]></referencenumber>
    <apijobid><![CDATA[r41651]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41651/associate-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[<p>At Regeneron, we are committed to developing and maintaining strategic relationships with clinical institutions that support our Clinical Development pipeline such as Academic Medical Centers (AMCs), Site Management Organizations (SMOs), Site Networks and Community Centers. The Global Partnerships team is responsible for establishing and managing relationships at the executive-level that enable operational and scientific engagement throughout the Global Development organization.</p><p>We are seeking an <strong>Associate Director Strategic Partnerships & Business Operations</strong> that will lead and optimize strategic relationships with clinical trial sites and site networks to drive executional and scientific excellence across the clinical development portfolio. This role will be responsible for establishing and managing governance frameworks with priority clinical trial sites including leading governance meetings, partnership metrics and day-to-day issue identification and resolution. You will report to the Director, Global Development Strategic Partnerships and will support across the Global Partnerships team to ensure the success of these strategic relationships.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Serve as the primary relationship owner for priority clinical trial sites</li><li>Establish a governance structure to manage relationships with high priority clinical trial sites including but not limited to:</li><li>Planning and facilitation of governance meetings such as joint research committees and portfolio reviews</li><li>Management of partnership metrics</li><li>Management of communication and issue escalation pathways</li><li>Manage the day-to-day activities to achieve the strategic objectives of the relationship</li><li>Act as a key internal and external point of contact for the relationship to proactively identify and resolve any potential issues</li><li>Act as an internal subject matter expert for the clinical institution to provide guidance to other departments within Regeneron</li><li>Manage critical initiatives with high priority clinical trial sites</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Previous experience in and a deep understanding of the drug development process</li><li>Previous experience maintaining relationships with clinical institutions including communication and stakeholder management at the executive level</li><li>Solid organizational and project management skills including strong attention to detail</li><li>A results-oriented, collaborative style</li><li>Experienced in planning and execution; thinks strategically and executes tactically to deliver results for the business</li><li>Demonstrates resiliency; able and willing to explore different paths to achieve an outcome</li><li>Consistently demonstrates good judgment and takes initiative to bring forward new ideas to improve processes</li><li>Previous experience operating across a matrix of teams and influencing without authority</li><li>Advanced skills in Microsoft Office Suite including Excel and PowerPoint</li></ul><p><strong>In order to be considered qualified for this role</strong> a minimum of a Bachelor’s Degree and 10+ years is required. Advanced degrees (MS, MBA) are preferred when accompanied by 8+ years of proven experience in pharma or a related field.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Facilities Engineer]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47148]]></requisitionid>
    <referencenumber><![CDATA[R47148]]></referencenumber>
    <apijobid><![CDATA[r47148]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47148/senior-facilities-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Facilities Engineer, you will provide engineering support, troubleshooting, & subject matter expertise to the Facilities Operations, Utilities & HVAC teams.</p><p><strong>A typical day might include, but is not limited to, the following:</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>This role might be for you if:</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>To be considered for this opportunity you should have:</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></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 05:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Critical Utilities]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47222]]></requisitionid>
    <referencenumber><![CDATA[R47222]]></referencenumber>
    <apijobid><![CDATA[r47222]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47222/director-critical-utilities/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director of Critical Utilities and Facility Management safeguards the reliability, safety, and compliance of the campus Central Utility Plant and all Mechanical, Electrical and Plumbing (MEP) systems, ensuring uninterrupted delivery of electricity, chilled water, steam, emergency power, and other crucial services for 24/7 research and operational needs. Reporting to senior facilities leadership, the role blends strategic planning with hands-on oversight, leading a hybrid workforce (internal technicians + outsourced FM provider), partnering with Engineering, EH&S, and Business Resilience teams, and requires occasional travel—up to 25%—to support off-site infrastructure and vendor audits.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Developing and implementing long-term operational strategies for Critical Utilities and Facilities Maintenance programs supporting a complex pharmaceutical/biotech campus environment.</p></li><li><p>Leading organizational development efforts including team structure design, role definition, workforce planning, and operational model optimization across internal staff and outsourced service providers.</p></li><li><p>Establishing and continuously improving maintenance, reliability, and capital planning programs to improve system performance, resiliency, compliance, and operational efficiency.</p></li><li><p>Providing executive oversight of Central Utility Plant and Powerhouse operations while partnering with operational leadership to ensure safe, reliable, and uninterrupted utility delivery.</p></li><li><p>Collaborating cross-functionally with Engineering, R&pD Operations, EH&S, Quality, Procurement, and Capital Projects teams to support site operations, infrastructure initiatives, and future campus growth.</p></li><li><p>Driving governance, performance management, and strategic vendor oversight activities including the development of critical metrics, operational reviews, budget planning, risk mitigation, and continuous improvement initiatives.</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Thrive on keeping utility plants, chillers, boilers, and generators running with zero unplanned downtime.</p></li><li><p>Balance hands-on problem solving with strategic planning, budgeting, and long-range asset management.</p></li><li><p>Motivate and coordinate a mixed team of internal technicians, union trades, and third-party providers.</p></li><li><p>Are comfortable making sure that rigorous safety and regulatory standards in high-risk environments.</p></li><li><p>Turn maintenance data into actionable reliability improvements.</p></li><li><p>Communicate clearly with researchers, engineers, and executives—and don’t mind hitting the road when needed.</p></li></ul><p><strong>In order to be considered for this role, you must have:</strong></p><ul><li><p>A bachelor’s degree in mechanical/electrical/Power/Marine/Energy Engineering—or—15 years of proven experience as an equivalent (Navy Nuclear Power School + 10 years accepted).</p></li><li><p>10+ years leading central utility or power-plant operations (chilled water, steam, emergency power) within a hybrid FM model, plus strong contract-management and vendor-governance skills.</p></li><li><p>Proficiency with BAS platforms (e.g., Metasys, EcoStruxure, Desigo).</p></li><li><p>Proven team-leadership abilities.</p></li><li><p>A valid NYS driver’s license to support up to 25% travel.</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[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Cardiovascular/Metabolism]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47613]]></requisitionid>
    <referencenumber><![CDATA[R47613]]></referencenumber>
    <apijobid><![CDATA[r47613]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47613/senior-medical-director-clinical-development-cardiovascularmetabolism/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Medical Director, Clinical Development, will play a key role in clinical development programs within the Cardiovascular/Renal/Metabolism portfolio focused on obesity and related comorbidities. This role serves as Scientific and Medical Lead for Clinical team(s) working closely with Operational Leads to guide and execute clinical development strategies and subsequent regulatory submissions. This role requires a high-performing and highly passionate individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research. The Senior Medical Director reports to an Executive Medical Director, Internal Medicine.</p><p>A typical day may include the following:</p><ul><li><p>Acts as medical expert and leader in interactions with external stakeholders</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 more efficient and innovative, yet robust Phase 2/3 programs.</p></li><li><p>Works closely with discovery teams to provide input on the next generation of targets in the field and leads the development of plans for Phase 1 clinical testing for initial characterization of the molecules PK/PD and safety.</p></li><li><p>Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety.</p></li><li><p>Plans and executes publication and clinical communication strategy in coordination with Publications team. Provides input to key external presentations.</p></li><li><p>Ensures quality of all clinical documents (e.g., Investigators’ Brochure, protocol, study report, clinical components of regulatory submissions, safety related documents). Develops written responses to regulatory agency questions and regulatory submission documents.</p></li></ul><p><strong>This may be the role for you if:</strong></p><ul><li><p>A minimum of an advanced degree in medicine (i.e., M.D. or D.O. or equivalent).</p></li><li><p>Clinical training in Endocrinology or Cardiology (board certified or eligible or equivalent) is strongly preferred.</p></li><li><p>A minimum of 4 years of relevant clinical development experience in industry leading clinical trials including: protocol design, managing study start-up, directing and guiding study team execution, data cleaning, medical monitoring/review, database locks.</p></li><li><p>Experience with regulatory filings and interactions with health authorities preferred</p></li></ul><p>This role requires 4 days a week / weekly on-site presence in Tarrytown, NY or Warren, NJ.</p><p>#MDJOBSCD, #MDJOBS, #GDTherapeuticJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Sciences, Internal Medicine]]></title>
    <date><![CDATA[Sun, 19 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43175]]></requisitionid>
    <referencenumber><![CDATA[R43175]]></referencenumber>
    <apijobid><![CDATA[r43175]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43175/associate-director-clinical-sciences-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Clinical Sciences contributes to the development, evaluation, planning and execution of Internal Medicine clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Works in a matrix environment as part of a cross-functional team (with internal and external vendor representation) and may contribute to candidate development projects through early and/or late phase development. Reports to the Sr Dir/Director, Clinical Science, Internal Medicine and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p>As an Associate Director, a typical day may include the following:</p><ul><li><p>May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Utilizes proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late-stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Contributes to planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators</p></li><li><p>Proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li></ul><p>This role may be for you:</p><ul><li><p>Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>You possess strong cross-functional management, interpersonal skills, and strong attention to detail</p></li></ul><p>To be considered for this role, a bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/PharmD/MSc). ≥ 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Metabolic disease and/or inflammatory disease areas. We are seeking proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills. We need an individual who is a strong team-player. Experience in all aspects of conducting global clinical trials and execution of clinical programs. Other levels considered depending on experience. Experience in managing trials in one or more of the following therapeutic areas - cardiovascular, renal, metabolic and/or inflammatory disease - required. #Obesity</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$173,500.00 - $283,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Summer 2026 MD Intern, Internal Medicine]]></title>
    <date><![CDATA[Wed, 22 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43354]]></requisitionid>
    <referencenumber><![CDATA[R43354]]></referencenumber>
    <apijobid><![CDATA[r43354]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43354/summer-2026-md-intern-internal-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>If you’re currently a medical school student interested in drug discovery and development, you may be a fit for an internship in our Internal Medicine Clinical Development Unit.</p><p><strong>In this role, a typical internship will include:</strong></p><ul><li><p>Achieving a general understanding of what happens in our global development organization</p></li><li><p>Completing a hands-on project that has an impact on the business</p></li><li><p>Engaging with Regeneron leadership</p></li><li><p>Collaborating with a specific hiring manager and other interns</p></li><li><p>Establishing connections with Regeneron’s diverse employee resource groups</p></li><li><p>Participating in professional development sessions</p></li><li><p>Showcasing the knowledge you gained through end of program presentation sessions</p></li><li><p>Getting paid for your hard work!</p></li></ul><p><strong>Internship Project Specifics:</strong></p><p>The summer intern will be placed on a project team in the Internal Medicine Clinical Development Unit at Regeneron. During this project the summer intern may visually and/or descriptively analyze clinical trial data from recent studies or databases. Disease areas that comprise the focus of the summer interns project may include: cardiovascular, pulmonary and/or immunological & inflammatory diseases.</p><p>The student will be trained on basic statistical modeling techniques using SAS JMP. The summer project may involve reviewing pharmacokinetic (PK) and pharmacodynamic (PD) data from clinical trials. Students will be trained on techniques for data cleaning, statistical analysis, and linear regression (univariate and multivariate). The student will work closely with the global program head, medical director and clinical pharmacology director during the project.</p><p>Additionally, students will be trained in Good Clinical Practice (GCP) standards for human clinical trials including relevant International Conference on Harmonization (ICH) and FDA Guidelines. The student will also attend relevant team meetings including: Strategic Project Team, Global Clinical Sub Team, Global Regulatory Sub Team and others as needed.</p><p>At the end of the summer internship period, the student will be expected to give a presentation/summary of their research experiences to an internal audience at Regeneron.</p><p>To be considered for this opportunity, you must be currently enrolled in medical school and returning to school the semester following the internship). A cumulative GPA of 3.0 is preferred. We want someone who is able to commit to 40 hours per week for a minimum of 6-8 weeks during a time-period from the end of May/ early June through August. The specific weeks of the internship are flexible and intended to accommodate the intern’s time out of school. Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community is also preferred.</p><p>Requirements:</p><ul><li><p>Medical student currently enrolled in an accredited US medical school (MD)</p></li><li><p>Must have completed at least the first-year basic science curriculum. Students who have completed the second year and beyond will also be considered but must have adequate time available during an elective or research rotation to be on site at Regeneron.</p></li><li><p>Familiarity with Microsoft Office tools (Word, Outlook, Powerpoint).</p></li><li><p>Prior research experience is preferred but not required. Understanding of biostatistics, experimental design and the scientific method is preferred. Experience with R studio, Python, SPSS, SAS or SAS JMP is a plus.</p></li><li><p>On site attendance at Regeneron offices in Tarrytown NY is expected 5 days per week</p></li></ul><p><strong><em>Please note our intern pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for Tarrytown, NY: $32.00-$40.70 per hour. </em></strong></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Procurement-Direct]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44723]]></requisitionid>
    <referencenumber><![CDATA[R44723]]></referencenumber>
    <apijobid><![CDATA[r44723]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44723/director-global-procurement-direct/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Director Global Procurement, Direct position within our team. In this role you will develop a holistic Category Strategy and provide strategic leadership and direction with a focus on CMO & External Manufacturing Procurement. The position focuses on a very exciting part of Regeneron’s molecule portfolio which includes Drug Product & Drug Substance for Mab’s, Advanced Therapies and other therapeutic areas. This role will be critical to driving performance across the IOPS External Manufacturing categories including alignment with stakeholder goals, driving towards competitive advantages (strategic and financial) and optimizing supplier relationships. This role works in close collaboration with IOPS Stakeholders to enable company revenue targets and the new product pipeline.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Lead the composition, development and execution of category strategies in CMO External Manufacturing, Drug Substance & Drug Product.</p></li><li><p>Translate category strategies into achievable and meaningful sourcing projects that deliver value to Regeneron and its patients.</p></li><li><p>Partner with Direct Procurement Leadership colleagues to ensure strategies evolve as Regeneron and its pipeline evolves.</p></li><li><p>Implement category strategies to meet objectives.</p></li><li><p>Collaborate with other parts of Global Procurement to best manage cross-category suppliers.</p></li><li><p>Anticipate needs and plan strategies to optimize achievement of corporate goals.</p></li><li><p>Collaborate and execute a best-in-class partner management program.</p></li><li><p>Implement and manage technology solutions to drive value via efficiency and effectiveness.</p></li><li><p>Build and manage a team that provides all CMO Procurement support globally.</p></li><li><p>Continually enhance capability and capacity through ongoing talent development establishing/communicating criteria for evaluating staff performance; managing direct reports, implementation of consistent work processes; and drive process excellence with a focus on stakeholder experience</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Believe that value can be driven through strategic partnerships and efficient ways of working.</p></li><li><p>Can tap into strong in-depth knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of a Global Procurement organization.</p></li><li><p>Enjoy successfully leading global categories or global teams, processes, and suppliers within a multi-national organization.</p></li><li><p>Serve as role-model leader consistently exhibiting behaviors across an organization of direct reports to create clarity, provide a clear and understandable vision with transparency and trust both within and outside of the organization.</p></li><li><p>Can demonstrate success leading cross-functional teams to drive results in CMO, External Manufacturing categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Can influence and partner with senior executives and peer functions to drive strategic change and efficiency.</p></li><li><p>Have working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Have experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><ul><li><p>Director: 12+ years of experience in relevant functions or industries. The ideal candidate will have in-depth knowledge of CMO’s & External Manufacturing, Raw Materials or Packaging Technologies in the Pharmaceutical field procurement categories.</p></li></ul><p>This role requires working onsite 5 days per week.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Regulatory Affairs Strategy - Oncology]]></title>
    <date><![CDATA[Thu, 15 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44633]]></requisitionid>
    <referencenumber><![CDATA[R44633]]></referencenumber>
    <apijobid><![CDATA[r44633]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44633/director-regulatory-affairs-strategy-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities will include support to some clinical study activities. The candidate will also supply, lead and/or supervise IND/CTA and BLA submissions activities.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide interpretation of regulatory authorities’ feedback, policies and guidelines.</p></li><li><p>Lead the development of regulatory strategic plans either directly in conjunction with project teams or through your reports. Own the preparation of major clinical submissions required for regulatory approval.</p></li><li><p>Work with project teams to resolve complex project issues. Utilize regulatory expertise and knowledge of regulatory requirements and regulations to strategically interpret, plan, and communicate requirements to ensure attainment of governmental approvals.</p></li><li><p>Responsible for quality and timeliness of IND/CTA and BLA submissions. Interact with other functions and partners, in the preparation, review, and completion of documents for regulatory submissions.</p></li><li><p>Successfully plan, prioritize, supervise and/or conduct activities in close collaboration with leads from other areas. Assure compliance with regulations and with project team timelines.</p></li><li><p>Provide interpersonal support and lead personnel.</p></li><li><p>Critical thinking, leadership skills, assertiveness, excellent negotiation and project management skills as evidenced by past performance on drug development project teams</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>If you bring strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices.</p></li><li><p>If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred</p></li><li><p>If you have a high attention to detail; ability to coordinate and prioritize assigned projects according to company goals</p></li><li><p>You bring strong interpersonal skills both written and verbally</p></li></ul><p><strong>To be considered,</strong> you must possess excellent written and verbal communication skills along with a MD, Ph.D. or Pharm D. degree. We expect a minimum of 10 years of pharmaceutical industry experience, at least 7 of which should include regulatory experience.</p><p><em>This role requires you to work onsite 4 days per week in either Warren, NJ, Tarrytown, NY or Cambridge, MA. If you are not local and qualify we can offer relocation support. </em></p><p>#MDJOBSRA #GDRAJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 16 Jan 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44660]]></requisitionid>
    <referencenumber><![CDATA[R44660]]></referencenumber>
    <apijobid><![CDATA[r44660]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44660/senior-manager-internal-medicine-clinical-scientist-immuneinflammatory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p></div><div><div><div><div><p><strong>As a Senior Manager in Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Develops/maintains understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Collaborates with internal functions and external vendors to promote clinical study integrity</p></li><li><p>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>Demonstrated ability to influence within team and may influence cross functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in one or more of the following therapeutic areas – Immune/Inflammatory related clinical trials.</p></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Global Program Head - Oncology]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45150]]></requisitionid>
    <referencenumber><![CDATA[R45150]]></referencenumber>
    <apijobid><![CDATA[r45150]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45150/vice-president-global-program-head-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Global Program Head (GPH) for Oncology leads integrated strategy and execution for one or more REGN oncology antibody programs from lead selection through Biologics License Application (BLA). The GPH co-leads the asset strategic team with a clinical co-leader, aligns cross-functional stakeholders, and ensures Executive Management has the right information to authorize program strategy decisions. This role spans discovery through late-stage development and interfaces broadly across research, development, and commercial functions to deliver high-quality, scientifically rigorous, and competitive development plans.</p><h3><strong>Key Responsibilities</strong></h3><ul><li>Drive creation and continuous refinement of an integrated, end-to-end program strategy from discovery through late-stage development and BLA submission</li><li>Co-lead the asset strategic team with the clinical co-leader; provide program oversight, execution discipline, and risk/issue management</li><li>Identify, engage, and align key stakeholders across REGN and partners to ensure input and accountability for program strategies and plans</li><li>Provide strategic guidance across research, nonclinical, clinical, medical safety, CMC/supply (toxicology, clinical and commercial materials), regulatory, and commercial needs</li><li>Ensure scientific rigor and innovation are embedded in program decision-making and development plans</li><li>Integrate cross-functional perspectives on scientific rationale, operational feasibility, budget, timeline, and competitive/commercial landscape</li><li>Translate strategy, recommendations, and trade-offs clearly between teams and senior leadership; prepare and deliver high-quality discussions and presentations to facilitate decisions</li><li>Represent Regeneron at joint development committees as needed and maintain productive external partner interactions</li></ul><h3><strong>Qualifications</strong></h3><ul><li>MD, PhD, or PharmD required</li><li>15+ years of broad oncology drug development experience, with substantial expertise in oncology clinical development</li><li>Proven track record advancing programs through key development milestones and/or approval in biotech/pharma; biologics experience strongly preferred</li><li>Deep knowledge of the competitive landscape and regulatory pathways for oncology drug approval</li><li>Demonstrated ability to build and lead high-performing, cross-functional teams in a highly matrixed environment without direct line authority</li><li>Strong strategic thinking, stakeholder management, and communication skills; adept at influencing across functions and levels</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (f/m/d) - Bremen - Osnabrück - Oldenburg]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45946]]></requisitionid>
    <referencenumber><![CDATA[R45946]]></referencenumber>
    <apijobid><![CDATA[r45946]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45946/sales-specialist-oncology-fmd-bremen-osnabrueck-oldenburg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>You will be responsible for a variety of customer engagement activities such as meeting with Healthcare Professionals (HCPs) and representing our Oncology division at key meetings. You will identify the key people in Oncology, understand the account context and tailor calls based on individual and account requirements and build KOL support for our Oncology portfolio in the territory Bremen - Osnabrück - Oldenburg.</p><div><p><strong>A typical day may include:</strong></p><ul><li><p>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and reliably implementing sales & marketing plans</p></li><li><p>Consistently deliver on the value proposition for the brand and ensure brand objectives are met through key message communication to HCPs</p></li><li><p>Act as a manager in your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach in line with regional/country level guidance</p></li><li><p>In line with the Germany Brand Plan, develop and implement a local account plan based on key data sources and local market insights</p></li><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs</p></li><li><p>Leverage all communication channels including digital channels, in collaboration with other functions, in order to achieve the best possible share of voice in the market</p></li><li><p>Report results and developments proactively and clearly to the Germany leadership team</p></li></ul><p><strong>This may be for you if:</strong></p><ul><li><p>You have a deep understanding of the local healthcare economy, with the ability to identify key players in Oncology</p></li><li><p>You have a “patient first” value system</p></li></ul><p>To be considered, you need a Bachelor’s Degree or equivalent experience and a "pharmaceutical sales representative" (Pharmaberater:in / Pharmareferent:in) qualification. We're looking for 5+ years of sales experience within the biotech/pharmaceutical sector including Oncology experience and proficiency in German as well as conversational English language skills. You need to be ready for very frequent travel and have a driver's license cl. 3/B.</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 04:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, QA Microbiology]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46191]]></requisitionid>
    <referencenumber><![CDATA[R46191]]></referencenumber>
    <apijobid><![CDATA[r46191]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46191/executive-director-qa-microbiology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is hiring! The Executive Director, QA Microbiology is responsible for the development and execution of the strategy and plan for the Regeneron GMP Microbiology program. The individual in this position is also responsible for providing direction to the function areas to ensure high-quality, safe, and effective products that are compliant with global regulatory expectations with respect to microbiological topics. This position will direct the efforts of the applicable functional areas in support of compliance and business objectives and will ensure that the Microbiology program remains current with industry expectations and help liaison with subject matter experts within the lines of businesses. </p><p>In this role, a typical day might include the following:</p><ul><li><p>Implement a value-added microbiology program based on sound science and the application of the appropriate quality, regulatory and legal requirements.</p></li><li><p>Monitor the performance of the microbiology program using the appropriate metrics and demonstrate a commitment to continuous improvement.</p></li><li><p>Embed quality tools and risk management processes within the microbiology program.</p></li><li><p>Stay abreast of changing requirements/expectations and proactively address within the microbiology program.</p></li><li><p>Use quality and risk management tools to make timely, science-based decisions to protect patient safety.</p></li><li><p>Implement appropriate solutions that address complex technical, legal and global regulatory standards.</p></li><li><p>Partners with QA Operations functions within the lines of business to translate strategy to implementation, and ensure compliant and robust aseptic practices.</p></li><li><p>Demonstrate confidence during difficult decision-making and influence internal and external business partners to ensure acceptable outcomes.</p></li><li><p>Lead as microbiology decision maker to ensure the safety and effectiveness of the products.</p></li><li><p>Represent as the face of Regeneron to internal and external stakeholders, including regulatory agencies and corporate partners regarding microbiological topics.</p></li><li><p>Translate the vision and business strategies of the microbiological program into executable action plans.</p></li><li><p>Ensure the Microbiological Control Strategy is transparent and the organization is engaged in its execution.</p></li><li><p>Allocate resources based on microbiology program priorities and corresponding business needs.</p></li><li><p>Establish high standards for performance management and accountability to achieve microbiological and organizational objectives.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Comprehensive knowledge of microbiological expectations throughout drug development process, pharmaceutical technology, drug manufacturing processes and related issues, drug laws, global regulations, and guidelines, particularly CMC and GMP.</p></li><li><p>Experience building up a quality culture and quality management capabilities.</p></li><li><p>Comprehensive knowledge and experience in CMC section content for investigational and marketed product submissions (IND, BLA, CBE, PAS) for FDA and equivalent submissions for Europe.</p></li><li><p>A sense of passion and commitment for delivering things as quickly and efficiently as possible.</p></li><li><p>The ability to think and operate in a rapidly evolving and ambiguous environment.</p></li><li><p>Ability to articulate and execute concepts for developing and ensuring the highest quality throughout the network (internal and external).</p></li><li><p>Intellect for quality risk identification, mitigation, and management.</p></li><li><p>Strong communication skills —written and oral.</p></li><li><p>Experience with businesses in different phases of the business lifecycle and the quality and validation issues associated with these phases.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Engineering, Chemistry, Biology or related science/technical field and the following amount of experience in a regulated industry (ie., Biotech, Pharma, Medical Device) for each level:</p><ul><li><p>Sr Director – 15+ years</p></li><li><p>Executive Director – 18+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role. Equivalent combination of education and experience will be considered.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$239,600.00 - $399,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 10:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46369]]></requisitionid>
    <referencenumber><![CDATA[R46369]]></referencenumber>
    <apijobid><![CDATA[r46369]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46369/drug-production-associate-manufacturing-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment.</p><p>A typical day for a Drug Production, Associate Manufacturing Specialist might include:</p><ul><li><p>Performing all aspects of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operating automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Supporting equipment start-up, troubleshooting, and validation</p></li><li><p>Partnering with R&D teams to implement new drug manufacturing processes and technologies</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Enjoy working in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients</p></li><li><p>Are highly organized, detail oriented and perform work accurately the first time</p></li><li><p>Value trust and transparency in everyday work</p></li><li><p>Work well in both small and large teams to accomplish tasks adhering to a schedule</p></li><li><p>Can operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients</p></li><li><p>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Are a good communicator and can give and receive feedback constructively</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p>Gowning and Environment</p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li></ul><p>Shift & Physical Requirements</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p>To be considered for this role you must meet the below minimum education and experience requirements:</p><p>Drug Production, Associate Manufacturing Specialist:</p><ul><li><p>HS diploma + 4 years of relevant work experience <strong>or</strong></p></li><li><p>AS, BS or BA in Life Sciences or related field</p></li></ul><p>Regeneron offers an exciting and competitive benefits package! For details check out: <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Statistical Genetics (Oncology)]]></title>
    <date><![CDATA[Wed, 08 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46218]]></requisitionid>
    <referencenumber><![CDATA[R46218]]></referencenumber>
    <apijobid><![CDATA[r46218]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46218/director-statistical-genetics-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an exceptional senior leader with deep expertise in cancer genetics and genomics to join our team at the Regeneron Genetics Center. This Director-level role carries full accountability for the strategy and execution of cancer genetic product development — from aligning the vision with senior leadership and translating it into an actionable operational plan, through overseeing product development and setting the strategy for commercialization. The ideal candidate will bring a demonstrated track record of independence and impact, and will serve as the driving force for bringing cancer risk genomics into clinical and commercial reality.</p><p><strong>In this role, a typical day might include the following:</strong></p><p>• Develop and deliver on cancer genetics testing opportunities, including germline testing partnerships, serving as the senior leader accountable for clinical cancer test development.</p><p>• Define and own the end-to-end strategy for germline genetic cancer risk product development, translating organizational vision — aligned with senior leadership — into a clear, actionable operational roadmap with measurable milestones.</p><p>• Develop and execute a comprehensive somatic genetics strategy for Regeneron’s oncology portfolio, identifying new opportunities for somatic profiling studies across tumor types and leveraging existing cancer genomics databases.</p><p>• Lead and execute large-scale somatic cancer sequencing analyses, including whole-exome and whole-genome sequencing of tumor samples, RNA-seq, and integrative multi-OMICS studies to identify driver mutations, therapeutic vulnerabilities, and mechanisms of resistance.</p><p>• Design and contribute to cancer molecular profiling and clinical correlation analyses that integrate germline and somatic mutational profiles with multi-modal transcriptomic, epigenetic, and proteomic data to support target discovery, indication selection, and patient stratification strategies.</p><p>• Oversee all phases of product development for cancer risk genomics programs, ensuring scientific rigor, cross-functional alignment, and on-time delivery against strategic objectives.</p><p>• Develop and execute the commercialization strategy for RGC cancer products, identifying market opportunities, go-to-market pathways, and partnerships that maximize clinical and commercial impact.</p><p>• Collaborate with and lead a multidisciplinary genetics team consisting of human genetics scientists, bioinformaticians, and statistical geneticists to design, execute, and interpret genetics studies related to cancer risk, somatic evolution, mechanisms, and therapeutic outcomes.</p><p><strong>This job might be for you if you:</strong></p><p>• Have a demonstrated ability to independently own and drive strategic programs in cancer risk genomics or oncology product development from conception through commercialization.</p><p>• Bring innovative thinking and hands-on leadership to large-scale somatic cancer sequencing studies and integrative genomic analyses.</p><p>• Have deep expertise in analyzing tumor sequencing data, including variant calling, mutational signature analysis, clonal evolution, copy number alterations, and structural variant detection.</p><p>• Have experience in developing or contributing to germline diagnostic tests for cancer predisposition, risk assessment, or clinical decision-making.</p><p>• Are a motivated senior leader with a desire to pursue genetic discovery in a fast-paced multidisciplinary environment and can effectively guide teams and align stakeholders toward strategic goals.</p><p>• Have demonstrated experience in quantitative problem solving, statistical analyses, and translating somatic and germline genetic findings into clinical applications.</p><p><strong>To be considered for this role</strong>, you must have an MD or MD/PhD with a strong background in quantitative biology applied to cancer genetics and genomics, and a proven ability to design and lead large-scale human cancer genomic programs delivering medically- and commercially-relevant outcomes.</p><p>A minimum of 12 years of research experience in cancer genetics, genomics, or oncology product development is required, with a commensurate level of independence, seniority, and demonstrated responsibility for program strategy and execution.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 08 Apr 2026 18:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Global Development IT & Digital Manager]]></title>
    <date><![CDATA[Wed, 08 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45997]]></requisitionid>
    <referencenumber><![CDATA[R45997]]></referencenumber>
    <apijobid><![CDATA[r45997]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45997/global-development-it-digital-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>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>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 08 Apr 2026 04:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Immunology Pharmaceutical Representative – Picardie]]></title>
    <date><![CDATA[Mon, 20 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46594]]></requisitionid>
    <referencenumber><![CDATA[R46594]]></referencenumber>
    <apijobid><![CDATA[r46594]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46594/immunology-pharmaceutical-representative-picardie/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>As an Immunology Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, while covering the <strong>Picardie</strong> region. You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>Immunology Pharmaceutical Representative – Picardie</strong></p><p><strong>As an Immunology Pharmaceutical Representative, a typical day might include the following:</strong></p><ul><li><p>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and optimally implementing sales & marketing plan.</p></li><li><p>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</p></li><li><p>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</p></li><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</p></li><li><p>Leverage all communication channels including digital channels, in collaboration with other functions, to achieve the best possible share of voice in the market.</p></li><li><p>Report results and developments proactively and clearly to the Immunology leadership team</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</p></li><li><p>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</p></li><li><p>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</p></li><li><p>You can operate effectively in a “start-up” model as this is a completely new team.</p></li></ul><p>To be considered for this opportunity you must hold a Carte Professionnelle with minimum <strong>5+ years of pharmaceutical sales experience in Immunology</strong>. You are happy with regular travel and have a valid driver's license. Conversational English would be desirable, but not required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Field Medical Affairs Oncology - France]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46686]]></requisitionid>
    <referencenumber><![CDATA[R46686]]></referencenumber>
    <apijobid><![CDATA[r46686]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46686/director-field-medical-affairs-oncology-france/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Director, Head of Field Medical Oncology to lead Regeneron’s field medical oncology organization in France and serve as a key medical leader within Global Medical Affairs.</p><p>In this role, you will guide in-country medical and clinical activities, align local execution with global strategy, and strengthen Regeneron’s scientific presence across Oncology. It is a meaningful opportunity to shape team performance, support innovation access, and influence how medical insights inform patient care and business decisions.</p><p><strong>Director, Head of Field Medical Oncology – Paris </strong></p><p><strong>(hybrid)</strong></p><p><strong>A Typical Day:</strong></p><ul><li>Leading the field medical oncology team across France.</li><li>Coaching direct reports through field visits and 1:1 discussions.</li><li>Recruiting, training, and developing team members for strong execution.</li><li>Guiding compliant medical initiatives, field activities, and performance metrics.</li><li>Supporting clinical development through site identification and investigator engagement.</li><li>Coordinating support for IIS proposals, AOIs, and potential EAP activities.</li><li>Partnering with Medical Directors on congresses, symposia, and advisory boards.</li><li>Contributing field medical insight to launch readiness, market access, and lifecycle plans</li></ul><p><strong>This Role May Be For You:</strong></p><ul><li>You enjoy leading and developing a field medical team.</li><li>You like balancing scientific depth with practical in-country execution.</li><li>You work comfortably across medical affairs, clinical, operations, regulatory, and commercial interfaces.</li><li>You are motivated by building trusted relationships with investigators and external experts.</li><li>You naturally keep compliance at the center of how work gets done.</li><li>You are energized by shaping strategy while staying close to field realities.</li><li>You can move between team leadership, scientific exchange, and operational support.</li><li>You value bringing clear, actionable medical insights into decision-making.</li></ul><p>To be considered, you will bring a PhD, PharmD, MD, DVM, or equivalent, along with 7+ years of relevant Medical Affairs Oncology experience, including experience as a Field Medical Manager in the biotech or pharmaceutical industry within oncology, especially lung and skin cancer. You will also need strong knowledge of in-country Medical Affairs and Clinical Development, a thorough understanding of the local healthcare environment, experience across product lifecycle development, and fluency in English.</p><p>The role requires willingness to travel 30–50%. Preferred experience includes immuno-oncology, new product launches in country, and an established external network with key opinion leaders in lung and skin cancer.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Marketing - Oncology]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44802]]></requisitionid>
    <referencenumber><![CDATA[R44802]]></referencenumber>
    <apijobid><![CDATA[r44802]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44802/manager-marketing-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>We’re Hiring: Manager, Marketing (Oncology Japan)</strong><br>Are you ready to make a meaningful impact in the oncology field? At Regeneron Japan, we are seeking an experienced Product Manager to lead our local oncology marketing initiatives. Reporting to the Senior Marketing Manager, you’ll play a pivotal role in shaping our brand strategy and executing impactful marketing campaigns for both current and future product launches. Join us in driving innovation and improving lives through cutting-edge therapies.</p><p><strong>A Typical Day:</strong><br>As Manager, Marketing (Oncology Japan), you will:</p><ul><li>Develop and execute the overarching brand marketing strategy in alignment with global objectives.</li><li>Collaborate with cross-functional teams to implement promotional activities that resonate with key target audiences.</li><li>Analyze market dynamics, competitive actions, and stakeholder feedback to identify opportunities and mitigate risks.</li><li>Partner with Medical Affairs to ensure an aligned brand strategy and seamless execution of the strategic brand plan.</li><li>Create tailored promotional materials for sales teams and digital channels, ensuring consistency with brand plans.</li><li>Lead the planning and execution of external stakeholder engagement activities, including national congresses and HCP meetings.</li><li>Manage the local promotional budget and ensure expenditures align with approved financial plans.</li><li>Uphold the highest ethical and compliance standards in all marketing activities.</li></ul><p><strong>This Role May Be For You If:</strong><br>You are:</p><ul><li>A strategic thinker with a proven track record in biotech/pharma brand marketing.</li><li>Skilled in managing agencies, suppliers, and developing annual budgets.</li><li>Proficient in planning, prioritization, and communication, with excellent presentation skills.</li><li>Comfortable working in complex, dynamic environments and taking initiative to drive results.</li><li>Experienced in oncology marketing and product launches (preferred but not required).</li><li>Willing to travel (30–40%, including some weekends) for conferences and meetings.</li><li>Knowledgeable about local healthcare compliance codes and promotional regulations.</li><li>Fluent in written and spoken English.</li></ul><p><strong>To Be Considered:</strong><br>Applicants must hold a Bachelor's degree, preferably in a science-related field, and have 5+ years of brand marketing experience within the biotech/pharma industry. Expertise in oncology marketing and product launches is preferred. A deep understanding of healthcare compliance codes and regulations is essential. Strong integrity, creativity, and adaptability are critical for success in this role.</p><p>This job advertisement has been designed to reflect the essential functions and qualifications outlined in the job description while maintaining a clear, professional, and inclusive tone.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 05:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology-Miami, Orlando, FL, Puerto Rico]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46693]]></requisitionid>
    <referencenumber><![CDATA[R46693]]></referencenumber>
    <apijobid><![CDATA[r46693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46693/medical-account-specialists-hematology-miami-orlando-fl-puerto-rico/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Miami]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Miami, Orlando, FL, Puerto Rico </strong></p><p>The Hematology Oncology Account Specialist, is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Hematology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of two bispecific agents to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 09:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician, Saturday-Wednesday 3rd shift]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46909]]></requisitionid>
    <referencenumber><![CDATA[R46909]]></referencenumber>
    <apijobid><![CDATA[r46909]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46909/hvac-technician-saturday-wednesday-3rd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a HVAC Technician to our growing team, working a Saturday-Wednesday 10:00pm – 8:30am shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment; troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for approximately 6 months. Working hours thereafter will be Saturday-Wednesday 10:00pm-8:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a HVAC Technician, a typical day might include the following:</p><ul><li><p>Maintaining coolers and freezers including Ultra Low temperature Freezer</p></li><li><p>Maintaining Centrifugal and Reciprocating refrigeration chillers</p></li><li><p>Maintaining Chilled water systems including distribution and condenser pumps</p></li><li><p>Maintaining Air Compressors</p></li><li><p>Electrical power systems and stand-by power generation equipment</p></li><li><p>Following current good manufacturing practices (cGMPs) and good business practices (G)</p></li><li><p>Participating in rotational on-call for site emergency work</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOP's, cGMP's, GDP’s and quality standards</p></li><li><p>Becoming fully gown qualified to work within Production areas</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</p></li><li><p>May plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Are able to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li></ul><p>To be considered for the HVAC Technician position you must be willing and able to work a Saturday-Wednesday 10:00pm – 8:30am schedule. Applicants ideally should have technical school training with field experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance and the following minimum amounts of experience for each level:</p><ul><li><p>HVAC Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>HVAC III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li><li><p>HVAC IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role. Will substitute relevant work experience in lieu of education. Electronic, PLC, mechanical and building automation systems experience in Pharmaceutical Industry preferred. EPA certified for refrigeration gases.</p><p>#REGENTOSK </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager-Artificial Intelligence- Global Development]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43358]]></requisitionid>
    <referencenumber><![CDATA[R43358]]></referencenumber>
    <apijobid><![CDATA[r43358]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43358/senior-manager-artificial-intelligence-global-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Global Development (GD) is embarking on a digital transformation project that will incorporate AI, machine learning, and automation into our processes to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. This position will play a key role in developing the platforms, processes and technologies that will incorporate AI effectively across GD. The AI engineer will work with a team of engineers and scientists to help bring transformative change to GD. The role will encompass a wide range of AI/ML-related activities, from data engineering and technical development to optimizing vendor systems for use at Regeneron to mentoring colleagues in best practices for adopting and AI in their everyday workflows. Development will not necessarily be limited to the use of generative AI, but may also include technical implementation of machine learning models, natural language processing, and other approaches. The engineer will work with stakeholders across GD and other groups to develop solutions and architectures that addresses our needs and integrate into the overall corporate strategy.</p><p><strong>As a Senior Manager, a typical day may include: </strong></p><ul><li><p>Implement, and refine novel algorithms and scalable AI /ML solutions tailored to GD applications such as clinical trial design, regulatory intelligence, patient identification and stratification, etc. Deploy these solutions to production environments as appropriate Implementation includes hands-on development and coding.</p></li><li><p>Develop, implement, and improve data architecture and engineering approaches for diverse data sources across GD</p></li><li><p>Contribute to initiatives with GDIT and enterprise IT to build the necessary infrastructure (software and hardware) to support advanced analytics</p></li><li><p>Collaborate with GD colleagues to help them approach AI/ML more effectively</p></li><li><p>Establish rigorous validation frameworks for AI models and monitor existing models for accuracy and efficiency</p></li><li><p>Stay up to date with the latest advances in the field and, as appropriate, evaluate them for adoption at Regeneron</p></li></ul><p><strong>This may be for you if you:</strong></p><ul><li>Can demonstrate expertise in AI And ML</li><li>Want to make an impact on patient lives</li><li>Are actively developing your skills in AI and ML</li><li>Capable of communicating to a technical and non-technical audience. <br> </li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Deep understanding of generative AI, machine learning, natural language processing, and statistical modeling</p></li><li><p>Deep expertise in programming (Python, R, etc.), with a focus on applying advanced technical skills to data analysis, pipeline creation, automation, and software development</p></li><li><p>Expertise in database platforms and cloud computing infrastructure</p></li><li><p>Track record of model development, implementation to scale, maintenance, and evaluation in a healthcare of life sciences setting</p></li><li><p>Experience managing and analyzing large-scale clinical datasets</p></li><li><p>Excellent communication skills, both technical and non-technical</p></li><li><p>Experience managing multiple projects</p></li><li><p>Experience working in cross-functional teams</p></li><li><p>May require travel up to 20%</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$148,300.00 - $241,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist - Quantitative Translational Scientist]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46821]]></requisitionid>
    <referencenumber><![CDATA[R46821]]></referencenumber>
    <apijobid><![CDATA[r46821]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46821/principal-scientist-quantitative-translational-scientist/]]></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>Regeneron’s Precision Medicine Quantitative Biomarker team (PMQBS) is seeking a Principal Scientist with a blend of deep biomarker and translational-science expertise coupled with advanced computational and analytical skills. This role will focus primarily on the Oncology portfolio, and 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 querying, visualizing, and cleaning data. The individual will work collaboratively with internal and external groups to assure data integrity, best practices for analytics and data visualization, and offering strategic insights to drive Precision Medicine objectives. </p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Set and refine quantitative biomarker strategies across multiple programs, aligning with Precision Medicine Strategy Leads and senior stakeholders.</p></li><li><p>Translate program objectives into testable hypotheses, analytical roadmaps, and decision criteria that inform clinical development and asset strategy.</p></li><li><p>Architect exploratory analyses of multi-modal datasets (genomic, transcriptomic, proteomic, metabolomic, clinical, and other biomarkers) to generate actionable insights.</p></li><li><p>Define and review statistical frameworks, including hypothesis testing, modeling approaches, and power/sample-size analyses, ensuring appropriate interpretation.</p></li><li><p>Oversee the correct application of statistical models on integrated datasets and drive clear, decision-oriented interpretation for translational and clinical teams.</p></li><li><p>Contribute to the vision for scalable, reproducible pipelines and automated workflows that support enterprise-wide biomarker discovery and clinical development.</p></li><li><p>Direct the design and enhancement of computational workflows for novel biomarkers; evaluate, integrate, or build tools as needed.</p></li><li><p>Provide guidance on data cleaning, integration, and visualization standards to enable robust, interpretable analyses.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Proficient in statistical modeling/regression, machine learning, and related data integration/blending techniques.</p></li><li><p>Experienced in implementing scalable workflows on cloud platforms (AWS, GCP, or Azure)</p></li><li><p>Experienced in Linux and/or cloud environments, shell scripting, and notebook-based workflows.</p></li><li><p>Knowledgeable of structured data and data mapping for systems integration, data provisioning, and consumption.</p></li><li><p>Experience with version control and AI coding assistants such as Claude Code is strongly preferred.</p></li><li><p>Knowledgeable of structured data and data mapping for systems integration, data provisioning, and consumption.</p></li></ul><p><strong>To be considered for this role,</strong> you must have at minimum a PhD with 2 years, or Masters with 5 years of relevant industry experience in one of the following or otherwise related quantitative fields: Computer Science, Computational Biology, Systems Biology, Quantitative Biology, Bioinformatics, Data Analytics, Biostatistics. A working understanding of Clinical trials is a strong plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47082]]></requisitionid>
    <referencenumber><![CDATA[R47082]]></referencenumber>
    <apijobid><![CDATA[r47082]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47082/medical-director-clinical-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Are you ready to make a meaningful impact on clinical development programs in Japan? At Regeneron, we are seeking a dedicated Medical Director, Clinical Sciences, to join our dynamic team. In this pivotal role, you will collaborate closely with the Japan Clinical Development Lead (J-CDL) to advance scientific and clinical aspects of our programs. From contributing to global clinical teams to supporting regulatory filings, your expertise will drive innovation and deliver results that matter.</p><p>Join us in shaping the future of clinical development, where your skills and insights will play a vital role in transforming lives.</p><p><strong>A Typical Day:</strong></p><p>As the Medical Director, Clinical Sciences, your day will be filled with impactful activities, such as:</p><ul><li><p>Supporting the clinical components of assigned clinical development programs (CDPs) in Japan.</p></li><li><p>Providing clinical and scientific input for regulatory documents, including J-NDA/J-CTD submissions.</p></li><li><p>Contributing to the development and adaptation of clinical trial protocols and related documentation for Japan-specific needs.</p></li><li><p>Collaborating with cross-functional teams to ensure clinical feasibility and address local medical needs in global studies.</p></li><li><p>Participating in investigator meetings, site initiation visits, and vendor kick-off meetings to drive study execution.</p></li><li><p>Offering medical/scientific input to resolve issues during study conduct and execution.</p></li><li><p>Staying current on scientific advancements in therapeutic areas and representing the company at national and international conferences.</p></li><li><p>Building and maintaining relationships with key opinion leaders (KOLs) and investigator sites.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You have a strong understanding of the drug development process, clinical trial design, and good clinical practice (GCP).</p></li><li><p>You excel in both Japanese and English, with business-level proficiency in English communication.</p></li><li><p>You enjoy collaborating across cross-functional teams, bringing diplomacy and influence to your interactions.</p></li><li><p>You are detail-oriented and possess exceptional analytical and problem-solving skills.</p></li><li><p>You thrive in dynamic environments and are adept at managing regulatory interactions effectively.</p></li><li><p>You value diversity, different perspectives, and are committed to fostering inclusive teamwork.</p></li></ul><p><strong>To Be Considered:</strong></p><p>We are looking for candidates with the following qualifications:</p><ul><li><p><strong>Required:</strong> MD or MD/PhD with at least 5 years of pharmaceutical industry experience, including 3 years of clinical development experience.</p></li><li><p>Expertise in regulatory filings and clinical document preparation, particularly CTN and J-NDA/J-CTD submissions.</p></li><li><p>Proven ability in protocol design, clinical data review, and familiarity with medical monitoring activities.</p></li><li><p>Strong knowledge of Phase I–III clinical trial design and objectives.</p></li><li><p><strong>Preferred:</strong> Experience with clinical feasibility assessments and Japan-specific enrollment considerations.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 02:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I (Gastro)-Pittsburgh, PA]]></title>
    <date><![CDATA[Sun, 26 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47115]]></requisitionid>
    <referencenumber><![CDATA[R47115]]></referencenumber>
    <apijobid><![CDATA[r47115]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47115/medical-specialist-i-gastro-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>Geography: Pittsburgh, PA</strong></p><p>The Medical Specialist (Sales Representative), Gastroenterology (MS) will report to the District Manager, Gastroenterology, and be responsible for engaging Gastroenterologists and other key customers within an assigned geographical universe, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies, and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US. </p><p><strong>A Typical Day May Include the Following:</strong></p><p>The MS is responsible for developing strategy and executing tactics within key accounts in the Gastroenterology therapeutic area to generate product utilization. The MS will develop strong working relationships with experts and all Gastroenterologists in assigned geography as well as nurses, office staff and other important health care personnel and key patient advocacy support groups as directed.</p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>This Role May Be for You If:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li></ul><p>To be considered you must possess a minimum of a ​Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in a subcutaneous self-injectable biologic specialty market. Experience with in-servicing and training office staff, nurses and office managers. Ability to partner and collaborate with other internal field teams and alliance partners. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 27 Apr 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Medical Affairs-Classical Hematology]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47118]]></requisitionid>
    <referencenumber><![CDATA[R47118]]></referencenumber>
    <apijobid><![CDATA[r47118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47118/senior-manager-medical-affairs-classical-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Manager, Medical Affairs -Classic Hematology you will serve as a scientific and strategic resource leading the execution of our medical plans across bleeding and clotting disorders. Take an active participation in an integral role to drug launch readiness and early access programs. </p><p>This position is at our Sleepy Hollow, NY offices and will require you to be onsite 4 days/week. If eligible, we can offer relocation benefits. We cannot offer a remote work option. </p><p><strong>A typical day may include the following: </strong><br>• Translating scientific and clinical insights into medical strategies supporting evidence generation and product positioning.<br>• Ensuring our medical activities are conducted in strict compliance with applicable regulations, company policies, and industry codes of practice.<br>• Establishing, developing, and sustaining peer-level relationships with KOLs and academic institutions. <br>• Support the development and oversight of company-sponsored clinical trials, including identification and selection of investigators and trial sites.<br>• Manage investigator-initiated studies with our Field Medical team. <br>• Gather and report relevant scientific, clinical, and competitive intelligence. <br>• Drive launch readiness activities, contributing medical expertise to cross-functional planning and execution.<br>• Support early access programs, including data collection, management, and reporting in alignment with regulatory requirements.<br>• Coordinate and facilitate advisory boards and scientific meetings, ensuring robust insight capture and actionable outputs.</p><p><strong>This may be for you if you:</strong><br>• Want to be a part of the early-stage buildout of a new team<br>• Have an exceptional ability to communicate clinical and medical data to clinical and non-clinical audiences.<br>• Demonstrated ability to work independently and effectively within a matrix organizational structure.<br>• Want to have an impact of patient health</p><p>To be consider it is required to have a doctorate level education in life sciences (MD, PharmD, PhD) and a clinical background in hematology. Your experience must 3+ years of experience in a Medical Manager or Medical Affairs role within the biotech or pharmaceutical industry. Solid understanding of anticoagulation or thrombosis along with their treatment guidelines, and clinical research processes is preferred. Willingness to travel including overnight and occasional weekend travel.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Compliance - Canada]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47219]]></requisitionid>
    <referencenumber><![CDATA[R47219]]></referencenumber>
    <apijobid><![CDATA[r47219]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47219/director-compliance-canada/]]></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 are looking for a <strong>Canada Compliance Director</strong> to join our International Compliance team, playing a central role in supporting business operations and strengthening our compliance program across Canada and selected international markets. Working closely with global teams, you will develop policies, guide business practices, and support ethical decision-making across the organization. This is a meaningful opportunity to influence compliance culture, partner with senior leadership, and help ensure our activities are aligned with industry standards and regulations.</p><p><strong>Compliance Director – Canada</strong></p><p><strong>(Office based – Toronto)</strong></p><p><strong>A Typical Day:</strong></p><ul><li>Leading compliance activities across Canada and selected international markets</li><li>Driving implementation of compliance programs with global and legal teams</li><li>Developing and refining policies, procedures, and compliance guidance</li><li>Delivering and improving training for employees and external partners</li><li>Advising on compliance risks related to business initiatives and HCP interactions</li><li>Supporting internal investigations and monitoring activities when required</li><li>Collaborating on audits, risk assessments, and remediation actions</li><li>Identifying emerging risks and proactively shaping mitigation strategies</li></ul><p><strong>This Role May Be For You:</strong></p><ul><li>You enjoy partnering with senior leaders to guide compliant business decisions</li><li>You are comfortable navigating sophisticated regulatory environments in pharma</li><li>You take a proactive approach to identifying and mitigating compliance risks</li><li>You value collaboration across cross-functional and international teams</li><li>You like translating regulatory requirements into practical business guidance</li><li>You are motivated by shaping training, policies, and compliance frameworks</li><li>You are confident providing oversight on activities involving HCPs and HCOs</li><li>You appreciate balancing critical thinking with hands-on execution</li></ul><p><strong>To Be Considered</strong></p><p>You bring a minimum of 7 years of experience working in or with pharmaceutical companies on healthcare compliance activities, along with deep knowledge of Canadian healthcare compliance laws, regulations, and industry codes of practice. You have experience drafting and implementing policies, as well as supporting monitoring, auditing, and training programs. A strong understanding of compliance across commercial, medical affairs, market access, and clinical development is required. Fluency in English is essential, and French is considered an asset. This role is based in Toronto with a hybrid working model and may require travel.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Laboratory Assistant, Bioanalysis]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45695]]></requisitionid>
    <referencenumber><![CDATA[R45695]]></referencenumber>
    <apijobid><![CDATA[r45695]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45695/senior-laboratory-assistant-bioanalysis/]]></url>
    <company><![CDATA[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 LabOps team is primarily responsible for managing and optimizing all aspects of the Lab Environment. This may include but not limited to ensuring labs are equipped, maintained and run efficiently in the areas of Lab Management, Process Optimization, Compliance and Safety, Resource Allocation & Coordination and Communication.</p><p>This role requires knowledge of laboratory procedures, ability to perform moderate complex tasks, make recommendations to enhance processes to do the job effectively, work cross-functionally with others in department.</p><p> <strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Performs daily routine tasks, which can include monitoring and re-stocking inventory in labs and storage areas, equipment managment, and recording appropriately in electronic lab notebooks</p></li><li><p>May have modified working schedule to include weekend days with purpose of providing general support to group.</p></li><li><p>Be adaptable to learning and supporting additional activities that may arise to continuously support the team through future growth and expansion</p></li><li><p>Anticipates and recognizes potential problems, presents them to supervisor, and works to identify key operational improvements and devise strategies to increase the speed and efficiency</p></li><li><p>Provide guidance to and/or assists others on non-routine or escalated issues</p></li><li><p>Participates effectively as a member of the team within functional area, may provide guidance to others within group</p></li><li><p>Communicate effectively with all functions and levels within the organization, exemplify strong interpersonal and customer service skills while leveraging prior technical experience/knowledge </p></li></ul><p><strong>This Role Might Be For You If You:</strong></p><ul><li><p>Possess good organization, communication, and collaboration skills; can work well within a team and individually</p></li><li><p>Have a service-oriented mindset and desire to provide quality customer service</p></li></ul><ul><li><p>Actively seeks opportunities for skill enhancement and knowledge enrichment</p></li></ul><ul><li><p>Possess strong operational skills to drive and execute core responsibilities with limited supervisory guidance</p></li></ul><p><strong> To Be Considered, You Must Have</strong>: High School Diploma and 2 - 4 years of experience, or combination of training and experience. A 2-year college degree may be preferred. Experience in inventory management is a plus. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$30.24 - $47.36]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:26:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Human Factors Engineer]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47279]]></requisitionid>
    <referencenumber><![CDATA[R47279]]></referencenumber>
    <apijobid><![CDATA[r47279]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47279/human-factors-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>Regeneron is currently looking for a Human Factors (HF) Engineer to join our Process Sciences Drug Product Engineering department. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. This non-lab based role is focused on human factors evaluation of delivery systems, ensuring that assigned devices, labelling and packaging are designed to be safe and effective for use by intended users. </p><p>When & where:</p><ul><li>Monday-Friday, 8am-4:30pm</li><li>Location: East Greenbush, New York, United States</li></ul><p>What you’ll do:</p><ul><li>Develops HF engineering strategies and leads HF activities on drug-device combination product program teams, including ethnography, requirements definition research, use-related risk analysis, formative usability studies and summative usability studies</li><li>Authors, reviews and edits study protocols and reports, research summaries, usability requirements and design control documentation</li><li>Performs task analysis, usability-related risk analyses, interface evaluations and provides design recommendations</li><li>Conducts user inquiries, user studies, data gathering and data analysis</li><li>Collaborates with internal cross-functional design team and external vendors as needed</li><li>Works with other HF team members to develop and implement continuous process improvements</li></ul><p>Let’s find out if we’re a fit:</p><ul><li>Requires B.S in Biomedical Engineering, Human Factors specific Psychology or another relevant engineering discipline<ul><li>Assoc Human Factors Engineer: 0-2 years of experience</li><li>Human Factors Engineer: 2+ years of experience</li></ul></li><li>Level will be determined based on experience</li><li>Working knowledge of: FDA Human Factors Guidance, Design Controls, HE75, ISO 62366 is preferred</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><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$66,200.00 - $123,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs-Neurology (northern CA, WA and OR)]]></title>
    <date><![CDATA[Sat, 09 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46426]]></requisitionid>
    <referencenumber><![CDATA[R46426]]></referencenumber>
    <apijobid><![CDATA[r46426]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46426/senior-manager-field-medical-affairs-neurology-northern-ca-wa-and-or/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Manager, you will play a pivotal role as a field-base/Medical Science Liaison providing scientific and Neurology therapeutic area expertise. The Senior Manager will become a scientific expert communicating accurate and applicable science to medical and health care professionals, and payers. In addition, you will support our strategic medical objectives by developing and maintaining professional relationships through facilitating collaboration opportunities.</p><p><strong>Territory: </strong> focus on northern CA, WA and OR (additional territory will include ID, MT, WY, NV, AK)</p><h3>A typical day may include the following:</h3><ul><li>Develop and maintain peer–to–peer collaborations and relationships with medical and scientific experts, and population health decision makers.</li><li>Participate on committees or project teams supporting field medical strategies and tactics.</li><li>Respond to unsolicited medical information requests, handle questions and liaise with headquarters personnel ensuring proper responses has been provided and data is fair and balanced.</li><li>Develop an understanding of the regional landscape including specialties involved in care of patients in that area & other landscape mapping activities.</li><li>Identify and bring actionable information & insights that enhance the value and appropriate use of our products back to appropriate internal collaborators.</li><li>Build and cultivate important working relationships across field partners to ensure an integrated approach when working with HCP’s or experts.</li><li>Collaborate with physicians on medical affairs initiatives including publications, Company– sponsored research (CSR), regional advisory boards, regional medical education opportunities, training and speaker development programs.</li><li>Develop and sustain expertise in product/molecule data, disease state management, emerging therapies, and the competitive landscape.</li><li>Respond to HCP inquiries with integrity, compliance, and adherence to legal, regulatory, and our guidelines, policies & procedures ensuring focused and balanced clinical and scientific information.</li><li>Support clinical research activities throughout the life cycle (phase 1-4), as well as Investigator Initiated Studies, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ experts and sites in alignment with Medical Affairs objectives</li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) along with a minimum of 3-5 years related work experience preferred (clinical, managed care, or industry experience) including experience as a Medical Science Liaison. Recent experience in Neurology is preferred. Experience communicating and disseminating scientific and clinical data in required. Travel withing the assigned territory and attendance at industry conference is required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 09:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Regulatory Intelligence]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47246]]></requisitionid>
    <referencenumber><![CDATA[R47246]]></referencenumber>
    <apijobid><![CDATA[r47246]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47246/senior-manager-regulatory-intelligence/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Senior Manager, Regulatory Intelligence to play a key role in monitoring, interpreting, and communicating changes in the global regulatory landscape, with a strong focus on EU regulatory strategy and pharmacovigilance.</p><p>In this role, we partner closely with cross‑functional teams to translate regulatory developments into clear, actionable insight that supports drug development, regulatory strategy, and GxP compliance across the organization.</p><h3>A Typical Day May Include</h3><ul><li>Monitoring and assessing new and emerging regulatory guidance, legislation, and policy from global health authorities and industry bodies.</li><li>Evaluating regulatory developments to determine relevance and impact on development programs, regulatory strategy, and internal processes.</li><li>Preparing concise regulatory intelligence summaries, reports, and presentations tailored to different stakeholder groups.</li><li>Acting as a point of contact for regulatory intelligence questions and ad‑hoc requests.</li><li>Identifying business‑critical regulatory changes and proactively communicating implications to cross‑functional stakeholders.</li><li>Supporting regulatory commenting activities, including review and drafting of submissions to health authorities and industry organizations.</li><li>Facilitating regulatory intelligence briefings, meetings, and knowledge‑sharing sessions.</li><li>Maintaining regulatory intelligence content and contributing to improvements in how intelligence is captured and shared.</li><li>Mentoring junior team members, as needed.</li></ul><h3>This Role May Be For You If You</h3><ul><li>Enjoy staying ahead of regulatory change and applying it in a practical, business‑focused way.</li><li>Have strong experience in regulatory affairs and/or pharmacovigilance within pharma or biotech.</li><li>Are confident interpreting regulatory guidance and understanding its impact across the drug development lifecycle.</li><li>Are comfortable working cross‑functionally and engaging with a range of stakeholders.</li><li>Can work independently, manage competing priorities, and deliver to deadlines.</li><li>Value clarity, accuracy, and quality in your work.</li><li>Are motivated to improve processes and contribute to how regulatory intelligence is delivered across the organization.</li></ul><h3>What You’ll Bring</h3><ul><li>8+ years’ experience in the pharmaceutical or biotech industry, or within a health authority, with a focus on Regulatory Affairs and/or Pharmacovigilance.</li><li>Strong understanding of EU and US regulatory and pharmacovigilance requirements across the drug development lifecycle.</li><li>Experience sourcing, monitoring, and interpreting regulatory information from health authority platforms and other intelligence sources.</li><li>Strong analytical skills, with the ability to identify key regulatory risks and implications.</li><li>Clear, concise written and verbal communication skills.</li><li>Strong organizational skills and attention to detail.</li><li>A collaborative, practical approach to working across teams and functions.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 03:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ultra-Pure Water Technician, Monday-Friday 1st shift]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46855]]></requisitionid>
    <referencenumber><![CDATA[R46855]]></referencenumber>
    <apijobid><![CDATA[r46855]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46855/ultra-pure-water-technician-monday-friday-1st-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking to fill an Ultra-Pure Water (Clean Utilities) Technician position with a Monday - Friday 6:00am-2:30pm shift. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Clean Utilities Technicians support the manufacturing process through involvement with start-up, operation, monitoring, maintaining and shutdown of clean utility systems and equipment within Clean Utility mechanical rooms.</p><p><strong>Please note training will be Monday-Friday 7:00am-3:30pm for the first few months. Working hours thereafter will be Monday - Friday 6:00am-2:30pm. </strong></p><p><strong>As a Clean Utilities Technician, a typical day might include the following:</strong></p><ul><li><p>Performing preventative and predictive maintenance on related clean utilities and systems that support manufacturing.</p></li><li><p>Maintaining water rooms and related equipment such as pumps, motors, Water for Injection (WFI) stills, Clean Steam Generators and related piping.</p></li><li><p>Performing activities such as troubleshooting, hands on repairs on all related clean utility equipment and systems, and WFI point of use flushing.</p></li><li><p>Maintaining documents and records on all validated equipment and systems.</p></li><li><p>Collaborating with other departments and contractors on scheduling repairs and maintenance of clean utility systems.</p></li><li><p>Perform monitoring and control of systems utilizing computer driven Building Automation System (BAS) and PLC controls</p></li><li><p>Communicating with management regarding change documentation as necessary.</p></li><li><p>Following current Good Manufacturing Practices (cGMPs) and Good Business Practices (G).</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur.</p></li><li><p>Participating in rotational on-call schedule.</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Can read and/or understand piping, electrical, and instrumentation drawings</p></li><li><p>Possess basic troubleshooting skills as they relate to the water room and mechanical aptitude</p></li><li><p>Demonstrate basic problem solving skills</p></li><li><p>Understand additional mechanical equipment and systems such as pharmaceutical compressed air, domestic water lines, plant steam and high/low pressure condensate return systems</p></li><li><p>Can learn and follow routine procedures independently as well as part of a team</p></li><li><p>Have the comfort and flexibility to work in a changing environment</p></li><li><p>Are capable of lifting, pushing, and/or pulling at least 50lbs</p></li><li><p>Have basic knowledge of Microsoft Office Suite</p></li></ul><p>To be considered for the Clean Utilities Technician position you must be willing and able to work Monday - Friday 6:00am-2:30pm. Applicants must meet the education and experience minimums listed below for each level: </p><ul><li><p>Clean Utilities Technician II: HSD/GED with 5+ years of related experience OR AAS degree and 2+ years of related experience</p></li><li><p>Clean Utilities Technician III: HSD/GED with 8+ years of related experience OR AAS degree and 5+ years of related experience</p></li><li><p>Clean Utilities Technician IV: HSD/GED with 11+ years of related experience OR AAS degree and 8+ years of related experience</p></li></ul><p>Prior experience in the maintenance and operation of large scale utilities plant is preferred but not required.</p><p>Level will be determined based on qualifications relevant to the role.</p><p>#REGENTOSK</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Project Manager (Quality Control)]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45581]]></requisitionid>
    <referencenumber><![CDATA[R45581]]></referencenumber>
    <apijobid><![CDATA[r45581]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45581/associate-project-manager-quality-control/]]></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 an Associate Project Manager to join our QC (Quality Control) AS (Analytical Sciences) team. The Associate Project Manager - QC works to identify, define and progress the clinical phase project deliverables for Analytical Sciences for advanced therapies programs. Working with internal subject matter experts, external contract manufacturing organizations, external contract labs and customer groups in a matrixed team environment, the Associate Project Manager ensures that analytical test methods and supporting quality deliverables are established to support product manufacturing.</p><p><strong>As an Associate Project Manager, a typical day might include the following:</strong></p><ul><li>Serves as the Analytical Sciences representative on advanced therapies CMC (Chemistry, Manufacturing and Controls) program teams, acting as the primary point of contact for analytical topics, program milestones, and risk/issue escalation.</li><li>Builds and nurtures strong partnerships with external contract laboratories, overseeing outsourced analytical programs to drive shared accountability, consistent communication, and high-quality, on-time deliverables.</li><li>Communicates cross-functionally within Analytical Sciences to align method development needs, resourcing, and timing for each clinical-phase program.</li><li>Ensures analytical activities (internal and external) adhere to appropriate phase-appropriate quality systems, data integrity principles, and regulatory expectations.</li><li>Develops a cohesive strategy for each clinical phase program and is responsible for the execution of that strategy.</li><li>Uses technical knowledge to ensure customer groups are provided with the appropriate analytical services including ensuring appropriate assays are in place for manufacturing sampling plans.</li><li>Partners with CMC Regulatory Sciences, Quality Assurance, Manufacturing, Process Sciences, and Technical Training to define analytical deliverables and supporting documentation (reports, protocols, method development plans, technical memos, forms).</li><li>Collaborates with CMC Reg Sci to support regulatory filings.</li><li>Identifies, implements, and scales tools and templates (e.g., dashboards, trackers, method development frameworks, tech transfer packages) to improve team quality and efficiency.</li><li>May own the implementation of CAPAs for Analytical Sciences and/or assist with quality events.</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You have excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company.</li><li>You can navigate a fast-paced and ambiguous environment to create a detailed program plan with defined deliverables and timelines.</li><li>Can resolve and negotiate conflicts or problems with tact, diplomacy and composure.</li><li>You have experience with MS Project, or related project management tools.</li></ul><p>To be considered for this position you must have a BS/BA in chemistry, biology or related field with 6+ years of relevant experience, preferably in the pharmaceutical or biotechnology industries. PMP certification is strongly preferred.</p><p>Level will be determined based on qualifications necessary for the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead RTL Oncology Lung]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47470]]></requisitionid>
    <referencenumber><![CDATA[R47470]]></referencenumber>
    <apijobid><![CDATA[r47470]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47470/regional-tumor-lead-rtl-oncology-lung/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Lung to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><h3>A Typical Day:</h3><ul><li></li><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><h3>This Role May Be For You:</h3><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Southeast]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47574]]></requisitionid>
    <referencenumber><![CDATA[R47574]]></referencenumber>
    <apijobid><![CDATA[r47574]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47574/regional-director-neurology-southeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Georgia]]></city>
    <state><![CDATA[Georgia]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the [INSERT] Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Southeast (Georgia, Florida & Alabama)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician]]></title>
    <date><![CDATA[Thu, 08 Jan 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42034]]></requisitionid>
    <referencenumber><![CDATA[R42034]]></referencenumber>
    <apijobid><![CDATA[r42034]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42034/hvac-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add an experienced HVAC Technician to our growing team at our SUNY campus with a Monday-Friday 8:00am-4:30pm shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment. We perform all tasks necessary for troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</p><div><p>As an HVAC Technician, a typical day might include the following:</p><ul><li>Maintenance of coolers and freezers including Ultra Low temperature Freezers</li><li>Operation of Centrifugal and Reciprocating refrigeration chillers</li><li>Maintenance of Chilled water systems including distribution and condenser pumps and Air Compressors</li><li>Participating in rotational on-call for site emergency work</li><li>Preventive maintenance and repair of industrial air handling systems</li><li>Operation of facility-wide BAS system</li><li>Conducting daily rounds on all HVAC and facilities related equipment</li></ul><p>This role might be for you if you:</p><ul><li>Follow current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Ensure safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, GDPs and quality standards</li><li>Can communicate and coordinate with each department and within Facilities Management when planned and unplanned work events occur</li><li>Are able to coordinate with outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li><li>Have a solid understanding of industrial HVAC systems including maintenance of industrial Air Handler Units</li><li>Are EPA certified for refrigeration gases</li><li>Have the ability to become fully gown qualified to work in production areas</li></ul><p>To be considered for the HVAC Technician you ideally should have an AAS and the following minimum experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance for each level. Electronic, PLC, mechanical and building automation systems experience in pharmaceutical industry is preferred.</p><ul><li>HVAC Technician II: AAS with 2+ years of relevant experience or equivalent combination of education and experience</li><li>HVAC Technician III: AAS with 5+ years of relevant experience or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44950]]></requisitionid>
    <referencenumber><![CDATA[R44950]]></referencenumber>
    <apijobid><![CDATA[r44950]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44950/director-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s) [asset(s)] assigned within a given therapeutic area (TA), and is the GPS representative on the cross functional strategic program team (SPT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety strategy. This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management. The GPS Director joins Regeneron’s industry leading scientific organization, and has a direct impact on drug development, operations, and commercialization in all relevant global territories.</p></div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)</p></li><li><p>Leads cross-functional Safety Monitoring Team (SMT) activities</p></li><li><p>Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)</p></li><li><p>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</p></li><li><p>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </p></li><li><p>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</p></li></ul><p><strong>This role might be for you if can/have:</strong></p><ul><li><p>Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.</p></li><li><p>Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.</p></li><li><p>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</p></li><li><p>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</p></li><li><p>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum 10+ years of total relevant experience in PV and/or relevant medical field or equivalent of industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content). </p></li><li><p>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</p></li><li><p>Clinical experience and/or industry experience in Oncology is a plus</p></li></ul><p>#MDJOBSPS #GDPSJobs</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Imaging Operations]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44913]]></requisitionid>
    <referencenumber><![CDATA[R44913]]></referencenumber>
    <apijobid><![CDATA[r44913]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44913/senior-manager-clinical-imaging-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Clinical Imaging Operations Lead, you will have a leading role in the design and execution of key strategic and operational aspects of complex early and late phase clinical trials across multiple therapeutic areas, where imaging is a primary or key endpoint. You will collaborate with Clinical Imaging Science Leads and be fully integrated within clinical study teams to ensure high-quality image acquisition, data integrity, and compliance with all study specific procedures. You should expect to work closely with our imaging vendor partners, the clinical operations function, the data management function, external clinical research organizations (CROs), and clinical sites to ensure the successful completion of startup activities, ongoing execution, and close-out of clinical studies. </p><p><strong>A day in the life may look like:</strong></p><ul><li><p><strong>Portfolio Oversight: </strong>Responsible for the execution, functional reporting, and imaging operational oversight of specific portfolios/assets through direct study management or indirect guidance of other team members working on the portfolio. Expected to develop an in-depth knowledge aligned to the portfolio and close relationships with cross-functional colleagues in similar supporting roles. </p></li><li><p><strong>Imaging Startup and Project Management Support:</strong> Collaborate with clinical operations study leads and cross-functional teams to manage the start-up activities of imaging components in clinical trials. Assist with imaging vendor selection, request for proposals, management, and performance tracking. </p></li></ul><ul><li><p><strong>Study Documentation and Compliance:</strong> Author, review, and/or manage essential study documents such as Imaging Manuals, Independent Review Charters, Communication plans, data transmittal forms, Standard Operating Procedures, and Work Instructions. Ensure all documentation is audit-ready and filed appropriately in the Trial Master File (TMF).</p></li><li><p><strong>Site Management and Training:</strong> Provide technical support and training to clinical site personnel, which may include conducting site initiation visits or Teleconferences. Review and approve training materials for imaging facilities and/or clinical site personnel. </p></li><li><p><strong>Process & Technology Improvement:</strong> Participate in process and technology improvement initiatives and ensure strict compliance with all procedures and regulations.</p></li></ul><p><strong>This may be the right role for you if you have:</strong></p><ul><li><p>A well-developed knowledge of clinical imaging across multiple indications alongside an in-depth knowledge of multiple imaging vendors.</p></li><li><p>Excellent communication and organizational skills alongside strong capabilities to provide succinct and impactful updates that demonstrate a developed understanding of the impact of imaging.</p></li><li><p>People management experience is highly preferred as the role will be expected to mentor other team members effectively and may have direct reports. </p></li></ul><p><strong>In Order to be considered qualified for this role you must have:</strong> <strong>:</strong></p><p>· BA/BS with 8+ years of clinical trial imaging experience</p><p>· Certification as a Registered Technologist (R.T.) with experience in modalities like CT, MRI, or Nuclear Medicine is highly preferred</p><p>· At least 3 years of imaging operational clinical trial experience in a pharmaceutical (sponsor) setting </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Mgr Global Procurement- Lab Consumables]]></title>
    <date><![CDATA[Sun, 22 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44951]]></requisitionid>
    <referencenumber><![CDATA[R44951]]></referencenumber>
    <apijobid><![CDATA[r44951]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44951/sr-mgr-global-procurement-lab-consumables/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Senior Manager for the Research and Pre-Clinical Development (R&pD) Lab Consumables team. In this role you will develop and manage strategies for our subcategories, as well as planning and executing strategic sourcing initiatives. The Senior Manager will be responsible for developing sourcing specifications, requirements, and scopes of work for RFIs, RFQs, and RFPs. They will gather and assess data through benchmarking, market intelligence reports, and Voice of the Customer (VoC) interviews, and perform analytics on spend, inventory levels, utilization, and KPI measurements. We are looking for a proactive and collaborative individual who can effectively manage supplier relationships, mitigate risks, and contribute to the success and development of our team.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Being accountable for supporting the definition and implementation of the global Lab Consumables Category strategy to serve global and regional business needs as assigned.</p></li><li><p>Work closely with stakeholders to manage discussions related to the Lab Consumables Categories and aligns category priorities with Procurement management and stakeholders.</p></li><li><p>Manage negotiations, supplier management activities, and stakeholder engagement activities for the Lab Consumables Category as assigned.</p></li><li><p>Take direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Represent Global Procurement by participating in organizational decisions in the Lab Consumables categories with critical short and long-term impact on the success, efficiency, growth, and results of Global Procurement.</p></li><li><p>Demonstrate knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li></ul><p>This role may be a fit for you if you:</p><ul><li><p>Have experience successfully managing category processes, and suppliers across a breadth of categories</p></li><li><p>Can demonstrate success working effectively with cross-functional teams to drive results in the Lab Consumables category or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Use external data sources, market information, and supplier engagement to constantly improve Regeneron’s knowledge of supply market dynamics.</p></li><li><p>Can support the primary relationship manager with key supplier relationship management activities.</p></li><li><p>Have knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Can leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Powerpoint)</p></li><li><p>Have working knowledge and hands on experience supporting sourcing platform technologies preferred (LabViva, Zageno, ScienceExhange, Scientist.com, others)</p></li><li><p>Ability to use data analytics, automation and visualization tools to drive insights and communicate to stakeholders and senior leadership (PowerBI, Tableau, Power Automate)</p></li><li><p>Management and implementation of inventory management programs including technology solutions (RFID, QR codes, others), consignment programs, VMI solutions, single use materials, bioreagents and media etc.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><p>Sr Manager Level: 8+ years of experience in relevant experience, functions or industries. The ideal candidate will have in-depth knowledge of managing global category processes, and suppliers.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Feb 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Quantitative Pharmacology]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45201]]></requisitionid>
    <referencenumber><![CDATA[R45201]]></referencenumber>
    <apijobid><![CDATA[r45201]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45201/director-quantitative-pharmacology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Director in Pharmacometrics (Quantitative Pharmacology), this individual is accountable for the delivery of support for one or more research & development programs, within their pharmacometrics discipline. In this capacity the Director is accountable for the timely and accurate delivery of needed quantitative analyses, interpretation, and messaging to PMx management, as well as the timely delivery of well-constructed and well-messaged reports for PMx review.</p><p><strong>A day in the life of a Director may look like:</strong></p><p>· Manages and is accountable for the PK/PD evaluation of a small portfolio of products or projects.</p><p>· Works independently, with guidance in only the most complex situations.</p><p>· Informs PMx management of important program and regulatory developments in a timely manner.</p><p>· Ensures analyses and documentation are of the highest quality and accuracy.</p><p>· Ensures that reports and other documents have the appropriate messaging and that a meaningful “story-line” is developed.</p><p>· Ensures that study reports and other documents have an appropriate functional review and are suitable for review by senior management.</p><p>· Solves complex problems; takes a broad perspective to identify solutions.</p><p>· Has a strong publication record and actively publishes work in scientific literature</p><p>· Makes contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p><p>· Has excellent interpersonal and communication skills, both written and oral, and has ability to communicate complex information succinctly.</p><p><strong>This may be the right role for you if you:</strong></p><p>· Are fully knowledgeable of pharmacokinetic /pharmacodynamic principles, pharmacology, biology, and quantitative aspects of drug development as well as having an advanced knowledge of pharmaceutical drug development.</p><p>· Possess a deep understanding of scientific literature and technical skills in a number of PK/PD methods and techniques. Has extensive knowledge base of the work in overall scientific community in own discipline.</p><p>· Recognized as an expert in own area within the organization.</p><p>· Have extensive regulatory experience through authoring of regulatory briefing books, CTD summaries, contribution at HA meetings, HA negotiations through regulatory reviews and approvals of BLA or equivalent.</p><p>· Decisions are guided by policies, procedures and business plan; receives guidance from head of function.</p><p><strong>In order to be considered qualified for this role, </strong>you must have a PhD +8 years with a degree in Quantitative Pharmacology (pharmacometrics) or related field.</p><ul><li><p>Hands on usage of a broad range of quantitative tools and systems is required, as is a strong publication record in the field.</p></li><li><p>A proven track record of displaying excellent interpersonal and communication skills both written and oral and ability to communicate complex information succinctly.</p></li><li><p>Proven experience developing QP elements of regulatory strategy and interacting with regulatory agencies without supervision.</p></li></ul><p>#PMx</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, R&D Thought Leadership and Reputation]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45847]]></requisitionid>
    <referencenumber><![CDATA[R45847]]></referencenumber>
    <apijobid><![CDATA[r45847]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45847/manager-rd-thought-leadership-and-reputation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As Manager, R&D Thought Leadership & Reputation Communications, you will play a key role in shaping and executing integrated external communications that strengthen Regeneron’s reputation, advance our scientific narrative, and position our Research & Development (R&D) senior leaders as industry authorities. You’ll translate complex science into compelling stories and orchestrate programs that engage key audiences across channels.</p><p><strong><em>This role is based at our Sleepy Hollow, NY or Tarrytown, NY location with a minimum of four days onsite per week required – this role is not open to fully remote or hybrid work arrangements.</em></strong></p><p><strong>Why it matters:</strong></p><p>You will bridge corporate reputation and stakeholder engagement through public-facing, above-brand R&D storytelling, reputation campaigns, and executive communications across owned, earned and social channels—elevating visibility, trust and impact among key audiences.</p><p>Reporting to the Director, Research Communications—with a dotted line to the Director, Global Development Communications—this role sits within the Corporate Communications team in Corporate Affairs. You will partner closely with the Product & Pipeline Communications, Patient Advocacy and R&D teams.</p><p><strong>A typical day might include:</strong></p><ul><li><p>Supporting development of a comprehensive external communications strategy aligned to R&D and enterprise objectives, clarifying goals and audiences, key messages, and the owned, earned, social and paid channel mix.</p></li><li><p>Collaborating with scientists, physician-scientists, medical affairs, regulatory, and operational teams to translate complex scientific topics into compelling stories for use on our corporate website, social media channels, and communications campaigns.</p></li><li><p>Identifying and securing speaking engagements, media opportunities, and events for R&D functional leaders; preparing spokespeople with briefing documents and message maps; and building and maintaining relationships with trade media by proactively pitching stories and responding to inquires, as appropriate. </p></li><li><p>Leading project management and execution of reputation-building campaigns including content planning and creation, managing reviews and approvals, and ensuring on-time delivery.</p></li><li><p>Overseeing external PR agencies/vendors and external partners to drive quality, timelines, budgets, and integration across workstreams. </p></li><li><p>Defining measurement plans and dashboards using data and feedback to optimize content and demonstrate impact.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You think strategically and execute tactically to deliver measurable business outcomes.</p></li><li><p>You have exceptional writing, storytelling, and editing skills, and can translate complex scientific concepts into engaging multimedia content.</p></li><li><p>You excel at project management and can lead multiple initiatives simultaneously within a matrixed organization.</p></li><li><p>You bring strong business acumen and a creative, innovative mindset to problem-solving.</p></li><li><p>You have experience shaping executive presence and social media campaigns (LinkedIn).</p></li><li><p>You thrive in a dynamic, fast-paced and collaborative team environment. </p></li><li><p>You are proactive and agile, adaptable, and comfortable navigating ambiguity.</p></li></ul><ul><li><p>You have experience managing agencies and/or multiple vendors with strong integration skills. </p></li><li><p>You take a data-driven approach to communications planning, optimization and measurement.</p></li><li><p>You are passionate about science and relentlessly curious.</p></li></ul><p><br><strong>To be consider for this role you have:</strong></p><p>A Bachelor’s degree in a related field is required. You bring 7+ years of professional experience in strategic corporate healthcare communications, with a focus on pharmaceutical or biotech communications preferred. Agency experience preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Mar 2026 20:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44853]]></requisitionid>
    <referencenumber><![CDATA[R44853]]></referencenumber>
    <apijobid><![CDATA[r44853]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44853/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A <strong>Manager Statistical Programming</strong> provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management.<br> </p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Develop an expertise within a therapeutic area or standard tool. Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project</li><li>Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)</li><li>Manage the effort, including esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Provide programming support for complex presentations and more complex statistical ad-hoc requests. </li><li>Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.</li><li>If applicable, lead an application development and act as the programming representative to the user audience.</li><li>Work with management to determine resource requirements for therapeutic area or department function <br>responsibilities. </li><li>Review and select resumes, screen and interview candidates for contractor and permanent positions.</li><li>Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals.</li><li>Advises all direct reports about the procedures surrounding retention of data, records, and information for <br>employees in their group.<br> </li></ul><p><strong>In order to be considered qualified for this role</strong></p><ul><li>Master’s Degree</li><li>8-10 years of relevant work experience</li><li>SAS Certification desirable.</li><li>Also acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Data Management]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44601]]></requisitionid>
    <referencenumber><![CDATA[R44601]]></referencenumber>
    <apijobid><![CDATA[r44601]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44601/associate-director-external-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Associate Director, External Data Services, plays a critical leadership role, overseeing team members to ensure all activities align with Regeneron’s procedures and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver structured external data in compliance with Regeneron SOPs. The role also involves coaching, mentoring, and managing the performance of direct reports, while contributing to the department's strategic direction. Additionally, the AD works with senior leadership to define goals, staffing needs, and departmental structure.</div><div><div><div><div><p><strong>A typical day in the life as an Associate Director, External Data Services includes: </strong></p><ul><li><p>Shape and implement the strategy for External Data Services.</p></li><li><p>Lead and manage a team of External Data Services Managers and Specialists.</p></li><li><p>Oversee the development and maintenance of all DTS documents, ensuring alignment with Regeneron standards, processes, and timelines.</p></li><li><p>Drive the External Data Vendor Oversight model, establishing effective communication, partnership-level processes, and portfolio-level transparency on DTS status and escalations.</p></li><li><p>Represent External Data Services in leadership forums and technology discussions.</p></li><li><p>Contribute to and execute the External Data Services technology strategy.</p></li><li><p>Provide expert-level guidance to CROs, stakeholders, and external vendors on External Data Services.</p></li><li><p>Identify process gaps and lead initiatives to improve processes.</p></li><li><p>Track milestones and deliverables, escalate issues, and communicate portfolio-level updates to stakeholders.</p></li><li><p>Lead or contribute to special projects requiring strategic input and expertise in External Data.</p></li><li><p>Serve as a subject matter expert (SME) for complex topics requiring leadership-level commitment.</p></li><li><p>Develop SOPs, Work Instructions, Guidance Manuals, and other DTS development tools.</p></li><li><p>Provide coaching, mentoring, and performance management for direct reports.</p></li><li><p>Manage resource allocation and planning for External Data Services.</p></li></ul><p><strong>This Role Might Be for You If You:</strong></p><ul><li><p>Have expert knowledge of regulations like 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards for data collection.</p></li><li><p>Possess deep expertise in Data Management, External Data processes, and industry best practices.</p></li><li><p>Demonstrate advanced experience with extracting data in SAS, CSV, and XML formats.</p></li><li><p>Can address complex External Data challenges and recommend actionable solutions.</p></li><li><p>Have a proven ability to develop best practices and processes to achieve objectives.</p></li><li><p>Exhibit strong problem-solving, analytical, and project management skills.</p></li><li><p>Thrive in a matrix environment with virtual teams and can motivate others effectively.</p></li><li><p>Possess an excellent understanding of cross-functional activities and their intersections with External Data.</p></li><li><p>Manage multiple priorities with attention to detail and deliver results within tight timelines.</p></li><li><p>Communicate effectively through strong interpersonal, oral, and written skills.</p></li><li><p>Adapt quickly in a fast-paced, dynamic environment.</p></li><li><p>Are open to travel up to 20%.</p></li></ul><p><strong>To be qualified for this role, you must meet the following requirements:</strong></p><ul><li><p>A minimum of <strong>10+ years of experience</strong> in External Clinical Data Management, with expert knowledge of database structures in biotechnology, pharmaceutical, or health-related industries.</p></li><li><p>At least <strong>4 years of people management experience</strong>.</p></li><li><p>A <strong>Bachelor’s degree</strong> in Science, Health, Computing, or a related field.</p></li><li><p>Hands-on experience with <strong>Imaging Data</strong> is required.</p></li><li><p>Advanced knowledge of <strong>Biomarker data types</strong> and/or Imaging Data for oncology and non-oncology studies is a plus.</p></li><li><p>Expert knowledge of database structures is preferred.</p></li></ul><p>This role is ideal for a seasoned professional who thrives at the intersection of leadership, technical expertise, and strategic vision. If you’re ready to make a significant impact in External Data Services, this position could be your next career milestone.</p></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 11:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development Quality Lead Japan (GDQL-J)]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45173]]></requisitionid>
    <referencenumber><![CDATA[R45173]]></referencenumber>
    <apijobid><![CDATA[r45173]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45173/senior-manager-global-development-quality-lead-japan-gdql-j/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a passionate and experienced Senior Manager to join our Global Development Quality & Regulatory Compliance team as the Global Development Quality Lead for Japan (GDQL-J). In this key role, you will lead quality and compliance initiatives within our local affiliate operations, supporting GCP, GVP, Medical, and Regulatory Affairs. This position offers an exciting opportunity to create strategic partnerships, drive proactive, risk-based quality activities, and foster a culture of continuous improvement. If you are ready to make a meaningful impact and grow with us, we encourage you to apply.</p><p><strong>A Typical Day:</strong><br>In this dynamic role, you will:</p><ul><li>Lead GVP-compliant quality activities in collaboration with the business and GDQM team.</li><li>Provide expert guidance on inspection readiness, preparation, and management at the local affiliate level.</li><li>Partner with cross-functional teams to implement and sustain quality processes.</li><li>Conduct audits and support issue management related to GVP, GCP, Regulatory, and Medical Affairs.</li><li>Mentor, coach, and manage junior team members, fostering their professional growth.</li><li>Collaborate with local and global stakeholders to align quality strategies and operations.</li><li>Act as a subject matter expert in GCP and GVP, providing training and consultations.</li><li>Drive process improvement initiatives to enhance efficiency and compliance.</li></ul><p><strong>This Role May Be For You If:</strong><br>You are someone who:</p><ul><li>Thrives in a collaborative environment and builds strong stakeholder relationships.</li><li>Has a proactive approach to quality management and risk assessment.</li><li>Excels in managing complex quality issues and compliance activities.</li><li>Enjoys mentoring and developing team members to achieve their full potential.</li><li>Is detail-oriented and committed to maintaining the highest standards of quality.</li><li>Values innovation and continuous learning to stay ahead in the pharmaceutical industry.</li><li>Communicates effectively and influences peers and senior leaders alike.</li><li>Is adept at managing multiple priorities and delivering results under tight deadlines.</li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor’s degree and at least 8 years of relevant experience in the healthcare or pharmaceutical industry, with a strong background in quality management or clinical development. Advanced knowledge of GCP and GVP guidelines, along with experience in regulatory inspection management, is essential. Preferred qualifications include expertise in risk-based quality management and proficiency in Microsoft Office tools. Native level Japanese proficiency and business level English proficiency is required.</p><p>This is your chance to be part of a team that values integrity, innovation, and excellence. Join us in shaping the future of quality and compliance in the pharmaceutical industry. Apply today!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Utilities Technician, Saturday - Wednesday Shift]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45762]]></requisitionid>
    <referencenumber><![CDATA[R45762]]></referencenumber>
    <apijobid><![CDATA[r45762]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45762/utilities-technician-saturday-wednesday-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a Utilities Technician to our growing team with a Saturday - Wednesday 10:00pm-8:30am shift. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Utility Technicians are responsible for operations and maintenance of High Purity Water/Steam systems and Plant Utility systems that support that manufacturing process. This is a diverse maintenance position with growth potential in a growing company.</p><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for the first few weeks. Working hours thereafter will be Saturday - Wednesday 10:00pm-8:30am. </strong><strong>Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p><strong>As a Utilities Technician, a typical day might include the following:</strong></p><ul><li>Maintaining water room and boiler room related equipment, including pumps, motors, clean and plant utilities pre-treatment systems, Water for Injection (WFI) stills, Clean Steam Generators, high pressure steam, plant steam boilers, boiler controls, condensate return, natural gas, domestic potable water, tepid water, wastewater, and related piping</li><li>Performing activities such as troubleshooting and hands on repairs on Clean Utility and Plant Utility equipment and systems</li><li>Following current good manufacturing practices (cGMPs)</li><li>Participating in rotational on-call schedule for site emergency work</li></ul><h3><strong>This role might be for you if you:</strong></h3><ul><li>Are adept at reading and/or understanding piping, electrical, and instrumentation drawings</li><li>Possess basic troubleshooting skills and mechanical aptitude as related to the utilities being maintained</li><li>Are capable of lifting, pushing, and/or pulling at least 50lbs</li><li>Are comfortable and flexible working in a changing environment</li><li>Can learn and follow routine procedures</li></ul><p>To be considered for the Utilities Technician position you must be willing and able to work Saturday - Wednesday 10:00pm-8:30am. Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies subject area and the following minimum amounts of relevant experience for each level, preferably in a cGMP environment:</p><ul><li>Utilities Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Utilities Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>#REGENTOSK</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - General Medicine]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45803]]></requisitionid>
    <referencenumber><![CDATA[R45803]]></referencenumber>
    <apijobid><![CDATA[r45803]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45803/director-global-patient-safety-sciences-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s)/asset(s) assigned within a given therapeutic area (TA), and is the GPS representative on the cross functional strategic program team (SPT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety strategy. This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management. The GPS Director joins Regeneron’s industry leading scientific organization, and has a direct impact on drug development, operations, and commercialization in all relevant global territories.</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)</p></li><li><p>Leads cross-functional Safety Monitoring Team (SMT) activities</p></li><li><p>Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)</p></li><li><p>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</p></li><li><p>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </p></li><li><p>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</p></li></ul><p><strong>This role might be for you if can/have:</strong></p><ul><li><p>Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.</p></li><li><p>Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.</p></li><li><p>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</p></li><li><p>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</p></li><li><p>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum 10+ years of total relevant experience in PV and/or relevant medical field or equivalent of industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content). </p></li><li><p>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</p></li><li><p>Clinical experience and/or industry experience in Oncology is a plus</p></li></ul><p>#MDJOBSPS #GDPSJobs</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Clinical Supply Operations]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46090]]></requisitionid>
    <referencenumber><![CDATA[R46090]]></referencenumber>
    <apijobid><![CDATA[r46090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46090/manager-clinical-supply-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Clinical Supply Operations is a key member of the team, responsible for leading clinical supply activities that support the development and operation of clinical supply logistics processes. Partnering with cross‑functional teams and external vendors, you will provide operational oversight, identify and implement improvements, and drive continuous optimization using data‑driven insights.</p><p><strong>A Typical Day</strong></p><ul><li><p>Coordinate Clinical Logistics Vendors in the execution of distribution; supervise performance, drive improvements, and resolve issues to meet study timelines and quality expectations.</p></li><li><p>Collaborate with cross‑functional partners (e.g., Clinical Operations, CMC, Quality, Regulatory, Finance) to develop and improve Clinical Supply operational processes that ensure timely, in‑full delivery of clinical trial materials.</p></li><li><p>Lead cross‑functional improvement initiatives to optimize operational efficiencies, streamline handoffs, and support strategic decision‑making and problem‑solving.</p></li><li><p>Represent the needs of the team in cross‑functional forums and initiatives; champion organisational change and adoption of new or improved processes and tools.</p></li><li><p>Create and lead performance metrics and dashboards to provide clarity into operational performance, trends, and opportunities; translate insights into action plans.</p></li><li><p>Act as an advisor to team members on operational tasks, process issues, projects, and initiatives; mentor and train others to achieve high‑quality results.</p></li><li><p>Maintain standardized SOPs, work instructions, playbooks, and templates; drive continuous improvement in planning processes and vendor management.</p></li><li><p>Identify and mitigate supply risks and dependencies early; propose pragmatic solutions and secure alignment on course corrections across collaborators.</p></li><li><p>Partner with digital/data and systems teams to harness IRT/RTSM, ERP/WMS, and analytics tools for planning and tracking; ensure data integrity and audit readiness.</p></li><li><p>May directly supervise staff; set priorities, coach performance, and support development.</p></li></ul><p><strong>This Role Might Be for You If You Have</strong></p><ul><li><p>Hands‑on experience leading clinical trial supply operations and distribution, including oversight of third‑party logistics providers and pack/label/ship activities.</p></li><li><p>Strong project management skills with the ability to lead multiple concurrent workstreams, deadlines, and collaborators in a matrixed environment.</p></li><li><p>Proven vendor management expertise, including service level oversight, performance management, and continuous improvement.</p></li><li><p>Excellent communication and relationship‑building skills; adept at influencing across functions and levels.</p></li><li><p>High attention to detail with creative, data‑driven problem‑solving.</p></li><li><p>Proficiency with clinical supply and data tools (e.g., IRT/RTSM, ERP, WMS) and Microsoft Excel, PowerPoint, and Word.</p></li><li><p>Familiarity with GxP/GDP requirements and best practices for clinical supply, distribution, and documentation.</p></li></ul><p><strong>To Be Considered</strong></p><p>Bachelor’s degree in supply chain, life sciences, engineering, or a related field with 6+ years of professional experience. Experience supporting global or multi‑region clinical studies is advantageous; . Fluency in English; additional languages are a plus.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Genetics Medicines, Auditory]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45891]]></requisitionid>
    <referencenumber><![CDATA[R45891]]></referencenumber>
    <apijobid><![CDATA[r45891]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45891/senior-medical-director-clinical-development-genetics-medicines-auditory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Senior Medical Director, Regeneron Genetic Medicines Clinical Development Unit (RGM CDU) is a qualified physician scientist with significant pharmaceutical/biotechnology sector and exceptional clinical trials experience. With oversight from Vice President manager, the Senior Medical Director works with other members of the cross-functional team to deliver translational and clinical programs from target nomination to registration. </p></div><div><p>A typical day in the life may include the following responsibilities: </p></div><div><ul><li><p>Serves as the clinical champion for research programs from target nomination to clinical candidate selection and contributes to the evaluation of novel targets and modalities </p></li></ul></div><div><ul><li><p>Leads the Global Clinical Sub-Team to deliver clinical programs from development candidate selection to registration </p></li></ul></div><div><ul><li><p>Designs human studies, including first-in-human, proof-of-concept, and registrational studies </p></li></ul></div><div><ul><li><p>Leads Cross-Functional Study Teams to deliver human studies </p></li></ul></div><div><ul><li><p>Maintains a high-trust, collaborative environment with team members at partner biotech companies across co-development programs </p></li></ul></div><div><ul><li><p>Mentors and develops team members </p></li></ul></div><div><ul><li><p>Contributes to RGM activities by interacting with scientists across the RGM Clinical Development Unit, Regeneron Genetics Center, and RGM Therapeutic Functional Area, presenting project work, fostering cross-project learning, best-practice adoption, and a culture of scientific excellence </p></li></ul></div><div><p>This job may be for you if you have the following: </p></div><div><ul><li><p>M.D. degree. (MD/Ph.D. preferred) Board Certification/Eligibility in a relevant therapeutic area (Neurology, NeuroPsychiatry, Pediatric Neurology) preferred </p></li></ul></div><div><ul><li><p>At least 4 – 8 years of clinical development pharmaceutical industry experience </p></li></ul></div><div><ul><li><p>Has authored and published in medical/scientific peer-reviewed journals. Interactions with Regulatory agencies or Common Technical Document (CTD or “dossier”) submission in any ICH region are an advantage </p></li></ul></div><div><ul><li><p> Effective communications (verbal & written) and presentation skills are essential </p></li></ul></div><div><ul><li><p> Must be able to work productively in a fast-paced collaborative environment </p></li></ul></div><div><ul><li><p>Demonstrated critical thinking skills and sound decision-making </p></li></ul></div><div><ul><li><p>Prior experience with mentoring and leading cross functional teams </p></li></ul></div><div><p>This role is based on-site in Tarrytown 4 days/week. </p></div><p>#MDJOBS, #MDJOBSCD, #GDTherapeuticJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Staff Engineer, Data Management]]></title>
    <date><![CDATA[Mon, 13 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45058]]></requisitionid>
    <referencenumber><![CDATA[R45058]]></referencenumber>
    <apijobid><![CDATA[r45058]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45058/senior-staff-engineer-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Data Enablement and Analytics (DEA) team, within the PAPD (Product, Analytics and Process Development) organization, is a multi-functional team that drives PAPD’s digitalization efforts by making data usable and useful!</p><p>The Data Management Architect defines and governs the end-to-end architecture of data systems that power preclinical science and operations. You will architect domain-driven data models, curated datasets, and integration patterns across data lakes, lab systems and analytical tools, while enabling self-service visualizations. You will drive data quality, lineage, metadata and data catalog standards, and platform patterns. To accomplish this, you will partner with numerous teams and departments and deliver value through Agile approaches.</p><div></div><p><strong>A Typical Day in the Role Might Involve:</strong></p><ul><li><strong>Enterprise Data Architecture (Preclinical):</strong><br>Define data models for preclinical entities (samples, assays, lots, batches, instruments, methods), harmonized across the data ecosystem; establish golden‑record, lineage, and System or record. </li><li><strong>Data Platform Design:</strong><br>Partner with IT teams to continue our journey to a central data platform like the Research data lake or connected data marts. Partner with data engineering teams to design streaming and batch data flow (ETL vs ELT) patterns and deliver such solutions.</li><li><strong>Visualization & Semantics:</strong><br>Publish governed, analysis‑ready semantic layers and reusable data marts; define KPI/metric definitions; enable self‑service in <strong>Spotfire</strong>/<strong>Tableau</strong> with certified data sources and good performance.</li><li><strong>Data Management & Governance:</strong><br>Stand up data catalog/metadata standards, reference/master data strategies, quality controls, and lifecycle policies; partner with business data stewards in PAPD.</li><li><strong>LIMS/ELN Architecture and Solution Delivery:</strong><br>Partner with platform owners and lab teams to model experiment workflows, capture structured context at source, and ensure compliant, scalable Lab platforms like <strong>Benchling or LabWare LIMS. </strong></li><li><strong>SAFe Ways of Working:</strong><br>Act as the overall product manager and program Lead – define our roadmap and continuous delivery mechanism using Scaled Agile Frameworks.</li><li><strong>Collaboration & Change Enablement:</strong><br>Co‑create roadmaps with PAPD functional leads and department data experts; conduct design reviews; mentor engineers and citizen developers.</li></ul><div></div><p><strong>Minimum Qualifications</strong></p><ul><li><strong>Education:</strong> Ph.D. with 6+ years OR Master’s with 12+ years in Computer Science, Data Science, Data Engineering, Applied Mathematics, Bioinformatics, or related discipline.</li><li>Strong understanding of <strong>LIMS/ELN</strong> systems like <strong>Benchling</strong>, <strong>LabWare</strong> or similar <strong>is mandatory.</strong></li><li><strong>Experience:</strong> 8+ years in data architecture/engineering in a scientific or manufacturing context; proven delivery in hybrid cloud/on‑prem data lakes/warehouses.</li><li><strong>Cloud data platforms: </strong>Expertise in AWS, Snowflake, Databricks or comparable cloud data platforms and ecosystems.</li><li><strong>Database Platforms:</strong> Expertise in NoSQL, in-memory, Graph and relational databases, which form the backbone of our operations.</li><li><strong>Tooling & Platforms:</strong> Expert in <strong>data lake</strong> architectures (curation/serving layers), metadata/catalog tools, ELT/ETL data transformation frameworks;</li><li><strong>Analytics Enablement:</strong> Delivered governed, reusable datasets powering visualization tools like <strong>Spotfire</strong>, <strong>Tableau or Power BI</strong>;</li><li><strong>Ways of Working:</strong> Working knowledge of <strong>Scaled Agile (SAFe)</strong> - backlog refinement, PI planning and release management.</li></ul><p><strong>Preferred Qualifications</strong></p><ul><li>Experience in <strong>preclinical/bioprocess</strong> domains (samples, assays, batches, equipment, methods).</li><li>Experience with Lab Systems for bioprocessing. </li><li>Prior work aligning data standards across R&D, QA, and Manufacturing (data integrity, traceability).</li></ul><div></div><p><strong>Core Competencies</strong></p><ul><li>Build<strong> Data Architectures</strong> that span lab, data, and analytics ecosystems.</li><li>Strong<strong> Communications </strong></li><li>Ability to <strong>Influence</strong>:</li><li>Build <strong>Roadmaps</strong>.</li><li><strong>Continuous delivery</strong> using Agile.</li></ul><div><div><div><p><br> </p></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 14 Apr 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I - Allergy-ENT - Salt Lake City N, UT]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46245]]></requisitionid>
    <referencenumber><![CDATA[R46245]]></referencenumber>
    <apijobid><![CDATA[r46245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46245/medical-specialist-i-allergy-ent-salt-lake-city-n-ut/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Salt Lake City North Allergy/ENT territory</strong></p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists and Otolaryngologists as well as other key customers. We need someone who is highly proficient in presenting clinically focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, result-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology and ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/Otolaryngology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings, and medical conferences.</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p><strong>Key Markets include: </strong>Bountiful, Farmington, Idaho Falls, Logan, Layton, Ogden, Park City, Pocatello, Salt Lake City, and West Valley City.</p><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with <strong>a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology and/or ENT market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. </strong>Allergy/Immunology/Otolaryngology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Boston  (Neurology)]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46425]]></requisitionid>
    <referencenumber><![CDATA[R46425]]></referencenumber>
    <apijobid><![CDATA[r46425]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46425/associate-director-field-medical-affairs-boston-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>As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging 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. You will be considered a scientific and clinical expert on our current and future Neurology assets. </p><p><strong>Territory:</strong> Boston area</p><p><strong>A typical day may include the following: </strong> </p><ul><li>Establish, foster, cultivate and maintain peer relationships with KOLs in Neurology </li><li>Act as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding. </li><li>Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans. </li><li>Support evidence generation (company sponsored trials and investigator-initiated studies) research initiatives. </li><li>Identify and report medical insights. </li><li>Identifies gaps in research and educational needs to inform medical strategy. </li><li>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. </li><li>Performs disease management and therapeutic area education with identified practitioners, payers and researchers. </li><li>Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence. </li><li>Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally. </li></ul><p>To be considered 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. Experience as a Neurology MSL or in Neurology is preferred. Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs is required. Established relationships with KOLs in neuromuscular centers is preferred, as is product launch experience. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Capable of frequent business travel (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends.</p><p>#msl #medicalscienceliaison</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 21:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Operations- Oncology]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44699]]></requisitionid>
    <referencenumber><![CDATA[R44699]]></referencenumber>
    <apijobid><![CDATA[r44699]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44699/senior-manager-commercial-operations-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Join Us in Driving Innovation and Excellence in Oncology Commercial Operations </p><p>We are seeking a dynamic and results-oriented Senior Manager, Commercial Operations (Oncology Japan) to join our team. In this pivotal role, you will empower our Sales & Marketing team by facilitating the local implementation of Commercial strategies and driving continuous improvements. Reporting directly to the Associate Director, Commercial Operations (Oncology Japan), you will play a key role in ensuring business optimization in a fast-paced and evolving environment. If you are passionate about making a meaningful impact in the oncology field, we invite you to be part of our journey.</p><p>---</p><p>A Typical Day: </p><p>- Lead continuous improvement of local Commercial processes to ensure scalability and quality for future organizational growth. </p><p>- Partner with Marketing and IT teams to oversee governance and content management for promotional materials and product websites, ensuring compliance with Medical, Legal, and Regulatory review processes (MLR). </p><p>- Facilitate and ensure governance of local Healthcare Professional (HCP) contracting requests for engagements, such as advisory boards and consulting agreements in collaboration with internal and external stakeholders. </p><p>- Collaborate with Meetings & Events management to ensure smooth execution of local oncology-related meetings, sponsorships, and events according to business needs. </p><p>- Execute local field sizing, alignments, targeting, and segmentation in partnership with analytics teams, both locally and above-market. </p><p>---</p><p>This Role May Be For You If: </p><p>- You thrive in a collaborative environment and excel in partnering with cross-functional teams, including vendors and field-based employees. </p><p>- You have strong organizational and project management skills, with the ability to deliver results against tight deadlines while balancing multiple projects. </p><p>- You are skilled in data visualization and storytelling, with a knack for turning insights into actionable strategies. </p><p>- You are proficient in tools such as Microsoft PowerPoint, Excel, Word, and Veeva, and have intermediate English communication skills. </p><p>- You are passionate about the oncology field and have experience navigating Japan’s biopharmaceutical Commercial market dynamics. </p><p>- You enjoy working in a fast-paced, evolving environment and are committed to driving continuous improvements. </p><p>---</p><p>To Be Considered: </p><p>Candidates must have at least 8 years of relevant pharmaceutical or biotech industry experience in Commercial roles with increasing responsibilities, including 5 years of global Commercial Operations experience. A Bachelor’s degree is required, with equivalent experience considered. Preferred qualifications include prior experience in the pharmaceutical industry or consulting, alongside expertise in change management, data storytelling, and cross-functional collaboration.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Precision Medicine]]></title>
    <date><![CDATA[Tue, 14 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46445]]></requisitionid>
    <referencenumber><![CDATA[R46445]]></referencenumber>
    <apijobid><![CDATA[r46445]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46445/senior-scientist-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Precision Medicine Quantitative Biomarker Team is seeking a Senior Scientist with a blend of deep biomarker and translational-science expertise coupled with advanced computational and analytical skills. Sitting within Precision Medicine, you will drive Translational Medicine initiatives that accelerate biomarker discovery and shape clinical development strategies across the entire internal medicine portfolio.</p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li><p>As a Senior Scientist, the candidate will serve as the Precision Medicine quantitative lead to inform internal medicine clinical studies and programs using innovative analytical, computational, and translational strategies.</p></li><li><p>The candidate will design and oversee exploratory analyses of multi-modal data—including genomic, transcriptomic, proteomic, metabolomic, clinical and other biomarker endpoints—to generate actionable insights.</p></li><li><p>The candidate will also help develop scalable, long-term solutions (pipelines, workflows, automation) that enhance biomarker‐discovery and clinical-development efforts enterprise-wide.</p></li><li><p>The Senior Scientist shall lead the development of scientific software for querying, visualizing, analyzing and interpreting data to advance the capabilities of the Precision Medicine department to answer scientific questions through computational means. </p></li><li><p>The candidate will help coordinate cross-functional projects, partnering with biostatisticians, bioinformaticians, epidemiologists, mathematicians, and clinical/research scientists, as well as external collaborators.</p></li><li><p>They will ensure the robustness and reproducibility of exploratory statistical and bioinformatic analyses performed in-house or by external vendors.</p></li><li><p>The candidate will monitor emerging literature, technologies, and industry trends in precision medicine, genomics, and bioinformatics to propose and implement novel strategies that advance drug development.</p></li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li><p>Develop and perform tailored analytic methods using AI with cross-functional partners (bioinformatics, biostatistics, pharmacometrics, outcomes, imaging) to interrogate multi-modal data sets—transcriptomic, proteomic, metabolomic, wearable, and imaging endpoints.</p></li><li><p>Partner with Molecular Profiling, RGC, and Therapeutic Area Scientists, to design and interpret analyses that impact understanding of disease biology, therapeutic mechanism of action, response prediction, etc.</p></li><li><p>Integrate internal and external datasets; perform bioinformatic and statistical analyses that support Precision Medicine programs across all omics and clinical endpoints. </p></li><li><p>Prepare and deliver data visualizations, manuscripts, reports, and presentations that communicate key findings to internal leadership and external collaborators.</p></li><li><p>Lead matrixed teams and juggle multiple projects, rapidly structuring complex, unfamiliar datasets into clear clinical insights and stakeholder-ready presentations. </p></li><li><p>Build- or oversee development of user-friendly tools using AI that give scientists seamless access to integrated biomarker results.</p></li><li><p>Mentor junior scientists and foster a culture of collaboration, innovation, and scientific rigor within the Precision Medicine department. </p></li></ul><p><strong>To be considered for this position, you must have: </strong></p><ul><li><p>Ph.D. in molecular biology, bioinformatics, computational biology, or a related discipline, with 0-2 post-doctoral or industry experience.</p></li><li><p>Proven track record of leading biomarker and translational-science initiatives in cardiovascular, metabolic, or internal-medicine indications with a preference in Obesity, Cardiovascular Disease, renal disease, neurodegenerative disorders, muscle and metabolism disorders, and/or rare genetic diseases.</p></li><li><p>Proficiency in statistical modeling, machine learning, and multi-omics data integration using R, Python, and relevant bioinformatics frameworks. </p></li><li><p>Experience implementing scalable workflows on cloud platforms (AWS, GCP, or Azure)</p></li><li><p>Experience with version control and AI coding assistants such as Claude Code is preferred.</p></li><li><p>Demonstrated ability to communicate complex scientific concepts to diverse stakeholders and translate insights into clinical-development decisions.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 15 Apr 2026 11:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Obesity (Cardiovascular/ Lipids)]]></title>
    <date><![CDATA[Mon, 20 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46850]]></requisitionid>
    <referencenumber><![CDATA[R46850]]></referencenumber>
    <apijobid><![CDATA[r46850]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46850/medical-director-clinical-development-obesity-cardiovascular-lipids/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Development, Obesity (Cardiology) should be a qualified physician with pharmaceutical industry experience, preferably in the area of related comorbidities, in relevant areas such as cardiovascular/ lipids. The Director will serve as Medical Lead for clinical trials and is responsible for the design of clinical study concepts leading to clinical trial protocols. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p><strong>A typical day in the life of a Medical Director may include the following responsibilities:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external stakeholders</p></li><li><p>Defines clinical trial-related Clinical Development Program (CDP) goals and objectives </p></li><li><p>Works closely with discovery teams to provide input on the next generation of targets in the field</p></li><li><p>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts </p></li><li><p>Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings</p></li><li><p>Leads the Global Clinical Study Team to produce high quality program deliverables on schedule </p></li><li><p>Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety </p></li></ul><p><strong>This job may be for you if you have the following: </strong></p><ul><li><p>An M.D. or equivalent with board eligibility or board certification in Cardiology preferred; relevant experience can be acceptable.</p></li><li><p>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</p></li><li><p>Experience in lipid/cardiovascular disorders drug development strongly preferred</p></li><li><p>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</p></li></ul><p>#MDJOBS, #MDJOBSCD#GDTherapeuticJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Business Operations Specialist]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45598]]></requisitionid>
    <referencenumber><![CDATA[R45598]]></referencenumber>
    <apijobid><![CDATA[r45598]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45598/senior-it-business-operations-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will be a vital part of the IOPS IT Business Operations function supporting core business services such as Procurement Management, Financial Management, License Management & Process Improvement.</p><p>As a Senior IT Business Operations Specialist, a typical day might include, but is not limited to, the following:</p><ul><li>Coordinating & Supporting Procurement activities for IOPS IT in collaboration with our IT user base.</li><li>Building partnerships with SS&P to ensure alignment with their procedures and adhering to spending controls.</li><li>Maintaining appropriate financial data to allow for data driven insights and analysis.</li><li>Providing support to the Budget and Forecasting Planning cycles.</li><li>Working with developers on our financial reports to ensure data is accurate and available.</li><li>Maintaining the License Management database to ensure on-time renewals occur.</li><li>Contributing to reports on IT Business Management progress to​ procurement, contractor management, project managers, and/or operations​ teams as necessary.</li><li>Implementing and maintaining processes and documentation to support efficiencies within the group.</li><li>Supporting the IT Business Operations Manager as required in continuous improvement initiatives.</li></ul><p>This role might be for you if you:</p><ul><li>Have broad experience in administering business practices to create the highest level of efficiency.</li><li>Have steered purchasing procedures and activities.</li><li>Have in-depth experience with financial management practices.</li><li>Are proficient in using asset management applications.</li><li>Have experience with developing and maintaining business processes and suggest improvements.</li><li>Have demonstrated experience of working on your own initiative and having work across diverse and global teams.</li><li>Are detail oriented and focused on maintaining data to a high standard & accuracy.</li></ul><p>To be considered for this opportunity you should have a BA/BS in Business, Financial, Management, or related field and 5+ years of Business Operations experience.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Associate Statistician]]></title>
    <date><![CDATA[Tue, 14 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46744]]></requisitionid>
    <referencenumber><![CDATA[R46744]]></referencenumber>
    <apijobid><![CDATA[r46744]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46744/temp-associate-statistician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Statistician will provide statistical support and promote the use of statistical thinking across the site. The role will involve establishing, organising and maintaining effective statistics and data evaluation services pertaining to process monitoring and modelling of biological drugs.</p><p><strong>As an Associate Statistician a typical day might include the following:</strong></p><p>· Completing protocol/report review and approval</p><p>· Fulfilling site-wide statistical analysis requests</p><p>· Conducting brief courses on statistical methods</p><p><strong>This role may be for you if: </strong></p><p>· You possess strong written and oral communication skills</p><p>· Have a working knowledge of word processing, spreadsheet and database management software</p><p>· Are familiar with the computer systems (JMP, Minitab, R) and support tools needed to conduct statistical analyses</p><p>· Are capable of working in a team atmosphere to develop standardized procedures concerning statistical acceptance criteria and analysis</p><p>· Have the ability to teach others with experience organizing and conducting statistical training</p><p>· Familiar with common methods such as Multivariate Regression, Equivalency Testing, Control Charts and Sampling Plans, DOE, Data Mining</p><p>To be considered for this role, you should have a BS/BA or higher in Mathematics/Statistics or related field, equivalent years’ experience in a similar role will be considered in lieu of education.</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 15 Apr 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Engineer, Synthetic and Bioconjugation Scale-Up Technologies (PMPD)]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44429]]></requisitionid>
    <referencenumber><![CDATA[R44429]]></referencenumber>
    <apijobid><![CDATA[r44429]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44429/staff-engineer-synthetic-and-bioconjugation-scale-up-technologies-pmpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Preclinical Manufacturing & Process Development group (PMPD), located in Tarrytown NY, is seeking a hardworking and dynamic <strong>Staff Engineer </strong>for its Synthetic and Bioconjugation Scale-up Technologies (SBST) group. In this exciting new role, you will provide scientific leadership and support for synthetic oligonucleotide process development using the principles of Quality by Design (QbD), process scale-up, and technology transfer of manufacturing-related workflows at Contract Development and Manufacturing Organizations (CDMOs) to ensure timely and reliable entrance to the clinic through product commercialization.</p><p><strong>A Typical Day in the Role of Staff Engineer might include:</strong></p><ul><li>Designing and developing scalable, robust and controlled GMP-ready processes for chemical synthesis of small-molecules. This includes purification development and establishing supporting analytical characterization techniques.</li><li>Proactively complying to lab safety and environmental safety expectations of both Regeneron and regulatory bodies such as Food and Drug Administration (FDA), Department of Transportation (DoT), etc.</li><li>Ensuring a team-based evaluation of processes by working closely with several groups such as R&D chemistry, Formulations Development, Analytical Chemistry, and Protein Biochemistry to ensure integrated program success.</li><li>Generating robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Partnering with External Manufacturing group and other key partners at Regeneron’s IOPS organization to vet CDMO’s and successfully transfer processes with immediate, first-time success.</li><li>Developing new technologies for process improvements and predictive process models, and pioneering novel at-line/in-line process analytical technologies to ensure robust processing.</li><li>Reviewing and providing domain expertise for all regulatory submissions.</li><li>Authoring publications, reports, tech transfer documents, regulatory support documents, patents.</li><li>Performing long-term planning for laboratory related personnel, supplies and equipment.</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Have strong initiative and aim to complete challenging tasks and learn new technologies.</li><li>Are capable of multi-tasking, working both independently and within a team environment.</li><li>Have excellent interpersonal, verbal and written communication skills.</li><li>Can think critically and demonstrate problem-solving skills.</li></ul><p>This role requires a Ph.D. or Master’s in organic chemistry or a related field. At least 3-6+ years of industrial experience post-PhD or a MS w/10+ years, or BS with 15+years in active pharmaceutical ingredient (API) process development is preferred. Experience with small-molecules in the bioconjugates space will be highly preferable. Hands on experience with organic molecule synthesis and characterization tools such as mass spectrometry, nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, high-performance liquid chromatography (HPLC) etc. is preferred. Candidate must be well-versed with purification techniques such as crystallization, extraction, chromatography etc. Experience with solid-phase and liquid phase peptide synthesis is preferable. Proven experience in scaling-up synthetic small-molecule reactions and technology transfer to a GMP manufacturing facility is a plus. Candidate should be well-versed with International Council for Harmonization (ICH)/regulatory guidelines and their impact on process development of synthetic</p><p><strong>A typical day in the role of Staff Engineer might include:</strong></p><ul><li>Designing and developing scalable, robust and controlled cGMP-ready processes for the chemical synthesis, purification, and isolation of oligonucleotides across early and late-stage process development.</li><li>Ensuring a team-based evaluation of processes by working closely with several groups such as R&D Chemistry, Formulations Development, Analytical Chemistry, Protein Biochemistry, CDMOs, and other key stakeholders to ensure integrated program success.</li><li>Generating robust technology transfer documentation and supporting production with onsite presence during scale-up/GMP manufacturing activities.</li><li>Partnering with the External Manufacturing group and other key partners at Regeneron’s Industrial Operations and Product Supply (IOPS) organization to vet CDMOs and successfully transfer processes with immediate, first-time success.</li><li>Promote new technologies for process improvements, predictive process models, and novel at-line/in-line process analytical technologies to ensure robust processing.</li><li>Reviewing and providing domain expertise for regulatory submissions.</li><li>Authoring publications, reports, tech transfer documents, regulatory support documents, patents.</li><li>Scientifically up-to-date on advances in process chemistry and related disciplines</li><li>Requires up to 20% travel</li></ul><p><strong>This role may be for you if you:</strong></p><ul><li>Have strong initiative and aim to complete challenging tasks and learn new technologies.</li><li>Are capable of multi-tasking, working both independently and within a team environment.</li><li>Have excellent interpersonal, verbal and written communication skills.</li><li>Can think critically and demonstrate problem-solving skills.</li></ul><p>This role requires a Ph.D. or Master’s in organic chemistry or a related field. At least 5 years of industrial experience post-PhD or at least 7 years of experience post-Masters in active pharmaceutical ingredient (API) process development is preferred. Experience with small-molecules in the bioconjugates space will be highly preferable. Hands-on experience with solid-phase oligonucleotide synthesis, purification, and characterization using techniques such as mass spectrometry (MS), nuclear magnetic resonance (NMR), infrared (IR) spectroscopy, and high-performance liquid chromatography (HPLC) is preferred. Proven experience in scaling-up synthetic oligonucleotide syntheses and technology transfer to a GMP manufacturing facility is a plus. Candidate should be well-versed with International Council for Harmonization (ICH)/regulatory guidelines and their impact on process development of synthetic molecules and bioconjugates. Experience in working with multi-functional Chemistry, Manufacturing and Control (CMC) teams and experience in authoring publications, reports, technical transfer documents, regulatory support documents, patents is a plus.</p><p>Note: title will be commensurate with experience</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 07:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director and Corporate Counsel, Regulatory & Commercial Product Attorney]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44229]]></requisitionid>
    <referencenumber><![CDATA[R44229]]></referencenumber>
    <apijobid><![CDATA[r44229]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44229/director-and-corporate-counsel-regulatory-commercial-product-attorney/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As Director and Corporate Counsel--Commercialization and Regulatory Law, you will provide proactive and collaborative legal advice to our rapidly growing and globally expanding Commercial Business Units in support of the commercialization of one or more of Regeneron’s biotechnology products. You will be an integral member of our Global R&D, Regulatory, and Commercialization Law Team. Our Law Department thrives on collaboration, trust, a commitment to growth and development, and helping to enable Regeneron to bring products to patients in need and deliver impactful results for our company. </p><p>You will be tasked with serving as a strategic and solutions-oriented partner to one or more of our Product Commercialization teams, including by acting as Product Counsel, providing legal advice to various cross-functional teams, including Marketing & Sales, Medical Affairs, Regulatory, Health Economics and Outcomes Research, Corporate Affairs, Market Access, and Compliance.</p><p><strong>This role is based at Regeneron's offices in Sleepy Hollow, NY (4 days a week onsite) - it is not open to hybrid or fully remote assignments</strong></p><p><strong>A typical day may include:</strong></p><ul><li>Providing day-to-day strategic and business-focused legal and risk counseling for one or more of Regeneron’s products, from development through commercialization</li><li>Advising on a broad range of healthcare regulatory matters, including regulatory labeling, advertising and promotion, drug safety, market research, scientific exchange, interactions with healthcare professionals and patients, and patient support programs</li><li>Counseling on strategic brand and medical planning and developing creative and innovative solutions considering both the business objectives and priorities as well as the legal and regulatory landscape</li><li>Advising on and serving as a member of Product and Medical cross-functional Review Committees</li><li>Counseling on all aspects of product commercialization, including launch preparation, data releases, launch execution, market development, disease awareness, product communication, advertising and promotion, and strategic brand planning.</li><li>Ensuring compliance with all relevant laws, regulations, policies, procedures and controls within relevant business areas supported</li><li>Advising on data disclosures and scientific publications, including press releases and US and/or international medical congresses, scientific exchange, and the review of key scientific publications</li><li>Liaising with other Law Department functions globally, including Dispute Resolution, IP, Compliance, and Transactions, to ensure integrated legal support and timely updates and information sharing,</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>A strong aptitude for math and science, including reading and understanding clinical studies and data</li><li>Excellent oral and written communication skills with proven ability to present complex information accurately and concisely</li><li>Strong interpersonal communication skills and an ability to build trust and influence at all levels</li></ul><ul><li>Ability to handle multiple priorities in a dynamic and evolving environment</li><li>Strategic thinker with excellent analytical and problem-solving skills, focusing on practical solutions</li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li>Have a JD with excellent law school credentials and be licensed to practice law in New York or eligible for licensure as a registered in-house counsel</li><li>Have at least 4-5+ years of legal experience at a top-tier and nationally recognized law practice</li><li>Preference given to candidates with solid understanding of the statutory and regulatory frameworks governing the biotech/pharmaceutical industry, healthcare laws, regulations and guidance (including the Food Drug and Cosmetics Act, FDA Guidance, anti-kickback statues, the False Claims Act, advertising and promotion, scientific exchange and the Lanham act.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Contracts & Trade Controls]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47099]]></requisitionid>
    <referencenumber><![CDATA[R47099]]></referencenumber>
    <apijobid><![CDATA[r47099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47099/associate-director-contracts-trade-controls/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Corporate Counsel serves as legal counsel and business partner for Regeneron's manufacturing division (IOPS – Industrial Operations and Product Supply), providing legal support across a broad range of business operations within this complex, global organization. As a member of the IOPS Law Group, this attorney will draft, review, and negotiate a wide array of contracts — including complex, international supply, material transfer, equipment purchase, consulting, confidentiality, and license agreements. We are looking for a business-savvy attorney who can effectively partner with Law Department colleagues and cross-functional teams across Regeneron, providing practical legal advice on contracts, trade laws and regulations, and other operational matters.</p><p><strong>As Associate Director, Corporate Counsel, a typical day might include the following:</strong></p><ul><li><p>Providing advice and counseling to IOPS business operations on legal issues related to manufacturing, supply, distribution, and other related areas</p></li><li><p>Guiding internal clients through the entire contract life cycle, including determination of internal form vs. vendor paper, coordination with procurement and business clients, negotiating with vendors, etc.</p></li><li><p>Identifying legal and business issues in contracts for resolution through negotiating, drafting, and internal client discussions</p></li><li><p>Working as an on-site corporate contract specialist for the Rensselaer sites, handling legal matters as they arise</p></li><li><p>Collaborating regularly with colleagues in the Regeneron Law Dept, IOPS Law group (including Rensselaer and Raheen, Ireland), business partners, and procurement professionals</p></li><li><p>Assisting the Export Trade Controls (ETC) function with policy and procedure drafting, training, assessments, and counsel on U.S. and international import and export regulatory matters — including Office of Foreign Assets Control (OFAC) sanctions programs; anti-boycott compliance; export control classification and export licensing under the Export Administration Regulations (EAR) and other applicable laws and regulations; tariff classification, customs valuation, country of origin determination, and preference programs/FTAs under Customs and Border Protection (CBP) regulations and other applicable laws and regulations; and Partner Government Agency (PGA) requirements impacting import and export compliance for biotech products, including those administered by the FDA, USDA, and CDC/APHIS</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven contract drafting skills and the ability to work in a fast-paced, dynamic environment requiring agility and emotional intelligence; some experience in real estate and regulatory law is helpful but not required</p></li><li><p>You have experience with, or a strong willingness to learn, U.S. and international import and export trade compliance laws, regulations, and agency requirements relevant to a global biotech company</p></li><li><p>You have exceptionally strong interpersonal and communication (written and spoken) skills</p></li><li><p>You can work efficiently with others cross-functionally, within the Law Department, and across business units</p></li><li><p>You demonstrate sound judgment in novel or evolving regulatory areas and are comfortable navigating ambiguity</p></li></ul><p><strong>To be considered for this role, you must have</strong> a BA/BS and JD with excellent law school credentials, and a license to practice law in New York or eligibility for licensure as registered in-house counsel. We need someone with at least 3 years of legal experience, including some pharmaceutical and/or biotech work, or an equivalent combination of education and experience. Law firm experience is strongly preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$147,800.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - Bioanalytical & Biomarker Technologies]]></title>
    <date><![CDATA[Fri, 01 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46725]]></requisitionid>
    <referencenumber><![CDATA[R46725]]></referencenumber>
    <apijobid><![CDATA[r46725]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46725/senior-scientist-bioanalytical-biomarker-technologies/]]></url>
    <company><![CDATA[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 bioanalytical scientist who can contribute to the development and implementation of state-of-the-art quantitative and qualitative analytical and bioanalytical methods to support biopharmaceuticals in discovery and preclinical development pipeline at Regeneron. The successful candidate need function well in a collaborative, fast-paced, multidisciplinary team environment.</p><p><strong>A Typical day in this role looks like:</strong></p><ul><li>Primarily responsible for developing LC‑MS–based bioanalytical methods in various biological matrices.</li><li>Apply these methods to quantify biotherapeutic levels, assess in vitro stability, evaluate in vivo biotransformation, and measure biomarkers (small molecules, peptides, and proteins).</li><li>Support characterization of drug candidates and critical reagents within the discovery pipeline.</li><li>Collaborate closely with chemistry, conjugation, biology, PK, and TK teams to ensure strong experimental design, accurate data interpretation, and informed decision‑making.</li><li>Contribute to advancing programs involving bioconjugates, oligonucleotides, bispecifics, and other therapeutic modalities.</li><li>Explore and evaluate innovative bioanalytical technologies and emerging platforms to support an evolving portfolio, including novel molecular modalities and therapeutic areas.</li><li>Document experiments, results, and findings in an electronic lab notebook.</li><li>Present scientific work at internal and external meetings.</li><li>Perform general lab and instrument maintenance.</li><li>Grow into the role of bioanalytical representative on cross‑functional project teams, effectively managing priorities to meet multiple project goals and timelines.</li></ul><p><strong>This role may be for you if you have experience:</strong></p><ul><li>Chemistry, Biochemistry, Pharmaceutical Science or a related discipline, B.S. with 10+ yrs, MS with 8+ yrs, or Ph.D. with 0-6 yrs postdoctoral experience.</li><li>Proven expertise and extensive experience in liquid chromatography and mass spectrometry is required, with demonstrated track record of successfully developing MS, LC-MS or LC-MS/MS method.</li><li>Hands on experience in sample preparation technique (LLE, SPE, Immunocapture, enzymatic digestion, homogenization etc.) and automation platform.</li><li>Scientific curiosity and strong capabilities in experimental design, execution, data interpretation and troubleshooting with limited supervision.</li><li>Ability to think critically and to prioritize and manage multiple projects under aggressive timeline in a fast-paced environment.</li><li>Detail-oriented, good interpersonal and effective technical writing and verbal communication skills.</li><li>Industrial experience in bioanalysis of LC-MS based small molecule, siRNA, biomarkers and biotherapeutics assay development is preferred. Job level may be adjusted based on the experience.</li><li>Previous experience in GLP lab and mass spectrometry applications in ADC analytics, metabolomics and proteomics would be advantageous.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 01 May 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Auditor]]></title>
    <date><![CDATA[Fri, 01 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47018]]></requisitionid>
    <referencenumber><![CDATA[R47018]]></referencenumber>
    <apijobid><![CDATA[r47018]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47018/senior-it-auditor/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior IT Auditor is responsible for contributing towards planning, executing, and reporting on operational IT audits, evaluating risks and controls, including application, infrastructure, cloud, data management, SDLC, change management, and IT operations, in accordance with IIA standards and department methodologies. Perform IT SOX control walkthroughs and testing, along with preparing the related documentation. Assess the effectiveness of cybersecurity controls, including identity and access management, vulnerability management, logging and monitoring, incident response, and security governance. <br> </p><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include the following:</strong> </p><div><ul><li><p>Review controls related to cloud computing (e.g., AWS, Azure), SaaS platforms, data lakes, and analytics environments, including shared responsibility models. </p></li></ul></div><div><ul><li><p>Design and execute data analytics‑driven audit procedures using tools such as Dataiku or equivalent, to identify anomalies, trends, and control gaps. </p></li></ul></div><div><ul><li><p>Apply automation, continuous auditing techniques, and responsible use of AI, where appropriate, to improve audit efficiency, coverage, and insight, including assessing AI‑enabled business processes and controls. </p></li></ul></div><div><ul><li><p>Manage timely completion of audit tasks, including communication of status to the auditee and the Manager/Director. </p></li></ul></div><div><ul><li><p>Identify, document, and communicate control deficiencies, root causes, technology risks, and opportunities for improvement, providing practical, actionable recommendations aligned with business objectives. </p></li></ul></div><div><ul><li><p>Present the results of audit work to Internal Audit Management and auditees, including practical recommendations to address identified risks and/or weaknesses in internal controls as well as opportunities to enhance operational efficiencies. </p></li></ul></div><div><ul><li><p>Prepare clear, concise, and professional audit reports and executive‑level presentations for Internal Audit leadership, management, and key stakeholders. </p></li></ul></div><p><strong>This role might be for you if have experience with :</strong></p><div><ul><li><p>Advanced knowledge of IT infrastructure, applications, cybersecurity, and automated controls </p></li></ul></div><div><ul><li><p>Strong understanding of SOX, COSO, COBIT, NIST, GxP, GDPR, and other relevant regulatory and governance frameworks. </p></li></ul></div><div><ul><li><p>Strong analytical, critical‑thinking, and problem‑solving skills, with the ability to independently assess risk and propose solutions. </p></li></ul></div><div><ul><li><p>Comfortable working and learning independently and as part of a team </p></li></ul></div><div><ul><li><p>Excellent interpersonal, communication and writing skills, strong organizational abilities, and attention to detail are required </p></li></ul></div><div><ul><li><p>Experience with data analytical tools (e.g. Dataiku, Alteryx, etc.) </p></li></ul></div><div><ul><li><p>Understanding of AI concepts, associated risks (e.g., model governance, data quality, access, ethical use), and internal controls relevant to AI‑enabled processes. </p></li></ul></div><p><strong>To be considered for this role</strong>, you must have a Bachelor's degree with a<strong> </strong>minimum of 3 - 4 years of progressive experience in IT audit, information security, or technology risk. CISA, CISM and/or CISSP certifications/license preferred. Experience auditing and evaluating infrastructure, cybersecurity risks/controls and auditing operating systems. Pharmaceutical, life sciences, or other regulated industry experience strongly preferred. Big 4 or public accounting experience preferred but not required. </p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 01 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Columbus, OH]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47139]]></requisitionid>
    <referencenumber><![CDATA[R47139]]></referencenumber>
    <apijobid><![CDATA[r47139]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47139/medical-specialist-i-pulmonology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Columbus, OH - representative must reside within or close to the territory.</strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include: physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Are confident in demonstrating strong and consistent sales performance that exceeds expectations related to goals</p></li><li><p>Are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>Can demonstrate a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>Collaborate effectively with internal and external partners</p></li><li><p>Share a passion and learning interest in science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li></ul><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 09:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II- Ophthalmology- Columbus/Cincinnati, OH]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47059]]></requisitionid>
    <referencenumber><![CDATA[R47059]]></referencenumber>
    <apijobid><![CDATA[r47059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47059/medical-specialist-ii-ophthalmology-columbuscincinnati-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Columbus</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p><strong>A typical day might include the following: </strong></p><p>The Ophthalmology Medical Specialist will report to the Regional Director and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you have:</strong></p><p>· Experience in biologics and buy and bill products</p><p>· Demonstrated history of high sales performance</p><p>· Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Buy and Bill experience. Ophthalmology with relevant retina experience is preferred. Must be based in or located in close proximity to the assigned territory (relocation will not be provided). Ability to travel (40-60%).</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 09:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Autoimmune Diseases]]></title>
    <date><![CDATA[Sun, 26 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46984]]></requisitionid>
    <referencenumber><![CDATA[R46984]]></referencenumber>
    <apijobid><![CDATA[r46984]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46984/associate-scientist-autoimmune-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>The Immunology and Inflammation group is seeking an Associate Scientist to support the development of therapeutics for autoimmune disease. This role involves joining a highly collaborative team working in autoimmunity, immune cell biology, and tissue immunity. You will have the opportunity to engage in cutting edge immunological research as part of our discovery efforts and to contribute to human health. </p><p><strong>As an associate scientist in the Immunology and Inflammation group, your typical day might include: </strong></p><ul><li><p>Handling and caring for mice, including performing procedures such as blood and/or tissue sample collection or injections (IP, IV and subcutaneous) </p></li><li><p>Processing of organs for immune cell isolation and analysis </p></li><li><p>Maintaining, expanding, and/or modulating cells in vitro </p></li><li><p>Evaluating cell phenotypes and function using ex vivo or in vitro assays such as flow cytometry and immunoassays. </p></li><li><p>Analysis of data using biological and statistical software such as Flowjo, OMIQ, Excel, Prism </p></li><li><p>Close collaborative interactions with teams across the organization </p></li><li><p>Documentation of experimental procedures and results </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, </strong>you should have a B.S. or M.S. degree in a relevant field with 0-2 years of experience in immunology or a related discipline. Relevant experience includes: </p><p>Experience in tissue culture, cell-based assays, flow cytometry, or immunoassays (e.g. ELISA, MSD, Luminex), as well as proficiency in basic computer applications and experience with biological data collection and analysis highly preferred </p><p>Experience in mouse handling is highly preferred. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 27 Apr 2026 10:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Automation Engineer]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46939]]></requisitionid>
    <referencenumber><![CDATA[R46939]]></referencenumber>
    <apijobid><![CDATA[r46939]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46939/associate-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>In this role you will be responsible for automation and controls systems project management towards specification, design, start-up, and commissioning in a cGMP environment.</p><p><strong>As an Associate Automation Engineer, a typical day might include the following:</strong></p><ul><li><p>Managing projects related to design, commissioning, and performance improvement of automated equipment</p></li><li><p>Providing design/approval of hardware, software, and controls for automated equipment</p></li><li><p>Providing technical and automation operational support to Manufacturing and Facilities</p></li><li><p>Implementing software/hardware changes and upgrades, understands impact of actions to Manufacturing and Facilities</p></li><li><p>Implementing modification/change control procedures and protocols</p></li><li><p>Supporting the Validation Department with initial design review, software testing, protocol execution and review</p></li><li><p>Programming PLC and HMI application for automated process equipment, capable of troubleshooting and demonstrates knowledge of instrumentation and controls</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Are a self-starter with high initiative and possess a data-driven approach to problem-solving</p></li><li><p>Have strong interpersonal skills</p></li><li><p>Have demonstrated adaptability and flexibility to working in different environments and teams</p></li></ul><p>In order to be considered for this position, you must hold a BS/BEng or higher in Science, Engineering, Instrumentation or Software Programming. May substitute relevant experience for education.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 04:26:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Clinical Development, Ophthalmology]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47444]]></requisitionid>
    <referencenumber><![CDATA[R47444]]></referencenumber>
    <apijobid><![CDATA[r47444]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47444/senior-medical-director-clinical-development-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Medical Director will play a key role in clinical development programs within the Ophthalmology portfolio, including being accountable for deliverables of the assigned program(s), supporting resourcing, budget, and timelines of these programs. This role serves as scientific and medical lead for clinical team(s) working closely with operational leads. This role requires a high-performing and highly passionate individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p>The incumbent will collaborate with multi-disciplinary clinical teams, assisting in guiding and executing clinical development strategies and subsequent regulatory submissions. This role is responsible for the design and execution of first-in-human through registration-enabling studies. This role will serve as a representative to a range of audiences, including Internal Medicine leadership, executive leadership, development partners, and US and global regulatory agencies. The Senior Medical Director, Ophthalmology reports to the Vice President, Ophthalmology Therapeutic Area Lead.</p><p><strong>A typical day in the life of a Senior Medical Director, Clinical Development may include the following: </strong></p><ul><li>Acts as medical expert and leader in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, advisory boards), internal stakeholders (e.g., Research, Global Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards.</li><li>Develops unique and innovative clinical strategies to significantly shorten the development cycle in the face of an evolving regulatory landscape. Designs and develops more efficient and innovative, yet robust Phase 1, 2, and 3 programs.</li><li>Works closely with the research and discovery teams to provide input on the next generation of targets in the field.</li><li>Ensures safety of the drug, including the safety aspects of patients in clinical studies and signal detection from post-marketing surveillance, with the support from Global Patient Safety.</li><li>Ensures quality of all clinical documents (e.g., investigators’ brochure, protocol, study report, clinical components of regulatory submissions, safety related documents).</li><li>Develops written responses to regulatory agency questions and prepares regulatory submission documents.</li><li>Has strong consensus-building skills and the ability to collaborate with multi-disciplinary teams towards sound decision-making. Key member of dynamic and matrixed clinical teams in a fast-paced and hands-on environment. </li></ul><p><strong>This role may be for you if you have the following:</strong></p><ul><li>A M.D. or D.O. or equivalent medical degree and relevant training</li><li>A trained Ophthalmologist (board certified or eligible or equivalent) is essential.</li><li>A minimum of 4 years of industry experience (early or late clinical development); however, a candidate with a strong academic background and less experience may be considered.</li><li>Experience in leading proof of concept and/or registrational clinical trials, including protocol design, managing study start-up, directing, and guiding study team execution, data cleaning, medical monitoring/review, database locks.</li><li>Solid knowledge of compliance and global regulatory requirements (ICH) for development of pharmaceutical candidate products is required.</li><li>A strong commitment to clinical research and the ability to work well within a team setting are essential.</li><li>This role requires 4 days a week on-site in Tarrytown, NY, Cambridge, MA, or Warren, NJ</li></ul><p>#MDJobs, #MDJOBSCD, #GDTherapeuticJobs, SKC</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, People Analytics & Insights]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45959]]></requisitionid>
    <referencenumber><![CDATA[R45959]]></referencenumber>
    <apijobid><![CDATA[r45959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45959/manager-people-analytics-insights/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, People Analytics & Insights will partner with colleagues from across human resources and internal customers to provide evidence-based insights on the people and organizational aspects of Regeneron’s business. The ideal candidate will have a fundamental technical background, strong project management skills, customer orientation and requisite HR experience. Expertise in data management, metrics and reporting, descriptive and predictive analytics, data visualization and storytelling are all critical for success in this role. We see this as a phenomenal opportunity to build people analytics expertise working closely with others who have been shaping an enterprise-wide people analytics program.</p><p><strong><em>This role could be based at our Sleepy Hollow, NY, Rensselaer, NY, or Warren, NJ location with a minimum of 4 days onsite required - this is not open to fully remote or hybrid work.</em></strong></p><p>As the Manager, People Analytics & Insights, a typical day might include the following:</p><ul><li>Building datasets and conducting custom analytics projects, spanning descriptive and predictive analytics</li><li>Leading open-ended text analysis to summarize survey comments and establish foundational AI capability</li><li>Supporting ongoing reporting for select leadership audiences, including opportunities for automation and efficiency</li><li>Translating metric priorities into new dashboards in Workday and key reports with compelling visualizations and storytelling to help guide decision-making regarding Regeneron’s talent and organizational practices</li><li>Identifying, prioritizing and implementing improved data quality and additional data capture opportunities in partnership with HR Technology, IT and Finance teams</li><li>Working closely with colleagues to build and integrate people data and HR analytical capability</li></ul><p>This job might be for you if:</p><ul><li>You have high attention to detail and can easily shift gears between ongoing work and ad hoc requests</li><li>You have the ability to balance multiple projects, while informing key partners of progress and outcomes</li><li>You can handle ambiguity and are highly adaptable and flexible to changing requirements and business demands</li><li>You are adept with large and complex datasets to answer business questions</li></ul><ul><li>You possess the demonstrated ability to tell a story through data and communicate effectively with key partners through advanced visualization techniques</li></ul><ul><li>You have learning agility and a desire to keep up with the latest developments in the field of HR reporting, analytics and related technology</li></ul><p>To be considered for this opportunity, you must have a minimum of an Advanced Degree (Masters, PhD) in an applied social science or quantitative field. Preferably with 7+ years of experience (for PhD, 3+ years) working with HR, People and Business data to generate critical insights for leaders and decision makers (including working with big data, integrated business data, global data, labor market data and third-party data). This includes expertise in managing data collection, organization and quality assurance for the purposes of building statistical models, leading metrics and sustainable reporting.</p><p>We need someone who is experienced in building supervised and unsupervised machine learning models, including understanding of use cases for alternative modeling methodologies. Advanced proficiency in statistical software packages (e.g., R, Python, SAS, SPSS) and data visualization tools (e.g., Tableau, Qlik) is required. Experience with global HR technology systems and human capital platforms (e.g., Workday) is also required. We would love to find someone with both quantitative and qualitative research, design and analysis experience, including natural language processing and sentiment analysis.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-Oncology-Seattle, WA]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47378]]></requisitionid>
    <referencenumber><![CDATA[R47378]]></referencenumber>
    <apijobid><![CDATA[r47378]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47378/medical-account-specialist-ii-oncology-seattle-wa/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Seattle]]></city>
    <state><![CDATA[Washington]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Seattle, WA</strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><h3><strong>A typical day may include the following:</strong></h3><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><h3><strong>This role might be for you if:</strong></h3><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Oncology Account Specialist -Oncology- Rochester, MN]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47524]]></requisitionid>
    <referencenumber><![CDATA[R47524]]></referencenumber>
    <apijobid><![CDATA[r47524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47524/oncology-account-specialist-oncology-rochester-mn/]]></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>Geography: Rochester, MN</strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Translational Pharmacokinetics and Pharmacokinetic/Pharmacodynamic]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47268]]></requisitionid>
    <referencenumber><![CDATA[R47268]]></referencenumber>
    <apijobid><![CDATA[r47268]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47268/associate-director-translational-pharmacokinetics-and-pharmacokineticpharmacodynamic/]]></url>
    <company><![CDATA[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 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>The daily responsibilities of this role include:</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 Might Be for You If You :</strong></p><ul><li><p>Thrive in a fast-paced, collaborative environment.</p></li><li><p>Are passionate about science and motivated to contribute to bringing new drugs to patients.</p></li><li><p>Desire exposure to multiple therapeutic areas and emerging modalities.</p></li><li><p>Excellent written and verbal communication, presentation, influencing, and leadership skills.</p></li></ul><p><strong>To be considered for this opportunity, you must have:</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><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Hematology]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47471]]></requisitionid>
    <referencenumber><![CDATA[R47471]]></referencenumber>
    <apijobid><![CDATA[r47471]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47471/regional-tumor-lead-marketing-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Hematology to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><p><strong>This Role May Be For You:</strong></p><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in hematology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</p><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Compliance Counsel]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47379]]></requisitionid>
    <referencenumber><![CDATA[R47379]]></referencenumber>
    <apijobid><![CDATA[r47379]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47379/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>Regeneron is looking for a Director, Compliance Counsel to investigate compliance matters across a global organization to ensure compliance with all laws, regulations, and company policies. This is a high-impact role at the intersection of law, ethics, and business - one for a seasoned attorney who is comfortable building relationships across the enterprise and identifying and addressing cross-border issues. This role will provide guidance to internal stakeholders and perform other compliance-related tasks, as needed, to support the company’s compliance program. A successful attorney for this role will be able to work across the organization, assess risk, and provide a neutral and informed perspective.</p><p><strong> </strong></p><p><strong>This role is based at Regeneron's office in Sleepy Hollow, NY (4 days a week onsite) - we offer a comprehensive relocation package.</strong></p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Lead end-to-end compliance investigations from evaluating initial allegations to recommending remedial action to ensure compliance with all laws, regulations, and company policies, across the U.S. and internationally.</p></li><li><p>Respond 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>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>Provide input into policies, procedures and guidance documents.</p></li><li><p>Monitor and assess legislative and regulatory developments impacting Regeneron’s global operations.</p></li></ul><p><strong> </strong></p><p><strong>This role might be for you if you:</strong></p><ul><li><p>Have experience conducting internal, compliance, and/or government investigations.</p></li><li><p>Possess high level of influencing skills and ability to inspire change as it relates to implementing remedial actions.</p></li><li><p>Have the ability to effectively deliver sound and clear Compliance advice in a business setting.</p></li><li><p>Have in-depth 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.</p></li></ul><p><strong>To be considered for this opportunity,</strong> you must have a JD with 8+ years of validated experience, with at least two years working in or with pharmaceutical companies on healthcare compliance related activities. Licensed to practice law in New York or eligible for licensure as a registered in-house counsel.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 19:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director Clinical Pharmacology]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47530]]></requisitionid>
    <referencenumber><![CDATA[R47530]]></referencenumber>
    <apijobid><![CDATA[r47530]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47530/executive-director-clinical-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>Reporting to the Vice President, Clinical Pharmacology, the Executive Director will be responsible for managing a team of scientists providing Clinical Pharmacology support in Oncology therapeutic focus areas of the corporate development portfolio. In this capacity, the Executive Director is accountable for the successful and timely completion of all assignments, encompassing a broad array of deliverables in support of corporate strategic goals. The Executive Director is expected to apply both logistical and strategic initiatives as well as incorporate novel and creative scientific approaches.</p><p>The Executive Director will support the professional development of Scientists in their team, provide executive guidance to managers in their team, and is accountable for adherence to all applicable SOPs, PMx working practices and the corporate code of ethical conduct.</p><p><strong>A day in the life may look like:</strong></p><ul><li><p>In concert with other PMx Executive Directors (particularly Quantitative Pharmacology and Clinical Pharmacology-Non-Oncology), manage and mentor a broad spectrum of individual contributing scientists and Directors.</p></li><li><p>Accountable for the PK/PD evaluation of assigned portfolio of products or projects that are highly complex and wide in scope.</p></li><li><p>Accountable for the performance and results of their team within the defined scope of functional responsibilities.</p></li><li><p>Responsible for performance management and assessment of staff and provides guidance and training to enable their success. Provides technical guidance and mentoring of colleagues within the function and across the organization.</p></li><li><p>Utilizing a mastery level of PK/PD knowledge and strategic leadership skills, works with their team to effectively develop and implement strategic analyses in support of development projects.</p></li></ul><p><strong>This may be the right role for you if you have:</strong></p><ul><li><p>Influential across the organization to include individual contributors (in and out of function), and other functional managers, as well as Sr Management, management within PMx, development program teams, and other Regeneron Functional areas across the organization.</p></li><li><p>Provides Functional level sign off for agreed documents as designated by the Vice President, Clinical Pharmacology</p></li><li><p>Contributes to the development of Clinical Pharmacology functional strategy.</p></li></ul><p><strong>In order to be considered qualified for this role you must have a </strong>PhD, in pharmacokinetics or a biological or related discipline (e.g. pharmacology, toxicology, biology. biochemistry, pharmaceutical science.) 20 years of experience in Clinical Pharmacology.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$285,600.00 - $475,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, CBU Operational Effectiveness - Pulmonology]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47559]]></requisitionid>
    <referencenumber><![CDATA[R47559]]></referencenumber>
    <apijobid><![CDATA[r47559]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47559/director-cbu-operational-effectiveness-pulmonology/]]></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>The Director, Marketing Operations supports strategic and operational activities of the Pulmonology Therapeutic Business Unit. Partners with sales leadership, marketing and market access to find opportunities, gaps and solutions to drive commercial success. Serves as the point person to connect activities across CBU functions as well as functions not reporting into CBU. Enables Therapeutic Business Unit Head to focus on critical strategic and operational issues.</div><div><div><div><div><div><div><div><div><div><h3>A typical day might include the following:</h3><ul><li><p>Supports 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 the organizational strategy and direction.</p></li><li><p>Analyzes existing business strategy and derives recommendations</p></li><li><p>Partners with senior leadership to set operational strategy</p></li><li><p>Tracks key deliverables for Pulmonology CBU and follows up with responsible individuals</p></li><li><p>Identifies solutions that support operational efficiencies/effectiveness of Pulmonology CBU</p></li><li><p>Provide Marketing Operations Support for the Marketing and CBU field teams.</p></li></ul><h3>This role might be for you if:</h3><ul><li><p>You are a strong program manager and able to track multiple projects</p></li><li><p>You can create presentation materials and design projects</p></li><li><p>You can collaborate and engage effectively with a global group</p></li><li><p>You communicate clearly and concisely across various groups</p></li><li><p>You are detail oriented and a self-starter </p></li></ul><p>To be considered for this opportunity, we are requiring 10+ years of pharmaceutical/biotech or related experience or an equivalent combination of education and experience. We would like to see Pulmonology experience. We are looking for someone who also has experience in field management (DM/RD) and home office experience (marketing and other relevant experiences). We need you to possess the business sense necessary to interpret and draw business insights from data analysis to formulate recommendations and complete action plans. Lastly, we require you to be in the Sleepy Hallow office a few times a week.</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 06:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Solid Tumor Oncology]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45090]]></requisitionid>
    <referencenumber><![CDATA[R45090]]></referencenumber>
    <apijobid><![CDATA[r45090]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45090/medical-director-clinical-development-solid-tumor-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. This role may work on studies in ovarian cancer.</p></div><div><p><strong>As a Medical Director, a typical day may include the following:</strong></p><ul><li><p>Defines clinical trial-related goals and objectives.</p></li><li><p>Conducts literature and database research on clinical trials as needed</p></li><li><p>Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.</p></li><li><p>Leads and supervises the Clinical Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role may be for you if:</strong></p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p><br><strong>To be considered for this role</strong>, you must have a MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience. Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.</p><div><p><em>This role has a 4-day onsite minimum requirement in Tarrytown, NY.</em></p></div><div><div><div><div></div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Quality Compliance Specialist]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47568]]></requisitionid>
    <referencenumber><![CDATA[R47568]]></referencenumber>
    <apijobid><![CDATA[r47568]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47568/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>In this role you will be responsible for maintaining site compliance of operations inclusive of Manufacturing, Quality Systems, Quality Control, Quality Assurance, Facilities Maintenance, Materials Handling, and QA Validation adhering to mandated regulatory requirements and site expectations.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li><p>Ensuring compliance with all aspects of Quality for the Raheen site and administration of site quality systems including Deviations, CAPA Change Control, Audits, Customer Complaints, Quality Risk Management</p></li><li><p>Reviewing failure investigations, change control documents, corrective/preventative action documents, standard operating procedures</p></li><li><p>Maintaining electronic systems, procedures, policies and other instructional documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements</p></li><li><p>Monitoring and trending metrics</p></li><li><p>Participating in regulatory and customer audits and quality risk assessments</p></li><li><p>Collaborating with functional departments to resolve issues and maintain compliance</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have a quality mindset and excellent attention to detail</p></li><li><p>You demonstrate strong interpersonal skills</p></li><li><p>You are comfortable working in a fast-paced setting</p></li></ul><p>To be considered for this opportunity you should have a BS/BA in a scientific discipline or related field with 2+ years of relevant work experience in pharmaceutical or related industry. Relevant experience may be substituted for education requirement.</p><br><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Worldwide Operations Office - Pharmacovigilance]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47622]]></requisitionid>
    <referencenumber><![CDATA[R47622]]></referencenumber>
    <apijobid><![CDATA[r47622]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47622/executive-director-worldwide-operations-office-pharmacovigilance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Executive Director, Worldwide Operations Office to join our PV Organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Executive Director, Worldwide Operations Office serves as the single point of accountability for Regeneron’s global-to-local pharmacovigilance model. This role ensures consistency, compliance and operational excellence across all regions and countries by defining the scope and governance of regional PV Hubs, establishes clear boundaries between global, regional, and local responsibilities, and translates regional insights into strategic guidance for GPS leadership. This role drives a unified, patient-centered approach to safety across Regeneron’s global footprint while enabling appropriate local adaptation to meet regional regulatory requirements. </p><p><strong>This role might be for you if can: ​</strong></p><ul><li><p>Partner with cross-functional US and International teams to embed a patient safety mindset across Regeneron’s global operations (e.g., gather feedback from regional leaders, establish knowledge sharing forums) </p></li><li><p>Provide functional oversight of WWOO and regional PV Hubs, ensuring operational performance, quality standards, regulatory compliance, and consistent application of global processes across markets </p></li><li><p>Define execution scope for regional PV Hubs, determining which processes require localization to meet requirements versus which can be executed through centralized global processes, including clear delineation of responsibilities between GPS and affiliate teams </p></li><li><p>Establish governance framework for local process adaptation, defining clear standards for when and how global PV processes may be tailored to meet local regulatory requirements </p></li><li><p>Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI </p></li><li><p>Aggregate insights and potential risks from regional and country-level activities to shape, influence, and prioritize objectives for the PV system </p></li><li><p>Coordinate across key GPS functions (e.g., QPPV, Case Management, Quality & Compliance) on matrixed activities, regional priorities, and global to local interdependencies </p></li><li><p>Adapt the international model to fit changing business needs, including assessing future needs for additional PV Hubs based on portfolio expansion, geographic growth, and regulatory landscape changes </p></li><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 raise capabilities across the organization </p></li><li><p>Influence cross-functional leaders to align priorities and drive enterprise results </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Advanced degree (PharmD, MD, MS, or MBA) in life sciences, healthcare, or related field preferred; Bachelor's degree required</p></li><li><p>17+ years of experience in pharmacovigilance, international operations within the life sciences industry </p></li><li><p>Minimum 7 years in leadership roles with demonstrated experience managing international or multi-regional operations </p></li><li><p>Proven ability to develop relationships and influence key decision making with GPS and Non-GPS functions (e.g., QPPV, Med Affairs, Regulatory), regions, and senior stakeholders </p></li><li><p>Strong background in PV compliance, inspection readiness, and quality oversight across multiple markets </p></li><li><p>Strategic mindset with the ability to translate regional complexity into clear governance, decisions, and executive-level insights </p></li><li><p>Preferred experience with AI technologies </p></li></ul><p>#GDPSJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Clinical Research Informatics]]></title>
    <date><![CDATA[Fri, 15 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45670]]></requisitionid>
    <referencenumber><![CDATA[R45670]]></referencenumber>
    <apijobid><![CDATA[r45670]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45670/associate-manager-clinical-research-informatics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Regeneron Genetics Center uses genetics and health data on millions of people to advance our understanding of human disease and guide Regeneron’s therapeutic programs. You will help us to organize, analyze and interpret health information aggregated from electronic health records, surveys, digital devices, and laboratory assays from multiple collaborators. This will require developing and implementing standards for health data as well as code repositories, pipelines and analysis tools that facilitate interacting with data.</p><p>You will need expertise in organizing and structuring large and complex datasets as well as top-notch software engineering and orchestration skills. You will help design data structures that store health data. You will implement the code and processes that populate, validate, and analyze these data. You will participate in the downstream analysis using machine learning, genomics, and epidemiology. This will be a dynamic, challenging position with lots of work and lots of opportunities.</p><p><strong>As an Associate Manager Clinical Research Informatics, a typical day might include</strong>:</p><ul><li><p>Developing and maintaining a toolkit with key functions, APIs, and summaries that help users understand, interpret, and interact with phenotype data. In addition to Python, knowledge of R, SQL and/or C++ is a definite plus.</p></li><li><p>Developing the tools and code that will transform electronic health records, surveys, laboratory assays, or digital device data into a harmonized tall and narrow format compatible with RGC analytical tools, applications and processes. You will probably be writing and updating code in Python and using associated data science libraries, such as pandas, Polars, NumPy, scikit, and others.</p></li><li><p>Reviewing the structure, content, and quality of phenotype data extracted from electronic health records, surveys, digital devices<strong>,</strong> or laboratory assays. Each of these datasets may include data on 100,000s of people and require coordination and input from multiple stakeholders with varied expertise.</p></li><li><p>Discussing the challenges and opportunities of using health data from electronic health records, surveys, digital devices<strong>,</strong> and laboratory assays to characterize human health and disease. Expertise in cutting-edge statistical methods for epidemiology is a definite plus.</p></li><li><p>Working with modern cloud environments and platforms. A knowledge of AWS and related toolkits will be useful for your day-to-day work. You will be using your computational skills to execute analysis and data processing at scale and to facilitate automation and repeatability of all key processes.</p></li><li><p>Presenting results and summaries of these datasets and data processing plans to a variety of technical audiences, ranging from experts in statistics, epidemiology, genetics, and computation to experts in biology, drug design, and medicine. You will need outstanding communication skills and an ability to summarize and present to a variety of technical audiences.</p></li><li><p>Working in a highly interactive environment with a team of colleagues. We highly value the ability to interact, learn, and teach so that you and other skilled individuals consistently achieve high levels of motivation, enthusiasm, and performance.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>A demonstrated knowledge of Python and key data science libraries is a must. Knowledge of R, SQL and/or C/C++ is also highly valued. If you have contributed to code in GitHub or another public repository, let us know.</p></li><li><p>Understanding strategies for mapping structured and unstructured data to ontologies such as ICD-10, RxNORM and LOINC.</p></li><li><p>Knowledge and experience applying best practices for data quality control, summarization and visualization.</p></li><li><p>A passion for learning. We are a fast-moving team in a fast-moving company. You should expect to encounter challenging work and to learn many new skills.</p></li></ul><p><strong>To be considered for this position </strong>you should have a PhD (or MS with additional years in lieu) in Computer Science, Health Informatics, Clinical Informatics, Biostatistics, or a related field with at least 0-2 years of relevant experience organizing large datasets in a research setting, whether in academia or industry, highly preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 16 May 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Physician Scientist – Obesity and Liver Disease Human Genetics]]></title>
    <date><![CDATA[Sun, 21 Sep 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39319]]></requisitionid>
    <referencenumber><![CDATA[R39319]]></referencenumber>
    <apijobid><![CDATA[r39319]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r39319/physician-scientist-obesity-and-liver-disease-human-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an exceptional Physician Scientist to join our Cardiometabolic Therapeutic Area Genetics (TAG) team at the Regeneron Genetics Center (RGC). Within the RGC, the Cardiometabolic TAG team is using massive scale human exome sequencing for discovery and validation of new therapeutic targets in obesity and obesity associated metabolic disease. The position holder will collaborate with various RGC teams and with pre-clinical and clinical development teams at Regeneron to accelerate therapeutic development for genetically-validated targets in obesity and metabolic disease via the generation of new human genetics and epidemiological insights.<br> </p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Accelerate therapeutic development for genetically-validated targets via the generation of new human genetics and epidemiological insights.</p></li><li><p>Generate key research questions and then design and execute studies and analyses to help address these questions, interpret the results of these studies and summarize ensuing insights in a variety of formats for different audiences (e.g. documents, presentations, patent applications, publications, etc.).</p></li><li><p>Understand and leverage RGC and Regeneron datasets, external resources and the scientific/medical literature to address key research questions at hand and summarize results giving appropriate weight to quantitative and qualitative strength of evidence.</p></li><li><p>Support target nominations and validation utilizing the RGC’s human genetics capabilities and leveraging Regeneron’s extensive internal therapeutics platforms and development modalities.</p></li><li><p>Partner with Clinical Development to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations.</p></li><li><p>Participate in the intellectual life of the Cardiometabolic TAG, the RGC and Regeneron at large and help build an inclusive work culture where everyone can perform at their best and fully develop their talent and potential.</p></li><li><p>Represent the Therapeutic Area Genetics team in cross-functional initiatives within RGC and Regeneron.</p></li></ul><p><strong>This job might be for you if you have:</strong></p><ul><li><p>Demonstrated ability to design and lead human genetics and epidemiological studies delivering medically-relevant findings in a team-based environment.</p></li><li><p>Ability to use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions. Familiarity with clinical genetics concepts and various genetic models of disease.</p></li><li><p>Strong computational and quantitative skills including ability to design and execute complex analyses using large scale datasets both with individual-level as well as result-level data (e.g. UK Biobank, All of US, MVP, Biobank Japan, meta-analysis of genome-wide summary statistics, etc). This includes proficiency with R or similar software and familiarity with high performance computing environments.</p></li><li><p>Experience leading complex human genetics research endeavors. Knowledge of different study designs and analyses including GWAS, exome or genome sequencing in cohort, case-control or family-based studies. Ability to integrate different data resources to translate initial findings.</p></li><li><p>Familiarity with the applications of genetics to gain medically-actionable insights including polygenic risk scores, quantitative traits analyses and Mendelian randomization.</p></li><li><p>Understanding of drug development and clinical trial design and execution. Experience as investigator in Randomized Controlled Trials is a plus. Experience in the clinical management or medical research relating to cardio-metabolic disease is not strictly required but is a plus.</p></li></ul><p>.</p><p><strong>To be considered for this role,</strong> you must have a MD with strong background in and knowledge of human genetics and genetic epidemiology. An outstanding candidate will be an MD/PhD with training and experience in translational human genetics, genetic epidemiology, epidemiology (or related disciplines) and strong quantitative skills.</p><p>#MDJOBSGG #MDJobs</p><ul></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$173,500.00 - $283,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Sun, 16 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43733]]></requisitionid>
    <referencenumber><![CDATA[R43733]]></referencenumber>
    <apijobid><![CDATA[r43733]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43733/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager Statistical Programming provides technical leadership and support to the project teams on all statistical programming matters according to the project strategies within therapeutic area(s). The incumbent manages the programming aspect of a project in collaboration with partnering functions, stakeholders, and external functional service providers for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards, regulatory safety reports, and other requests. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. The incumbent will lead or participate in process and methodology development for department goals and SME topics. Maybe responsible for goal setting and performance management.</p><p><strong>In this role, a typical day might include: </strong><strong>​</strong></p><ul><li>Manage and lead programming support within multiple studies/projects in various study activities to ensures timely and high-quality programming deliverables in assigned projects and areas. Lead and coordinate programming documentation including specifications, as appropriate, for multiple studies following programming standards and processes</li><li>Demonstrate company values and act as a role model by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability</li><li>Ensure the commitment and reinforcement of the roles and responsibilities of the statistical programming function</li><li>Proactive communication with study and project teams to clarify requirements and specifications, guide direct reports or support programmers on assignment status</li><li>Lead and support global regulatory authority submissions including preparing programming deliverable for submission and working closely with partnering functions to address health authority requests.</li><li>Lead and manage department goals and SME topics</li><li>May oversee development of direct reports by setting goals, managing performance, evaluating, and monitoring training needs, supporting development plans, mentoring, and coaching</li><li>May participate in screening and interviewing candidates for contractor and permanent positions.</li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 10+ (12+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience.</li><li>Advanced SAS programming skills in a clinical data environment with expertise in at least one, preferably multiple, therapeutic areas. Knowledge of other programming languages such as R, Python etc. is a plus.</li><li>Understanding of pharmaceutical clinical development across multiple therapeutic areas (i.e. understanding of statistical concepts, techniques and clinical trial principles) and good knowledge of regulatory submissions and requirements</li><li>Ability to work on global interdisciplinary teams. Good organizational, interpersonal, communication, and leadership skills. Establish and maintain effective working relationships with coworkers, managers, and clients</li><li>Ability to effectively manage multiple tasks and projects</li><li>Problem solving and innovative skills that demonstrate initiative and motivation</li><li>Ability to influence others, mentor, and coach junior programmers to achieve results</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HEOR (Classical Hematology)]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45181]]></requisitionid>
    <referencenumber><![CDATA[R45181]]></referencenumber>
    <apijobid><![CDATA[r45181]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45181/associate-director-heor-classical-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director you will develop HEOR strategies and plans, conduct HEOR and RWE studies and develop publications and deliverables. We work closely with Market Access, Medical Affairs, Clinical Development, Commercial, Regulatory and other groups to ensure evidence needs are identified and addressed to demonstrate the value of our classical hematology portfolio. </p><p>This position is at our Sleepy Hollow, NY location and will require you to be onsite 4 days/week. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Develop and implement global HEOR strategies and programs for our portfolio throughout the product’s lifecycle, to inform and support clinical development and regulatory needs during early pipeline phase and ensuring optimal market access. <br>• Collaborate with business partners to develop and support compelling product value propositions with aim to optimize future patient access to our therapeutics<br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation. <br>• Leverage RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams generating insights to inform development programs and key business questions. <br>• Co-lead conduct of regulatory-grade real world evidence studies and provide education on emerging opportunities for employing RWE across the solid tumor portfolio.<br>• Collaborate on conduct and communication of epidemiology and pharmacoepidemiology analyses and studies in support of development and regulatory goals.<br>• Provide relevant input into selection of patient population, comparators and endpoints within clinical trials to enable demonstration of robust incremental value over standard of care that can facilitate optimal future patient access. <br>• Develop and implement Clinical Outcomes Assessment (COA) measurement strategies and plans in support of product labeling, patient access and product differentiation. Develop and validate COA endpoints for integration in clinical studies; analyze and communicate data from clinical trials. Produce COA evidence dossiers for regulatory submissions. Interact as necessary with Agencies on those matters and keep track of competitor PRO developments with regulators and payers. <br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.</p><p><strong>This may be for you if you: </strong><br>• Want to have an impact on patient lives<br>• Enjoy working in a ‘rapid response’ environment<br>• Would like an opportunity to present to senior leaders<br>• Want to be part of a growing high performing team</p><p>To be considered it is required to have an Advanced graduate degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field (e.g. pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health). 4+ years with PhD or 6+ years with MS in HEOR; at least 3 years of life science company or healthcare consulting experience is a plus. Strong technical expertise required in design and conduct of HEOR studies and models. Solid understanding of regulatory (e.g. FDA, EMA) considerations. Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Business Operations (IT)]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42096]]></requisitionid>
    <referencenumber><![CDATA[R42096]]></referencenumber>
    <apijobid><![CDATA[r42096]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42096/vice-president-business-operations-it/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Vice President position in our Business Operations organization to lead both the strategic transformation and daily operational management of all information technology functions supporting Manufacturing operations at Regeneron. This role encompasses dual leadership responsibilities—managing established IT functional areas while simultaneously leading implementation of new critical and migration from old to new systems across global operations sites.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Global IT Leadership: Lead IT functions such as Application Management, Infrastructure, Data, Digital Products, Software Development, Compliance, and Security. Ensure high system performance for manufacturing-critical systems.</p></li><li><p>Strategic Transformation: Jointly with respective function leaders, plan transformation of key processes and coordinate implementation of core systems (MES, LIMS, eQMS, ERP, etc.) to deliver significant uplift in operational performance of respective functions and cross functional processes.</p></li><li><p>Digitization: Collaborate with core business functions to design and implement digital data solutions to enable business intelligence and advanced analytics</p></li><li><p>Compliance & Risk Management: Ensure alignment to FDA, cGMP, and global regulations while mitigating IT risks.</p></li><li><p>Corporate Collaboration: Partner with Corporate IT for enterprise alignment while maintaining operations-specific independence.</p></li><li><p>Organizational Development: Build and develop a high-performing global IT team, ensuring internal availability of critical development capabilities, while outsourcing occasional and non-critical work, encouraging continuous improvement.</p></li><li><p>Budget & Vendor Management: Manage IT budgets and vendor relationships for seamless system integration, selective outsourcing of non-core and temporary activities for cost and performance optimization</p></li><li><p>Executive Leadership: Represent IT in Site Management teams and communicate progress to collaborators.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have led implementation and migration of core IT systems in operations and other business-critical functions, enterprise applications.</p></li><li><p>Have solved major business challenges and significantly improved business outcomes through identification, design and successful deployment of the newest information technologies and solutions.</p></li><li><p>Led successful digitization and automation of processes, data integration, development of business intelligence and AI solutions.</p></li><li><p>Are able to lead global teams that include IT and business partners, to manage dual operational/strategic responsibilities, and to drive cross-functional change initiatives.</p></li><li><p>Have strong interpersonal skills to collaborate across all organizational levels.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in IT or related field, 20+ years of experience in IT and business operations / transformations; biotechnology/pharmaceutical experience is a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 07:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Statistical Genetics]]></title>
    <date><![CDATA[Wed, 25 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45060]]></requisitionid>
    <referencenumber><![CDATA[R45060]]></referencenumber>
    <apijobid><![CDATA[r45060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45060/senior-manager-statistical-genetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and talented Senior Manager, Analytical Genetics and Data Science (AGDS) to join the AGDS team at the Regeneron Genetics Center (RGC). In this individual contributor role, you will conduct analyses of large-scale human genetic and phenotypic datasets for the discovery and validation of new therapeutic targets. Your work will use both in-house and public data resources, and your responsibilities will include integrating genetic data with other multi-omics data, applying state of the art statistical tools and methodologies, performing QC, and identifying and interrogating data driven hypotheses related to analytic and translational genetics. In addition to designing and executing analytic studies, you will collaborate with groups across Regeneron’s R&D functions, including both pre-clinical and clinical development teams.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Demonstrated expertise in genetic association analyses using large-scale genetic data. </p></li><li><p>Strong understanding of multi-omic data integration and its application in therapeutic target discovery. </p></li><li><p>Experience in developing and implementing methods for data harmonization and normalization. </p></li><li><p>Experience with cutting edge genetic analysis approaches, such as genome-wide association analysis, exome-wide association analysis, rare variant analysis, Mendelian randomization, LD Score regression, polygenic risk score modelling, pleiotropy analysis, meta-analysis, and the use of functional data to prioritize variants and genes of interest.</p></li><li><p>Proven ability to independently lead and manage research projects from conception to completion. </p></li><li><p>Excellent communication and collaboration skills, with a track record of working effectively in interdisciplinary teams.</p></li></ul><p><strong>This role might be for you if have:</strong></p><ul><li><p>A PhD in a relevant field (e.g., statistical genetics, bioinformatics, computational biology, genetics, or related disciplines). </p></li><li><p>5 years of post-PhD experience in analyzing large-scale omics datasets.</p></li><li><p>Outstanding communication skills and an ability to summarize and present the results of human genetic studies to a variety of technical audiences, ranging from specialists in statistical genetics and computation to specialists in biology, drug design, and medicine.</p></li></ul><p>​#RGC</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Feb 2026 13:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Statistical Programming]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44857]]></requisitionid>
    <referencenumber><![CDATA[R44857]]></referencenumber>
    <apijobid><![CDATA[r44857]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44857/manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A <strong>Manager Statistical Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. As an integral part of a study team, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan, programming specification or user requirements document using internal standards and guidelines. The incumbent provides guidance in implementing and executing the programming and project standards. The incumbent will be responsible for leading the programming aspect of a project, both internally or CROs, for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards and annual reports. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. Meets statistical ad hoc requests of senior management.<br> </p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Develop an expertise within a therapeutic area or standard tool. Work with minimal supervision to perform, coordinate and oversee the preparation, execution, reporting and documentation of a project</li><li>Function as a lead programmer in the development and QC of tables, listings, graphs, or systems in support of analysis requirements utilizing Regeneron tools and methodologies and current industry standards (i.e. CDISC SDTM / ADaM)</li><li>Manage the effort, including esubmssion deliverables, using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Provide programming support for complex presentations and more complex statistical ad-hoc requests. </li><li>Act as programming representative in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports.</li><li>If applicable, lead an application development and act as the programming representative to the user audience.</li><li>Work with management to determine resource requirements for therapeutic area or department function <br>responsibilities. </li><li>Review and select resumes, screen and interview candidates for contractor and permanent positions.</li><li>Provide feedback to management regarding team member’s contributions to the work effort for evaluating individual's performance and recommend yearly goals.</li><li>Advises all direct reports about the procedures surrounding retention of data, records, and information for <br>employees in their group.<br> </li></ul><p><strong>In order to be considered qualified for this role</strong></p><ul><li>Master’s Degree</li><li>8-10 years of relevant work experience</li><li>SAS Certification desirable.</li><li>Also acceptable - 5+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience with a Master’s Degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Data Science]]></title>
    <date><![CDATA[Mon, 23 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46197]]></requisitionid>
    <referencenumber><![CDATA[R46197]]></referencenumber>
    <apijobid><![CDATA[r46197]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46197/process-development-engineer-iii-data-science/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Data Enablement and Analytics (DEA) team within Preclinical Manufacturing and Process Development (PMPD) is seeking a Machine Learning Engineer to develop, build and deploy analyses and machine learning models that support bioprocess development. This role is ideal for a data scientist with a strong foundation in chemical or biomedical engineering and a passion for building impactful solutions in close collaboration with scientists and process engineers.</p><p>You will work at the intersection of software engineering, data science, and bioprocess domain expertise—developing models that will be put into action within PMPD’s laboratory and manufacturing operations. You will mentor and coordinate citizen data scientists. Your work will streamline workflows, enable automation, and accelerate decision-making across PMPD.</p><h3>A Typical Day in the Role Might Look Like:</h3><ul><li><p>Partner closely with scientists, engineers, and analysts to understand bioprocess workflows and identify high‑impact data science opportunities.</p></li><li><p>Acquire, clean, and structure complex datasets to enable scalable, repeatable analyses.</p></li><li><p>Design, develop, and apply advanced analytics and machine learning models to drive data‑informed decision‑making.</p></li><li><p>Deploy models into production environments, enabling automated and autonomous operations where appropriate.</p></li><li><p>Lead, mentor, and coordinate citizen data scientists on critical initiatives across PMPD</p></li><li><p>Enhance, maintain, and extend existing analytics tools and platforms to support new use cases and evolving business needs.</p></li><li><p>Contribute as an active member of Agile teams within a Scaled Agile Framework, supporting planning, delivery, and continuous improvement.</p></li><li><p>Continuously evaluate emerging technologies and methodologies to strengthen data science capabilities within the organization</p></li></ul><h3>What You Bring</h3><ul><li><p>Bachelor’s or Master’s degree in Chemical Engineering, Biomedical Engineering, or a related discipline. 5-7 years of experience in bioprocess development, pharmaceutical manufacturing, or a closely related domain.</p></li><li><p>Demonstrated ability to apply machine learning and predictive analytics to complex, real‑world problems.</p></li><li><p>Strong programming skills in Python and SQL, with a solid understanding of data modeling and database design.</p></li><li><p>Experience working in Linux/Unix environments and using Git for version control and collaboration.</p></li><li><p>Excellent communication skills and a collaborative mindset, with the ability to partner effectively with scientists, engineers and analysts, while mentoring citizen data scientists.</p></li><li><p>Familiarity with DevOps and deployment technologies such as Kubernetes, NixOS, and Jenkins.</p></li><li><p>Experience with Operational Technology and analytics platforms (e.g., PI Historian, OPC, MQTT, Dataiku, Seeq) is a plus.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Mar 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Quality Control Scientist (Chemistry)]]></title>
    <date><![CDATA[Sun, 15 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46048]]></requisitionid>
    <referencenumber><![CDATA[R46048]]></referencenumber>
    <apijobid><![CDATA[r46048]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46048/sr-quality-control-scientist-chemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Sr Quality Control Scientist in the Technical Resources Department. This position performs assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.</p><p>As a Sr QC Scientist for Chemistry in the Technical Resources Department, a typical day might include the following:</p><ul><li><p>Performs assay development/validation for QC.</p></li><li><p>Reviews new test procedures and assays.</p></li><li><p>Evaluates and bring in new methodologies/techniques when needed.</p></li><li><p>Facilitate assay transfer from R&D and to business partners</p></li><li><p>Organize analytical assay transfer internally and externally.</p></li><li><p>Set product specification.</p></li><li><p>Participates in technical troubleshooting and problem investigation.</p></li><li><p>Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.</p></li><li><p>Participates in training programs for analysts.</p></li></ul><p>This job might be for you if:</p><ul><li><p>You have in-depth knowledge with HPLC based assays.</p></li><li><p>You like dealing with technical issues, troubleshooting, and constant change</p></li><li><p>You are a team player who can work with a variety of different people on different tasks</p></li><li><p>You have strong written and verbal communication skills</p></li><li><p>You enjoy mentoring and training others on systems, processes and problem solving</p></li><li><p>You enjoy working in a fast-paced environment and are flexible to changing requirements</p></li><li><p>You can take on new and sometimes ambiguous challenges and learn quickly</p></li></ul><p>To be considered for a Sr QC Scientist (Chemistry) Technical Resources role you must have a BS in Chemistry, Biochemistry, Biology, or a related field, and 6+ years of relevant experience. Higher level degree preferred.</p><p>Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred.</p><p>Level is determined based on experience relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 16 Mar 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Program Management Process and Standards]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46277]]></requisitionid>
    <referencenumber><![CDATA[R46277]]></referencenumber>
    <apijobid><![CDATA[r46277]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46277/director-program-management-process-and-standards/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director, Development Program Operations</strong> will have a leadership role in the building and optimization of the Strategic Program Team’s (SPTs) operating model and Development capabilities (processes, tools, services) that contribute to the company’s performance and operational excellence. Under this role’s leadership, the team is accountable for generating actionable insights and recommendations to senior leadership to drive how we scale our operating model, for example our team membership composition, roles/responsibilities, deliverables.</p><p>Additionally, this role is responsible for designing, building and managing cross-functional business-critical initiatives that drive the acceleration of portfolio delivery. These initiatives require strong matrix leaders with drug development and business acumen and are passionate about applying robust strategic change execution methods and best practices. The role will need to anticipate business needs through strategic planning and trend analysis and with alignment of key stakeholders across Development with interfaces in Research, Manufacturing and Commercial. Operates with a continuous improvement mindset to enable cross functional operational efficiencies.</p><p>This role is a hands-on contributor and people manager responsible to build relationships at all levels of the organization in order to solicit and action stakeholder input regarding the SPT operating model. This role will navigate the fast-paced and agile environment of Regeneron in a collaborative and innovative manner.</p><p><em>***Note: this role requires 4-days onsite in either Tarrytown, NY or Warren, NJ and is not eligible fully remote. </em></p><p><strong>A typical day in this role looks like: </strong></p><ul><li>Identify, create and drive strategic initiatives related to the DPM and SPT operating model with direct impact to drive Development portfolio and pipeline </li><li>Partner with Program and Portfolio Management (PPM) Leadership Team and Development functional areas to monitor and measure implementation impacts and take action when needed </li><li>Develop, maintain and implement project/program management methodology, including processes, tools, metrics and policies to ensure efficiency, quality and business success </li><li>Drive consistency and standardization across program strategy execution and ensures compliance to the application of these execution methodologies and standards </li><li>Design and implement the operating cadence, including running coordination meetings, project updates and overall oversight of projects </li><li>Work with Development and PPM Leadership to define innovative operational Key Performance Indicators (KPIs) for the projects and services delivered, tracking these KPIs across the department and projects to ensure goals are consistently achieved </li><li>Build strong, interdependent partnerships and manages the communication effectively with functional area heads in Development, key stakeholders in Research, Commercial and Manufacturing </li><li>Responsible for the coaching and development of department members as well as ensuring that the organizational strategy delivers the skills, capabilities and processes that enable portfolio delivery are present in his/her team </li></ul><p><strong>This role may be for you if you have: </strong></p><ul><li>Significant experience in the biotechnology or pharmaceutical industry with a strong understanding of drug development activities in context of line functions and project teams </li><li>Consulting experience and experience with developing a Project Management Office (PMO) is desirable </li><li>Proven experience in a similar role; understanding of Operational Excellence, Six Sigma/LEAN and business process management preferred </li><li>Proven leadership skills with the ability to innovate and drive framework and change in a matrixed environment, amidst ambiguity </li><li>Lead the department with a customer-first demeanor </li><li>Strong analytical, problem-solving and strategic thinking abilities </li><li>Strong organizational and multitasking abilities, overseeing multiple projects simultaneously </li><li>Excellent interpersonal skills with a proven ability to negotiate, influence and work effectively with individuals at all levels of the organization, including senior leadership </li><li>Excellent communication skills (written/verbal), including presenting complex information and insights effectively </li><li>Experience in building and leading high performing teams and driving cross-functional initiatives </li><li>IT proficiency with MS software and project management tools, analytics and visual reporting applications (e.g. SharePoint, MS Project, PowerPoint, Word, Excel, PowerBI, etc) </li><li>Ability to travel (<10%) </li></ul><p><strong>In order to be considered qualified</strong>, a minimum of a Bachelor’s degree (Bachelor of Science) and 12+ years industry experience with a minimum of 5+ years in project management experience required. MBA preferred. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 17:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Aggregate Reporting Management]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46482]]></requisitionid>
    <referencenumber><![CDATA[R46482]]></referencenumber>
    <apijobid><![CDATA[r46482]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46482/senior-manager-aggregate-reporting-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><p>Regeneron's Patient Safety organization is seeking a Senior Manager, Aggregate Reporting Management to join our team!</p></div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><p>This position in the Global Patient Safety (GPS) Operations is responsible for management of aggregate safety reporting activities across all phases of the product lifecycle. This role supports the consistent, compliant, and scientifically robust preparation, distribution and submission of periodic and ad-hoc safety reports to health authorities, collaborators and contract research organizations worldwide.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Drives preparation, development and maintenance of Aggregate Reporting (i.e., PSURs/PBRER, PAER, DSURs, Local Periodic Reports, SUSARs) Deliverables</p></li><li><p>Leads Aggregate Report planning, production and distribution activities across GPS and other functions across US, EU, Japan and other ICH regions, as well as non-ICH regions</p></li><li><p>Provides expertise and guidance to authors and contributors of aggregate reports</p></li><li><p>Maintains compliance metrics and contributes to implementation of Quality Events and Corrective Action and Preventive Action (CAPA) for non-compliance</p></li><li><p>Implements effective structure, procedures and tools to ensure aggregate reports and other functional deliverables are completed timely and with high quality</p></li><li><p>Develops and oversees functional specifications of data requirements for aggregate deliverables from the safety and clinical databases</p></li><li><p>Collaborates with Global Patient Safety (GPS) and with other functional areas (Epidemiology, Clinical Development, Regulatory Affairs, Statistics, etc.) contributing to aggregate safety reports</p></li><li><p>Acts as subject matter expert during audits and inspection.</p></li><li><p>Provides oversight, and training as needed of CRO respective activities in support of high quality and timely aggregate reports</p></li><li><p>Acts as a functional vendor management overseeing and driving high quality outputs from our vendors</p></li><li><p>Develops and maintains aggregate report procedural package (SOPs, Work Instructions), reports’ templates, KPIs</p></li><li><p>Drives process improvement through automation and other tech initiatives.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required (advanced degree or HCP‑focused background preferred) and 5+ years of Pharmacovigilance experience, with a demonstrated focus on Aggregate Safety Reporting.</p></li><li><p>Project management experience strongly preferred, PMP preferred</p></li><li><p>Experience with health authority inspections (PV and GCP)</p></li><li><p>Medical writing experience with regulatory documentation</p></li><li><p>Strong project management skills</p></li><li><p>Excellent strategic decision-making and analytical skills</p></li><li><p>Strong communication and writing skills</p></li><li><p>Strong understanding of Scientific content</p></li><li><p>Proven experience with technology implementations allowing for streamlined process execution.</p></li></ul><p>#GDPSJobs</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology (Iowa/Western Illinois)]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43133]]></requisitionid>
    <referencenumber><![CDATA[R43133]]></referencenumber>
    <apijobid><![CDATA[r43133]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43133/medical-specialist-ii-ophthalmology-iowawestern-illinois/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Peoria]]></city>
    <state><![CDATA[Illinois]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Territory: Iowa/Western Illinois</strong></h3><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets several medicines, including for eye diseases, and has product candidates in development in other areas of high unmet medical need.</p><p><strong>A typical day might include the following:</strong><br>The Medical Specialist II will report to the Regional Director and will be responsible for daily development and management of relationships with Retina Specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The primary focus on this role will be the approved indications suffered by patients as it relates to conditions of the eye. The Medical Specialist II will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you:</strong><br>• Have experience in biologics and buy and bill products<br>• Can demonstrate history of high sales performance<br>• Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Ophthalmology and/or Buy & Bill with relevant retina experience is preferred. Residency in the territory is required.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$152,300.00 - $195,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44572]]></requisitionid>
    <referencenumber><![CDATA[R44572]]></referencenumber>
    <apijobid><![CDATA[r44572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44572/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>At Regeneron, we are driven by innovation and a commitment to improving lives. As part of our global expansion, we are seeking a dedicated <strong>Regulatory Affairs Manager</strong> to join our growing regulatory team in Japan. This role offers a unique opportunity to shape the regulatory landscape for biological products and regenerative medicines in Japan, while collaborating with a diverse team of experts locally and globally. If you’re passionate about navigating regulatory processes and making a meaningful impact, we’d love to hear from you.</p><br><h3><strong>A Typical Day:</strong></h3><ul><li><p>Lead the preparation, submission, and maintenance of clinical trial applications to PMDA.</p></li><li><p>Coordinate and execute health authority meetings, including PMDA consultations and MHLW meetings.</p></li><li><p>Manage timely submissions of marketing authorization applications and post-approval changes for assigned projects.</p></li><li><p>Ensure compliance with Japan’s regulatory requirements and local standards.</p></li><li><p>Collaborate with cross-functional teams, including clinical, commercial, medical, and patient safety colleagues.</p></li><li><p>Assist in the development of local labeling and patient information for key programs.</p></li><li><p>Support the regulatory review of promotional materials as needed.</p></li></ul><br><h3><strong>This Role May Be For You If:</strong></h3><ul><li><p>You have a Bachelor’s degree in a scientific discipline, with a Master’s degree in Science or Pharmacy being preferred.</p></li><li><p>You bring approximately 5 years of experience in regulatory affairs, particularly with J-NDA submissions and approvals in Japan.</p></li><li><p>You take pride in your ability to prepare and review documents like J-CTDs and briefing materials for PMDA consultations.</p></li><li><p>You are eager to learn about regulatory strategies and drug development across multiple products.</p></li><li><p>You have a strategic mindset, strong commercial awareness, and excellent communication skills in English.</p></li><li><p>You thrive in a global, matrixed team environment and enjoy fostering collaboration.</p></li><li><p>You are familiar with advising on regulatory requirements for clinical trials (advantageous but not mandatory).</p></li></ul><br><h3><strong>To Be Considered:</strong></h3><p>To excel in this role, you must have a <strong>Bachelor’s degree in a relevant scientific field</strong> and <strong>approximately 5 years of regulatory experience</strong>, including expertise in <strong>J-NDA submissions</strong> and <strong>document preparation</strong> for PMDA consultations. Candidates with a <strong>Master’s degree in Science or Pharmacy</strong> and experience advising on clinical trial requirements will be highly regarded. Strong communication skills in English and the ability to work effectively in a global team are essential.</p><p>Join us in shaping the future of medicine and making a difference in patients' lives. Apply now to become a part of our inspiring journey. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 02:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Scientist (Technical Resources)]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45795]]></requisitionid>
    <referencenumber><![CDATA[R45795]]></referencenumber>
    <apijobid><![CDATA[r45795]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45795/sr-scientist-technical-resources/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Sr Quality Control Scientist in the Technical Resources (Chemistry) Department. This position performs assay development, characterization, optimization, transfer, validation, and investigations for QC. You would provide technical support, guidance and supervision for release, stability, and in-process testing and assay development.</p><p>As a Sr QC Scientist for Chemistry a typical day might include the following:</p><ul><li><p>Performs assay development/validation for QC.</p></li><li><p>Reviews new test procedures and assays.</p></li><li><p>Evaluates and bring in new methodologies/techniques when needed.</p></li><li><p>Facilitate assay transfer from R&D and to business partners</p></li><li><p>Organize analytical assay transfer internally and externally.</p></li><li><p>Set product specification.</p></li><li><p>Participates in technical troubleshooting and problem investigation.</p></li><li><p>Review analytical development report, assay and process validation report and other technical documents for technical correctness and regulatory compliance.</p></li><li><p>Participates in training programs for analysts.</p></li></ul><p>This job might be for you if:</p><ul><li><p>You have in-depth knowledge with HPLC based assays.</p></li><li><p>You like dealing with technical issues, troubleshooting, and constant change</p></li><li><p>You are a team player who can work with a variety of different people on different tasks</p></li><li><p>You have strong written and verbal communication skills</p></li><li><p>You enjoy mentoring and training others on systems, processes and problem solving</p></li><li><p>You enjoy working in a fast-paced environment and are flexible to changing requirements</p></li><li><p>You can take on new and sometimes ambiguous challenges and learn quickly</p></li></ul><p>To be considered for a Sr QC Scientist (Chemistry) Technical Resources role you must have a BS in Chemistry, Biochemistry, Biology, or related field, and 6+ years of relevant experience.</p><p>PhD strongly preferred.</p><p>Experience with cell or gene therapy in a Biopharmaceutical environment is strongly preferred.</p><p>Level is determined based on experience relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Applications Analyst - Oracle]]></title>
    <date><![CDATA[Sun, 26 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46999]]></requisitionid>
    <referencenumber><![CDATA[R46999]]></referencenumber>
    <apijobid><![CDATA[r46999]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46999/principal-it-applications-analyst-oracle/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal IT Applications Analyst is a technical expert responsible for the configuration, implementation, maintenance, and ongoing support of Oracle Supply Chain IT applications and systems, including the Oracle ERP. The position requires expertise in Oracle ERP systems, including system architecture, integration, and performance monitoring, as well as the ability to lead strategic initiatives and deliver solutions that improve user experience and operational efficiency.</p><p>As a Principal IT Applications Analyst, a typical day might include the following:</p><ul><li>Lead the technical configuration and deployment of Oracle Supply Chain modules within Oracle ERP, ensuring alignment with business requirements and compliance with regulatory standards.</li><li>Support and manage system integrations with other enterprise applications, including middleware tools, APIs, and EDI configurations and are in compliance with applicable regulatory guidelines and all Regeneron procedures and policies.</li><li>Develop and implement customizations, extensions, and workflows using Oracle Application Development Framework (ADF), Business Process Management (BPM), and other Oracle tools.</li><li>Collaborate with IT and business teams to design and implement scalable solutions, including the creation of technical documentation, test plans, and deployment strategies.</li><li>Coordinate ongoing maintenance of Oracle EBS or Fusion ERP systems, including monitoring system performance, solving issues, and ensuring high availability and reliability of applications.</li><li>Manage application upgrades, patches, and security configurations while adhering to change management protocols.</li><li>Provide technical support and guidance to users, including root cause analysis and resolution of complex system issues.</li><li>Monitor system metrics and performance indicators to proactively identify areas for optimization and improvement.</li><li>Follows the methodologies and standards for IT project documentation and implementation, which includes guidelines, procedures, standards, and monitoring for organizational compliance.</li><li>Works with IOPS IT team and applicable vendors to develop and drive a strategic roadmap related to the application.</li><li>Works with business partners to develop and deploy system functionality to applicable user communities.</li><li>May manage and oversees a small staff of specialists on department projects and initiatives.</li><li>Recommends, negotiates and manages vendor contracts and ensures relationships are managed in an effective manner.</li><li>May serve as an SME or spokesperson for IOPS IT during a regulatory inspection.</li><li>Provides leadership in continuous improvement of GMP training programs including the methodologies for delivery, maintenance, and tracking of all GMP training, such as Standard Operating Procedure (SOP) training assessment and on-the-job training (OJT), through Kaizen and other continuous improvement approaches.</li><li>Maintains strong relationships with key business leaders to ensure acceptance and operational applicability of key processes and programs.</li></ul><p>This role may be for you if you have:</p><ul><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 like 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 regulatory guidelines, including GMP compliance, and experience supporting audits and inspections.</li><li>Proven track record of supporting complex ERP, upgrades, and customizations.</li><li>Excellent leadership, communication, and problem-solving skills.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Senior IT Applications Analyst: 5 years of progressive industry/relevant experience.</li><li>Principal IT Applications Analyst: 8 years of progressive industry/relevant experience.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Pharmaceuticals, life sciences or medical device manufacturing industry experience highly preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 27 Apr 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, GxP Enterprise Architecture]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44202]]></requisitionid>
    <referencenumber><![CDATA[R44202]]></referencenumber>
    <apijobid><![CDATA[r44202]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44202/director-gxp-enterprise-architecture/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, GxP Enterprise Architecture leads the IT architecture practice for manufacturing and operations (e.g., manufacturing, QA, QC, process sciences, supply chain). This role defines technology strategy and standards, governs platform decisions, and ensures solutions meet GxP and data integrity requirements while advancing business capabilities and long-term platform health.</p><p>As a Director, GxP Enterprise Architecture, a typical day might include the following:</p><ul><li>Define and evolve EA governance, standards, reference architectures, and reusable patterns across application, integration, data, and infrastructure.</li><li>Own the multi-year technology roadmap aligned to business capability priorities and lifecycle plans.</li><li>Lead architecture reviews, maintain the application portfolio, and manage technical debt and end‑of‑life risk.</li><li>Ensure alignment with enterprise-wide architecture, avoid redundant platform investments while identifying capability gaps.</li><li>Translate market trends (ERP, MES, LIMS, QMS, data, cloud, integration) into actionable guidance and adoption plans.</li><li>Manage business strategy enablement options, and trade-offs met by technology with business leaders.</li><li>Collaborate with corporate IT's Architecture team to ensure architectural standards are in place and enforced.</li><li>Ensure Architecture Standards are aligned with 21 CFR Part 11, Annex 11, data integrity, and CSV/CSA requirements.</li><li>Produce and maintain target-state architectures, capability maps, roadmaps, solution blueprints, integration diagrams, and ADRs.</li></ul><p>This role may be for you if you have knowledge in:</p><ul><li>GMP systems landscape: ERP (e.g., Oracle EBS, Oracle Fusion), MES, LIMS/ELN, QMS, WMS, EDMS; familiarity with SCADA/DCS and shop-floor integration.</li><li>Integration patterns and platforms: APIs, event-driven architecture, EDI, ETL/ELT; iPaaS/ESB (e.g., MuleSoft, Boomi), OPC UA; canonical data models.</li><li>Data and analytics: data lakehouse (e.g., Snowflake, Databricks), MDM, data governance, metadata lineage, BI platforms; ISA-95 data layers.</li><li>Cloud and infrastructure: AWS/Azure services, hybrid architectures, VPC/VNet design, containerization (Kubernetes), IaC (Terraform), CI/CD, microservices.</li><li>Security and compliance: identity and access management (Azure AD), segregation of duties, network segmentation/OT boundary patterns, NIST/ISO 27001 controls, backup/DR.</li><li>Architecture practice: TOGAF/ArchiMate, modeling tools (e.g., LeanIX, Lucidchart), solution blueprinting, ADRs, and traceability for audits.</li><li>SDLC and delivery: Agile/SAFe, DevOps in regulated environments, validation documentation (URS/FS/DS), risk-based CSA.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with 12 years of experience in a relevant industry or equivalent combination of education and experience. Biotechnology/Life Sciences industry experience, preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$192,900.00 - $321,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II-Ophthalmology-Ft. Worth, TX]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46891]]></requisitionid>
    <referencenumber><![CDATA[R46891]]></referencenumber>
    <apijobid><![CDATA[r46891]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46891/medical-specialist-ii-ophthalmology-ft-worth-tx/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>MEDICAL SPECIALIST II - OPHTHALMOLOGY - FT. WORTH, TEXAS</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets medicines for eye diseases, colorectal cancer, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including hypercholesterolemia, oncology, rheumatoid arthritis, allergic asthma, and atopic dermatitis.</p><p><strong>A typical day might include the following: </strong></p><p>The Ophthalmology Medical Specialist will report to the Regional Director and will be responsible for developing and managing relationships with retina specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The Medical Specialist will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you have:</strong></p><p>· Experience in biologics and buy and bill products</p><p>· Demonstrated history of high sales performance</p><p>· Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Buy and Bill experience. Ophthalmology with relevant retina experience is preferred. Must be based in or located in close proximity to the assigned territory, covering DFW, Waco, Midland/Odessa, Lubbock, and East Texas (relocation will not be provided). Ability to travel (40-60%)</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Development Program Management]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47295]]></requisitionid>
    <referencenumber><![CDATA[R47295]]></referencenumber>
    <apijobid><![CDATA[r47295]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47295/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>We are seeking a Senior Manager to join our Development Program Management team. Using prior program management knowledge and experience in the drug development industry, the Sr. Manager provides operational direction as the leader for one or more development programs [within a given Therapeutic Area]. The Sr. Manager Development Program Management executes the strategic direction of a program from preclinical through commercialization by driving the development and implementation of integrated [project] program plans, goals, budgets, and timelines. The Sr. Manager Development Program Management is responsible for forming and managing effective cross functional teams and leads a network of functional area project managers. You will be responsible for supporting the development of a program throughout its lifecycle, by integrating key stakeholders from Discovery, Manufacturing, Preclinical, Global Development and Commercial.</p><h3>As a Senior Manager, a typical day may include the following:</h3><ul><li><p><strong>Teams:</strong> Partners with the Strategic Program Lead to provide operational leadership of program (s) and supports development and execution of overall program strategy by facilitating cross functional Strategic Development Team. Assesses and proactively addresses the needs of the program from pre-IND through commercialization and makes operational decisions to support requirements for success. Actively aims to strengthen and lead high performance teams</p></li><li><p><strong>Planning and Tracking:</strong> By working with and through functional Project Management teams, with oversight develops an integrated project / program plan relevant to the team deliverables and ensures alignment across relevant functions and smooth transitions among pipeline stages. Leads annual goal setting sessions to develop project / program level goals that align with Regeneron’s overall goals and monitors progress against these goals. Develops contingency and risk mitigation plans. Oversees the development of integrated project / program plans and actively monitors progress against the approved baselines. Responsible for oversight of the integrated program timeline and budget, including management of variances and escalation where appropriate</p></li><li><p><strong>Collaborations:</strong> Manages the project / program interactions and deliverables between Regeneron and our strategic alliance partners and collaborators (where applicable). Fosters collaborative relationships across the alliance program teams to develop and execute strategic development plans</p></li><li><p><strong>Information:</strong> Has technical expertise in, and business ownership of, existing program management and planning systems and tools. Manages an existing system and/or tool, including championing the system/tool improvement</p></li><li><p><strong>Communication:</strong> Independently leads and facilitates collaboration between functional areas to ensure effective, accurate, and timely scientific / technical and program-related communication. Adept at tailoring communications based on audience, effectively framing and communicating nuanced context for stakeholders and capturing rationale for decisions</p></li><li><p><strong>Problem Solving:</strong> Creates/identifies new processes and/or leads the development of innovative solutions, collaborating with impacted stakeholders to gain alignment. Can identify risks and develops risk mitigation strategies, and manages programmatic challenges facing project teams. Champions process improvement initiatives, ensuring they meet the business needs</p></li></ul><h3>This role may be for you if you:</h3><ul><li><p>Have excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company in order to establish credibility with professionals on the project teams</p></li><li><p>Understand and motivate others and build effective teams</p></li><li><p>Have strong presentation and critical thinking skills</p></li><li><p>Actively promote constructive interactions among team members in order to address difficult situations</p></li><li><p>Resolve and negotiate conflicts or problems with tact, diplomacy and composure</p></li><li><p>Handle multiple projects and priorities with exceptional organizational and time management skills (both project and self)</p></li></ul><p>To be considered for this role, you must have a BS + 7 years of relevant project management experience, preferably in the drug development/pharmaceutical industry. We need an individual who can independently manage multiple development programs, often working under consultative direction.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Medical Director, Clinical Development, Hematology Cell Therapy]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47077]]></requisitionid>
    <referencenumber><![CDATA[R47077]]></referencenumber>
    <apijobid><![CDATA[r47077]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47077/executive-medical-director-clinical-development-hematology-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[<p>The Executive Medical Director, Hematology, will provide overall clinical scientific leadership for the cell therapy program and have responsibility for our clinical development strategy and execution of clinical trials in this area. This role will be a key partner with the Global Program Head to design the optimal development strategy for this portfolio. This role requires an impactful and highly hard-working individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to hematology clinical research. The Executive Medical Director, Hematology reports directly to the VP, Therapeutic Area Lead, Hematology.</p><p><strong>A typical day in the life may include the following:</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 easily 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 for 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 personal and business needs</p></li></ul><p><strong>This job may be for you if you have the following:</strong></p><ul><li><p>Demonstrated consistent track record in a range of leadership roles that include working with senior clinical development staff, establishing credibility with external collaborators such as opinion leaders and regulators, and demonstrating substantial experience in drug development (including experience with both IND and BLA/NDA submission).</p></li><li><p>Experience in leading study start-up, directing and guiding study team execution, data cleaning, medical review, database locks, handling health authority responses are also required.</p></li><li><p>A strong commitment to impacting patients through drug development and the ability to work well within a team setting are critical</p></li></ul><p>In order to be considered for this position, you must have an advanced degree in medicine (MD or equivalent), with a MD/PhD strongly preferred. Specialized fellowship training Hematology or Oncology is preferred. The incumbent will have a minimum of 6-8 years of industry experience in related therapeutic area clinical development. Cell therapy drug development experience is preferred. People management experience is a plus. This role requires a minimum of 4 days on-site weekly in Tarrytown, NY or Warren, NJ.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$390,000.00 - $527,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Director Medical Communications - Switzerland]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47245]]></requisitionid>
    <referencenumber><![CDATA[R47245]]></referencenumber>
    <apijobid><![CDATA[r47245]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47245/assoc-director-medical-communications-switzerland/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Basel]]></city>
    <state><![CDATA[Basel-City]]></state>
    <country><![CDATA[Switzerland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p><p>We are looking for an <strong>Associate Director, Medical Communications</strong> to bring high-quality medical information and scientific communications to healthcare professionals, patients, and internal partners across Switzerland & the Nordic hub. </p><p>In this role, you’ll shape and maintain audience-appropriate medical response documents and scientific Q&As, provide medical/scientific review of materials, and deliver communication strategies aligned with global medical direction. If you enjoy connecting science to real-world decisions—while keeping quality, compliance, and clarity at the center—this is a meaningful place to grow your impact. </p><p><strong>Associate Director, Medical Communications - Basel, Switzerland </strong></p><p><strong>A Typical Day may include:</strong> </p><ul><li>Developing and updating standard medical response documents / Q&As and custom response documents </li></ul><ul><li>Guiding MedicaI Information call center colleagues on inquiries and response quality </li></ul><ul><li>Reviewing promotional and medical materials for scientific accuracy and compliance </li></ul><ul><li>Preparing country-specific analytics from case trends and call volumes </li></ul><ul><li>Partnering with Medical Director, Field Medical, and Global Comms teams </li></ul><ul><li>Driving congress communication opportunities, scientific communications strategy at local level and contributing to the above countries strategy, supporting booth medical information </li></ul><ul><li>Keeping inspection-ready records to support audits and health authority reviews </li></ul><p><strong>This role may be for you if:</strong> </p><ul><li>You enjoy translating complex science for diverse audiences </li></ul><ul><li>You like owning content end-to-end, from creation through maintenance to delivery </li></ul><ul><li>You feel confident advising others on medical information inquiry management </li></ul><ul><li>You are comfortable balancing several communication assets and priorities at once </li></ul><ul><li>You value strong governance, quality processes, audit readiness, and documentation </li></ul><ul><li>You enjoy spotting scientific communication opportunities, including at congresses </li></ul><ul><li>You are agile, collaborative and love to connect with colleagues at the local, regional and global level located in different time zones </li></ul><p><strong>To be considered</strong> </p><p>A <strong>PhD, MD, or PharmD</strong> is required, along with <strong>5+ years of Medical Communications experience</strong> including <strong>at least 3 years in Medical Information</strong>, and <strong>5+ years</strong> in biotech/pharma (Medical Affairs, Clinical R&D, or related fields). You’ll also need an <strong>advanced understanding of Switzerland’s healthcare regulatory environment</strong> relevant to medical practice and the pharmaceutical industry, plus strong knowledge of <strong>European medical information/scientific communications requirements</strong> (with a focus on <strong>Swissmedic</strong> and Nordic countries). Preferred qualifications include proficiency in <strong>English</strong> and at least one of <strong>German, French, or Italian</strong>, as well as depth in medical communication strategy, congress strategy, scientific content development, and medical education. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Accountant, Corporate Accounting]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47371]]></requisitionid>
    <referencenumber><![CDATA[R47371]]></referencenumber>
    <apijobid><![CDATA[r47371]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47371/staff-accountant-corporate-accounting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>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>This position will perform accounting duties primarily within the Product Revenue and SG&A expense areas. Responsibilities include timely completion of activities within the monthly and quarterly close process, such as recording journal entries and preparing revenue, expense, and balance sheet account analyses. This is a highly visible role that works closely with Accounting, Finance, Commercial, Trade, and other departments to gather information, prepare schedules, and ensure accurate accounting for assigned areas.</p><p><strong>A Typical Day in the Role Might Look Like</strong><strong>:</strong></p><p><strong> </strong></p><ul><li><p>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</p></li><li><p>Prepare SG&A expense schedules and balance sheet account reconciliations for assigned areas</p></li><li><p>Partner with Finance to ensure completeness and accuracy of accruals and reclasses</p></li><li><p>Ensure compliance with the Company’s Prepaid Expense Accounting Policy and other relevant accounting policies</p></li><li><p>Perform fluctuation analyses and prepare variance explanations for Management</p></li><li><p>Maintain knowledge of and compliance with Company accounting policies and internal controls</p></li><li><p>Support compliance with Sarbanes‑Oxley (SOX) requirements, including maintaining documentation and supporting control execution</p></li><li><p>Assist with internal and external audit requests, as needed</p></li><li><p>Support cross‑functional requests and initiatives related to areas of responsibility</p></li><li><p>Participate in the Oracle Fusion Cloud Financials ERP implementation, including user acceptance testing (UAT) and updates to process documentation and workpapers</p></li><li><p>Assist with special projects, analyses, and process improvement initiatives, as needed</p></li></ul><p><strong>This Role May Be for You If You:</strong></p><ul><li><p>Are a team player who collaborates effectively, thinks independently, and proactively proposes solutions with a continuous improvement mindset</p></li><li><p>Have a solid understanding of accounting principles and can apply them to real‑world operational processes</p></li><li><p>Are analytical and able to organize and interpret large data sets to support sound accounting conclusions</p></li><li><p>Have strong organizational skills and a high level of attention to detail and accuracy</p></li><li><p>Can operate in a fast‑paced environment and comfortably manage multiple priorities</p></li><li><p>Have strong written and verbal communication skills</p></li></ul><p>To be considered for this role, you must have a Bachelors degree in Accounting or Finance and 2+ years of relevant accounting experience. Prior product revenue (gross to net) accounting experience preferred. Big 4 Accounting experience and CPA or CPA track are preferred. High proficiency with Microsoft applications is required, specifically Microsoft Excel. Experience with Oracle GL, SmartView, and Hubble are a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$71,800.00 - $116,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Tuscon, AZ]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47207]]></requisitionid>
    <referencenumber><![CDATA[R47207]]></referencenumber>
    <apijobid><![CDATA[r47207]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47207/medical-specialist-i-allergyent-tuscon-az/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tucson]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Tucson (Allergy/ENT)</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>A typical day might include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings, and medical conferences.</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 09:26:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director External Manufacturing Planning]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46664]]></requisitionid>
    <referencenumber><![CDATA[R46664]]></referencenumber>
    <apijobid><![CDATA[r46664]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46664/director-external-manufacturing-planning/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Director of External Manufacturing (EM) Planning. The Director of External Manufacturing Planning is accountable for global clinical and commercial manufacturing planning and scheduling, logistics coordination, and EM systems (i.e., ERP). This is a global leadership role with teams located in US and EU with the primary focus of delivering clinical and commercial medicines to all patients on-time and in-full. The Associate Director builds and develops a global team of production schedulers that collaborates with CMOs as well as internal manufacturing operations, owns S&OP processes with strategic manufacturing partners and ensures manufacturing readiness milestones.</p><p>A typical day in this role may include the following:</p><ul><li><p>Accountable for the global External Manufacturing production planning and scheduling through external and internal manufacturing network.</p></li><li><p>Establishes and maintains a strategic plan for the External Manufacturing department in support of activity requested by the business, including supporting a business continuity plan to ensure continued external production during disruptive local or worldwide events.</p></li><li><p>Develops and implements systems and reports that track and measure production readiness and supply metrics, component and WIP inventories meet defined safety stock targets, track the progression of every externally manufactured lot through release and ensure global capacity meets production requirements in the short and long terms for both clinical and commercial medicines.</p></li><li><p>Leads the Logistics area to ensure material is shipped in a timely manner to meet finished goods delivery dates and/or downstream activities.</p></li><li><p>Supports and collaborates with the External Manufacturing Project Management and Quality Assurance organizations to ensure accurate scheduling of manufacturing activities in support of technical transfers, process validations and CapEx project executions within the global External Manufacturing network.</p></li><li><p>Travel up to 25% (domestic and international), as required.</p></li></ul><p>This role might be a fit for you if:</p><ul><li><p> Demonstrated leader with expert knowledge of GMP production planning and scheduling processes for parenteral manufacturing, device assembly and finished label and package. </p></li><li><p>Deep knowledge ERP systems (Oracle preferred).</p></li><li><p>Knowledge of the challenges and lead times involved when transferring aseptic parenteral filling, device assembly and finish label & pack operations.</p></li><li><p>Working knowledge of industry practices and regulations (e.g. GxP, ISO, ICH, etc.) across multiple health authorities (e.g. FDA, IMB, etc.).</p></li><li><p>APICS, ISM, ASQ or SME professional certification preferred.</p></li><li><p>Competencies in German, French and/or Spanish (oral and written) preferred. <br> </p></li></ul><p>To be considered for the role you must have a BS/BA in a scientific discipline and 10 years of related experience in a biopharmaceutical cGMP environment, including 5 years management and/or leadership experience, or equivalent combination of education and experience. A MSc/MBA is a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$172,200.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Manager, Medical Device Quality Assurance]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47283]]></requisitionid>
    <referencenumber><![CDATA[R47283]]></referencenumber>
    <apijobid><![CDATA[r47283]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47283/sr-manager-medical-device-quality-assurance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Build our future together:</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 engineer and quality specialists.</p><p>When & where:</p><ul><li>Monday-Friday, 8am-4:30pm</li><li>Location: East Greenbush, New York, United States</li></ul><p>What you'll do:</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>This role requires:</p><ul><li>B.S 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><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Part_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Great Lakes]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47579]]></requisitionid>
    <referencenumber><![CDATA[R47579]]></referencenumber>
    <apijobid><![CDATA[r47579]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47579/regional-director-neurology-great-lakes/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Michigan]]></city>
    <state><![CDATA[Michigan]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Great Lakes Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Great Lakes (Michigan, Indiana, Illinois and Wisconsin)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Commercial Insights & Analytics - Neurology]]></title>
    <date><![CDATA[Tue, 12 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46486]]></requisitionid>
    <referencenumber><![CDATA[R46486]]></referencenumber>
    <apijobid><![CDATA[r46486]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46486/executive-director-commercial-insights-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>Regeneron is seeking an Executive Director, Commercial Insights and Analytics (I&A), Neurology to join our organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Executive Director, Commercial Insights and Analytics (I&A), Neurology, 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 Neurology Commercial Business Unit (CBU) to drive deeper insights that inform business decisions. </p><p><strong>This role might be for you if can: ​</strong></p><p><em>Lead</em></p><p>1) Lead and mentor the CSI&A Neurology 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 Neurology 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 for business decision-making</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 upcoming launch plans; and <strong>b)</strong> enhance brand differentiation and impact at launch and beyond</p><p><em>Partnership and collaboration</em></p><p>8) Collaborate with the Neurology CBU and other members of senior leadership to contribute to Commercialization roadmap, 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 Neurology 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 Neurology 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 Neurology CBU and with CSI&A leadership</p><p>14) Manage third-party vendor relationships</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>20+ years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with launch 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, preferably across both buy-and-bill and Rx environments</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution with hands on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li></ul><p>Preferred skills:</p><ul><li><p>Master’s (MBA, MPH, MS) preferred</p></li><li><p>Neurology disease category experience is desired</p></li><li><p>Experience with forecasting, especially the use of launch analogs</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>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Scientist, Biologics Characterization]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45916]]></requisitionid>
    <referencenumber><![CDATA[R45916]]></referencenumber>
    <apijobid><![CDATA[r45916]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45916/sr-scientist-biologics-characterization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><br>Regeneron’s Product Biochemistry in Tarrytown, NY is seeking a motivated and innovative Senior Scientist to drive late-stage development (Phase II through commercialization) of biologics. You will develop and deploy analytical methods and purification strategies, enrich and characterize product variants, and help onboard new technologies that deepen product understanding and improve processes across the pipeline. This role is for you if you are scientifically creative, hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment.<br><br> </p><h3>Key Responsibilities:</h3><ul><li>Develop analytical methods and purification protocols to support extended characterization of therapeutic proteins and gene therapy vectors.</li><li>Conduct biochemical/biophysical characterization to support development, regulatory submissions, and commercialization.</li><li>Apply DOE, advanced statistics, and risk assessments to evaluate and optimize methods and processes.</li><li>Author high-quality technical documents (protocols, reports, memos) and contribute to regulatory sections and publications. Ensure timely documentation of experiments following established SOPs and guidelines.</li><li>Maintain instruments, troubleshoot issues, and improve lab/data workflows within your area of expertise. Adhere to procedures, guidance, and best practices to ensure lab safety.</li></ul><ul><li>Proactively identify process improvement opportunities across Product Biochemistry and Regeneron and help drive implementation.</li></ul><br><h3>A Typical Day in the Role Might Look Like:</h3><ul><li>Design and execute experiments to enrich, purify, and characterize size/charge variants, complexes, and high-concentration formulations.</li><li>Integrate learnings from internal data and external literature to make science-based study design recommendations.</li><li>Documents experiments, results and findings in electronic laboratory notebook; presents work at group and department meetings; contributes to drafting of protocols, method development reports, regulatory submission sections, and peer-reviewed articles for publication.</li><li>Lead or participate in technology initiatives and continuous improvement projects; may also mentor and guide junior analysts in a matrix-based environment.</li><li>Maintain instruments, troubleshoot instrumental/experimental problems, and order/maintain supplies.</li></ul><h3>This Role Might Be For You If:</h3><ul><li>Possess strong lab skills in protein separation, purification, and tangential flow filtration (TFF). Possess skills in protein/product identification using mass spectrometry.</li><li>Thrive in a fast-paced, team environment and can also work independently across multiple projects.</li><li>Demonstrate initiative, calculated risk-taking, and a passion for innovation and continuous improvement.</li><li>Communicate clearly, manage projects effectively, and solve complex problems with data-driven rigor.</li><li>Mentor others and contribute to a safe, efficient, and inclusive lab environment.</li></ul><p>This role requires a BS/MS/Ph.D. in Biochemistry/Biophysics, or related field plus 8-10 yrs+ (BS/MS) or 0-2 yrs+ of proven experience (Ph.D.). Technical proficiency in automated FPLC and/or HPLC (SEC, IEX, affinity), electrophoresis (capillary or microchip, SDS-PAGE, western blots), spectroscopy and light scattering is recommended. A fundamental understanding of protein structure/function, mass spectrometry, and immunology/immunogenicity preferred. Preference will be given to candidates who have experience working in the biopharmaceutical industry. Excellent oral and written communication skills and evidence of teamwork are required. This role is fully onsite.</p><p>The ideal candidate must have strong initiative to complete tasks, learn new technologies, and demonstrate a commitment to continuous learning. This role requires the ability to manage multiple priorities in a fast‑moving R&D environment, operate effectively both independently and within a collaborative team environment, and communicate clearly, transparently, and in a timely manner with key stakeholders.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, CMC Regulatory Affairs (Hematology/Oncology)]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45185]]></requisitionid>
    <referencenumber><![CDATA[R45185]]></referencenumber>
    <apijobid><![CDATA[r45185]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45185/associate-director-cmc-regulatory-affairs-hematologyoncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.</p><p>For US locations, this role is on-site 4 days in the office and 1 day from home. For Uxbridge, UK or Dublin, Ireland this role would be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position . If eligible, we can offer relocation benefits.</p><p><strong>A typical day may include the following: </strong><br>• Lead product development activities from a CMC regulatory standpoint with input from senior management.<br>• Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post-approval activities.<br>• Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work-arounds, and obtain consensus. <br>• Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.<br>• Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).<br>• Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country-specific regulatory guidance documents; <br>• Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.<br>• Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.<br>• Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.<br>• Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.<br>• Find opportunities to initiate operational changes and policy modifications.<br>• Manage and coach team member(s). </p><p><strong>This may be for you if you: </strong><br>• Have a strong grasp of CMC worldwide regulations and guidelines.<br>• Have been successful in building collaboration and teamwork across cross-functional teams.<br>• Can demonstrate a proven track record managing and mentoring people.<br>• Demonstrated skill in managing multiple priorities.</p><p><br>To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred. Proven track record supporting biological products through development and approval is a distinct advantage. It is required to have a good understanding of current CMC worldwide regulations and guidelines. Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff Quality Control Lab Operations Specialist]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46643]]></requisitionid>
    <referencenumber><![CDATA[R46643]]></referencenumber>
    <apijobid><![CDATA[r46643]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46643/staff-quality-control-lab-operations-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>Quality Control External Testing is currently looking to fill a Staff QC Lab Operations Specialist position with a 1st shift, Monday-Friday, 8:00am – 4:30pm schedule. This position performs data review of analytical test results to support QC External Testing operations. In this role, a typical day might include the following:</p><ul><li><p>Provide oversight, lead, and manage the data review function within QC External Testing, establishing priorities and workflow processes to maximize efficiency and quality outcomes.</p></li><li><p>Conduct comprehensive data review for Release, In-Process, and Stability testing in Advanced Therapies, ensuring adherence to quality standards.</p></li><li><p>Perform thorough evaluation of analytical test method Qualification, Verification, Transfer, and Validation documentation.</p></li><li><p>Ensure all data complies with cGMP, GDP, FDA, EMA, and ICH Guidelines through meticulous review processes.</p></li><li><p>Verify analytical data meets ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, plus Complete, Consistent, Enduring, and Available).</p></li><li><p>Monitor testing compliance with established laboratory procedures, test methods, and approved protocols.</p></li><li><p>Collaborate with laboratory personnel to address documentation errors and omissions while fostering a cGMP-oriented culture.</p></li><li><p>Demonstrate exceptional attention to detail, focus, and multitasking capabilities when reviewing complex analytical laboratory data.</p></li><li><p>Apply strong technical expertise in various analytical methodologies including liquid chromatography, pH measurement, iCIEF, ELISA, SEC, and CE-SDS.</p></li><li><p>Engage with team members to implement continuous improvements to data review processes and methodologies.</p></li><li><p>Provide strategic guidance to QC analysts for enhancing Good Documentation Practices within cGMP frameworks and applicable SOPs.</p></li><li><p>Complete assigned tasks within established timeframes while managing organizational responsibilities including tracking open tasks and timelines.</p></li><li><p>Support the development and review of QA events, deviations, and investigations as required.</p></li><li><p>Maintain effective communication with QC Analysts, Group Leaders, and departmental managers to ensure seamless operations and quality compliance.</p></li></ul><p>This role might be for you if:</p><ul><li><p>You have management / supervisory experience.</p></li><li><p>You can effectively communicate issues and ideas with direct reports, peers, and with management</p></li><li><p>You have a strong ability to achieve thoroughness and accuracy when performing tasks</p></li><li><p>You have strong prioritization / organizational skills and are detailed-oriented.</p></li><li><p>You have the capability to adjust to shifting priorities, manage multiple tasks and meet deadlines</p></li><li><p>You have excellent written and oral communication skills</p></li><li><p>You have experience in a GMP setting</p></li></ul><p>To be considered for this role, you must have a BS/BA in a scientific field or equivalent combination of education and experience.</p><ul><li><p>Staff Specialist: Requires a BS/BA in a scientific field and 10 years of related experience or equivalent combination of education and experience.</p></li><li><p>Level is determined based on qualifications relevant to the role.</p></li></ul><p>Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for employees at all levels!</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager - Dermatology - Cleveland/Akron, OH]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47585]]></requisitionid>
    <referencenumber><![CDATA[R47585]]></referencenumber>
    <apijobid><![CDATA[r47585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47585/field-reimbursement-manager-dermatology-clevelandakron-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cleveland]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<h3><strong>Field Reimbursement Manager - Dermatology (Cleveland/Akron OH) </strong></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><p><strong>A typical day may include the following:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</p></li><li><p>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</p></li><li><p>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</p></li><li><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p></li><li><p>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</p></li><li><p>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</p></li><li><p>You are an ethical, standout colleague and have can grow in a cross-functional team environment - contributing creative ideas and positive energy to the group.</p></li><li><p>You possess excellent organizational, project management, and communication skills.</p></li><li><p>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><li><p>Established ability to work within an Account Management based structure.</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience. Experience working with products delivered through a Specialty Pharmacy network is essential. Collaboration and proactive communication skills required. Background in leadership and effective cross functional partnership a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Immuno Assay]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46562]]></requisitionid>
    <referencenumber><![CDATA[R46562]]></referencenumber>
    <apijobid><![CDATA[r46562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46562/senior-associate-scientist-immuno-assay/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Assay Development Group (ADG), located in Tarrytown, NY, is seeking a highly motivated <strong>Senior Associate Scientist</strong> to join the team. The ADG in Bioanalytical sciences develops preclinical and clinical assays to support program pipeline. In this role, you will support ongoing work, sample preparation, assay runs, data processing ensuring compliance with current GxP guidance documentation.</p><p><strong>A Typical Day in This Role Looks Like:</strong></p><p>· Designs and executes immunoassays (e.g., ELISA) with minimal supervision, based on protocols provided by literature, seminars and other scientists. Troubleshoots assay-related problems with minimal guidance of his/her supervisor and performs follow-up experiments. Suggests modifications to protocols or alternative protocols.</p><p>· Develops immunoassay methods and writes assay validation protocols for review with minimal supervision by supervisor and/or Study Director.</p><p>· Routinely multi-tasks and can work on multiple projects simultaneously.</p><p>· Summarizes and presents results to supervisor in a logical manner, verbally and in written reports or presentations.</p><p>· Expertly performs validation experiments, summarizes results in a tabular manner. Writes/reviews validation reports and procedure documents for review by the Study Director.</p><p>· Communicates effectively with supervisor and other members of the Assay Development Group.</p><p><strong>This Role May Be for You If You Have Experience:</strong></p><p>· Overseeing the preparation of reagents and buffers for use within the Assay Development Group and may coordinate the re-ordering of laboratory supplies and reagents when needed.</p><p>· Effectively operating a range of laboratory instrumentation and may oversee instrument verifications and/or maintenance, if required.</p><p>· Evaluating new technologies for the development of immunoassays using new formats or techniques.</p><p>· Maintaining GLP compliance for all laboratory work and documentation related to assay validations in accordance with FDA regulations and company SOPs. Assists in maintaining GLP compliance in the laboratory.</p><p>· Maintaining cleanliness of individual and communal work areas.</p><p>· Learning and complingwith safety requirements of his/her laboratory. Recognizes potential safety problems and takes action to correct them.</p><p><strong>To be considered for this role,</strong> <strong>you must have</strong> a Bachelor's degree (Master's preferred) in Biology or a related field with 3-6+ years of proven experience. Hands-on knowledge in immunoassays using a variety of detection systems and a proven understanding of additional methodologies to measure proteins and immunogenicity is needed. Prior experience in bioanalytical assay development is highly desirable.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Thought Leader Liaison (Neuro)]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47711]]></requisitionid>
    <referencenumber><![CDATA[R47711]]></referencenumber>
    <apijobid><![CDATA[r47711]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47711/director-thought-leader-liaison-neuro/]]></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 Director, Thought Leader Liaison Lead for Rare Neurology is a non-sales position for someone passionate about leading a team of Thought Leader Liaisons (TLLs) across the nation. The Director will work closely with U.S Thought Leaders in Rare Neurology. We are seeking an individual who will be a key member of the Rare Neurology marketing leadership team and will collaborate with cross-functional teams to ensure alignment with the overall brand strategy and tactical execution. The TLL Director will report to the Executive Director of Rare Neurology Marketing.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Guide and define the culture, structure, and strategic direction of Regeneron’s Rare Neurology TLL Team</p></li><li><p>Build a high performing team, capable of generating quality insights with Thought Leaders</p></li><li><p>Create a compliant environment which challenges, motivates and develops team members to reach optimum performance and potential</p></li><li><p>Set clear objectives, coach/ mentor, and assess performance and skill-level to develop future leaders within Regeneron</p></li><li><p>Provide strategic customer insights to the Marketing Leadership team to assist in the further development of the Rare Neurology brand strategy</p></li><li><p>Work collaboratively with multiple matrix partners in developing and refining business plans to achieve brand objectives</p></li><li><p>Manage budget and TLL operations to ensure the TLL team is appropriately resourced</p></li><li><p>Champion and lead the TLL team in a compliant manner</p></li><li><p>Build and cultivate collaboration within alliance</p></li></ul><p><strong>This role may be for you, if you can:</strong></p><ul><li><p>Lead from the front, demonstrating visible, engaged leadership that sets the standard for performance, professionalism, and expected behaviors</p></li><li><p>Operate as a key member of the marketing leadership team, contributing strategic perspective and driving alignment across brand, field, and cross‑functional partners</p></li><li><p>Develop and inspire talent, actively coaching the team and building a strong pipeline of future leaders</p></li><li><p>Foster strong collaboration and trust, creating an inclusive, high‑performing culture aligned with company values</p></li><li><p>Drive innovation and continuous improvement, elevating the impact of field marketing insights, execution, and customer engagement</p></li><li><p>Adapt and evolve with the business, proactively recalibrating the scope, focus, and capabilities of the TLL team in response to brand needs</p></li></ul><p>To be considered, you must have a Bachelor's degree, Master’s degree or other advanced education/certification a plus. We also seek Specialty pharmaceutical/ biopharmaceutical experience with a minimum of 12 years of work experience in one or more of the following: field sales, product marketing, or medical/ clinical experience including people management experience in Rare Neurology or a similar biologic/specialty/REMS market. Lastly we expect you to have the ability to travel to congresses, meetings, programs, etc. (50-80% travel).</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Immunology & Inflammation]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47486]]></requisitionid>
    <referencenumber><![CDATA[R47486]]></referencenumber>
    <apijobid><![CDATA[r47486]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47486/associate-scientist-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Immunology and Inflammation group is seeking an Associate Scientist to support the development of therapeutics for autoimmune disease. This role involves joining a highly collaborative team working in autoimmunity, immune cell biology, and tissue immunity. You will have the opportunity to engage in cutting edge immunological research as part of our discovery efforts and to contribute to human health. </p><p><strong>As an Associate cientist in the Immunology and Inflammation group, your typical day might include: </strong></p><ul><li><p>Handling and caring for mice, including performing procedures such as blood and/or tissue sample collection or injections (IP, IV and subcutaneous) </p></li><li><p>Processing of organs for immune cell isolation and analysis </p></li><li><p>Maintaining, expanding, and/or modulating cells in vitro </p></li><li><p>Evaluating cell phenotypes and function using ex vivo or in vitro assays such as flow cytometry and immunoassays. </p></li><li><p>Analysis of data using biological and statistical software such as Flowjo, OMIQ, Excel, Prism </p></li><li><p>Close collaborative interactions with teams across the organization </p></li><li><p>Documentation of experimental procedures and results </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>re 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 0-2 years of experience in immunology or a related discipline. </p></li><li><p>Experience in tissue culture, cell-based assays, flow cytometry, or immunoassays (e.g. ELISA, MSD, Luminex), as well as proficiency in basic computer applications and experience with biological data collection and analysis highly preferred </p></li><li><p>Experience in mouse handling is highly preferred. </p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs - Hematology - Ontario]]></title>
    <date><![CDATA[Thu, 13 Nov 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42140]]></requisitionid>
    <referencenumber><![CDATA[R42140]]></referencenumber>
    <apijobid><![CDATA[r42140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42140/senior-manager-field-medical-affairs-hematology-ontario/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p></div><div><p>We are seeking a <strong>Senior Manager, Field Medical Affairs – Hematology</strong> to join our team and strengthen our partnerships with experts in hematologic malignancies. In this role, you will engage with key opinion leaders, healthcare providers, and investigators, serving as a trusted scientific resource and strategic partner. You’ll play a meaningful role in the understanding of Regeneron’s therapies, supporting clinical development and investigator-initiated research, and contributing to impactful new therapies. </p></div><div><p>We are looking for our next team member to join our passionate & dedicated Medical Affairs team in Canada. This is a remote, field-based role located in the Greater Toronto Area, Ontario, Canada.</p></div><div><p><strong>Senior Manager, Field Medical Affairs, Hematology</strong></p><p><strong>Greater Toronto Area, Ontario, Canada</strong></p></div><div><p><strong>A Typical Day:</strong> </p></div><div><ul><li><p>Building and maintaining relationships with KOLs in malignant hematology. </p></li></ul></div><div><ul><li><p>Acting as a primary clinical/scientific contact for HCPs and investigators. </p></li></ul></div><div><ul><li><p>Generating medical insights to advise strategy and development plans. </p></li></ul></div><div><ul><li><p>Supporting clinical trial execution by identifying investigators and trial sites. </p></li></ul></div><div><ul><li><p>Collaborating on abstracts, posters, and manuscripts to communicate data. </p></li></ul></div><div><ul><li><p>Contributing to investigator-initiated study programs and research collaborations. </p></li></ul></div><div><ul><li><p>Attending medical congresses to support scientific exchange. </p></li></ul></div><div><ul><li><p>Partnering cross-functionally with Medical Affairs, Commercial, and Market Access. </p></li></ul></div><div><p><strong>This Role May Be For You:</strong> </p></div><div><ul><li><p>You thrive on scientific exchange and are confident discussing complex data with KOLs. </p></li></ul></div><div><ul><li><p>You have established background in hematology and understand the oncology landscape. </p></li></ul></div><div><ul><li><p>You enjoy balancing independent field work with cross-functional collaboration. </p></li></ul></div><div><ul><li><p>You adapt easily to changing priorities and field-based challenges. </p></li></ul></div><div><ul><li><p>You are motivated by opportunities to contribute to country readiness and new research. </p></li></ul></div></div><div><div><ul><li><p>You value compliance and integrity while working with investigators and partners. </p></li></ul></div><div><ul><li><p>You are comfortable with frequent travel and engaging in high-level conversations. </p></li></ul></div><div></div><div></div><div><p>To be considered, you should bring at least 5 years of field medical or medical manager experience in biotech or pharma, with a strong background in hematology. Knowledge of malignant hematology is required, and experience in lymphoma or multiple myeloma is preferred. Country readiness experience and established KOL relationships are highly valued. You should also have solid knowledge of treatment guidelines, clinical research, and Canadian regulations. Strong communication, organizational skills, and the ability to travel up to 70% are essential. </p></div></div><ul></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Sciences, Hematology]]></title>
    <date><![CDATA[Wed, 29 Oct 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43418]]></requisitionid>
    <referencenumber><![CDATA[R43418]]></referencenumber>
    <apijobid><![CDATA[r43418]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43418/medical-director-clinical-sciences-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Sciences functions as clinical leader of a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase), under leadership of Program Lead Medical Director (Program Lead MD) or Sr. Medical Director.</p><p>A day in the life may include the following responsibilities:</p><ul><li><p>Provides clinical leadership and responsible for all clinical deliverables within the assigned section of a clinical program with minimal supervision from Program Lead MD. </p></li><li><p>Manages all operational aspects and drives execution of the section of the clinical program in partnership with global line functions, assigned Clinical Scientist and Clinical Operations associates.</p></li><li><p>Supports Program Lead MD (and/or Sr. MD) and frequently lead interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Medical Affairs, Marketing, HE&OR), and internal decision boards.</p></li><li><p>Serves occasionally as member for Global Clinical Development training programs, author or reviewer for clinical SOPs and may contribute to GCD strategy by serving on taskforces or other panels.</p></li></ul><p>This job may be for you if:</p><p>· You are passionate about impacting entire populations of patients</p><p>· You want to develop innovative new therapies</p><p>· You enjoy collaborating with team members towards a common goal.</p><p>In order to be considered for this position, you must have an MD or equivalent, ideally with Hematology Oncology fellowship training. More than 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV is strongly preferred. Medical/scientific expertise in disease area of assigned program is preferable. </p><p>#MDJOBS #heme</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Patent Attorney]]></title>
    <date><![CDATA[Tue, 20 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44376]]></requisitionid>
    <referencenumber><![CDATA[R44376]]></referencenumber>
    <apijobid><![CDATA[r44376]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44376/director-patent-attorney/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Patent Attorney will act as legal counsel on matters related to the development, protection, and management of Regeneron’s valuable intellectual property pertaining to its manufacturing. The role will be responsible for patent activities relating to manufacturing and bioprocessing at all stages of the development pipeline including cell line technologies, purification, formulations, assay and media development. This position will partner closely with our world-class scientists and manufacturing development leaders around key strategies for our rapidly growing patent portfolio, patent filings, trade secret protection, and patent actions.<br><br><strong>As a Director Patent Attorney, a typical day may include:</strong></p><ul><li><p>Identifying, capturing and prosecuting new inventions relating to manufacturing and bioprocessing; Preparing and prosecuting global patent applications relating to all aspects of manufacturing & bioprocessing including cell development, cell culture, purification, assay development, formulation, packaging and delivery; Leading outside counsel on various projects as appropriate;</p></li><li><p>Conducting patent landscape overviews, freedom-to-operate analyses, validity assessments and patentability assessments in relation to Regeneron pipeline products, and presenting the results and analyses to senior members of the Law Department and senior management;</p></li><li><p>Leading US and foreign administrative patent actions (e.g., oppositions, third party observations, inter partes reviews, etc.);</p></li><li><p>Assisting in litigation activities as needed</p></li><li><p>Supporting due diligence projects, agreements and other transactional work, administrative initiatives, and policy questions.</p></li></ul><p><strong>This role might be for you if you have experience:</strong></p><ul><li><p>Advising on emerging legal issues, including monitoring and reviewing case law and legislative developments.</p></li><li><p>Possess strong interpersonal skills and the ability run multiple projects against competing priorities.</p></li><li><p>Excel at handling a large and sophisticated docket with minimal direction.</p></li><li><p>Have exceptional communication skills, including presentation, interpersonal, writing and conflict resolution.</p></li></ul><p><strong>To be considered for this position, you must possess</strong> a Ph.D. in the life sciences (e.g., biochemistry, molecular biology, cell biology, or related fields) is required with a Juris Doctorate from an accredited law school. Admitted to practice before the USPTO and licensed to practice law in at least one state (member of the NY bar or eligible for in-house licensure in NY); 5- 10 years of proven experience in a law firm setting (with or without corporate law department experience) preparing and prosecuting patent applications in the biological arts.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 21 Jan 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Marketing, Neurology Customer Experience]]></title>
    <date><![CDATA[Mon, 02 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44931]]></requisitionid>
    <referencenumber><![CDATA[R44931]]></referencenumber>
    <apijobid><![CDATA[r44931]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44931/senior-director-marketing-neurology-customer-experience/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Director Marketing, Neurology Customer Experience, will contribute to the success of our emerging Neurology Business Unit and will report to the Executive Director, Marketing. This person will implement the approved Brand plan, and have primary responsibility to lead the development and implementation of the strategic and tactical plans/programs as it relates to our customer experience across the omnichannel environment for both HCP and consumer for our upcoming launch in Myasthenia Gravis.</p><p>This important role is responsible for leading the creation of an omnichannel strategy and execution across both HCP and consumer audiences. This includes the development and implementation of content strategy across customer groups: Physician / physician groups, Patients / caregivers. Develop deep insights through an understanding of customer preferences to shape our content strategy and direct team to implement across customers. Lead a team to deliver HCP and patient content with a passion for curated customized content across the customer journey.</p><p><strong>In this position a typical day may include the following:</strong></p><ul><li>For HCPs, the focus will be content production delivered through all digital channels for non-personal from home office initiatives as well as Next Best Action through Veeva CRM for field communication to their customers.</li><li>For patients the focus will be to activate the patients demonstrating the broad awareness while continuing to drive/maintain brand awareness. This includes advertising across all relevant media channels. Significantly increase our digital content offerings as well as enhancing our CRM program to include: lead generation and adherence.</li><li>Ensuring that marketing processes and programs align with corporate guidance, as well as regulatory, legal, and ethical guidelines.</li><li>Leading and providing development opportunities for direct reports.</li><li>This person will work closely with many cross functional teams including across the entire brand team, Market Access team, Insights and Analytics, Commercial IT</li><li>Monitoring spending against budget and managing projects to agreed-upon timelines, budgets, and scope.</li></ul><p><strong>This May Be the Right Role for You If you:</strong></p><ul><li>You have experience with a digital asset management system and Sales Force Cloud</li><li>You have expertise in behavioral science would be a plus.</li><li>You can demonstrate leadership qualities and have experience managing teams.</li><li>You are a strong communicator and can present well, capable of articulating complex strategies to partners of all levels, including Senior Leaders, regardless of their technical background.</li><li>You can complete and manage multiple projects in a fast-paced environment where quick decision making and clear direction is a must.</li><li>You bring organizational agility and the capability to reprioritize based on external or internal changes.</li><li>You can work effectively and efficiently with team members, across departments, and managing agencies.</li></ul><p>To be considered for this role,<strong> </strong>you must have a Bachelor's Degree, MBA preferred. The ideal candidate must have a minimum 15 years of progressive experience in biologics marketing and omnichannel strategy development and execution in the life sciences. Neurology experience is preferred and Myasthenia Gravis or Neurology Rare Disease experience a plus. Lastly, you will need to be onsite in Sleepy Hollow, NY 4 days a week.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Feb 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Epidemiology-Health Economics & Outcomes Research]]></title>
    <date><![CDATA[Mon, 02 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44671]]></requisitionid>
    <referencenumber><![CDATA[R44671]]></referencenumber>
    <apijobid><![CDATA[r44671]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44671/director-epidemiology-health-economics-outcomes-research/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Director, Epidemiology (HEOR) you will develop and drive real world evidence (RWE) that influences the development and commercialization of our innovative therapies. You will lead high impact epidemiologic research, apply innovative methods, and work with rich real world data sources answering complex questions for patients, clinicians, regulators, and payers.</p><p>This position is located at our Sleepy Hollow, NY offices and will require you to be on-site 4 days week. If eligible, we can offer relocation benefits. We cannot offer a fully remote option. </p><p><strong>A typical day may include the following: </strong><br>• Generate high quality observational research using RWD to support development and commercial strategies.<br>• Apply epidemiologic expertise to clinical development and trial design discussions, including opportunities for external control arms or hybrid evidence approaches.<br>• Support global HTA, payer, and regulatory submissions by generating epidemiology and RWE inputs for reimbursement packages and regulatory and value dossiers.<br>• Synthesize and critically evaluate scientific evidence to generate epidemiologic evidence for regulatory and payer submissions, press releases, and internal needs.<br>• Evaluate and implement emerging design and analytic methods enhancing our RWE capabilities.<br>• Stay current with evolving regulatory and payer expectations for RWE, guiding internal teams on implications for evidence strategy and generation.<br>• Represent the organization in external scientific, industry, and other forums, including peer reviewed publications and conference presentations to strengthen external visibility.</p><p><strong>This may be for you if you:</strong> <br>• You thrive in a team first environment and want to see your work inform decision making at scale.<br>• Have an innovation approach and enjoy developing solutions to complex problems<br>• Are at ease with an abundance of detail and complexity, yet mindful of the big picture.<br>• Can operate successfully in a ‘rapid response” environment<br>• Exceptional communication abilities that allow you to translate complex designs and findings into clear, actionable insights for a wide range of audiences.</p><p>To be considered it is required to have a PhD in Epidemiology or a related subject area supported by 7+ years of experience across academia, pharma/biotech, or consulting. Hands on leadership in developing study protocols and statistical analysis plans using real world data sources with a record of peer-reviewed publications is required. Expertise in advanced analytical methods for large healthcare datasets to apply or expand skills in machine learning. Familiarity with global HTA and payer evidence is advantageous.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 02 Feb 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director,  Program Operations Leader - Ophthalmology/Renal]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45092]]></requisitionid>
    <referencenumber><![CDATA[R45092]]></referencenumber>
    <apijobid><![CDATA[r45092]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45092/director-program-operations-leader-ophthalmologyrenal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>For US Locations, this position is on-site 4 days per week and 1 day from home. For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position. </em></p><p>The Program Operations Leader (POL) is responsible for leadership of and setting and implementation of the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional strategy of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence.</p><p>In a typical day, you will:</p><ul><li>Be responsible for the overall success of the clinical study team(s) within a program(s)</li><li>Maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested</li><li>Provide operational insight into feasibility, timeline and cost estimates during clinical program/study development</li><li>Oversee clinical study timelines within a clinical program(s)</li><li>Provide input and operational insight into Clinical Study Concepts (CSC)</li><li>Be responsible for development and implementation of operational strategy, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol </li><li>Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency within the program and development of best practices within CTM</li><li>Oversee clinical study budgets within a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate</li><li>Ensure timely delivery of quality operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams within the clinical program(s). </li><li>Drive decision making and integrates all operational considerations for studies within a clinical program(s) to ensure goals are attainable prior to implementation</li><li>Act as point of contact for clinical program and study level escalation</li><li>Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress</li><li>Provide proactive creation and implementation of risk mitigation strategies</li><li>Provide innovative and flexible operational solutions and options to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges</li><li>Drives the strategy and oversight for vendor selection and management within a clinical program(s)</li><li>Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts</li><li>May require up to 25% travel</li></ul><p>To be considered, you must possess a Bachelor's degree and a minimum of 12 years of related in-house sponsor-side pharmaceutical experience, with 8 years in clinical operations.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 09 Feb 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sample Management Associate]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44409]]></requisitionid>
    <referencenumber><![CDATA[R44409]]></referencenumber>
    <apijobid><![CDATA[r44409]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44409/sample-management-associate/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A Sample Management Associate supports biobanking operations efficiently and effectively while beginning to independently manage sample data processes. Possesses a thorough knowledge and understanding of clinical/non-clinical study protocols and associated documentation. Is fully capable of multi-tasking across assignments. Works with clients directly in a team environment. The incumbent may help in assessing and investigating new opportunities that will lead to increased efficiencies and improved productivity with regards to biobanking operations.</p><h3>As a Sample Management Associate, a typical day may include:</h3><ul><li><p>Trains on clinical/non-clinical study protocols and associated study documentation to build knowledge of study conduct as it pertains to biospecimen management. Executes study reference file creation by interpreting protocols and other applicable data inputs with guidance.</p></li><li><p>Performs the accessioning and receipt of non-clinical/clinical samples by assessing and verifying data, both manually and with automated platforms such as Microsoft VBA and Streamlit. May identify and communicate issues with automated platforms to drive resolution.</p></li><li><p>Has an in-depth knowledge of Microsoft Excel and can analyze discrepancies in sample metadata using complex formulas with limited guidance.</p></li><li><p>Executes necessary operations in applicable software systems (e.g., LIMS, ELN, etc.) to perform specimen and data management. Has the ability to identify and troubleshoot routine challenges.</p></li><li><p>Fulfills clinical/non-clinical sample requests to support bioanalysis deliverables as well as company-wide research initiatives.</p></li><li><p>Facilitates the completion and review sample transfer documentation, as applicable.</p></li><li><p>Responsible for assigning and coordinating sample management activities for assigned programs under limited guidance.</p></li><li><p>Under supervision, executes the reconciliation and data cleaning of biospecimens to drive deliverables forward.</p></li><li><p>May be responsible for the review of study documents to support study start up and protocol amendments.</p></li></ul><h3>This role may be for you if you:</h3><ul><li><p>Collaborates and maintains effective verbal and written communication with internal and/or external stakeholders to facilitate data discrepancy resolution. Communicates with CRO’s and third-party vendors to support biospecimen operations.</p></li><li><p>Is capable of identifying and troubleshooting problems pertaining to clinical/non-clinical protocols and associated documents as well as routine sample management processes and/or procedures.</p></li><li><p>Ensures a state of audit readiness. Assists in the preparation of supporting documents for Quality Audits, as applicable. May participate in study audit activities.</p></li><li><p>Handles high priority and high volume tasks within the appropriate timeframe while maintaining accuracy. Adapts to changing priorities. Is capable of multi-tasking across assignments.</p></li><li><p>Provides cross-functional support to other sample management teams, as needed.</p></li><li><p>May assist with the training of other laboratory staff.</p></li><li><p>Participates in sub-group meetings and may shares results or progress of work with others.</p></li><li><p>Ensures compliance and proper documentation in accordance with SOPs, and applicable regulations.</p></li><li><p>Communicates effectively with his/her manager and actively seeks out feedback to deepen self-development.</p></li><li><p>Responsible for his/her own safety in the laboratory, as well as for the safety of co-workers and visitors.</p></li></ul><h3>To be considered, you must have:</h3><p>Minimum of a Bachelors Degree + 2+ years experience</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Feb 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Change Communications]]></title>
    <date><![CDATA[Thu, 12 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45838]]></requisitionid>
    <referencenumber><![CDATA[R45838]]></referencenumber>
    <apijobid><![CDATA[r45838]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45838/manager-internal-change-communications/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an internal communications pro at the Manager level to help develop and drive communications targeting our 15,000+ colleagues globally. The successful candidate will join a dynamic and high-performing Internal Communications team that thinks strategically and executes at a high level to support our fast-growing company -- where colleagues are passionate about their work and our mission to bring important new medicines to patients in need. Internal Communications is part of the Corporate Affairs organization, which is focused on strengthening Regeneron’s reputation by developing strategies and programs that (1) distinguish our science, medicines and patient focus, (2) sustain culture and drive employee engagement, and (3) advance and differentiate our corporate responsibility commitments.</p><p><em><strong>This role will require 4 days per week onsite at our Global HQ Campus in Westchester, NY. This is not available as a fully remote / hybrid work.</strong></em></p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li><p>Support the development and execution of global communications programs that advance the goals of our key corporate functions (HR, IT, etc.) that are advancing critical innovation and digital transformation programs across the company.</p></li><li><p>Serve as trusted internal communications partner to leaders within G&A functions, advising on communications approaches that support enterprise priorities and initiatives.</p></li><li><p>Plan and coordinate key internal communications initiatives, demonstrating project management know-how and creative approaches that effectively inform, inspire and engage employees.</p></li><li><p>Draft compelling messaging – including project briefs, key messages, talking points, FAQ and other materials – that connect to company goals and priorities.</p></li><li><p>Develop informative and creative ways to communicate and engage employees about critical enterprise change initiatives, including digital transformation, global expansion, culture storytelling, and more.</p></li><li><p>Build strong relationships with colleagues at all levels of the organization to support collaboration.</p></li><li><p>Measure the effectiveness of communications and translate insights into actionable recommendations to improve reach, clarity and impact. </p></li><li><p>Identify and implement opportunities to elevate the strategic focus of communications, streamline processes, and improve overall efficiency and effectiveness.</p></li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li><p>Experienced in planning and executing communications initiatives, including storytelling and content management, that engage a busy, global employee base.</p></li><li><p>Knowledge and understanding of change communication principles that help employees navigate organizational change and connect to the opportunity that change presents.</p></li></ul><ul><li><p>Outstanding verbal and written communication skills, with the ability to translate complex topics into clear, accessible messaging tailored to diverse audiences.</p></li><li><p>Knowledge of and experience with channels, approaches and technologies that are used to communicate and connect with employees (intranets, enterprise social platforms, email distribution tools, etc.)</p></li><li><p>Ability to manage and prioritize multiple tasks and projects, adapt quickly to changing priorities and needs, and meet deadlines in a fast-paced environment.</p></li><li><p>Exceptional project management skills, strong attention to detail, sound judgment and curiosity to learn.</p></li></ul><p><strong>To be considered you must have a:</strong></p><ul><li><p>Bachelor's degree</p></li><li><p>Minimum 4+ relevant experience in internal communications and employee engagement.</p></li></ul><ul><li><p>Previous employment in a PR/Communications agency and/or the pharma/biotech industry preferred but not required.</p></li><li><p>Experience in a communications role supporting corporate or business functions, including HR, IT, etc.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Mar 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, External Clinical Data Management]]></title>
    <date><![CDATA[Tue, 17 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42183]]></requisitionid>
    <referencenumber><![CDATA[R42183]]></referencenumber>
    <apijobid><![CDATA[r42183]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42183/associate-director-external-clinical-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, External Data Services, plays a critical leadership role, overseeing team members to ensure all activities align with Regeneron’s procedures and industry best practices. This position collaborates closely with Clinical Data Management teams and External Data Vendors to deliver structured external data in compliance with Regeneron SOPs. The role also involves coaching, mentoring, and managing the performance of direct reports, while contributing to the department's strategic direction. Additionally, the AD works with senior leadership to define goals, staffing needs, and departmental structure.</p><p><strong>A typical day in the life as an Associate Director, External Data Services includes: </strong></p><ul><li><p>Shape and implement the strategy for External Data Services.</p></li><li><p>Lead and manage a team of External Data Services Managers and Specialists.</p></li><li><p>Oversee the development and maintenance of all DTS documents, ensuring alignment with Regeneron standards, processes, and timelines.</p></li><li><p>Drive the External Data Vendor Oversight model, establishing effective communication, partnership-level processes, and portfolio-level transparency on DTS status and escalations.</p></li><li><p>Represent External Data Services in leadership forums and technology discussions.</p></li><li><p>Contribute to and execute the External Data Services technology strategy.</p></li><li><p>Provide expert-level guidance to CROs, stakeholders, and external vendors on External Data Services.</p></li><li><p>Identify process gaps and lead initiatives to improve processes.</p></li><li><p>Track milestones and deliverables, escalate issues, and communicate portfolio-level updates to stakeholders.</p></li><li><p>Lead or contribute to special projects requiring strategic input and expertise in External Data.</p></li><li><p>Serve as a subject matter expert (SME) for complex topics requiring leadership-level commitment.</p></li><li><p>Develop SOPs, Work Instructions, Guidance Manuals, and other DTS development tools.</p></li><li><p>Provide coaching, mentoring, and performance management for direct reports.</p></li><li><p>Manage resource allocation and planning for External Data Services.</p></li></ul><p><strong>This Role Might Be for You If You:</strong></p><ul><li><p>Have expert knowledge of regulations like 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards for data collection.</p></li><li><p>Possess deep expertise in Data Management, External Data processes, and industry best practices.</p></li><li><p>Demonstrate advanced experience with extracting data in SAS, CSV, and XML formats.</p></li><li><p>Can address complex External Data challenges and recommend actionable solutions.</p></li><li><p>Have a proven ability to develop best practices and processes to achieve objectives.</p></li><li><p>Exhibit strong problem-solving, analytical, and project management skills.</p></li><li><p>Thrive in a matrix environment with virtual teams and can motivate others effectively.</p></li><li><p>Possess an excellent understanding of cross-functional activities and their intersections with External Data.</p></li><li><p>Manage multiple priorities with attention to detail and deliver results within tight timelines.</p></li><li><p>Communicate effectively through strong interpersonal, oral, and written skills.</p></li><li><p>Adapt quickly in a fast-paced, dynamic environment.</p></li><li><p>Are open to travel up to 20%.</p></li></ul><p><strong>To be qualified for this role, you must meet the following requirements:</strong></p><ul><li><p>A minimum of <strong>10+ years of experience</strong> in External Clinical Data Management, with expert knowledge of database structures in biotechnology, pharmaceutical, or health-related industries.</p></li><li><p>At least <strong>4 years of people management experience</strong>.</p></li><li><p>A <strong>Bachelor’s degree</strong> in Science, Health, Computing, or a related field.</p></li><li><p>Hands-on experience with <strong>Imaging Data</strong> is required.</p></li><li><p>Advanced knowledge of <strong>Biomarker data types</strong> and/or Imaging Data for oncology and non-oncology studies is a plus.</p></li><li><p>Expert knowledge of database structures is preferred.</p></li></ul><p>This role is ideal for a seasoned professional who thrives at the intersection of leadership, technical expertise, and strategic vision. If you’re ready to make a significant impact in External Data Services, this position could be your next career milestone.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,800.00 - $252,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Mar 2026 11:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Product Management, Delivery & Operations]]></title>
    <date><![CDATA[Sun, 22 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45153]]></requisitionid>
    <referencenumber><![CDATA[R45153]]></referencenumber>
    <apijobid><![CDATA[r45153]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45153/director-product-management-delivery-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Global Development IT Director, Product Management is a key member of the GDIT Delivery & Operations organization, responsible for overseeing and guiding their team members in delivering, maintaining & enhancing all technology products in their defined business domain. This resource will also partner with key business stakeholders to intake, design, implement and enhance technology products. This role will work closely with Business Solution Partners (BSP) to deliver projects and technology product improvements. The role will also be responsible for line management of product owners aligned to the domain and will assume product owner responsibilities for a specific set of technologies, including end-to-end implementation and support for all products that fall within the domain. This role will be responsible for the Development Operations & Portfolio Management (DO&PM) domain. </p><p><em><strong>The role will be based onsite at our offices in Warren, NJ or Armonk, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><strong>In this role, a typical day might include the following:</strong></p><div><ul><li><p>Lead & coach the Product Leads and Product Analysts within GDIT Delivery & Operations assigned to the domain, ensuring delivery on team commitments, collaboration across members, and definitions of processes, tools and competencies needed to further build the domain capabilities. </p></li></ul></div><div><ul><li><p>Oversee all operational support for products and domain providing line leadership and guidance to individual product owners while thinking across product lines. </p></li></ul></div><div><ul><li><p>Ensure alignment with product model processes and standards while customizing to meet domain-specific needs as applicable, including being responsible for product backlog and incidents management, including insights into enhancements and incidents trends over time. </p></li></ul></div><div><ul><li><p>Partner with the Business Process Owners and BSPs to implement new/enhanced technologies, and take ownership of products including end-to-end support, performance, and commitment to continuous improvement. </p></li></ul></div><div><ul><li><p>Intake, assess, prioritize and validate domain specific needs/requirements including partnership with BSPs to ensure alignment between technology roadmaps and product priorities. </p></li></ul></div><div><ul><li><p>Responsible for identifying resourcing needs and for oversight of internal and vendor delivery, and managed service vendor associates in support of product. </p></li></ul></div><div><ul><li><p>Work collaboratively with GDS functions, Corporate IT, and other relevant functions in the management of enterprise systems, including development and adherence to standards and governance. </p></li></ul></div><p><strong>This Job Might Be For You If You Have:</strong></p><div><ul><li><p>Proven ability to manage competing priorities across a multitude of stakeholders and to direct teams to deliver value-oriented, prioritized solutions. </p></li></ul></div><div><ul><li><p>Excellent communication skills and the ability to indirectly influence key partners and stakeholders with clear, concise, and well-formed message tailored to the audience </p></li></ul></div><div><ul><li><p>Strong record of accomplishment in technology project management, stakeholder management, budget management and value engineering. </p></li></ul></div><div><ul><li><p>Ability to effectively manage multiple priorities with a sense of urgency, and effectively manage ambiguity and changing priorities </p></li></ul></div><div><ul><li><p>Experience managing technology capability identification, selection, implementation, and operations </p></li></ul></div><div><ul><li><p>Excellent problem-solving skills to address day-to-day challenges associated with business solutions </p></li></ul></div><div><ul><li><p>Knowledge of pharmaceutical Global Development business capabilities, processes, systems, and key trends in the industry. </p></li></ul></div><div><ul><li><p>Experience growing and motivating a team, coaching members through career milestones and progression. </p></li></ul></div><div><ul><li><p>Exposure to delivering presentations and engaging with senior leadership. </p></li></ul></div><p><strong>To be considered for this role, you must have:</strong></p><div><ul><li><p>BS/BA Degree with 12+ years relevant experience </p></li></ul></div><div><ul><li><p>MS Degree with 10+ years relevant experience </p></li></ul></div><div><ul><li><p>Deep knowledge of Development Operations & Portfolio Management business processes, including but not limited to Drug Development Program and Portfolio Management; Resource Management; Clinical Trial Feasibility, Planning, Execution, and Closeout; Clinical Monitoring; Study Start-up; Site Management; and Clinical Drug Supply Management. </p></li></ul></div><div><ul><li><p>Experience managing technology teams and driving business value in the Clinical Operations space with specific technologies like Veeva Clinical Vault (CTMS, TMF, SSU, etc.), CluePoints, Planisware, etc., a plus. </p></li></ul></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 23 Mar 2026 12:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Software Engineer]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43915]]></requisitionid>
    <referencenumber><![CDATA[R43915]]></referencenumber>
    <apijobid><![CDATA[r43915]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43915/principal-software-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Regeneron Genetics Center is one of the largest human genetics sequencing programs in the world. We study human DNA at massive scale to understand why diseases happen and how we can stop them. Using genetics to improve human health, our research has contributed directly to medicines helping patients today.</p><p>The RGC IT team builds and maintains shared services, platform tooling, and APIs that our research teams depend on. We approach development with an AI-first mindset, utilizing LLM-powered tooling to move faster, explore more ideas and quickly turn complex problems into working solutions for our scientists.</p><p><strong>A Typical Day As a Principal Software Engineer, you’ll contribute to:</strong></p><ul><li><p>API and service development across a shared platform that research teams use to access and work with large-scale genetic data.</p></li><li><p>Cloud-based data pipeline work on AWS, keeping high-volume genomic data moving reliably and performantly.</p></li><li><p>Integrating and applying AI tooling across development workflows — from LLM-assisted coding and review to building AI-powered capabilities into the platform itself.</p></li><li><p>Working directly with scientists and engineers to understand requirements and deliver meaningful solutions to improve our scientific discovery process.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Strong fundamentals at the API and data layer. You’ve built production APIs, integration services, and pipelines in the cloud as microservices.</p></li><li><p>Comfortable with AI-first development. You use tools like Claude Code as a core part of how you work — not occasionally, but throughout planning, implementation, and review.</p></li><li><p>Technical depth across the stack. API design patterns, distributed systems, cloud-native development on AWS — you can contribute without needing everything handed to you.</p></li><li><p>Works well as part of a team. Decisions here are collaborative. You do good work in that kind of environment.</p></li><li><p>Takes quality seriously. You write things that can be tested and maintained, and you know why that matters at scale.</p></li></ul><p><strong>To be considered for this opportunity,</strong> you must have a Bachelor’s Degree or higher with at least 6 years of relevant IT experience building cloud-native applications. Candidates must have hands-on experience with:</p><ul><li><p>Languages & Runtimes: Python, TypeScript</p></li><li><p>API & Integration: REST API design and development, service integration patterns</p></li><li><p>AI Tooling: LLM-assisted development tools (e.g. Claude Code, GitHub Copilot), AI/ML service integration</p></li><li><p>Data & Databases: PostgreSQL or MySQL, Redshift or Snowflake, ETL orchestration</p></li><li><p>Infrastructure: Docker, AWS cloud services</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 09:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Sr Payroll Analyst]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46044]]></requisitionid>
    <referencenumber><![CDATA[R46044]]></referencenumber>
    <apijobid><![CDATA[r46044]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46044/temp-sr-payroll-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role, you will report to the Payroll Manager. The Payroll Analyst will support the wider team in the completion of all payroll tasks.</p><p>This is a 12 month temporary contract. </p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li>Reviewing and inputting all administrative payroll data changes to records for processing of our bi- weekly and monthly payroll and maintain records</li><li>Working with other departments such as Comp & Bens and HRPB’s to ensure payroll data is correct and processed accordingly</li><li>Reconciling each payroll, reviewing all entries and forward for approval</li><li>Ensuring accuracy in all tax information, reconciliations and payments</li><li>Undertaking Time & Labour processing and administration of time cards</li><li>Managing the internal inbox with responsibility for responding to employees’ queries</li><li>Assisting with audit queries related to payroll</li><li>Updating SOPs and training documents for a variety of payroll processes</li><li>Working with the team to evaluate and test system enhancements to Core Pay</li></ul><p><strong>This role might be for you if you have: </strong></p><ul><li>A positive can do approach to work</li><li>A proven track record at completing projects and assigned tasks</li><li>Experience in European payroll (preferred but not required)</li><li>Strong Excel experience including Pivot Tables, VLookups and Macros</li></ul><p>To be considered for this role you should have an IPASS qualification with a minimum of 5 years’ experience in a high-volume environment and years’ experience with Core Pay and Core Insight. Experience in Oracle and Workday preferred but not required.</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Oncology Lung Cancer Marketing]]></title>
    <date><![CDATA[Mon, 06 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46333]]></requisitionid>
    <referencenumber><![CDATA[R46333]]></referencenumber>
    <apijobid><![CDATA[r46333]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46333/director-us-oncology-lung-cancer-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, US Oncology HCP Lung Cancer Marketing, is a member of the Oncology Business Unit with accountability for working closely with the Senior Director to develop commercial HCP promotion strategy and tactical plans for Non-Small Cell Lung Cancer (NSCLC) within the US. Also responsible for collaborating with the International team for Global commercialization and promotion.</p><p>This position will report directly to the Senior Director, US HCP Lung Cancer Marketing. The Director will work collaboratively across the Franchise Team, International teams, internal cross-functional colleagues, while effectively managing external agency partners to ensure alignment and to drive optimal integration and execution of personal and non-personal initiatives.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Lead HCP marketing for the NSCLC indications in the US. This includes defining US market opportunities, analyzing the competitive landscape, identifying key site of care and key account segmentation and needs, developing customer-focused and differentiated product and indication positioning, and customizing messages to key target audiences.</li><li>Works in close collaboration with Clinical, Medical Affairs and Field Medical to ensure alignment with Medical Education strategic plans.</li><li>Engage with physician experts and attend key congresses to support Scientific Marketing team efforts and assess important disease and treatment data.</li><li>Work closely with the Insights and Data Analytics team to design and implement promotional strategies, while tracking brand performance, share of voice, market dynamics and competitive actions & response. Provide business assumptions input to forecasting.</li><li>Oversee and collaborate with Digital/Media Strategy team for optimization and implementation of the multi-channel marketing mix, including omni-channel digital & media strategy and implementation, and creation and deployment of educational resources towards brand objectives and developing indicators/metrics for high-impact engagements with HCP key target audiences.</li><li>Develop and coordinate NSCLC HCP Marketing inputs and key sections of brand plan, identify and prioritize business opportunities.</li><li>Responsible for the development of the Field Plan of Action and training plan, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/collaborators.</li><li>Maintain strong collaborative relationships with cross-functional areas and internal strategic partners (i.e., Field Sales, Training, Promotional Review Committee, Medical Affairs, Regulatory, Clinical, Legal, Compliance, Market Access etc.)</li><li>Ensures that the marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines.</li><li>Manages and develops a direct report to ensure their continued development and growth.</li><li>Works cross functionally to create, manage and track budget to ensure operating within the approved budget and phasing.</li></ul><h3><strong>This job might be for you if:</strong></h3><ul><li>You are effective collaborator and communicator both written and verbal</li><li>You can navigate regularly in ambiguity</li><li>You excel in a fast paced environment</li></ul><p>To be considered for this role, we expect you to have a Bachelors degree; 12+ years of pharmaceutical marketing focused on Oncology. Along with leading and developing long range brand plans, budgets and forecasts for commercial teams in the pharmaceutical/biotech industry. Lastly, this role requires you to travel 30% of the time and to be in the office in Sleepy Hollow, NY 4 days a week.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Apr 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Medicine, Clinical Scientist (Immune/Inflammatory)]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44657]]></requisitionid>
    <referencenumber><![CDATA[R44657]]></referencenumber>
    <apijobid><![CDATA[r44657]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44657/manager-internal-medicine-clinical-scientist-immuneinflammatory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>We are seeking a Manager, Clinical Scientist to join our team. The Manager Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Manager works in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to the Associate Director/Director Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p></div><div><div><div><div><div><div><div><div><p><strong>As a Manager within Clinical Sciences, a typical day may include the following:</strong></p><ul><li><p>Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings</p></li><li><p>May contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments</p></li><li><p>Develops/maintains basic understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and limited knowledge of disease and drug landscape</p></li><li><p>Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets</p></li><li><p>May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborate with others for scientific and foundational guidance</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)</p></li><li><p>Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Supports identification of data trends and potential inconsistencies in data across assigned studies and raises</p></li><li><p>Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study</p></li></ul><p><strong>This role may be for you if: </strong></p><ul><li><p>Demonstrated basic knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills</p></li><li><p>Demonstrate some ability to influence within study team</p></li><li><p>Independently resolves most issues and complex matters, requiring advanced analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven track record in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related area. Additionally, ≥ 6 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in immune/inflammatory related clinical trials. Basic knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 11:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Manager Workday]]></title>
    <date><![CDATA[Sun, 12 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42066]]></requisitionid>
    <referencenumber><![CDATA[R42066]]></referencenumber>
    <apijobid><![CDATA[r42066]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42066/sr-manager-workday/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Bengaluru]]></city>
    <state><![CDATA[Karnātaka]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>We are seeking a highly motivated Senior Functional Product Owner with expertise in Workday HCM solutions, particularly in Compensation, Advanced Compensation, and Benefits modules, to support both US and international operations. This role requires a combination of technical competence, functional product design expertise, and strong collaboration skills to deliver impactful solutions.</p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Act as the subject matter expert for Workday modules, focusing on Total Rewards (Compensation, Advanced Compensation), Benefits, and Time Tracking & Absence.</p></li><li><p>Collaborate with stakeholders to build product roadmaps and design innovative, scalable solutions that align with business needs.</p></li><li><p>Partner with business teams to capture requirements, document processes, and translate them into technical solutions.</p></li><li><p>Lead system-specific implementations, including integrations with third-party vendors for benefits solutions.</p></li><li><p>Be responsible for quality assurance testing, support user acceptance testing (UAT), and ensure timely delivery of solutions.</p></li><li><p>Provide hyper-care support after go-live, troubleshoot issues, and ensure smooth transitions.</p></li><li><p>Work closely with IT, boundary systems, and other technical teams to deliver effective solutions.</p></li><li><p>Identify gaps in existing processes and recommend improvements to enhance efficiency and scalability.</p></li><li><p>Build and maintain strong relationships with internal customers, keeping them informed of progress, risks, and delivery timelines.</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>8+ years of HR functional lead experience, with a strong background in Workday HCM.</p></li><li><p>6+ years of hands-on experience in Workday Compensation and Advanced Compensation modules, including supporting annual compensation cycles.</p></li><li><p>Experience with Workday Benefits modules, including integrations with third-party vendors.</p></li><li><p>Proficiency in creating advanced Workday reports and understanding security configurations for functional modules.</p></li><li><p>Exposure to other Workday modules like Time & Absence is a plus.</p></li><li><p>Strong understanding of system design, implementation, and integration processes.</p></li><li><p>Familiarity with ServiceNow or similar cloud-based applications is an advantage.</p></li><li><p>Experience documenting business processes, system flowcharts, and testing traceability (SIT, UAT).</p></li><li><p>Excellent communication and collaboration skills.</p></li><li><p>Analytical mindset with a proactive approach to problem-solving.</p></li><li><p>Ability to challenge and influence technical designs for simplicity and scalability.</p></li><li><p>Strong organizational skills with the ability to prioritize tasks and manage multiple priorities effectively.</p></li><li><p>Bachelor’s Degree is required.</p></li><li><p>Certifications in cloud-based technologies (e.g., Workday, AWS, ServiceNow) are a plus.</p></li></ul><p>Connect with us, so we can learn more about you, and you can learn more about our medicines. And join us in crafting the future of healthcare.</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 13 Apr 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Oncology (Skin) - Manchester]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46312]]></requisitionid>
    <referencenumber><![CDATA[R46312]]></referencenumber>
    <apijobid><![CDATA[r46312]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46312/sales-specialist-oncology-skin-manchester/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is growing its newly established International Oncology organisation and is seeking a Sales Specialist to join the UK sales team. This role focuses on engaging oncology healthcare professionals, supporting effective clinical practice through high‑quality scientific exchange, and representing Regeneron Oncology across the local healthcare system. The position offers the opportunity to contribute to a developing oncology portfolio while working closely with cross‑functional colleagues.</p><h3><strong>When and where</strong></h3><ul><li><strong>Location & work model:</strong> UK‑based, field‑facing role</li><li><strong>Travel:</strong> Frequent travel required, including attendance at meetings and congresses</li></ul><h3><strong>Discover your role</strong></h3><ul><li>Engage oncology healthcare professionals through compliant, scientific discussions</li><li>Understand local healthcare environments and account context</li><li>Communicate agreed brand messages to support objectives</li><li>Develop and implement territory and account plans using data and insights</li><li>Manage key accounts in line with regional and country guidance</li><li>Work closely with medical colleagues on regional activities</li><li>Represent Regeneron Oncology at national and international meetings</li><li>Report performance and market insights to UK leadership</li></ul><h3><strong>This role requires</strong></h3><ul><li>Comfort managing a defined territory and multiple accounts</li><li>A planned and structured approach to customer engagement</li><li>Flexibility to adapt activity based on account and market needs</li><li>Confidence using face‑to‑face, remote, and digital engagement channels</li><li>Consistent adherence to industry codes and company procedures</li><li>Professional conduct grounded in integrity and ethics</li></ul><h3><strong>Required qualifications</strong></h3><p>A Bachelor’s degree, or recognised equivalent for sales professionals, is required. The role requires experience in customer engagement and disease‑ or concept‑led selling, with the ability to present effectively to varied audiences. Strong planning and prioritisation capability and competence using CRM systems and multiple IT platforms are essential. Qualification in the relevant pharmaceutical industry Code of Practice (such as ABPI or EFPIA), fluency in English, and willingness to travel frequently are required.</p><p><strong>Preferred:</strong> Experience within the biotech or pharmaceutical sector, oncology sales exposure, and launch experience.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 10:26:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Specialist (Oligonucleotides/VLPs)]]></title>
    <date><![CDATA[Mon, 13 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46552]]></requisitionid>
    <referencenumber><![CDATA[R46552]]></referencenumber>
    <apijobid><![CDATA[r46552]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46552/qa-specialist-oligonucleotidesvlps/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Quality Assurance Specialist (Oligonucleotides/Virus-like particles (VLPs)) position. This position performs activities supporting dispositioning product and/or raw materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Reviewing and approving batch records from Contract Manufacturing Organizations (CMO) manufacturing bulk drug substance including VLPs and small interfering RNAs (si-RNA)</p></li><li><p>Representing Quality Assurance in support of sophisticated Deviations, Change Controls, CAPAs, etc., including active participation in investigation, evaluation, and problem resolution</p></li><li><p>Providing consultation or advice in alignment with QA policies</p></li><li><p>Performing activities associated with disposition of raw materials and product (e.g. receipt, inspection, document review, shipping, etc.)</p></li><li><p>Reviewing, editing, or approving Regeneron controlled documents</p></li><li><p>Reviewing and approving of investigations associated with raw materials, product, laboratory, facilities, and materials</p></li><li><p>Performing status labeling of raw materials and product</p></li><li><p>Continually evaluating Regeneron processes and procedures with an eye toward continuous improvement</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have an understanding of VLP or si-RNA manufacturing operations</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li><li><p>Are able to learn and utilize computerized systems for daily performance of tasks</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and the following amount of relevant experience for each level:</p><ul><li><p>Associate QA Specialist – 2+ years</p></li><li><p>QA Specialist – 4+ years</p></li><li><p>Sr QA Specialist - 6+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 14 Apr 2026 13:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Automation]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45447]]></requisitionid>
    <referencenumber><![CDATA[R45447]]></referencenumber>
    <apijobid><![CDATA[r45447]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45447/senior-manager-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Senior Automation Manager who will be responsible for leading the design, implementation, validation, and lifecycle management of automation systems supporting bioprocessing, laboratory, and manufacturing operations. This role will ensure operational efficiency, regulatory compliance, data integrity, and continuous improvement across all automated platforms within a regulated biotech environment.</p><p><strong>As a Senior Manager Automation, a typical day might include the following: </strong></p><ul><li>Managing a team in order to meet end user requirements</li><li>Working with System Owners to prioritize change control requests, releases and enhancements</li><li>Providing oversight for the design, implementation, and support of automation equipment</li><li>Maintaining adherence to ALCOA+ data integrity principles</li><li>Developing, implementing and driving operational rigor and discipline using metrics and other operational controls as needed</li><li>Presenting status of System Operations and Project Status to executive stakeholders and ensuring alignment of resources to key priorities</li><li>Developing continuous improvement ideas that improve team performance and efficiencies</li><li>Ensuring projects are completed on time and within budget</li></ul><ul><li>Performing monthly staff performance reviews and developing annual performance evaluation of staff</li><li>Developing and executing the site automation strategy aligned with business and operational goals</li><li>Capable of leading cross-functional automation projects from concept through commissioning and validation</li><li>Overseeing automation budgets, project timelines, and external vendor partnerships</li><li>Ensuring compliance with 21 CFR Part 11 and GxP requirements</li><li>Supporting internal and external regulatory audits</li><li>Ensuring automation systems comply with regulatory agencies, IOPS policies and procedures requirements</li><li>Supporting digital transformation and Industry 4.0 initiatives</li><li>Coordinating preventative and corrective maintenance programs</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>You are a self-starter with high initiative and possess a data-driven approach to problem-solving</li><li>You demonstrate strong interpersonal skills and have previous experience managing a team</li><li>You are experienced operating with integrity, focus, and clarity in an environment of ambiguity to drive change and improvement</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better</li><li>Can balance changing priorities with increasing workload by making/communicating timely decisions</li></ul><p>To be considered for this position you should have a BSc/BA/BEng in IT/Automation/Analytics or related field and the following minimum years of relevant industry experience for each level:</p><p>Manager: 7+ years</p><p>Senior Manager: 8+ years</p><p>#REGNIRLTO #LI-Onsite #JOBSIEST #IRELIM </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 03:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Electrical Project Engineer]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46892]]></requisitionid>
    <referencenumber><![CDATA[R46892]]></referencenumber>
    <apijobid><![CDATA[r46892]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46892/senior-electrical-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Senior Electrical Engineer who will design, specify and commission new and renovated electrical systems. This individual will provide engineering support and problem solving for new capital projects, existing equipment and manufacturing processes and work in conjunction with the electrical maintenance team to ensure operational availability of electrical distribution networks. </p><p><strong>As a Senior Electrical Engineer a typical day might include the following:</strong></p><p>- Designing and maintaining LV (e.g. Lighting, General Services, UPS, Protection Settings incl. Arc Flash) and ELV (e.g. Fire Alarm, Data points, Building Automation) systems</p><p>- Managing small projects related to electrical systems infrastructure</p><p>- Assisting in the design review, site acceptance and installation of electrical equipment</p><p>- Preparing and maintaining electrical drawings and related documentation</p><p>- Designing and specifying cGMP E&I equipment and process controls</p><p>- Managing electrical systems residing on the business IT network</p><p>- Supporting validation department by preparation of design documents and assisting in protocol execution</p><p>- Assisting in investigations of equipment and control system anomalies, incl. power quality events</p><p>- Preparing engineering evaluations for and executing modification change control documentation</p><p>- Supervising electrical contractors and confirming works are to the required standard</p><p>- Preparing risk assessments, method statements and all aspects relating to Health and Safety on site</p><p>- Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p><p>- Can safely operate and manage HV network</p><p>- Maintaining company reputation by enforcing compliance with all relevant laws, policies, standards and regulations</p><p><strong>This role may be for you if:</strong></p><ul><li><p>You have excellent technical and analytical skills</p></li><li><p>You are skilled at problem-solving and continuous improvement</p></li><li><p>You possess strong communication and collaboration skills</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p>To be considered for this position, you must hold a Bachelors degree in Electrical Engineering or relevant discipline and have 5+ years' experience working in regulated industry. Level will be determined based on qualifications and experience relevant to the role</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 03:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist, Viral Delivery Technologies (AAV)]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46365]]></requisitionid>
    <referencenumber><![CDATA[R46365]]></referencenumber>
    <apijobid><![CDATA[r46365]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46365/senior-associate-scientist-viral-delivery-technologies-aav/]]></url>
    <company><![CDATA[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 Viral Delivery Technologies group is seeking a highly motivated Senior Associate<strong> </strong>Scientist to support development of an antibody-retargeted adeno-associated virus (AAV) delivery platform. This role will support the design, characterization, and in vitro/in vivo validation of novel AAVs, further expanding the company’s gene therapy vector delivery portfolio.</p><p><strong>As a Senior Associate Scientist within the Viral Delivery Technologies group, a typical day might include:</strong></p><ul><li><p>Design, execute, analyze, and troubleshoot in vitro experiments to characterize and validate antibody-retargeted viral vector designs, screening protocols, and performance.</p></li><li><p>Perform basic molecular biology and protein analysis techniques (e.g., cloning, SDS-PAGE, Western blotting, ELISA, DNA extraction, PCR, qPCR, protein chromatography).</p></li><li><p>Partner with the bioinformatics team to translate vector designs into screening platforms.</p></li><li><p>Execute rAAV production protocols and expand our understanding of AAV biology to inform novel vector optimizations.</p></li><li><p>Collaborate with cross-functional team members, collaborators in analytical groups, and core facilities across Research and Discovery.</p></li><li><p>Participate in team meetings and prepare regular updates and presentations for departmental forums.</p></li></ul><p><strong>This role may be a good fit if you:</strong></p><ul><li><p>Enjoy working in an innovation-driven, highly collaborative, fast-paced environment.</p></li><li><p>Have an affinity for bioengineering and technology-development projects.</p></li><li><p>Are highly motivated and seek continual improvement.</p></li><li><p>Are rigorous, have strong attention to detail, and can effectively balance multiple projects.</p></li><li><p>Have excellent presentation and communication skills.</p></li></ul><p><strong>To be considered for this role,</strong> you must have, at minimum, a B.A./B.S. and 5+ years of relevant industry or academic experience. An M.S. in cell biology, molecular biology, biochemistry, protein purification, and/or antibodies is preferred. Required experience includes mammalian cell culture; manipulation and purification of viruses and/or proteins; DNA isolation from tissues and cells; plasmid cloning; use of antibodies in various applications; and maintenance of accurate, up-to-date electronic lab records. Familiarity with key antibody properties, protein engineering, viral vector production, and relevant research software (e.g., Microsoft Office, GraphPad Prism, Benchling, MacVector) is desired. Level will be commensurate with experience.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist, Hearing Loss and Vestibular Disorders]]></title>
    <date><![CDATA[Tue, 14 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44687]]></requisitionid>
    <referencenumber><![CDATA[R44687]]></referencenumber>
    <apijobid><![CDATA[r44687]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44687/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>We are seeking a highly skilled, motivated, and innovative Principal Scientist to lead the development of therapies to treat 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.</p><p><strong>A typical day in the life of a Principal Scientist on this team may include:</strong></p><ul><li><p>Lead the design of rigorous and appropriate experiments to address core questions of hearing biology, that can drive drug discovery and preclinical programs.</p></li><li><p>Develop and characterize novel animal models to better understand mechanisms of hearing loss and evaluate the potential of novel therapeutics to mitigate hearing phenotypes.</p></li><li><p>Design and execute <em>in vivo</em> and <em>in vitro</em> functional assays to understand the mechanisms of 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>Carefully analyze and evaluate data.</p></li><li><p>Present data both internally and externally, and participate in discussions in our collaborative, cross-functional team environment.</p></li><li><p>Independently draft and review protocols and articles for publication.</p></li><li><p>Motivate, develop, and supervise junior scientists, research associates and other trainees.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You enjoy a dynamic, fast-paced environment</p></li><li><p>Can work well both independently and in a team, and communicate effectively with colleagues across all levels</p></li><li><p>Maintain a rigorous approach to scientific work</p></li><li><p>You are resilient in overcoming challenges and can adapt to shifting priorities</p></li><li><p>You are excited to learn on the fly and expand your areas of expertise</p></li></ul><p><strong>To be considered for this role, you must have the following</strong>:</p><p>Ph.D. with a strong record of innovation and publication and 5+ years of experience. Proven expertise in drug development is required. Managerial experience is highly desirable. In vivo experimental experience is desirable. Strong understanding of human and mouse genetics and/or auditory physiology is an advantage.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 15 Apr 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs, North Center]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46698]]></requisitionid>
    <referencenumber><![CDATA[R46698]]></referencenumber>
    <apijobid><![CDATA[r46698]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46698/senior-manager-field-medical-affairs-north-center/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced Field Medical Affairs professional specializing in Hematology to join our team in Spain. In this pivotal role, you will serve as a scientific and clinical resource, engaging with key opinion leaders, healthcare professionals, and internal stakeholders to advance disease awareness and support innovative research initiatives. By collaborating across Medical Affairs, Clinical Development, Market Access and Commercial, you’ll help drive impactful strategies that shape the future of hematological care. This is your chance to create a meaningful difference in patient outcomes while growing your expertise in a dynamic, matrix-driven environment.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Building and nurturing peer relationships with leading experts in Hematological Malignancies.</p></li></ul><ul><li><p>Presenting scientific and clinical data to healthcare professionals and investigators.</p></li></ul><ul><li><p>Supporting and managing clinical trials by identifying investigators and trial sites.</p></li></ul><ul><li><p>Collaborating with internal teams and cross-functional partners to align strategies.</p></li></ul><ul><li><p>Responding to requests for information about disease states and Regeneron’s products.</p></li></ul><ul><li><p>Ensuring compliance with company policies and regulatory guidelines.</p></li></ul><ul><li><p>Assisting with the development of abstracts, posters, and manuscripts for scientific communication.</p></li></ul><ul><li><p>Providing support to the commercial team</p></li></ul><p><strong>This Role May Be For You, if you:</strong></p><ul><li><p>Thrive in a collaborative, matrix environment and enjoy cross-functional teamwork.</p></li></ul><ul><li><p>Value building and maintaining positive relationships with healthcare professionals and investigators.</p></li></ul><ul><li><p>Are committed to scientific integrity and professional communication at all times.</p></li></ul><ul><li><p>Excel at organizing, planning, and balancing multiple priorities, both independently and as part of a team.</p></li></ul><ul><li><p>Are passionate about advancing hematological research and supporting innovative clinical initiatives.</p></li></ul><p><strong>To Be Considered</strong></p><p>Applicants must hold a Bachelors degree with preferably 5+ proven experience, including at least 3 years in a Field Medical or Medical Manager role within the biotech or pharmaceutical industry, focusing on Oncology or Hematology. Expertise in the Hematology therapeutic area is required, with experience in lymphoma and/or multiple myeloma strongly preferred. Established relationships with key opinion leaders in malignant hematology and familiarity with institutions specializing in Hematologic Malignancies are advantageous. Drug launch experience, knowledge of treatment guidelines, clinical research processes, EU and pharma regulations, and strong communication skills are essential. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Portfolio Management]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45484]]></requisitionid>
    <referencenumber><![CDATA[R45484]]></referencenumber>
    <apijobid><![CDATA[r45484]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45484/executive-director-portfolio-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>This position is based on-site in Tarrytown, NY.</em></p><p>The <strong>Executive Director, Portfolio Management</strong> is a key member of the Program and Portfolio Management (PPM) Leadership Team. This function plays an important role in optimizing the portfolio of programs in Regeneron’s product pipeline. The Executive Director will lead a group that integrates the entire development portfolio makeup and cross functional resourcing of post-research assets through lifecycle management to enable efficient portfolio decision making by executive leadership. The role will interface with senior management across Research, Development, Manufacturing and Commercial to ensure Portfolio Management excellence to drive pipeline delivery & portfolio value. This role will partner with Clinical Development Unit Heads, Functional Leaders, Global Program Heads and Program Management to deliver portfolio level information and analysis across the integrated development plans for all assets in development. The candidate will also be responsible for influencing asset and portfolio level decisions through identification of interdependencies and downstream implications of drug development decisions. </p><p><strong>In a typical day, you will:</strong></p><ul><li>Provide leadership and strategic vision for the Portfolio Management group, supporting Clinical Development Units, cross-functional Strategic Program Teams (SPT’s) for all clinical assets.</li><li>Partner with Global Program Heads (GPH’s) and key functional leaders to ensure data enabled, timely portfolio and asset level decision making with key inputs from Research, Development, Manufacturing and Commercial. </li><li>Identify and champion Portfolio and Asset Development best practices, including the use of dashboards, templates, tools, systems and processes to drive efficiency, alignment, decision making, and communication - all leading to effective product planning and delivery.</li><li>Leverage Program and organizational knowledge, leadership, and facilitation skills to enable Program and Portfolio Management Teams to drive alignment, collaboration, and accountability within the SPTs and across corporate functions resulting in achievement of company and program goals.</li><li>Drive portfolio level program planning, including cross-functional resource planning, financial, and capacity assessments; contribute to long-range and budgetary planning.</li><li>Ensure effective communication of Program and Portfolio Management information to the broader organization.</li><li>Lead program and portfolio communication and reporting in partnership with executives and functional leaders, including developing and delivering monthly dashboards and program and portfolio reviews to the Executive Team, key business partners, and the Board of Directors. This covers pipeline content, portfolio metrics, development and portfolio reporting across all Therapeutic Areas (TA’s).</li><li>Develop strong working relationships with key stakeholders within and outside of Regeneron (functional leaders, peers, vendors, pharma industry community, and external opinion leaders).</li><li>Provide information to support portfolio decision making aligned with decisions on progression of individual assets.</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Extensive knowledge of research and development and thorough understanding of the tasks required in all stages of drug development.</li><li>A strong understanding of the people, processes and infrastructure involved in managing across the drug development lifecycle.</li><li>Comprehensive knowledge of Program, Portfolio and Resource Management methodologies and techniques.</li><li>Ability to prioritize multiple tasks and options with a strong attention to detail.</li><li>Excellent written and verbal communication skills; strong communicator and influencer within all levels of the organization, including executive leadership. Knows what information and discussions are needed to help drive decisions and solve issues.</li><li>Strong analytical capabilities, including quantitative and qualitative assessment skills and demonstrated critical thinking skills.</li><li>Ability to distill complex issues and ideas down to simple comprehensible terms and issue resolution.</li><li>Exceptional ability to lead people and multidisciplinary functional groups, identify and develop talent, and delegate effectively.</li><li>Strong conflict resolution and problem-solving skills.</li><li>Strong leadership and team building skills.</li><li>Demonstrated capability to drive transformational change at the divisional and Enterprise scale.</li></ul><p><strong>To be considered, you must possess: </strong></p><ul><li>17+ years of pharmaceutical/biotech industry experience and a minimum of six years in program, portfolio and/or alliance management.</li><li>BA/BS in business, finance, science/technology, or related field required, advanced degree strongly preferred but not required. MS/PhD or MBA with experience working within a science-based life sciences organization.</li><li>Ability to work effectively in a fast-paced, rapidly changing and expanding environment and to juggle multiple large-scale projects, programs and enterprise- wide initiatives in a global organization.</li><li>Outstanding work ethic and integrity, including high ethical and quality standards.</li><li>Strong interpersonal skills particularly motivational, negotiation, listening, judgment, analytic, and conflict management skills, demonstrated by ability to lead teams.</li><li>Ability to engage in collaborative decision making, complete tasks in a timely fashion, and function in a rapid-paced environment. Must be a practical thinker, able to identify simple, realizable solutions.</li><li>Proven ability to develop and lead a successful business plan, along with the flexibility and humility to “roll up your sleeves” to execute with excellence.</li><li>Comfortable with ambiguity and occasional chaos; cool under fire.</li><li>For best fit, the candidate must have the ability and strong desire to “make things happen”; and must have a results-oriented work ethic, a positive can-do attitude and be a bold, critical, and collaborative thinker.</li><li>Advanced knowledge of MS Project, Planisware, Planview and/or other project and portfolio planning and tracking software programs is required.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 19:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Neuroscience & Ophthalmology Genetics]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46973]]></requisitionid>
    <referencenumber><![CDATA[R46973]]></referencenumber>
    <apijobid><![CDATA[r46973]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46973/associate-director-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[<p>We are seeking a Physician Scientist to join our Neuroscience and Ophthalmology Therapeutic Area Genetics (TAG) team. We see this role as a subject matter authority in the translation of human genetic evidence into actionable insights in neurological, psychiatric, ophthalmological, hearing- and aging-related diseases. You will work closely with other teams in the Regeneron Genetics Center and Regeneron at large and be primarily responsible for designing, contributing to the execution of, and interpreting large and complex human genetic studies in the therapeutic areas. We hope you are excited by the opportunity to play a role in the development and implementation of innovative translational sciences and identify new therapeutic targets through genetic approaches. </p><p>As a Physician Scientist in Neurology/Ophthalmology, a typical day might include the following:</p><ul><li><p>Applying human genetics to target discovery, selecting indications for drug programs, and identifying subgroups of patients who are more likely to respond to treatment through genetic analyses.</p></li><li><p>Working with a multidisciplinary genetics team consisting of human genetics scientists, bioinformaticians, statistical geneticists, and other team members to design, execute, and interpret genetics studies in ophthalmology.</p></li><li><p>Working in close collaboration with other Therapeutic Area Genetics team members and forming a strong partnership with Genome Informatics, Analytical Genomics, Clinical Informatics, and other RGC teams to deliver on complex, top-quality scientific endeavors in these Therapeutic Areas.</p></li><li><p>Generating, summarizing, and presenting results in internal and external meetings to a variety of audiences.</p></li><li><p>Leading or contributing to the writing of scientific reports and publications.</p></li><li><p>Representing the TAG team in cross-functional initiatives within RGC and Regeneron.</p></li><li><p>Collaborating with external industry and academic partners in scientific consortia.</p></li></ul><p>This job may be for you if:</p><ul><li><p>You have demonstrated the ability to design and lead human genetics studies delivering medically relevant findings in a team-based environment.</p></li><li><p>You use medical knowledge to define relevant phenotypes for genetic association studies and to formulate innovative and important research questions. You have familiarity with clinical genetics concepts and various genetic models of disease.</p></li><li><p>You have experience leading complex human genetics research endeavors, have knowledge of different study designs and analyses including GWAS, exome, or genome sequencing in cohort, case-control, or family-based studies, and have the ability to integrate different data resources to translate initial findings.</p></li><li><p>You have an interest in understanding the genetic basis and causes of Neurological, Psychiatric, Ophthalmological, Hearing- and Aging-related diseases and translating this knowledge into therapeutic insights. An outstanding candidate will have previous experience with phenotypes related to these diseases.</p></li><li><p>You thrive working in a highly interactive environment with a diverse team of colleagues.</p></li><li><p>You have outstanding communication skills and an ability to summarize and present the results of human genetic studies to a variety of audiences.</p></li></ul><p>To be considered for this opportunity, you must have an MD or MD/Ph.D. with a strong background in and knowledge of human genetics or genetic epidemiology. An outstanding candidate will be an MD/Ph.D. with training and experience in translational human genetics, genetic epidemiology (or related disciplines), and strong quantitative skills. Familiarity with the applications of statistical genetics to gain medically actionable insights including polygenic risk scores, quantitative traits analyses, and Mendelian randomization, and familiarity with command-line interface, programming languages, and statistical software (eg. Python, R) is preferred. The outstanding candidate will have experience with the use of genetics in combination with other “omics” technologies (eg. epigenetics, proteomics, RNA-seq).</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Corporate Strategy]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47067]]></requisitionid>
    <referencenumber><![CDATA[R47067]]></referencenumber>
    <apijobid><![CDATA[r47067]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/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[<p>The Corporate Strategy team at Regeneron is responsible for conceiving and conducting analyses to help senior leadership make critical decisions for our business. The Manager, Corporate Strategy 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. This role requires strong analytical and communication skills and the ability to generate clear insights from complex information for leaders across the organization.</p><p><em><strong>This is a great opportunity to support a leading biotech company by delivering cross-functional insights to senior leadership. The role is based at our Global HQ campus in Tarrytown NY - it is not eligible for remote work. Occasional travel may be required for this role.</strong></em></p><p>As a Manager in Corporate Strategy, job duties include:</p><ul><li><p>Collaborating with all key functions of the company to gather information and data about our business</p></li><li><p>Planning and conducting interviews with functional groups to understand needs and problems, and help find solutions</p></li><li><p>Analyzing internal and external data to evaluate strategic options for Regeneron</p></li><li><p>Assessing market opportunities and potential return for key R&D investment decisions</p></li><li><p>Modeling future scenarios at the program and corporate level to inform business decisions</p></li><li><p>Contributing 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</p></li><li><p>Communicating conclusions and recommendations of analyses to senior management</p></li></ul><p>While no two days in Corporate Strategy are alike, a typical day might include:</p><ul><li><p>Building a financial model for the CEO or Head of Business Development to inform discussions on a business development deal</p></li><li><p>Leading a discussion with research, development, or commercial leaders to better understand a specific challenge and potential solutions for an upcoming senior leadership presentation</p></li><li><p>Investigating an emerging issue in the external landscape and how other biopharmaceutical companies are reacting to it</p></li><li><p>Conducting an NPV analysis to assess the potential return on a Phase 3 development program</p></li><li><p>Addressing ad hoc questions from senior leaders on specific Regeneron programs</p></li></ul><p>This role might be for you if you possess:</p><ul><li><p>Problem-solving skills and the ability to think through complex business problems and propose a path to a solution</p></li><li><p>Strong interest in understanding “the big picture” of how drugs are developed and deliver meaningful impact to patients</p></li><li><p>Experience analyzing complex data, including scientific, clinical, and financial data</p></li><li><p>Strong command of financial modeling and valuation</p></li><li><p>Strong written and verbal communication skills</p></li><li><p>Team player attitude with a desire to work collaboratively with other functions to reach an end goal</p></li><li><p>Comfort working independently and taking action on projects when limited guidance has been provided</p></li></ul><p>To be considered for this opportunity, a minimum of a Bachelor’s degree is required and 5+ years of work experience in consulting, equity research, or investment banking, or in a strategy role within the biopharmaceutical industry. Strong analytical skills, including extensive experience using Microsoft Excel and PowerPoint, are critical to be successful in this role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$114,800.00 - $187,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 09:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[IT Lead, Manufacturing GxP]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46064]]></requisitionid>
    <referencenumber><![CDATA[R46064]]></referencenumber>
    <apijobid><![CDATA[r46064]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46064/it-lead-manufacturing-gxp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a skilled IT professional to serve as the IT Lead for Regeneron's Cell Medicines (RCM) Manufacturing operation to support and maintain all Clinical Manufacturing Equipment and data acquisition/monitoring systems. This role will require strong management skills to effectively manage the support needed from multiple Regeneron Corporate IT services groups and external support vendors as needed, in addition to strong technical skills as the primary On-Site IT SME for the Clinical Manufacturing area.</p><p>This individual will ensure seamless communication, service delivery, and networking of points of contact across multiple IT groups and the business. The ideal candidate will have leadership and communication skills, experience in a GMP (Good Manufacturing Practices) environment, and the ability to troubleshoot on-site IT issues related to all Manufacturing and QC equipment and facilities IT systems.</p><p><strong>As an IT GxP Manufacturing Lead, a typical day may include: </strong></p><ul><li><p>Serve as the primary point of contact between RCM and Corporate IT, coordinating support across internal groups and external vendors.</p></li><li><p>Align IT services with RCM’s needs by facilitating clear stakeholder communication on requirements, timelines, and deliverables.</p></li><li><p>Lead planning and execution of IT projects and initiatives within a GMP environment, ensuring effective cross-team coordination.</p></li><li><p>Provide regular operational and project status updates, metrics, and risk/issue reports to leadership.</p></li><li><p>Manage and direct contracted IT personnel and oversee vendor performance for service delivery.</p></li><li><p>Troubleshoot and resolve on-site IT issues for manufacturing, QC equipment, and facilities systems (hardware/software), ensuring rapid restoration.</p></li><li><p>Ensure high availability and resilience of critical systems through monitoring, preventive maintenance, backups/archiving, and recovery readiness.</p></li><li><p>Develop and maintain GxP documentation, including specifications, test protocols, validation/CSV records, and system administration SOPs.</p></li><li><p>Support integration of equipment and systems with LIMS and other enterprise platforms in coordination with Corporate IT; supervise EMS for compliance and reliability.</p></li><li><p>Ensure GMP/regulatory compliance by partnering with QA, managing IT tasks in CMMS, maintaining audit readiness, and driving continuous improvement of workflows and support processes.</p></li></ul><p><strong>This role could be for you if you: </strong></p><ul><li><p>Strong management and leadership abilities.</p></li><li><p>Excellent written and verbal communication skills.</p></li><li><p>Ability to collaborate effectively with cross-functional teams.</p></li><li><p>Proven track record of collaborating with corporate IT teams.</p></li><li><p>Ability to adapt to a fast-paced, multifaceted work environment.</p></li></ul><p><strong>To be considered for this role, you must meet the following:</strong></p><ul><li><p>Bachelor’s degree in information technology, Computer Science, or a related field.</p></li><li><p>5 – 10 years' demonstrated ability in an IT role, preferably within a GMP-regulated environment.</p></li><li><p>Proficiency in troubleshooting all IT aspects of manufacturing/QC equipment and other data collection/monitoring systems (e.g. EMS)</p></li><li><p>Familiarity with GMP requirements and IT compliance standards.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:26:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ophthalmology Account Director (OAD) North Central – Great Lakes]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47304]]></requisitionid>
    <referencenumber><![CDATA[R47304]]></referencenumber>
    <apijobid><![CDATA[r47304]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47304/ophthalmology-account-director-oad-north-central-great-lakes/]]></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 Ophthalmology Account Director (OAD) North Central – Great Lakes will represent the entire Regeneron ophthalmology product portfolio. The OAD connects to the key business decision-makers and all other relevant Key Opinion Leaders (KOLs) within their assigned accounts and will be a critical liaison between their customers and Regeneron. Leveraging their account and contract management capabilities, the OAD will be required to lead and appropriately educate and influence customers including large provider practices and private equity groups, as well as internal audiences including senior Regeneron Market Access, Brand and Executive leadership teams.</p><p>Working in the context of an integrated account business plan, the OAD will play an important account management role working both independently and closely with the ED Ophthalmology Accounts to educate on, administer, and pull-through provider contracts as well as other partnership opportunities targeted at financial, operational, and other relevant business decision-makers and their teams. The OAD will be an expert in customer engagement and contract management and will work closely with other Regeneron internal team members within Market Access and the Brand sales force.</p><p>Additionally, OADs will have a strong understanding of the customer healthcare environment and will play a pivotal role not only in effective customer and contract education and management, but also in navigating both the external complexity and the internal dynamics of product and customer priorities. The OAD will represent current and potentially future contracted ophthalmology products within their customer base and provide relevant customer feedback to internal stakeholders and leadership in a timely manner.</p><p><strong>In this role, a typical day may include:</strong></p><ul><li>MBO Driven, customer facing role</li><li>Focused on maximizing customer executive engagement, reach and frequency, and contract education and pull-through efforts within assigned customers and geography to help customers and patients understand the GPO contracts</li><li>Works collaboratively as a partner with Sales, Marketing, Reimbursement, and other internal colleagues to appropriately and efficiently develop and execute account plans for assigned customers within their assigned geography</li><li>Seeks to maximize depth of customer engagements by identifying, engaging, and educating all relevant audiences at the customer about the GPO program including as appropriate C-suite, KOLs, and business and reimbursement staff</li><li>Thoroughly explains quarterly GPO program changes, if any, to customers</li><li>Delivers regular contract performance updates to customers</li><li>Performs quarterly business reviews with customers</li><li>Seeks customer feedback on the Regeneron GPO program and shares with Market Access and Brand leadership</li><li>Looks for opportunities to engage customers at regional and national retinal meetings</li><li>Fully understands other elements of customer considerations such as payer mix, ensure customer awareness of existing inventory levels, operational challenges, and reimbursement dynamics</li><li>Spends 75% of time in customer facing activities, prioritizing in-person meetings when possible</li></ul><p>To be considered for this role you must have:</p><ul><li><p>10-12 years of "progressive" industry/relevant professional experience</p></li><li><p>10+ years of pharmaceutical/biotech or related experience</p></li><li><p>Additional broad-based experience valued: sales operations, corporate partnerships, marketing, and/or sales management, and/or supply chain.</p></li><li><p>Previous experience in launching new Specialty Pharmaceutical/Biologics products or indications. Proven knowledge and relationships with key Executive level decision makers from retina and other market GPOs and institutional trade partners. Prior retina account or brand experience. Demonstrated ability to work collaboratively with and influence peers and management. Demonstrated communication skills, including presentation, negotiation and content development. Demonstrated results orientation. Demonstrated strategic planning capabilities, including event planning and meeting facilitation. Understanding of financial concepts and contracting issues and demonstrated ability to measure contract performance. Demonstrated outsourced vendor management skills.</p></li><li><p>Ability to travel 50-75%, including weekends as necessary.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 07:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, HCP Marketing - Oncology (Skin)]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47350]]></requisitionid>
    <referencenumber><![CDATA[R47350]]></referencenumber>
    <apijobid><![CDATA[r47350]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47350/associate-director-hcp-marketing-oncology-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Oncology HCP Marketing will provide strategic & operational support for the US congresses and peer-to-peer education for the Non-Melanoma Skin Cancer (NMSC) indications. The Associate Director will work to increase brand equity and presence at key congresses, and will help build relationships & loyalty with customers. This role will provide an opportunity to gain marketing experience in a competitive space and make meaningful change in the ways we meet our business needs.</p><h3><strong>A Typical Day Might Look Like:</strong></h3><ul><li>Support & implement US congress & convention plans, creative vision, and communication strategy</li><li>Coordinate with marketing team, medical affairs, and thought leader liaisons (TLLs) to ensure cohesion across congress plans</li><li>Partner with Thought Leader Liaisons (TLLs) & Non-Small Cell Lung Cancer (NSCLC) congress point on Pan-tumor congress execution (eg. ASCO, ESMO)</li><li>Analyze the competitive landscape, identifying key promotions opportunities, and develop customer-focused and differentiated messages to key target audiences at congresses</li><li>Support all operational aspects for Peer-to-Peer education & Speaker Programs including content development/updates, new engagement tactics/formats, HCP contracting, training, logistics, communications, and act as key liaison with Commercial Operations group</li><li>Develop professional relationships with external medical experts & speakers</li><li>Contribute to US Advisory Board and Ad Council planning, including project management/timelines, content development, & contracting</li><li>Support management of promotional medical education, including content updates, execution, rollout of new promotional displays & tactics, pull-through with the sales team, vendor management, & budgets</li><li>Support management of agency involved in key projects with quarterly assessment and budget tracking</li><li>Support management of third party KOL programs</li><li>Planning & participation in relevant Brand Team Meetings</li><li>Ensuring marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines</li><li>Ensuring project timelines and expenses are kept on scope and budget</li><li>Ensuring cost effective delivery of all programs while tracking and monitoring metrics</li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li>You can lead strategically, drive performance, and align across multiple functions</li><li>You bring strong project and process skills with attention to detail, proactivity, and ability to prioritize effectively</li><li>You are standout colleague with ability to navigate & collaborate cross-functionally</li><li>You thrive in a fast paced launch environment</li><li>You are innovative thinking and problem solving ability</li><li>You effectively communicate to a wide variety of scientific and commercially oriented individuals</li></ul><p>To be considered, you have 10 years of life science related marketing or slales experience along with a Bachelor's degree. We would like to see you have Oncology or Dermatology experience with a focus on Biologic products. We would prefer you to have Congress & Peer-to-Peer experience as well. Lastly, this will be a role that requires you to be onsite 4 days a week in Sleepy Hollow, NY.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Medical Affairs (Oncology)]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47167]]></requisitionid>
    <referencenumber><![CDATA[R47167]]></referencenumber>
    <apijobid><![CDATA[r47167]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47167/associate-director-medical-affairs-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Medical Affairs Oncology, you will lead the development and execution of our US medical strategy for solid tumors. You will serve as a key scientific and medical resource, providing leadership across evidence generation, external engagement, and internal strategic guidance. A core responsibility is to ensure US medical/clinical activities are aligned with global strategies, goals, and operations driving high-quality, compliant execution.<br>This position is on-site in Sleepy Hollow, NY, 4 days per week. If eligible, we can offer relocation benefits. A remote work option is not available for this role</p><p><strong>A typical day may include: </strong><br>• Representing Medical Affairs in cross-functional forums aligning closely with Headquarters Medical Affairs and other functions optimizing strategic and tactical plans.<br>• Defining and delivering the US tumor area strategy and annual objectives.<br>• Partnering with Field Medical to translate strategy into action, including scientific exchange and insight generation. <br>• Providing medical support for our clinical development and research activities, including identifying centers of excellence and key investigators/sites, contributing to investigator meetings, and supporting targeted patient recruitment efforts.<br>• Leading US scientific engagement with external collaborators advancing appropriate understanding and use of our medicines and improve patient care.<br>• Developing and implementing US medical strategies for congresses, symposia, advisory boards, and other scientific forums.<br>• Delivering clear, credible scientific presentations to diverse audiences including physicians, pharmacists, payers and agency partners.<br>• Providing medical input with scientific integrity into commercialization strategies. <br>• Leading medical reviewer on the Medical Review Committee (MRC) for review/approval of promotional, educational, and related materials, ensuring accuracy, balance, and compliance.<br>• Reviewing US Investigator-Initiated Study (IIS) proposals, protocols, and concepts in Medical Affairs Review Committee (MARC) meetings. <br>• Supporting development and review of US clinical pathways and guideline submissions in partnership with cross-functional teams.<br>• Translating US insights to inform global strategy; ensure bi-directional communication and alignment with global Medical Affairs and clinical development.<br>• Managing relevant budgets, timelines, and vendor/agency partners to deliver initiatives on time and within scope.<br>• Uphold the highest ethical, scientific, and compliance standards across all activities</p><p><strong>This may be for you if you: </strong><br>• Want to work at the intersection of science, strategy, and patient care.<br>• Can demonstrate extensive cross-functional collaboration and visibility with senior leaders<br>• Want an opportunity to shape US medical strategy and influence our direction<br>• Have the capability to deal with scientific concepts and complexity comfortably.</p><p>To be considered a doctorate level healthcare degree is required (MD, PharmD, PhD) degree with demonstrated expertise in Oncology (solid tumors) in clinical, research or drug-development. A minimum of 6+ years of experience in Medical Affairs required. Proven medical communication skills with the ability to tailor complex scientific content to audiences of varying expertise. Ability and willingness to travel approximately 40%, including some international travel.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Scientist - Precision Medicine]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46826]]></requisitionid>
    <referencenumber><![CDATA[R46826]]></referencenumber>
    <apijobid><![CDATA[r46826]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46826/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>The Precision Medicine group at Regeneron is responsible for designing, implementing, executing, analyzing and interpreting the overarching clinical biomarker strategies for therapeutic candidates during clinical development. We are seeking to hire a Precision Medicine Strategy Lead (PMSL) at the Principal Scientist level to oversee the development and execution of biomarker strategies for multiple clinical stage assets across diverse therapeutic areas including solid tumor oncology, heme malignancies, immune oncology, rare genetic disorders and/or neurodegenerative conditions.</p><p><strong>As a Principal Scientist, a typical day may include the following:</strong></p><ul><li><p>Program-level PM lead for implementation of strategic vision for clinical biomarkers in one or more therapeutic areas that will broadly enable advances in target identification, indication selection, early indication of biological activity and patient stratification/selection</p></li><li><p>Serve as an individual contributor and representative of Precision Medicine on development teams and deliver biomarker strategies to key programs from initial concept to execution, data delivery and results interpretation</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine and clinical biomarker strategies for molecules in discovery phases (leading to candidate molecule selection)</p></li><li><p>Represent Regeneron and work with colleagues from allied companies to develop and implement strategies for partnered alliances</p></li><li><p>Collaborate with clinical operations teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Design, oversee and manage internal and external research collaborations in areas of clinical technologies and translational research</p></li><li><p>Accountability for ensuring clinical assays used in programs are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with internal Regeneron laboratories (e.g. Discovery Research, Molecular Profiling, Regeneron Genetics Center, DNA Core, BioAnalysis, etc.) to develop plan for validation and application of research assays</p></li><li><p>Contribute to and ensure the quality of Precision Medicine technical reports, study memos and clinical study reports, data reviews and interpretations, scientific publications and recommendations to development teams and management</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You have the ability to drive, manage, execute and deliver results for complex multi-functional projects</p></li><li><p>You have excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills</p></li><li><p>You have a strategic understanding of the application of biomarker technologies to basic, translational or clinical research</p></li><li><p>You have demonstrated ability to ensure timely delivery of results across selected programs</p></li></ul><p><strong>To be considered for this position,</strong> you must have a Master's degree with 7 years of experience (Ph.D. DrPH, M.D. with 4+ years of experience) participating effectively on cross-disciplinary teams in pharmaceutical or biotech industry. We are seeking candidates with experience in clinical assay development, validation and implementation, with a track record of high impact in drug development. Experience in solid tumor oncology or heme malignancies with exposure to clinical development experience is preferred. Familiarity with complex datasets, molecular epidemiology and/or statistics a plus. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director , Field Medical Affairs--Gastroenterology (GA, AL, KY, TN)]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47174]]></requisitionid>
    <referencenumber><![CDATA[R47174]]></referencenumber>
    <apijobid><![CDATA[r47174]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47174/associate-director-field-medical-affairs-gastroenterology-ga-al-ky-tn/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs, you will play a pivotal role as a field-based professional within Gastroenterology to support the clinical and business objectives across the product life cycle. We deliver strategic and operational support by establishing, developing and maintaining scientific exchange with medical specialists, health care professionals, and payers, aligned with our strategic objectives. We provide clinical and health economic information that enhances the value and appropriate use of Regeneron products. You will work with clinical research sites and investigators, and support of research activities as directed by the Global Medical Functional head.</p><p>Responsibilities of this role are to ensure accurate exchange and distribution of clinical and scientific information relevant to in-line and pipeline products in a timely, ethical and customer-focused manner.</p><p><strong>Territory:</strong> GA, AL, KY, TN</p><p><strong>A typical day may include:</strong><br>• Engaging in scientific discussions with medical and scientific specialists, including Healthcare Professionals and population health decision makers (“payers”) consistent with Medical Affairs objectives.<br>• Demonstrating deep scientific expertise related to assigned molecules/products and the associated therapeutic area to exchange relevant information and insights with specialists within a region.<br>• Building and developing relationships with key external scientific and medical specialists and organizations in a region to ensure strong understanding of evolving healthcare trends across the relevant therapeutic area landscape.<br>• Shaping and executing local medical strategy based on Global Medical Affairs strategy within planned timelines.</p><p><strong>This may be for you if you:</strong><br>• Enjoy working independently in the field, while having an impact on our mission.<br>• Are passionate about developing knowledge of and sharing clinical scientific data.<br>• Enjoy working collaboratively and building relationships in academic and clinical practice settings.<br>• Possess the innate ability to balance multiple initiatives, prioritize them and execute them independently, while excelling at keeping all partners advised and engaged.</p><p>To be considered for this position, you must have an advanced Clinical/Science Degree (e.g., MD, PharmD, PhD) with a minimum of 5 years related work experience (clinical, managed care, or industry experience). Experience as a Medical Science Liaison is required. Experience in Immunology is required; Gastroenterology experience is preferred. It is required to have the ability to communicate and disseminate scientific and clinical data.</p><p>Residency in the territory is required.</p><p>#msl #medicalscienceliaison<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 11:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Principal Scientist - Bioanalytical Sciences]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46556]]></requisitionid>
    <referencenumber><![CDATA[R46556]]></referencenumber>
    <apijobid><![CDATA[r46556]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46556/senior-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>Regeneron's Assay Development Group (ADG) in Bioanalytical Sciences, located in Tarrytown, NY, is seeking a Senior Principal Scientist. In this exciting role, you will create and execute novel assay strategies for all biotherapeutic modalities, designing experiments, troubleshooting problems, organizing and interpreting experimental results and performing follow-up experiments.</p><br><h3>A Typical Day in the Role Might Look Like:</h3><ul><li><p>Develop bioanalytical assay approaches for pharmacokinetic, biomarker assays and immunogenicity assays for a diverse pipeline of novel biotherapeutics, including monoclonal antibodies, bispecifics, antibody-drug conjugates (ADC), adeno-associated virus (AAV), CAR-T, RNA as well as drug target biomarkers to support non-clinical and clinical studies.</p></li><li><p>Supervise a team of scientists in the development and validation of immunoassays for the measurement of drug, drug complexes and anti‑drug antibodies to support new programs.</p></li><li><p>Guides the designs and execution of immunoassays (PK, PD and ADA) by direct reports, based on protocols provided by literature, seminars and other scientists. Suggests troubleshooting experiments for assay-related problems follow-up experiments to further assay development and optimize assays.</p></li><li><p>Routinely reviews data for multiple developmental projects, working on these projects simultaneously.</p></li><li><p>Summarizes and presents results internally to management and externally in industry meetings.</p></li><li><p>Writes/reviews assay validation protocols, reports and SOPs prior to submission to Quality Auditing (QA). Functions as Study Director for assay validation studies conducted by direct reports.</p></li></ul><h3><strong>This Role Might Be For You If You:</strong></h3><ul><li><p>Stimulates, develops, and promotes the scientific and career development of direct and indirect reports.</p></li><li><p>Can act as a leader within the group that effectively drives projects forward to meet aggressive timelines</p></li><li><p>Can communicate effectively with supervisor, upper management/senior leaders and other members within the company and/or outside vendors to obtain assay-related reagents or discuss reagents needs.</p></li><li><p>Propose innovative solutions and troubleshooting to address scientific complexity and challenges.</p></li></ul><p><strong>To be considered for this opportunity, you must have a </strong>PhD degree with 5+ or a MS with 8+ or a BS with 10+ years meaningful experience. An in-depth understanding of the science and technology on the development and validation of immunoassays is required. The ability to perform sophisticated technical tasks to pursue projects that incorporate a diverse set of skills and work on multiple projects/experiments simultaneously is helpful.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, GMP Counsel Regulatory]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46969]]></requisitionid>
    <referencenumber><![CDATA[R46969]]></referencenumber>
    <apijobid><![CDATA[r46969]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46969/senior-director-gmp-counsel-regulatory/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Director, GMP Counsel Regulatory provides legal advice and counsel to global manufacturing operations (including Quality Assurance, Quality Control and other IOPS leadership) regarding GMP-related matters in Regeneron’s manufacturing, quality, and supply chain operations that constitute Regeneron’s Industrial Operations and Product Supply (“IOPS”) organization.</p><p>This role serves as a subject matter expert and key advisor on U.S. and global GMP legal and regulatory requirements, supporting GMP compliance across manufacturing, development, clinical, and commercial programs. The Senior Director partners closely with Quality (including Data Integrity), Manufacturing, Technical Operations (including Automation), IT (including AI), Supply Chain, Regulatory and other Law Department colleagues to support inspections, filings, and ongoing inspection readiness.</p><br><p><strong>A typical day may include:</strong></p><ul><li><p>Interpret and advise on GMP regulations to inform strategy and execution for manufacturing and quality-related regulatory activities throughout IOPS.</p></li><li><p>Counsel and apply U.S. and global GMP law regulations to business operations.</p></li><li><p>Serve as primary legal counsel on GMP compliance matters impacting development, clinical and commercial manufacturing across all operations - - bulk/API, fill-finish/packaging, etc.</p></li><li><p>Advise and support preparation, management, and response activities for regulatory GMP inspections and partner/collaborator audits.</p></li><li><p>Provide legal guidance on regulatory GMP inspection findings, CAPAs, remediation strategies, and enforcement risk mitigation.</p></li><li><p>Partner with IOPS key functions (e.g., QA, Manufacturing and Automation, IT) to ensure continuous inspection readiness.</p></li><li><p>Collaborate with QA, Manufacturing and Automation, IT, Supply Chain, Technical Operations, Regulatory and Law teams.</p></li><li><p>Advise internal stakeholders on legal regulatory risk, strategy, and compliance considerations related to GMP manufacturing operations and, as applicable, remediation and recall activity.</p></li></ul><br><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Excellent oral and written communication skills with proven ability to present complex information accurately and concisely</p></li><li><p>Strong interpersonal communication skills and an ability to build trust and influence at all levels</p></li></ul><ul><li><p>Ability to handle multiple priorities in a dynamic and evolving environment</p></li><li><p>Strategic thinker with excellent analytical and problem-solving skills, focusing on practical solutions</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>JD required with significant experience in pharmaceutical, biotechnology, or highly regulated environment.</p></li><li><p>15+ years of progressive regulatory affairs legal counsel or related government (or industry) experience with significant GMP exposure.</p></li><li><p>5+ years of demonstrated experience supporting FDA and/or global regulatory inspections, 483 response and corrective actions/remediation, recall and other regulatory significant activity.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$203,000.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Medical Operations, Expanded Access Programs]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47170]]></requisitionid>
    <referencenumber><![CDATA[R47170]]></referencenumber>
    <apijobid><![CDATA[r47170]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47170/senior-manager-medical-operations-expanded-access-programs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Expanded Access Programs will be responsible for all operational aspects of multiple projects/programs such as Expanded Access Programs, individual patient expanded access, and post-trial access managed by Medical Affairs. Based on team assigned, this role may include supervision of staff. Additionally, this role will support other MA projects, as requested.</p><h3>As a Senior Manager, a typical day may include:</h3><h3>Program Management:</h3><ul><li><p>Operational responsibility across multiple projects/program(s) with minimal direction: Expanded Access Programs, individual patient expanded access, post-trial access</p></li></ul><h3>Meetings & Committees:</h3><ul><li><p>Participates in team review meetings, product team alignment meetings, and program budget & status update meetings as needed</p></li></ul><h3>Budget Management:</h3><ul><li><p>Accountable for financial forecasting accuracy of Managed Access Programs within span of responsibility</p></li><li><p>Maintenance of program budget trackers for each molecule/activity, ensuring all communicated actuals and accruals are captured, projections are reforested as necessary, and brand give back are fully assessed</p></li><li><p>Maintains financial forecast for programs for quarterly for reporting to Accounting & Finance, and responsible for ensuring issue resolution for all discrepancies</p></li></ul><h3>Drug Supply:</h3><ul><li><p>Responsible for managing drug supply for Expanded Access Programs and individual patient expanded access, as appropriate</p></li></ul><h3>Metrics & Reporting:</h3><ul><li><p>Responsible for ongoing analyses, tracking and reporting of projects/programs support, timelines for completion, expected or assessed delays, solutions for streamlining processes for greater efficiency, and other related metrics in support of program activities</p></li></ul><h3>Vendor Management:</h3><ul><li><p>Manages vendors and financial tracking as required per program</p></li></ul><h3>Essential Documents:</h3><ul><li><p>Ensures appropriate archiving of projects’/programs’ essential documents</p></li></ul><h3>Systems Management:</h3><ul><li><p>Utilizes appropriate systems to contribute to cross-functional communication, planning and transparency, including but not limited to:</p></li><li><p>Ensures ongoing QC of SharePoint document storage for completeness and audit readiness</p></li><li><p>Expertise required in the utilization of QlikSense, QlikView, SharePoint, Oracle and ESRA portal to support team needs</p></li></ul><h3>Process:</h3><ul><li><p>Adheres to all relevant processes, trainings, and SOPS to ensure consistency, efficiency, and compliance. Exercises' judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions; Continued process improvements</p></li></ul><h3>Organizational goals:</h3><ul><li><p>Development of objectives in order to quantify success and attainment of goals. Ensures optimal structure, procedures, and adequate resources supporting growth of multiple projects/programs. Knows when to escalate issues, and involve senior levels of management to obtain adequate resolution</p></li></ul><h3>Alliance Management:</h3><ul><li><p>Ensures financial transparency and alignment with both Alliance and internal stakeholders, supporting the product team financial reviews</p></li></ul><p>To be considered a bachelor’s degree is required and an advanced degree preferred. You are to have 5- 8 years’ experience working in clinical research or medical operations within the pharmaceutical or biotech industry. Active working experience and/or courses pertaining to clinical research and/or MA areas (such as GCP, Investigator Initiated Studies; medical/educational grants administration; medical information; registries; OIG/PhRMA guidance.). Compassionate Use or Managed Access programs preferred. We are seeking strong communication and presentation skills for senior management audiences.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Scientist, Drug Product Development]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47481]]></requisitionid>
    <referencenumber><![CDATA[R47481]]></referencenumber>
    <apijobid><![CDATA[r47481]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47481/sr-scientist-drug-product-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a highly skilled and motivated <strong>Senior Scientist </strong>to join our Drug Product Development and Technology (DPDT) Group. This Sr. Scientist position offers an exciting opportunity to work on various aspects of Drug Product development including high throughput formulation screening, characterization & development, lyophilization & other drug product process development activities for biologics, including monoclonal antibody (mAb), peptides, fusion proteins etc.</p><p><strong>A Typical Day In The Role Might Look Like:</strong></p><ul><li><p>Lead design and execution of high-throughput (HT) formulation studies to rapidly screen excipients for desirable physicochemical characteristics and stability for mAbs, peptides and fusion proteins etc. Perform HT analytical characterization and leverage statistical tools (e.g., JMP) to process large data sets efficiently.</p></li><li><p>Lead development and optimization of lyophilization cycles for various modalities across different phases of development</p></li><li><p>Perform biophysical and biochemical characterization of liquid and lyophilized formulations using techniques such as DSC, FDM, TGA, SE-UPLC, and others.</p></li><li><p>Support and lead process development, scale-up, technology transfer, and troubleshooting activities with Contract Manufacturing Organizations (CMOs) in collaboration with Industrial Operations & Product Supply (IOPS).</p></li><li><p>Collaborate cross-functionally with colleagues from Product, Analytical & Preclinical Development (PAPD) and IOPS organizations to advance the program needs.</p></li><li><p>Participate and contribute in cross-functional meetings to provide technical expertise and contribute to project planning and decision-making. Communicate effectively with stakeholders to ensure timely delivery of project milestones and objectives.</p></li><li><p>Draft and review protocols, technical reports, and supporting documents towards regulatory filings.</p></li><li><p>Stay abreast of advancements in DP Development technologies including novel process tools, HT methodologies, analytical tools and industry trends to drive innovation within the group.</p></li><li><p>Identify and implement process improvements to enhance efficiency, scalability, and quality in lyophilization and formulation development.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Strong problem-solving skills and ability to address technical challenges in a fast-paced environment.</p></li><li><p>Ability to work independently and in team settings to drive the challenging task efficiently</p></li><li><p>Excellent technical writing, communication, and project management skills. Demonstrated ability to collaborate cross-functionally.</p></li></ul><p>This position requires a Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemical and Biomolecular Engineering, or a related field with 0 - 3 years of relevant industry experience; OR M.S. with 8+ years of experience. Experience working with monoclonal antibodies and peptides is highly desirable with hands-on experience with biochemical and biophysical techniques for protein characterization using chromatography (SE-UPLC, IEX, RP-UPLC), electrophoresis (CE-SDS, MCE, cIEF, iCE), particle size (DLS, HIAC, MFI), UV-Vis, Viscosity and thermostability characterization (DSC, DSF). Expertise in lyophilization process development, including design, execution, and troubleshooting is desired as well. Experience with statistical software (e.g., JMP) for design of experiments and data analysis preferred. Ability to build efficient workflows for formulation screening and analytical testing and experience with automation tools is a plus.</p><p>This is a unique opportunity to contribute to cutting-edge drug product development initiatives and work on innovative technologies that will shape the future of the organization. You will join a dynamic and collaborative team committed to excellence and innovation in pharmaceutical development.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Precision Medicine]]></title>
    <date><![CDATA[Sat, 09 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47135]]></requisitionid>
    <referencenumber><![CDATA[R47135]]></referencenumber>
    <apijobid><![CDATA[r47135]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47135/manager-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Precision Medicine Clinical Laboratory Study Management (CLSM Manager) will lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Non-Immuno-Oncology (non-IO). In this role, you will be a key driver of precision medicine operational execution partnering with Precision Medicine Strategy Lead (PMSL), clinical study teams, data management (DM), Samples, Kits, Data, Logistics (SKDL), Clinical Laboratory Study Manager (CLSM), and Clinical Laboratory Project Management (CLPM) groups to deliver high-quality samples and data. Through strong cross functional collaboration and operational excellence, you will help ensure biomarker and non-biomarker strategies are executed seamlessly, enabling the translation of innovative science to medicines for patients.</p><h3><strong>As a CLSM Manager, a typical day may include the following:</strong></h3><ul><li><p>Works with project manager and set-up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics</p></li><li><p>Monitor’s acquisition of clinical trial samples (including human tissue, bone marrow aspirate, whole blood, plasma, serum, etc.) and ensure compliance with ICF permissions</p></li><li><p>Supports individual clinical study teams as required for all technical and operational sample-related matters for assigned projects by liaising with internal stakeholders working on ICF and other trial documents impacting samples and testing </p></li><li><p>Work closely with central lab and/or specialty lab project managers, clinical trial management team, and CRO to ensure samples are collected per protocol and assist with resolving any sample related issues or queries.</p></li><li><p>Oversees Study start up, closeout and overall life-cycle activities for assigned studies at central lab/specialty labs to support all samples and testing</p></li><li><p>Provides input on sample-related section in clinical trial-related (e.g. protocols and ICF) and other supporting documents</p></li><li><p>Works closely with data management lead and SKDL to determine how sample and testing data will be captured, blinded and transferred for clinical trials.</p></li><li><p>Enables transfer of sample/testing data from vendors through development and review of appropriate data transfer specification and related documents in collaboration with SKDL.</p></li><li><p>Provides guidance to clinical teams and clinical sites regarding collection and storage of samples acquired during clinical trials or other human sample acquisition projects</p></li><li><p>Works with scientists and clinical team to ensure sample collection and usage is in compliance with study protocol and applicable ICF</p></li></ul><br><h3><strong>This role may be for you if:</strong></h3><ul><li><p>You possess strong leadership tendencies, ability to proactively identify problems, determine resolutions, set priorities, and direct projects and work cross-functionally to manage expectations with excellent communication and collaborative skills and work well in a team-based environment. The CLSM Manager will be responsible for day-to-day oversight of multiple CLSMs, including responsibility for coaching, mentoring and performance management ensuring applicable key trial level milestones are achieved on schedule.</p></li><li><p>You demonstrate strong leadership skills and possess high level of emotional intelligence and effectively work collaboratively with colleagues, vendors and internally at Regeneron to ensure program success.</p></li></ul><p><strong>To be considered for this role,</strong> you must have a Bachelors, Minimum of 8 years pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams. Minimum of 5 years’ experience with Clinical Trials, focus on clinical sample collection. Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested. We need a strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required. We are seeking clinical study knowledge, demonstrated by knowledge in science and technology.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 10 May 2026 13:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[International Compliance Assistant (f/m/d) - 12 months contract, part-time]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47149]]></requisitionid>
    <referencenumber><![CDATA[R47149]]></referencenumber>
    <apijobid><![CDATA[r47149]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47149/international-compliance-assistant-fmd-12-months-contract-part-time/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The International Compliance Assistant plays a key role in supporting the smooth and effective operation of the International Compliance function. This position provides essential administrative, logistical, and coordination support, helping the team stay organized, connected, and on track.</p><p>Working closely with Compliance colleagues across regions and countries, the Compliance Assistant helps manage schedules, meetings, travel, documentation, and vendors, enabling the timely delivery of compliance activities and initiatives.</p><p>This is an ideal role for someone who enjoys keeping things running efficiently, working with multiple stakeholders, and contributing behind the scenes to a high‑impact function.</p><p><strong>International Compliance Assistant - Munich </strong></p><p>This is a part-time position on <strong>a 20 hours per week work schedule</strong>. The contract duration will be 12 months.</p><br><p><strong>A Typical Day:</strong></p><ul><li><p>Manage travel arrangements and support accurate expense reporting for team members</p></li><li><p>Coordinate logistics for compliance initiatives and events (e.g., team meetings, Integrity at Work day)</p></li><li><p>Support vendor coordination, including third‑party training providers</p></li><li><p>Maintain team and departmental calendars, including scheduling meetings and coordinating availability</p></li><li><p>Prepare meeting agendas, document outputs, and track follow‑up actions</p></li><li><p>Provide editorial support for correspondence, reports, and presentations</p></li><li><p>Plan and support in‑person team meetings</p></li><li><p>Coordinate cross‑functional meetings, including Country and Regional Compliance Committees</p></li><li><p>Consolidate data from multiple sources to support monitoring and reporting activities</p></li><li><p>Provide general administrative support to meet evolving team needs</p></li></ul><p><strong>This Role May Be For You, If You Have:</strong></p><ul><li><p>Strong organizational skills and the ability to manage multiple administrative tasks simultaneously</p></li><li><p>Excellent attention to detail, particularly when preparing meeting materials, tracking actions, and maintaining calendars</p></li><li><p>Strong written and verbal communication skills</p></li><li><p>Confidence coordinating logistics for meetings, events, and cross‑functional groups</p></li><li><p>Proficiency in Microsoft Office tools (Outlook, Word, Excel, PowerPoint) and comfort using digital tools for scheduling and data consolidation</p></li><li><p>Experience managing travel arrangements and supporting expense processes</p></li><li><p>Strong interpersonal skills and the ability to collaborate effectively with internal teams and external vendors</p></li><li><p>A high level of professionalism and discretion when handling confidential or sensitive information</p></li><li><p>Strong time‑management skills and the ability to work independently while meeting deadlines</p></li><li><p>A proactive, adaptable mindset, with the ability to anticipate needs and adjust to changing priorities</p></li></ul><p><strong>To Be Considered:</strong></p><ul><li><p>Fluency in English is required</p></li><li><p>A bachelor’s degree is preferred; equivalent professional experience (approximately 5 years) may be considered in lieu of a degree</p></li></ul><br><p>You’ll be part of a collaborative, international Compliance team where organization, teamwork, and attention to detail make a real difference. This role offers exposure to a broad range of compliance activities and stakeholders, with the opportunity to develop strong coordination and operational skills in a global environment.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Part_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 05:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Government Affairs Europe]]></title>
    <date><![CDATA[Sat, 09 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47381]]></requisitionid>
    <referencenumber><![CDATA[R47381]]></referencenumber>
    <apijobid><![CDATA[r47381]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47381/director-government-affairs-europe/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. </p><p>We are looking for a <strong>Director, Government Affairs Europe</strong> to help shape and advance our public policy strategy across key European markets. In this role, you will lead government affairs activities, build trusted stakeholder relationships, and navigate complex healthcare systems to support business objectives. You will play a central role in aligning policy initiatives with organisational priorities while representing our interests externally. This is a unique opportunity to influence policy environments and drive meaningful impact across the region.</p><p><strong>Director, Government Affairs Europe</strong></p><p><strong>Dublin, Madrid, Milan, Paris (Office based)</strong></p><p><strong>A Typical Day:</strong></p><ul><li>Leading government affairs and public policy activities across assigned European markets</li><li>Managing relationships with consultants to strengthen advocacy and policy influence</li><li>Developing advocacy strategies to support policy priorities and mitigate risks</li><li>Monitoring legislative developments and assessing impact on business operations</li><li>Representing the organisation in external forums and stakeholder engagements</li><li>Coordinating cross-functional teams to align policy activities with business goals</li><li>Supporting implementation of EU policies at national level to ensure compliance</li><li>Preparing policy analyses and briefing materials to inform strategic decisions</li></ul><p><strong>This Role may be for you:</strong></p><ul><li>You enjoy working across multiple countries and navigating diverse healthcare systems</li><li>You are comfortable influencing policy through stakeholder engagement and advocacy</li><li>You value building and maintaining strong external and internal relationships</li><li>You are motivated by translating complex legislation into strategic insights</li><li>You appreciate balancing strategic planning with operational execution</li><li>You thrive when coordinating with cross-functional and international teams</li><li>You are attentive to detail when tracking policy developments and compliance requirements</li><li>You enjoy representing an organisation in high-level external discussions</li></ul><p>To be considered, you must hold a Bachelor’s degree, with a minimum of <strong>7–10 years of experience in government affairs</strong>, public policy, or a related field within the pharmaceutical or healthcare industry. Demonstrated experience working with European healthcare systems and policy environments, along with managing external stakeholders or consultants, is required. Fluency in English is essential. An advanced degree in public policy, international relations, political science, law, or a related field is preferred, and proficiency in an additional European language such as German, French, Italian, or Spanish would be an advantage.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 09 May 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Technician, Sunday-Wednesday 1st shift]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47289]]></requisitionid>
    <referencenumber><![CDATA[R47289]]></referencenumber>
    <apijobid><![CDATA[r47289]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47289/process-technician-sunday-wednesday-1st-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Process Technician position with a Sunday-Wednesday 6:00am-4:30pm schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Process Technicians play a vital role in supporting our manufacturing operations. They provide operational, maintenance, and troubleshooting support for manufacturing process area maintenance through strict compliance with Standard Operating Procedures (SOPs) and cGMPs.</p><div><p><strong>Please note training will take place Monday-Friday 1st shift 6:00am-2:30pm for several weeks. Working hours thereafter will be Sunday-Wednesday 6:00am-4:30pm.</strong></p><p>As a Process Technician, a typical day might include the following:</p><ul><li><p>Performing daily operations, maintenance and repairs on utility systems, manufacturing equipment and building systems in a cGMP environment</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment</p></li><li><p>Identifying any off-nominal conditions with mechanical equipment and mechanical troubleshooting of manufacturing/utility equipment in a clean room environment</p></li><li><p>Performing daily Work Orders (WOs) and PMs and efficiently coordinating the workflow and documentation of PMs and WOs</p></li><li><p>Troubleshooting electrical equipment during off-nominal conditions; locating the source of trouble and arranging for/performing all necessary repairs</p></li><li><p>Coordinating with each impacted department and within Facilities Management when planned and unplanned work events occur</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Can interpret P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</p></li><li><p>Have prior experience in equipment maintenance or a related position requiring mechanical skills and abilities</p></li><li><p>Are safety-minded while looking for opportunities to continuously improve</p></li><li><p>Strive for compliance with regulatory, corporate, and site-specific policies and procedures</p></li><li><p>Can fully gown as required when entering and working on production floor</p></li><li><p>Are able to support a rotational on-call schedule</p></li></ul><p>To be considered for this position you must be willing and able to work Sunday-Wednesday 6:00am-4:30pm. Applicants should have an AAS degree, preferably in an Engineering or Construction Technologies related field, and the following minimum amounts of proven experience for each level:</p><ul><li><p>Process Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>Process Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role</p><p>#REGENTOSK</p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Precision Medicine Associate]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47375]]></requisitionid>
    <referencenumber><![CDATA[R47375]]></referencenumber>
    <apijobid><![CDATA[r47375]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47375/senior-precision-medicine-associate/]]></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 role will support the development, execution, and maintenance of automation and data solutions across Samples, Kits, Data, and Logistics (SKDL) within Precision Medicine Operations. This role is a hands-on technical contributor focused on building, maintaining, and improving tools, dashboards, and data workflows that support clinical sample and data operations.</p><p>The individual will apply programming and data engineering skills to help streamline operational workflows, improve data quality and visibility, and support timely delivery of biomarker samples and data. The role works closely with senior SKDL leaders, study teams, and lab partners to execute defined automation and data initiatives and to resolve operational issues related to samples and data.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Develop, enhance, and maintain automation tools, scripts, and code workflows to reduce manual effort across sample, kit, data, and logistic operations.</p></li><li><p>Co-design, build and maintain reporting documents and dashboard to support routine sample and data tracking, issue identification, and operational reporting.</p></li><li><p>Implement automated coding pipelines to perform data cleaning, transformation, and integration routines under guidance from senior technical leads.</p></li><li><p>Support extraction and consolidation of data from lab vendor reports, operational trackers, and internal systems.</p></li><li><p>Data Engineering & Integration</p></li><li><p>Support development of dataset frameworks, mappings, and metadata across samples, kits, and lab data. Assist with API-based or file-based data integra</p></li><li><p>Adhere to established data governance and security practices to ensure compliant handling of confidential clinical data.</p></li><li><p>Support operational oversight of biosamples and related data across clinical studies, including tracking collection, shipment, storage, and data completeness.</p></li><li><p>Participate in investigation and resolution of sample or data-related issues in collaboration with senior team members and lab vendors.</p></li><li><p>Maintain operational documentation and metrics related to sample status, data quality, and logistics events.</p></li><li><p>Support study meetings, documentation, and routine communications with labs and internal stakeholders.</p></li></ul><p><strong>This role may be for you, if you:</strong></p><ul><li><p>Working proficiency in one or more programming languages such as Python, R, SQL, MATLAB, or Perl.</p></li><li><p>Experience with data processing, basic database concepts, and dashboarding or visualization tools.</p></li><li><p>Foundational understanding of structured data concepts (tables, entities, relationships, metadata).</p></li><li><p>Exposure to clinical sample workflows, lab data, LIMS, or operational tracking systems preferred.</p></li></ul><p><strong>To be considered for this role, you must have a</strong> Bachelor’s degree (or higher) in a scientific, computational, engineering, or related discipline. 5+ years of relevant experience in clinical research, data operations, laboratory operations, or a related setting (biotech, pharma, CRO, academic research).</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$83,800.00 - $136,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Engineer]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47030]]></requisitionid>
    <referencenumber><![CDATA[R47030]]></referencenumber>
    <apijobid><![CDATA[r47030]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47030/senior-automation-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Our Automation Engineers keep our cutting-edge process controls and process monitoring systems running at peak efficiency. We provide unsurpassed expertise in designing, developing, implementing, and optimizing Regeneron’s sophisticated biopharmaceutical manufacturing processes.</p><p>As a Senior Automation Engineer, a typical day might include the following:</p><ul><li>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures.</li><li>Using PLCs and HMIs to provide technical support and solutions to Manufacturing, Quality Control, and Facilities according to established SOPs and departmental practices.</li><li>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems.</li><li>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines.</li><li>Supporting small manufacturing, engineering, and validation projects.</li><li>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action.</li><li>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols.</li></ul><p>This job might be for you if you:</p><ul><li>Want to support our extraordinary team to produce the highest quality medicines for patients as efficiently as possible to change people’s lives.</li><li>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better.</li><li>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly.</li><li>Have a knack for compiling documentation and enjoy it!</li><li>Don’t get frustrated with a meticulous process of change control, investigations and corrective actions.</li></ul><p>To be considered for this position, we prefer a BS in Engineering or a related field and 5+ years of relevant experience. Equivalent experience with process control systems and/or data acquisition systems may be considered in lieu of degree. </p><p>We look for experience in the design and maintenance of process control systems and/or data acquisition systems. We may consider candidates with limited experience programming and troubleshooting PLCs. Some experience in a regulated manufacturing environment is preferred. We use Allen-Bradley and Siemens control system products and video graphic chart recorders; specific knowledge with these products is ideal.​ Experience programming and troubleshooting with DeltaV DCS is desirable.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 09:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Associate, Analytics: Synthetic and Bioconjugation Scale-Up Technologies (SBST) (1 of 2)]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47642]]></requisitionid>
    <referencenumber><![CDATA[R47642]]></referencenumber>
    <apijobid><![CDATA[r47642]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47642/process-development-associate-analytics-synthetic-and-bioconjugation-scale-up-technologies-sbst-1-of-2/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated <strong>Process Development Associate </strong>(PDA) to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group. In this hands-on, lab-based role, you will generate high-quality, robust analytical data, support method development, and help characterize bioconjugates and critical intermediates to advance our growing and diverse bioconjugate pipeline. You will partner closely with cross-functional teams and external collaborators by generating key data to drive data-driven decisions that supports drug development in clinical to commercial stage.</p><p><em><strong>A Typical Day in the Role of Process Development Associate Might Look Like:</strong></em></p><ul><li><p>Perform hands-on analytical testing, method development, and characterization of bioconjugates and critical intermediate raw materials.</p></li><li><p>Analyze and present key data clearly to enable timely, data-driven decisions across a broad audience.</p></li><li><p>Partner with internal and external analytical groups to execute, establish and transfer fit-for-purpose analytical methods.</p></li><li><p>Communicate plans and results within cross-functional teams to enable program success.</p></li><li><p>Capture and document data in ELN entries in a timely manner to support program timelines.</p></li><li><p>Help with building business workflows to standardize sample and data management</p></li><li><p>Maintain compliance with lab and environmental safety requirements and promote a safe lab environment.</p></li><li><p>Be a responsible lab citizen by supporting equipment upkeep, maintaining an organized workspace, and proactively planning for lab resources.</p></li><li><p>Help with troubleshooting equipment and scheduling with Vendor service engineers</p></li></ul><p><em><strong>This Role May Be For You If You:</strong></em></p><ul><li><p>Enjoy working in the lab, and committed to generating high quality, reproducible data</p></li><li><p>Have strong initiative and aim to complete challenging tasks and learn new technologies in a timely manner.</p></li><li><p>Have strong fundamental understanding with analytical techniques and method development for antibody, bioconjugates, and/or small-molecule characterization.</p></li><li><p>Are capable of working in a fast-paced and collaborative environment involving cross-functional teams.</p></li><li><p>Communicate clearly (written and verbal) and build strong working relationships.</p></li><li><p>Can think critically and demonstrate problem-solving skills and comfortable navigating ambiguity.</p></li></ul><p>B.S. in chemistry, biochemistry, biology, chemical engineering, or a related field with 0–1 year of relevant laboratory experience (academic or industry); hands-on wet lab experience required. Fundamental knowledge of synthetic molecules (e.g., small molecules, PEG, peptides, and/or oligos) and/or protein analytical techniques. Strong communication skills (written and verbal) and the ability to present data clearly. Ability to work independently and collaboratively across cross-functional teams; strong attention to detail and documentation practices. Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment.</p><p><strong> </strong></p><p><strong>Preferred Qualifications</strong></p><ul><li><p>Experience with analytical characterization tools such as electrophoresis, HPLC separation, and UV spectroscopy.</p></li><li><p>Knowledge or experience in working with biological therapeutics, bioconjugates, or related modalities.</p></li></ul><p><strong> </strong></p><p><strong>#pmpd</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III,  Analytics: Synthetic and Bioconjugation Scale-Up Technologies (SBST)]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47644]]></requisitionid>
    <referencenumber><![CDATA[R47644]]></referencenumber>
    <apijobid><![CDATA[r47644]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47644/process-development-engineer-iii-analytics-synthetic-and-bioconjugation-scale-up-technologies-sbst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron’s Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated <strong>Process Development Engineer III</strong> to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group. In this role, you will serve as the analytical lead to develop fit-for-purpose analytical methods, transfer, and provide troubleshooting support to advance diverse bioconjugate pipeline. You will lead and implement analytical deliverables working closely with bioconjugation teams and internal/external collaborators (CDMOs) to advance bioconjugate programs from development to commercialization.</p><p><em><strong>A Typical Day in the Role of Process Development Engineer III Might Look Like:</strong></em></p><ul><li><p>Independently design and execute analytical testing, method development and characterization to enable bioconjugate process development.</p></li><li><p>Serve as the subject matter expert to lead and design analytical deliverables: robust method development, method transfer to internal/external receiving labs, training, and troubleshooting to move program forward.</p></li><li><p>Connect, interpret, communicate complex results into clear actionable next steps to technical and non-technical audiences to persuade and drive timely decisions.</p></li><li><p>Author high-quality documentation (i.e., procedures, development and characterization reports, ELN entries) in a timely manner to support program timelines.</p></li><li><p>Drive, build and improve business workflows: documentation standardization, data digitization, and sample management.</p></li><li><p>Maintain compliance with lab and environmental safety requirements and promote a safe lab environment.</p></li><li><p>Proactively scout, evaluate, and implement new or improved technologies for high-throughput analytics and real-time decision making</p></li><li><p>Lead equipment upkeep, troubleshooting, maintain an organized workspace, and proactively plan for lab resources.</p></li><li><p>Mentor and support peers and junior team members (direct and/or indirect via matrix).</p></li></ul><p><em><strong>This Role May Be For You If You:</strong></em></p><ul><li><p>Enjoy working in the lab to advance exciting new drug modalities to patients</p></li><li><p>Posses strong initiative and aim to complete challenging tasks and learn new technologies quickly.</p></li><li><p>Possess strong hands-on experience and fundamental understanding of analytical techniques and method development for antibody, bioconjugates, and/or synthetic molecule (small molecule, peptides, and oligos) characterization, including relevant software.</p></li><li><p>Lead with customer centric mindset with providing analytical support to advance drug development in different phases of the program</p></li><li><p>Thrive in a fast-paced, highly collaborative environment working on complex problems.</p></li><li><p>Communicate clearly (written and verbal), simplify messages for impact, and build strong working relationships.</p></li><li><p>Think critically and apply strong problem-solving skills, and comfortable navigating ambiguity.</p></li></ul><p>This role requires a B.S. with 10+ years of relevant experience, or M.S. with 7+ years or recent PhD with 0-3 years of relevant experience in chemistry, biochemistry, biology, chemical engineering, or a related field. Hands-on experience with analytical method development for antibody, bioconjugate, and/or synthetic molecules (e.g., small molecule, PEG, peptides, and/or siRNA) such as electrophoresis, HPLCs, LC-MS, UV spectroscopy, plus associated software (e.g., Empower). Hands-on experience in transferring methods to internal/external labs, and troubleshooting. Demonstrated experience serving as an analytical lead for bioconjugate programs, collaborating effectively with internal teams and external CDMOs. Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences. Experience drafting analytical methods, development and characterization reports to support regulatory filing. Ability to work independently and collaboratively across cross-functional teams to persuade and drive data-based decision. Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment.</p><p><strong>#pmpd</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Sample Management]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47309]]></requisitionid>
    <referencenumber><![CDATA[R47309]]></referencenumber>
    <apijobid><![CDATA[r47309]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47309/associate-scientist-sample-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Serves as an Associate Scientist to support the operation of automated lab equipment. Under the direct supervision of management, performs routine technical tasks and will begin to manage, organize, and troubleshoot more independently. Has operational knowledge of laboratory equipment. Has a basic understanding of clinical study protocols and procedures for specimen handling and storage. </p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li><p>Operating automated laboratory systems, including biospecimen storage/retrieval equipment and liquid handlers</p></li><li><p>Troubleshooting system errors and performing routine maintenance under supervision</p></li><li><p>Assisting in training and supporting teams who use automated systems</p></li><li><p>Communicating with internal groups and external vendors to resolve equipment‑related needs</p></li><li><p>Supporting qualification and validation activities for new automated systems</p></li><li><p>Working with automation programs with guidance</p></li><li><p>Using LIMS to accurately track sample movement in real time</p></li><li><p>Using ELN for documenting equipment‑related activities</p></li><li><p>Using VBA macros to estimate and record run times; may write simple macros to support workflow organization</p></li><li><p>Maintaining GLP compliance for all lab work, documentation, and sample handling</p></li><li><p>Keeping individual and shared lab spaces clean and organized</p></li><li><p>Following all laboratory safety requirements and helping identify and correct safety concerns</p></li><li><p>Sharing information effectively with management and team members</p></li><li><p>Participating in team or sub‑team meetings and occasionally presenting work</p></li><li><p>Demonstrating professionalism, integrity, and a strong work ethic</p></li><li><p>Engaging in ongoing professional development and communicating regularly with management regarding performance</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Work well in a team‑oriented environment and can manage multiple tasks effectively</p></li><li><p>Communicate clearly and professionally with colleagues across departments</p></li><li><p>Are organized, detail‑oriented, and proactive in your work</p></li><li><p>Are comfortable learning new systems, tools, and automated technologies</p></li><li><p>Can follow established procedures while also identifying opportunities for improvement</p></li><li><p>Are committed to maintaining high standards of quality, safety, and compliance</p></li><li><p>A Bachelor’s degree with 0–4 years of relevant experience</p></li><li><p>A Master’s degree with 0–2 years of relevant experience</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Statistical Programming - Pharmacometrics]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47328]]></requisitionid>
    <referencenumber><![CDATA[R47328]]></referencenumber>
    <apijobid><![CDATA[r47328]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47328/associate-director-statistical-programming-pharmacometrics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Associate Director Pharmacometrics Programming </strong>provides timely support to the study team on all programming matters according to the project strategies. Provides project leadership, resource planning/coordinating deliverables within project or across multiple projects. Lead programming support for processing/analyzing/storing data from clinical studies according to a Statistical Analysis Plan, clinical pharmacology report requirement and programming specifications using internal standards and guidelines. Providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. The incumbent is responsible for addressing administrative functions required for project management such as compilation of resource requirements and milestones, identifying/communicating changes in project requirements that may affect key deliverables at the project level, and working with the department head to develop resource strategies.</p><p><strong><em>This position requires 4 days onsite presence based out of our Tarrytown, NY or Warren, NJ location.</em></strong></p><p><strong>A typical day might include the following:</strong></p><ul><li><p>Lead the programming and QC of analysis datasets, TFL's across multiple projects or standard tools following Regeneron standard data models or user requirements. Representation of PMX programming functions and coordination of activities with cross line functions and support planning/coordinating timelines in data exchange, deliverables. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies.</p></li><li><p>Lead the integration of data across studies in support of Exposure-response, PopPK and PopPKPD analysis and 2.7.2.</p></li><li><p>Provide programming support for all PMX deliverable in HAR request, data driven analysis, publications, conference</p></li><li><p>Plan and lead the creation and validation of electronic submission requirements (i.e. annotated CRF, data export files, define documents).</p></li><li><p>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Expert SAS programming skills (SAS (Base, Stat, Macro, graph) in a clinical data environment</p></li><li><p>Understanding of relational database structure and reporting systems utilizing multiple data delivery applications</p></li><li><p>Strong Experience/knowledge with implementing standardization methodology, creation of current CDISC data standards.</p></li><li><p>Comprehensive understanding of biostatistics, pharmaceutical clinical development (i.e. safety deliverables, efficacy analysis), experienced in data handling, process and analysis and able to understand/perform Pharmacokinetics, immunogenicity, exposure response analysis in timely manner</p></li><li><p>Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.</p></li><li><p>Good Skilled in use of relevant software, including Window SAS, SAS studio (Base, Stat, Macro, graph), MS-Excel, R programming and/or Python.</p></li><li><p>Good knowledges in AI use case in statistical programming and data sciences.</p></li></ul><p><strong>To be considered for this opportunity</strong> you must have a Master in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline. 10+ years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. Experience in project and people management, and expertise in one or more therapeutic areas is also preferred. SAS Certification desirable in statistics, computer science.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Scientist, Bispecifics and Antibody Engineering]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46800]]></requisitionid>
    <referencenumber><![CDATA[R46800]]></referencenumber>
    <apijobid><![CDATA[r46800]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46800/sr-scientist-bispecifics-and-antibody-engineering/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a motivated and result-driven Sr. Scientist to join our fast-paced and innovative Antibody Engineering team of Bispecifics and Antibody Engineering Department. You will be part of a group of diverse talents responsible for designing, producing, and characterizing novel next-gen antibody and protein therapeutics across multiple therapeutic areas, including obesity & muscle metabolism, connective tissue diseases, and immunology/inflammation, at Regeneron. This position will directly impact both pipeline advancement and innovative platform development at this exciting time, as significant advances in antibody engineering have already propelled approvals of multiple next-gen antibody-based therapies in many indications. </p><p><strong>As a Sr. Scientist, a typical day may include the following:</strong></p><ul><li><p>Independently design and construct novel bispecific or multi-specific antibodies.</p></li><li><p>Express (transfect), purify, and characterize novel antibodies.</p></li><li><p>Develop and perform in vitro high-throughput biochemical and cell-based assays (ELISA, flow cytometry binding, reporter assay, AlphaLISA, receptor degradation assay)</p></li><li><p>Apply molecular biology techniques (cloning, PCR, SDS-PAGE, Western blotting) for DNA and protein generation and characterization.</p></li><li><p>Analyze data, troubleshoot experiments, provide accurate presentations to the management and communicate results in multi-functional team and department meetings.</p></li><li><p>Ability and enthusiasm for independently learning new methods and software.</p></li><li><p>Maintain up-to-date data analysis, Benchling database, and a timely record of the electronic notebook (ELN)</p></li></ul><p><strong> </strong></p><p><strong>This role may be for you if:</strong></p><ul><li><p>You enjoy working in a highly collaborative and fast-paced environment</p></li><li><p>You have a desire to learn new skills and advance your career in a cutting-edge environment </p></li><li><p>You have strong communication and presentation skills</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this role</strong>, <strong>you must have:</strong> a PhD in biology, molecular biology, biochemistry, cell biology, or immunology. We need someone with expertise in cell culture, flow cytometry /FACS, and Bioassays. Experience with cell-free expression, high-throughput bioassays, protein purification, and/or molecular biology is preferred, but we are willing to train. You should have experience designing well-controlled experiments that yield reliable results, and be able to analyze data and draw conclusions. You will help support the increasing and exciting unmet demand for the design, production, and functional characterization of novel bispecific or multispecific antibody projects. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 13:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Customer Insights & Analytics - Neurology]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45023]]></requisitionid>
    <referencenumber><![CDATA[R45023]]></referencenumber>
    <apijobid><![CDATA[r45023]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45023/director-customer-insights-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>Regeneron is seeking a Director, Insights & Analytics (I&A) to join our team! As part of an exciting upcoming launch in generalized myasthenia gravis (gMG), this role will play a critical role in shaping analytics, insights, and decision-making during a pivotal moment for the organization</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, I&A will report into an Executive Director, I&A within the Commercial Strategy and Insights and Analytics (CSI&A) department. This role will oversee a high-performing team (internal and external) responsible for generating actionable insights from a broad set of I&A sources, to inform business decisions. The role will partner with and serve as a strategic advisor to the Neurology Commercial Business Unit (CBU) and will partner with other leaders to grow and develop talent within the CSI&A team.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><p>1) Lead the I&A Neurology team in providing business analytics, customer insights and competitive intelligence to address all commercialization needs</p><p>2) Collaborate with the ED, I&A to set the strategic I&A direction that aligns with overarching priorities and helps drive launch excellence</p><p><em>Develop</em></p><p>3) Foster innovative solutions and a design-thinking approach aligned with strategies for the Neurology business.</p><p>4) Develop people from both a functional skills and leadership perspective, with the goal of growing internal talent</p><p>5) Assess and implement novel methodologies and frameworks to <strong>a)</strong> garner meaningful insights to inform business decisions a rapidly developing Neurology CBU; and <strong>b)</strong> enhance brand differentiation and impact</p><p><em>Partnership and collaboration</em></p><p>6) Lead efforts to identify and crystalize insights that inform strategic plans</p><p>7) Collaborate with the Neurology CBU and other members of leadership to identify, predict and inform business decisions relating to the competitive outlook for gMG</p><p>8) Develop and maintain a mutually beneficial partnership with CBU stakeholders; ensure insight generation and feedback are embraced; strike a balance between project rigor, timelines and ability to influence decisions</p><p>9) Coordinate alignment with stakeholders on all insights and analytics agendas</p><p>10) Work with other CSI&A leaders to develop standardized adoption of capabilities such as marketing mix, promotional optimization, data science, market structure analysis, patient/treatment flow modeling, analog modeling and ML/AI methodologies across I&A</p><p><em>Execute</em></p><p>11) Proactively communicate with the Neurology CBU and provide strategic recommendations and insights as well as anticipated future needs</p><p>12) Construct and deliver integrated business reviews, I&A summary overviews with leadership from Neurology and CSI&A</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum BS with 12+ (or MS with 10+) years of pharmaceutical/biotech commercial experience, in roles of increasing accountability; prior experience with market-leading brands required and neurology or rare disease experience is desired</p></li><li><p>Functional expertise in business analytics, HCP consumer/patient insights, primary research methods, analog forecast development and competitive intelligence</p></li><li><p>Prior experience managing I&A groups with responsibility for analytics, HCP consumer/patient insights, market access analytics, and competitive intelligence</p></li><li><p>Demonstrated knowledge of the legal and regulatory environment, as it relates to commercialization in the pharmaceutical/biotechnology industry</p></li><li><p>Knowledge of data industry standards</p></li><li><p>Proven ability to influence, communicate and negotiate with all levels of management across functional and business unit boundaries</p></li><li><p>Extensive experience with managing numerous projects concurrently against stringent deadlines</p></li><li><p>Prior experience working with I&A projects and initiatives where a balance between project rigor and timeliness was needed</p></li><li><p>Ability to think strategy to execution, with hands-on experience in implementing large initiatives with cross-functional stakeholders</p></li><li><p>Expertise in data visualization and data storytelling</p></li><li><p>Strong interpersonal, facilitation and communication skills, with the ability to resolve conflict, drive consensus and work across multiple departments</p></li><li><p>Strong organizational, project management, influencing and change management skills </p></li><li><p>Proven ability to manage multiple project and priorities concurrently, while meeting stringent deadlines</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[MR（Medical Representatives）- Oncology *Saitama Area]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47140]]></requisitionid>
    <referencenumber><![CDATA[R47140]]></referencenumber>
    <apijobid><![CDATA[r47140]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47140/mr-medical-representatives-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>We’re Hiring: Medical Representative (Oncology)</strong></p><p>At Your Company Name, we are driven by the philosophy of prioritizing patients first and advancing the field of oncology. As a Medical Representative specializing in oncology, you’ll play a pivotal role in expanding our business while delivering value to patients and healthcare providers. This is an exciting opportunity to contribute to meaningful innovations in healthcare while building strong relationships with key stakeholders. Join us and be part of a team committed to making a difference in patients’ lives.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Build and maintain relationships with medical professionals in the oncology field, collaborating closely to meet patients’ needs.</p></li><li><p>Develop and execute area-specific sales strategies and manage budgets to achieve sales targets effectively.</p></li><li><p>Monitor market trends and adapt activity plans to align with changing dynamics.</p></li><li><p>Strategically utilize data to craft and implement actionable plans aimed at achieving business objectives.</p></li><li><p>Manage administrative tasks such as expense reports and activity documentation with precision and timeliness.</p></li><li><p>Attend and actively participate in regional and national business meetings.</p></li><li><p>Complete company-provided training programs to stay updated on industry knowledge and best practices.</p></li><li><p>Represent the company at conferences and events, fostering meaningful connections in the oncology space.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You have over five years of experience as an MR and a proven track record of building relationships with Key Opinion Leaders (KOLs) or Area Opinion Leaders (AOLs).</p></li><li><p>You are passionate about putting patients first and excel at engaging clients with empathy and professionalism.</p></li><li><p>You thrive in a role that requires strategic planning, execution, and adaptability to changing market conditions.</p></li><li><p>You are skilled at delivering impactful presentations and communicating effectively in both individual and group settings.</p></li><li><p>You have experience working with oncology products, diseases, or treatment concepts and can articulate their value.</p></li><li><p>You possess general proficiency with PC tools and Office software.</p></li><li><p>You enjoy a dynamic work environment that includes occasional travel, including weekends, when necessary.</p></li></ul><p><strong>To Be Considered:</strong></p><p>Candidates must have at least five years of MR experience, a bachelor’s degree or equivalent, and a valid driver’s license. Preferred qualifications include experience in the oncology domain, familiarity with competitive products, and knowledge of biological drugs. While English proficiency is a plus, it is not mandatory for this role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager-Immunology-Missouri]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47676]]></requisitionid>
    <referencenumber><![CDATA[R47676]]></referencenumber>
    <apijobid><![CDATA[r47676]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47676/field-reimbursement-manager-immunology-missouri/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Missouri]]></city>
    <state><![CDATA[Missouri]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The 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><p><strong>When & where: </strong></p><ul><li><p>Remote role</p></li><li><p>Location: Missouri</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment. 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></li><li><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></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, in efforts to streamline the coverage and specialty pharmacy processes to acquire alliance products</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></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelors 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.</p></li><li><p>You have biologic expertise (Specialty Pharmacy/Buy & Bill)</p></li><li><p>You are a standout colleague and able to collaborate</p></li><li><p>You can optimally communicate across multiple regions via different mediums</p></li><li><p>You can get results with your activity</p></li><li><p>You are capable with meeting the expectations of internal and external customers</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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 17:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Mid South]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47573]]></requisitionid>
    <referencenumber><![CDATA[R47573]]></referencenumber>
    <apijobid><![CDATA[r47573]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47573/regional-director-neurology-mid-south/]]></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[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the [INSERT] Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Mid South (North Carolina, Virginia, South Carolina, Tennessee</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Device Development Engineer (Project Leadership)]]></title>
    <date><![CDATA[Mon, 26 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44516]]></requisitionid>
    <referencenumber><![CDATA[R44516]]></referencenumber>
    <apijobid><![CDATA[r44516]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44516/sr-device-development-engineer-project-leadership/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Sr. Device Development Engineer to join our project lead team. The Sr. Device Development Engineer will drive the end-to-end development of a device combination product and/or platform delivery system, within a specific therapeutic area (Ophthalmic, Immunology/Inflammation, Cardiometabolic, etc.). They will provide comprehensive leadership in engineering product management, regulatory compliance (design controls), and multi-functional collaboration with internal and external partners, for the combination product device.</p><p>A typical day for a Sr. Device Development Engineer might include:</p><ul><li>Leads multidisciplinary engineering project teams (Human Factors, V&V Engineering, Manufacturing Engineer, Quality Engineering) through the complete device design and development lifecycle of a combination product development within the Regeneron Pipeline.</li><li>Defines detailed product requirements and specifications with commercial, clinical, and other development/strategy collaborators.</li><li>Defines technical specifications and design requirements in collaboration with engineering teams (manufacturing, verification, packaging etc.)</li><li>Responsible for all user needs and requirements to be validated through design and development.</li><li>Develops, manages, and communicates development program plans, risks, timelines, and budgets to internal and external team members.</li><li>Integrate device development activities with Chemistry Manufacturing Controls (CMC) and Global development timing and goals.</li><li>Supports global internal manufacturing and external manufacturing teams around relevant design and process development information transfers.</li><li>Leads all aspects of product testing and quality assurance processes for the specific device development.</li><li>Ensures comprehensive and compliant Design History File (DHF) is developed and ensures to meet regulatory and quality requirements (21CFR Part 3 and 21 CFR 820.30).</li><li>Supports management in related clinical and commercial regulatory activities that is related to the device development (ie: IND/IMPD, BLA Submission, Clinical Pharmacy Manuals etc.)</li><li>Understands design inputs and outputs of multiple delivery systems and how it can impact end users.</li><li>Supports management and/or therapeutic area device project leads, in strategic product launch and go-to-market plans for the device development.</li></ul><p>This role might be for you if you:</p><ul><li>Understand relevant FDA regulations, particularly 21 CFR Part 3 and 21 CFR 820.30.</li><li>Have experience with design history file management (21 CFR 820.30).</li><li>Possess strong project management and interpersonal skills and strong analytical and problem-solving capabilities.</li><li>Can balance business objectives with technical constraints.</li><li>Can work effectively across multiple functional teams.</li><li>Enjoy working in a fast-paced, multifaceted research and development environment.</li><li>Are willing and able to travel for partner meetings, audits, and project coordination activities.</li></ul><p>To be considered for the Device Development Engineer you must have a B.S in Engineering and 5+ years or relevant experience; or equivalent combination of education & experience. Previous experience in product management/project management/ and/or project leadership related activities is required. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $143,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 27 Jan 2026 09:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ICSR Knowledge & Process Optimization]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45882]]></requisitionid>
    <referencenumber><![CDATA[R45882]]></referencenumber>
    <apijobid><![CDATA[r45882]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45882/director-icsr-knowledge-process-optimization/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director, ICSR Knowledge & Process Optimization to join our organization.</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director of ICSR Knowledge & Process Optimization is accountable for developing, maintaining, and continuously improving global procedures, standards, and tools that enable high-quality, compliant, and efficient individual case safety report (ICSR) processing and adverse event reporting across both developmental and marketed products. This role ensures end-to-end ICSR process robustness—from intake through expedited submissions and periodic reporting—by driving harmonized procedures, risk-based quality controls, and technology-enabled automation. The Director partners closely with GPS Standards and Training, Signal Management, Safety Sciences, Clinical Development, Quality/QA, Regulatory, Medical Information, IT, and Commercial to ensure timely compliance with global regulations while advancing operational excellence.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Ability to further develop and maintain processes for high quality and compliant</p></li><li><p>ICSR case processing from all sources for reporting to all applicable destinations. This includes owning the global ICSR process framework: standards, SOPs, Work Instructions (WIs),</p></li><li><p>Job aides, data entry conventions (DECs), templates, decision trees, and training curricula for all case types for the various resources performing case evaluation, medical assessment, and submissions.</p></li><li><p>Ensure procedural alignment to global regulations and guidance.</p></li><li><p>Map end-to-end processes (intake → triage → data entry → medical review → case finalization → submissions → follow-up → reconciliation); identify waste, bottlenecks, and process failures. This includes partnering with IT/Safety Systems to evaluate, pilot, and scale technologies and automation.</p></li><li><p>Define and review key performance indicators to ensure training compliance and effectiveness (e.g. first time right (FTR); rework/cycle time; quality event/CAPA closure timelines, etc.)</p></li><li><p>Curate and maintain the ICSR Knowledge Base (product/study-specific conventions, seriousness criteria, causality heuristics, MedDRA coding conventions, follow-up rules, local regulatory nuances, partner agreements).</p></li><li><p>Standardize and deploy role-based training and certification for internal teams and vendors; measure learning effectiveness and error reduction.</p></li><li><p>Partner with Vendor Relationship Management/QA/other stakeholders to ensure vendor procedures align to sponsor standards; define hand-offs, SLAs, and reconciliation controls (e.g., MI/Call Center, literature vendors, third party vendors).</p></li><li><p>Oversee readiness for internal audits and Health Authority inspections; lead remediation plans and CAPAs related to ICSR processes.</p></li><li><p>Performs other related duties as assigned or requested per business needs.</p></li><li><p>Able to independently identify, analyze, and resolve moderate to complex issues and trends. </p></li><li><p>Strong knowledge of global pharmacovigilance regulations, systems, and processes and ability to translate those into efficient and auditable procedures. </p></li><li><p>Previous people management experience with the ability to mentor and develop direct reports. </p></li><li><p>Excellent written and verbal communication skills. Able to express complex ideas. </p></li><li><p>Able to align diverse stakeholders and influence across teams, departments and geographies. </p></li><li><p>Able to identify and document regulatory non-compliance and any related issues. </p></li><li><p>Plans and executes change management; measures adoption and outcomes. </p></li><li><p>Uses metrics to prioritize and verify improvements; comfortable with data and dashboards. </p></li><li><p>Excellent organizational and interpersonal skills. </p></li><li><p>Attention to detail; able to identify and resolve discrepancies on compliance reports.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor's Degree in one of the life sciences or clinical research and/or a licensed healthcare professional required.</p></li><li><p>Minimum of 12 years of experience in safety and safety reporting.</p></li><li><p>Equivalent combination of relevant education and experience.</p></li><li><p>Computer literacy and experience working with Microsoft Office (Word, Excel, PowerPoint) required</p></li><li><p>Excellent knowledge of Argus and its applications.</p></li><li><p>Excellent verbal and written communication skills required.</p></li><li><p>Excellent interpersonal and organizational skills required.</p></li><li><p>Ability to work independently, prioritize effectively and work in a matrix team environment required.</p></li><li><p>Ability and willingness to travel domestically as required.</p></li></ul><p>#GDRAJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 08:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Inspection Management (GCP)]]></title>
    <date><![CDATA[Tue, 10 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R38901]]></requisitionid>
    <referencenumber><![CDATA[R38901]]></referencenumber>
    <apijobid><![CDATA[r38901]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r38901/associate-director-inspection-management-gcp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management of GCP, GVP and GLP inspections. The GDQIM IML will engage with key stakeholders, build strategic partnerships working and liaising with Clinical Study teams, relevant functions and other GDQ functions to support teams with inspection preparation activities on all Regeneron-sponsored clinical trials.</p><p><strong>In this role, a typical day might include the following:</strong></p><p>Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.<br>• Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.<br>• Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.<br>• Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.<br>• Identifying and discussing with the Clinical Study Teams potential issues and/or gaps, in advance of an impending inspection, that may require strategies to mitigate risk and/or provide additional clarification to an inspector.<br>• Ensuring the preparation, management and conduct of inspection preparation sessions which include mock inspections, trainings, and clinical site preparation visits working with GDQA team to identify and mitigate risks to clinical programs.<br>• Serving as the back room lead/co-lead or front room co-lead, responsible for explaining, managing,and ensuring the execution of all activities, including managing the tracking of requests and inquiries, and coordinating requests for responses from relevant personnel during any regulatory inspection conducted worldwide.<br>• Responsible for managing the preparation and provision of timely inspection updates and daily/end of inspection summaries to GD Executive and Senior Management, in addition to any other key relevant internal and external stakeholders.<br>• Responsible for managing inspection response development, and Corrective Actions/Preventive Actions (CAPA) follow-up activities alongside other GDQIM colleagues, cross-functional stakeholders, and process owners.<br>• Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.</p><h3><strong>This role may be for you if have:</strong></h3><p>• Advanced knowledge, understanding and application of GCP, and/or GVP <br>guidelines including the management of significant/complex quality issues <br>and compliance activities.<br>• Extensive experience with participating in, and supporting, Regulatory <br>Agency Inspections of Investigator Sites, Sponsors and Clinical Research <br>Organizations (CROs) in a GxP environment, including inspection <br>preparation, facilitation, and follow-up.<br>• Effective management of interpersonal relationships, stakeholder <br>engagement, and collaborations.<br>• Demonstrated ability to interface and collaborate effectively with other <br>Managers and Directors within, and external to, the organization.<br>• Extensive experience in providing training and presenting information on <br>key quality and regulatory compliance information.</p><p><strong>To be considered for this opportunity we are looking for:</strong></p><p>Bachelor's degree with a minimum of 10 years of relevant <br>healthcare/pharmaceutical industry experience.<br>• Experience working in either a quality/compliance role (e.g., Quality <br>Management, Quality Assurance etc.), or in a Clinical Development role <br>with expertise and/or transferable skills related to Good Clinical Practice <br>(GCP), and/or Good Pharmacovigilance Practice (GVP).<br>• Experience in training, supervising, line management, mentoring and <br>development of staff, and leading a small team</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 11 Mar 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Regeneron Genetics Medicines]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46057]]></requisitionid>
    <referencenumber><![CDATA[R46057]]></referencenumber>
    <apijobid><![CDATA[r46057]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46057/manager-clinical-scientist-regeneron-genetics-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a Manager, Clinical Scientist to join our Genetics Medicines team. The Manager, Clinical Scientist assists in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Manager works in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to the Sr Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p><strong>As a Manager within Clinical Sciences, a typical day may include the following:</strong></p><ul><li>Member of the Clinical Study Team and the Global Clinical SubTeam; regularly attends and actively participates in study team meetings</li><li>May contribute to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments</li><li>Develops/maintains basic understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and limited knowledge of disease and drug landscape</li><li>Applies basic scientific expertise to support execution of clinical research and development studies for early and/or late stage assets</li><li>May assist with preparation of documents related to trials, such as medical monitoring plans, SAPs, informed consents, clinical components of the Clinical Study Reports and regulatory documents; collaborate with others for scientific and foundational guidance</li><li>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</li><li>May contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority)</li><li>Supports clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</li><li>Supports identification of data trends and potential inconsistencies in data across assigned studies and raises</li><li>Exhibits basic research and analytical knowledge to understand how study objectives and design impact data analysis; supports identification of critical risks and mitigations to study</li></ul><p><strong>This role may be for you if:</strong></p><ul><li>Demonstrated basic knowledge of the drug development process, Good Clinical Practice, study design and clinical research methodology; beginner level medical writing skills</li><li>Demonstrate some ability to influence within study team</li><li>Independently resolves most issues and complex matters, requiring advanced analytical skill, training and/or education. Raises highly complex problems or out-of-policy issues</li><li>Strong management, interpersonal and problem-solving skills</li><li>Proven track record in clinical trial process improvements</li><li>Considerable organizational awareness, including significant experience working cross-functionally</li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related area. Additionally, ≥ 6 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in immune/inflammatory related clinical trials. Basic knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 22:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, US Oncology Skin Cancer Marketing]]></title>
    <date><![CDATA[Mon, 06 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46356]]></requisitionid>
    <referencenumber><![CDATA[R46356]]></referencenumber>
    <apijobid><![CDATA[r46356]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46356/director-us-oncology-skin-cancer-marketing/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, US Oncology HCP Skin Cancer Marketing, is a member of the Oncology Business Unit with accountability for working closely with the Senior Director to develop commercial HCP promotion strategy and tactical plans for Non-Melanoma Skin Cancer (NMSC) within the US. Also responsible for collaborating with the International team for Global commercialization and promotion.</p><p>This position will report directly to the Senior Director, HCP Skin Cancer Marketing. The Director will work collaboratively across the Franchise Team, International teams, internal cross-functional colleagues, while effectively managing external agency partners to ensure alignment and to drive optimal integration and execution of personal and non-personal initiatives<strong>.</strong></p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li>Lead HCP marketing for the NMSC indications in the US. This includes defining US market opportunities, analyzing the competitive landscape, identifying key site of care and key account segmentation and needs, developing customer-focused and differentiated product and indication positioning, and customizing messages to key target audiences.</li><li>Works in close collaboration with Clinical, Medical Affairs and Field Medical to ensure alignment with Medical Education strategic plans.</li><li>Engage with physician experts and attend key congresses to support Scientific Marketing team efforts and assess important disease and treatment data.</li><li>Work closely with the Insights and Data Analytics team to design and implement promotional strategies, while tracking brand performance, share of voice, market dynamics and competitive actions & response. Provide business assumptions input to forecasting.</li><li>Oversee and collaborate with Digital/Media Strategy team for optimization and implementation of the multi-channel marketing mix, including omni-channel digital & media strategy and implementation, and creation and deployment of educational resources towards brand objectives and developing indicators/metrics for high-impact engagements with HCP key target audiences.</li><li>Develop and coordinate NMSC HCP Marketing inputs and key sections of brand plan, identify and prioritize business opportunities.</li><li>Responsible for the development of the Field Plan of Action and training plan, national/regional sales meeting execution and Field communications in collaboration with internal and external partners/collaborators.</li><li>Maintain strong collaborative relationships with cross-functional areas and internal strategic partners (i.e., Field Sales, Training, Promotional Review Committee, Medical Affairs, Regulatory, Clinical, Legal, Compliance, Market Access etc.)</li><li>Ensures that the marketing processes, programs, and internal reports are developed, implemented, and effectively administered to be consistent with corporate guidance and all regulatory, legal, ethical guidelines.</li><li>Manages and develops a direct report to ensure their continued development and growth.</li><li>Works cross functionally to create, manage and track budget to ensure operating within the approved budget and phasing.</li></ul><h3><strong>This job might be for you if:</strong></h3><ul><li>You are effective collaborator and communicator both written and verbal</li><li>You can navigate regularly in ambiguity</li><li>You excel in a fast paced environment</li></ul><p>To be considered for this role, we expect you to have a Bachelors degree; 12+ years of pharmaceutical marketing focused on Oncology. Along with leading and developing long range brand plans, budgets and forecasts for commercial teams in the pharmaceutical/biotech industry. Lastly, this role requires you to travel 30% of the time and to be in the office in Sleepy Hollow, NY 4 days a week.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Apr 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Field Medical Affairs (Neurology)]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46413]]></requisitionid>
    <referencenumber><![CDATA[R46413]]></referencenumber>
    <apijobid><![CDATA[r46413]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46413/director-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>As a Director, Field Medical Affairs, you will be responsible for regional hiring, deployment, and leadership responsibilities for Neurology focused Medical Science Liaisons. You will collaborate with the Senior Director, Field Medical, Medical Directors, and others in setting Field Medical strategy. Responsible for oversight of activities in accordance with current regulatory and health care compliance guidelines. Other responsibilities include providing scientific exchange and collaboration with therapeutic area opinion leaders on disease and product information as well as research initiatives. Participate in the development and management of company and investigator sponsored clinical trials</p><p><strong>A typical day may include the following: </strong><br>• Responsible for the management of a regional Field Medical team including. <br>• Conduct routine field visits and 1:1 meeting, providing observation and coaching <br>• Recruitment, coaching, training, development of direct reports <br>• Monitor compliant execution of initiatives and other permissible field activities <br>• Track team field activity level and field metrics <br>• Ensure each field medical members’ territory plan is strategic, up to date and actionable <br>• Manage the team through special projects and cross-functional support activities <br>• Neurology Field Medical direct line leadership including, hiring, goal setting, performance evaluation and all other aspects related to direct report supervision. <br>• Collaborate with internal team members to ensure alignment and communication of Medical Affairs (MA) field medical goals and team value proposition. <br>• Participate in the development of educational materials/evidence communication tools and champions the regulatory/legal/health care compliance approvals. <br>• Identifies gaps in research needs and strategies of the company and creates opportunities to fill gaps with potential and existing investigators. <br>• Assists with management of clinical data through support of abstracts, posters, presentations and manuscript development to ensure rapid and accurate communication of scientific and clinical results. <br>• Appropriately engages healthcare professionals and attends medical conferences to collect and report relevant medical insights. <br>• Develop strategic plans and coordinates activities for Neurology scientific meetings and congresses. <br>• Collaborates with Clinical and other study staff to develop, implement plans and strategies established by Medical Affairs to support Neurology Development Plans. <br>• Develop strategies for, maintain lists of Neurology experts/investigator targets and associated plans of action. <br>• Collaborate with Medical Information to develop, plan, and review materials used for response to scientific inquiries. </p><p>To be considered an Advanced medical and/or scientific degree required (e.g., MD/DO, PhD, PharmD, DVM) along with 10+ years’ work experience in Medical Affairs. Previous experience as an MSL and leading a team of MSLs is required. 5+ years Neurology pharmaceutical work experience is preferred; in myasthenia gravis (MG) is helpful. Prior experience developing assets such as slide decks, FAQs or related MSL materials and launch experience is preferred. Must be proficient in Microsoft Word, Excel and PowerPoint and Veeva. </p><p>#msl #medicalscienceliaison<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs, Allergy & Respiratory (Asthma)]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46160]]></requisitionid>
    <referencenumber><![CDATA[R46160]]></referencenumber>
    <apijobid><![CDATA[r46160]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46160/medical-director-medical-affairs-allergy-respiratory-asthma/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron seeks a dedicated Medical Director, Medical Affairs, who prioritizes patient care above all else. The successful candidate will drive the development and execution of medical strategies and activities related to Regeneron's strategic assets in the Allergy & Respiratory disease area, ensuring integrity and scientific accuracy. This role requires deep expertise in asthma and related diseases, and clinical trial execution.</p><p><strong>A typical day in the life of a Medical Director, Medical Affairs may include the following responsibilities: </strong></p><p>• Develops and oversees implementation of US and ex-US focused medical strategy and tactics, including scientific communications and publications, annual medical planning, field communications, and collaborations with experts.<br>• Supports the design, conduct, oversight, analysis, and reporting of Medical Affairs post-approval interventional and non-interventional respiratory clinical trials.</p><p>• Attends clinical study team meetings, data oversight review sessions, and works closely with CRO medical monitors in support of medical affairs clinical trials.</p><p>• Oversees and provides hands on support in management, generation and dissemination of clinical and non-clinical data that supports the medical strategy and results in high quality publications.</p><p>• Collaborates effectively within a multifunctional, matrix organization which includes field medical teams, medical operations, education, information, HEOR, publication management, and statistics.<br>• Develops and cultivates long-term strategic partnerships with clinical experts, societies, collaborative groups, advocacy groups, and other external stakeholders.</p><p>• Supports commercial activities such as promotional materials review, speaker training, colleague training, etc.</p><p><strong>This role may be for you if you have the following:</strong></p><p>• Physician (MD/MBBS or equivalent medical degree) with specialized training AND experience in pulmonology or allergy, specifically asthma</p><p>• 0-4 years of industry experience in Allergy/Respiratory Medical Affairs and/or Clinical Development (academic research experience will be considered)</p><p>• Demonstrated experience in clinical trial execution</p><p>• Experience working in an alliance setting is strongly preferred</p><p>• Lead complex business and technical discussions internally and externally and explain scientific/medical concepts to all levels<br>• Cultivate relationships and establish trust with internal and external Medical Experts in pulmonology.</p><p>• Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management.</p><p>• You thrive in a very dynamic environment in a therapeutic area with other competing treatment options.</p><p>#MDJobs, #MDJOBSMA, #GDMAJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 21:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Product Biochemistry (NMR)]]></title>
    <date><![CDATA[Sun, 12 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46495]]></requisitionid>
    <referencenumber><![CDATA[R46495]]></referencenumber>
    <apijobid><![CDATA[r46495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46495/associate-scientist-product-biochemistry-nmr/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Our Product Biochemistry team is seeking a highly motivated Associate to join our dynamic and collaborative group. In this role, you will be responsible for implementing biophysical assessment strategies on different drug modalities such as oligonucleotides, peptides, and small molecule payloads, including collecting and analyzing NMR data, to support research and development efforts. You will play an integral part in technology innovation efforts aimed at enhancing our understanding of therapeutic agents through advanced NMR methodologies.</p><h3>A Typical Day as an Associate Scientist Looks Like:</h3><ul><li>Conduct NMR experiments and analyze data to elucidate the structural and chemical properties of oligonucleotide, peptide, and small molecule candidates.</li><li>Develop and optimize NMR protocols and methods to support both upstream and downstream research initiatives.</li><li>Document all analytical work in electronic laboratory notebooks according to defined protocols with accuracy and attention to detail.</li><li>Communicate experimental findings and data interpretation to supervisors and project teams.</li><li>Summarize results in a concise format for presentations and regulatory documents.</li><li>Present findings at group, departmental, and cross-functional meetings.</li><li>Maintain and troubleshoot instruments and other essential laboratory equipment.</li><li>Utilize additional analytical methods characterize therapeutic candidates alongside NMR studies, and participate in protein purification/enrichment activities.</li></ul><h3>This Role May Be for You If You Have:</h3><ul><li>Experience in the general operations of a laboratory and the ability to manage and organize scientific data under managerial supervision.</li><li>Technical competencies in NMR spectroscopy, with hands-on experience in collecting and interpreting NMR data on oligonucleotides, peptides, and small molecules.</li><li>Experience operating a range of NMR instruments and troubleshooting instrumentation issues.</li><li>Strong organizational skills and the ability to prioritize multiple tasks in a fast-paced environment.</li><li>Ability to contribute to lab equipment maintenance and safety to help create a safe, effective and efficient working environment.</li><li>Familiarity with related analytical techniques such as chromatography or mass spectrometry is a plus.</li></ul><p>This role requires a Bachelor’s or Master’s degree in Chemistry, Biochemistry, Biophysics, or a related field plus 0-3 yrs+ experience with an emphasis on NMR data collection and analysis of oligonucleotides, peptides, or small molecules. Preference will be given to candidates who have experience working in the biopharmaceutical industry. Excellent oral and written communication skills and evidence of teamwork are required. Experience with SEC-MALS, iCE, CE-SDS, DSC, or general protein purification and chromatography techniques is highly desirable and considered a plus for this role.</p><p>The ideal candidate must have strong initiative to complete tasks, learn new technologies, and demonstrate a commitment to continuous learning. This role requires the ability to manage multiple priorities in a fast-moving R&D environment, operate effectively both independently and within a collaborative team environment, and communicate clearly, transparently, and in a timely manner with key stakeholders.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 12:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Corporate Counsel (Privacy Counsel: Digital Cyber AI)]]></title>
    <date><![CDATA[Sun, 12 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46433]]></requisitionid>
    <referencenumber><![CDATA[R46433]]></referencenumber>
    <apijobid><![CDATA[r46433]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46433/director-corporate-counsel-privacy-counsel-digital-cyber-ai/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a key member of the Privacy Office in Regeneron’s Law Department, this role will enable our rapidly growing and globally expanding business to develop and execute innovative data-driven strategies in accordance with data privacy law, and related cybersecurity and AI requirements. This role will support our Digital and Information Technology functions, including Information Security, AI, and Data Governance. This position will report to Regeneron’s Chief Privacy Officer.</p><p><strong>This role is based at Regeneron's offices in Sleepy Hollow, NY or Cambridge, MA (4 days a week onsite) - it is not open to hybrid or fully remote assignments.</strong></p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Strategically assessing potential privacy risks associated with innovative new initiatives and developing appropriate controls, training and guidance to enable compliance with applicable regulations.</p></li><li><p>Providing legal advice on cybersecurity and information incidents and working with internal stakeholders to prepare for and respond to cyber/information incidents, including managing the incident response process</p></li><li><p>Providing legal guidance at the intersection of privacy and AI adoption including participation in AI use case assessments. </p></li><li><p>Drafting policies, procedures and guidance related to the foregoing subject matter areas in partnership with Law Department colleagues, Digital/IT and business functions.</p></li><li><p>Monitoring developments in the US and globally (including related legislation and industry practices) and supporting operationalization of compliance with regional and local laws such as CCPA/CPRA, NIS2 Directive, etc.</p></li><li><p>Advising on the application and solutions for complying with biometric and other emerging data-related laws.</p></li><li><p>Representing the Privacy Office as a member of Regeneron's technology-related committees and working groups.</p></li><li><p>Partnering with Privacy Office colleagues to contribute to the implementation and advancement of the Regeneron Privacy Program.</p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p>Strong knowledge of local and global privacy, cybersecurity and AI laws and familiarity with associated risk management frameworks and standards (e.g., NIST).</p></li><li><p>Excellent relationship building skills.</p></li><li><p>Demonstrated ability to work collaboratively and with all levels of the organization.</p></li><li><p>Exceptional oral, written, and presentation communication skills, with the ability to effectively communicate and translate complex legal analysis into practical guidance for a varied audience.</p></li><li><p>High level of business acumen, influencing skills and ability to drive change.</p></li><li><p>Willingness to take on a leadership role in an important, dynamic and challenging field.</p></li><li><p>Experience with privacy-enhancing technologies is a plus.</p></li><li><p>Pharmaceutical/biotechnology industry preferred.</p></li></ul><p><strong>To be considered for this role,</strong> you must have a JD and be licensed to practice law in New York State or eligible for licensure as a registered in-house counsel. At least 12 years of legal experience at a law firm and/or in-house, with at least 5 years of experience of directly relevant experience. Biotechnology, pharmaceutical or related life science experience strongly preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist (External CRO Management)]]></title>
    <date><![CDATA[Sun, 19 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46523]]></requisitionid>
    <referencenumber><![CDATA[R46523]]></referencenumber>
    <apijobid><![CDATA[r46523]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46523/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>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><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide scientific and operational oversight on all aspects of bioanalytical activities conducted at Contract Research Organizations (CROs), independently and in collaboration with representative of the Bioanalytical Outsourcing Team.</p></li><li><p>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</p></li><li><p>Work with internal and external SMEs (Subject Matter Experts) to address any/all issues that may occur during assay development and/or sample analysis</p></li><li><p>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</p></li><li><p>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</p></li><li><p>Facilitate with the review of GLP and GCLP compliance status at CROs</p></li></ul><p><strong>This job might be for you if you:</strong></p><ul><li><p>Previous experience managing external CROs- coordinating bioanalysis, assay validation etc is a plus</p></li><li><p>Experience with novel drug candidates (gene therapies, CAR-T, mAbs, ADCs etc) is a plus</p></li><li><p>Excellent documentation skills with attention to detail and overall data quality</p></li><li><p>Ability to clearly and concisely communicate project goals, deliverables internally and externally</p></li><li><p>Ability to multi-task and work under tight timelines.</p></li></ul><p><strong>To be considered for this role</strong>, <strong>you must have:</strong></p><ul><li><p>BS/MS with 10+yrs experience in an industry setting</p></li><li><p>Hands-on experience with regulated bioanalysis</p></li><li><p>Hands-on experience with assay validation/qualification relevant under multiple platforms: LBA, LC/MS, PCR-based methods</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Supervisor Process Maintenance, Wednesday-Saturday 2nd shift]]></title>
    <date><![CDATA[Sun, 12 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44046]]></requisitionid>
    <referencenumber><![CDATA[R44046]]></referencenumber>
    <apijobid><![CDATA[r44046]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44046/supervisor-process-maintenance-wednesday-saturday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking to add a Supervisor Process Maintenance to our growing team working a Wednesday-Saturday 2:00pm-12:30am schedule. This role primarily oversees the operations of the Large Scale 10k process area maintenance functions.</p><p>As a Supervisor Process Maintenance, a typical day might include the following:</p><ul><li>Planning and scheduling maintenance repairs/modifications of facility and process equipment.</li><li>Troubleshooting process equipment problems and making required changes.</li><li>Advising supervision of Regeneron Process Maintenance Technicians and Process Maintenance Leads to high performance goals in a cGMP - FDA regulated environment.</li><li>Leading team in continuous improvement, 5S, and Lean initiatives.</li><li>Coaching, counseling and managing performance of a team.</li><li>Reviewing departmental operations and recommending changes to management.</li><li>Forecasting resource requirements and submitting budget recommendations to management.</li><li>Supervising, coordinating and assuring compliance with contractors and Regeneron employees on all applicable codes and standards.</li><li>Supporting Deviation Management process including NOE, EOE and DNF investigations and reviews.</li></ul><p>This position might be for you if you:</p><ul><li>Have at least 3 years of leadership experience.</li><li>Consistently demonstrate adept interpersonal and communication abilities as a leader and provide thoughtful and decisive decision making.</li><li>Have a strong attention to detail including experience with budgeting management.</li><li>Are able to see the “Big Picture” and demonstrate the ability to respond accordingly.</li><li>Ensure the highest level of customer service for both internal and external customers.</li><li>Are skilled in the use of Microsoft office applications (Word, Excel, PowerPoint, Visio and Project) and other related software.</li></ul><p>To be considered for the Supervisor Production Maintenance position, you should have an AS in engineering, science or related field and 5+ years’ experience in pharmaceutical production operations for aseptic formulations, filling and lyophilization. Equivalent combination of education and experience may be considered.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 14:56:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Obesity]]></title>
    <date><![CDATA[Sun, 19 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46851]]></requisitionid>
    <referencenumber><![CDATA[R46851]]></referencenumber>
    <apijobid><![CDATA[r46851]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46851/medical-director-clinical-development-obesity/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Development, Obesity should be a qualified physician with pharmaceutical industry experience, preferably in the area of metabolism, in relevant areas such as obesity or Type 2 diabetes. The Director will serve as Medical Lead for clinical trials in the CDP and is responsible for the design of clinical study concepts leading to clinical trial protocols. This role requires a high-performing and highly passionate physician scientist who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to clinical research.</p><p><strong>A typical day in the life of a Medical Director may include the following responsibilities:</strong></p><ul><li><p>Acts as medical expert and leader in interactions with external stakeholders</p></li><li><p>Defines clinical trial-related Clinical Development Program (CDP) goals and objectives </p></li><li><p>Works closely with discovery teams to provide input on the next generation of targets in the field</p></li><li><p>Responsible for the relevance and accuracy of medical science underpinning of clinical study concepts (CSC) based on thorough scientific review and consultation with internal and external experts </p></li><li><p>Reviews and finalizes clinical study concepts for presentation to Therapeutic Head, Strategic Program Teams, and internal governance meetings</p></li><li><p>Leads the Global Clinical Study Team to produce high quality program deliverables on schedule </p></li><li><p>Responsible for the medical content of clinical study reports, the analysis of clinical data, including safety monitoring, and all activities and procedures that ensure patient safety </p></li></ul><p><strong>This job may be for you if you have the following: </strong></p><ul><li><p>An M.D. or equivalent with board eligibility or board certification in Pediatric Endocrinology preferred; relevant experience can be acceptable.</p></li><li><p>At least 2 years pharmaceutical industry experience (equivalent research in academia will be considered)</p></li><li><p>Experience in metabolic disorders drug development strongly preferred</p></li><li><p>Previous interactions with regulatory agencies or common technical document (CTD or “dossier”) submission in an ICH region is an advantage</p></li></ul><p>#MDJOBS, #MDJOBSCD#GDTherapeuticJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Hiroshima Area]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47083]]></requisitionid>
    <referencenumber><![CDATA[R47083]]></referencenumber>
    <apijobid><![CDATA[r47083]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47083/medical-representative-mr-dermatology-starhiroshima-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong></p><p>You will primarily work in the Hiroshima area.</p><p>Your residence is expected to be in Hiroshima.</p><p>Are you ready to make a meaningful impact in the pharmaceutical industry? At Regeneron, we’re committed to putting patients first, and we’re looking for a passionate Sales Representative to join our Dupixent ROW Commercial Team in Japan. This role is your opportunity to drive dermatology sales objectives while working with a team dedicated to innovation and excellence. With a focus on delivering value to healthcare professionals and patients alike, this position offers the chance to grow your career while making a difference in people’s lives.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Achieve sales objectives by effectively managing territory budgets and resources.</p></li><li><p>Develop and implement an annual territory business plan that incorporates market insights and aligns with marketing strategies.</p></li><li><p>Regularly update business plans to adapt to changing market dynamics.</p></li><li><p>Utilize key data sources to create strategic action plans for the territory.</p></li><li><p>Conduct disease and concept selling to engage healthcare professionals and deliver tailored solutions.</p></li><li><p>Perform administrative tasks, including expense reporting, marketing feedback, and call reporting.</p></li><li><p>Collaborate with alliance partners to meet overall objectives and ensure compliance with regulatory guidelines.</p></li><li><p>Attend local, regional, and national meetings as required, and complete all training programs provided by Regeneron.</p></li><li><p>Maintain company property in good order and adhere to safe driving practices.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You excel at building strong relationships with customers and delivering value-driven solutions.</p></li><li><p>You have a knack for strategic thinking and can manage your time effectively to achieve goals.</p></li><li><p>You thrive in independent work environments and can execute plans under tight timelines.</p></li><li><p>You’re organized, detail-oriented, and comfortable with administrative responsibilities.</p></li><li><p>You enjoy collaborating with others to achieve shared objectives.</p></li><li><p>You’re adaptable and willing to travel, including evenings and weekends, as needed.</p></li></ul><p><strong>To Be Considered:</strong></p><p>Candidates must have a Bachelor’s degree (or equivalent) and at least five years of sales representative experience in the pharmaceutical industry. A valid driver’s license and MR certification are required. While fluency in English is a plus, it is not essential for this role. Preferred qualifications include therapy area knowledge in dermatology, sales experience in biologics, and established relationships with key opinion leaders in dermatology.</p><p>Join us at Regeneron, where your expertise and dedication can make a real difference. Apply today to become a part of a team that’s revolutionizing healthcare and improving lives worldwide.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist, Analytical Drug Product Development and Technology (DPDT)]]></title>
    <date><![CDATA[Mon, 20 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46918]]></requisitionid>
    <referencenumber><![CDATA[R46918]]></referencenumber>
    <apijobid><![CDATA[r46918]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46918/scientist-analytical-drug-product-development-and-technology-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[<p>We are seeking a highly motivated Scientist to support the laboratory based analytical method development and qualification within the Drug Product Development and Technology (DPDT) group. The DPDT team supports all stages R&D work through commercial. You will be responsible for developing and qualifying analytical methods that will be assessing drug product stability of various drug products from pre-clinical to commercialization development.</p><h3><strong>A Typical Day in the Role Might Look Like:</strong></h3><ul><li>Support analytical strategy development for drug products, with primary focus on peptides, and supporting focus on antibody–drug conjugates, siRNA, monoclonal antibodies, and bispecific antibodies</li><li>Develop and qualify analytical methods for critical quality attributes to support formulation development, DP process development, and stability testing for programs in preclinical and clinical stage.</li><li>Prepare, author, and review critical analytical technical documents, including analytical method procedures (SOPs), method performance reports, method transfer documents and chip into pharmaceutical development reports for completeness and correctness.</li><li>Guide and work with team members in conducting research and developmental activities. Investigates and solves problems related to the methods used to assess product quality and stability. Sets goals, assigns tasks, and provides performance management and development as needed.</li><li>Maintain full working knowledge of analytical techniques and instruments and applies appropriately to projects and identify and assess novel analytical methods and technologies.</li><li>Evaluate, interpret and present data at team meetings.</li><li>Collaborate with other team members in DPDT and other functional groups at Regeneron in supporting the program development.</li><li>Maintain accurate and complete laboratory record, participate in general lab instrument maintenance, and perform trouble shooting independently.</li></ul><h3><strong>This Role Might Be For You If You Have:</strong></h3><ul><li>Enthusiasm in science with a motivation for making contributions in a team environment is necessary.</li><li>Demonstrated communication skills, collaborative attitude and strong multi-tasking capabilities to thrive in matrix teams.</li><li>Strong collaboration, teamwork, and communication skills.</li><li>Independent, motivated, and detail-oriented with excellent problem-solving abilities.</li></ul><p>This role requires a BS degree in Chemistry, Chemical Engineering, Biochemistry, or related field with ≥7 years of research experience, or MS degree in the above mentioned fields with ≥ 5-years of hands-on research experience. Familiarity with the quantitative and qualitative techniques used in peptide and/or biologic drug products, including capillary and microchip electrophoresis, HPLC/UPLC, mass spectrometry. Experience in biophysical characterization techniques such as DLS, HIAC, fluorescent labeling assays s is a plus. The ability to work independently to design experiments, as well as interpret, document and communicate results is required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sourcing Manager]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44844]]></requisitionid>
    <referencenumber><![CDATA[R44844]]></referencenumber>
    <apijobid><![CDATA[r44844]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44844/sourcing-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we are passionate about transforming science into life-changing medicines. As a leading biotechnology company, our mission is to improve lives through groundbreaking research and innovative solutions. We are looking for a <strong>Manager, Global Procurement – International Markets: Japan</strong> to join our Tokyo-based team and play a vital role in enabling our international expansion and local market priorities.</p><p>As part of our Global Procurement team, you will collaborate with international stakeholders and category teams to address Japan’s unique regulatory, cultural, and commercial requirements. This is your opportunity to make a meaningful impact, drive strategic sourcing initiatives, and contribute to Regeneron’s vision of building a procurement capability that serves as a competitive advantage.</p><p><strong>A Typical Day:</strong></p><ul><li>Partner with stakeholders and the Global Procurement organization to align global priorities with local needs.</li><li>Implement global category strategies within Japan to ensure consistency in sourcing, contracting, and supplier relationship management.</li><li>Provide input to global strategies to incorporate Japan’s market-specific requirements effectively.</li><li>Execute sourcing, negotiation, and contracting activities to support business objectives.</li><li>Collaborate with country stakeholders to understand strategy, budgets, and annual spend requirements.</li><li>Analyze local contracts and monitor spend trends to identify opportunities for efficiency.</li><li>Leverage data for decision-making and to drive successful category projects.</li><li>Foster relationships with suppliers and stakeholders to deliver cost savings, improve cash flow, and enhance operational efficiency.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You thrive in a collaborative environment and enjoy working closely with international teams.</li><li>You have a keen understanding of Japan’s unique regulatory, legal, and cultural landscape.</li><li>You are passionate about driving value through strategic procurement and supplier engagement.</li><li>You excel at analyzing data to identify trends and inform decision-making.</li><li>You are an effective communicator and can build influential relationships with stakeholders and suppliers.</li><li>You are adaptable, focused, and able to navigate ambiguity to drive change and improvement.</li><li>You are committed to maintaining the highest ethical standards and delivering excellence in all you do.</li></ul><p><strong>To Be Considered:</strong></p><p>The ideal candidate will have a bachelor’s degree in a relevant field and at least 5 years of experience in indirect procurement, preferably in the Pharma/BioPharma industry. Experience in Commercial, Corporate/Indirect, and R&D categories is highly desirable, along with a proven ability to lead global category teams and processes. Proficiency with sourcing and contracting tools (e.g., Oracle, Zycus, GEP, Ariba) and standard business applications (Word, Excel, PowerPoint) is required.</p><p><strong>Why Join Regeneron?</strong></p><p>At Regeneron, we lead with science and are committed to fostering a culture of integrity, excellence, and innovation. Our Global Procurement team is at the forefront of enabling our scientific advancements and driving value for the organization. Join us to be part of a dynamic team that is shaping the future of procurement while making a difference in the lives of patients worldwide.</p><p>This job ad has been crafted to align with the provided guidelines, ensuring clarity, inclusivity, and a professional tone while strictly adhering to the job description.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 10:56:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Mon, 20 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46894]]></requisitionid>
    <referencenumber><![CDATA[R46894]]></referencenumber>
    <apijobid><![CDATA[r46894]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46894/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>We are seeking a Senior Project Engineer who will be responsible for designing, specifying and commissioning new and renovated biopharmaceutical process equipment. This position will provide engineering support and problem solving support for existing equipment and manufacturing processes.</div></div><div><div><div><div><div><div><div><div><div><p><strong>As a Sr Project Engineer, a typical day might include the following: </strong></p><ul><li><p>Designing and specifying cGMP process equipment, piping, and controls</p></li><li><p>Managing small-to-mid-sized projects related to process equipment and manufacturing</p></li><li><p>Assisting in the design review, site acceptance, and installation of equipment</p></li><li><p>Preparing piping and instrumentation diagrams (P&IDs) and other related drawings</p></li><li><p>Developing Process Flow Diagrams (PFDs) for manufacturing processes</p></li><li><p>Supporting the QA Validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Reviewing and approving lifecycle documentation, cleaning validation protocols, and summary reports</p></li><li><p>Assisting with investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</p></li><li><p>Assisting management with tracking of department throughput and efficiency</p></li><li><p>Representing the engineering department at cross-functional meetings</p></li><li><p>Supervising direct reports as needed</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations and test plans, and executing change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors as needed</p></li><li><p>Maintaining a clean and safe working environment by enforcing procedures, policies, and regulations</p></li><li><p>Maintaining company reputation by ensuring compliance with all relevant laws, policies, and regulations</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You have excellent technical and analytical skills.</p></li><li><p>You are skilled at problem-solving and continuous improvement.</p></li><li><p>You possess strong communication and collaboration skills.</p></li><li><p>You are adaptable and can work in a fast-paced, regulated environment</p></li></ul><p>To be considered for this opportunity you should have a BS/BEng or higher in chemical/process/mechanical engineering with 5+ years of related experience. Direct experience with biopharmaceutical process equipment is preferred. May substitute relevant experience for education.</p><p>#LI-Onsite #JOBSIEPR #IRELIM #REGNIRLTO</p></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>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 05:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HR Operations Specialist - Temporary contract, 9 months]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46692]]></requisitionid>
    <referencenumber><![CDATA[R46692]]></referencenumber>
    <apijobid><![CDATA[r46692]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46692/hr-operations-specialist-temporary-contract-9-months/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The HR Operations Specialist is responsible for the initiating, auditing, correcting and troubleshooting of employee data into Workday and Oracle. Overall, you will be ensuring the quality, integrity and quick resolution of issues within HR Operations with a focus on consistency and quality of employee core data entry, day to day operational transactions for Workday, Oracle, HireRight, ServiceNow and other systems used within the HR Operations team. You will serve as a subject matter expert in troubleshooting and problem solving for HR Operations as it relates to the systems and quality for HR data management.</p><p>This is a temporary contract for 9 months.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Conduct final audits within HR Operations prior to actual data entry into the system – with a goal of zero errors.</p></li><li><p>Conduct audits of the process, identify deviations from the process, keep an updated log of issues, work with coordinators to ensure compliance with the process.</p></li><li><p>Work with rest of team across all sites collecting monthly updates of the operations metrics for the group (volume/error rate).</p></li><li><p>Work with key stakeholder groups such as payroll and IT to resolve issues, identify solutions to problems and implement those solutions. Escalate to the Manager HR Operations as needed.</p></li><li><p>Take direction and carry out activities as directed by the Manager HR Operations as it relates to issues such as mass uploads of employee data, communications, and onboarding activities.</p></li><li><p>Work with Manager HR Operations to develop solutions to complex problems, plan of action, and then execution to resolve issues as they arise.</p></li><li><p>Responsible for level one support (troubleshooting, remedying) for end users on business issues.</p></li><li><p>Perform data analysis, identify key metrics, and present to leadership.</p></li></ul><p><strong> </strong></p><p><strong>This Role May Be For You, If You:</strong></p><ul><li><p>Are knowledgeable in Background Checks and Leave of Absence Administration. </p></li><li><p>Demonstrate strong working knowledge of HR information systems, preferably Workday, which enable and support all HR transaction processing.</p></li></ul><p><strong>To be considered</strong>, you have a Bachelor's degree and three or more years of progressive experience with business operations and/or HR systems. Three or more years of experience within one or more HR operational functions are strongly preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant, Global Patient Safety]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46569]]></requisitionid>
    <referencenumber><![CDATA[R46569]]></referencenumber>
    <apijobid><![CDATA[r46569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46569/executive-assistant-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Executive Assistant to join our Global Patient Safety Organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Global Patient Safety (GPS) Executive Assistant is a dynamic role that requires tenured experience in administrative support at Regeneron. The Executive Assistant will report to and support the Senior Vice President (SVP) of GPS who oversees a global leadership team and functions in their remit. The incumbent will provide advanced calendar management, travel and all associated logistics to the SVP of GPS to ultimately ensure leaders of Regeneron and associated teams can effectively carry out high level business objectives. Given business need, the incumbent will lead team event planning, cross functional team building and town halls, order department supplies, become involved with space planning and may take in additional client support in a highly proactive, professional, collaborative and efficient manner. The Executive Assistant should have advanced experience in Microsoft 365 applications, Concur, and is able to learn new technologies with ease for themselves and their client.</p><p><strong>This role might be for you if can: ​</strong></p><ul><li><p>Proactively manages and responsible for time management and calendars of Executive using thorough understanding of department and leadership priorities.</p></li><li><p>Ability to anticipate the needs of leaders and teams in order to manage and problem solve all logistics with a larger scope and greater impact if scheduling conflicts occur.</p></li><li><p>May lead all logistics/execution of internal meetings including but not limited to cross functional team buildings and town halls. Acts as the contact for external meetings and is responsible for collaborating with Strategic Sourcing and Procurement to manage and negotiate contracts for off-site meetings as well as managing meeting/event budgets within the approval limit. May act as point person to gather agenda items and may collect slides from multiple individuals in order to provide a complete slide deck and materials for meetings/events.</p></li><li><p>May assist with managing budgets within functional department supported.</p></li><li><p>Handles travel and expense reports for their client, and additional clients in the department if necessary. Assists guests with travel, where applicable. </p></li><li><p>Advanced knowledge of company policies, procedures and resources and acts as a point person for leader(s)/department(s) taking the lead to raise potential continuous improvement efforts to current processes. </p></li><li><p>Actively manages department contact lists/org charts. Proactively manages and updates content on department SharePoint sites and/or internal pages.</p></li><li><p>Responsible for proactively monitoring purchase order requests and may be responsible for gathering expense requests. May also submit requisitions and coordinate tracking of departmental deadlines. </p></li><li><p>May lead the preparation, onboarding and assimilation for new employees within GPS, including coordination with IT, Facilities, and Procurement. Assists with department space planning and may assist in headcount tracking. </p></li><li><p>Anticipate and make recommendations for catering for meetings and events scheduled over meal periods.</p></li><li><p>May act as SME for junior Administrative colleagues, create best practices and proactively works with other administrative coordinators to ensure coverage while Admins are out of the office.</p></li><li><p>All other duties as assigned.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Associates or BA preferred; 8+ years administrative experience with a minimum of 4 years of executive administrative experience desirable.</p></li><li><p>Years of experience may be considered in lieu of degree.</p></li><li><p>Highly collaborative within the department(s) of support as well as being sought out by peers cross-functionally. Skillful written and verbal communication skills are essential; ability to interact across all levels of employees and management while maintaining confidentiality. Demonstrated organizational knowledge and ability to understand department and leader priorities while potentially supporting groups with increasingly complex responsibilities.</p></li><li><p>Highly independent and shows advanced judgment and problem-solving skills. Comfortable leading projects. Ability to coordinate team members cross-functionally.</p></li><li><p>Is a quick learner, can cope and make good decisions despite change and ambiguity; skillfully handles risk and uncertainty with composure and shifts gears with ease. </p></li><li><p>Works comfortably with all levels in the organization including senior managers. Understands how senior leaders think and what they expect. </p></li><li><p>Advanced knowledge and proficiency in MS Office, SharePoint, Concur and teleconference systems with the ability to assist with more advanced troubleshooting. May be responsible for training new employees on internal systems</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$38.61 - $63.03]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 19:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Governance and Contract Compliance, Regeneron Genetics Center (RGC)]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47043]]></requisitionid>
    <referencenumber><![CDATA[R47043]]></referencenumber>
    <apijobid><![CDATA[r47043]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47043/director-data-governance-and-contract-compliance-regeneron-genetics-center-rgc/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Data Governance and Contract Compliance lead and ensures compliance across a large portfolio of global data licensing collaborations involving genetic and associated health data. You will serve as RGC’s internal resource on data privacy, genomic data governance, and cross-border data transfer; partnering with RGC counsel, research and technology teams, and the Privacy Office, to uphold the highest standards of data stewardship. You will develop and implement operational policies, procedures, and risk mitigation strategies that enable scientific collaboration, while safeguarding individual data rights worldwide.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead compliance across approximately 150 global data licensing collaborations related to genetic and associated health data, including ongoing monitoring, risk assessment, and remediation.</p></li><li><p>Partner with counsel to interpret and ensure compliance with international privacy regulations (GDPR, HIPAA, CCPA/CPRA), and genomic data governance frameworks (NIH Genomic Data Sharing Policy, GA4GH), in data collaboration agreements and research operations.</p></li><li><p>Drive the development and operationalization of RGC data governance policies, procedures, consent frameworks, and data use agreements specific to genetic and health data.</p></li><li><p>Lead all aspects of data security stewardship practices, evaluating and integrating emerging privacy-preserving technologies with the IT Security team.</p></li><li><p>Monitor the evolving global regulatory landscape for genetic data governance, advising leadership on compliance risks and policy adaptations.</p></li><li><p>Lead, mentor, and develop a team of data governance and compliance professionals; championing a culture of accountability, transparency, inclusion, and continuous learning.</p></li><li><p>Collaborate cross-functionally with Legal, IT Security, Research, and Business Development to embed privacy-by-design into data collaboration workflows and initiatives.</p></li></ul><p><strong>This job might be for you if you have:</strong></p><ul><li><p>Experience with GDPR, HIPAA, CCPA/CPRA, and other applicable privacy regulations.</p></li><li><p>Solid understanding of genomic data governance frameworks, including the NIH Genomic Data Sharing Policy and GA4GH standards.</p></li><li><p>Clear written and verbal communication skills, with the ability to relay complex regulatory requirements to scientific and executive audiences.</p></li><li><p>Validated experience building and leading high-performing compliance teams.</p></li><li><p>IRB experience. Familiarity with federated learning, and secure multi-party computation technologies is preferred.</p></li></ul><p><strong> In order to be considered for this role, you must have:</strong></p><ul><li><p>A PhD in Genetics, Genomics, Bioethics, Life Sciences, or a related field; or a relevant degree with experience in data governance and compliance.</p></li><li><p>An equivalent combination of advanced education and 10+ years of experience in data governance, compliance, or regulatory affairs; with at least 5 years focused on genetic or health data in research, biopharmaceutical, or biotech settings.</p></li><li><p>CIPP/E or CIPP/US certifications are strongly preferred.</p></li></ul><br><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as 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[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 12:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[ITOT Infrastructure Support Technician]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47012]]></requisitionid>
    <referencenumber><![CDATA[R47012]]></referencenumber>
    <apijobid><![CDATA[r47012]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47012/itot-infrastructure-support-technician/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>ITOT Infrastructure Support Technician is responsible for providing IT support to Manufacturing. Work closely with Manufacturing to provide IT expertise and troubleshooting of issues while ensuring smooth operation of IT equipment & applications in MFG. Support the implementation of IT projects in MFG involving end users and adhering to all clean room standards & procedures ensuring a state of compliance at all times.</p><p>As a ITOT Infrastructure Support Technician, a typical day might include the following:</p><ul><li><p>Oversees the performance of all IT hardware and applications across the Manufacturing areas.</p></li><li><p>Conduct trouble-shooting and support investigations associated with IT equipment & applications used in Manufacturing.</p></li><li><p>Support the implementation of new IT hardware and applications and liaise with stakeholders and vendors.</p></li><li><p>Prepare reports by collecting, analyzing, summarizing information and trends on the performance of IT equipment and applications.</p></li><li><p>Support communication of, preparation for and the execution of IT systems & applications downtime so impact to Manufacturing is minimized.</p></li><li><p>Liaise closely with the end users of IT equipment and applications supporting resolution of issues keeping Manufacturing & IT Management informed as required.</p></li><li><p>Issue trouble shooting guides and/or training material around IT applications & equipment as required.</p></li><li><p>Identify IT related continuous improvement ideas & projects through discussions with end users and implement opportunities of value within Manufacturing operations.</p></li><li><p>Attend all relevant Manufacturing and IT meetings, including the daily Manufacturing MDI (Managing for Daily Improvement).</p></li><li><p>Required to liaise with cross functional depts in the organization on behalf of Manufacturing in relation to IT equipment and applications.</p></li><li><p>Demonstrate strong communication skills, with the ability to clearly and concisely convey technical information to both technical and non-technical stakeholders across Manufacturing and IT teams.</p></li></ul><p>This role may be for you if you are:</p><ul><li><p>Technically competent with IT hardware in MFG e.g. Laptops, Phones, Scanners, Printers, Nova Units etc.</p></li><li><p>Technically competent on IT applications such as OPM, Orchestrate, MES, LIMS etc.</p></li><li><p>Familiar with regulatory requirements in relation to Data Integrity for IT infrastructure.</p></li></ul><p>In order to be considered for this position, you must hold an Associate's in information technology or related field along with:</p><ul><li><p>IT Support Technician III: 5 years of relevant experience.</p></li><li><p>IT Support Technician IV: 8 years of relevant experience.</p></li><li><p>IT Support Technician V: 10 years of relevant experience.</p></li><li><p>Experience in a cGMP manufacturing facility preferred.</p></li><li><p>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</p></li></ul><p>Gowning and Environment</p><ul><li><p>Full cleanroom attire (Examples 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>Physical</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours).</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lb.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 11:26:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Trade Analyst - Customs Brokerage]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46522]]></requisitionid>
    <referencenumber><![CDATA[R46522]]></referencenumber>
    <apijobid><![CDATA[r46522]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46522/senior-trade-analyst-customs-brokerage/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Trade Analyst will be responsible for executing daily trade compliance activities related to Regeneron import/exports, new product classification, licensing/permits, shipping operations support and over program activities. This is a highly interactive role that requires excellent soft skills and the ability to maneuver through complex Pharmaceutical classification procedures routinely.</p><p>As a Senior Trade Analyst, a typical day might include the following:</p><ul><li>Primary support and point of contact for all tactical trade compliance related functions.</li><li>Work daily with Regeneron’s Customs Brokers for Regeneron Trade Compliance.</li><li>Act as business liaison for Customs (CBP), FDA, and USDA including issue resolutions.</li><li>Review, validate, and confirm US harmonized tariff system (HTS) and export commodity control classifications (ECCN) for all formulated drug substance products and raw materials as necessary. This includes but is not limited to collaboration within the organization, brokerage and vendors/partners.</li><li>Ensure trade compliance best practices are executed. Advise business of trade regulatory changes, updates and keep business current on trade practices.</li><li>Manage and update Export and Import Trade Compliance Manuals.</li><li>Assist business with export or import permits. This includes conducting classification research to verify needs for licensing/permits, as well as completing the actual applications.</li><li>Create Trade Compliance related SOPs as needed.</li><li>Provide professional customer service at all times. This role interacts daily with multiple internal/external customers and requires strong soft skills.</li><li>Providing periodic training on Trade Compliance to the business.</li><li>Approximately 5% travel required.</li></ul><p>This role may be for you if you have:</p><ul><li>Knowledge of Export, Import procedures, permit applications etc. ideally within the pharmaceutical industry.</li><li>Ability to handle Customs and entry related issues and escalate when required.</li><li>Ability to manage relationships with Customs Brokers and cross functional teams.</li><li>Current knowledge of trade compliance best practices.</li><li>Licensed Customs Broker (preferable).</li></ul><p>In order to be considered for this position, you must hold a Bachelor's degree in related field and</p><ul><li>Analyst: 2+ years of experience.</li><li>Senior Analyst: 5+ years of experience.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Customs brokerage experience or trade compliance practices with exporter/importer, in chemical and/or FDA regulated industry.</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>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Enterprise Integration]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44136]]></requisitionid>
    <referencenumber><![CDATA[R44136]]></referencenumber>
    <apijobid><![CDATA[r44136]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44136/associate-director-enterprise-integration/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of Enterprise Integration is a strategic and hands-on leader responsible for defining the integration vision, establishing governance, and delivering reliable, scalable, and secure integration capabilities across the enterprise. This role owns the integration platform and services as a product, sets design principles and leading practices, orchestrates work across application and corporate shared service teams, and ensures the portfolio delivers measurable business outcomes. They will inform technical and architecture strategy, stand up and qualify new technologies, and drive continuous improvement by reducing technical debt and standardizing work.</p><p>As an Associate Director, a typical day might include the following:</p><ul><li>Inform and define the technical and architecture strategy for enterprise integration (roadmaps, tools/technology selection, platforms, patterns, standards).</li><li>Establish design principles and leading practices for APIs, architecture, data movement, orchestration, and security.</li><li>Support standing up new technology and qualifying through proofs of concept, pilots, and vendor evaluations.</li><li>Lead decisions on “which bus to get on” (e.g., ESB, event bus, streaming backbone) aligned to use cases and scalability goals.</li><li>Create and maintain an Integration “Pattern” Decision Framework to guide synchronous vs. asynchronous, pub/sub vs. request/response, batch vs. streaming, ETL vs. ELT, and choreography vs. orchestration choices.</li><li>Establish and run governance processes including intake, prioritization & work management; create and maintain Standard Work (SOPs, playbooks, runbooks, checklists) for design, build, test, deploy, and support.</li><li>Maintain an authoritative Integration Catalog of APIs, events, integrations, schemas, SLAs, and ownership.</li><li>Serve as Product Owner for the Integration Platform and shared integration services, defining vision, roadmap, backlog, and success metrics.</li><li>Orchestrate work across application teams, corporate functions (security, compliance, finance), and programs to ensure alignment and remove blockers.</li><li>Provide project management oversight across the integration portfolio: scope, timeline, budget, dependencies, risk management, and status reporting.</li><li>Drive integration quality through design reviews, pattern adherence, testing standards, and observability.</li><li>Identify, prioritize, and remediate integration technical debt (legacy patterns, brittle point-to-point, insufficient observability, poor documentation).</li><li>Implement practices for reusability, versioning, deprecation, and lifecycle management of integrations.</li><li>Own integration financials: annual budgeting, forecasting, vendor/software costs, cloud consumption, and chargeback models.</li><li>Measure and communicate ROI, TCO, and value realization of integration investments.</li></ul><p>This role may be for you if you have:</p><ul><li>Proven experience with integration platforms (iPaaS, ESB, API gateway, event streaming), such as IBM MQ, MuleSoft, Boomi, Azure Integration Services, Kafka/Confluent, AWS/GCP integration suites, or similar.</li><li>Strong grasp of integration patterns (EDA, pub/sub, CQRS, SAGA, orchestration/choreography), data movement (ETL/ELT), and API lifecycle management; knowledge of integration platforms such as Oracle Integration Cloud (OIC), middleware, and APIs.</li><li>Familiarity with enterprise architecture frameworks (e.g., TOGAF), agile at scale (e.g., SAFe), and ITIL service management practices.</li><li>Solid understanding of security, compliance, privacy, identity, and data governance as they apply to integrations.</li><li>Demonstrated success in establishing governance, standard work, and cross-functional orchestration with measurable outcomes.</li><li>Familiarity of regulatory guidelines, including GxP compliance, Sox, and security.</li><li>Expertise in Oracle SQL, PL/SQL, and reporting tools like Oracle BI Publisher and OTBI.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Senior Manager: 8+ years in enterprise integration, middleware, or API/platform architecture; 4+ years in leadership roles.</li><li>Associate Director: 10+ years in enterprise integration, middleware, or API/platform architecture; 5+ years in leadership roles.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 08:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ultra-Pure Water Technician, Sunday-Thursday 3rd shift]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46858]]></requisitionid>
    <referencenumber><![CDATA[R46858]]></referencenumber>
    <apijobid><![CDATA[r46858]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46858/ultra-pure-water-technician-sunday-thursday-3rd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking to fill an Ultra-Pure Water (Clean Utilities) Technician position with a Sunday-Thursday 10:00pm-8:30am shift. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Clean Utilities Technicians support the manufacturing process through involvement with start-up, operation, monitoring, maintaining and shutdown of clean utility systems and equipment within Clean Utility mechanical rooms.</p><p><strong>Please note training will be Monday-Friday 7:00am-3:30pm for the first few months. Working hours thereafter will be Sunday-Thursday 10:00pm-8:30am. </strong></p><p>As a Clean Utilities Technician, a typical day might include the following:</p><ul><li><p>Performing preventative and predictive maintenance on related clean utilities and systems that support manufacturing.</p></li><li><p>Maintaining water rooms and related equipment such as pumps, motors, Water for Injection (WFI) stills, Clean Steam Generators and related piping.</p></li><li><p>Performing activities such as troubleshooting, hands on repairs on all related clean utility equipment and systems, and WFI point of use flushing.</p></li><li><p>Maintaining documents and records on all validated equipment and systems.</p></li><li><p>Collaborating with other departments and contractors on scheduling repairs and maintenance of clean utility systems.</p></li><li><p>Perform monitoring and control of systems utilizing computer driven Building Automation System (BAS) and PLC controls</p></li><li><p>Communicating with management regarding change documentation as necessary.</p></li><li><p>Following current Good Manufacturing Practices (cGMPs) and Good Business Practices (G).</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur.</p></li><li><p>Participating in rotational on-call schedule.</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Can read and/or understand piping, electrical, and instrumentation drawings</p></li><li><p>Possess basic troubleshooting skills as they relate to the water room and mechanical aptitude</p></li><li><p>Demonstrate basic problem solving skills</p></li><li><p>Understand additional mechanical equipment and systems such as pharmaceutical compressed air, domestic water lines, plant steam and high/low pressure condensate return systems</p></li><li><p>Can learn and follow routine procedures independently as well as part of a team</p></li><li><p>Have the comfort and flexibility to work in a changing environment</p></li><li><p>Are capable of lifting, pushing, and/or pulling at least 50lbs</p></li><li><p>Have basic knowledge of Microsoft Office Suite</p></li></ul><p>To be considered for the Clean Utilities Technician position you must be willing and able to work Sunday-Thursday 10:00pm-8:30am. Applicants must meet the education and experience minimums listed below for each level: </p><ul><li><p>Clean Utilities Technician II: HSD/GED with 5+ years of related experience OR AAS degree and 2+ years of related experience</p></li><li><p>Clean Utilities Technician III: HSD/GED with 8+ years of related experience OR AAS degree and 5+ years of related experience</p></li><li><p>Clean Utilities Technician IV: HSD/GED with 11+ years of related experience OR AAS degree and 8+ years of related experience</p></li></ul><p>Prior experience in the maintenance and operation of large scale utilities plant is preferred but not required.</p><p>Level will be determined based on qualifications relevant to the role.</p><p>#REGENTOSK</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Phoenix North]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47133]]></requisitionid>
    <referencenumber><![CDATA[R47133]]></referencenumber>
    <apijobid><![CDATA[r47133]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47133/medical-specialist-i-allergyent-phoenix-north/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Phoenix]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Phoenix N (Allergy/ENT)</strong></p><p>Key Markets include Phoenix, Scottsdale</p><p>Our Medical Specialists are at the forefront of engaging Allergists and Immunologists as well as other key customers. We need someone who is highly proficient in presenting clinically focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, result-oriented, customer-focused team if you are up for the challenge.</p><p>As a Allergy/ENT Medical Specialist, a typical day might include the following:</p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology health care professionals including physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups as directed</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings, and medical conferences.</p></li></ul><p>This role may be for you if:</p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Precision Medicine (Cell Medicine)]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46672]]></requisitionid>
    <referencenumber><![CDATA[R46672]]></referencenumber>
    <apijobid><![CDATA[r46672]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46672/director-precision-medicine-cell-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking to hire a Precision Medicine Scientific Lead to oversee the development and execution of biomarker strategies for novel cell therapies, cell transfer conditioning agents and combinations with bispecific antibodies across multiple disease areas (Oncology and Immunology). In this highly matrixed role, they will design, develop, communicate across levels and operationally implement clinical biomarker strategies to support selecet programs in early and late stage drug development. Clinical biomarker assays include pharmacokinetic assays, mechanism of action, patient stratification assays and pharmacodynamic assays. The candidate will collaborate with teams internal to RCM and more broadly Regeneron or with contract research organizations to develop and implement clinical biomarker assays.</p><p><strong>As a Director, a typical day may include the following:</strong></p><ul><li><p>Program-level Precision Medicine lead that develops and implements the strategic vision for pharmacokinetic, pharmacodynamic, and exploratory biomarkers for clinical studies enabling indication and/or patient selection, early indication of biological activity, and to identify potential novel combinations.</p></li><li><p>String collaboration with Biomarker and clinical operation teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Key individual contributor and precision medicine representative to development and Cell therapy characterization teams with a remit to integrate, influence and deliver biomarker strategies from initial concept to execution, data delivery and results interpretation.</p></li><li><p>Collaborate with internal Regeneron laboratories and groups (e.g. BioAnalytical, Clinical Pharmacology, Molecular Profiling, CDX, Discovery Research, Analytical Innovations, DMSQ etc.) to develop plan for validation and application of assays in the clinic.</p></li><li><p>Accountability for ensuring complex clinical assays used in programs are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine biomarker strategies for molecules in discovery phases (leading to candidate molecule selection) through to the clinic.</p></li><li><p>Represent Regeneron externally thorough collaborations and/or presentations.</p></li><li><p>Contribute to Clinical Protocol, schedule of Assessments, clinical study reports, technical reports, data agreements, scientific publications and make recommendations to development teams and management</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>The ability to drive, manage, complete and deliver results for complex multi-functional projects</p></li><li><p>Excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills</p></li></ul><p><strong>To be considered for this role, you must have a </strong>PhD and 10+ years of experience participating effectively on cross-disciplinary teams in pharmaceutical or biotech industry. Experience in clinical assay development, validation and implementation with strong experience in Immunology is preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Legal Data Privacy Operations]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47119]]></requisitionid>
    <referencenumber><![CDATA[R47119]]></referencenumber>
    <apijobid><![CDATA[r47119]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47119/senior-manager-legal-data-privacy-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an experienced and forward-thinking Senior Manager Legal Data Privacy Operations to lead privacy program operations within the Law Dept. / Privacy Office. As a key member of the Privacy Office within Regeneron’s Law Department, you will play an important role in advancing our data privacy program. This includes managing complex privacy projects, delivering tactical operational support, and supporting governance initiatives. By leading well-designed and executed privacy operations, this role plays a central part in building the organizational foundation that enables Regeneron to manage data responsibly, maintain trust, and support the company's overall mission.</p><p><strong><em>A typical day might include:</em></strong></p><ul><li><p>Managing and identifying opportunities to improve core privacy operations, including PIA, ROPA, and DSAR processes across multiple business units, geographies, and regulatory frameworks.</p></li><li><p>Leading complex privacy program initiatives that involve coordinating and aligning privacy processes with other business functions and leveraging technology and AI to automate, find efficiencies, and enhance how privacy operations are managed and executed.</p></li><li><p>Documenting advice and implementation of online privacy notices and controls, tracking technologies, and privacy-enhancing tools.</p></li><li><p>Developing and maintaining privacy program metrics and KPIs.</p></li><li><p>Maintaining and developing internal policies, procedures, guidance documents, training and awareness, including our Intranet site.</p></li><li><p>Coordinating Privacy Steward engagement to advance enterprise-wide privacy initiatives in alignment with organizational objectives and regulatory requirements.</p></li><li><p>Managing vendor relationships by overseeing the execution of Statements of Work and ensuring timely processing of requisitions, purchase orders, and invoices.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Knowledge of privacy laws and understanding of privacy risk management technologies</p></li><li><p>Demonstrated ability to critically evaluate privacy processes and implement innovative, practical improvements.</p></li><li><p>Experience collaborating with teams outside of privacy or legal function to integrate privacy requirements into business operations.</p></li><li><p>Strong project management skills and ability to manage multiple priorities and deliverables simultaneously</p></li><li><p>Excellent relationship building skills and demonstrated ability to work collaboratively</p></li><li><p>Exceptional oral, written, and presentation communication skills</p></li><li><p>AI literacy and experience leveraging technology to support or enhance privacy operations</p></li></ul><p><strong>To be considered for this role</strong>, you must have a bachelor's degree, advanced degree in a related field preferred. At least 8 years of experience in privacy, with a preference for at least 3 years managing privacy operations (including PIA, ROPA, and DSAR processes) within a legal or compliance privacy function.</p><p>Certified Information Privacy Manager (CIPM) or Certified Information Privacy Technologist (CIPT) Project Management Professional (PMP) or equivalent certification.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 20:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Technical Analyst - Manufacturing Systems]]></title>
    <date><![CDATA[Fri, 01 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45572]]></requisitionid>
    <referencenumber><![CDATA[R45572]]></referencenumber>
    <apijobid><![CDATA[r45572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45572/principal-technical-analyst-manufacturing-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal Technical Analyst - Manufacturing Systems will serve as a technical expert responsible for implementing and integrating manufacturing technologies across our biopharmaceutical facilities. You will execute hands-on technical builds and integrations spanning Nymi biometric systems, IBM Maximo EAMS (Enterprise Asset Management System), and related manufacturing technologies, ensuring compliant deployment that supports operational excellence and predictive maintenance capabilities.</p><p>As a Principal Technical Analyst - Manufacturing Systems , a typical day might include the following:</p><ul><li>Execute technical builds and integrations for manufacturing systems including Nymi biometric authentication, IBM Maximo EAMS, MES platforms, and associated technologies across designated facilities or project portfolios.</li><li>Implement integration solutions connecting Maximo with predictive maintenance systems, MES workflows, and biometric access controls, following established architectural frameworks.</li><li>Configure IBM Maximo EAMS modules including work management, asset management, and predictive maintenance capabilities for future release implementations.</li><li>Build and test Nymi biometric integration points with manufacturing systems to enable secure, compliant user authentication workflows.</li><li>Execute validation protocols (SDLC Framework aligned to CSA) for manufacturing technology implementations in FDA-regulated environments, ensuring documentation meets regulatory standards.</li><li>Implement change control procedures for system modifications, maintaining compliance throughout the development lifecycle.</li><li>Configure master data elements within assigned systems following established data architecture standards.</li><li>Support transformation of paper-based processes into digital workflows while maintaining regulatory compliance requirements.</li><li>Diagnose integration problems between Maximo, biometric systems, MES platforms, and automation equipment (Ignition, DeltaV, Rockwell).</li><li>Partner with senior technical leads, automation engineers, and site stakeholders to understand requirements and deliver technical solutions aligned with business objectives.</li></ul><p>This role may be for you if you have:</p><ul><li>Practical experience dealing with project management, particularly dealing with the implementation of new technology and ways of doing things.</li><li>Ability to understand and engage broader business strategy, work with key department leaders and stakeholders and align activities and initiatives.</li><li>A demonstrated ability in creation of requirements, design documents and test scripts.</li><li>Must be competent to work at the technical level of all phases of system design and implementation.</li><li>Ability to communicate at all levels with clarity and precision both written and verbally together with strong presentation skills.</li><li>Ability to anticipate client needs and propose alternative business solutions</li><li>Knowledge of GMP, 21 CFR Part 11 and Annex 11.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field required along with </p><ul><li>Principal: 8+ years of progressive industry/relevant experience. </li><li>Staff: 10+ years of progressive industry/relevant experience. </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 have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 01 May 2026 06:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[District Manager Florida (Allergy ENT)-Florida]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46690]]></requisitionid>
    <referencenumber><![CDATA[R46690]]></referencenumber>
    <apijobid><![CDATA[r46690]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46690/district-manager-florida-allergy-ent-florida/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Florida]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Orlando, Miami, Fort Lauderdale, West Palm, Sarasota, and Naples</strong></p><p>The District Manager (DM), Allergy/ENT will report to the Regional Director, Allergy/ENT and be responsible for hiring, leading, developing and retaining Allergy/ENT 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>A Typical Might Look Like This:</strong></p><ul><li><p>Successful leadership record of hiring, coaching, developing, promoting, and retaining top talent within span of control and ability to effectively manage performance of the team.</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a District Sales Manager in complex markets within complex systems required.</p></li><li><p>Strong understanding of Payer environment, reimbursement and challenges within National, Regional and local payer market including; government programs, managed health care and evolving health care systems.</p></li><li><p>Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners.</p></li></ul><p><strong>This Position Might Be for You If:</strong></p><ul><li><p>Successful leadership record of hiring, coaching, developing, promoting, and retaining top talent within span of control and ability to effectively manage performance of the team.</p></li><li><p>Proven success and positive track record of performance with a high degree of integrity as a District Sales Manager in complex markets within complex systems required.</p></li><li><p>Strong understanding of Payer environment, reimbursement and challenges within National, Regional and local payer market including; government programs, managed health care and evolving health care systems.</p></li><li><p>Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p></li><li><p>Ability to partner and collaborate with other internal field teams and alliance partners.</p></li></ul><p>To be considered for this opportunity you will have the following: Bachelor’s degree required, Master’s degree or other advanced education/certifications a plus (Focused degree in science or clinical experience is a plus). Minimum of 7 years of pharmaceutical/biopharmaceutical experience with 3 years of sales leadership/management in sub-cutaneous self-injectable biologic markets required. Experience in the market strongly preferred. Ability to travel extensively with local and regional influence.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$175,300.00 - $218,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 08:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II, Advanced Therapy Project Management (ATPM)]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47142]]></requisitionid>
    <referencenumber><![CDATA[R47142]]></referencenumber>
    <apijobid><![CDATA[r47142]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47142/process-development-engineer-ii-advanced-therapy-project-management-atpm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron, located in Tarrytown, NY, is seeking a Process Development Engineer II to support project management, technology transfer, and business operations for Regeneron Advanced Therapy Programs. This representative will work in the Advanced Therapy Project Management (AT-PM) group within Product, Analytical, and Process Development Operations (PAPD Ops) to help drive successful development and tech transfer of advanced therapies (e.g., AAV, bioconjugates, and synthetic chemistry programs) by enabling clear cross-functional ways of working, disciplined planning, and operational excellence with our internal partners and Contract Development & Manufacturing Organizations (CDMOs).</p><h3><strong>A Typical Day in This Role Might Look Like:</strong></h3><ul><li>Lead cross-functional tech transfer teams and independently own workstreams to establish production processes at CDMOs. Drive readiness for manufacturing start-up and execution by clarifying scope, securing inputs/approvals, tracking deliverables, and escalating risks/issues with proposed mitigations.</li><li>Own communication strategy and operating cadence for assigned programs (e.g., core team meetings, technical forums, and stakeholder updates). Provide concise, decision-ready status reporting (scope/timeline/cost/risk) tailored to different audiences, including senior stakeholders.</li><li>Build, maintain, and continuously improve integrated plans across development and transfer activities. Facilitate scenario planning and tradeoff discussions to protect key milestones and support portfolio-level prioritization.</li><li>Anticipate and address risks to manufacturing readiness related to process. Define mitigation plans and help ensure teams execute with rigor expected for successful CDMO campaign execution.</li><li>Lead recurring and ad-hoc technical forums to drive timely decisions, resolve issues, and capture lessons learned. Translate learnings into tools to improve repeatability across modalities and CDMOs.</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 (RFPs, scope alignment, contracting coordination, and invoice tracking).</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, bringing energy, a strategic mindset, and an action-oriented approach while navigating ambiguity and changing priorities.</li><li>You enjoy and excel at problem solving and can break down complex technical and operational challenges, propose well-thought-out plans, and drive decisions.</li><li>You like building structure and scalable frameworks that help cross-functional teams execute efficiently and with the right balance of rigor and flexibility.</li><li>You proactively identify risks/roadblocks, communicate tradeoffs, and know when and how to escalate.</li><li>You are willing to try, learn, and iterate to keep programs moving forward and partners aligned.</li></ul><p>This role requires a B.Sc., with 5+, or M.Sc. with 3+ years of biochemistry/ chemical/biochemical engineering or a related field, including demonstrated ownership of cross-functional deliverables. A strong customer-service mindset is essential. The ideal candidate can independently facilitate team collaboration, build and maintain integrated plans, and design/improve repeatable business processes. Experience supporting CMC development and/or technology transfer to CDMOs (e.g., process development, analytics, documentation readiness) is preferred. Prior experience or knowledge of bioconjugation, gene therapy/AAV, or related advanced therapy process development is a plus.</p><p>If applicable, candidates may include GPA on their resume.</p><p>#pmpd</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 12:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Business Office]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47016]]></requisitionid>
    <referencenumber><![CDATA[R47016]]></referencenumber>
    <apijobid><![CDATA[r47016]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47016/director-global-patient-safety-business-office/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director, Global Patient Safety Business Office to join our organization!!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, GPS Business Office, serves as a strategic partner to the SVP of Global Patient Safety, driving execution of GPS’ overarching strategic plan, including the annual department operating plan, long-term roadmap, and key transformation initiatives for pharmacovigilance (PV) enablement (e.g., Global Capabilities Center (GCC)). This role leads business planning, execution and enablement of GPS initiatives, communication strategies, resource management, PV forecasting and capacity planning, talent calibration, and the PV functional-level vendor strategy.</p><p><strong>This role might be for you if can/have:</strong></p><ul><li><p>Define and communicate the GPS vision and strategy in alignment with enterprise goals and business priorities </p></li><li><p>Serve as a strategic thought partner to the SVP of Global Patient Safety regarding PV strategy, and operating model </p></li><li><p>Act as a strategic connector across GPS teams to enable execution of GPS vision, strategy and priorities </p></li><li><p>Lead strategy and governance for the Global Capabilities Center (GCC) across GPS functions, aligning scope, resourcing, and metrics to GPS priorities and enterprise objectives, to expand PV capacity and drive measurable outcomes </p></li><li><p>Lead development of annual department operating plans and strategic roadmaps for GPS </p></li><li><p>Drive operational excellence in collaboration with GPS leaders, through benchmarking and continuous improvement </p></li><li><p>Partner with GPS interfacing functions to enable PV operational alignment </p></li><li><p>Collaborate with GPS leadership on goal setting, initiative tracking, and performance dashboards </p></li><li><p>Lead delivery of key GPS functional meetings (e.g., GPS Leadership Team, All Hands, Mid-Year meetings). </p></li><li><p>Prepare and maintain regular delivery of GPS communications </p></li><li><p>Organize and manage mid-year and year-end talent calibration exercises in collaboration with stakeholders and HR Business Partners (HRBPs) </p></li><li><p>In partnership with RA GPS DQ Strategy and Operations and Portfolio Management, establish operational portfolio forecasting for GPS </p></li><li><p>Lead resource planning and optimization across GPS functions (internal staffing, GCC expansion, vendor utilization) in partnership with stakeholder functions (e.g., Vendor Relationship Management, GD Resource Management, RA GPS DQ Strategy Planning & Operations, and Portfolio Management) </p></li><li><p>Collaborate cross-functionally in support of GPS with Development Services & Operational Excellence (DS&OE) team, and Learning Center of Excellence (LCoE) functions. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum Bachelor’s Degree (Advanced Degree preferred) in business, strong preference for degree in life sciences or healthcare with 10+ years of relevant PV planning and operations experience in the pharmaceutical area and specific industry experience in managing and providing oversight of operations within a global patient safety organization highly preferred. </p></li><li><p>Proven ability to lead and develop a diverse remit in a constructive, goal-oriented environment, with continuous improvement and innovation mindset. </p></li><li><p>Demonstrated pharmacovigilance (PV) and Safety Risk Management (RM) expertise, including end-to-end safety processes, regulatory expectations, and cross-functional governance within a global patient safety organization </p></li><li><p>Demonstrated problem-solving with the ability to “flex” across different complexities, business situations and cross functional partners of GPS </p></li><li><p>Proven ability to drive results through strong cross-functional partnerships and stakeholder engagement </p></li><li><p>Demonstrated ability and track-record to lead PV operational and planning initiatives with excellence, including governance activities </p></li><li><p>Highly detail-oriented, ensuring accuracy, consistency, and quality across deliverables, documentation, and communications, while maintaining strategic perspective. </p></li></ul><p>#GDPSJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as 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[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 15:56:13 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs-Chicago/St Louis (Neurology)]]></title>
    <date><![CDATA[Sat, 09 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46422]]></requisitionid>
    <referencenumber><![CDATA[R46422]]></referencenumber>
    <apijobid><![CDATA[r46422]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46422/senior-manager-field-medical-affairs-chicagost-louis-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>As a Senior Manager, you will play a pivotal role as a field-based/Medical Science Liaison providing scientific and Neurology therapeutic area expertise. The Senior Manager will become a scientific expert communicating accurate and applicable science to medical and health care professionals, and payers. In addition, you will support our strategic medical objectives by developing and maintaining professional relationships through facilitating collaboration opportunities. </p><p><strong>Territory: </strong>Chicago, St Louis, including IL, MO, KS, MN, NE, IA, WI ND, SD</p><p><strong>A typical day may include the following: </strong></p><ul><li>Develop and maintain peer–to–peer collaborations and relationships with medical and scientific experts, and population health decision makers. </li><li>Participate on committees or project teams supporting field medical strategies and tactics. </li><li>Respond to unsolicited medical information requests, handle questions and liaise with headquarters personnel ensuring proper responses have been provided and data is fair and balanced. </li><li>Develop an understanding of the regional landscape including specialties involved in care of patients in that area & other landscape mapping activities. </li><li>Identify and bring actionable information & insights that enhance the value and appropriate use of our products back to appropriate internal collaborators. </li><li>Build and cultivate important working relationships across field partners to ensure an integrated approach when working with HCP’s or experts. </li><li>Collaborate with physicians on medical affairs initiatives including publications, Company– sponsored research (CSR), regional advisory boards, regional medical education opportunities, training and speaker development programs. </li><li>Develop and sustain expertise in product/molecule data, disease state management, emerging therapies, and the competitive landscape. </li><li>Respond to HCP inquiries with integrity, compliance, and adherence to legal, regulatory, and our guidelines, policies & procedures ensuring focused and balanced clinical and scientific information. </li><li>Support clinical research activities throughout the life cycle (phase 1-4), as well as Investigator Initiated Studies, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ experts and sites in alignment with Medical Affairs objectives </li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) along with a minimum of 3-5 years related work experience preferred (clinical, managed care, or industry experience) including experience as a Medical Science Liaison. Recent experience in Neurology is preferred. Established relationships with KOLs in neuromuscular centers is preferred. Experience communicating and disseminating scientific and clinical data required. Travel within the assigned territory and attendance at industry conferences is required. </p><p>#msl #medicalscienceliaison</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 10 May 2026 19:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II-Ophthalmology-Denver]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47329]]></requisitionid>
    <referencenumber><![CDATA[R47329]]></referencenumber>
    <apijobid><![CDATA[r47329]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47329/medical-specialist-ii-ophthalmology-denver/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Denver]]></city>
    <state><![CDATA[Colorado]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Territory: Denver Territory (Colorado/Nebraska)</strong></p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets several medicines, including for eye diseases, and has product candidates in development in other areas of high unmet medical need.</p><p><strong>A typical day might include the following:</strong><br>The Medical Specialist II will report to the Regional Director and will be responsible for daily development and management of relationships with Retina Specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The primary focus on this role will be the approved indications suffered by patients as it relates to conditions of the eye. The Medical Specialist II will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you:</strong><br>• Have experience in biologics and buy and bill products<br>• Can demonstrate history of high sales performance<br>• Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Ophthalmology and/or Buy & Bill with relevant retina experience is preferred. Residency in the territory is required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Commercial Data Science - Immunology]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47027]]></requisitionid>
    <referencenumber><![CDATA[R47027]]></referencenumber>
    <apijobid><![CDATA[r47027]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47027/associate-director-commercial-data-science-immunology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Associate Director, Commercial Data Science to join the Immunology Advanced Analytics team within CSI&A. This portfolio-level role supports multiple indications within the Immunology portfolio across a co-promote alliance. In collaboration with the Director, this individual will leverage data science, machine learning, and AI to drive marketing and sales execution effectiveness — owning end-to-end MMM delivery, advanced analytics workstreams, and an active mandate to evaluate and integrate AI capabilities into commercial workflows.</p><p><strong>In this role, a typical day might include:</strong></p><p>Reporting into the Director, Advanced Analytics – Immunology, this individual will serve as a primary day-to-day owner of deliverables while collaborating with the Director on strategic direction, stakeholder engagement, and prioritization. The role involves helping manage external vendor relationships, coordinating with alliance counterparts, and applying AI and data science capabilities to drive efficiency and innovation — all within a team culture of analytical rigor and continuous improvement.</p><p><strong>This role might be for you if you can / have:</strong></p><p><em>Lead</em></p><p>1) Own end-to-end delivery of Marketing Mix Modeling (MMM) across multiple indications within the Immunology portfolio — including data validation, KBQ alignment with marketing stakeholders, high-level readouts, media deep dives, alliance model coordination, and sales leader presentations — in collaboration with the Director.</p><p>2) Contribute to the ongoing standardization and continuous improvement of the MMM process, partnering with external modeling and media agency partners to support a repeatable, scalable workflow.</p><p>3) Lead advanced analytics workstreams — including promotional response modeling, HCP targeting, Next Best Action (NBA), and attribution/referral modeling — leveraging data science and machine learning techniques to drive marketing and sales execution effectiveness across the Immunology portfolio.</p><p>4) Lead the evaluation and integration of AI and data science capabilities into commercial analytics workstreams and deliverables, identifying opportunities to drive efficiency, analytical depth, and business value.</p><p>5) Lead communication of analytical outputs to VP-level and cross-functional commercial audiences, translating complex model results into clear, actionable business implications.</p><p><em>Develop</em></p><p>6) Develop structured data pipelines and analytics-ready datasets supporting portfolio and indication-level advanced analytics using SQL, Python/PySpark, or equivalent tools.</p><p>7) Develop analytical frameworks that address priority commercial business questions using syndicated pharmaceutical data assets including IQVIA NPA, DDD, APLD, and CRM data.</p><p>8) Contribute to analytics-ready dataset governance and semantic layer development within cloud-based data environments (Databricks, Snowflake), ensuring data assets are structured, validated, and fit for downstream use.</p><p>9) Develop and apply AI, machine learning, and data science methodologies to enhance the depth, scalability, and commercial impact of marketing and sales analytics deliverables.</p><p><em>Partnership and Collaboration</em></p><p>10) Help manage external analytics vendor relationships — including modeling partners, media measurement vendors, and data collection partners — ensuring deliverables are accurate, timely, and aligned with business goals.</p><p>11) Coordinate MMM and analytics deliverables with alliance counterparts at Sanofi, including side-by-side model comparisons and cross-partner alignment on methodology and business implications.</p><p>12) Partner with Immunology commercial stakeholders across Marketing, Sales, Finance, and Market Access to translate analytical outputs into strategic and tactical decisions.</p><p>13) Collaborate with Data Management and platform teams to ensure analytics infrastructure supports current and future use cases across the Immunology portfolio.</p><p>14) Ensure compliance with privacy, regulatory, and legal requirements across all analytical workstreams and data assets.</p><p><em>Execute</em></p><p>15) Execute indication-level and cross-portfolio analytics including MMM readout cycles, promotional sensitivity analyses, HCP targeting models, and search/media ROI assessments.</p><p>16) Execute rigorous data analysis using SQL, Python/PySpark, R, or equivalent tools within Databricks or Snowflake environments.</p><p>17) Measure and track promotional performance against success metrics across indications; develop insights that guide investment optimization and course correction.</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Bachelor’s degree required; MBA/Master’s degree desired.</p></li><li><p>MBA/Master’s degree and 7+ years of commercial analytics experience OR Bachelor’s degree and 10+ years of experience in pharmaceutical or biotech commercial analytics, data science, or a related field. Immunology or biologics experience preferred.</p></li><li><p>Demonstrated hands-on expertise with structured pharmaceutical data assets, including syndicated datasets such as IQVIA, APLD, claims, or equivalent Rx data sources.</p></li><li><p>Familiarity with omnichannel data assets and platforms supporting DTC and HCP engagement measurement, including media delivery, digital touchpoint, and clean room data sources (e.g., LiveRamp, Crossix, or equivalent).</p></li><li><p>Proficiency in SQL and Python/PySpark or R within a cloud analytics environment (Databricks, Snowflake, or equivalent).</p></li><li><p>Experience owning or significantly contributing to Marketing Mix Modeling (MMM) engagements — including full-cycle delivery from data validation through stakeholder readout and vendor coordination.</p></li><li><p>Familiarity with analytics-ready data architecture, semantic layer concepts, and cloud-based data platform governance in a commercial pharma context.</p></li><li><p>Experience with advanced analytics techniques including promotional response modeling, HCP targeting, attribution modeling, or Next Best Action (NBA) frameworks.</p></li><li><p>Demonstrated experience with AI and machine learning methodologies and their application to commercial analytics use cases; experience integrating AI tools, predictive models, or automation into marketing and sales analytics workflows required.</p></li><li><p>Ability to translate complex analytical outputs into clear business implications for marketing, sales, and senior leadership audiences.</p></li><li><p>Strong communication, presentation, and data storytelling skills with demonstrated ability to influence across functions and seniority levels.</p></li><li><p>Proven success managing multiple concurrent analytical workstreams and external vendor relationships in a fast-paced, deadline-driven environment.</p></li><li><p>Experience working within or alongside an alliance or co-promote structure preferred.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Precision Medicine]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47367]]></requisitionid>
    <referencenumber><![CDATA[R47367]]></referencenumber>
    <apijobid><![CDATA[r47367]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47367/senior-manager-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, SKDL Automation & Programming Lead, will drive the technical strategy, development, and implementation of automation solutions across Samples, Kits, Data, and Logistics (SKDL) within Precision Medicine Operations. This role serves as the technical authority for clinical sample/data workflows and leads the design, programming, and deployment of scalable tools, integrations, and dashboards to modernize SKDL operations.</p><p>The individual will combine deep knowledge of clinical sample/data processes with strong computational programming expertise to enable high‑quality, timely, and compliant biomarker sample and data delivery. Responsibilities include architecting automation pipelines, building analytical dashboards, optimizing data flows, and ensuring operational readiness for database locks and biomarker deliverables. Preferred background includes familiarity with central and specialty labs, LIMS, data operations, APIs, database design, and sample tracking systems. Proficiency in Python, R, SQL, and/or MATLAB is required.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Lead the design and implementation of automation solutions to streamline SKDL processes and reduce manual effort across samples, kits, and clinical data workflows.</p></li><li><p>Develop, maintain, and scale dashboards, data pipelines, and computational tools for real‑time sample/data tracking and issue resolution.</p></li><li><p>Build automated data cleaning, transformation, and integration workflows using industry‑standard programming languages and platforms.</p></li><li><p>Design programmatic extraction and aggregation of key insights from operational reports and lab vendor outputs.</p></li><li><p>Architect structured data models, ontologies, and mappings across samples, kits, lab data, and metadata.</p></li><li><p>Develop and support API‑based integrations between central labs, specialty labs, LIMS, EDC, and internal systems.</p></li><li><p>Provide end-to-end oversight of clinical trial biosamples and data generation—from collection through storage and disposal—per study requirements.</p></li><li><p>Serve as the point of contact for resolving complex technical and sample/data issues with central and specialty labs.</p></li><li><p>Maintain and review operational metrics across studies related to samples, kits, data quality, and logistics.</p></li></ul><p><strong>This role may be for you, if you have:</strong></p><ul><li><p>Advanced proficiency in one or more programming languages: Python, R, SQL, MATLAB, or Perl.</p></li><li><p>Experience with APIs, database development, dashboard/visualization tools, and Linux/Unix environments.</p></li><li><p>Knowledge of structured data concepts such as entities, classes, hierarchies, relationships, and metadata.</p></li><li><p>Experience with central/specialty labs, LIMS, kit management systems, and sample tracking workflows.</p></li><li><p>Strong ability to evaluate sample/data interdependencies, risks, and upstream/downstream impacts on clinical programs.</p></li></ul><p><strong>To be considered for this role, you must have a </strong>Bachelor’s or Master’s degree in a scientific, computational, or engineering discipline. 10+ years of relevant experience in clinical research within academic, CRO, biotech, or pharmaceutical settings, with strong knowledge of clinical trials, sample/data workflows, and clinical databases.</p><ul></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 20:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs, Advertising & Promotion]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45490]]></requisitionid>
    <referencenumber><![CDATA[R45490]]></referencenumber>
    <apijobid><![CDATA[r45490]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45490/manager-regulatory-affairs-advertising-promotion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Manager, of Advertising and Promotion to join our Regulatory Affairs team!!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidances to the development of key product messages presented in Biologic License Applications (BLAs) and Marketing Authorization Applications (MAAs). This individual will provides regulatory advertising and promotion expertise to relevant stakeholders, typically carrying out the responsibilities with guidance from the Regulatory Affairs, Advertising and Promotion Director. The Manager Regulatory Affairs, Advertising and Promotion will oversee therapeutic area(s) and ensure that messages are translated into advertising and promotion initiatives that meet the commercial team’s objectives, while maintaining the necessary state of compliance and corporate integrity.</p><p><strong>This role might be for you if you can/Have</strong></p><ul><li><p>Management of US regulatory activities associated with advertising and promotion of the company’s marketed products. Manages commercial activities from a regulatory advertising and promotion perspective with guidance from the Regulatory Affairs, Advertising & Promotion Director.</p></li><li><p>Creatively contribute to the advise on the development of product messages and materials across multiple functional areas.</p></li><li><p>Provide timely regulatory advice and guidance, with guidance from Regulatory Affairs, Advertising & Promotion Director, to Commercial teams and Medical Affairs with respect to conference exhibit activities, disease awareness and speaker programs</p></li><li><p>Provide review of US and Global (if applicable) product and disease state materials/communications, with guidance from Regulatory Affairs, Advertising & Promotion Director, to support corporate goals and comply with applicable laws, regulations, and guidance.</p></li><li><p>Collaborate cross functionally with key stakeholders in areas such as Marketing, Medical Affairs, and Legal.</p></li><li><p>Responsible for establishing working relationship and managing communication with regulatory advertising and promotion professionals at co-promote partner companies</p></li><li><p>Help lead and assist in all interactions with the FDA Office of Prescription drug Promotion (OPDP) for assigned company products, responsible for helping to maintain working relationship and effective communication with FDA OPDP reviewers with respect to advertising and promotion matters, including request for advisory submissions.</p></li><li><p>Responsible for compliance with promotional material submissions to FDA on Form 2253</p></li><li><p>Monitor the external environment to advise product teams on evolving regulatory requirements related to product and disease state communications</p></li><li><p>Maintain vigilance with respect to FDA promotional enforcement activities; provide stakeholders with updates on a regular basis; in partnership with management, provide guidance to stakeholders with respect to impact of enforcement activities on the company policies.</p></li><li><p>Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization of policies</p></li><li><p>Ability to cross train across products/indications to ensure continuous Regulatory A&P support is provided to stakeholders</p></li><li><p>Collaboration with Regulatory Therapeutic Area Leads to review key marketing application summary documents and study reports</p></li><li><p>With guidance from management, help provide input during review cycles to reflect commercialization objectives and messages in the submission documents/reports that are submitted to health authorities</p></li><li><p>Provide input to management during labeling development and negotiation to reflect commercialization objectives and messages that impact promotion and advertising.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>A minimum of 2 total years relevant experience, preferably within Regulatory Advertising and Promotion</p></li><li><p>At minimum, a Bachelor's degree (BS) from an accredited college or university in Life Sciences. An Advanced Scientific degree (i.e., Masters, PharmD, Ph.D) is preferred.</p></li><li><p>Knowledge of regulations, guidelines and precedents related to pharmaceutical product development and marketing, with focus in the area of advertising and promotion</p></li><li><p>Experience with pharmaceutical products required, biologics experience is a plus</p></li><li><p>Experience working directly/indirectly with the FDA, specifically OPDP/APLB is preferred</p></li><li><p>Ability to review promotional materials and interact with FDA OPDP/APLB and support launch products/campaigns, while maintaining excellent written/verbal communication skill when giving strategic regulatory advice</p></li><li><p>Ability to support global promotional review, understanding of clinical trial recruitment materials, and familiarity with labeling regulations is desirable</p></li><li><p>Contributes to the influence of cross-functional teams and may interact with senior management</p></li></ul><p>#GDRAJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Novel Oligonucleotide Delivery Platforms]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47616]]></requisitionid>
    <referencenumber><![CDATA[R47616]]></referencenumber>
    <apijobid><![CDATA[r47616]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47616/associate-scientist-novel-oligonucleotide-delivery-platforms/]]></url>
    <company><![CDATA[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 scientist to join the Non-Viral Delivery Technologies group within Regeneron Genetic Medicines. You will support production, purification, and characterization of proteins and larger macromolecular protein-based nanocarriers to be used in next-generation delivery technology development, further expanding the company’s growing genetic medicines portfolio.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Maintenance and manipulation of bacterial and mammalian cells for protein expression</p></li><li><p>Designing and cloning constructs into appropriate expression vectors</p></li><li><p>Operation of AKTA systems for small scale purification by liquid chromatography-based techniques (e.g. affinity, ion exchange, size exclusion)</p></li><li><p>In vitro reporter assays with adherent and suspension cell lines or primary cells</p></li><li><p>Characterization of proteins (e.g. SDS-PAGE, SE-UPLC, CE, DLS)</p></li><li><p>Working collaboratively with other team members and groups around the company</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Enjoy working in a fast-paced environment with rapid hypothesis generation and testing</p></li><li><p>Can troubleshoot through logistical and technical hurdles as they arise</p></li><li><p>Can work independently and show initiative to continually improve protocols and processes</p></li><li><p>Can tolerate failure, ambiguity, data-driven pivots on changing priorities and project direction</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this role, you must have:</strong></p><ul><li>A BS/MS in molecular biology, biochemistry, bioengineering, or related fiel</li><li>Previous experience in cloning, bacterial-based expression systems, self-assembled VLPs are a plus. </li><li>Experience with aseptic technique used in mammalian cell culture, chromatography, running an AKTA Pure, and SDS-PAGE/CE are distinct advantages. </li><li>To be successful in this role, you need to work collaboratively, have attention to detail, and be organized. </li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)]]></title>
    <date><![CDATA[Sat, 20 Sep 2025 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42074]]></requisitionid>
    <referencenumber><![CDATA[R42074]]></referencenumber>
    <apijobid><![CDATA[r42074]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42074/medical-director-clinical-development-oncology-lung-breast-colorectal-gastric-cancers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials. This role may work on studies in melanoma, lung, breast, gastric, or colorectal cancers.</p></div><div><p><strong>As a Medical Director, a typical day may include the following:</strong></p><ul><li><p>Defines clinical trial-related goals and objectives.</p></li><li><p>Conducts literature and database research on clinical trials as needed</p></li><li><p>Collaborates with Clinical Project Managers and Clinical Trial Managers at the study level and with the Therapeutic Area Program Manager</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.</p></li><li><p>Leads and supervises the Clinical Team to produce high quality program deliverables on schedule</p></li><li><p>Maintains and develops relationship with key study investigators</p></li></ul><p><br><strong>This role may be for you if:</strong></p><ul><li><p>You are passionate about impacting entire populations of patients</p></li><li><p>You want to learn innovative approaches to drug development</p></li><li><p>You want to be a part of a collaborative, growing team</p></li></ul><p><br><strong>To be considered for this role</strong>, you must have a MD or MD/PhD with a minimum of 3 to 5 years of relevant research experience. Oncology clinical fellowship training with translational and/or clinical research experience is strongly preferred.</p><div><p><em>This role has a 4-day onsite minimum requirement in Tarrytown, NY or Warren, NJ.</em></p></div><div><div><div><div></div></div></div></div><p>#MDJOBSCD, #MDJOBS, #GDTher, #Oncology</p></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!</p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$280,700.00 - $379,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:43 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Reporting and Analytics Lead (Oracle Fusion)]]></title>
    <date><![CDATA[Thu, 18 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44208]]></requisitionid>
    <referencenumber><![CDATA[R44208]]></referencenumber>
    <apijobid><![CDATA[r44208]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44208/director-erp-reporting-and-analytics-lead-oracle-fusion/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oracle Fusion ERP Reporting and Analytics Lead oversees the reporting and analytics strategy for the Oracle Fusion Cloud implementation. This role partners closely with SI partners, GPOs, Product Leads, Data Engineering, and Business SMEs to rationalize reporting requirements and guide the design and development of reporting solutions across Oracle Fusion Cloud reporting tools and Fusion Data Intelligence (FDI). The role ensures that reporting architecture, data sourcing, and analytics approaches align with enterprise standards, support phased modernization—from Oracle EBS to Oracle Cloud—and comply with data governance and AI policies, including the responsible use of Oracle AI Agents.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Provide leadership and subject-matter expertise across Oracle Fusion Cloud reporting tools, including OTBI, BI Publisher, Fusion Data Intelligence (FDI), OAC within FDI, Financial Reporting Center, Account Inspector/Monitor, Smart View, and embedded dashboards/KPIs.</p></li><li><p>Work closely with the SI partner to guide reporting design, validate deliverables, and ensure solutions meet business requirements and align with Oracle Cloud capabilities.</p></li><li><p>Lead the report rationalization strategy, determining the appropriate placement of reporting across Fusion-native tools, FDI, the Data Lake, or external BI platforms.</p></li><li><p>Support reporting strategy across a phased implementation, where some functions transition to Oracle Fusion Cloud while other modules remain in Oracle EBS.</p></li><li><p>Ensure reporting continuity during Chart of Accounts (CoA) redesign, including mapping, harmonization, and alignment of reporting structures across EBS and Oracle Cloud during coexistence.</p></li><li><p>Guide reporting solutions that require combined data from Fusion Cloud and external systems, determining where best to perform data blending (FDI vs. Data Lake).</p></li><li><p>Oversee Data Lake extract designs and data sourcing strategies, ensuring required datasets from Oracle Cloud and legacy systems are modeled accurately and consistently.</p></li></ul><h3><strong>This Job Might Be For You If You Have:</strong></h3><ul><li><p>Deep expertise with Oracle Fusion Cloud reporting tools: OTBI, BIP, Fusion Data Intelligence (FDI), OAC within FDI, Financial Reporting Center, Account Monitor/Inspector, Smart View, and embedded KPIs.</p></li><li><p>Strong ability to rationalize reporting requirements and determine appropriate placement across Fusion-native tools, FDI, Data Lake, or external BI platforms.</p></li><li><p>Ability to guide SI partner designs and influence architectural decisions.</p></li><li><p>Knowledge of key business domains including P2P, R2R, O2C, Plan to Make, PLM/PDH, WMS, OTM/GTM.</p></li><li><p>Experience designing, reviewing, and governing Standard and Custom Oracle AI Agents for reporting and analytics use cases.</p></li><li><p>Strong knowledge of SOX, audit controls, data integrity, and security/role-based access models.</p></li></ul><h3><strong>To be considered for this role, you must have:</strong></h3><ul><li><p>Bachelor’s degree in Information Systems, Data Analytics, Computer Science, Engineering, or related field.</p></li><li><p>15+ years of experience in enterprise reporting and analytics.</p></li><li><p>10+ years of experience with Oracle Fusion Cloud reporting tools.</p></li><li><p>3+ years of experience with Oracle AI Agents.</p></li><li><p>Experience supporting large-scale ERP transformations and phased modernization (EBS → Fusion)</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety - General Medicine]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44959]]></requisitionid>
    <referencenumber><![CDATA[R44959]]></referencenumber>
    <apijobid><![CDATA[r44959]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44959/senior-manager-global-patient-safety-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases in the assigned Therapeutic Area. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.</p><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>Complete signal detection activities in line with approved safety surveillance plan</p></li><li><p>Perform signal evaluation for any identified signals and author the safety evaluation reports</p></li><li><p>Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries</p></li><li><p>Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned compounds</p></li><li><p>Participate in other risk management activities as appropriate for assigned compounds</p></li><li><p>We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron</p></li><li><p>Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents</p></li></ul><p><strong>This role might be for you if can/have the:</strong></p><ul><li><p>Ability to apply relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments</p></li><li><p>Ability to work with a safety system database for purposes of medical case review and simple queries</p></li><li><p>Able to be proactive and self-disciplined, you can meet deliverables, and effectively use your time and prioritize</p></li><li><p>Ability to effectively communicate (verbal and written) safety findings</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum a Master's, PhD, or PharmD</p></li><li><p>Offers 7+ years of relevant risk management experience in the pharmaceutical/ biotech industry or health authority</p></li></ul><p>#GDPSJobs </p></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Vice President, Quality Assurance]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44609]]></requisitionid>
    <referencenumber><![CDATA[R44609]]></referencenumber>
    <apijobid><![CDATA[r44609]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44609/vice-president-quality-assurance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is hiring! The Vice President, Quality Assurance will lead the strategic development, execution, and oversight of key quality and compliance programs across Regeneron GMP operations. This role blends deep expertise in microbiology, data governance, and quality systems to safeguard patient safety, ensure product effectiveness, and uphold global regulatory compliance. This position will guide cross-functional teams, drive innovation, and champion a culture of quality across the organization. </p><p>In this role, a typical day might include the following:</p><p>Microbiology Program Leadership:</p><ul><li><p>Oversee the development and implementation of a value-added microbiology program aligned to global regulatory and legal requirements.</p></li><li><p>Monitor program performance via metrics; embed quality tools and risk management for continuous improvement.</p></li><li><p>Stay ahead of evolving industry standards and proactively adapt program strategy and execution.</p></li><li><p>Make science-based decisions that protect patient safety and ensure product quality and effectiveness.</p></li><li><p>Act as a microbiology decision-maker with internal stakeholders, regulators, and corporate partners.</p></li><li><p>Partner with lines of business to drive operational performance and compliance.</p></li><li><p>Allocate resources and set high-performance standards to meet microbiological and organizational objectives.</p></li></ul><p>Data Governance & Integrity (DGI) Program Leadership:</p><ul><li><p>Lead strategic vision of the of the DGI Program, including engagement, culture, monitoring, and operational leadership.</p></li><li><p>Develop and implement policies and procedures aligned with global regulatory standards and industrial best practices.</p></li><li><p>Drive a mature data quality culture through change management and stakeholder engagement.</p></li><li><p>Ensure DGI standards are continuously met and the function is properly resourced and equipped.</p></li></ul><p>Quality Systems Oversight:</p><ul><li><p>Establish and lead quality systems across Regeneron with clear roles, responsibilities, workflows, and metrics.</p></li><li><p>Provide leadership, tools, and coaching to quality system owners for effective execution.</p></li><li><p>Oversee Right to Operate Review meetings; ensure management review expectations are met.</p></li><li><p>Represent the Quality Management System Office in initiatives and program meetings, aligned to organizational goals.</p></li><li><p>Coach and mentor staff; collaborate with Information Systems to support quality systems and the Quality Plan.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven expertise in microbiology, data governance, and quality systems within GMP environments.</p></li><li><p>Experience leading enterprise quality transformations across multi-site operations.</p></li><li><p>Familiarity with digital quality systems, data analytics, and industry best-in-class tools.</p></li><li><p>Strong knowledge of global regulatory standards and quality management principles.</p></li><li><p>Demonstrated ability to drive change management and foster a culture of quality and compliance.</p></li><li><p>Skilled in resource allocation, strategic planning, and decision-making in complex technical and regulatory settings.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and 20+ years in a GMP-regulated industry (Biotech, Pharma, Medical Device), including at least 5+ years in a managerial capacity, or equivalent education and experience.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$300,000.00 - $500,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Predictive Analytics]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45118]]></requisitionid>
    <referencenumber><![CDATA[R45118]]></referencenumber>
    <apijobid><![CDATA[r45118]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45118/senior-manager-predictive-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated and talented Senior Manager of Predictive Analytics to join the Regeneron Genetics Center (RGC) to pioneer clinical use cases for proteomic and genomic data. In this role, you will develop and apply predictive models on the world’s largest integrated datasets of genomics, proteomics, and electronic medical records. </p><p>The role involves partnering with cross-functional teams, including Business Development, Laboratory staff, and other scientific groups, to foster collaboration and advance key initiatives. The candidate must have the ability to influence, with strong interpersonal skills. Excellent communication and interpersonal skills are also required as this candidate will be expected to work productively in a collaborative, team working environment.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Plan, develop, and execute large-scale analyses of proteomic and genomic datasets, with an emphasis on aging and age-related diseases.</p></li><li><p>Develop and implement methods for data harmonization and normalization across distinct cohorts to ensure consistency and reproducibility of results.</p></li><li><p>Evaluate statistical methods for disease risk prediction, and if necessary, develop new methods</p></li><li><p>Turn disease prediction needs from other teams and collaborators into concrete project/budget proposals</p></li><li><p>Stay informed on emerging market trends in disease prediction and applications of genomics data to continuously refine research directions</p></li><li><p>Deliver clear and concise presentations of genomics and proteomic findings to leadership, ensuring alignment with organizational goals and priorities</p></li><li><p>Ability to provide data to internal, external, and non-scientific audience </p></li><li><p>Design, implement, and optimize data pipelines for high-throughput genomic and proteomic workflows, ensuring efficient processing of large-scale proteomic datasets.</p></li><li><p>Develop and integrate robust quality control (QC) measures at multiple stages of analysis pipelines to ensure data accuracy, consistency, and reproducibility.</p></li></ul><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Demonstrated expertise in statistics, machine learning and predictive analytics applied to biological data.</p></li><li><p>Demonstrated aptitude for translating research results into products or prototypes</p></li><li><p>Proven ability to independently lead and manage research projects from conception to completion.</p></li><li><p>Excellent communication and collaboration skills, with a track record of working effectively in interdisciplinary teams</p></li><li><p>Demonstrated ability to present data, insights, and recommendations effectively to stakeholders at all levels of the organization</p></li></ul><p><strong>To be considered for this role, we require:</strong></p><ul><li><p>A PhD in a relevant field (e.g., human genetics, statistics, computational biology, or related disciplines) and at least five years of experience analyzing large-scale genomics data, or a bachelor's degree with at least 8 years of relevant experience.</p></li><li><p>Candidates with prior industry experience are preferred</p></li><li><p>Experience in exploratory data analysis, applied statistics, or software engineering is preferred in one or more of these domains</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 19:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Procurement - Direct]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45462]]></requisitionid>
    <referencenumber><![CDATA[R45462]]></referencenumber>
    <apijobid><![CDATA[r45462]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45462/associate-director-global-procurement-direct/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill an Associate Director Global Procurement, Direct position within our team. In this role you will develop a holistic Category Strategy and provide strategic leadership and direction with a focus on Packaging Components and Device Category. This role will work closely with stakeholders to lead discussions related to Packaging Components and Device Categories while aligning priority needs with procurement management and stakeholders. This position will be critical to driving performance across the IOPS External Manufacturing categories including alignment with stakeholder goals, driving towards competitive advantages (strategic and financial) and optimizing supplier relationships. This role works in close collaboration with IOPS Stakeholders to enable company revenue targets and the new product pipeline.</p><p>In this role, a typical day may include the following:</p><ul><li><p>Help define and implement the global Packaging Components and Devices Category strategy to serve global and regional business needs.</p></li><li><p>Manage negotiations, supplier management activities, and stakeholder engagement activities for the Packaging Components and Devices Category as assigned.</p></li><li><p>Work with leadership to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities.</p></li><li><p>Represent Global Procurement by participating in organizational decisions in the Packaging Components and Devices categories with critical short and long-term impact on the success, efficiency, growth, and results of Global Procurement.</p></li><li><p>Demonstrate knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities.</p></li><li><p>Manage category activities to ensure compliance with appropriate GxPs and other applicable regulations, as applicable.</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements.</p></li><li><p>May provide coaching and guidance on job performance and career development to direct reports (if applicable) and provides leadership examples for the organization.</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Believe that value can be driven through strategic partnerships and efficient ways of working.</p></li><li><p>Can tap into strong in-depth knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of a Global Procurement organization.</p></li><li><p>Enjoy successfully leading global categories or global teams, processes, and suppliers within a multi-national organization.</p></li><li><p>Serve as role-model leader consistently exhibiting behaviors across an organization of direct reports to create clarity, provide a clear and understandable vision with transparency and trust both within and outside of the organization.</p></li><li><p>Can demonstrate success managing cross-functional teams to drive results in Packaging Components and Devices categories or related categories through effective sourcing, negotiations, contracting, and supplier relationship management.</p></li><li><p>Can influence and partner with senior executives and peer functions to drive strategic change and efficiency.</p></li><li><p>Have working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li><li><p>Have experience successfully leading global categories teams, processes, and suppliers across a breadth of categories</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in a relevant field of study plus progressive experience in procurement, preferably including substantial experience in Pharma/BioPharma.</p><ul><li><p>Director: 10+ years of experience in relevant functions or industries. The ideal candidate will have in-depth knowledge of Packaging Components and Device Category experience.</p></li></ul><p> This role requires working onsite 5 days per week.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$147,800.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 08:56:27 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Pulmonology-Dayton, OH/Northern Cincinnati]]></title>
    <date><![CDATA[Wed, 04 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45789]]></requisitionid>
    <referencenumber><![CDATA[R45789]]></referencenumber>
    <apijobid><![CDATA[r45789]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45789/medical-specialist-i-pulmonology-dayton-ohnorthern-cincinnati/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dayton]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Dayton, OH/Northern Cincinnati -representative must reside within or close to the territory.</strong></p><p>The Medical Specialist (Sales Representative), Pulmonology (MS) will be responsible for engaging Pulmonologists and other key customers within an assigned geography, presenting clinically focused selling messages to create and grow revenue, and consistently delivering product goals. The MS will demonstrate strong and consistent sales performance that exceeds forecast and expectations related to product goals. The MS will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>As a Medical Specialist, a typical day might include the following:</strong></p><ul><li><p>Developing strategy and implementing tactics within key accounts in our Pulmonary therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong relationships with Pulmonary health care professionals. This will include physicians, advanced practitioners, nurses, office staff and other important personnel as well as key patient advocacy support groups. </p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Participating in initiatives to support sales success such as industry-related congresses, local and regional meetings and medical conferences.</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Are confident in demonstrating strong and consistent sales performance that exceeds expectations related to goals</p></li><li><p>Are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>Can demonstrate a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>Collaborate effectively with internal and external partners</p></li><li><p>Share a passion and learning interest in science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li></ul><p>To be considered you will need a bachelor’s degree (required); Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Respiratory market and/or a similar subcutaneous self-injectable biologic specialty market also required. Demonstrate advanced clinically-based selling skills and be results oriented with a proven track record of success with product launches. Experience with in-servicing and training office staff, nurses and office managers and the ability to partner and collaborate with other internal field teams and alliance partners. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 04 Mar 2026 09:56:45 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Global Procurement- Advanced Therapies]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46026]]></requisitionid>
    <referencenumber><![CDATA[R46026]]></referencenumber>
    <apijobid><![CDATA[r46026]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46026/senior-manager-global-procurement-advanced-therapies/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Senior Manager, Global Procurement-Advanced Therapies, with experience in end-to-end procurement strategies/processes and with proven successful global category execution in Contract Development and Manufacturing Operations. Regeneron is a leading biotechnology company that invents, develops, and commercializes life-transforming medicines for people with serious diseases. Founded and led for 36 years by physician-scientists, Regeneron's unique ability to translate science repeatedly and consistently into medicine has led to numerous FDA-approved treatments and products in development, almost all of which were homegrown in Regeneron's laboratories.</p><p>A typical day might include the following:</p><ul><li><p>Accountable for supporting the definition and implementation of the global CMO Category strategy to serve global and regional business needs as assigned</p></li><li><p>Works closely with partners to manage discussions related to the CMO Categories and aligns category priorities with Procurement management and business partners</p></li><li><p>Manage negotiations, supplier management activities, and partner engagement activities for the Packaging Category as assigned</p></li><li><p>Takes direction to drive value in terms of cost savings, cash flow improvement, and other efficiency savings from category management activities</p></li><li><p>Supports Global Procurement by participating in organizational decisions in the CMO categories with critical short and long-term impact on the success, efficiency, growth, and results of the category team</p></li><li><p>Demonstrates knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of the Global Procurement organization and leverages this knowledge to drive improvements within Regeneron, aligned with corporate priorities</p></li></ul><p>The Role Might be for you if have:</p><ul><li><p>Experience leading category activities to ensure compliance with appropriate GxPs and other applicable regulations</p></li><li><p>Negotiates contract terms and conditions in consultation with Law department aligned with Regeneron’s priorities and business requirements</p></li><li><p>Managed teams of professional level employees responsible for performing category management tasks (if applicable.)</p></li><li><p>Uses data to drive decision-making for successful category projects.</p></li><li><p>Working knowledge with sourcing contracting tools, ERP’s, and eRFx systems preferred. (Oracle, Zycus, Ariba, Other)</p></li></ul><p>We are looking for someone with a bachelor's degree in a relevant field of study plus relevant, progressive experience in procurement, including experience in Pharma/BioPharma or science in general.</p><ul><li><p>Sr Manager level: 8+ years of experience in relevant functions or industries, demonstrating growth in experience, scale, and development throughout.</p></li></ul><p>*This role requires working onsite 5 days per week</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Medical Affairs]]></title>
    <date><![CDATA[Mon, 16 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R42160]]></requisitionid>
    <referencenumber><![CDATA[R42160]]></referencenumber>
    <apijobid><![CDATA[r42160]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r42160/medical-director-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we are dedicated to addressing unmet medical needs through groundbreaking therapies. We are seeking a strategic and accomplished <strong>Medical Director, Medical Affairs</strong> to join our team in Tokyo, Japan.</p><p>This role is pivotal in shaping medical strategies and activities for our genetic medicine and rare disease portfolio, with a focus on gene therapy and auditory neuropathy. You will work at the intersection of science, medicine, and innovation, collaborating with internal teams and external stakeholders to ensure scientific excellence and patient-centered outcomes.</p><p>This is a unique opportunity to lead in a cutting-edge field and contribute to therapies that transform lives.</p><br><h3><strong>A Typical Day:</strong></h3><p>As the Medical Director, Medical Affairs, you will:</p><ul><li>Develop and implement medical strategies, including scientific communications, publications, and annual planning.</li><li>Build and maintain partnerships with healthcare professionals, researchers, and advocacy groups to enhance patient care and outcomes.</li><li>Provide medical and scientific leadership to cross-functional teams, ensuring alignment with global and regional strategies.</li><li>Support clinical study sites and regulatory activities, including J-NDA filings and post-approval processes.</li><li>Oversee the generation and dissemination of clinical and non-clinical data to support medical objectives and high-quality publications.</li><li>Organize advisory board meetings to gather insights and inform strategic decisions.</li><li>Ensure scientific accuracy and compliance in medical materials and communications.</li><li>Represent Regeneron Japan in global medical impact teams and external collaborations.</li><li>Attend surgeries or medical procedures to offer technical and scientific guidance when required.</li></ul><br><h3><strong>This Role May Be For You If:</strong></h3><ul><li>You excel in building relationships with diverse stakeholders, including healthcare providers and researchers.</li><li>You thrive in collaborative environments and can align cross-functional teams toward shared goals.</li><li>You possess expertise in translating complex scientific concepts into actionable strategies.</li><li>You are detail-oriented and committed to maintaining high standards of compliance and ethics.</li><li>You have experience in gene therapy and rare diseases, particularly auditory neuropathy.</li><li>You can provide technical and scientific guidance during surgical interventions when required.</li></ul><br><h3><strong>To Be Considered:</strong></h3><p>Candidates must hold an MD or equivalent, with at least 5 years of related industry experience. A strong background in drug development, regenerative medicine, and rare diseases is essential. Fluency in Japanese and English is required, along with the ability to lead technical and business discussions with internal and external stakeholders. Preferred candidates will have experience in gene therapy and auditory disease, as well as a proven track record of medical affairs leadership.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Mar 2026 02:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Internal Medicine, Clinical Scientist (Cardio, Metabolic, & Renal)]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44795]]></requisitionid>
    <referencenumber><![CDATA[R44795]]></referencenumber>
    <apijobid><![CDATA[r44795]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44795/manager-internal-medicine-clinical-scientist-cardio-metabolic-renal/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3>As a Manager in Clinical Sciences, a typical day may include the following:</h3><ul><li>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</li><li>Develops/maintains understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</li><li>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</li><li>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</li><li>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</li><li>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</li><li>Collaborates with internal functions and external vendors to promote clinical study integrity</li><li>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</li><li>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li>Demonstrated ability to influence within team and may influence cross functionally</li><li>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</li><li>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</li><li>Strong management, interpersonal and problem-solving skills</li><li>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements</li><li>Considerable organizational awareness, including significant experience working cross-functionally</li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 5 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in one or more of the following therapeutic areas – cardiovascular, renal, metabolic disease.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46083]]></requisitionid>
    <referencenumber><![CDATA[R46083]]></referencenumber>
    <apijobid><![CDATA[r46083]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46083/senior-manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>We are hiring a Senior Clinical Study Lead (CSL) to join our dynamic Clinical Trial Management team in Tokyo, Japan.</strong> As a pivotal member of our team, you will lead large-scale and complex clinical trials globally and regionally, ensuring excellence in execution and compliance with industry standards. This role offers opportunities to contribute to innovative solutions and drive process improvements, making an impactful difference in clinical study operations.</p><p><strong>A Typical Day:</strong><br>As a Senior Clinical Study Lead, you will:</p><ul><li><p>Lead cross-functional study teams to ensure clinical study delivery.</p></li><li><p>Provide operational input into protocol development and oversee study-specific documentation.</p></li><li><p>Manage clinical trial systems such as CTMS and TMF, ensuring compliance with registry requirements.</p></li><li><p>Identify outsourcing needs, engage vendors, and oversee contracting and management.</p></li><li><p>Develop and manage study budgets and timelines while mitigating risks.</p></li><li><p>Oversee site evaluation, selection, and activation, including investigator meetings.</p></li><li><p>Monitor patient recruitment strategies and ensure data quality.</p></li><li><p>Supervise study close-out activities, including database lock and reconciliation of vendor contracts.</p></li><li><p>Contribute to clinical study report writing and process improvement initiatives.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You thrive in leadership roles, with the ability to build and guide productive study teams.</p></li><li><p>You excel in managing complex clinical trials and balancing direct leadership with oversight responsibilities.</p></li><li><p>You have advanced technical proficiency in trial management systems and MS applications such as Excel, PowerPoint, and Word.</p></li><li><p>You possess exceptional communication skills, both written and verbal, and are adept at influencing and negotiating across diverse stakeholders.</p></li><li><p>You are proactive, self-disciplined, and skilled at prioritizing tasks to meet deadlines effectively.</p></li><li><p>You demonstrate expertise in global clinical trial operations and regulatory guidelines.</p></li><li><p>You are passionate about driving innovation and continuous improvement in clinical study execution.</p></li></ul><p><strong>To Be Considered:</strong><br>Candidates must possess a Bachelor’s degree and have at least 8 years of relevant industry experience. Advanced project management skills, cross-functional leadership, and knowledge of ICH/GCP guidelines are essential. Preferred qualifications include line management experience and proficiency in vendor management.</p><p>This is your opportunity to lead groundbreaking clinical trials and contribute to the advancement of global healthcare. Join us and be part of a team dedicated to excellence and innovation in clinical trial management.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 02:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager GMP Compliance and Inspections]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46546]]></requisitionid>
    <referencenumber><![CDATA[R46546]]></referencenumber>
    <apijobid><![CDATA[r46546]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46546/manager-gmp-compliance-and-inspections/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>We are seeking a Manager for GMP Compliance & Inspections who will work with cross-functional teams to drive activities that will ensure a state of continuous GMP compliance in Regeneron. This individual will play a leading role in the preparation and execution of regulatory inspections, partner audits and internal audits, as well as follow up post audit/inspection on any items requiring response and action. This role will also promote and drive compliance by building inspection readiness processes across the organization. </p></div><div></div><div><p><strong>As the Manager GMP Compliance & Inspections a typical day might include the following: </strong></p></div><div><ul><li><p>Ensuring readiness for regulatory inspections and partner/other audits in the creation, maintenance and management of inspection content, ensuring it is organized, current and readily accessible at all times</p></li></ul></div><div><ul><li><p>Planning all inspection and audit logistics and scenarios: communication plan, room allocations, backroom/frontroom configuration, technology checks & personnel assignments</p></li></ul></div><div><ul><li><p>Performing a lead role in the audit/inspection Backroom and responding to incoming requests during inspections and audits and ensuring timely and accurate responses</p></li></ul></div><div><ul><li><p>Evaluating outcomes of regulatory authority inspections/partner and other audits to identify near misses, lessons learned and other best practices and working cross-functionally to ensure identified process or system improvement opportunities are sustainably implemented</p></li></ul></div><div><ul><li><p>Coordinating inspection/audit responses and actively managing commitments to regulatory authorities/audit bodies in response to inspection/audit findings</p></li></ul></div><div><ul><li><p>Working collaboratively with commitment owners to ensure that all commitment timelines are met via proactive CAPA tracking, and confirming their timely closure and ensuring suitable effectiveness checks are in place</p></li></ul></div><div><ul><li><p>Maintaining and enhancing communication processes to site management on the status of regulatory inspection readiness and CAPA commitments, including development of appropriate KPIs</p></li></ul></div><div><ul><li><p>Generating, developing and reporting metrics / trends for program adherence to requirements and effectiveness </p></li></ul></div></div><div><div><ul><li><p>Participating in proactive evaluation and education of site GMP compliance against current and emerging regulatory trends</p></li></ul></div><div><ul><li><p>Utilising strong critical thinking skills to serve as a thought partner to the GMP Compliance and Inspections leadership with regard to complex problems</p></li></ul></div><div><ul><li><p>Supporting and leading teams implementing practices and improvements to make IOPS inspection-ready at all times</p></li></ul></div><div><ul><li><p>Building and implementing tools to improve IOPS inspection readiness; determining system improvements through effective project management</p></li></ul></div><div><ul><li><p>Developing and delivering training on inspection conduct, backroom/frontroom protocols, and regulatory expectations</p></li></ul></div><div><ul><li><p>Working with department leaders and cross functional teams to educate, building and maintaining an inspection readiness structure across the organization</p></li></ul></div><div><ul><li><p>Liaising with partners on audit/inspection and quality related matters to provide guidance and advice</p></li></ul></div><div><ul><li><p>Participating on internal committees/teams, as required</p></li></ul></div><div><ul><li><p>Cross-site support of inspection readiness and inspection activities</p></li></ul></div><div><ul><li><p>Coordinating Regeneron information to support regulatory requests for paper inspections and/or observation responses</p></li></ul></div><div><ul><li><p>Additional duties may be assigned as required. </p></li></ul></div><div><p><strong>This role might be for you if:</strong></p><ul><li>You have strong project management, interpersonal, cross- cultural, communication, negotiation, and problem-solving skills</li><li>You understand and listen to team members and stakeholders while fostering a productive team environment to one common objective</li><li>You are driven for proactive resolution of issues with tact, diplomacy and composure</li><li>You show resiliency and flexibility in the face of challenges and adversarial situations</li><li>You are able to provide clear direction to others in ambiguous situations and environments</li><li>You possess knowledge of industry practices and regulations</li></ul></div><div><p>To be considered for this role you should have a BA/BS degree in Life Sciences and the following minimum years of relevant experience for each level: </p></div><div><ul><li><p>Assoc Manager: 6+ years of relevant experience, preferably in the pharmaceutical or biotech industries or related field or equivalent combination of education and experience. </p></li></ul></div><div><ul><li><p>Manager: 7+ years of relevant experience, preferably in the pharmaceutical or biotech industries or related field or equivalent combination of education and experience. </p></li></ul><p>Level will be determined based on qualifications and experience relevant to the role.</p><p>#IRELIM #JOBSIEST #LI-Onsite</p></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 03:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, IT Product Management – Source to Pay]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45507]]></requisitionid>
    <referencenumber><![CDATA[R45507]]></referencenumber>
    <apijobid><![CDATA[r45507]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45507/associate-director-it-product-management-source-to-pay/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, IT Product Management – Source to Pay, you will lead the IT execution, delivery, and operational ownership of Regeneron’s Source-to-Pay (S2P) capabilities within a modern, global ecosystem. This role is accountable for translating product strategy and roadmap direction into high-quality, scalable, and compliant solutions that support Global Procurement, Finance, and Supply Chain operations.</p><p>Success in this role requires not only deep Oracle EBS and Fusion S2P expertise, but also deep Procurement industry knowledge.</p><div></div><div></div><p>A typical day in this role might look like:</p><ul><li>Serve as IT Product Owner for Oracle EBS and Fusion Cloud Source-to-Pay and associated boundary systems, including but not limited to Procurement (Direct and Indirect), Purchasing, Sourcing/eRFx, Supplier Portal, Supplier Qualification Management, Third Party Risk Management initiatives and Accounts Payable.</li><li>Be a Strategic and trusted IT Partner to business to understand Global Procurement, AP, and Supplier (including ASL and Qualification Management) needs in support of the digital strategy, corporate objectives, and functional priorities.</li><li>Drive S2P end-to-end process, supplier master data and governance (along with Supply Chain) and technology deliverables supporting global growth including standardization.</li><li>Lead IT deliverables for multi-year Procurement Technology Transformation Roadmap and Strategy, deliver on Business outcomes</li><li>Partnering strategically with business for Vendor Selections, RFPs, Cost benefit analysis, application rationalization on an ongoing basis.</li><li>Prepare and maintain project and day-to-day business requirements, functional and system designs, solution documentation, and test plans.</li><li>Provide oversight of system integrators and vendors, ensuring delivery aligns with enterprise standards, Oracle best practices, and future‑state architecture.</li><li>Execute and enforce application, integration, and data architecture standards.</li><li>Partner with technical leads on integrations and extensions involving OIC, APIs, file-based integrations, and data exchanges with upstream and downstream systems.</li><li>Provide techno-functional ownership and oversight for procurement-related boundary systems including Icertis (contract management), ORO (procurement orchestration), Sievo (spend analytics), and Trustpair (supplier bank validations).</li><li>Lead participation in Integration Testing, SIT, UAT, regression testing, and quarterly Oracle patch impact assessments for all P2P-related functionality.</li><li>Maintain strong Identity and Access Management controls (RBAC / ABAC) across sensitive procurement and financial systems.</li><li>Partner with Infosec and other technology teams to ensure alignment with Regeneron security standards and ensure compliance on ERP platforms, SaaS, and third-party applications for patching, data security, privacy.</li></ul><p>This role might be for you if you have:</p><ul><li>Proven experience delivering global S2P implementations, ERP modernizations, or complex rollouts.</li><li>Experience across Oracle ERP Procurement, Finance, and Supply Chain applications.</li><li>Deep experience with Direct Procurement and Supplier Onboarding specifically related to complex ASL and Supplier Qualification process.</li><li>Oracle Fusion Cloud Procure-to-Pay process areas.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in a related field (Business, Finance, Supply Chain, Information Systems) and 10+ years of experience across Oracle ERP Procurement, Finance, and Supply Chain applications with deep experience with Direct Procurement and Supplier Onboarding specifically related to complex ASL and Supplier Qualification process plus 4+ years of hands-on experience with Oracle Fusion Cloud Procure-to-Pay process areas.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Scientific Communications - Oncology]]></title>
    <date><![CDATA[Tue, 14 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46231]]></requisitionid>
    <referencenumber><![CDATA[R46231]]></referencenumber>
    <apijobid><![CDATA[r46231]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46231/director-scientific-communications-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Scientific Communications- ONCOLOGY- will assume a pivotal role in leading and aligning strategic, integrated medical communications efforts, The Director will be responsible for the development of the global scientific communication platform(s), which will serve as the foundational resource(s) for cross-functional teams to harmonize and deliver evidence-based internal and external communications. Ensuring content is accurate, concise and accessible, the Director will drive and create meaningful scientific communications tailored to diverse audience needs and lead the collation of Integrated Medical Communications Plans (IMCP). Together, these collective efforts will position the Director, Scientific Communications at the heart of galvanizing stakeholder engagement, advancing medical knowledge, and ultimately improving clinical care for patients.</p><p>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits. </p><p>A typical day may include the following:</p><ul><li>For the asset/program(s) under the purview of responsibility, the Director, Scientific Communications will:</li><li>Lead the development and alignment of a comprehensive Integrated Medical Communication Plan(s)</li><li>Establish and effectively communicate clear Scientific Communication objectives and goals to internal stakeholders, and formulate a tactical plan for compliant execution</li><li>•Partner with Medical Director(s) and other key internal stakeholders to devise an overarching Congress strategy and align on Congress presence and key deliverables for Tier 2 congresses.</li><li>Drive the creation and development of Scientific and Digital Communications materials with a focus on:</li><li>Scientific Communication Platform, Lexicon and Narrative</li><li>Congress Presence: Coordinate and Collaborate with the Congress Strategy and Planning team on Tier 1 medical booth design and content/material; Tier 2 end-to-end planning & execution.</li><li>Program and Scientific Slides</li><li>Disease-State Education materials</li><li>Data/Publication updates</li><li>In collaboration with the therapeutic area medical directors and Field Medical Leads, assess medical education gaps and needs of external stakeholders</li><li>Identify and prioritize scientific educational opportunities to reach targeted stakeholders in an impactful manner</li><li>Address knowledge gaps, or Clinical Impact Opportunities, with tailored, targeted and timely content creation which can be adapted for engagement across geographic regions as well as multiple platforms, including digital</li><li>Lead projects within the scope of responsibility through medical review committees, facilitating the endorsement of appropriate materials</li><li>Ensure medical and scientific integrity and accuracy of created content and ensure materials have a fair and balanced representation</li><li>Work with Project Manager to supervise all materials are delivered within the allocated budget, and tracks budget spend in a systematic manner</li><li>Maintain adherence to rigorous ethical and compliance standards, upholding an uncompromising level of personal ethics rooted in a “patient first” value framework.</li></ul><p>To be considered it is required to have a PhD, MD, or PharmD with at least 8 years of relevant medical communication experience with Oncology is required. . Demonstrated expertise in medical communication strategies, congress planning, scientific content development, and medical education is required. Strong project management skills, ethical integrity, and the ability to work in a matrix organization are essential. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 15 Apr 2026 13:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician, Tuesday-Saturday 3rd shift]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46910]]></requisitionid>
    <referencenumber><![CDATA[R46910]]></referencenumber>
    <apijobid><![CDATA[r46910]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46910/hvac-technician-tuesday-saturday-3rd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>We are currently looking to add a HVAC Technician to our growing team, working a Tuesday-Saturday 10:00pm – 8:30am shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment; troubleshooting, preventative maintenance, calibration, and repair work of all mechanical related systems.</div></div><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for approximately 6 months. Working hours thereafter will be Tuesday-Saturday 10:00pm-8:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a HVAC Technician, a typical day might include the following:</p><ul><li>Maintaining coolers and freezers including Ultra Low temperature Freezer</li><li>Maintaining Centrifugal and Reciprocating refrigeration chillers</li><li>Maintaining Chilled water systems including distribution and condenser pumps</li><li>Maintaining Air Compressors</li><li>Electrical power systems and stand-by power generation equipment</li><li>Following current good manufacturing practices (cGMPs) and good business practices (G)</li><li>Participating in rotational on-call for site emergency work</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOP's, cGMP's, GDP’s and quality standards</li><li>Becoming fully gown qualified to work within Production areas</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>May plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</li></ul><h3>This role might be for you if you:</h3><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Are able to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li></ul><p>To be considered for the HVAC Technician position you must be willing and able to work a Tuesday-Saturday 10:00pm – 8:30am schedule. Applicants ideally should have technical school training with field experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance and the following minimum amounts of experience for each level:</p><ul><li><p>HVAC Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>HVAC III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li><li><p>HVAC IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role. Will substitute relevant work experience in lieu of education. Electronic, PLC, mechanical and building automation systems experience in Pharmaceutical Industry preferred. EPA certified for refrigeration gases. </p><p>#REGENTOSK </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46213]]></requisitionid>
    <referencenumber><![CDATA[R46213]]></referencenumber>
    <apijobid><![CDATA[r46213]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46213/principal-statistical-programmer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A <strong>Principal Statistical </strong>P<strong>rogrammer </strong>provides timely support to the study team on all programming matters according to the project strategies.</p><p><strong>In this role, a typical day might include:</strong> ​</p><p>As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.</p><p><strong>This role might be for you if can:</strong> ​</p><ul><li><p>Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. </p></li><li><p>Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. </p></li><li><p>Support creation and validation of 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. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.</p></li><li><p>Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</p></li><li><p>Participate in department working groups; provide input in development of tools and improvement of processes.</p></li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Masters Degree</p></li><li><p>SAS, (Base, Stat, Macro, graph). </p></li><li><p>3 + Years experience</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager Material & Supplier Quality]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46568]]></requisitionid>
    <referencenumber><![CDATA[R46568]]></referencenumber>
    <apijobid><![CDATA[r46568]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46568/manager-material-supplier-quality/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will lead all aspects of a team of QA employees within the Material and Supplier Quality area. You will be responsible for ensuring quality standards and excellence internally and externally.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li><p>Responsible for review and approval of the following types of documents, relating to area functions including QC test data, specifications, failure investigations, change controls, SOPs, validation protocols and summary reports and SCAR records (Supplier Corrective Action Request)</p></li><li><p>Coordinating QA resources assigned to functional area to meet goals and timings; coordinates prioritization of activities with area management</p></li><li><p>Performing compliance monitoring of area operations, including trending of SCARS/MARS and evaluating effectiveness of corrective actions</p></li><li><p>Generating monthly trend data on release cycle times and SCAR/MAR cycle times</p></li><li><p>Supporting Supplier Quality Group</p></li><li><p>Reviewing customer requirements and implementing required processes to meet customer expectations regarding Quality</p></li><li><p>Participating in regulatory and customer audits</p></li></ul><p><strong>This role may be for you if you:</strong></p><ul><li><p>Demonstrate excellent people management experience</p></li><li><p>Have a strong quality mindset</p></li><li><p>Enjoy working in a dynamic and fast-paced environment</p></li><li><p>Can collaborate and build successful partnerships internally and externally</p></li></ul><p>To be considered for this role, you should hold a Requires BSc/BEng in scientific discipline or related field with 8+ years of relevant work experience in pharmaceutical or related industry. Supervisory experience required.</p><p>Manager: Minimum 7 years of experience</p><p>Senior Manager: Minimum 8 years of experience</p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 09:56:20 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Representative (MR) - Dermatology *Okayama, Hiroshima Area]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47551]]></requisitionid>
    <referencenumber><![CDATA[R47551]]></referencenumber>
    <apijobid><![CDATA[r47551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47551/medical-representative-mr-dermatology-starokayama-hiroshima-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong></p><p>You will primarily work in the Okayama and Hiroshima area.</p><p>Your residence is expected to be in Okayama or Hiroshima.</p><p>Are you ready to make a meaningful impact in the pharmaceutical industry? At Regeneron, we’re committed to putting patients first, and we’re looking for a passionate Sales Representative to join our Dupixent ROW Commercial Team in Japan. This role is your opportunity to drive dermatology sales objectives while working with a team dedicated to innovation and excellence. With a focus on delivering value to healthcare professionals and patients alike, this position offers the chance to grow your career while making a difference in people’s lives.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Achieve sales objectives by effectively managing territory budgets and resources.</p></li><li><p>Develop and implement an annual territory business plan that incorporates market insights and aligns with marketing strategies.</p></li><li><p>Regularly update business plans to adapt to changing market dynamics.</p></li><li><p>Utilize key data sources to create strategic action plans for the territory.</p></li><li><p>Conduct disease and concept selling to engage healthcare professionals and deliver tailored solutions.</p></li><li><p>Perform administrative tasks, including expense reporting, marketing feedback, and call reporting.</p></li><li><p>Collaborate with alliance partners to meet overall objectives and ensure compliance with regulatory guidelines.</p></li><li><p>Attend local, regional, and national meetings as required, and complete all training programs provided by Regeneron.</p></li><li><p>Maintain company property in good order and adhere to safe driving practices.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You excel at building strong relationships with customers and delivering value-driven solutions.</p></li><li><p>You have a knack for strategic thinking and can manage your time effectively to achieve goals.</p></li><li><p>You thrive in independent work environments and can execute plans under tight timelines.</p></li><li><p>You’re organized, detail-oriented, and comfortable with administrative responsibilities.</p></li><li><p>You enjoy collaborating with others to achieve shared objectives.</p></li><li><p>You’re adaptable and willing to travel, including evenings and weekends, as needed.</p></li></ul><p><strong>To Be Considered:</strong></p><p>Candidates must have a Bachelor’s degree (or equivalent) and at least five years of sales representative experience in the pharmaceutical industry. A valid driver’s license and MR certification are required. While fluency in English is a plus, it is not essential for this role. Preferred qualifications include therapy area knowledge in dermatology, sales experience in biologics, and established relationships with key opinion leaders in dermatology.</p><p>Join us at Regeneron, where your expertise and dedication can make a real difference. Apply today to become a part of a team that’s revolutionizing healthcare and improving lives worldwide.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Drug Development Program Management]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44486]]></requisitionid>
    <referencenumber><![CDATA[R44486]]></referencenumber>
    <apijobid><![CDATA[r44486]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44486/director-drug-development-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director Development Program Management</strong> 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><em>***Note this role is based in office in either Tarrytown, NY / Warren, NJ / or Cambridge, MA and not eligible remote. </em></p><p><strong>A typical day in this role looks like: </strong></p><div><ul><li><strong>Development</strong><strong> </strong><strong>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<strong> </strong>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 may be for you if you have:</strong></p><ul><li>Have excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company in order to establish credibility with professionals on the project teams. </li><li>Understand and motivate others and build effective teams. </li><li>Have strong presentation and critical thinking skills. </li><li>Actively promote constructive interactions among team members in order to address difficult situations. </li><li>Resolve and negotiate conflicts or problems with tact, diplomacy and composure. </li><li>Handle multiple projects and priorities with exceptional organizational and time management skills (both project and self) </li><li>Thrive in fast paced organizations; expert in dealing with ambiguity and uncertainty </li></ul><p><strong>In order to be considered qualified</strong>, you must have a Bachelor's degree and 12+ years of in-house pharmaceutical program management with knowledge of the drug development process as well as understanding of clinical trials.</p></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[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager-(Gastro)-Tallahassee, FL, Montgomery, AL & Mobile, AL]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47237]]></requisitionid>
    <referencenumber><![CDATA[R47237]]></referencenumber>
    <apijobid><![CDATA[r47237]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47237/reimbursement-business-manager-gastro-tallahassee-fl-montgomery-al-mobile-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[<p><strong>Field Reimbursement Manager, Immunology – Pulmonology and Gastroenterology (Tallahassee, FL - Montgomery, AL - Mobile, AL) </strong></p><p><strong> </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 stakeholders, sales teams, Payer teams, Alliance partners, HUBs, etc. The Field Reimbursement Management reports to the District Manager of Field Market Access. </p><p>Regeneron has an Alliance partner for commercializing Dupixent. As a result, members of the Regeneron Field Reimbursement Team must demonstrate the ability to in a proactive and highly collaborative environment across an Alliance team. </p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</p></li><li><p>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>Execute against established performance parameters and monitor personal performance against these agreed parameters:</p></li><li><p>Work closely with REGN and Sanofi partners as assigned; REGN and Sanofi District Sales Managers, Medical Specialists, other FRM, Reimbursement, Marketing and Access team members in assigned geographical areas to ensure optimal coverage and customer knowledge of this process and all REGN patient services within defined accounts</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, in efforts to streamline the coverage and specialty pharmacy processes to obtain alliance products</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 complies with Regeneron policies, processes, and standard operating procedures</p></li></ul><p><strong>This role may be for you if:</strong> </p><ul><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 complies with Regeneron policies, processes, and standard operating procedures</p></li><li><p>Maintain knowledge base necessary to ensure support of all access and patient/payer support programs and resources offered for all products.</p></li><li><p>Assist in providing appropriate field insights throughout the development of Market Access marketing support materials as needed</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><li><p>Ensure training is completed and kept up to date with appropriate clinical knowledge of the respective products</p></li><li><p>Develop and execute annual budget, with allocation within respective territory</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>A Minimal educational requirement: Bachelor’s Degree. Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience. Experience working with products delivered through a Specialty Pharmacy network is critical. Knowledge of CMS policies and processes with expertise in Part D (Pharmacy Benefit design and coverage policy).This is a field-based position. Candidates must live within the geographical territory that includes Tallahassee, FL, Montgomery, AL, and Mobile, AL. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Global Commercial Strategy & Operations - Immunology]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47419]]></requisitionid>
    <referencenumber><![CDATA[R47419]]></referencenumber>
    <apijobid><![CDATA[r47419]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47419/associate-director-global-commercial-strategy-operations-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><em>This position is required on-site at Sleepy Hollow, currently 4 days per week with 1 day work from home. A fully remote role is not possible. This role cannot be based in Tarrytown NY nor Basking Ridge NJ.</em></p><p>The Associate Director, Global Commercial Strategy & Operations Immunology will work closely with Global Senior Brand Leadership including SVP, CBU VPs and cross-functional teams to support strategic planning and execution. This role will support the integration and coordination of franchise business planning and analytics, develop global and market brand strategies and lead strategic projects. This role will be based in Sleepy Hollow NY and will report to the Senior Director, Global Commercial Strategy.</p><h3><strong>A Typical Day May Look Like:</strong></h3><ul><li>Support Global, Cross-Functional and Cross-Regional Immunology Commercial integration efforts. Responsible for maintaining cross brand alignment of indications in the U.S., key international markets and HQ teams.</li><li>Evaluate and provide brand leadership with key trends, industry/category/ performance data to support delivery of brand performance against forecasts and assumptions. Helps guide adaptation as necessary to deliver on key brand objectives.</li><li>Support efforts to expand the global impact and reach of product by providing analytic support, investment, strategy, and planning.</li><li>Synthesize data available and build data driven models where needed to analyze and gather insights to help senior leaders better understand business potential for new indications in a given market.</li><li>Lead analysis to measure global business performance by providing valuable insights and recommendations backed by data/</li><li>Collaborate with global leadership on establishing and tracking global performance incentives (including consolidation / calculation).</li><li>Support Immunology Global and U.S. strategic projects in support of overall Immunology brand goals and objectives.</li><li>Participate and where needed lead key partnering meetings, activities and actions.</li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li>You have familiarization with commercial strategy, deep understanding in analytics and proven track record in operations with new product indications and/or launch experience preferred.</li><li>You bring strong analytic skills, learning agility, excellent verbal and written communication skills. Data driven with the ability to visualize, articulate and derive insights by making decisions that are sensible given available information.</li><li>You are able to build positive, productive and sustainable work relationships with internal partners and working with cross functional matrix team across various organizational functions; alliance experience preferred.</li><li>You can operate and define priorities based on business with a result focused approach.</li></ul><p>To be considered, we expect you to have Bachelor’s degree ideally in a scientific field with 10+ years of progressive consulting and/or industry/relevant professional experience including pharmaceutical/biotech. MBA strongly preferred. We also expect you to have the ability to travel 20%</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[CAD Operator]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47041]]></requisitionid>
    <referencenumber><![CDATA[R47041]]></referencenumber>
    <apijobid><![CDATA[r47041]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47041/cad-operator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a customer service oriented individual to join our team as a CAD Operator. As part of an engineering support group, the CAD team produces and maintains design drawings, piping & instrumentation diagrams, wiring diagrams, equipment layouts, and architectural drawings for fabrication and Technical Operations projects. We support the entire site through a variety of tasks including proposal drawings, red line mark ups, and sketches.</p><br><p>In this role, a typical day might include:</p><ul><li><p>Setting priorities for editing and creating engineering drawings in CAD format based on red-line mark ups and sketches.</p></li><li>Creating drawings, updating associated metadata, and coordinating workflows in an electronic document control system.</li><li>Producing and distributing architectural and engineering prints in support of manufacturing operations, regulatory filings, validation projects, and engineering projects.</li><li>Developing and implementing drafting standards and use of standard object libraries across all IOPS (Industrial Operations and Product Supply) sites.</li><li>Performing field verification of installed equipment and systems and generates “as-built” CAD drawings based on findings.</li><li>Authoring department Standard Operating Procedures and Work Instructions.</li><li>Supporting large capital projects by maintaining all drawing responsibility during project execution.</li><li>Creating engineering drawings, such as 3D modeling of process equipment/vessels, to support investigations or corrective actions.</li><li>Coordinating with outside contractors and Architectural & Engineering Firms to confirm and issue Engineering Drawing File numbers and ensuring alignment to the Engineering Drawing Standards.</li><li>Acting as a main point of contact for drawing questions and drawing requests.</li><li>Ensuring on-site and off-site contractors are provided with appropriate Engineering Documents (design documents, P&IDs, specifications, etc.) required for successful project execution and providing supervision to contractors, as needed.</li></ul><p>This role might be for you if you:</p><ul><li>Have experience with AutoCAD or related Autodesk Computer Aided Design software and drawing standards.</li><li>Are able to evaluate drawing redlines/punch list items and GMP evidence provided and determine a path forward for drawing updates.</li><li>Possess knowledge of engineering and architectural drawings.</li><li>Understand project plans and schedules.</li><li>Have an interest in training others within the Engineering department on Engineering Drawing Program procedures.</li><li>Have the ability to prioritize work independently to ensure expectations are met in a timely fashion.</li><li>Can communicate effectively across all levels of the business, both verbally and written, with a keen focus on providing exceptional customer service</li><li>Have a solid understanding of word processing, spreadsheets, database management software, and PCs.</li><li>Are passionate about working in a tight-knit team</li></ul><p>Applicants ideally should have an Associate’s degree in Computer Aided Drafting or another relevant field and the below minimum amounts of experience for each level. We may substitute relevant CAD experience in an engineering and/or construction industry in lieu of a degree.</p><ul><li>CAD Operator II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>CAD Operator III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li><li>CAD Operator IV: 8+ years of related experience or HSD/GED with 12+ years of related experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Analytical Scientist]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45517]]></requisitionid>
    <referencenumber><![CDATA[R45517]]></referencenumber>
    <apijobid><![CDATA[r45517]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45517/sr-analytical-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 Sr. 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>A Typical Day in this Role May Include:</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></ul><p><strong>This job may be for you if:</strong></p><ul><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>To be considered for this position you must have a BS/BA in Chemistry, Biochemistry, Biology, or related field, with 5+ years of relevant industry experience in analytical development and QC method lifecycle.</p><ul><li>PhD degree is preferred.</li><li>Level determined based on qualifications.</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>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 14:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Project Engineer]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46962]]></requisitionid>
    <referencenumber><![CDATA[R46962]]></referencenumber>
    <apijobid><![CDATA[r46962]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46962/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[<p>We are looking for an experienced Engineer to join our growing Project Engineering team. Our team designs, specifies and commissions new and renovated biopharmaceutical process and clean utility equipment. We provide engineering support and lead deviation investigations for existing equipment and manufacturing processes to support the production of our life-changing medications.</p><p>As a Project Engineer, a typical day might include the following:</p><ul><li><p>Designing and specifying cGMP process equipment, piping, and/or controls including development and review of engineering documentation</p></li><li><p>Managing mid-to-large sized projects related to process equipment and clean utilities including start-up and commissioning</p></li><li><p>Assisting in and leading the design review, site acceptance and installation of equipment</p></li><li><p>Preparing piping and instrumentation diagrams and other related drawings</p></li><li><p>Developing Process Flow Diagrams for manufacturing processes</p></li><li><p>Supporting QA/Validation department by preparing design documents and assisting in protocol execution</p></li><li><p>Assisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</p></li><li><p>Implementing corrective/preventative actions for existing equipment and manufacturing processes</p></li><li><p>Preparing engineering evaluations and test plans for and executing modification change control documentation</p></li><li><p>Supervising mechanical, electrical, and automation contractors</p></li><li><p>Traveling up to 10% of the time, both domestically and internationally</p></li></ul><p>This position might be for you if you:</p><ul><li><p>Are interested in having a broad scope with a variety of tasks, seeing the entire process, not just specific equipment or processes</p></li><li><p>Enjoy solving puzzles and challenges, supporting investigations across the business</p></li><li><p>Have a desire to contribute to elements of design work by helping to specify and translating customer needs into equipment</p></li><li><p>Want to do more than just project management or troubleshooting, balancing your technical and project management skills</p></li><li><p>Have a solid understanding of process control systems and automation</p></li><li><p>Are skilled at planning and tracking project activities and schedules</p></li><li><p>Are thoroughly knowledgeable with engineering documentation required for cGMP process equipment as well as sanitary equipment design requirements</p></li><li><p>Have working knowledge of biopharmaceutical equipment</p></li><li><p>Have demonstrated strengths with strong interpersonal, cross-cultural communication</p></li><li><p>Are adept at building and maintaining relationships and leading without direct authority</p></li><li><p>Show resiliency and flexibility in the face of challenging situations</p></li></ul><p>Qualified candidates must have a Bachelor's degree Chemical Engineering or Biochemical Engineering (or another relevant Engineering discipline) and the following minimum years of experience in project/process engineering or an equivalent combination of education and experience. Direct experience with biopharmaceutical process equipment is preferred.</p><ul><li><p>Project Engineer: 2+ years</p></li><li><p>Senior Project Engineer: 5+ years</p></li><li><p>Principal Project Engineer: 8+ years</p></li></ul><p>Level will be determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$75,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Administrative Coordinator]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47141]]></requisitionid>
    <referencenumber><![CDATA[R47141]]></referencenumber>
    <apijobid><![CDATA[r47141]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47141/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>We are seeking an organised and people‑focused Admin Coordinator to support our Immunology team across the UK/NL Cluster, while also providing administrative partnership to the General Manager of the International Region. This role supports collaboration, coordination, and day‑to‑day effectiveness across teams and geographies, helping leaders stay focused on delivering life‑transforming medicines.</p><p>We rely on this role to anticipate needs, manage logistics, and bring clarity to increasingly complex administrative processes, while maintaining accuracy, discretion, and strong working relationships.</p><h3><strong>A Typical Day:</strong></h3><ul><li>Coordinating calendars and meeting logistics across regions</li><li>Supporting internal and external meetings and off‑site events</li><li>Managing requisitions, purchase orders, and expense tracking</li><li>Partnering with Procurement on vendors and meeting budgets</li><li>Maintaining SharePoint content, org charts, and contact lists</li><li>Supporting travel coordination and expense submissions</li><li>Assisting with onboarding and space planning activities</li></ul><h3><strong>This Role May Be For You If You…</strong></h3><ul><li>Enjoy being a central point of coordination</li><li>Like bringing structure to complex schedules and processes</li><li>Are comfortable working across countries and teams</li><li>Value accuracy, discretion, and follow‑through</li><li>Prefer a role that blends routine with problem‑solving</li></ul><h3><strong>To Be Considered</strong></h3><p>Experience in an administrative or coordination role supporting teams or senior leaders is required. Familiarity with requisitioning, purchase orders, and expense processes is expected, with experience using systems such as Concur, MarkView, or Oracle considered beneficial. Experience with meeting and contract tools including Cvent, iCertis, or Zycus is an advantage. Confidence using Microsoft Teams and maintaining SharePoint or similar collaboration platforms is required</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 08:56:16 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp - Senior Supply Logistics Analyst]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47526]]></requisitionid>
    <referencenumber><![CDATA[R47526]]></referencenumber>
    <apijobid><![CDATA[r47526]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47526/temp-senior-supply-logistics-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will support the effective management and development of Regeneron’s external (3PL) warehousing network, ensuring materials are available to meet manufacturing needs.</p><p>You will work closely with internal teams and external partners to support material flow, maintain compliance standards, and improve overall performance. The role also involves analysing data and providing insights to support decision-making in a modern, data-driven supply chain network.</p><p>This is a 12 month contract position.</p><p><strong>A typical day might include, but is not limited to, the following: </strong></p><ul><li>Supporting the day-to-day operation of external warehousing partners</li><li>Ensuring services are delivered in line with quality, compliance, and service agreements</li><li>Collaborating with partners to maintain effective material flow and inventory availability</li><li>Ensuring adherence to established procedures and qualification to required training for the 3PL resource pool</li><li>Providing analysis and insights via KPIs to support operational and strategic decisions</li><li>Acting as a key point of contact for 3PL-related activities</li><li>Working with cross-functional teams (Quality, Planning, Warehouse & Logistics)</li><li>Supporting forward planning for capacity, capability, and service levels</li><li>Managing costs for the 3PL network against agreed budget</li><li>Initiating and executing projects aimed at optimising our supply chain</li><li>Managing Warehouse Management Systems (WMS) linked to enterprise resource planning platforms and automation control systems</li><li>Using data analytics and reporting tools</li><li>Overseeing electronic documentation and workflow management systems</li><li>Utilising learning management systems</li></ul><p><strong>This role might be for you if you:</strong><strong>​</strong> </p><ul><li>You enjoy working collaboratively across teams and organisations</li><li>You are focused on compliance, and high standards of execution</li><li>You are comfortable using data to support decision-making</li><li>You communicate clearly and build strong working relationships</li><li>You are organised and able to manage shifting priorities</li><li>You take a structured, solution-focused approach</li><li>You are comfortable with a balance between on-site work and travel to our 3PL network partners</li></ul><p>To be considered for this opportunity, you must hold a degree in Supply Chain, Operations, Business or a related field, with experience in supply chain, logistics or operations (ideally 5+ years), and experience working with external partners and within regulated industries considered advantageous.<br><br> </p><p>#IRELIM #JOBSIEST #LI-Onsite</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 06:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists-Hematology-New York]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47625]]></requisitionid>
    <referencenumber><![CDATA[R47625]]></referencenumber>
    <apijobid><![CDATA[r47625]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47625/medical-account-specialists-hematology-new-york/]]></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>Geography: New York, New York</strong></p><p>The Hematology Oncology Account Specialist, is responsible for engaging Hematologist and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Hematology Experts and other key Oncology customers within the assigned geographical universe and deliver clinically focused selling messages to support the launch of two bispecific agents to treat malignancies in MM, respectively, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p>​</p><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>​</p><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Associate - Purification Development]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47100]]></requisitionid>
    <referencenumber><![CDATA[R47100]]></referencenumber>
    <apijobid><![CDATA[r47100]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47100/process-development-associate-purification-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Preclinical Manufacturing & Process Development Group (PMPD) is seeking a <strong>Process Development Associate </strong>as a full-time position to work in the Purification Development group. In this role, you will contribute to the development of platforms aimed to accelerate process development, including high-throughput screening and mechanistic modeling. You will also be responsible for using such platforms to design and execute experiments to support the Purification Development group. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Purification of a diverse array of proteins at microliter scale to support many of Regeneron’s research and discovery groups</p></li><li><p>Utilization of automated liquid handling to perform experiments.</p></li><li><p>Development of technology and automation to increase process throughput and efficiency of preclinical manufacturing</p></li><li><p>Calibration of <em>in silico</em> unit operation models to inform development and increase mechanistic understanding</p></li><li><p>Documentation of experiments, results, and findings in an electronic laboratory notebook; presentation of work at group and department meetings.</p></li><li><p>Maintenance of instruments and troubleshooting of instrumental/experimental problems</p></li><li><p>Collaboration with peers to complete core deliverables while exhibiting independence in experimental execution and troubleshooting</p></li></ul><p><strong>This Role Might Be For You If You :</strong></p><ul><li><p>Enjoy a fast-paced bench-scale laboratory setting where sound science and teamwork are priorities.</p></li><li><p>Contribute to lab equipment maintenance and safety to help create a safe, effective, and efficient working environment.</p></li><li><p>Have an eye for development of efficient workflows and best practices.</p></li><li><p>Are well organized and can juggle competing priorities and multiple ongoing projects</p></li><li><p>Anticipate and recognize potential problems with laboratory supplies / equipment and act to prevent and tackle problems.</p></li><li><p>Keep up with SOP training and/or compliance responsibilities.</p></li><li><p>Are scientifically curious, enthusiastic, and proactively ask questions to learn or seek clarification.</p></li></ul><p>The role requires a Bachelor’s and/or Master’s degree in either Chemical Engineering, Biochemical Engineering, or Biochemistry, and 0 - 2+ years’ experience in the biotech or pharmaceutical industry. A strong fundamental understanding of various protein purification techniques a plus. Experience with Downstream Development and with equipment like Akta Explorers/Avants/Pilots, chromatography columns, HPLCs and UPLCs, as well as software such as Empower, Unicorn, JMP, and LIMS is a plus. Experience with liquid handlers, such as Hamiltons or Tecans, is a plus. Experience with mechanistic modeling and GoSilico Chromatography Modeling Software is a plus.</p><p><strong>#pmpd</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - DNA Core]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47230]]></requisitionid>
    <referencenumber><![CDATA[R47230]]></referencenumber>
    <apijobid><![CDATA[r47230]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47230/associate-scientist-dna-core/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an <strong>Associate Scientist</strong> to join the DNA Core Lab. DNA Core facility provides Regeneron laboratories with services necessary for conducting scientific research. These services include, but not limited to, Nucleic Acid isolation and purification, Gene Expression and Genotyping. As a member of the DNA Core team, an individual is expected to perform the assignment in timely fashion and follow scientific protocols. In addition to daily responsibility, each Research Associate is expected to contribute to technology development by conducting experiments, leading to process improvement. Successful candidates should be able to troubleshoot technical issues and be able to clearly communicate with other team members as well as collaborate with scientists both within DNA Core and outside.</p><p><strong>Responsibilities during a typical day might include the following:</strong></p><ul><li>Homogenizing Tissues on automated machines.</li><li>Working with mice tissue and/or cells for RNA/DNA / Protein Extraction</li><li>Running quality control on the RNA/DNA/Protein to measure quantity and quality<br>Contribute to lab and equipment maintenance and order supplies/reagents to help create a safe efficient working environment.</li><li>Laboratory work involves pipetting, computer work and communication with researchers.</li><li>Maintain accurate and complete records consistent with company policy and legal requirements. <br> </li></ul><p><strong>This role may be for you, if you: </strong></p><ul><li>Familiar with Liquid Handling Systems such as Hamilton.</li><li>RNA Purification techniques</li><li>Flexible with multi-tasking while shifting priorities</li><li>Must have a minimum of B.S. in Molecular Biology, Cellular Biology or related field with 0+ years of laboratory experience.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Non-Viral Delivery Tech]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47529]]></requisitionid>
    <referencenumber><![CDATA[R47529]]></referencenumber>
    <apijobid><![CDATA[r47529]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47529/associate-scientist-non-viral-delivery-tech/]]></url>
    <company><![CDATA[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 scientist to join the Non-Viral Delivery Technologies group within Regeneron Genetics Medicines. You will support production, purification, and characterization of protein reagents to be used in next-generation delivery technology development, further expanding the company’s growing genetic medicines portfolio.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Maintenance and manipulation of suspension cells</p></li><li><p>Operation of AKTA systems for small scale purification by liquid chromatography-based techniques (e.g. affinity, ion exchange, size exclusion)</p></li><li><p>Develop high-throughput protein purification and conjugation workflows</p></li><li><p>Characterization of purified proteins (e.g. SDS-PAGE, SE-UPLC, CE)</p></li><li><p>Working collaboratively with other team members and groups around the company</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Enjoy working in a fast paced, highly collaborative environment</p></li><li><p>Have an affinity for protein purification</p></li><li><p>Manage and organize data and workflows</p></li><li><p>Can troubleshoot through logistical and technical hurdles as they arise</p></li><li><p>Can work independently and show initiative to continually improve protocols and processes</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this role, you must have: </strong></p><ul><li><p>A BS/MS in molecular biology, biochemistry, bioengineering, or related field.</p></li><li><p>Experience with aseptic technique used in mammalian cell culture, chromatography, running an AKTA Pure/Avant, and SDS-PAGE/CE are distinct advantages. </p></li><li><p>To be successful in this role, you need to work collaboratively, have attention to detail, and be organized. </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>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Medical Affairs-Oncology]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47331]]></requisitionid>
    <referencenumber><![CDATA[R47331]]></referencenumber>
    <apijobid><![CDATA[r47331]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47331/senior-manager-medical-affairs-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Manager, Medical Affairs you will represent medical affairs in Review Committees related to our the Oncology franchise. A key component is to lead the execution of our medical symposia and maintaining up-to-date scientific and medical knowledge of the oncology landscape. The role involves understanding patient and physician perspectives, clinical decision-making, and their medical impact. <br>This position is located at our Sleepy Hollow, NY offices and will require you to be on-site 4 days/week. If eligible, we can offer relocation benefits. We cannot offer a fully remote option. </p><p><strong>A typical day may include the following</strong>: <br>• Serving as the medical representative in Medical and Promotional Review Committees, ensuring medical/scientific accuracy of medical, promotional, educational, and external-facing materials with fair balanced representation of medical data<br>• Leading the execution of symposia, managing vendors, budget, content review and approval, and engaging with external thought leaders under Medical Director(s) guidance<br>• Supporting our Medical Plan, including congress strategy, scientific communications, scientific engagements, publications, and HEOR activities. <br>• Facilitating Key Opinion Leader (KOL) engagements at medical congresses adhering to high ethical and compliance standards <br>• Assisting in the development and execution of advisory boards<br>• Planning and support training on products and disease aspects, including field medical, medical information, commercial, and sales teams<br>• Presenting scientific and medical materials to diverse audiences such as physicians, pharmacists, marketing/medical agencies, and other collaborators in various settings</p><p><strong>This may be for you if you: </strong><br>• Want to have an impact on patient health<br>• Can demonstrate an understanding of immuno-oncology treatment approaches<br>• Are comfortable communicating to a medical and non-medical audience <br>• Pro-active in your learning approaches to innovative clinical outcomes</p><p>To be considered a PharmD, M.D., or PhD with minimum of 4+ years of experience in the pharmaceutical industry is required. Clinical understanding of oncology/immune-oncology treatment and guidelines is required. . Experience in Medical Review Committees and developing symposia and congress engagement strategies. Extensive clinical and scientific expertise in oncology/immuno-oncology in Medical Affairs is preferred. Willingness to travel occasionally for medical meetings. Ability to critically review medical and scientific information<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Reimbursement Manager-Immunology-Columbus, OH]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47677]]></requisitionid>
    <referencenumber><![CDATA[R47677]]></referencenumber>
    <apijobid><![CDATA[r47677]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47677/field-reimbursement-manager-immunology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong></p><p>The 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><p><strong>When & where: </strong></p><ul><li><p>Remote role</p></li><li><p>Location: Columbus, OH</p></li></ul><p><strong>Discover your role:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment. 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></li><li><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></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, in efforts to streamline the coverage and specialty pharmacy processes to acquire alliance products</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></ul><p><strong>This role requires:</strong></p><ul><li><p>Bachelors 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.</p></li><li><p>You have biologic expertise (Specialty Pharmacy/Buy & Bill)</p></li><li><p>You are a standout colleague and able to collaborate</p></li><li><p>You can optimally communicate across multiple regions via different mediums</p></li><li><p>You can get results with your activity</p></li><li><p>You are capable with meeting the expectations of internal and external customers</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>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 17:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-West]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47572]]></requisitionid>
    <referencenumber><![CDATA[R47572]]></referencenumber>
    <apijobid><![CDATA[r47572]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47572/regional-director-neurology-west/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - California]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the West Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: West (California, Oregon Washington)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 19:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Tax Planning]]></title>
    <date><![CDATA[Thu, 18 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43986]]></requisitionid>
    <referencenumber><![CDATA[R43986]]></referencenumber>
    <apijobid><![CDATA[r43986]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43986/associate-director-tax-planning/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director Tax Planning role will be responsible for developing, implementing and maintaining tax planning opportunities across Regeneron’s business and supply chain. This is a highly collaborative role, interfacing with leaders and colleagues from all functional areas to optimize Regeneron’s tax positions, in alignment with Regeneron’s evolving business and expanding footprint. This role provides critical leadership and support across all aspects of tax planning including supply chain planning, domestic and international planning and governance, and business development and special projects. This role works closely with internal and external subject matter experts to identify opportunities, execute strategies and document positions. </p><div></div><div><p>The ideal candidate will have the personal drive and enthusiasm to both understand and successfully navigate a fast-growing company in a rapidly evolving marketplace. The ideal candidate will have a hands-on and entrepreneurial style and be willing assist the team and manage projects from development through to finalization. This person is a strategic thinker who approaches challenges with a positive attitude and drives the team towards solutions. This is a visible position with direct contact with Regeneron business leads and senior management. </p></div><p><em><strong>This role will require 4 days per week onsite at our HQ Campus in Sleepy Hollow, NY. This is not available as a fully remote / hybrid work.</strong></em></p><div><p><strong>As an Associate Director, Tax Planning a typical day may include</strong> </p></div><div><ul><li><p>Identify, develop and implement tax planning opportunities in support of Regeneron’s expanding business and supply chain, including modeling financial impact, leading cross-functional assessment and execution, and identifying risk mitigation strategies. </p></li></ul></div><div><ul><li><p>Lead tax aspects of supply chain planning, including optimization of clinical and commercial supply chains, external manufacturing arrangements and distribution models, in alignment with business needs and taking into account domestic and foreign income taxes and indirect taxes. </p></li></ul></div><div><ul><li><p>Research, review and / or draft documentation involving complex tax issues and strategies as may be required in an expanding business, including but not limited to tax technical memoranda, operating manuals, governance policies and reports, and intercompany and third-party agreements. </p></li></ul></div><div><ul><li><p>Support tax efficient international operations and expansion, including optimization of local tax planning and tax incentives, collaborating cross-functional subject matter experts to ensure that finance and business goals are met and reporting is accurate. </p></li></ul></div><div><ul><li><p>Provide end-to-end tax support to Business Development on third-party deals (licenses, collaborations, acquisitions and divestitures and other agreements) including leading diligence to identify risks and opportunities, development of optimal deal structures, review and negotiation of legal documents, and implementation. </p></li></ul></div><div><ul><li><p>Collaborate closely, both internally and externally, with advisors and subject matter experts to ensure tax strategies and implementation contemplate cross-functional impact and are properly documented (including transfer pricing and tax operations). </p></li></ul></div><div><ul><li><p>Monitor U.S. and foreign tax proposals, including OECD BEPS/Pillar Two, working with tax subject matter experts to determine the financial and operational impacts of proposed changes on Regeneron’s tax positions. </p></li></ul></div><div><ul><li><p>Establish strong relationships, demonstrate organizational and interpersonal skills to build a collaborative environment, foster open communication, and educate the business on tax considerations. </p></li></ul></div><div><ul><li><p>Foster a culture of excellence, integrity, and accountability for a growing team. </p></li></ul></div><div><ul><li><p>Interface and interact effectively with personnel at all levels of Regeneron’s organization, including senior leadership, finance leaders, collaborators, external advisors and members of the tax department. </p></li></ul></div><div><div><p><strong>This role may be for you if you have: </strong> </p></div><div><ul><li><p>Mastery of US tax rules, in particular US international tax rules, mergers and acquisitions </p></li></ul></div><div><ul><li><p>Exposure to international supply chain structures, global complexity and foreign tax rules including OECD BEPS and other proposals. </p></li></ul></div></div><div><div><ul><li><p>Ability to research and interpret complex US and non-US tax rules. </p></li></ul></div><div><ul><li><p>Excellent analytical and problem-solving skills required, with the ability to plan and execute at strategic and tactical levels. </p></li></ul></div><div><ul><li><p>Strong communication and interpersonal skills with an ability to effectively relate tax issues to non-tax personnel and upper management. </p></li></ul></div><div><ul><li><p>Strong creative and analytical thought processes, with ability to work in a fast-paced environment with excellent prioritization and organizational skills. </p></li></ul></div><div><ul><li><p>Confident and personable individual, able to work collaboratively inside and outside the tax department and build bridges at all levels of the enterprise. </p></li></ul></div><div><ul><li><p>A superior work ethic, positive attitude, and willingness to jump into projects and assist the team in all areas of tax as may be required at a growing company. </p></li></ul></div><div><ul><li><p>Dedication to the highest work quality and job excellence. </p></li></ul></div><div><ul><li><p>Proficiency with MS Office, in particular, PowerPoint and Excel. </p></li></ul></div></div><p><strong>To be considered for this role you must possess a Bachelor’s degree with 10+ years of experience in tax planning and strategy, including experience in a corporate environment in addition to law firm and/or accounting firm experience. A J.D., CPA or equivalent required, MBA, LLM or Master’s degree in finance a plus.</strong> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff IT Compliance Analyst]]></title>
    <date><![CDATA[Tue, 20 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43076]]></requisitionid>
    <referencenumber><![CDATA[R43076]]></referencenumber>
    <apijobid><![CDATA[r43076]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43076/staff-it-compliance-analyst/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Staff IT Compliance Analyst plays a critical role in ensuring that the Manufacturing IT group operates in full compliance with regulatory requirements, industry standards, and Regeneron’s internal quality procedures. This role also oversees the preparation and management of internal and external audits to maintain a state of inspection readiness.</p><p>As a Staff IT Compliance Analyst, a typical day might include the following:</p><ul><li>Providing expert guidance and analysis to the Manufacturing IT team on regulatory compliance, quality assurance, and inspection readiness, while managing internal programs to ensure audit preparedness.</li><li>Evaluating, developing, and refining Manufacturing IT policies, standard operating procedures (SOPs), and practices to align with regulatory requirements, corporate quality standards, and industry best practices.</li><li>Representing and supporting Manufacturing IT subject matter experts (SMEs) during internal and external audits, while leading the development and execution of responses to audit findings.</li><li>Establishing, maintaining, and improving metrics to monitor IT compliance, inspection readiness, and audit outcomes, and effectively communicating these findings to stakeholders.</li><li>Collaborating with global sites to ensure deployed systems comply with business needs, regulatory expectations, and data integrity requirements, while promoting a culture of quality and continuous improvement.</li><li>Monitoring industry trends in audit observations and regulatory changes, identifying potential compliance gaps, and implementing timely corrective or preventive actions.</li><li>Supporting IT quality processes, including managing IT deviations, change controls, and the creation or revision of IT quality documents, while demonstrating flexibility and cross-functional expertise.</li></ul><p>This role may be for you if you have:</p><ul><li>A deep understanding of GxP regulations (e.g., FDA 21 CFR Part 11, EU Annex 11) and expertise in IT system validation and qualification processes.</li><li>Proven ability to apply quality assurance principles to IT compliance activities, ensuring systems and processes meet both regulatory and corporate quality standards.</li><li>Strong analytical and problem-solving skills, with a proactive approach to identifying and resolving compliance risks.</li><li>Excellent communication and collaboration skills to work effectively across global teams and interact with regulatory inspectors or auditors.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field required along with</p><ul><li>Principal IT Compliance Analyst: 8 years of relevant experience.</li><li>Staff IT Compliance Analyst: 10 years of relevant experience.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Quality Assurance (QA) experience strongly desired.</li><li>Experience in the pharmaceutical or biotechnology industry preferred.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 21 Jan 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Global Patient Safety Sciences - Neurology]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44952]]></requisitionid>
    <referencenumber><![CDATA[R44952]]></referencenumber>
    <apijobid><![CDATA[r44952]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44952/director-global-patient-safety-sciences-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>The Global Patient Safety (GPS) Lead role (Director of GPS) serves as the first point of contact (POC) for all safety related issues for the compound(s) [asset(s)] assigned within a given therapeutic area (TA), and is the GPS representative on the cross functional strategic program team (SPT) for the compound. The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety strategy. This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management. The GPS Director joins Regeneron’s industry leading scientific organization, and has a direct impact on drug development, operations, and commercialization in all relevant global territories.</p></div><div><div><div><div><div><div><div><div><div><div><div><div><div><div><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>This Director position is directly responsible for all aspects of Global Patient Safety activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)</p></li><li><p>Leads cross-functional Safety Monitoring Team (SMT) activities</p></li><li><p>Represent Global Patient Safety for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)</p></li><li><p>Proactively identify and develop safety strategies and planning for non-compound specific Global Patient Safety activities (mechanism of action etc.)</p></li><li><p>Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds</p></li><li><p>Actively participate in the development and maintenance of relevant SOPs, working practices and guides </p></li><li><p>Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists</p></li></ul><p><strong>This role might be for you if can/have:</strong></p><ul><li><p>Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.</p></li><li><p>Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.</p></li><li><p>A proven ability to lead and develop a diverse team of Safety Professionals in a constructive, goal-oriented environment.</p></li><li><p>An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.</p></li><li><p>Ability to utilize GPS safety database for purposes of medical case review and simple queries. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum 10+ years of total relevant experience in PV and/or relevant medical field or equivalent of industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content). </p></li><li><p>5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree required.</p></li><li><p>Clinical experience and/or industry experience in Oncology is a plus</p></li></ul><p>#MDJOBSPS #GDPSJobs</p></div></div></div></div></div></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 13:26:34 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Precision Medicine]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44954]]></requisitionid>
    <referencenumber><![CDATA[R44954]]></referencenumber>
    <apijobid><![CDATA[r44954]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44954/director-precision-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Precision Medicine group at Regeneron is responsible for designing, implementing, executing, analyzing and interpreting the overarching clinical biomarker strategies for therapeutic candidates during clinical development. We are seeking to hire a hands-on Precision Medicine Strategy Lead (PMSL) roles at the director level, with backgrounds in one or more therapeutic areas within the group. We are seeking someone to independently oversee the development and execution of biomarker strategies across one (or more) therapeutic areas depending on their areas of expertise, with a preference in obesity / metabolism pharmaceutical development.. The following therapeutic areas are in scope: Neurodegenerative Disorders, Cardiovascular Disease, Muscle and Metabolism Disorders, and/or Rare Genetic Diseases). In this highly matrixed role, they will design, develop, communicate at senior levels and operationally implement clinical biomarker strategies to support key programs in early and late stage drug development. Clinical technologies applied include biomarker assays, pharmacogenetic assessments, as well as other clinical and physiological testing devices. </p><p><strong>A typical day may include:</strong></p><ul><li><p>Enhancing our understanding of indications at a cellular and molecular level</p></li><li><p>Conducting novel biomarker discovery, qualifying new biomarkers/approaches to expedite proof-of-concept for new drug candidates.</p></li><li><p>Optimizing label claims for later stage candidates, enabling personalized medicine principles to be applied, as appropriate, in full development. </p></li><li><p>With a focus in therapeutic areas outside of Oncology, broad understanding of disparate biomarker technologies, and deep experience in biomarker assay development and validation in clinical drug development </p></li><li><p>Responsible for conducting in-depth literature and technology reviews pertinent to assigned clinical development programs within the TFA, identifying and pulling in experts in multiple disease areas, navigating and supporting the logistical and regulatory factors pertaining to clinical technologies.</p></li></ul><p><strong>This role may be for you if have experience with the following:</strong></p><ul><li><p>TA--level lead for implementation of strategic vision for clinical biomarkers in one or more therapeutic areas across multiple programs with multiple studies that will broadly enable advances in target identification, indication selection, early indication of biological activity and patient stratification/selection</p></li><li><p>Serve as an individual contributor and senior-level representative of Precision Medicine on development teams and deliver biomarker strategies to key programs from initial concept to execution, data delivery and results interpretation</p></li><li><p>Collaborate with Discovery Research and product development teams to facilitate appropriate incorporation of Precision Medicine and clinical biomarker strategies for molecules in discovery phases (leading to candidate molecule selection)</p></li><li><p>Represent Regeneron and work with colleagues from allied companies to develop and implement strategies for partnered alliances</p></li><li><p>Collaborate with clinical operations teams to implement specific biomarker and exploratory sample collection and analyses in all relevant clinical studies in selected programs</p></li><li><p>Design, oversee and manage internal and external research collaborations in areas of clinical technologies and translational research</p></li><li><p> Accountability for ensuring complex clinical assays used in programs in the TFA portfolio of clinical development are fit-for-purpose (whether developed and validated internally or externally)</p></li><li><p>Collaborate with internal Regeneron laboratories (e.g. Discovery Research, Molecular Profiling, Regeneron Genetics Center, DNA core, BioAnalysis, etc.) to develop plan for validation and application of research assays</p></li><li><p>Ensure timely delivery of results across selected programs, consistent with program team and senior management expectations in a way that increases the potential impact of Precision Medicine deliverables on Global Development programs</p></li><li><p> Contribute to and ensure the quality of Precision Medicine technical reports, study memos and clinical study reports, data reviews and interpretations, scientific publications and recommendations to development teams and management.</p></li></ul><p><strong>To be considered for this role</strong>, you must have a PhD and 10+ years of experience driving, managing, executing and delivering results for complex multi-functional projects. You have excellent communication and presentation skills and high emotional intelligence, organizational skills and effective team skills. Strong track record in mentorship and development of direct reports.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 21:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Program Operations Leader, Oncology]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45269]]></requisitionid>
    <referencenumber><![CDATA[R45269]]></referencenumber>
    <apijobid><![CDATA[r45269]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45269/director-program-operations-leader-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director Program Operations Leader</strong> (POL) is responsible for leadership of and setting and implementation of the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional strategy of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence.</p><p><strong>Director Program Operations Leader - Oncology </strong></p><p><em>(For US Locations, this position is on-site 4 days per week and 1 day from home. For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days from home. A fully remote role is NOT possible for this position.)</em></p><p><strong>In a typical day, you will:</strong></p><ul><li>Be responsible for the overall success of the clinical study team(s) within a program(s)</li><li>Maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested</li><li>Provide operational insight into feasibility, timeline and cost estimates during clinical program/study development</li><li>Oversee clinical study timelines within a clinical program(s)</li><li>Provide input and operational insight into Clinical Study Concepts (CSC)</li><li>Be responsible for development and implementation of operational strategy, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol </li><li>Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency within the program and development of best practices within CTM</li><li>Oversee clinical study budgets within a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate</li><li>Ensure timely delivery of quality operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams within the clinical program(s). </li><li>Drive decision making and integrates all operational considerations for studies within a clinical program(s) to ensure goals are attainable prior to implementation</li><li>Act as point of contact for clinical program and study level escalation</li><li>Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress</li><li>Provide proactive creation and implementation of risk mitigation strategies</li><li>Provide innovative and flexible operational solutions and options to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges</li><li>Drives the strategy and oversight for vendor selection and management within a clinical program(s)</li><li>Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts</li><li>May require up to 25% travel</li></ul><p><strong>To be considered, you must possess</strong> a Bachelor's degree and a minimum of 12 years of related in-house sponsor-side pharmaceutical experience, with 8 years in clinical operations.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Medical Director, Medical Affairs, MASH]]></title>
    <date><![CDATA[Tue, 03 Mar 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45729]]></requisitionid>
    <referencenumber><![CDATA[R45729]]></referencenumber>
    <apijobid><![CDATA[r45729]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45729/senior-medical-director-medical-affairs-mash/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>The Senior Medical Director, Medical Affairs – MASH, will play a pivotal and highly visible strategic leadership role within the organization, reporting directly to the VP, Medical Affairs, General Medicine. This role is responsible for driving the medical strategy and execution for MASH assets, with a strong focus on strategic planning, cross-functional leadership, and external engagement. The Senior Medical Director will ensure all medical affairs activities are delivered with scientific excellence, integrity, and patient-centricity.</div></div><div><div><div><div><p><strong>A typical day in this role might look like: </strong></p><ul><li>Provides visionary leadership in the development, execution, and continuous refinement of medical strategy and tactics for assigned assets, ensuring alignment with corporate and global objectives. Champions the integration of scientific communications, publications, annual medical planning, and field communication strategies in partnership with key internal and external stakeholders.</li><li>Apply deep therapeutic area expertise and strategic business acumen to proactively identify and address evolving medical needs in clinical practice. Ensures the medically appropriate use of investigational medicines and anticipates future trends impacting patient care, policy, and access.</li><li>Directs and oversees the generation, management, and dissemination of robust clinical and non-clinical data. Drives high-impact publication strategies and ensures scientific content supports both the medical strategy and external stakeholder needs, maintaining the highest standards of accuracy and scientific rigor.</li><li>Leads cross-functional and cross-alliance teams with a focus on strategic alignment, collaboration, and excellence in execution. Fosters a culture of innovation and accountability, ensuring seamless coordination across medical, commercial, regulatory, and alliance partners.</li><li>Serves as a key strategic advisor and leader on global and US cross-functional teams, providing authoritative scientific and medical perspectives that inform and shape organizational strategy and decision-making.</li><li>Oversee the design, conduct, and reporting of Medical Affairs studies, ensuring scientific integrity, regulatory compliance, and alignment with strategic priorities. Provides mentorship and guidance to teams executing these initiatives.</li><li>Cultivates and expands long-term, strategic partnerships with clinical experts, societies, collaborative groups, advocacy organizations, payers, policy makers, and other external stakeholders. Acts as the primary ambassador for Regeneron, building trust and advancing shared goals in the MASH therapeutic area.</li><li>Leads prioritization and support for investigator-initiated studies, serving as a key decision-maker and member of internal Scientific Review Committees. Ensuring alignment with overall medical strategy and organizational objectives.</li><li>Overseas and ensures the scientific accuracy and compliance of all medical materials, including promotional and non-promotional content. Provides final approval and guidance to uphold the highest standards of scientific and ethical integrity.<br> </li></ul><p><strong>This role might be for you if: </strong></p><ul><li>Must have an MD or MD equivalent with a preference for specialized fellowship training in Gastroenterology or Hepatology</li><li>5 years of related industry experience in global or US medical affairs</li><li>Solid background and experience in drug development and life-cycle management</li><li>Experience with working in an alliance setting strongly preferred</li><li>Ability to lead technical and business discussions internally and externally and explain scientific/medical concepts to all levels</li><li>Ability to cultivate and maintain relationships with leading medical/scientific experts in the relevant fields</li><li>Ability to establish trust through the consistent demonstration of scientific expertise and satisfactory follow-through on requests from key opinion leaders</li><li>Strong leadership and management skills</li><li>Attention to detail in analyses, deliverables, and communications</li><li>Strong presentation and communication skills; must be able to provide succinct, strategic, and actionable insights to senior management</li><li>A proactive self-starter who can lead work and manage others independently, with the ability to see the next step and take actions without prompting</li><li>Ability to juggle multiple projects</li><li>Thorough understanding of the healthcare environment including all external stakeholders</li></ul><p>#MDJOBSMA, #MDJOBS, #GDMAJobs</p></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$333,300.00 - $450,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 03 Mar 2026 16:26:12 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Omnichannel Customer Experience, Consumer Marketing (Ophthalmology)]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46178]]></requisitionid>
    <referencenumber><![CDATA[R46178]]></referencenumber>
    <apijobid><![CDATA[r46178]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46178/associate-director-omnichannel-customer-experience-consumer-marketing-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Marketing will contribute to the financial success of the Ophthalmology franchise. Main area of responsibility will be to implement and manage key elements of the U.S. Consumer Marketing plan, ultimately to drive demand for the product.</p><p>Specifically, this will include omnichannel campaign implementation including, Television, Print/Mail, digital and social media marketing execution, patient engagement tool/material development, patient education plan development and implementation, strategic content creation, Agency collaboration, materials and inventory management, budget management, management of review materials schedule and process.</p><p><strong>A Typical Day Might Look Like This:</strong></p><ul><li><p>Contributing to, and implementing consumer strategy, communications planning and tactical plans</p></li><li><p>Implementation of consumer initiatives and tactical plans</p></li><li><p>Delivering against omnichannel strategy and optimizing performance media programs against business goals and priorities</p></li><li><p>Manage & provide strategic input to Agency-led media planning that delivers against the goals of the business</p><ul><li><p>Evaluate, and provide feedback to, performance of media buys in an ongoing way ensure alignment with brand objectives</p></li><li><p>Work with internal Insights & Analytics Teams to expand our approach to measurement of campaigns and other omnichannel initiatives</p></li></ul></li><li><p>Developing innovative digital and social media programs that accelerate brand awareness and drive consumer action</p></li><li><p>Extend omnichannel strategies through an understanding of technical, data, and media system integration points and underlying platforms in a way that delivers incremental value to our customers, patients, and prospects</p><ul><li><p>Expand on compliant first-party data strategy that enriches our customer experience and drives value for our brand</p></li><li><p>Continue to refine our view of our customer, personas, segmentation, and related – business-critical user journeys</p><ul><li><p>Mature our approach to customer journeys in a way that delivers data, insights, and an evolution of our marketing activities</p></li></ul></li><li><p>Develop SEO-inspired content planning that delivers on the needs of our customers in a way that ladders up to critical success factors for our brand</p><ul><li><p>Content development in various formats including: long form, short form, video, social channel specific (Reddit vs Facebook vs LinkedIn), and email</p></li></ul></li><li><p>Develop a seamless holistic digital experience that fulfills on tactical goals including key site actions, engagement, and customer registrations for CRM programs</p></li><li><p>Enrich existing CRM strategy to be more inclusive of additional user needs, journeys, and conversion stages</p></li></ul></li><li><p>Driving selection of patient ambassadors and developing patient testimonials and videos</p></li><li><p>Implementing targeted communication programs</p></li><li><p>Representing promotional tactics for medical, legal, and regulatory team reviews and ensuring final deliverables are accurate and compliant.</p></li><li><p>Working closely with the cross functional marketing team</p></li><li><p>Managing budgets and closely monitoring performance, ensuring cost effective delivery of all programs while tracking and monitoring KPIs</p></li><li><p>Developing and managing patient education and engagement tools and materials- and related promotion through personal and digital distribution channels</p></li></ul><p><strong>If This Looks Like You:</strong></p><ul><li><p>Demonstrated competency in managing consumer/patient marketing programs</p></li><li><p>Demonstrated digital and social marketing experience</p></li><li><p>Demonstrated ability to work effectively, efficiently, and collaboratively with team members and across departments to develop and execute programs and materials</p></li><li><p>Demonstrated competency in agency management and budget management</p></li><li><p>Proven ability to work within regulatory, legal, and compliance guidelines</p></li><li><p>Demonstrated project management skills</p></li></ul><p>To be considered you have a Bachelor's Degree, MBA a plus. Demonstrated experience in marketing of biologics preferred. You have 10+ years of progressive marketing experience including at least 5 years in the Consumer space in pharmaceutical marketing. Demonstrated omnichannel digital marketing experience. Demonstrated Consumer marketing competencies in the pharmaceutical/biotech areas. Prior U.S. launch experience a plus. Strong interpersonal & presentation skills. Ability to communicate with all levels of the organization. Must be willing to travel ~10% (including weekend travel as needed). This is an office-based role, and the expectation will be to work in the office 4-days a week.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 06:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Program Operations Leader, Internal Medicines]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44524]]></requisitionid>
    <referencenumber><![CDATA[R44524]]></referencenumber>
    <apijobid><![CDATA[r44524]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44524/director-program-operations-leader-internal-medicines/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Director Program Operations Leader</strong> (POL) is responsible for leadership of and setting and implementation of the operational strategy for delivery of one or more complex programs in Clinical Trial Management (CTM). This individual is responsible for clinical operations activities and decisions including quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable regulations, ICH/GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The POL is a member of the Clinical Trial Management extended leadership team, and as such interacts with senior level management, external vendors, collaboration partners and clinical study personnel for clinical research project and department initiatives. The POL is responsible for line management of clinical trial management staff (including AD POL), and has responsibility for staff recruitment, development, coaching, mentoring and performance management. Plays a key role in driving the functional strategy of Clinical Trial Management in partnership with Functional leadership. The Director POL is expected to operate with autonomy and high-degree of independence.</p><p><strong>Director Program Operations Leader - Specialty Medicine, Rare Disease</strong></p><p><em>(For Uxbridge and Dublin, colleagues must be on-site 3 days per week and 2 days from home. A fully remote role is NOT possible for this position.)</em></p><p><strong>In a typical day, you will:</strong></p><ul><li>Be responsible for the overall success of the clinical study team(s) within a program(s)</li><li>Maintain an overview of clinical program(s) status and issues and proactively communicates progress, risks, issues or changes that may impact quality, timelines and/or budget; provide clinical program level updates to stakeholders as requested</li><li>Provide operational insight into feasibility, timeline and cost estimates during clinical program/study development</li><li>Oversee clinical study timelines within a clinical program(s)</li><li>Provide input and operational insight into Clinical Study Concepts (CSC)</li><li>Be responsible for development and implementation of operational strategy, driving early study planning budget and timelines from Clinical Study Concept through Final Protocol </li><li>Review plans and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies. Ensure consistency within the program and development of best practices within CTM</li><li>Oversee clinical study budgets within a program: ensures review, presentation and approval of initial study budget and manages the budget through the lifecycle of the program by communicating changes to TA Operations Leader, as appropriate</li><li>Ensure timely delivery of quality operational deliverables and accountable for ensuring consistency of process and approaches across clinical study teams within the clinical program(s). </li><li>Drive decision making and integrates all operational considerations for studies within a clinical program(s) to ensure goals are attainable prior to implementation</li><li>Act as point of contact for clinical program and study level escalation</li><li>Review key metrics and Key Performance Indicators (KPIs) across studies and within clinical program(s) to track study progress</li><li>Provide proactive creation and implementation of risk mitigation strategies</li><li>Provide innovative and flexible operational solutions and options to the cross functional and development teams; assists in preparing scenarios for creative solutions to operational challenges</li><li>Drives the strategy and oversight for vendor selection and management within a clinical program(s)</li><li>Manages the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables and relationship with key CRO (functional and project) and vendor counterparts</li><li>May require up to 25% travel</li></ul><p><strong>To be considered, you must possess</strong> a Bachelor's degree and a minimum of 12 years of related in-house sponsor-side pharmaceutical experience, with 8 years in clinical operations.</p><p><em>For US Locations, this position is on-site 4 days per week and 1 day from home. </em></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 04:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Drug Production, Associate Manufacturing Specialist]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46370]]></requisitionid>
    <referencenumber><![CDATA[R46370]]></referencenumber>
    <apijobid><![CDATA[r46370]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46370/drug-production-associate-manufacturing-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently looking for a Drug Production, Associate Manufacturing Specialist in the Global Manufacturing department. In this role, you will focus on manufacturing life changing medicines for patients around the world while working in a clean room environment. Please continue to review the job duties if you are interested in working 3rd shift (10pm-8:30am) with the potential for weekends.</p><p>A typical day for a Drug Production, Associate Manufacturing Specialist might include:</p><ul><li><p>Performing all aspects of drug production in a clean room including cell culture and purification of monoclonal antibodies</p></li><li><p>Completing and reviewing batch records and logbooks in accordance with Current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP)</p></li><li><p>Performing in-process sampling and analysis of buffer solutions, cell culture, and drug substance</p></li><li><p>Operating automated equipment such as bioreactors, chromatography columns, and filtration skids</p></li><li><p>Supporting equipment start-up, troubleshooting, and validation</p></li><li><p>Partnering with R&D teams to implement new drug manufacturing processes and technologies</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Enjoy working in a fast-paced setting where your priorities can quickly change based on the needs of the business and our patients</p></li><li><p>Are highly organized, detail oriented and perform work accurately the first time</p></li><li><p>Value trust and transparency in everyday work</p></li><li><p>Work well in both small and large teams to accomplish tasks adhering to a schedule</p></li><li><p>Can operate in a highly regulated environment strive to continuously improve processes and maintain compliance to manufacture safe and effective medicines for patients</p></li><li><p>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Are a good communicator and can give and receive feedback constructively</p></li></ul><p>If this sounds like you check out this video to view 'A Day in the Life': <a href="https://regeneronmax.widen.net/s/z2p5kvcjvv/20220706_iops_001">A Day in the Life</a></p><p>Gowning and Environment</p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li></ul><p>Shift & Physical Requirements</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours) in a clean room environment</p></li><li><p>To enable a healthy work life balance we offer multiple shifts that are 4 working days (10 hours) to support 24/7 production.</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p>To be considered for this role you must meet the below minimum education and experience requirements:</p><p>Drug Production, Associate Manufacturing Specialist:</p><ul><li><p>HS diploma + 4 years of relevant work experience <strong>or</strong></p></li><li><p>AS, BS or BA in Life Sciences or related field</p></li><li><p>Able to work 3rd shift (10pm-8:30am) with the potential for weekends</p></li></ul><p>Regeneron offers an exciting and competitive benefits package! For details check out: <a href="https://careers.regeneron.com/en/working-at-regeneron/total-rewards/">https://careers.regeneron.com/en/working-at-regeneron/total-rewards/</a></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$21.78 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation Integration Engineer]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44508]]></requisitionid>
    <referencenumber><![CDATA[R44508]]></referencenumber>
    <apijobid><![CDATA[r44508]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44508/senior-automation-integration-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><p>We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems. </p></div><div><p>As a Senior Automation Systems Integration Engineer<strong>,</strong> a typical day might include the following: </p></div><div><ul><li><p>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures. </p></li></ul></div><div><ul><li><p>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems. </p></li></ul></div><div><ul><li><p>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines. </p></li></ul></div><div><ul><li><p>Supporting small manufacturing, engineering, and validation projects. </p></li></ul></div><div><ul><li><p>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action. </p></li></ul></div><div><ul><li><p>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols. </p></li></ul></div><div><ul><li><p>Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure </p></li></ul></div><div><ul><li><p>Creation, modification, and maintenance of automation system documentation </p></li></ul></div><div><p>This role might be for you if you: </p></div><div><ul><li><p>Have experience with OT applications, including SCADAs, HMIs, Historians, etc. </p></li></ul></div><div><ul><li><p>Are familiar with standing up large systems at the enterprise level </p></li></ul></div><div><ul><li><p>Have core knowledge related to ISE S95 and S88 principles and IT/Automation integration </p></li></ul></div><div><ul><li><p>Have familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure </p></li></ul></div><div><ul><li><p>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better </p></li></ul></div><div><ul><li><p>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly </p></li></ul></div><div><ul><li><p>Can balance changing priorities with increasing workload by making/communicating timely decisions </p></li></ul></div><div><p>To be considered for the Senior Automation Systems Integration Engineer position you ideally should have a bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level: </p></div><div><ul><li><p>Senior Engineer: 5+ years </p></li></ul></div></div><div><div><ul><li><p>Principal Engineer: 8+ years</p></li></ul></div><div><p>Level will be determined based on qualifications relevant to the role</p></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 11:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director,  Scientific Communications ( Oncology)]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46060]]></requisitionid>
    <referencenumber><![CDATA[R46060]]></referencenumber>
    <apijobid><![CDATA[r46060]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46060/associate-director-scientific-communications-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Associate Director, Scientific Communications, to join our dynamic Global Medical Affairs team supporting out Oncology portfolio. In this pivotal role, you will shape and implement comprehensive scientific communication strategies for oncology, ensuring alignment with therapeutic goals and delivering impactful educational materials. This position offers the opportunity to collaborate within a matrix organization, influence medical communications globally, and contribute meaningfully to advancing patient care. </p><p>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits.</p><p><strong>A typical day may include the following: </strong><br>• Developing and maintaining scientific communication platforms, lexicons, and disease-state education materials.<br>• Collaborating with Medical Affairs Franchise Directors aligning on congress deliverables and educational content.<br>• Driving quality control and endorsement of scientific assets like program slides and publication updates.<br>• Leading projects through medical review committees to ensure compliance and scientific accuracy.<br>• Managing vendor interactions to ensure timely delivery of high-quality materials.<br>• Creating innovative digital scientific assets for diverse medical channels, including portals and social media.<br>• Assessing internal and external medical education needs to develop impactful educational activities.<br>• Supervising budget allocations and ensuring systematic tracking of expenditures.<br>• Maintaining centralized, searchable resource repositories to support internal teams.</p><p><strong>This may be for you if you:</strong> <br>• Are highly self-motivated with a hands-on execution mentality and a “can-do” spirit. <br>• Excel in a fast-paced, constantly evolving organization and value adaptability. <br>• Are passionate about ensuring scientific integrity and accuracy in all medical and scientific assets. <br>• Enjoy collaborating across multifunctional teams and driving innovative approaches to medical education. <br>• Are committed to ethical standards and prioritize patient-first values in your work. <br>• Are adept at using digital channels to enhance the reach and impact of scientific communications. </p><p>To qualify for this position, you must hold a PhD, MD, or PharmD and have a minimum of 6 years of experience in the pharmaceutical industry, including at least 4 years in Scientific Communications or Medical Affairs. A strong background in oncology and general medicines is essential. Preferred qualifications include proficiency in managing vendor relationships, developing innovative digital assets, and navigating medical review processes. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Scientific Communications- General Medicine]]></title>
    <date><![CDATA[Wed, 25 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46059]]></requisitionid>
    <referencenumber><![CDATA[R46059]]></referencenumber>
    <apijobid><![CDATA[r46059]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46059/director-scientific-communications-general-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Join our passionate team as the Director of Scientific Communications for General Medicine. In this pivotal role, you will lead the creation and alignment of our integrated medical communication strategies to advance medical knowledge and improve clinical care for patients. Collaborating with cross-functional teams, we develop evidence-based scientific communication platforms, ensuring content accuracy, accessibility, and impact. With a focus on innovation and collaboration, this role offers the opportunity to make meaningful contributions to partner engagement and patient outcomes.<br>This position requires on-site presence 4 days a week in Warren, NJ or Sleepy Hollow, NY, with occasional travel between sites. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong> <br>• Lead the development and execution of comprehensive Integrated Medical Communication Plans. <br>• Establish and communicate clear scientific communication of our objectives and tactical plans<br>• Partner with medical directors and key collaborators to devise congress strategies and oversee deliverables. <br>• Drive the creation of scientific and digital communication materials, including scientific communication platforms, lexicons, narratives, and disease-state education.<br>• Collaborate with the Congress Strategy and Planning team to ensure impactful booth designs and materials.<br>• Assess medical education gaps and find opportunities to create tailored, targeted, and timely content for diverse platforms and regions.<br>• Oversee the medical review process to ensure scientific accuracy, compliance, and ethical integrity of all materials.<br>• Manage project budgets and timelines in collaboration with the project manager.</p><p>T<strong>his may be for you if you: </strong><br>• Thrive in a collaborative, cross-functional environment. <br>• Can manage multiple projects, vendors, and priorities in a fast-paced environment. <br>• Are committed to ethical and compliance standards and have a “patient-first” value framework. <br>• Bring critical thinking and analytical skills to assess data and inform strategic decision-making. </p><p>To be considered it is required to have a PhD, MD, or PharmD with at least 8 years of relevant medical communication experience. Demonstrated expertise in medical communication strategies, congress planning, scientific content development, and medical education is required. Strong project management skills, ethical integrity, and the ability to work in a matrix organization are essential. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 26 Mar 2026 14:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist - Flow Cytometry]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45896]]></requisitionid>
    <referencenumber><![CDATA[R45896]]></referencenumber>
    <apijobid><![CDATA[r45896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45896/associate-scientist-flow-cytometry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated<strong> Associate Scientist – Flow Cytometry</strong> to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as perform data analysis using various flow cytometric software programs.</p><p><strong>As an Associate Scientist – Flow Cytometry, a typical day might include:</strong></p><ul><li><p>Ensuring proper maintenance, alignment, and calibration of cell sorting equipment</p></li><li><p>Analyzing flow cytometric data</p></li><li><p>Maintaining and organizing schedules for cell sorting equipment</p></li><li><p>Maintaining adequate inventory of flow cytometry supplies and reagents</p></li><li><p>Supporting maintenance of flow cytometry equipment, such as LSRFortessa X-20, FACSymphony A3/A5, FACSDiscover A8, Aurora, CytoFLEX (LX), IntelliCyt iQue, and Amnis ImageStreamX MkII cytometers</p></li><li><p>Operating a Sony MA900, FACSAria Fusion, FACSymphony S6, and FACSDiscover S8 high-speed cell sorters</p></li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li><p>You are able to critically analyze and troubleshoot scientific problems</p></li><li><p>You have a customer-centric viewpoint</p></li><li><p>You have good scientific initiative and ability to multi-task, prioritize work, and balance multiple projects</p></li><li><p>You can work independently but also within a collaborative team environment and have flexibility to work on changing priorities</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS in a scientific field and 1-3 years of relevant experience using cytometric instrumentation. Experimental laboratory work and cell sorting is strongly preferred. Must be flexible and willing to perform flow cytometric duties that expedite and support scientific staff's flow cytometric goals and objectives. Experience with cell sorting, tissue culture, cytometry staining, assay development, and data analysis is advantageous. Additionally, we need someone with analytical problem-solving experience. </p><p><strong>#regncyto</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 12:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Biostatistics - Genetic Medicine]]></title>
    <date><![CDATA[Mon, 06 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46282]]></requisitionid>
    <referencenumber><![CDATA[R46282]]></referencenumber>
    <apijobid><![CDATA[r46282]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46282/associate-director-biostatistics-genetic-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>This position is for a qualified statistician/biostatistician to support Clinical Biostatistics with Global Development. </p><p><strong>In this role, a typical day might include:</strong> ​</p><p>The incumbent will lead efforts of the Biostatistics department with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. The incumbent will represent statistical issues in regulatory agency meetings. The incumbent will lead the development and delivery of training to non-statistical colleagues, lead the development of new infrastructure and processes, and be active in representing the company in professional associations, conferences, and publications. As an Associate Director, the incumbent will be responsible for mentoring and overseeing less experienced statisticians, with the potential to manage full-time staff. </p><p><strong>This role might be for you if can:</strong> ​</p><ul><li><p>Represent Biostatistics at Global Clinical sub-teams. </p></li><li><p>Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.</p></li><li><p>Lead contributions to the preparation of material to be used in regulatory interactions, including drafting analysis plan and reviewing TFLs to be used in regulatory meetings, slides for advisory committee meetings, etc.</p></li><li><p>Lead and contributes to process improvement and technical working groups and sets timelines and expectations for the deliverables. Authors new/revised SOPs and contributes to cross-functional EPIC workstreams. </p></li><li><p>Evaluate appropriateness of available software for planned analyses and determines needs for use of novel statistical methodology or tools.</p></li><li><p>Prepare presentations and written reports to effectively communicate results to the project team, management, and regulatory agencies. Co-presents findings to management. </p></li><li><p>Is involved in research activities for innovative statistical methods and applications in clinical trial development as well as providing training to non-statisticians. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD or equivalent degree in statistics/biostatistics with >6 years of experience in the pharmaceutical industry OR MS degree in statistics/biostatistics with >11 years of experience</p></li><li><p>Preferred: Hematology, IO, non-oncology, Multiple Myeloma experience or similar Therapeutic Area.</p></li><li><p>Time to Event (TTE) experience.</p></li><li><p>Knowledge of drug discovery and development and ability to integrate statistical concepts into drug discovery and development strategies.</p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>Must be able to work productively in a fast-paced collaborative environment, with demonstrated critical thinking skills, time management skills, and effective communication skills.</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Expertise in statistical software</p></li></ul><p>#GDBDMJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 06 Apr 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Thoracic Oncology (GA, FL, TN, AL, MS)]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46555]]></requisitionid>
    <referencenumber><![CDATA[R46555]]></referencenumber>
    <apijobid><![CDATA[r46555]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46555/associate-director-field-medical-affairs-thoracic-oncology-ga-fl-tn-al-ms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director, Field Medical Affairs you will engage in scientific exchange and collaborate with Oncology disease experts and product information as well as research initiatives. We provide scientific and/or medical expertise by thoroughly understanding Oncology as a therapeutic area serving as a scientific/medical resource. We present scientific and clinical data and disease state awareness in response to requests for information to therapeutic area specialists, practitioners, investigators, research coordinators, site personnel and internal partners.</p><p><strong>Territory:</strong> GA, FL, TN, AL, MS ( with a preference of candidates residing in FL or Atlanta)</p><p><strong>A typical day may include the following</strong><br>• Identifies and maintains a list of relevant medical/therapeutic area professionals, investigator targets and associated plans of action.<br>• Participates in the development and management of clinical trials.<br>• Review of concept proposals and development of protocols<br>• Identifies and assists in selection of investigators and trial sites<br>• Supports site initiation and enrollment activities<br>• Acts as a resource for area healthcare professionals within the surrounding trial site community<br>• Collaborates with Clinical Development and other trial staff to implement plans and strategies. <br>• Establishing scientific relationship with investigators and Medical Affairs, supporting investigator-initiated study (IIS) concept program.<br>• Identifies gaps in research needs of company and creates opportunities by collaborating with potential and existing investigators and site personnel.<br>• Performs disease education with identified practitioners, payers and researchers.<br>• Attends medical conferences to collect and report relevant, scientific, clinical, & competitive intelligence<br>• Assists with management of clinical data to ensure rapid and accurate communication of scientific/clinical results supporting abstract, poster, presentation, and manuscript development.</p><p><strong>This may be for you if you:</strong><br>• Enjoy working independently in the field, while having an impact on the company’s mission.<br>• Are passionate about developing knowledge of and sharing clinical scientific data<br>• Like working corroboratively and developing relationships in academic and clinical practice settings<br>• Have the highly developed ability to balance and prioritize multiple initiatives and excel while implementing them independently</p><p>To be considered for this an advanced Clinical/Science Degree required (MD, PharmD, PhD) is required. A minimum of 5 years related work experience in Oncology as a Field Medical Affairs representative or Medical Science Liaison required. Residence must be within the assigned territory. </p><p>#msl #medicalscienceliaison</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 20:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Quality Compliance Specialist (Quality Risk Management)]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46551]]></requisitionid>
    <referencenumber><![CDATA[R46551]]></referencenumber>
    <apijobid><![CDATA[r46551]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46551/quality-compliance-specialist-quality-risk-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Quality Compliance Specialist (Quality Risk Management) position. This position is responsible for supporting Regeneron’s Internal Drug Product Manufacturing operations through the use of quality risk management (QRM). Job functions will primarily consist of the broad application of patient centered QRM across a full spectrum of processes vital to the operations. Specifically, the active facilitation of quality risk assessments, risk reviews and other quality risk-based programs supporting the Quality System (e.g., change control, deviation management, etc.). The person in this role will be consistently challenged with assignments, touching almost every phase of our process.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Providing technical expertise in quality risk management to a broad base of customers throughout the organization, including Quality Assurance, Quality Control, Manufacturing, Medical Device and Facilities</p></li><li><p>Facilitating data driven risk assessments and risk reviews using appropriate methodologies (e.g., FMEA, RBIA, REM and HACCP)</p></li><li><p>Partnering with Risk Assessment Owners to define scope, acceptance criteria, and evaluation scales</p></li><li><p>Guiding teams through risk identification, analysis, control/mitigation, and residual risk evaluation</p></li><li><p>Preparing and revising QRM documents</p></li><li><p>Developing and improving the quality risk management program</p></li><li><p>Contributing to contamination control strategy (CCS) and aseptic processing risk assessments for fill/finish operations; interface with EM, utilities, and equipment owners.</p></li><li><p>Preparing for and supporting regulatory, customer, and internal audits/inspections</p></li><li><p>Coaching colleagues on QRM principles and driving consistency in application</p></li><li><p>Tracking metrics (e.g., on-time risk reviews, cycle time) and identifying opportunities for continuous improvement.</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have excellent collaboration, influence, and communication skills</p></li><li><p>Are effective at facilitating cross-functional discussions</p></li><li><p>Proficient digital literacy in Microsoft (MS) Word, Excel and PowerPoint required. Experience with Veeva heavily preferred.</p></li><li><p>Have an understanding of QRM principles</p></li><li><p>Are able to interpret complex technical and systems information and make sound risk-based decisions.</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Biological Sciences, Chemistry, Biochemistry, Engineering or related field and at least 2 years of relevant experience. May substitute proven experience for education requirement.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$67,400.00 - $110,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Sourcing Specialist Global Procurement]]></title>
    <date><![CDATA[Wed, 08 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46412]]></requisitionid>
    <referencenumber><![CDATA[R46412]]></referencenumber>
    <apijobid><![CDATA[r46412]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46412/sr-sourcing-specialist-global-procurement/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking for a Sr Sourcing Specialist Global Procurement. In this role, you will be responsible for end-to-end management of assigned categories, including the category strategy development, category sourcing plan execution, and projects to optimize value. You will also support the planning and execution of strategic sourcing initiatives. This person will develop sourcing specifications, requirements and related scope of work, conducting data gathering, support spend analytics, assist in delivering measurable cost savings, and monitor savings against contracts.</p><p>In this role, a typical day may include the following:</p><p> Strive towards continuous vendor improvement and effectively manage relationships with key category vendors and business stakeholders.</p><p>· Develop and sustain vendor and customer relationships as well as assist in ensuring accountability exists within the managed category and performance is tracked.</p><p>· Align with stakeholders and business leaders on their needs and provide Project Management and support for multiple projects within budget and on time</p><p>· Responsible for continuous quality and service from suppliers to support efficient business operations</p><p>· Accountable for category spend savings targets and objectives</p><p>This role may be a fit for you if you:</p><p>· Are responsible for sound contract management and drive continuous value out of the contract</p><p>· Are accountable for contract agreements and addendums and ensure valid contracts are in place</p><p>Can lead category supplier relationships and sourcing opportunities, including RFPs, negotiations, etc.</p><p>To be considered for this role you must possess a Bachelor’s degree in a relevant field of study with at least 5 years of relevant experience. Pharmaceutical industry experience preferred. Will substitute relevant experience for education requirement.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 08 Apr 2026 12:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[SALES MANAGER – RESPIRATORY　※Chugoku and Shikoku area]]></title>
    <date><![CDATA[Sun, 19 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45705]]></requisitionid>
    <referencenumber><![CDATA[R45705]]></referencenumber>
    <apijobid><![CDATA[r45705]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45705/sales-manager-respiratory-chugoku-and-shikoku-area/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Location:</strong></p><p>You will be responsible for the Chugoku and Shikoku area.</p><p>Your residence is expected to be in Hiroshima or Okayama.(Hyogo or Osaka also available for consultation)</p><p><br>Are you ready to lead, inspire, and drive results in a dynamic commercial immunology team? At Regeneron, we are seeking a Sales Manager to co-create and embed a high-performance team culture aligned with our vision, values, and strategic direction. As a pivotal member of our team, you will manage a group of Sales Specialists within a designated region, coaching and performance-managing them to achieve commercial goals. This role offers the opportunity to make a meaningful impact while fostering growth and innovation in the pharmaceutical industry.</p><p><strong>A Typical Day:</strong><br>As Sales Manager, your day will be filled with exciting challenges and meaningful contributions. You can expect to:</p><ul><li><p>Lead and coach the Sales Specialist Team to deliver on commercial objectives.</p></li><li><p>Develop and implement regional and local account plans with clear tactical strategies.</p></li><li><p>Monitor key performance indicators to ensure targets are met, adjusting strategies as needed.</p></li><li><p>Manage budgets effectively to demonstrate return on investment across the region.</p></li><li><p>Foster productive working relationships with co-commercialization partners and key healthcare professionals (HCPs).</p></li><li><p>Ensure full adherence to industry codes of practice and company procedures.</p></li><li><p>Provide performance overviews to relevant business functions, supporting organizational success.</p></li><li><p>Identify and share best practices to enhance team performance and collaboration.</p></li></ul><p><strong>This Role May Be For You If:</strong><br>You thrive in a leadership role and possess the qualities to excel in this position. You:</p><ul><li><p>Have previous experience in 1st Line Management, preferably within the pharmaceutical industry.</p></li><li><p>Are passionate about coaching and developing teams to achieve their best.</p></li><li><p>Demonstrate strong commercial acumen and account management expertise.</p></li><li><p>Excel at strategic planning, prioritization, and execution to achieve goals.</p></li><li><p>Are skilled at networking, influencing, and building high-credibility relationships.</p></li><li><p>Have a proven ability to spot business opportunities and turn them into solutions.</p></li><li><p>Value collaboration and have experience working with cross-functional teams.</p></li><li><p>Are comfortable with frequent travel and adapting to diverse environments.</p></li></ul><p><strong>To Be Considered:</strong><br>Qualified candidates will hold a bachelor’s degree, preferably in life sciences, pharmacy, chemistry, or biology, and have at least 7 years of progressive industry experience. MR certification and a valid driver’s license are required. Proficiency in working with data, CRM systems, and tools like Excel and PowerPoint is essential. Preferred qualifications include therapy area knowledge in respiratory and ENT, biologics sales experience, and established relationships with key opinion leaders in these fields. Fluency in English is advantageous but not mandatory.</p><p>Join us in shaping the future of immunology, where your leadership will drive innovation and success. Apply today to become a part of Regeneron’s transformative journey!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 20 Apr 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Scientist, Genetics Medicine]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46823]]></requisitionid>
    <referencenumber><![CDATA[R46823]]></referencenumber>
    <apijobid><![CDATA[r46823]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46823/associate-director-clinical-scientist-genetics-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. Leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Associate Director reports to the RGM CDU Senior Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3><strong>As an Associate Director, a typical day may include:</strong></h3><ul><li><p>May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead Clinical Scientist</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; able to conceive and communicate strategy proposals well-grounded in supporting literature</p></li><li><p>Develops the Expanded Synopsis and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve; adjudicate and resolve cross functional comments with minimal support</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Leads planning and prepares information for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority); Presents data and information to external investigators (SIV) and internal collaborators</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Applies proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; Identifies risks and designs mitigation strategies</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across studies/programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies/program</p></li><li><p>May serve as a peer coach learning how to mentor and provides guidance to junior members of department and cross-functional team members as appropriate</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Ability to lead activities within a matrix environment; Exhibits confidence and professional diplomacy, while effectively relating to people at all levels internally and externally; Demonstrated ability to Influence within team and may influence across functionally</p></li><li><p>Demonstrates initiative, creativity and innovation skills. Directly or indirectly contributes to the development of innovations; Identifies opportunities for process improvements</p></li><li><p>Resolves novel problems requiring creative application of advanced skill, training, and education</p></li><li><p>Demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs</p></li><li><p>Strong cross-functional management, interpersonal and problem-solving skills</p></li><li><p>Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines</p></li><li><p>Proven track in clinical trial process improvements</p></li><li><p>Considerable organizational awareness, including substantial experience working cross-functionally</p></li></ul><p>To be considered, you must have a Bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc) and ≥ 10 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. Demonstrate proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrates solid medical writing skills.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 13:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists - Hematology - Minnesota]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46705]]></requisitionid>
    <referencenumber><![CDATA[R46705]]></referencenumber>
    <apijobid><![CDATA[r46705]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46705/medical-account-specialists-hematology-minnesota/]]></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>The Hematology Oncology Account Specialist, is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><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 R/R Multiple Myeloma, to grow brand share and revenue and to deliver product goals.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 11:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Scientist - AAV (CDMS) - Analytical and Biological Mass Spectrometry (ABMS)]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46347]]></requisitionid>
    <referencenumber><![CDATA[R46347]]></referencenumber>
    <apijobid><![CDATA[r46347]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46347/senior-scientist-aav-cdms-analytical-and-biological-mass-spectrometry-abms/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Pharmaceutical's Analytical and Biological Mass Spectrometry Group (ABMS), located in Tarrytown, NY, is seeking a highly motivated Sr. Scientist. In this role, you will work in an innovative mass spectrometry (MS) lab and develop LC-MS methods for characterizing biotherapeutic products to support all stages of drug development, from early-stage candidate selections to late-stage regulatory submissions. You will conduct and develop innovative technologies to support a diverse Regeneron's R&D pipeline. </p><p><strong>A Typical Day in the Role Might Look Like:</strong> </p><ul><li><p>Design, execute, and clearly communicate analytical characterization for biotherapeutics, including adeno-associated virus (AAV), monoclonal and bispecific antibodies, Fc-fusion proteins, and other modalities, to support drug development. </p></li></ul><ul><li><p>Lead and execute characterization activities to evaluate and elucidate critical quality attributes such as charge variants, size variants, and post-translational modifications, with an emphasis on charge detection mass spectrometry (CDMS) and related native-MS approaches. </p></li></ul><ul><li><p>Provide analytical support for cross-functional teams, including formulation development, upstream/downstream process development, and manufacturing to solve drug development challenges. </p></li></ul><ul><li><p>Proactively advance LC-MS characterization of biotherapeutics by developing innovative techniques that address evolving developmental needs and improve operational efficiency. </p></li></ul><ul><li><p>Independently conduct sample preparation and LC-MS analyses in compliance with SOPs, and document experimental procedures and results in electronic laboratory notebook (ELN). </p></li></ul><ul><li><p>Author and review regulatory submission documents, including IND, comparability, and BLA reports, and contribute to manuscripts for peer-reviewed publications. </p></li></ul><ul><li><p>Represent analytical development on project teams, provide subject matter expertise, and communicate results at internal and external meetings.<strong> </strong> </p></li></ul><p><strong>This Role Might Be For You If You:</strong> </p><ul><li><p>You thrive in a fast-paced, collaborative environment and consistently deliver results with efficiency and ownership. </p></li></ul><ul><li><p>You quickly learn new technologies, tackle complex problems, and have a passion for science. </p></li></ul><ul><li><p>You are self-motivated and proactive, prioritizing effectively, and driving work forward with minimal supervision. </p></li></ul><p><strong>To be considered for this role, you must have</strong> a BS (10+ years), MS (7+ years) or PhD degree (0-3+ years) in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related field. Experience with charge detection mass spectrometry (CDMS) is strongly preferred. Experience applying LC-MS to extended characterization of AAV and monoclonal antibodies to support product and process development is a plus. Extensive experience with advanced mass spectrometers (Q Exactive Plus, Q Exactive UHMR, Q-TOF, etc.), liquid chromatography, and data processing software (Protein Metrics, Skyline, UniDec etc.) is desired. Experience with experimental design and data analysis (e.g., molecular modeling, graphing, and statistical analysis) is a plus. 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><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 14:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Flow Cytometry]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45522]]></requisitionid>
    <referencenumber><![CDATA[R45522]]></referencenumber>
    <apijobid><![CDATA[r45522]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45522/associate-scientist-flow-cytometry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated Associate Scientist – Flow Cytometry to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as data analysis using various flow cytometric software programs.</p><p><strong>As a Associate Scientist – Flow Cytometry, A Typical Day Might Include:</strong></p><ul><li><p>Ensuring proper maintenance, alignment, and calibration of cell sorting equipment</p></li><li><p>Analyzing flow cytometric data</p></li><li><p>Maintaining and organizing schedules for cell sorting equipment</p></li><li><p>Maintaining adequate inventory of flow cytometry supplies and reagents</p></li><li><p>Supporting maintenance of flow cytometry equipment, such as LSRFortessa X-20, FACSymphony A3/A5, FACSDiscovery A8, Aurora, CytoFLEX (LX), IntelliCyt iOue, and Amnis ImageStreamX MkII cytometers</p></li><li><p>Operating a Sony MA900, FACSFusion, FACSymphony S6, and FACSDiscovery S8 high-speed cell sorters</p></li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li><p>You are able to critically analyze and troubleshoot scientific problems</p></li><li><p>You have a customer-centric viewpoint</p></li><li><p>You have good scientific initiative and ability to multi-task, prioritize work and balance multiple projects</p></li><li><p>You can work independently but also within a collaborative team environment and have flexibility to work on changing priorities</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS in a scientific field and 1-3 years of relevant experience using cytometric instrumentation. Experimental laboratory work and cytometry sorting is strongly preferred. Must be flexible and willing to perform flow cytometric duties that expedite and support scientific staff's flow cytometric goals and objectives. Experiences with cell sorting, tissue culture, cytometry staining, assay development, and data analysis is advantageous. Additionally, we need someone with analytical problem-solving experience. </p><p><strong>#regncyto</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:26:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Study Lead]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47254]]></requisitionid>
    <referencenumber><![CDATA[R47254]]></referencenumber>
    <apijobid><![CDATA[r47254]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47254/manager-clinical-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Clinical Study Lead (CSL) 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. The CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies 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>As a Manager, Clinical Study Lead, a typical day may include the following:</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 escalating 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>Oversees study drug and clinical supplies forecasting, drug accountability, and reconciliation.</p></li><li><p>Oversees data quality, including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Ensures audit and inspection readiness throughout the study; supports internal audits and external inspections and contributes to CAPAs as required</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><li><p>May require up to 25% travel</p></li></ul><p>This role may be for you if:</p><ul><li><p>Demonstrated interpersonal & leadership skills</p></li><li><p>Ability to understand and implement the operational strategic direction and guidance for respective clinical studies</p></li><li><p>A data driven approach to planning, executing, and problem solving</p></li><li><p>Effective communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across key stakeholders</p></li></ul><p>To be considered for this role, candidates must hold a Bachelor’s degree and have at least six years of relevant industry experience. We seek extensive budget management expertise; a proven ability to build productive study teams and collaborations; and demonstrated vendor management experience. 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. The role also requires 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><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Allergy/ENT-Las Vegas]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47199]]></requisitionid>
    <referencenumber><![CDATA[R47199]]></referencenumber>
    <apijobid><![CDATA[r47199]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47199/medical-specialist-i-allergyent-las-vegas/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Las Vegas]]></city>
    <state><![CDATA[Nevada]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Las Vegas (Allergy/ENT)</strong></p><p>Key Markets include Las Vegas, Henderson, Reno, Sparks, Carson City</p><p>Our Medical Specialists are at the forefront of engaging Allergists, Immunologists, and ENTs 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 act. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, result-oriented, customer-focused team if you are up for the challenge.</p><p> As an Allergy/ENT Medical Specialist, a typical day might include the following:</p><ul><li><p>Developing strategy and executing tactics within key accounts in our Allergy/Immunology/ENT therapeutic areas to generate product utilization</p></li><li><p>Establishing and fostering strong working relationships with Allergy/Immunology/ENT 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>This role may be for you if:</p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease states, treatment options and healthcare trends</p></li><li><p>You can effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a bachelor’s degree. A master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years’ pharmaceutical sales experience. Having a minimum of 2 years’ sales in the Immunology or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role. Allergy/Immunology/ENT experience preferred. We need someone with demonstrated success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Associate Scientist - Bioanalytical & Biomarker Technologies]]></title>
    <date><![CDATA[Fri, 01 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47134]]></requisitionid>
    <referencenumber><![CDATA[R47134]]></referencenumber>
    <apijobid><![CDATA[r47134]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47134/senior-associate-scientist-bioanalytical-biomarker-technologies/]]></url>
    <company><![CDATA[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 dynamic <strong>senior associate scientist</strong> to join bioanalytical & biomarker technologies group. The candidate will design and execute analytical and bioanalytical method to support biotherapeutics discovery and preclinical development. The individual should be experienced in executing HPLC and/or LC-MS based methods from sample preparation, instrument operation to data analysis. The successful candidate will be expected to work cross-functionally in a collaborative, fast-paced, multidisciplinary team environment and have the opportunity to explore new technologies while growing technical depth.</p><p><strong>A Typical day in this role looks like:</strong></p><div><ul><li>Design, execute, and troubleshoot LC‑MS and HPLC methods for analytical characterization of bioconjugates and bioanalytical quantification of therapeutics.</li><li>Support a range of modalities—including monoclonal antibodies (mAbs), antibody–drug conjugates (ADCs), siRNA/oligonucleotides, and endogenous biomarkers—across diverse biological matrices.</li><li>Perform end‑to‑end sample preparation (e.g., LLE, SPE, affinity capture, enzymatic digestion, homogenization) and operate LC‑MS/MS workflows from instrument setup to data analysis.</li><li>Analyze and interpret results; summarize findings, propose next steps, and present data at internal meetings.</li><li>Document experiments, methods, and results in electronic lab notebooks (ELNs) with clarity and rigor; contribute to SOPs and method documentation.</li><li>Maintain instruments and general lab readiness; troubleshoot systems and ensure data integrity and instrument uptime.</li><li>Evaluate and implement new platforms, workflows, and automation to improve throughput, sensitivity, and robustness.</li><li>Prioritize effectively across multiple projects and timelines, collaborating closely with colleagues in discovery biology, DMPK/PK‑PD, and process/analytical teams.</li></ul></div><p><strong>This role may be for you, if you have experience: </strong></p><ul><li>BS or MS degree in Chemistry, Biochemistry, Pharmaceutical Science or a related discipline with 3+ years hand-on experience.</li><li>Experience in liquid chromatography and/or mass spectrometry is preferred, with the ability to execute, qualify and optimize analytical methods.</li><li>Hands on experience in sample preparation techniques (LLE, SPE, affinity capture, enzymatic digestion, homogenization, etc.); experience with automation platforms is a plus.</li><li>Detail-oriented, good interpersonal and effective technical communication skills (written and verbal).</li><li>Ability to manage multiple projects in a fast-paced environment.</li><li>Collaborative team player with a growth mindset to quickly adapt to evolving priorities and continuously learn to embrace new challenges.</li><li>Previous exposure in bioanalysis of LC-MS based small molecule, oligonucleotides, biomarkers and biotherapeutics assay development is beneficial.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$80,300.00 - $131,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 01 May 2026 14:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Automation Integration Engineer]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47031]]></requisitionid>
    <referencenumber><![CDATA[R47031]]></referencenumber>
    <apijobid><![CDATA[r47031]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47031/principal-automation-integration-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly skilled, experienced software Integration Engineer with experience in real-time data collection and analysis to join a diverse team of engineers, developers, analysts, and administrators to design, implement and support Data Acquisition and Analysis Systems. </p><p>As a Principal Automation Systems Integration Engineer<strong>,</strong> a typical day might include the following: </p><ul><li><p>Designing, developing, and implementing software/hardware improvements to existing automated equipment and new equipment according to change control procedures. </p></li></ul><ul><li><p>Performing troubleshooting and investigations relating to manufacturing deviations and anomalies associated with automated control systems. </p></li></ul><ul><li><p>Developing and editing engineering design documents, technical evaluations, and test plans for cGMP process equipment while following GAMP 5 guidelines. </p></li></ul><ul><li><p>Supporting small manufacturing, engineering, and validation projects. </p></li></ul><ul><li><p>Providing support to process control and process monitoring equipment software design, commissioning, testing, and corrective action. </p></li></ul><ul><li><p>Authoring or updating system specifications, user and functional requirements specifications, generating and executing vital Factory Acceptance Tests (FAT) and (Site Acceptance Testing) SAT protocols. </p></li></ul><ul><li><p>Reviewing cyber security vulnerabilities and risk pertaining to automation systems, software, and infrastructure </p></li></ul><ul><li><p>Creation, modification, and maintenance of automation system documentation </p></li></ul><p>This role might be for you if you: </p><ul><li><p>Have experience with OT applications, including SCADAs, HMIs, Historians, etc. </p></li></ul><ul><li><p>Are familiar with standing up large systems at the enterprise level </p></li></ul><ul><li><p>Have core knowledge related to ISE S95 and S88 principles and IT/Automation integration </p></li></ul><ul><li><p>Have familiarity with PLC communication, HMIs, computerized system design and maintenance of automation process control infrastructure </p></li></ul><ul><li><p>Want to challenge the status-quo and champion an environment where continuous improvement is not just metrics - it's a mentality for everyone, every day, to do better </p></li></ul><ul><li><p>Enjoy project-oriented work with a career goal of being regarded as an expert in keeping a biopharmaceutical process running smoothly </p></li></ul><ul><li><p>Can balance changing priorities with increasing workload by making/communicating timely decisions </p></li></ul><p>To be considered for this position you ideally should have a bachelor's degree in Computer Science, Chemical, Mechanical, or Electrical Engineering and the following minimum years of relevant experience for each level: </p><ul><li><p>Senior Engineer: 5+ years </p></li></ul><ul><li><p>Principal Engineer: 8+ years</p></li></ul><p>Level will be determined based on qualifications relevant to the role</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 16:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior IT Applications Analyst - Labware]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45599]]></requisitionid>
    <referencenumber><![CDATA[R45599]]></referencenumber>
    <apijobid><![CDATA[r45599]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45599/senior-it-applications-analyst-labware/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior IT Applications Analyst is responsible for the configuration, implementation, maintenance, and ongoing support of various IT applications and systems. This role will be primarily focused on performing System Administration, Application troubleshooting, solution design and implementation, and ensuring adherence to compliant processes with some software development opportunities as projects arise.</p><p>As a Senior IT Applications Analyst, a typical day might include the following:</p><ul><li>Develop software and enterprise system solutions by studying information needs, analyzing user requirements, assessing impact and integration with existing information flow between Systems, following the Regeneron software development lifecycle (SDLC).</li><li>Coordinates across business departments and stakeholders, gathering, and implementing requirements and enhancement requests for various applications.</li><li>Responsible for IT Applications documentation, including, converting User Requirement Specifications to a Detail Design Specification, Configuration Test Plans, and Summary Reports.</li><li>Perform design, code, and architecture reviews, processes IT Applications change control requests.</li><li>Providing end-user support for IT Applications including troubleshooting problems at the application, server, and infrastructure level.</li><li>Coordinates with other IT Application team members to administer and support production systems in an efficient and compliant manner.</li><li>Participates or may lead IT Applications systems security access and periodic audit trail reviews.</li><li>Performs recurring system administrative tasks and assists with the maintenance of existing AWS infrastructure.</li><li>Monitoring of development and production service issues to assist support teams.</li><li>Writes and executes queries against large-scale enterprise-level databases.</li><li>Configures reports (tabular, trend, and labels).</li></ul><p>This role may be for you if you have:</p><ul><li>Enjoy both collaborating with a team as well as working independently to develop solutions to complex problems.</li><li>Enjoy driving a creative mindset and collaborating to design, implement, and modify code or configuration, or discover ways to simplify business processes.</li><li>Exhibit a degree of ingenuity, creativity, and resourcefulness in an evolving and sometimes ambiguous environment.</li><li>Have strong analytical and organizational skills, as well as excellent written and verbal communication skills.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and</p><ul><li>Senior 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><li>Certificates in LabWare Configuration Using LIMS Basic and/or LabWare ELN V4: Experiments, Templates and Configuration highly preferred</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp Manager Payroll]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44748]]></requisitionid>
    <referencenumber><![CDATA[R44748]]></referencenumber>
    <apijobid><![CDATA[r44748]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44748/temp-manager-payroll/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role, you will report to the Payroll Manager. The Manager will be responsible for supporting the Payroll Manager and the wider team with all day‑to‑day activities involved in delivering the end‑to‑end payroll process.</p><p>This is a 18-month temporary contract.</p><p><strong>A typical day might include, but is not limited to, the following:</strong></p><ul><li><div>Conducting payroll audits and reviews prior to Associate Director Approval</div></li><li>Working with accounting to ensure all payroll data required for month end is provided in a timely and accurate manner</li><li>Preparing and/or reviews and inputs all administrative payroll data changes to records for processing of our bi- weekly and monthly payroll</li><li>Working with other departments such as Comp & Bens and HRPB’s to ensure payroll data is correct and processed accordingly</li><li>Reconciling each payroll, reviews all entries and forwards for approval</li><li>Ensuring all tax information, reconciliations and payments</li><li>Managing the internal inbox with responsibility for responding to employees’ queries </li><li>Assisting with audit queries related to payroll</li><li>Performing other duties or projects as assigned by management<br> </li></ul><p><strong>This role may be for you:</strong></p><ul><li>You thrive in a fast-paced, deadline-driven environment and can juggle multiple priorities</li><li>You communicate clearly and effectively with internal teams and external partners</li><li>You are comfortable working hands-on while providing strategic oversight</li><li>You have strong analytical skills and a keen eye for detail</li></ul><p><br>To be considered this opportunity you should a bachelor’s degree in accounting, finance, or business as well as 6/7 years of experience. Advanced Excel skills (including pivot tables, formulas, and lookups), experience with Workday, Oracle or Core is strongly preferred have a payroll experience, including having worked as a payroll manager with direct people management responsibilities.</p><p>Education and Experience:</p><ul><li>Associate Manager: Minimun 6 years of experience</li><li>Manager: Minimun 7 years of experience</li></ul><p>#LI-Onsite #IREADV #JOBSIEPR</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 09:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist Immunology - Montreal North/West]]></title>
    <date><![CDATA[Sat, 09 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47397]]></requisitionid>
    <referencenumber><![CDATA[R47397]]></referencenumber>
    <apijobid><![CDATA[r47397]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47397/sales-specialist-immunology-montreal-northwest/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></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>As a Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, while covering<strong> Montreal North/West</strong> territory. You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>As a Pharmaceutical Representative, a typical day might include the following:</strong></p><ul><li>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and optimally implementing sales & marketing plan.</li><li>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</li><li>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</li><li>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</li><li>Leverage all communication channels including digital channels, in collaboration with other functions, to achieve the best possible share of voice in the market.</li><li>Report results and developments proactively and clearly to the Immunology leadership team</li></ul><p><strong>This role might be for you if:</strong></p><ul><li>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</li><li>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</li><li>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</li><li>You can operate effectively in a “start-up” model as this is a completely new team.</li></ul><p>To be considered for this opportunity you must hold a Bachelor’s Degree with minimum 5+ years of pharmaceutical sales experience including 1-2 years specialty biologic experience, <strong>preferably GI, ENT and/or Allergy</strong>. You are happy with regular travel and have a valid driver's license. French & English language is required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sat, 09 May 2026 11:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47243]]></requisitionid>
    <referencenumber><![CDATA[R47243]]></referencenumber>
    <apijobid><![CDATA[r47243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47243/senior-manager-field-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron Japan, we are expanding our Field Medical Affairs team to bring innovative solutions in oncology and hematology oncology to the forefront. As a Senior Manager, Field Medical Affairs, you will play a pivotal role in advancing scientific exchange, collaborating with therapeutic area experts, and supporting clinical development initiatives. Join us in shaping the future of healthcare while contributing to meaningful, impactful work in a dynamic and collaborative environment.</p><p><strong>A Typical Day:</strong><br>As part of your role, you will:</p><ul><li><p>Identify and maintain relationships with medical and therapeutic area experts, investigators, and other stakeholders.</p></li><li><p>Respond to scientific and clinical inquiries in compliance with industry regulations.</p></li><li><p>Perform disease management and therapeutic area education for practitioners, payers, and researchers.</p></li><li><p>Attend medical conferences to gather and report scientific, clinical, and competitive intelligence.</p></li><li><p>Collaborate with investigators and internal medical affairs teams to support investigator-initiated studies (IIS).</p></li><li><p>Assist in the development and communication of clinical data through abstracts, posters, presentations, and manuscripts.</p></li><li><p>Support site initiation and enrollment activities for clinical trials.</p></li><li><p>Ensure adherence to company policies, procedures, and compliance standards.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You are passionate about oncology and have deep knowledge in lung cancer, solid tumors, or hematology oncology.</p></li><li><p>You thrive in a collaborative, matrix organization and enjoy building relationships in academic and clinical practice settings.</p></li><li><p>You have excellent communication skills and are fluent in both Japanese and English.</p></li><li><p>You are experienced in immuno-oncology and clinical trials, and possess a strong commitment to compliance.</p></li><li><p>You are comfortable traveling 30–50% of the time to engage with stakeholders and attend conferences.</p></li></ul><p><strong>To Be Considered:</strong><br>We’re looking for healthcare or scientific professionals with:</p><ul><li><p>A PhD, PharmD, or MD preferred, though a Master’s Degree with extensive oncology experience may be considered.</p></li><li><p>At least 6 years of relevant experience in pharmaceutical industry or clinical settings, such as drug information or disease management programs.</p></li><li><p>Proven expertise in oncology, particularly lung cancer, solid tumors, or hematology oncology.</p></li><li><p>Immuno-oncology experience is preferred.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 02:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer III, Operational Technology (OT) Data]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46099]]></requisitionid>
    <referencenumber><![CDATA[R46099]]></referencenumber>
    <apijobid><![CDATA[r46099]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46099/process-development-engineer-iii-operational-technology-ot-data/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Data Enablement and Analytics (DEA) team drives the future of digitalization within the Product, Analytics and Process Development (PAPD) organization. By making data usable, useful, and impactful DEA accelerates process development, supporting Regeneron’s mission to use the power of science to bring new medicines to patients over and over again.</p><p>In this role, you will drive the design, evolution, and governance of Operational Technology (OT) data systems, platforms, and tools that deliver high-quality data to lab specialists for real-time decision-making and offline analysis. You’ll implement value-focused data management solutions that increase asset value, meet immediate business needs, and build scalable data capabilities for the future.</p><h3>Responsibilities:</h3><ul><li>Provide technical leadership for OT data platforms by defining architecture principles, reference designs, and best practices that improve reliability, availability, and usability for manufacturing process development teams.</li><li>Ensure OT data availability, integrity, quality, security and accessibility by establishing and enforcing standards, controls, and audits that reduce incidents and outages.</li><li>Coach and mentor distributed data managers and junior engineers; set technical direction, review designs, and drive consistent execution against objectives and key results (OKRs).</li><li>Partner with lab specialists and IT to integrate process control and data acquisition systems into a unified architecture to advance data analytics capabilities and digital maturity.</li><li>Lead IT/OT convergence initiatives to align cybersecurity posture, compliance requirements, and network segmentation.</li><li>Communicate progress and decisions to stakeholders and leadership—create clear technical narratives, roadmaps, and status updates that enable informed decisions.</li></ul><h3>What A Typical Day in the Role Might Look Like:</h3><ul><li>Continuous Improvement: Translate user requests into prioritized backlog items; run grooming and planning sessions to deliver high-impact features.</li><li>Project Management: Design, lead, and implement cross-functional DEA programs (agile and waterfall); coach junior resources, unblock teams, ensure delivery against commitments.</li><li>Administration: Standardize and automate equipment onboarding; systematize access management with role-based controls; delegate routine tasks while instituting guardrails.</li><li>Support & Maintenance: Perform software updates and patching. Proactively monitor system health issues. Drive incident triage and root-cause remediation.</li><li>Knowledge Sharing: Serve as OT subject matter expert to PAPD and partner functions; lead evaluations of new applications and platforms; present proof-of-concept outcomes with clear recommendations.</li></ul><h3>This Role May Be for You If:</h3><ul><li>You are a champion for data-driven decision making and can articulate trade-offs across performance, security, compliance, and cost.</li><li>You uphold high standards for accuracy, quality and attention to detail.</li><li>You balance near-term delivery with long-term platform health, managing technical debt deliberately.</li><li>You enjoy mentoring, growing talent, and building repeatable processes that elevate team capabilities and outcomes.</li><li>You thrive in cross-functional environments—communicating clearly with technical and non-technical partners, and translating complex requirements into secure, scalable, maintainable data solutions.</li></ul><br><p>This role requires BS in Computer Science, Information Systems, Biomedical/Chemical/Electrical Engineering, or related field with 10+ years of proven experience, or MS with 7+ years or a PhD with 0-3 years. Preferably, with 5+ years with AVEVA PI System (Data Archive, Asset Framework) and Ignition SCADA, including high-availability design, data modeling, and integrations. Other preferred experience: SQL experience in a database owner role, demonstrated proficiency in design, deployment, and lifecycle management of OT data systems across high-availability industrial architectures, and familiarity with control systems architecture, industry standards and communication protocols (ISA-95, S88, OPC, MQTT). A working knowledge of continuous and batch manufacturing processes, associated data sources, software integration, consumption and data analytics tools and a foundational knowledge of lab-based automation software (e.g. Unicorn, Biobrain Supervise, FactoryTalk, Empower) is a plus. Growing proficiency in Python for automation, data pipelines, and tooling. Familiarity with the concepts of Industry 4.0, digitalization, and IT systems that drive IT/OT convergence</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-southern California/Arizona- (Neurology)]]></title>
    <date><![CDATA[Sat, 09 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46424]]></requisitionid>
    <referencenumber><![CDATA[R46424]]></referencenumber>
    <apijobid><![CDATA[r46424]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46424/associate-director-field-medical-affairs-southern-californiaarizona-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>As an Associate Director, Field Medical Affairs (Medical Science Liaison) responsibilities include engaging 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. You will be considered a scientific and clinical expert on our current and future Neurology assets. </p><p>Territory: Los Angeles; Southern CA, AZ, CO, NM, UT, HI</p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Establish, foster, cultivate and maintain peer relationships with KOLs in Neurology </p></li><li><p>Act as a primary clinical/scientific resource to HCPs for information pertaining to disease state and our products to ensure awareness and understanding. </p></li><li><p>Identifies and maintains a list of relevant medical/therapeutic area experts, investigators and develop engagement plans. </p></li><li><p>Support evidence generation (company sponsored trials and investigator-initiated studies) research initiatives. </p></li><li><p>Identify and report medical insights. </p></li><li><p>Identifies gaps in research and educational needs to inform medical strategy. </p></li><li><p>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. </p></li><li><p>Performs disease management and therapeutic area education with identified practitioners, payers and researchers. </p></li><li><p>Attends conferences to collect and report relevant, scientific, clinical, & competitive intelligence. </p></li><li><p>Ensures company policies, procedures, principles and financial controls are maintained with integrity and professionalism is displayed internally and externally. </p></li></ul><p>To be considered 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. Experience as a Neurology MSL or in Neurology is preferred. Demonstrated experience communicating complex data sets and the ability to be seen as a scientific peer while educating top KOLs is required. Established relationships with KOLs in neuromuscular centers is preferred, as is product launch experience. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines are required. Capable of frequent business travel (approximately 70% of time), including air travel, ability to travel overnight and occasionally on weekends</p><p>#msl #medicalscienceliaison</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 10 May 2026 19:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager,   GCP Quality Management- Global Development]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44852]]></requisitionid>
    <referencenumber><![CDATA[R44852]]></referencenumber>
    <apijobid><![CDATA[r44852]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44852/senior-manager-gcp-quality-management-global-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Global Development Quality Management (GCP) acting as a Quality Management Lead (QML) is a key position that will provide guidance and leadership for all aspects of quality and compliance within Global Development Quality (GDQ) systems. The GDQM (GCP) QML will engage with key stakeholders, build strategic partnerships working and liaising with study teams, relevant functions and other GDQ functions to lead risk-based quality management activities on all Regeneron-sponsored clinical trials, inclusive of issue management and providing continuous support of inspection readiness.</p><p>For US locations (Armonk, NY or Warren, NJ), this role is on-site 4 days in the office and 1 day from home. For Uxbridge, UK or Dublin, Ireland this role would be on-site 3 days per week and 2 days from home. A fully remote role is not possible for this position.</p><p><strong>A day in the life may look like:</strong></p><p>• Acting as a Subject Matter Expert (SME) and key liaison to GDQ to provide support and advise on any quality issues to ensure compliance and for the Quality Risk Assessment process.<br>• Ensuring and responsible for Risk-Based Quality Management (RBQM) initiatives and process improvements, in partnership with other functional areas.<br>• Responsible for the management of GCP-compliant activities from a quality perspective in conjunction with the business and the GDQM (GCP) team.<br>• Providing day-to-day quality and compliance support to cross-functional stakeholders, including issue management (triage/investigation/actions), audit responses, proactive quality management, Corrective Action/Preventive Action (CAPA) oversight, audit/issue trending.<br>• Engaging with, supporting, and liaising with multiple cross-functional stakeholders whose work impacts the GDQ system.<br>• Leading Quality Risk Assessment and Control Tracker (QRACT) activities at the time of Protocol development predicated on ICHGCP.</p><p><strong>This may be the right role for you if you have experience:</strong></p><p><strong>•</strong> Bachelor's degree with a minimum of 8 years of relevant healthcare/pharmaceutical industry experience.<br>• Experience working in either a quality/compliance role (e.g., Quality Management, Quality Assurance etc.), or in a Clinical Development role with expertise and/or transferable skills related to Good Clinical Practice (GCP), and/or Good Pharmacovigilance Practice (GVP).<br>• Providing consultation, mentorship, training, and support in respect to compliance with applicable international regulations, practices, and guidelines.<br>• Advising on the escalation of any quality issues that potentially represent serious non-compliances (or serious breach) via the issue escalation process.<br>• Supporting the collection and reporting of data (e.g., metrics).<br>• Contributing to and supporting process improvement initiatives and workgroups, as assigned.<br>• Exemplifying a quality mindset and behaviors in all interactions with internal and external colleagues, serving as an ambassador for GDQ.<br><br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 08:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[IT Product Manager – HCM & ERP (Japan)]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R39293]]></requisitionid>
    <referencenumber><![CDATA[R39293]]></referencenumber>
    <apijobid><![CDATA[r39293]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r39293/it-product-manager-hcm-erp-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>Location:</strong> Tokyo, Japan</p><p><br><strong>About the Role</strong><br>We are Regeneron, a global leader in biotechnology, dedicated to transforming lives through innovation. We are seeking an experienced IT Product Manager to join our dynamic General & Administrative IT team in Tokyo, Japan. This pivotal role focuses on supporting and enhancing our global Human Capital Management (HCM) systems and Enterprise Resource Planning (ERP) systems. As part of our team, you will collaborate with global and regional stakeholders to deliver innovative solutions that drive seamless integration and continuous improvement across technology platforms.</p><p>This is your opportunity to contribute to impactful projects, ensure efficient delivery processes, and make a meaningful difference in how technology supports our business goals.</p><p><strong>A Typical Day:</strong></p><ul><li>Act as the functional subject matter expert for Workday HCM and/or Oracle ERP systems, including modules such as Time and Absence, Finance, Compensation, and Procurement.</li><li>Collaborate with business partners to gather, document, and refine requirements that effectively address business processes and capabilities.</li><li>Lead project delivery for the Japan team, ensuring timely updates to global project managers and tracking risks and issues.</li><li>Oversee the full delivery lifecycle, from solution design and build oversight to quality assurance, testing, go-live, and post-production support.</li><li>Manage software/service contracts and vendor relationships, ensuring compliance with best practices and standards.</li><li>Troubleshoot and resolve post go-live issues with delivery teams, applying critical thinking under pressure.</li><li>Build and maintain strong relationships with Japan-based business stakeholders and global IT teams.</li><li>Translate technical concepts into practical business terms for diverse audiences, fostering collaboration and mutual understanding.</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You have 6+ years of proven experience as a technical lead or systems analyst, specializing in HCM or ERP systems.</li><li>You possess hands-on expertise in Workday HCM modules (e.g., Core HCM, Compensation, Time and Absence) or Oracle ERP (e.g., Finance, OTC, Procurement).</li><li>You are skilled in facilitating requirements traceability during testing phases such as SIT and UAT.</li><li>You thrive in fast-paced environments, managing multiple high-priority tasks with a “get-it-done” attitude.</li><li>You excel in both independent work and cross-functional team collaborations, leveraging an agile mindset to drive efficient use of technology.</li><li>You are well-organized, with the ability to prioritize tasks and deliver high-quality solutions on time.</li><li>You possess strong business-level English communication skills (written and spoken).</li></ul><p><strong>To Be Considered:</strong><br>Candidates must hold a Bachelor’s Degree in Computer Science, Information Systems, Business, or a related field. Certifications in cloud technology applications such as Workday or Oracle are advantageous. Experience with Jira, ServiceNow, or other cloud-based service management applications is a plus.</p><p>Join us in Tokyo and be part of a team that values innovation, collaboration, and the transformative power of technology. Apply now to make an impact with Regeneron!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 05:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Project Engineer]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47175]]></requisitionid>
    <referencenumber><![CDATA[R47175]]></referencenumber>
    <apijobid><![CDATA[r47175]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47175/senior-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an experienced Engineer to join our growing Project Engineering team. Our team designs, specifies and commissions new and renovated biopharmaceutical process and clean utility equipment. We provide engineering support and lead deviation investigations for existing equipment and manufacturing processes to support the production of our life-changing medications.</p><p>As a Senior Project Engineer, a typical day might include the following:</p><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls including development and review of engineering documentation</li><li>Managing mid-to-large sized projects related to process equipment and clean utilities including start-up and commissioning</li><li>Leading the design review, site acceptance and installation of equipment</li><li>Preparing piping and instrumentation diagrams and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting QA/Validation department by preparing design documents and assisting in protocol execution</li><li>Assisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations and test plans for executing modification change control documentation</li><li>Supervising mechanical, electrical, and automation and engineering contractors</li><li>Traveling up to 10% of the time, both domestically and internationally</li></ul><p>This position might be for you if you:</p><ul><li><p>Are interested in having a broad scope with a variety of tasks, seeing the entire process, not just specific equipment or processes</p></li><li>Enjoy solving puzzles and challenges, supporting investigations across the business</li><li>Have a desire to contribute to elements of design work by helping to specify and translating customer needs into equipment</li><li>Want to do more than just project management or troubleshooting, balancing your technical and project management skills</li><li>Have a solid understanding of process control systems and automation</li><li>Are skilled at planning and tracking project activities and schedules</li><li>Are thoroughly knowledgeable with engineering documentation required for cGMP process equipment as well as sanitary equipment design requirements</li><li>Have working knowledge of biopharmaceutical equipment</li><li>Have demonstrated strengths with strong interpersonal, cross-cultural communication</li><li>Are adept at building and maintaining relationships and leading without direct authority</li><li>Show resiliency and flexibility in the face of challenging situations</li></ul><p>Qualified candidates must have a Bachelor's degree Chemical Engineering or Biochemical Engineering (or another relevant Engineering discipline) and the following minimum years of experience in project/process engineering or an equivalent combination of education and experience. Direct experience with biopharmaceutical process equipment is preferred.</p><ul><li>Senior Project Engineer: 5+ years</li><li>Principal Project Engineer: 8+ years</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr. Manager QA Drug Product (Filling)]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46662]]></requisitionid>
    <referencenumber><![CDATA[R46662]]></referencenumber>
    <apijobid><![CDATA[r46662]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46662/sr-manager-qa-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[<p>Regeneron is currently seeking a Sr Manager Quality Assurance 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>As a Sr. Manager QA, a typical day might include the following:</p><ul><li>Provide leadership to multiple teams under your supervision, including being responsible for</li><li>Quality oversight of all equipment prep, formulation, and filling (multiple lines)</li><li>Responsible for programs that support the department, for example: area walkthroughs</li><li>Support development and growth of team, including your people leaders</li><li>Leadership point of contact for escalation of events, process updates, etc.</li></ul><p>This role might be for you if you have:</p><ul><li>Proven leadership in cGMP environments, including experience speaking and preparing for regulatory inspections and audits.</li><li>Strong collaboration and communication cross-functionally</li><li>Ability to think critically, and continuously improve processes</li><li>Ability to lead a department through a fast-paced and dynamic environment</li></ul><p>Gowning and Environment </p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </p></li></ul><p>To be considered for the Sr. Manager Quality Assurance you must be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Life Sciences or related field and 8+ years of experience. Experience in fill/finish manufacturing is preferred. Previous supervisory/ people leadership experience is required. May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Preclinical & Translational PK/PD]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47275]]></requisitionid>
    <referencenumber><![CDATA[R47275]]></referencenumber>
    <apijobid><![CDATA[r47275]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47275/associate-director-preclinical-translational-pkpd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of Translational/Preclinical Modeling develops and implements quantitative and mechanistic PK/PD models to aid in the understanding of target biology, therapeutic modality selection/optimization, and contributes to early clinical trial dose selection and/or design and advancement and strategic direction of modeling and simulation sciences.</p><p><strong>A Typical Day May Include:</strong></p><ul><li><p>Independently develops and implements quantitative and mechanistic mathematical PK/PD models that inform preclinical-to-early clinical translation, including human efficacious dose predictions and first-in-human dose selection.</p></li><li><p>Actively contributes to the advancement and strategic direction of modeling and simulation sciences</p></li><li><p>Provides expert support to pre-clinical PK/PD project representatives and R&D project teams to design, execute and interpret in vitro and in vivo quantitative pharmacology studies. This included working with the Research PK group to optimize use of mouse PK data to inform translation to nonhuman primate and human PK.</p></li><li><p>Effectively integrates and summarizes modeling and simulation analyses into useable information for multidisciplinary project teams.</p></li><li><p>Remains apprised of emerging science and literature, and effectively collaborates with subject matter experts in Clinical Pharmacology, Quantitative Pharmacology and R&D to advance modeling and simulation sciences.</p></li><li><p>Presents work at internal/external scientific meetings and publishes work in scientific journals</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>Experience using one or more modeling and simulation platforms (e.g., Phoenix NLME, NONMEN, Monolix, ADAPT, MATLAB, SimBiology, etc.)</p></li><li><p>Strong theoretical and practical foundation in pharmacokinetics, including non-compartmental, compartmental, PK/PD and PBPK.</p></li><li><p> Effectively work in a fast-paced, highly-matrixed team-based environment and leverages scientific reasoning to influence key stakeholders.</p></li><li><p>Ability to learn new areas of biological sciences to develop quantitative and mechanistic PK/PD models for emerging therapeutic modalities.</p></li><li><p>Familiarity with biotherapeutic modalities, including monoclonal and bispecific antibodies, gene therapy, CAR-T, siRNAs and other targeting agents preferred</p></li></ul><p><strong>To be considered for this position, you must have:</strong></p><p>Ph.D. or M.S. in pharmacokinetics, pharmaceutical sciences, engineering, applied mathematics or related disciplines with a track record of applying quantitative and mechanism-based PK/PD modeling and simulation approaches to advance the discovery and development of therapeutics. Greater than 6 years of pharmaceutical industry or related experience in developing and applying mechanism-based PK/PD models to guide R&D teams from early discovery to IND-stage clinical development.</p><p><strong> </strong></p><p><strong> </strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Pharmaceutical Sales Specialist Immunology - Alsace]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47580]]></requisitionid>
    <referencenumber><![CDATA[R47580]]></referencenumber>
    <apijobid><![CDATA[r47580]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47580/pharmaceutical-sales-specialist-immunology-alsace/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Chez Regeneron, nous croyons que lorsque la bonne idée trouve la bonne équipe, un réel changement est possible. Alors que nous travaillons activement à travers notre réseau pour inventer, développer et commercialiser des médicaments transformant la vie des personnes atteintes de maladies graves, nous établissons de nouvelles façons de penser la science, la fabrication et la commercialisation. </p></div><div><p>En tant que <strong>Délégué(e) Hospitalier(e) Immunologie</strong>, vous jouerez un rôle central dans la réalisation de nos objectifs et encouragerez une culture de haute performance. </p></div><div><p>De nature curieuse et proactive, vous serez responsable de la gestion du <strong>secteur Alsace (Strasbourg – Mulhouse - Colmar)</strong>, en assurant une planification et une gestion professionnelles des différents interlocuteurs/rices clés dans le domaine de l’Immunologie sur votre secteur, comprendre le fonctionnement des établissements hospitaliers et développer la croissance de Regeneron dans le respect du bon usage du médicament. </p></div><div></div><div><p><strong>En tant que Délégué(e) Hospitalier(e), une journée typique pourrait inclure les activités suivantes</strong> : </p></div><div><p>- Établir des interactions de haute qualité avec les Professionnels de Santé (PDS) en maintenant continuellement à jour les connaissances scientifiques autour du produit, de l'indication et des messages tout en mettant en œuvre de manière optimale le plan de vente et de marketing. </p></div><div><p>- Délivrer constamment la proposition de valeur de la marque à travers la communication des messages clés aux PDS. </p></div><div><p>- Travailler en alignement avec le plan de marque, développer et mettre en œuvre un plan stratégique local basé sur des sources de données clés et des insights du marché local. </p></div><div><p>- Collaborer étroitement avec les équipes médicales pour mettre en œuvre des programmes régionaux et des activités pertinentes pour soutenir les besoins des PDS. </p></div><div><p>- Optimisez tous les canaux de communication, y compris les canaux numériques, en collaboration avec d'autres fonctions, pour obtenir la meilleure part de voix possible sur le marché. </p></div><div><p>- Développer et mettre en œuvre, en ligne avec la stratégie de l’alliance Regeneron, un plan sectoriel reposant sur des données clés et le développement d’une connaissance assidue du marché local. </p></div><div><p><strong>Ce rôle pourrait être pour vous si</strong> : </p></div><div><p>- Vous êtes passionné(e) par le fait de garantir que les objectifs de l'actif sont atteints en communiquant les messages clés aux PDS, conformément aux bonnes pratiques. </p></div><div><p>- Vous êtes engagé(e) à travailler en collaboration et à développer d'excellents partenariats en interne et en externe, une expérience préalable dans une alliance est utile. </p></div><div><p>- Vous êtes enthousiaste à l'idée de gérer plusieurs canaux pour optimiser l'engagement des clients (par exemple, en face à face, appels à distance, e-mails approuvés, plateformes de communication numérique, etc.). </p></div><div><p>- Vous pouvez opérer efficacement dans un environnement naissant au sein d’une équipe collaborative, performante et ambitieuse. </p></div><div></div><div><p>Pour être considéré(e) pour cette opportunité, vous devez détenir un Diplôme de la Visite Médicale avec un minimum de 5+ années d'expérience professionnelles en vente pharmaceutique dans le domaine de l'Immunologie, idéalement en Pneumologie. Vous êtes mobile géographiquement et possédez un permis de conduire valide. L'anglais conversationnel serait souhaitable, mais non requis. </p></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Electrician, 1st shift Wednesday-Saturday]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47112]]></requisitionid>
    <referencenumber><![CDATA[R47112]]></referencenumber>
    <apijobid><![CDATA[r47112]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47112/electrician-1st-shift-wednesday-saturday/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking for an Electrician to join our growing team, working Wednesday-Saturday 6:00am-4:30pm. 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.</p><p>As an Electrician, a typical day might include the following:</p><ul><li>Maintaining electrical power systems and stand-by power generation equipment, as well as accurate electrical one-line drawings.</li><li>Maintaining an inventory of essential fuses and circuit breakers.</li><li>Directing outside service providers to provide and install electrical work and PMs.</li><li>Assisting Mechanical Technicians on facility or process equipment electrical issues.</li><li>Installing lighting, electrical and computer wiring when appropriate.</li><li>Scheduling work and maintaining all preventative maintenance for on-site emergency generators utilizing contracted services.</li><li>Scheduling and maintaining documentation on infrared scans for all electrical enclosures.</li><li>Developing, establishing and conducting annual employee training classes on electrical safety procedures and practices.</li><li>May involve working off-shift to support 24/7 coverage.</li></ul><p>This role might be for you if you:</p><ul><li><p>Are proficient with electrical and mechanical schematics and blueprints</p></li><li>Have the flexibility to work independently in a constantly evolving collaborative environment</li><li>Are a self-starter with a resilient, can-do demeanor</li><li>Enjoy working in the field as well as at a desk, processing documentation and correspondence</li><li>Communicate effectively both verbally and in writing while providing outstanding customer service</li><li>Have the ability to build effective working relationships with contacts inside and outside of the organization at all levels</li><li>Have some exposure to MS Office Suite, specifically Excel</li></ul><p>To be considered for the Electrician position you should have an AAS in Engineering or Construction Technologies and the following minimum experience for each level. You must be willing and able to work Wednesday-Saturday, 6:00am-4:30pm. Relevant experience at the Journeyman level may be substituted for degree. Experience with high voltage beneficial.</p><ul><li>Electrician II: 2+ years or equivalent combination of education and experience</li><li>Electrician III: 5+ years or equivalent combination of education and experience</li><li>Electrician IV: 8+ years or equivalent combination of education and experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $52.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Biostatistics - Oncology]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47599]]></requisitionid>
    <referencenumber><![CDATA[R47599]]></referencenumber>
    <apijobid><![CDATA[r47599]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47599/manager-biostatistics-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>This position is for a qualified Statistician/Biostatistician to support Clinical Biostatistics within Global Development Thrombosis.</p></div><div><div><div><div><div><div><div><div><div><p><strong>A typical day might include:</strong></p><p>The incumbent will work with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. The incumbent will co-author clinical study protocols, statistical analysis plans, and perform statistical analyses for interim and final reports. The incumbent will also develop and deliver training to non-statistical colleagues, collaborate on development of new infrastructure and processes, and influence the external pharmaceutical industry and regulatory environment through participation in professional associations, conferences, and publications.</p><p><strong>This role might be for you if you can:</strong></p><ul><li><p>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>To be considered for this opportunity, you must have the following:</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>#GDBDMJobs</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 15:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, PV Innovation]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47621]]></requisitionid>
    <referencenumber><![CDATA[R47621]]></referencenumber>
    <apijobid><![CDATA[r47621]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47621/director-pv-innovation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director of PV Innovation to join our Patient Safety Organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, PV Innovation is responsible for leading the development, implementation, and governance of AI capabilities that deliver measurable operational value and align to broader pharmacovigilance (PV) technology strategy. They are the primary point of contact for translating PV business needs into scalable digital solutions, while ensuring responsible, compliant, and secure adoption of AI technologies. </p><p><strong>This role might be for you if can/have: ​</strong></p><ul><li><p>Define and communicate the AI function vision, strategy and governance structure in alignment with business goals </p></li><li><p>Identify opportunities to leverage AI across PV processes to improve efficiency, insights, and scalability </p></li><li><p>Support the definition and execution of the GPS digital innovation strategy, providing AI expertise and technical input to the Executive Director, PV Innovation, GPS </p></li><li><p>Translate PV business requirements into scalable AI-enabled solutions and digital capabilities </p></li><li><p>Establish and maintain architecture, data, security, and Responsible AI standards and guardrails for PV AI initiatives </p></li><li><p>Oversee the implementation and scaling of AI solutions across GPS, ensuring solutions are fit-for-purpose and deliver measurable value </p></li><li><p>Ensure AI-enabled solutions comply with GxP, validation, data integrity, privacy, and regulatory requirements </p></li><li><p>Partner with key technology teams (e.g., GD IT, Cloud, Dev Ops, AI & Digital, Compliance) to ensure technology alignment, platform integration, and scalable deployment </p></li><li><p>Provide operational insights and emerging technology opportunities to inform the broader PV digital innovation roadmap </p></li><li><p>Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines. </p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Minimum Bachelor's degree with 12+ years of experience in pharmacovigilance, safety systems, digital innovation, data science, or AI-enabled technology within the life sciences industry </p></li><li><p>Demonstrated experience working at the intersection of safety operations and technology </p></li><li><p>Strong knowledge of AI and advanced analytic applications within regulated environments </p></li><li><p>Strong understanding of pharmacovigilance processes and safety systems (e.g., safety databases, signal detection tools, reporting platforms) </p></li><li><p>Knowledge of AI governance, Responsible AI frameworks, and data security standards </p></li><li><p>Ability to lead cross-functional initiatives across Safety, IT, and digital teams </p></li></ul><p>#GDPSJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-South Central]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47577]]></requisitionid>
    <referencenumber><![CDATA[R47577]]></referencenumber>
    <apijobid><![CDATA[r47577]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47577/regional-director-neurology-south-central/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Texas]]></city>
    <state><![CDATA[Texas]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the South Central Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: South Central (Texas and Louisiana)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-New York Metro]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47569]]></requisitionid>
    <referencenumber><![CDATA[R47569]]></referencenumber>
    <apijobid><![CDATA[r47569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47569/regional-director-neurology-new-york-metro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the [INSERT] Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: New York Metro</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><ul><li></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>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 20:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation System Administrator]]></title>
    <date><![CDATA[Sun, 21 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43991]]></requisitionid>
    <referencenumber><![CDATA[R43991]]></referencenumber>
    <apijobid><![CDATA[r43991]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43991/senior-automation-system-administrator/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Automation System Administrator, you will be embedded in a tight-knit team responsible for administration of automated/computerized system software and firmware to meet cGMP and policy requirements. In this critical role our team specifies and maintains software configuration for biopharmaceutical process, monitoring, and testing systems. This involves evaluation of new software for functional equivalence, validation activities to demonstrate suitability of software/process and maintaining the qualified state of systems throughout their lifecycle through change control.</p><p>In this role, a typical day might include:</p><ul><li>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</li><li>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</li><li>Utilizing configuration management and recipe/method management.</li><li>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</li><li>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</li><li>Conducting system integration with existing systems (e.g. LIMS, Historian).</li><li>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and/or design specifications, test plans, technical evaluation, and quality risk assessments.</li><li>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</li><li>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</li><li>Leading aspects of the work for contractors and providing guidance as applicable.</li></ul><p>This role might be for you if you:</p><ul><li>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</li><li>Have interest in manufacturing process within a regulated technical environment.</li><li>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</li><li>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</li><li>Understand process control systems and product release testing systems.</li><li>Are familiar with regulatory and quality policies, procedures, documentation methods.</li><li>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</li><li>Enjoy project management and have strong organizational skills.</li><li>Are motivated to participate in continuous process improvement.</li></ul><p>Applicants ideally should have a BS/BA in Science, Engineering or related field and the following minimum relevant experience for each level:</p><ul><li>Senior Automation System Administrator: 5+ years</li><li>Principal Automation System Administrator: 8+ years</li></ul><p>Equivalent combination of education and experience may be considered. Level will be determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Internal Medicine, Clinical Scientist (Ophthalmology)]]></title>
    <date><![CDATA[Tue, 27 Jan 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44659]]></requisitionid>
    <referencenumber><![CDATA[R44659]]></referencenumber>
    <apijobid><![CDATA[r44659]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44659/senior-manager-internal-medicine-clinical-scientist-ophthalmology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director/Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><h3>As a Senior Manager in Clinical Sciences, a typical day may include the following:</h3><ul><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; participates in collaborative activities with other departments; Member of the Clinical Study Team and Global Clinical SubTeam</p></li><li><p>Develops/maintains understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets; Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety</p></li><li><p>Collaborates with internal functions and external vendors to promote clinical study integrity</p></li><li><p>Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis; supports identification and/or identifies critical risks and mitigations</p></li><li><p>Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies; Reviews clinical data review plan and medical monitoring plan for assigned studies</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Demonstrated ability to influence within team and may influence cross functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li><li><p>Strong management, interpersonal and problem-solving skills</p></li><li><p>Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills. Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Proven track in clinical trial process improvements.</p></li><li><p>Considerable organizational awareness, including significant experience working cross-functionally.</p></li></ul><p>To be considered for this role, you must have a BS/MS/PhD/PharmD in a related field. Additionally, ≥ 8 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. We are seeking experience in Ophthalmology clinical trials.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 28 Jan 2026 14:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44611]]></requisitionid>
    <referencenumber><![CDATA[R44611]]></referencenumber>
    <apijobid><![CDATA[r44611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44611/principal-statistical-programmer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies.</p><p><strong>In this role, a typical day might include:</strong> ​</p><p>As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.</p><p><strong>This role might be for you if can:</strong> ​</p><ul><li>Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. </li><li>Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. </li><li>Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).</li><li>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.</li><li>Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</li><li>Participate in department working groups; provide input in development of tools and improvement of processes.</li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>Masters Degree</li><li>SAS, (Base, Stat, Macro, graph). </li><li>3 + Years experience</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Clinical Study Lead (Genetics Medicine, Hepatology)]]></title>
    <date><![CDATA[Tue, 17 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45358]]></requisitionid>
    <referencenumber><![CDATA[R45358]]></referencenumber>
    <apijobid><![CDATA[r45358]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45358/senior-manager-clinical-study-lead-genetics-medicine-hepatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Clinical Study Lead</strong> (CSL) is expected to operate with high-degree of independence and is accountable for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study budget, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs) and ICH/GCP. This role applies to internally sourced studies and studies out-sourced to Clinical Research Organizations (CROs) and the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives.</p><p>This role is not eligible fully remote. This role is required to be onsite in one of our locations.</p><h3><strong>A typical day in this role looks like: </strong></h3><ul><li><p>Leads the cross-functional study team responsible for clinical study delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</p></li><li><p>Provides operational input into protocol development</p></li><li><p>Oversees and provides input to the development of study specific documentation including but not limited to: case report forms (CRF), data management plan, monitoring plan, monitoring oversight plan, project specific training plan, data review plan, statistical analysis plan, etc.</p></li><li><p>Oversees set-up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS), Trial Master File (TMF) etc.</p></li><li><p>Ensures compliance with the clinical trial registry requirements</p></li><li><p>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors</p></li><li><p>Provides input into baseline budget development and management</p></li><li><p>Provides input into baseline timeline development and management</p></li><li><p>Leads risk assessment and identifies risk mitigation strategies at the study level</p></li><li><p>Leads the feasibility assessment to select relevant regions and countries for the study</p></li><li><p>Oversees/conducts site evaluation and selection</p></li><li><p>Leads investigator meeting preparation and execution</p></li><li><p>Monitors progress for site activation and monitoring visits and acts on any deviations from plan</p></li><li><p>Leads the development of and oversees implementation of patient recruitment and retention strategies and acts on any deviations from plan</p></li><li><p>Monitors data entry and query resolution and acts on any deviations from agreed metrics</p></li><li><p>Ensures accurate budget management and scope changes for internal and external studies</p></li><li><p>Oversees and provides input to the study drug and clinical supplies forecasting, drug accountability and drug reconciliation</p></li><li><p>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</p></li><li><p>Oversees the execution of the clinical study against planned timelines, deliverables and budget</p></li><li><p>Oversees data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations, and suspected serious non-compliance by sites</p></li><li><p>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the scope of work</p></li><li><p>Ensure clinical project audit and inspection readiness through the study lifecycle</p></li><li><p>Supports internal audit and external inspection activities and contributes to CAPAs as required</p></li><li><p>Manages and oversees study close-out activities including but not limited to database lock, reconciliation of vendor contracts, budget, TMF, and study drug accountability</p></li><li><p>Contributes to clinical study report writing and review</p></li><li><p>Facilitates and contributes to study level lessons learned</p></li><li><p>Assigns tasks to Clinical Study Management staff and supports their deliverables</p></li><li><p>Recommends and participates in cross-functional and departmental process improvement initiatives</p></li><li><p>Responsible for identification of innovative approaches to clinical study execution including global considerations and continuous improvement of CTM SOPs</p></li><li><p>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</p></li><li><p>Responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</p></li><li><p>May require 25% travel</p></li></ul><h3><strong>This role may be for you if you have:</strong></h3><ul><li><p>Exceptional interpersonal & leadership skills</p></li><li><p>Applies advanced expertise and implements the operational strategic direction and guidance for respective clinical studies</p></li><li><p>Demonstrates expert knowledge and a data driven approach to planning, executing, and problem solving</p></li><li><p>Advanced communication skills via verbal, written and presentation abilities</p></li><li><p>Proactive and self-disciplined, ability to meet deadlines, effective use of time, and prioritization</p></li><li><p>Ability to influence and negotiate across a wide range of stakeholders</p></li><li><p>Strong budget management experience</p></li><li><p>An awareness of relevant industry trends</p></li><li><p>Ability to build, lead and develop productive study teams and collaborations</p></li><li><p>Applies advanced negotiation and interpersonal skills to vendor management</p></li><li><p>Advanced technical proficiency in trial management systems and MS applications including (but not limited to) Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC</p></li><li><p>Extensive experience in global clinical trial operations with unique knowledge and skills to contribute to the development of protocols and key study documents</p></li><li><p>Knowledge of ICH/GCP and regulatory guidelines/directives</p></li><li><p>Advanced project management skills, cross-functional team leadership and organizational skills</p></li><li><p>Line management experience</p></li></ul><p><strong>In order to be considered qualified, </strong>a minimum of a Bachelor's degree is required and a minimum of 8 years relevant clinical trial experience.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 18 Feb 2026 12:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Deployment & Incentives]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45419]]></requisitionid>
    <referencenumber><![CDATA[R45419]]></referencenumber>
    <apijobid><![CDATA[r45419]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45419/associate-director-field-deployment-incentives/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking an Associate Director of Field Deployment and Incentives to join our organization!</p><p><strong>In this role, a typical day might include:</strong></p><p>The Associate Director of Field Deployment and Incentives serves as a strategic leader, responsible for enhancing field engagement and performance by designing and implementing IC plans, contests, and awards, and optimizing field force structure and territory alignments to achieve organizational objectives.</p><p>As a key member of the field enablement team, you will be the primary point of contact for your designated therapeutic areas, serving as a trusted strategic partner to field leadership and internal stakeholders. You will proactively provide essential insights and develop strategies for IC, contests, awards, and field force alignments by transforming complex data into clear, actionable recommendations that facilitate data-driven decision-making. Your expertise in project and vendor management will ensure that all deliverables meet the highest standards of quality and timeliness.</p><p>This role presents a unique opportunity to directly impact field performance and corporate outcomes, fostering professional growth and expanding skill sets within a dynamic team environment.</p><p><strong>This role might be for you if you can/have:</strong></p><ul><li><p>Lead end‑to‑end IC design (plans, contests, awards) aligned to brand and corporate objectives, ensuring solutions are motivational, equitable, compliant, and fiscally responsible.</p></li><li><p>Engage with field force structure and sizing projects, leading expansions, re-structures, and quarterly alignments changes to optimize field deployment and minimize field disruption.</p></li><li><p>Develop and execute robust models and simulations to assess incentives, contests, awards, and field structure design options and their trade-offs, effectively communicating implications and recommendations to facilitate real-time, data-driven decision-making for field leaders and senior stakeholders.</p></li><li><p>Partner with Insights/Marketing/Advanced Analytics to inform IC and award strategy, contest design and objectives, territory coverage and workload, aligning on methodologies and assumptions across teams.</p></li><li><p>Develop communication/training materials to ensure a high level of field understanding of their IC plans, contests, awards, and territory/geography design.</p></li><li><p>Liaise with external vendors and internal partners to ensure the design and delivery of high-quality, fit-for-purpose, actionable tools and reports.</p></li><li><p>Establish and maintain IC governance (policies, business rules, SOPs), partner across Legal/Compliance/Finance/HR/Marketing/Data-Management teams, and drive quality, accuracy, and timeliness in all deliverables.</p></li><li><p>Ensure a unified metric framework and consistent definitions across IC, contests, and performance reporting measures.</p></li><li><p>Address data discrepancies and collaborate with Commercial Data Management to uphold high data integrity. Prioritize, triage, and resolve issues swiftly and clearly, maintaining field trust in our processes and deliverables.</p></li><li><p>Own operations calendar and cross-functional operating rhythm, covering everything from territory design to performance tracking and payouts. Ensure that key timelines are consistently communicated to both field personnel and internal stakeholders and leaders.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong> </p><ul><li><p>Minimum BA/BS with 10+ years (or MBA/MS with 7+ years) of progressive experience in the pharmaceutical industry, focusing on IC, field force size, structure, and alignments, field analytics, targeting, or call planning, with 6+ years directly related to IC and field force structure and alignments.</p></li><li><p>Bachelor’s degree in a quantitative field, business, or related discipline; an advanced degree is preferred. </p></li><li><p>Subject-matter expertise in pharmaceutical incentive compensation and field deployment best practices.</p></li><li><p>Hands-on experience in analytics and modeling using large, complex datasets to solve intricate business challenges.</p></li><li><p>Proven ability to distill complex analyses into clear and actionable recommendations.</p></li><li><p>Strong QC/validation rigor.</p></li><li><p>Exceptional communication and interpersonal skills, with a demonstrated ability to influence without authority and collaborate effectively with diverse teams.</p></li><li><p>Excellent project management and prioritization skills to effectively balance multiple projects and priorities.</p></li><li><p>Able to thrive in fast-paced and ambiguous environments while consistently delivering exceptional results.</p></li><li><p>Solid understanding of open/closed pharma distribution models.</p></li><li><p>Proficient in Excel and PowerPoint for executive‑ready deliverables.</p></li><li><p>Expertise with key pharmaceutical data sources, including Xponent, DDD, 867, specialty pharmacy, patient-level, Hub, among others.</p></li><li><p>Knowledge of programming languages such as SQL, R, and Python.</p></li></ul><p><em>Preferred Qualifications include:</em></p><ul><li><p>Experience in sub-national performance analytics, including territory/region KPIs, execution diagnostics, and pull-through measurement.</p></li><li><p>Familiarity with data management and analytics platforms like Databricks or Snowflake, as well as business intelligence and visualization tools such as Power BI or Tableau.</p></li><li><p>Experience applying AI / Machine Learning to field deployment tools and design.</p></li><li><p>Knowledge of CRM Systems such as Veeva and Salesforce.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Clinical Study Lead (Clinical Experimental Sciences)]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44465]]></requisitionid>
    <referencenumber><![CDATA[R44465]]></referencenumber>
    <apijobid><![CDATA[r44465]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44465/senior-manager-clinical-study-lead-clinical-experimental-sciences/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><em>This role is not eligible remote, and must be onsite in one of our US office locations.</em></p><p>The <strong>Senior Clinical Study Lead (CSL) – Clinical Experimental Sciences Operations (CES Ops)</strong> is accountable for the execution of assigned clinical studies/research collaborations from study design, through execution, to study close out. Additionally, there are responsibilities for initiation, oversight and completion of CES Ops continuous improvement and Strategic Imperatives workstreams. The Sr. CSL is accountable for oversight of the contract and budget execution, study timelines, study budget management, and ensuring study conduct is in accordance with, Regeneron Standard Operating Procedures (SOPs), CES Ops Business Practice Tool processes and ICH/GCP, as applicable. The CES Ops portfolio is dynamic in nature; study types include, but are not limited to, less complex data transfer agreements, retrospective sample/data acquisition studies to more complex prospective studies including sample/data acquisition, biomarker/technology/method validation, genotypic/phenotypic call back studies, and challenge/screening studies. This role will interface heavily with Basic Research/Discovery as well as with clinical site staff, predominately at academic institutions. In rare instances the more complex studies may require out-sourcing to Clinical Research Organizations (CROs); the balance of direct leadership versus oversight will vary accordingly. Contributes and drives ongoing process improvement initiatives. This role may be responsible for direct line management.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>Leads the cross-functional study team responsible for clinical study/research collaboration delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study</li><li>Provides operational input into research plan and/or study protocol development</li><li>Ensures development of study specific documentation such as samples management plans and data management plans are completed on time and in accordance with the study protocol.</li><li>Oversees set-up and maintenance of study systems which may include Clinical Trial Management System (CTMS), Trial Master File (TMF), study SharePoint etc.</li><li>Identifies outsourcing needs of the study and leads and oversees engagement, contracting and management of required vendors, if appropriate</li><li>Provides input into baseline timeline development and management</li><li>Provides input into baseline budget development and management, facilitates internal review of the study budget for assessment of Fair Market Value</li><li>Ensures accurate budget management and scope changes for internal and external studies</li><li>Escalates issues related to study conduct, quality, timelines or budget to Program Operations Leader (POL) and other stakeholders and develops and implements appropriate actions to address issues</li><li>Oversees the execution of the clinical study against planned timelines, deliverables and budget</li><li>Oversees and ensures the CROs and Third Party Vendors are in alignment and are delivering per the</li><li>scope of work</li><li>Manages and oversees study close-out activities</li><li>Ensures End of Study Summary is delivered and properly archived</li><li>Facilitates and contributes to study level lessons learned</li><li>Assigns tasks to Clinical Study Management staff and supports their deliverables</li><li>Recommends and participates in cross-functional and departmental process improvement initiatives</li><li>Responsible for identification of innovative approaches to clinical study execution including global considerations and continuous improvement departmental processes and procedures</li><li>Works with Therapeutic Focus Area groups within Basic Research/Discovery</li><li>Works closely with clinical site staff, predominantly at academic institutions</li><li>Expected to maintain higher volume and/or greater complexity studies</li><li>Expected to communicate learnings, best practices and relevant information to other study leads at all levels, ensures consistency and internal alignment across staff</li><li>May be responsible for direct supervision of CTM staff. Line management responsibilities include work assignments, performance management, staff recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of a Bachelor's degree and8+ years of relevant clinical experience is required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 18:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations (GMP IT/OT)]]></title>
    <date><![CDATA[Tue, 24 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43879]]></requisitionid>
    <referencenumber><![CDATA[R43879]]></referencenumber>
    <apijobid><![CDATA[r43879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43879/associate-director-of-it-operations-gmp-itot/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of IT Operations (GMP IT/OT) ensures the reliable operation, delivery, and management of IT/Operational Technology (IT/OT) infrastructure and services, with a focus on supporting a highly regulated GxP environment. This role provides strategic direction, operational management, and administrative oversight for the daily IT operational activities, including hardware, communications & WiFi infrastructure, and service delivery. The position also ensures integration and alignment with corporate IT systems and infrastructure while maintaining robust compliance, security, and service standards.</p><div><div><div><div><p>As an Associate Director of IT Operations (IT/OT), a typical day might include the following:</p><ul><li>Ensure the reliable operation of IT/OT infrastructure, including but not limited to servers, hardware, communications and desktop support, plus oversight of daily operational activities.</li><li>Define, implement, and lead IT/OT infrastructure architecture, with a focus on hyper-converged systems, advanced networking, and wireless technologies, to ensure robust connectivity and security.</li><li>Build scalable and secure wireless networks to support industrial and enterprise needs. </li><li>Provide operational management for data centre operations, network services, telecom, asset management, and security plus ensure systems and procedures are in place for effective monitoring and reporting. </li><li>Maintain compliance with industry standards, including experience with automation systems such as DeltaV/Emerson and Rockwell/Allen-Bradley.</li><li>Manage service providers to ensure high-quality service delivery and alignment to service level agreements (SLAs) and act as the escalation point for major incidents.</li><li>Ensure compliance with relevant regulations and standards, including GxP, FDA and other global regulatory requirements. </li><li>Maintain robust security measures to protect IT/OT infrastructure, including data integrity and disaster recovery planning. </li><li> Lead and mentor a diverse technical team and run recruitment, training, performance evaluations, and target setting for the IT Operations team. </li><li>Collaborate with partners to ensure seamless integration between IT and OT systems. </li><li>Provide regular management reporting on service performance and IT operations. </li></ul><p>This role may be for you if you:</p><ul><li>Management and delivery experience required including management of a diverse technical team, including Helpdesk, Desktop, Server and Network staff. Experiencing managing vendors and managed services.</li><li>Experience in developing and deploying SLA's, Metrics and other best practices as well as having successfully implemented ITIL practices into an organization.</li><li>Experience with Business Continuity and Disaster Recovery planning.</li><li>Strong background in Microsoft OS in particular Server and GPO elements.</li><li>Strong understanding of Data Integrity and associated tools.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with</p><ul><li>Senior Manager: 8+ years of progressively more responsible experience, including 8+ years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment.</li><li>Associate Director: 10 years of progressively more responsible experience, including 10 years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Preferred knowledge of understanding of IT compliance guidelines, including PICS, CFR21 Part 11, Annex 11, and GAMP.</li></ul></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Feb 2026 04:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Quality Technical Operations]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45585]]></requisitionid>
    <referencenumber><![CDATA[R45585]]></referencenumber>
    <apijobid><![CDATA[r45585]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45585/director-quality-technical-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is hiring! As the Director of Quality Technical Operations you will lead a high-impact Quality function spanning QA MES, QA Validation Oversight, and QA Tech Transfer. You’ll define and implement cGMP best practices, set quality standards and metrics, and ensure clinical and commercial manufacturing operations meet and exceed regulatory compliance requirements.</p><p>In this role, a typical day might include the following:</p><ul><li><p>Define and implement quality standards, systems, and metrics across clinical and commercial manufacturing operations.</p></li><li><p>Provide quality oversight to activities related to validation and ensure that they are effectively administered and comply with regulatory requirements.</p></li><li><p>Oversee QA tasks related to electronic manufacturing record management and tech transfer.</p></li><li><p>Compile, organize, and present quality metrics and trends to senior leadership.</p></li><li><p>Plan and allocate QA resources to meet program goals, timelines, and priorities.</p></li><li><p>Coordinate prioritization of activities with area management to optimize execution.</p></li><li><p>Prepare for regulatory and customer audits; ensure observations are addressed effectively and on schedule.</p></li><li><p>Maintain safety and operational standards and approve documents related to QA functions.</p></li></ul><p>This role might be for you if you have:</p><ul><li><p>Proven leadership in cGMP environments with hands-on experience in QA systems and metrics.</p></li><li><p>A track record of successful audit readiness, execution, and response management.</p></li><li><p>Strong collaboration, communication, and stakeholder engagement skills.</p></li><li><p>An understanding of bulk API biologics manufacturing operations.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Life Sciences or related field and the following amount of relevant pharmaceutical manufacturing experience for each level:</p><ul><li><p>Director – 12+ years</p></li><li><p>Sr Director – 15+ years</p></li></ul><p>Level to be determined based on qualifications relevant to the role. May substitute proven experience for education requirement.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$172,200.00 - $338,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 17:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Délégué(e) Hospitalier(e) Oncologie - Bourgogne Franche-Comté]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45656]]></requisitionid>
    <referencenumber><![CDATA[R45656]]></referencenumber>
    <apijobid><![CDATA[r45656]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45656/delegue-e-hospitalier-e-oncologie-bourgogne-franche-comte/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>As an Oncology Pharmaceutical Sales Representative, you will play a pivotal role in driving our commercial goals and encouraging a high-performance culture, while covering <strong>Bourgogne Franche-Comté</strong>. You will be responsible for running your territory, ensuring professional account planning and management of all key accounts and implementing a professional targeting & segmentation approach.</p><p><strong>Oncology Pharmaceutical Representative - Bourgogne Franche-Comté</strong></p><p><strong>As an Oncology Pharmaceutical Representative, a typical day might include the following:</strong></p><ul><li><p>Establish and lead high quality HCP interactions by continuously keeping scientific knowledge around the product, indication and brand sales messaging up to date and optimally implementing sales & marketing plan.</p></li><li><p>Consistently deliver on the value proposition for the brand through key message communication to HCPs.</p></li><li><p>Work in alignment with the Brand Plan, develop and implement a local account plan based on key data sources and local market insights.</p></li><li><p>Collaborate closely with medical colleagues to implement regional programs and relevant activities to support HCP needs.</p></li><li><p>Leverage all communication channels including digital channels, in collaboration with other functions, to achieve the best possible share of voice in the market.</p></li><li><p>Report results and developments proactively and clearly to the Immunology leadership team</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You are passionate about ensuring that the asset’s objectives are met by communicating key messages to HCPs, in line with good practice.</p></li><li><p>You are committed to work in collaboration and develop excellent partnership internally & externally, previous experience in an alliance is helpful.</p></li><li><p>You are thrilled about handling multiple channels to optimize customer engagement (e.g. F2F, remote calls, approved e-mails, digital communication platforms, etc.).</p></li><li><p>You can operate effectively in a “start-up” model as this is a completely new team.</p></li></ul><p>To be considered for this opportunity you must hold a Carte Professionnelle with minimum <strong>5+ years of pharmaceutical sales experience in Oncology</strong>. You are happy with regular travel and have a valid driver's license. Conversational English would be desirable, but not required.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 03:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Calibration Technician, Tuesday-Saturday 3rd Shift]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45542]]></requisitionid>
    <referencenumber><![CDATA[R45542]]></referencenumber>
    <apijobid><![CDATA[r45542]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45542/calibration-technician-tuesday-saturday-3rd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a Calibration Technician to our growing team, working a Tuesday-Saturday 10:00pm – 8:30am shift. Our Calibration Technicians support our manufacturing by performing mechanical, electrical, calibration, electronic, or utility related tasks.</p><p><strong>Please note training will take place Monday-Friday 8:00am-4:30pm for approximately 6 months. Working hours thereafter will be Tuesday-Saturday 10:00pm-8:30am. </strong><strong>Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a Calibration Technician, a typical day might include the following:</p><ul><li>Calibrating various types of instrumentation including temperature, pressure, level, flow and analytical instruments</li><li>Performing loop check, tune, troubleshoot, and start-up of instrumentation</li><li>Working with medium and low voltages</li><li>Performing basic plumbing and tube bending jobs</li><li>Assisting the Facilities Management-Maintenance (FM-M) process and Clean Utility technicians in troubleshooting facilities and process related issues</li><li>Performing daily Work Orders (WO) and Preventative Maintenance (PM) and efficiently coordinate the workflow and documentation of PMs and WOs</li><li>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</li><li>Following current Good Manufacturing Practices (cGMPs)</li><li>Occasionally working on other facility related work tasks/issues that are outside the calibration department’s normal work duties</li><li>May include planning and scheduling outside contractors/vendors to perform scheduled and/or non-scheduled PM or general work</li><li>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOPs, cGMPs, and quality standards</li><li>Participation in compliance investigations if and when necessary</li><li>Full gowning required when entering and working on production floor</li><li>Participating in rotation on-call schedule</li></ul><h3>This role might be for you if you:</h3><ul><li>Demonstrate basic problem-solving skills</li><li>Are able to learn and follow routine procedures independently as well as part of a team</li><li>Are comfortable and have the flexibility to work in a changing environment</li><li>Can lift, push, and pull at least 50lbs</li><li>Seek to build and maintain positive working relationships with the business</li><li>Possess strong written and verbal communication skills</li><li>Maintain effective time management skills to allow deadlines to be met in a timely manner</li><li>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</li></ul><p>To be considered for the Calibration Technician position you must be willing and able to work a Tuesday-Saturday 10:00pm – 8:30am schedule. Applicants ideally should have an AAS degree, preferably in an Engineering or Construction Technologies related area and the following minimum amounts of experience for each level:</p><ul><li>Calibration Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</li><li>Calibration Technician III: 5+ years of related experience or HSD/GED with 8+ years of related experience</li><li>Calibration Technician IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</li></ul><p>Level will be determined based on qualifications relevant to the role.</p><p>Prior experience in the maintenance and operation of large-scale utilities plant preferred and ISA CCST Certification is strongly preferred but not required.</p><p>#REGENTOSK </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$28.46 - $44.42]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 10:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Field Medical Affairs-Hematology ( TN, AL, MS, AR)]]></title>
    <date><![CDATA[Wed, 08 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46458]]></requisitionid>
    <referencenumber><![CDATA[R46458]]></referencenumber>
    <apijobid><![CDATA[r46458]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46458/associate-director-field-medical-affairs-hematology-tn-al-ms-ar/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>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. We are expected to demonstrate a thorough understanding of B-Cell Malignancies (NHL and Multiple Myeloma) aligned with our strategic medical plans. </p><p><strong>Territory:</strong> Tennessee, Alabama, Mississippi and Arkansas (residency in the territory is required with a preference of TN and AL. </p><p><strong>A typical day may include the following:</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 may be for you if you:</strong><br>• Want to be a part of a pre-launch stage team potentially for multiple launches.<br>• Are skilled in the art of strategic conversation along with a proven ability to assess issues adapting appropriately.<br>• Can demonstrate an understanding of “know your audience” and ability to tailor information appropriately.<br>• Have demonstrated the ability to anticipate, organize, plan and handle multiple priorities, while adapting to the needs of the company.</p><p>To be considered a terminal scientific degree (MD, PharmD, PhD, DNP or DVM) is required. 8+ years of experience with a minimum of 4 years’ experience within a Hematology/Oncology Medical Science Liaison function is required. Knowledge of treatment guidelines, clinical research processes, FDA regulations, pharma regulations/compliant practices, and OIG guidelines. </p><p><strong>Additional requirements: </strong><br>• Residency in the assigned territory <br>• Travel: Capable of engaging in frequent business travel (approximately 70% of time), including air travel, overnight and occasionally on weekends.<br>• Possesses and maintains a valid driver’s license and clean driving record.</p><p><strong>Preferred experiences include: </strong><br>• Established relationships with KOLs and institutions focused on Hematologic Malignancies<br>• Drug launch experience. <br> </p><p><strong> </strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 08 Apr 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Clinical Scientist, Hematology]]></title>
    <date><![CDATA[Thu, 02 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46313]]></requisitionid>
    <referencenumber><![CDATA[R46313]]></referencenumber>
    <apijobid><![CDATA[r46313]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46313/manager-clinical-scientist-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Clinical Sciences, Hematology leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.</p><p>As a Manager, a typical day may include the following:</p><ul><li><p>Member of the Clinical Study Team and Global Clinical sub-team</p></li><li><p>Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments</p></li><li><p>Develops/maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape</p></li><li><p>Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late-stage assets</p></li><li><p>Assists with development of the Expanded Synopsis and may author clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments</p></li><li><p>Assists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review</p></li><li><p>Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety</p></li><li><p>Contributes to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority). Presents data and information to external investigators (SIV) and internal collaborators</p></li></ul><p>This role may be for you if:</p><ul><li><p>Possess demonstrated knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrate solid medical writing skills</p></li><li><p>Proven ability to influence within team and may influence across functionally</p></li><li><p>Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills</p></li><li><p>Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways</p></li></ul><p>To be considered for this position, you must have a minimum of Bachelor’s Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). We are seeking ≥ a minimum of 3 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. You have a basic knowledge of oncology or hematology therapeutic areas as well as a proven track in clinical trial process improvements. We need an individual with demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Resolves novel problems requiring creative application of advanced skill, training, and education.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 02 Apr 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Operations Specialist (IT Business Process Automation)]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44091]]></requisitionid>
    <referencenumber><![CDATA[R44091]]></referencenumber>
    <apijobid><![CDATA[r44091]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44091/principal-operations-specialist-it-business-process-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Principal Operations Specialist (IT Business Process Automation) to lead workflow automation across ServiceNow and ProcessX, partnering with IAM and QAR stakeholders to streamline processes, strengthen compliance, and improve reliability. You’ll own the end-to-end lifecycle—from design and integration to operations, incident response, and audit readiness—so teams can move faster with confidence.</p><p>As a Principal Operations Specialist, a typical day might include the following:</p><ul><li>Design, build, and maintain automated workflows in ServiceNow and ProcessX to improve operational efficiency and service delivery.</li><li>Identify, scope, and prioritize automation opportunities across IAM and QAR aligned to business goals and regulatory standards.</li><li>Optimize platform configurations and integrations for performance, scalability, and compliance, following ITIL and GxP best practices.</li><li>Monitor and continuously improve service availability, reliability, and throughput against defined SLAs/OLAs; publish clear metrics and dashboards.</li><li>Define and enforce operational guardrails, SOPs, CSV/validation artifacts, and documentation to ensure GxP, security, and audit readiness.</li><li>Lead major incident response for automation services; coordinate triage, stakeholder communications, root cause analysis, and post-incident reviews.</li><li>Create and execute Service Improvement Plans; use data and analytics to measure impact and recommend enhancements.</li><li>Act as a trusted advisor—translate requirements into practical roadmaps and automation solutions; align platform capabilities with stakeholder needs.</li><li>Partner with Security, QA, and Compliance to meet requirements such as data integrity, access controls, and change governance.</li><li>Own the automation platform roadmap; evaluate new features, apps, and integrations that extend value across the enterprise.</li></ul><p>This role may be for you if you have:</p><ul><li>Deep hands-on experience with ServiceNow workflow configuration, Flow Designer, IntegrationHub, CMDB, and custom development/integrations.</li><li>Proven success implementing automation that improves efficiency and compliance in GxP contexts; familiarity with 21 CFR Part 11 and Annex 11.</li><li>Strong familiarity with IAM and QAR processes in regulated environments and experience operating validated systems using GAMP 5 concepts.</li><li>Expertise with core ITIL disciplines: Incident, Problem, Change, Request, Monitoring/Reporting; strong operational rigor.</li><li>Experience creating validation packages and audit-ready documentation; understanding of data integrity controls and operational guardrails.</li><li>Service management operations at scale, including escalation procedures and on-call/major incident leadership.</li><li>Technical breadth across operating systems (Windows, Linux), virtualization (VMware), and monitoring/security tools (e.g., Splunk, Claroty, next-gen OT tools).</li><li>ServiceNow certifications (e.g., CSA, CAD, CIS in relevant modules) or equivalent demonstrable expertise.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field and</p><ul><li>Senior: 5 years of experience delivering IT/OT services to business or consumers.</li><li>Principal: 8 years of experience delivering IT/OT services to business or consumers.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Strong GxP experience and proven experience in highly regulated environments required.</li><li>Service Management or support in a large-scale and diverse environment of incident management, escalation procedures and related disciplines.</li><li>Experience with delivering projects and initiatives in the IT or OT space.</li><li>Deep experience with ITIL disciplines.</li><li>Experience with operating systems (Microsoft Windows & Linux), VMware.</li><li>Experience with monitoring and security tools such as Splunk, Claroty and next Gen OT tools.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff External Manufacturing Specialist]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46633]]></requisitionid>
    <referencenumber><![CDATA[R46633]]></referencenumber>
    <apijobid><![CDATA[r46633]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46633/staff-external-manufacturing-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>We are currently looking to fill a Staff External Manufacturing Specialist position within the Advanced Therapies External Manufacturing Team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. This role strategically manages Regeneron’s business relationships and supports end-to-end operations oversight with key Contract Manufacturing Organizations (CMOs) within Regeneron’s Bioconjugation portfolio. </p><p>As a Staff Specialist of External Manufacturing, a typical day might include the following: </p><ul><li><p>Lead Quarterly Business Reviews and other governance touchpoints with CMOs to drive performance, transparency, and continuous improvement.</p></li></ul><ul><li><p>Lead RFP, SOWs, project plans, and change order management associated with contractor operations.</p></li></ul><ul><li><p>Support and inform strategic initiatives and contract negotiations that drive long-term relationship stability and supply security.</p></li></ul><ul><li><p>Provide regulatory filing support across global clinical and/or commercial submissions as it pertains to CMO activities. </p></li></ul><ul><li><p>Lead external manufacturing activities at CMO and partner sites, including batch scheduling, material supply, product shipment, and cycle time monitoring.</p></li><li><p>Support all External Manufacturing activities, including technical transfer, validation plans, Master Manufacturing Records (MRs), SOPs, and other documentation required for clinical and commercial manufacturing execution.</p></li></ul><ul><li><p>Resolve supply issues with CMO/Partners affecting product quality or availability, including evaluating cost/benefit scenarios, making sound recommendations, and coordinating internal and external resources.</p></li><li><p>Serve as the liaison between Regeneron Quality Control, Quality Assurance, Supply Chain, MSAT, Operations/Logistics, and CMO/Partner sites.</p></li><li><p>Collaborate with Tech Transfer, New Product Launch, Life Cycle Management teams to enable efficient product introductions and transitions.</p></li><li><p>Ensure all manufacturing activities at CMO/Partner sites comply with cGMP requirements and applicable regulatory standards.</p></li></ul><ul><li><p>Assist in monitoring cGMP compliance at contract manufacturers to protect product integrity and Regeneron's regulatory standing.</p></li></ul><ul><li><p>Maintain current training status on all Regeneron-specific work instructions and SOPs.</p></li><li><p>Develop and maintain metrics to analyze CMO network performance, departmental workload, and operational health.</p></li></ul><p>This role might be for you if:</p><ul><li><p>You have Drug Substance/API manufacturing experience in Antibody Drug Conjugates (ADCs)/ other bioconjugate modalities (peptides, Peptides, Synthetic Oligonucleotides, or Monoclonal Antibodies.</p></li></ul><ul><li><p>You have Sterile Drug Product filling experience.</p></li><li><p>You thrive in environments where the scope is broad, the problems are ambiguous, and the expectation is that you build structure.</p></li><li><p>You communicate with influence; you can align a CMO executive and a QA investigator in the same week without changing who you are.</p></li></ul><ul><li><p>You are comfortable with travel to CMO/Partner sites as required (approximately 10–25%).</p></li></ul><ul><li><p>You have led, or are ready to lead, direct reports or cross-functional teams</p></li></ul><ul><li><p>You enjoy leading continuous improvements, system implementations and/or strategy development to reduce cycle times and improve efficiencies for area.</p></li></ul><p>To be considered for the Staff Specialist of External Manufacturing, a BS/BA in business or scientific discipline and 10 years of related experience in either cGMP manufacturing operations (clinical and/or commercial) or supplier management or equivalent combination of education and experience.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$108,000.00 - $176,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 10:56:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Study Associate Manager (CSAM)]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45359]]></requisitionid>
    <referencenumber><![CDATA[R45359]]></referencenumber>
    <apijobid><![CDATA[r45359]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45359/clinical-study-associate-manager-csam/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Armonk]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Associate Manager Clinical Study</strong> (CSAM) role supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct execution versus oversight of CROs deliverables will vary accordingly. The Assoc Mgr Clinical Study works with the study team internally and externally with vendors such as CROs in feasibility, planning, initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and Regeneron Standard Operating Procedures (SOPs). Travel to study sites may be required to assist with monitoring clinical studies.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the study</li><li>Contributes to risk assessment and helps identify risk mitigation strategies</li><li>Supports feasibility assessment to select relevant regions and countries</li><li>Oversees and provides input to the development of study specific documentation including but not limited to: case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc.</li><li>Reviews site level informed consents and other patient-facing study start-up materials</li><li>Oversees setting up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and Trial Master File (TMF) Contributes to investigator meeting preparation and execution</li><li>Oversees engagement, contracting and management of required vendors for the study</li><li>Oversees and provides input to study drug and clinical supplies forecasting, drug accountability and drug reconciliation</li><li>Provides regular status reports to stakeholders as requested by the Clinical Study Lead</li><li>Contributes to development of and oversees implementation of recruitment and retention strategies</li><li>Monitors recruitment and retention</li><li>Monitors progress for site activation and monitoring visits</li><li>Supports data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites</li><li>Escalates data flow and data quality issues to Clinical Study Lead</li><li>Oversees the execution of the specific clinical study deliverables against planned timelines</li><li>Escalates issues related to timelines or budget to Clinical Study Lead</li><li>Supports accurate budget management and scope changes</li><li>Contributes to clinical project audit and inspection readiness throughout the study lifecycle</li><li>Supports internal and external inspection activities and contributes to CAPAs as required</li><li>Manages aspects of study close-out activities including but not limited to database lock, reconciliation of vendor contract, study budget, TMF and study drug accountability</li><li>May be responsible for mentoring clinical trial management staff </li><li>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</li></ul><p><strong>In order to be considered qualified for this role, </strong>a minimum of Bachelor's degree and 4+ years of relevant clinical trial expereince is required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 13:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, QA Validation Oversight]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43170]]></requisitionid>
    <referencenumber><![CDATA[R43170]]></referencenumber>
    <apijobid><![CDATA[r43170]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43170/manager-qa-validation-oversight/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div><div><div><p>Regeneron is hiring a Manager, QA Validation Oversight to lead a team dedicated to ensuring the integrity of our process validation processes. This role is integral in supporting process validation activities, ensuring global consistency, addressing recurring themes in process documentation, and playing a pivotal role in regulatory inspections and compliance. </p></div><div></div><div><p>In this role, a typical day might include the following: </p></div><div><ul><li><p>Ensuring alignment between validation activities and Process Sciences initiatives to support successful transition of processes from development to manufacturing. </p></li></ul></div><div><ul><li><p>Collaborate closely with internal Process Sciences team to provide technical expertise and ensure consistency in Process Validation strategies. </p></li></ul></div><div><ul><li><p>Presenting/defending validation strategies, documentation, and processes to FDA and other regulatory agencies. </p></li></ul></div><div><ul><li><p>Reviewing and approving process validation documents, procedures, and protocols, proposing modifications and corrections where necessary to meet regulatory requirements and expectations. </p></li></ul></div><div><ul><li><p>Overseeing all aspects of QA Validation including review and approval of failure investigations, change controls, SOPs, Validation protocols and summary reports, and validation master plans. </p></li></ul></div><div><ul><li><p>Conduct one-on-one discussions with team members to review their performance feedback and set development goals, fostering professional growth within the team. </p></li></ul></div><div></div><div><p>This role might be a for you if you: </p></div><div><ul><li><p>Bring hands-on validation experience in a GMP-regulated environment. </p></li></ul></div><div><ul><li><p>Possess deep understanding and expertise in Process Validation. </p></li></ul></div><div><ul><li><p>Enjoy building strong, collaborative relationships across global internal teams. </p></li></ul></div><div><ul><li><p>Have a continuous improvement mindset. </p></li></ul></div><div><ul><li><p>Are an experienced leader who inspires and guides a multi-tiered team. </p></li></ul></div><div></div><div><p>To be considered for this role, you must hold a Bachelor’s degree in Engineering, Chemistry, or Life Sciences degree and the following minimum years of experience for each level: </p></div><div><ul><li><p>Associate Manager: 6+ years </p></li></ul></div></div><div><div><ul><li><p>Manager: 7+ years </p></li></ul></div><div></div><div><p>May substitute relevant experience in lieu of education requirement. Level is determined on qualifications relevant to the role. </p></div><div></div><div><p>#REGNQA </p></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$90,800.00 - $173,400.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Development  AI Engineer]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43611]]></requisitionid>
    <referencenumber><![CDATA[R43611]]></referencenumber>
    <apijobid><![CDATA[r43611]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43611/senior-manager-global-development-ai-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Global Development (GD) is embarking on a digital transformation project that will incorporate AI, machine learning, and automation into our processes to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. This position will play a key role in developing the platforms, processes and technologies that will incorporate AI effectively across GD. The AI engineer will work with a team of engineers and scientists to help bring transformative change to GD. The role will encompass a wide range of AI/ML-related activities, from data engineering and technical development to optimizing vendor systems for use at Regeneron to mentoring colleagues in best practices for adopting and AI in their everyday workflows. Development will not necessarily be limited to the use of generative AI, but may also include technical implementation of machine learning models, natural language processing, and other approaches. The engineer will work with stakeholders across GD and other groups to develop solutions and architectures that addresses our needs and integrate into the overall corporate strategy.</p><p><strong>As a Senior Manager, a typical day may include: </strong></p><ul><li><p>Implement, and refine novel algorithms and scalable AI /ML solutions tailored to GD applications such as clinical trial design, regulatory intelligence, patient identification and stratification, etc. Deploy these solutions to production environments as appropriate Implementation includes hands-on development and coding.</p></li><li><p>Develop, implement, and improve data architecture and engineering approaches for diverse data sources across GD</p></li><li><p>Contribute to initiatives with GDIT and enterprise IT to build the necessary infrastructure (software and hardware) to support advanced analytics</p></li><li><p>Collaborate with GD colleagues to help them approach AI/ML more effectively</p></li><li><p>Establish rigorous validation frameworks for AI models and monitor existing models for accuracy and efficiency</p></li><li><p>Stay up to date with the latest advances in the field and, as appropriate, evaluate them for adoption at Regeneron</p></li></ul><p><br><strong>This may be for you if you:</strong></p><ul><li><p>Can demonstrate expertise in AI And ML</p></li><li><p>Want to make an impact on patient lives</p></li><li><p>Are actively developing your skills in AI and ML</p></li><li><p>Capable of communicating to a technical and non-technical audience. </p></li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>Deep understanding of generative AI, machine learning, natural language processing, and statistical modeling</p></li><li><p>Deep expertise in programming (Python, R, etc.), with a focus on applying advanced technical skills to data analysis, pipeline creation, automation, and software development</p></li><li><p>Expertise in database platforms and cloud computing infrastructure</p></li><li><p>Track record of model development, implementation to scale, maintenance, and evaluation in a healthcare of life sciences setting</p></li><li><p>Experience managing and analyzing large-scale clinical datasets</p></li><li><p>Excellent communication skills, both technical and non-technical</p></li><li><p>Experience managing multiple projects</p></li><li><p>Experience working in cross-functional teams</p></li><li>May require travel up to 20%</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 09:26:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Global Finance Operations & Technology]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46449]]></requisitionid>
    <referencenumber><![CDATA[R46449]]></referencenumber>
    <apijobid><![CDATA[r46449]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46449/director-global-finance-operations-technology/]]></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 <strong>Director, Global Finance Operations & Technology</strong> is a leader who combines strong operational execution with strategic leadership to advance Regeneron’s global finance transformation agenda. This role sits between tactical delivery and enterprise strategy—owning critical finance technology initiatives, leading global process modernization, and shaping a scalable, data‑driven finance ecosystem.</p><p>The Director is expected to be hands‑on where needed, while also setting direction, influencing stakeholders, and leading cross‑functional teams across regions. This role plays a key part in translating finance strategy into executable solutions that improve efficiency, compliance, and insight generation.</p><p><em><strong>This role will require 4 days per week onsite at our Campus in Sleep Hollow, NY. This is not available as a fully remote / hybrid work.</strong></em></p><p><strong>A typical day may include:</strong></p><ul><li><p>Lead and deliver major global finance technology initiatives, including Oracle Fusion, automation, and advanced analytics programs.</p></li><li><p>Design and implement standardized global finance operations frameworks that balance enterprise consistency with regional requirements.</p></li><li><p>Provide operational leadership across core finance processes, ensuring accuracy, compliance, and continuous improvement.</p></li><li><p>Drive adoption of cloud platforms, AI, and automation by partnering closely with Finance, IT, HR, and other business functions.</p></li><li><p>Serve as a key liaison between business stakeholders and technology teams to translate requirements into scalable solutions.</p></li><li><p>Own finance data enablement efforts, including master data governance, metadata management, and data quality improvements.</p></li><li><p>Develop actionable insights from operational and financial data to support senior leadership decision‑making.</p></li><li><p>Identify process gaps, risks, and control issues; implement remediation plans to strengthen governance and compliance.</p></li><li><p>Mentor and develop managers and senior individual contributors, building digital fluency and operational excellence across the organization.</p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p><strong>Finance Technology & Transformation Leadership:</strong> Ability to bridge strategy and execution across finance systems and operations.</p></li><li><p><strong>Global Systems Expertise:</strong> Experience supporting multi‑country finance platforms and operating models.</p></li><li><p><strong>ERP & Cloud Platforms:</strong> Hands‑on experience with modern ERP solutions (e.g., Oracle Fusion, Workday) and cloud‑native technologies.</p></li><li><p><strong>Data & Analytics Enablement:</strong> Experience building dashboards, operational metrics, and insight‑driven reporting capabilities.</p></li><li><p><strong>Architecture & Integration:</strong> Working knowledge of finance system architecture, integrations, and data flows.</p></li><li><p><strong>Change & Talent Development:</strong> Passion for building high‑performing teams and fostering a culture of innovation and continuous improvement.</p></li></ul><p><strong>To be considered for this role you must possess:</strong></p><ul><li><p>Bachelor’s degree in Finance, Accounting, Information Systems, or related field; MBA preferred</p></li><li><p><strong>10+ years</strong> of progressive experience in finance operations, finance technology, or large‑scale transformation initiatives.</p></li><li><p>Demonstrated success delivering global ERP implementations, automation programs, or finance modernization efforts.</p></li><li><p>Strong understanding of end‑to‑end finance processes, shared services models, and regulatory/compliance frameworks.</p></li><li><p>Proven ability to lead cross‑functional, multinational teams in complex environments.</p></li><li><p>Excellent communication, stakeholder management, and change leadership skills.</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[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 11:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Commercial Finance]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46819]]></requisitionid>
    <referencenumber><![CDATA[R46819]]></referencenumber>
    <apijobid><![CDATA[r46819]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46819/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>This role leads Commercial Financial Planning & Analysis (FP&A) consolidation activities for monthly close and quarterly forecasts, ensuring a single source of truth across brands, functions, and geographies. In addition to core consolidation responsibilities, the role will help drive standardization and automation across commercial finance. The Senior Manager sets cadence, standards, and systems discipline to deliver accurate, timely, and insight-driven outputs for decision-making.</p><p><strong>A day in the life may look like:</strong></p><p>• Own end-to-end consolidation of monthly actuals and forecast updates for the Commercial organization</p><p>• Govern calendars, milestones, templates, and submission protocols to drive accountability and on-time deliverables</p><p>• Standardize definitions and mappings for revenue, GTN components, OpEx categories, and headcount across brands and geographies</p><p>• Review, challenge, and synthesize brand and functional submissions; ensure alignment with corporate guidance and macro assumptions</p><p>• Deliver executive-ready materials: bridges, variance analyses, trend diagnostics, and scenario views</p><p>• Partner with Corporate FP&A and Accounting on close deliverables, accrual processes, and policy alignment</p><p>• Lead rapid-turnaround ad hoc analyses for Finance and Commercial leadership, translating ambiguous asks into structured scenarios that quantify revenue and P&L impacts across GTN, pricing and contracting strategies, channel inventory dynamics, and forecast sensitivities</p><p>• Deliver concise, executive-ready options with assumptions, risks, and recommendations</p><p><strong>This may be the right role for you if you:</strong></p><p>• Drive automation of recurring reporting, dashboards, and forecast quality checks; partner with IT on enhancements and UAT</p><p>• Define model structures, hierarchies, and master data standards that enable efficient consolidation and flexible scenario planning</p><p>• Identify and implement improvements that shorten cycle time, reduce errors, and improve insights</p><p><strong>To be considered for this role</strong>, <strong>you must have:</strong></p><p>• 7+ years of experience, preferably in a pharmaceutical/biotech environment with a US-listed public company or exposure through Big 4 service engagements</p><p>• Knowledge of generally accepted accounting principles, financial reporting and analysis, and compliance</p><p>• Extensive knowledge of ERP/Planning tools is required; Oracle/Hyperion a plus</p><p>• Hands-on experience with BI tools in Finance is highly preferred (MS Power BI, Tableau, etc.)</p><p>• Experience with driving standardization and automation in finance is highly preferred</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[QA Investigation Specialist]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43465]]></requisitionid>
    <referencenumber><![CDATA[R43465]]></referencenumber>
    <apijobid><![CDATA[r43465]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43465/qa-investigation-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Rensselaer]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a QA Investigation Specialist position with our Bulk Drug Substance Manufacturing Quality Assurance team. This position performs all compliance related tasks vital to complete investigations and implementation of robust corrective actions for supporting manufacturing operations.<br><br>In this role, a typical day might include the following:</p><ul><li><p>Independently investigating non conformances and preventing reoccurrences in support of manufacturing operations</p></li><li><p>Preparing investigation reports that include recommendations on investigation findings for medium/high severity non conformances</p></li><li><p>Analyzing and evaluating information captured through investigations, summarizes information and trends in investigation reports</p></li><li><p>Communicating findings and recommendations at group meetings</p></li><li><p>Reviewing completed batch records and logbooks in accordance with cGMP standards in support of investigations</p></li><li><p>Reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures</p></li><li><p>Monitoring production processes to acquire vital data in support of investigations and track efficiency of changes</p></li><li><p>Participating in and/or leading cross-functional study teams to get results, support and or author investigations</p></li><li><p>Gathering, trending, and analyzing process related data to drive consistency and timeliness</p></li><li><p>Documenting all training</p></li><li><p>Training new employees on investigative processes and techniques</p></li><li><p>Coordinating and/or leading cross-functional meetings with multiple departments</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Have an understanding of biologics manufacturing operations</p></li><li><p>Are organized and have an attention to detail</p></li><li><p>Can prioritize multiple assignments and changing priorities</p></li><li><p>Are able to learn and utilize computerized systems for daily performance of tasks</p></li></ul><p>Gowning and Environment:</p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA) </p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire </p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree in Life Sciences, Engineering, or related field and the following minimum amounts of relevant experience for each level:</p><ul><li><p>Associate Specialist – 0-2 years</p></li><li><p>Specialist – 2+ years</p></li><li><p>Senior Specialist – 5+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$59,700.00 - $126,800.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Corporate Counsel - Privacy/ Transactions]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47353]]></requisitionid>
    <referencenumber><![CDATA[R47353]]></referencenumber>
    <apijobid><![CDATA[r47353]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47353/senior-director-corporate-counsel-privacy-transactions/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Cambridge]]></city>
    <state><![CDATA[Massachusetts]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>Regeneron Pharmaceuticals is seeking a highly experienced transactions attorney for a pivotal role to serve as a transactional attorney and liaison to the Regeneron Data Privacy Office. This position will act as a privacy expert within the Transactions & Contracts team offering guidance to colleagues on privacy law and ensuring that privacy provisions are seamlessly integrated into our contracts. The position also involves drafting, reviewing, negotiating, and providing strategic counsel on a diverse portfolio of significant agreements across our innovative business units, overseeing the operations of Regeneron’s contract lifecycle management system, including managing the group’s Associate Director, Contracts and Systems Operations.</p></div><div><div><div><div><div><div><div><div><div><p>Your expertise will be instrumental in advising the Transactions Team on complex privacy issues, requiring a deep understanding of life sciences, business transactions, and data privacy. We are looking for a candidate with exceptional drafting and negotiation skills, life sciences law expertise, leadership capabilities and a proven track record of progressive experience in contract law and data privacy. The ideal candidate thrives in collaborative settings, working alongside multiple stakeholders to provide comprehensive legal solutions that drive Regeneron's success.</p><p><em><strong>The role will be based onsite at our offices in Cambridge, MA or Sleepy Hollow, NY. This is not open to fully remote-based work arrangements. If eligible, we can offer relocation benefits. </strong></em></p><p><br><strong>A typical day might include the following:</strong></p><ul><li><p>Providing legal support for a particular area of business transactions, which may include research collaboration agreements, master services agreements, consulting services agreements, license agreements, data use agreements, laboratory services agreements and confidentiality agreements, among others.</p></li><li><p>Maintaining subject matter expertise in data privacy laws and the Regeneron privacy policies and advising Transaction Law colleagues and clients on developments of importance.</p></li><li><p>Providing ongoing one-on-one support to members of the Transaction Law team and coordinating with internal teams and external resources to negotiate and finalize data privacy language in third-party agreements.</p></li><li><p>Responding to U.S. and ex-U.S. contracting questions.</p></li><li><p>Managing updates to the group’s data privacy contracting playbook.</p></li><li><p>Creating data privacy contracting tools and training materials.</p></li><li><p>Managing office hours with internal business partners.</p></li><li><p>Developing and training on privacy contracting tools and requirements.</p></li><li><p>Acting as liaison for the Transactions Law Group with the Data Privacy Office on data privacy policy questions and approaches.</p></li><li><p>Providing strategic direction and oversight for Regeneron’s contract lifecycle management system, including serving as the manager of the team’s Associate Director, Contracts Systems and Operations.</p></li><li><p>Providing contract law support for the Regeneron Cell Medicines team in Cambridge.</p></li></ul><p><br><strong>This role might be for you if:</strong></p><ul><li><p>You have the ability to work independently, while meeting aggressive deadlines and juggling multiple matters.</p></li><li><p>You are able to maintain an objective perspective while developing and maintaining strong partnerships with key stakeholder / client organizations and protecting Regeneron’s interests.</p></li><li><p>You are an effective leader and can work effectively and professionally with colleagues and clients at all levels of the organization and in a collaborative, team-oriented environment.</p></li><li><p>You have the ability to effectively convey to, and respond to questions from, colleagues and key stakeholders, on data privacy law and other general legal concepts. </p></li></ul><p><br><strong>To be considered for this position</strong> you must possess a JD with excellent law school credentials. Licensed to practice law in New York or be eligible for licensure as a registered in-house counsel is preferred. At least 15 years of legal experience at a law firm and/or in-house, with biotech/pharmaceutical and/or health care experience. Solid understanding of contracts and related law. Experience with contracts involving data privacy and intellectual property. Experience in strategic leadership of contract management systems or similar role is preferred. You should also have a high level of business acumen, excellent contract drafting and negotiation proficiency, exceptional oral and written communication skills and interpersonal and conflict resolution capability.</p></div></div></div></div></div></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$242,000.00 - $403,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 19:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Ophthalmology Account Director (OAD) Mid-Atlantic]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47306]]></requisitionid>
    <referencenumber><![CDATA[R47306]]></referencenumber>
    <apijobid><![CDATA[r47306]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47306/ophthalmology-account-director-oad-mid-atlantic/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Ophthalmology Account Director (OAD) will represent the entire Regeneron ophthalmology product portfolio. The OAD connects to the key business decision-makers and all other relevant Key Opinion Leaders (KOLs) within their assigned accounts and will be a critical liaison between their customers and Regeneron. Leveraging their account and contract management capabilities, the OAD will be required to lead and appropriately educate and influence customers including large provider practices and private equity groups, as well as internal audiences including senior Regeneron Market Access, Brand and Executive leadership teams.</p><p>Working in the context of an integrated account business plan, the OAD will play an important account management role working both independently and closely with the ED Ophthalmology Accounts to educate on, administer, and pull-through provider contracts as well as other partnership opportunities targeted at financial, operational, and other relevant business decision-makers and their teams. The OAD will be an expert in customer engagement and contract management and will work closely with other Regeneron internal team members within Market Access and the Brand sales force.</p><p>Additionally, OADs will have a strong understanding of the customer healthcare environment and will play a pivotal role not only in effective customer and contract education and management, but also in navigating both the external complexity and the internal dynamics of product and customer priorities. The OAD will represent current and potentially future contracted ophthalmology products within their customer base and provide relevant customer feedback to internal stakeholders and leadership in a timely manner.</p><p><strong>In this role, a typical day includes: </strong></p><ul><li>MBO Driven, customer facing role</li><li>Focused on maximizing customer executive engagement, reach and frequency, and contract education and pull-through efforts within assigned customers and geography to help customers and patients understand the GPO contracts</li><li>Works collaboratively as a partner with Sales, Marketing, Reimbursement, and other internal colleagues to appropriately and efficiently develop and execute account plans for assigned customers within their assigned geography</li><li>Seeks to maximize depth of customer engagements by identifying, engaging, and educating all relevant audiences at the customer about the GPO program including as appropriate C-suite, KOLs, and business and reimbursement staff</li><li>Thoroughly explains quarterly GPO program changes, if any, to customers</li><li>Delivers regular contract performance updates to customers</li><li>Performs quarterly business reviews with customers</li><li>Seeks customer feedback on the Regeneron GPO program and shares with Market Access and Brand leadership</li><li>Looks for opportunities to engage customers at regional and national retinal meetings</li><li>Fully understands other elements of customer considerations such as payer mix, ensure customer awareness of existing inventory levels, operational challenges, and reimbursement dynamics</li><li>Spends 75% of time in customer facing activities, prioritizing in-person meetings when possible</li></ul><p><strong>To be considered for this role you must have</strong></p><ul><li><p>10-12 years of "progressive" industry/relevant professional experience</p></li><li><p>10+ years of pharmaceutical/biotech or related experience</p></li><li><p>Additional broad-based experience valued: sales operations, corporate partnerships, marketing, and/or sales management, and/or supply chain.</p></li><li><p>Previous experience in launching new Specialty Pharmaceutical/Biologics products or indications. Proven knowledge and relationships with key Executive level decision makers from retina and other market GPOs and institutional trade partners. Prior retina account or brand experience. Demonstrated ability to work collaboratively with and influence peers and management. Demonstrated communication skills, including presentation, negotiation and content development. Demonstrated results orientation. Demonstrated strategic planning capabilities, including event planning and meeting facilitation. Understanding of financial concepts and contracting issues and demonstrated ability to measure contract performance. Demonstrated outsourced vendor management skills.</p></li><li><p>Ability to travel 50-75%, including weekends as necessary.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Biostatistics - Medical Affairs]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47321]]></requisitionid>
    <referencenumber><![CDATA[R47321]]></referencenumber>
    <apijobid><![CDATA[r47321]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47321/manager-biostatistics-medical-affairs/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Manager, Biostatistics to join our team! This individual will be responsible for statistical support for oncology compounds within Medical Affairs.</p><p><strong> </strong></p><p><strong>In this role, a typical day may include:</strong></p><p>As part of a collaborative medical affairs team, you will implement the statistical function’s role in the oncology compounds’ medical impact plans. Together with medical directors, HEOR, medical writing, market access, and other colleagues within medical affairs, you will plan and execute evidence generation efforts, such as post-hoc analysis with innovative analytical approaches, respond to payer and reimbursement needs, review investigator initiated studies, and design and execute Phase IV studies as the study biostatistician, and ensure statistical rigor in all these duties. You will also work with fellow clinical development biostatisticians and programmers to deep dive into the clinical trial data for comprehensive understanding. You will be responsible for following departmental guidelines of collaboration, innovation, and intrinsic motivation. Working in a dynamic team with a wide range of interfaces, the role requires both strategic and operational skills combining innovative statistical thinking with a strong sense of business acumen, and excellent communication and interpersonal skills. Your manager will work with you to manage stakeholders, learn about oncology and the company’s compounds, develop Regeneron cultural understanding, and general industry knowledge.</p><p><strong> </strong></p><p><strong>This role might be for you if you have:</strong></p><ul><li><p>Strong interest and motivation in exploring existing clinical trial data for post-hoc analysis and innovative idea investigations</p></li><li><p>Experience with clinical trial design, including observational studies</p></li><li><p>Exposure to oncology study endpoints and analysis techniques</p></li><li><p>Strong communication skills to interpret, explain, and discuss results of complex statistical concepts and analyses to both technical and non-technical audiences.</p></li><li><p>Desire to present and share results with internal and external stakeholders.</p></li><li><p>Comfort with providing scientific/statistical input into study design, formulating novel methods to problem solving, and independently developing the statistical analysis plan to implement those solutions.</p></li><li><p>Authored Statistical Analysis Plans (SAP) and Protocols</p></li><li><p>Generated tables, listings, and figures for external communication use in publications/presentations and for internal purposes.</p></li><li><p>Ability translate and apply relevant innovative statistical methodology to everyday work.</p></li><li><p>Educate and disseminate knowledge throughout the organization for areas within the expertise of medical affairs.</p></li></ul><p><strong> </strong></p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>PhD / DrPH in statistics/biostatistics or related disciplines with >2 years experience in the pharmaceutical/biotech industry or MS degree in statistics/biostatistics with >7 years’ experience in the pharmaceutical industry as a statistician. </p></li><li><p>Knowledge of drug discovery/development/life cycle management(LCM) and ability to integrate statistical concepts into drug discovery/development/LCM strategies</p></li><li><p>Prior experience or knowledge of oncology is strongly preferred</p></li><li><p>Excellent influence and leadership skills, and a demonstrated ability to collaborate in a cross-functional environment. </p></li><li><p>Demonstrated critical thinking skills, time management skills, and effective communication skills.</p></li><li><p>Solid knowledge of statistical analysis methodologies, experimental and clinical trial design</p></li><li><p>Ability to write code in at least one common statistical software is required (i.e. SAS, R, Python). Ability to read SAS code is required</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 15:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Clinical Study Associate Manager (CSAM)]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44482]]></requisitionid>
    <referencenumber><![CDATA[R44482]]></referencenumber>
    <apijobid><![CDATA[r44482]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44482/clinical-study-associate-manager-csam/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Associate Manager Clinical Study</strong> (CSAM) role supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. This role applies to internally sourced studies and studies outsourced to Clinical Research Organizations (CROs) and the balance of direct execution versus oversight of CROs deliverables will vary accordingly. The Assoc Mgr Clinical Study works with the study team internally and externally with vendors such as CROs in feasibility, planning, initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and Regeneron Standard Operating Procedures (SOPs). Travel to study sites may be required to assist with monitoring clinical studies.</p><p><strong>A typical day in this role looks like:</strong></p><ul><li>May lead/oversee the planning and management of a clinical study in an assigned region(s) in alignment with the global study plans and may contribute to global planning and management of the study</li><li>Contributes to risk assessment and helps identify risk mitigation strategies</li><li>Supports feasibility assessment to select relevant regions and countries</li><li>Oversees and provides input to the development of study specific documentation including but not limited to: case report form (CRF), data management plan, monitoring plan, monitoring oversight plan, etc.</li><li>Reviews site level informed consents and other patient-facing study start-up materials</li><li>Oversees setting up and maintenance of study systems including but not limited to Clinical Trial Management System (CTMS) and Trial Master File (TMF) Contributes to investigator meeting preparation and execution</li><li>Oversees engagement, contracting and management of required vendors for the study</li><li>Oversees and provides input to study drug and clinical supplies forecasting, drug accountability and drug reconciliation</li><li>Provides regular status reports to stakeholders as requested by the Clinical Study Lead</li><li>Contributes to development of and oversees implementation of recruitment and retention strategies</li><li>Monitors recruitment and retention</li><li>Monitors progress for site activation and monitoring visits</li><li>Supports data quality including regular review of data metrics and listings, protocol deviations, eligibility violations, dosing deviations and suspected non-compliance by sites</li><li>Escalates data flow and data quality issues to Clinical Study Lead</li><li>Oversees the execution of the specific clinical study deliverables against planned timelines</li><li>Escalates issues related to timelines or budget to Clinical Study Lead</li><li>Supports accurate budget management and scope changes</li><li>Contributes to clinical project audit and inspection readiness throughout the study lifecycle</li><li>Supports internal and external inspection activities and contributes to CAPAs as required</li><li>Manages aspects of study close-out activities including but not limited to database lock, reconciliation of vendor contract, study budget, TMF and study drug accountability</li><li>May be responsible for mentoring clinical trial management staff </li><li>May be assigned unmasked tasks for studies, which may include but is not limited to, assisting with masked investigational product, set up and management of unmasked trial master file, review of unmasked data in the electronic data capture system, point of contact for IVRS issues, and support oversight of unmasked clinical monitoring</li></ul><p><strong>In order to be considered qualified for this role, </strong>a minimum of Bachelor's degree and 4+ years of relevant clinical trial expereince is required.<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 11:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Senior Manager, Commercial Operations]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44875]]></requisitionid>
    <referencenumber><![CDATA[R44875]]></referencenumber>
    <apijobid><![CDATA[r44875]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44875/temporary-senior-manager-commercial-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Amsterdam]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Netherlands]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager Commercial Operations (Contractor) drives data‑led decision‑making across Commercial Operations by developing and delivering business intelligence strategies, leading analytics projects, and translating sophisticated data into actionable insights.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Lead the build and execution of strategies in partnership with Commercial Operations, Sales, Marketing, and external partners.</p></li><li><p>Scope and handle analytics projects that extract, integrate, and analyze customer and market data from multiple sources to answer strategic and tactical business questions.</p></li><li><p>Own and improve critical commercial tools and platforms, ensuring high data quality, reliability, and usability.</p></li><li><p>Conduct sophisticated analyses to identify performance trends, generate insights, and advise resource allocation, channel mix, and sales force efficiency.</p></li><li><p>Define, track, and communicate critical metrics and leading indicators across teams; maintain dashboards and reporting cadences for collaborators and senior leadership.</p></li><li><p>Deliver clear, compelling presentations and insight narratives that influence decision‑making and drive action.</p></li><li><p>Ensure compliance with corporate policies, privacy, and data governance standards; implement controls and documentation for reproducibility and audit readiness.</p></li><li><p>Collaborate with IT and global analytics teams to build scalable data solutions, automate data pipelines, and modernize analytics products.</p></li><li><p>Support forecasting, segmentation, and targeting initiatives using sophisticated modeling and experimentation techniques.</p></li><li><p>Partner with alliance and above‑market teams to harmonize definitions, share standard processes, and enable consistent measurement across regions.</p></li><li><p>Establish analytics SOPs, playbooks, and reviewer guides; standardize code, QA processes, and release management for dashboards and models.</p></li><li><p>Proactively identify issues, risks, and data gaps; recommend pragmatic solutions and secure alignment across cross‑functional collaborators.</p></li></ul><p><strong>This Role Might Be for You If You Have:</strong></p><ul><li><p>Experience leading commercial analytics and business intelligence initiatives from concept through deployment and adoption.</p></li><li><p>Hands‑on expertise with CRM and marketing platforms (e.g., Veeva CRM, PromoMats) and modern BI tools (e.g., Power BI, Tableau, Qlik) to build and scale dashboards.</p></li><li><p>Strong proficiency in data wrangling and analysis (e.g., SQL and one or more of Python or R), and familiarity with data modeling and automation practices.</p></li><li><p>methodologies to support sales and marketing planning.</p></li><li><p>Deep understanding of data governance, privacy, and compliance principles; comfortable working with cross‑functional IT, Data, and Compliance partners.</p></li><li><p>Excellent storytelling, presentation, and collaborator leadership skills; ability to translate analytics into clear business recommendations.</p></li><li><p>A track record of building collaboration across matrixed teams and influencing without direct authority.</p></li><li><p>This role is a 12-month contract.</p></li></ul><p><strong>To Be Considered:</strong><br>You bring a bachelor’s degree in a quantitative or relevant field with 8+ years of relevant experience, with at least 5+ in pharmaceutical or life‑science.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 05:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Project Engineer]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47032]]></requisitionid>
    <referencenumber><![CDATA[R47032]]></referencenumber>
    <apijobid><![CDATA[r47032]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47032/principal-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[<p>We are looking for an experienced Engineer to join our growing Project Engineering team. Our team designs, specifies and commissions new and renovated biopharmaceutical process and clean utility equipment. We provide engineering support and lead deviation investigations for existing equipment and manufacturing processes to support the production of our life-changing medications.</p><p>As a Principal Project Engineer, a typical day might include the following:</p><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls including development and review of engineering documentation</li><li>Managing mid-to-large sized projects related to process equipment and clean utilities including start-up and commissioning</li><li>Leading the design review, site acceptance and installation of equipment</li><li>Preparing piping and instrumentation diagrams and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting QA/Validation department by preparing design documents and assisting in protocol execution</li><li>Assisting in investigations of process equipment, utility systems, and control system anomalies, as well as safety incidents</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations and test plans for executing modification change control documentation</li><li>Supervising mechanical, electrical, and automation and engineering contractors</li><li>Traveling up to 10% of the time, both domestically and internationally</li></ul><p>This position might be for you if you:</p><ul><li><p>Are interested in having a broad scope with a variety of tasks, seeing the entire process, not just specific equipment or processes</p></li><li>Enjoy solving puzzles and challenges, supporting investigations across the business</li><li>Have a desire to contribute to elements of design work by helping to specify and translating customer needs into equipment</li><li>Want to do more than just project management or troubleshooting, balancing your technical and project management skills</li><li>Have a solid understanding of process control systems and automation</li><li>Are skilled at planning and tracking project activities and schedules</li><li>Are thoroughly knowledgeable with engineering documentation required for cGMP process equipment as well as sanitary equipment design requirements</li><li>Have working knowledge of biopharmaceutical equipment</li><li>Have demonstrated strengths with strong interpersonal, cross-cultural communication</li><li>Are adept at building and maintaining relationships and leading without direct authority</li><li>Show resiliency and flexibility in the face of challenging situations</li></ul><p>Qualified candidates must have a Bachelor's degree Chemical Engineering or Biochemical Engineering (or another relevant Engineering discipline) and the following minimum years of experience in project/process engineering or an equivalent combination of education and experience. Direct experience with biopharmaceutical process equipment is preferred.</p><ul><li>Senior Project Engineer: 5+ years</li><li>Principal Project Engineer: 8+ years</li></ul><p>Level will be determined based on qualifications relevant to the role. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Facilities Compliance Specialist (Technical Writer)]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46956]]></requisitionid>
    <referencenumber><![CDATA[R46956]]></referencenumber>
    <apijobid><![CDATA[r46956]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46956/facilities-compliance-specialist-technical-writer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to add a Facilities Compliance Specialist (Technical Writer) to our growing team. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Facilities Compliance Specialists ensure cGMP compliance for the Facilities Management Department.</p><p><br>As a Facilities Compliance Specialist, a typical day might include the following:</p><ul><li>Facilitating creation, review and revision of Facilities Department related Standard Operating Procedures, Work Instructions, Risk Assessments, and ILCs, Job Aids for each group within the Department</li><li>Acting as a liaison between the Facilities Department and onsite quality and regulatory groups to define and address all issues of non-compliance</li><li>Managing and participating in Facilities Department issues of non-compliance to ensure all activities related to the investigation and resolutions of non-conformities are performed in a timely manner and in compliance with Regeneron procedures and regulatory requirements</li><li>Supporting development of CAPAs</li><li>Owning Change Controls</li><li>Managing and providing support, information, and assistance to individuals and groups with the initiation, review, submission, and follow-up of documents related to Change Controls and Corrective and Preventive Action plans</li><li>Participating in, and obtaining results of, all Facilities Department quality and regulatory audits</li><li>May oversee contractors</li></ul><p>This role might be for you if you: </p><ul><li>Have technical writing experience in a manufacturing environment, pharmaceutical industry preferred</li><li>Can prioritize multiple assignments and changing priorities in a fast-paced environment</li><li>Have experience with Veeva</li><li>Have knowledge of:<ul><li>CFR Part 11 and conformance requirements for data integrity</li><li>Regulations pertaining to asset maintenance, cleaning and operational control, asset lifecycles,</li><li>Annex 11 regulations</li></ul></li><li>Have an understanding of equipment and terminology used in a manufacturing operation</li><li>Are organized and have an attention to detail</li><li>Excel in a collaborative, cross functional environment </li></ul><p>To be considered for this role you must hold a Bachelor’s degree and the following minimum amounts of relevant experience for each level:</p><ul><li>Associate Specialist: 1+ year</li><li>Specialist: 2+ years</li><li>Senior Specialist: 5+ years</li></ul><p>Level will be determined based on qualifications relevant to the role</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$62,355.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 16:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager Payroll Service Delivery]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47441]]></requisitionid>
    <referencenumber><![CDATA[R47441]]></referencenumber>
    <apijobid><![CDATA[r47441]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47441/associate-manager-payroll-service-delivery/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. We continue to strengthen our global payroll and finance capabilities to support accuracy, compliance, and consistent employee experience.</p><p>As an Associate Manager – Payroll Service Delivery, you will support accurate, compliant, and timely payroll delivery across multiple countries within Regeneron’s Global Capability Center. You will work closely with Payroll, HR, Finance, and external vendors to support end‑to‑end payroll operations, maintain strong controls, and contribute to process standardization and service improvement.</p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Support day‑to‑day international payroll operations across assigned countries</p></li><li><p>Review payroll inputs, validations, audit checks, reconciliations, and approval workflows</p></li><li><p>Coordinate with external payroll vendors to support timely delivery and issue resolution</p></li><li><p>Partner with HR and Finance teams to ensure payroll data accuracy and completeness</p></li><li><p>Monitor payroll variances and highlight observations for follow‑up</p></li><li><p>Support payroll accounting activities and alignment with month‑end close processes</p></li><li><p>Ensure adherence to payroll controls, governance standards, and regulatory requirements</p></li><li><p>Track regulatory or statutory changes and coordinate updates with internal teams and vendors</p></li><li><p>Prepare documentation, reports, and data to support internal and external audits</p></li><li><p>Maintain and update payroll standard operating procedures and process documentation</p></li><li><p>Support process improvement, standardization, and system optimization initiatives</p></li><li><p>Guide and support payroll operations analysts in day‑to‑day execution.</p></li></ul><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Experience supporting payroll operations or payroll service delivery in a shared services environment</p></li><li><p>Working knowledge of payroll compliance, statutory requirements, and internal controls</p></li><li><p>Experience working with global payroll vendors and payroll or HR systems</p></li><li><p>Ability to review payroll data, identify issues, and support resolution</p></li><li><p>A structured, detail‑oriented approach to managing operational activities</p></li><li><p>Clear written and verbal communication skills</p></li><li><p>Comfort working with global stakeholders across time zone<strong>s.</strong></p></li></ul><p><strong>To be considered for this role:</strong></p><ul><li><p>Bachelor’s degree in Accounting, Finance, Business Administration, HR, or a related field</p></li><li><p> Typically 6–8+ years of experience in payroll operations, including exposure to multi‑country or international payroll</p></li><li><p> Experience working in a Shared Services Center or Global Capability Center is preferred</p></li><li><p> Payroll or professional certifications are an advantage</p></li><li><p> Proficiency in English and experience supporting global teams and stakeholders</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 05:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior CMC Regulatory Sciences Specialist]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47491]]></requisitionid>
    <referencenumber><![CDATA[R47491]]></referencenumber>
    <apijobid><![CDATA[r47491]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47491/senior-cmc-regulatory-sciences-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>We are seeking a highly motivated and experienced CMC Regulatory Sciences Specialist to join our dynamic team. This role will involve managing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies across clinical and commercial phases, ensuring compliance with US and international regulatory requirements. The ideal candidate will possess strong technical writing skills, a proactive approach, and the ability to work collaboratively with cross-functional teams.</p><p>As a Senior CMC Regulatory Sciences Specialist, a typical day might include the following:</p><ul><li>Develop and execute CMC regulatory strategies for clinical trial applications, amendments, commercial submissions, and marketing applications globally.</li><li>Prepare and oversee the coordination and compilation of CMC dossiers, including Module 3: Quality, ensuring alignment with applicable regulations and guidelines.</li><li>Author, review, and finalize CMC documents and responses to inquiries from global health agencies, maintaining submission timelines.</li><li>Develop submission strategies, including timelines, approaches, and defining deliverables, while maintaining clear communication with stakeholders.</li><li>Stay informed on regulatory trends, agency feedback, and global best practices, updating submission processes accordingly.</li><li>Collaborate with cross-functional teams and external partners to ensure alignment between regulatory submissions and product supply plans.</li><li>Engage with regulatory authorities as needed to support CMC-related modules and submissions.</li></ul><p>This role may be for you if you have:</p><ul><li>Experience in regulatory writing, technical writing (non-SOP related), or pharmaceutical development documentation</li><li>Strong knowledge of CMC regulatory requirements, FDA regulations, ICH guidelines, and Current Good Manufacturing Practices.</li><li>Experience in managing CMC submissions for clinical and commercial phases preferred.</li><li>Excellent written and verbal communication skills, particularly in technical writing.</li><li>Strong project management, critical thinking, and problem-solving skills.</li><li>Ability to work independently and within a team, adapting to shifting priorities and strategies.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in a scientific discipline and </p><ul><li>Senior CMC Regulatory Sciences Specialist: 5 years of relevant experience</li><li>Principal CMC Regulatory Sciences Specialist: 8 years of relevant experience in a biopharmaceutical and/or CMC regulatory or industry setting</li><li>Advanced degree preferred (MS or PhD). May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 08:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, EDC Development]]></title>
    <date><![CDATA[Thu, 19 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45329]]></requisitionid>
    <referencenumber><![CDATA[R45329]]></referencenumber>
    <apijobid><![CDATA[r45329]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45329/senior-manager-edc-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New Jersey]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><p>We’re growing our Clinical Database Development team, and we’re looking for a thoughtful leader to help us deliver reliable, inspection‑ready EDC solutions that support our key development programs. We provide clear direction, consistent processes across studies, and caring mentorship so our developers and CRO partners can do their best work. We champion quality standards and regulatory requirements, and we celebrate practical, elegant builds in Medidata Rave. We’ll support you as you guide strategy, develop talent, and shape the standards that move our portfolio forward!</p><p><strong>A Typical Day:</strong></p><ul><li>Oversee CRO EDC database builds and ensure process compliance.</li><li>Build and configure Rave studies using our Global Library.</li><li>Program edit checks, dynamics, derivations, and custom functions.</li><li>Lead UAT setup in Cloud Administration and drive resolution to go‑live.</li><li>Configure Coder, TSDV, and Clinical Views as protocols require.</li><li>Manage amendments, migrations, and quick publishes with Rave tools.</li></ul><p><strong>This Role May Be For You if you:</strong></p><ul><li>Balance standards with protocol nuances to craft dependable Rave builds.</li><li>Guide CRO partners with clarity while maintaining consistent practices.</li><li>Value compliance—21 CFR Part 11, ICH‑GCP, and CDISC are second nature.</li><li>Move comfortably between strategy, oversight, and hands‑on configuration.</li><li>Enjoy coaching developers and contributing to a high‑quality global library.</li></ul><p><strong>To Be Considered</strong><br>A bachelor’s degree in mathematics, science, or a related field is required, along with <strong>8+ years of EDC development</strong> experience in biotechnology, pharmaceutical, or health‑related industries and <strong>3+ years of people‑management</strong> experience. <strong>Medidata Rave</strong> experience is required, and you bring thorough knowledge of Data Management and Clinical Database Development processes and of applicable regulations (<strong>21 CFR Part 11, ICH‑GCP, CDISC</strong> standards for data collection). Preferred qualifications include <strong>Medidata Builder Certification</strong>, <strong>C#</strong> programming knowledge, and <strong>TrialGrid</strong> familiarity, plus experience with Rave Amendment Manager and Medidata Cloud Administration.</p></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[ITOT Infrastructure Support Technician]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47009]]></requisitionid>
    <referencenumber><![CDATA[R47009]]></referencenumber>
    <apijobid><![CDATA[r47009]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47009/itot-infrastructure-support-technician/]]></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>ITOT Infrastructure Support Technician is responsible for providing IT support to Manufacturing. Work closely with Manufacturing to provide IT expertise and troubleshooting of issues while ensuring smooth operation of IT equipment & applications in MFG. Support the implementation of IT projects in MFG involving end users and adhering to all clean room standards & procedures ensuring a state of compliance at all times.</p><p>As a ITOT Infrastructure Support Technician, a typical day might include the following:</p><ul><li>Oversees the performance of all IT hardware and applications across the Manufacturing areas.</li><li>Conduct trouble-shooting and support investigations associated with IT equipment & applications used in Manufacturing.</li><li>Support the implementation of new IT hardware and applications and liaise with stakeholders and vendors.</li><li>Prepare reports by collecting, analyzing, summarizing information and trends on the performance of IT equipment and applications.</li><li>Support communication of, preparation for and the execution of IT systems & applications downtime so impact to Manufacturing is minimized.</li><li>Liaise closely with the end users of IT equipment and applications supporting resolution of issues keeping Manufacturing & IT Management informed as required.</li><li>Issue trouble shooting guides and/or training material around IT applications & equipment as required.</li><li>Identify IT related continuous improvement ideas & projects through discussions with end users and implement opportunities of value within Manufacturing operations.</li><li>Attend all relevant Manufacturing and IT meetings, including the daily Manufacturing MDI (Managing for Daily Improvement).</li><li>Required to liaise with cross functional depts in the organization on behalf of Manufacturing in relation to IT equipment and applications.</li><li>Demonstrate strong communication skills, with the ability to clearly and concisely convey technical information to both technical and non-technical stakeholders across Manufacturing and IT teams.</li></ul><p>This role may be for you if you are:</p><ul><li>Technically competent with IT hardware in MFG e.g. Laptops, Phones, Scanners, Printers, Nova Units etc.</li><li>Technically competent on IT applications such as OPM, Orchestrate, MES, LIMS etc.</li><li>Familiar with regulatory requirements in relation to Data Integrity for IT infrastructure.</li></ul><p>In order to be considered for this position, you must hold an Associate's in information technology or related field along with:</p><ul><li>IT Support Technician III: 5 years of relevant experience.</li><li>IT Support Technician IV: 8 years of relevant experience.</li><li>IT Support Technician V: 10 years of relevant experience.</li><li>Experience in a cGMP manufacturing facility preferred.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li></ul><p>Gowning and Environment</p><ul><li>Full cleanroom attire (Examples 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>Physical</p><ul><li>Ability to perform physical requirements for entirety of shift (up to 10 hours).</li><li>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lb.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$28.46 - $61.88]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Statistical Programming]]></title>
    <date><![CDATA[Wed, 17 Dec 2025 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43877]]></requisitionid>
    <referencenumber><![CDATA[R43877]]></referencenumber>
    <apijobid><![CDATA[r43877]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43877/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A Sr. Manager provides timely support to the project team on all programming matters according to the project strategies within a therapeutic area. As an integral part of a project team, the incumbent provides project leadership and contributes to the programming support for processing data from clinical studies. Project requirements will be identified according to a Statistical Analysis Plan, programming specifications or user requirements/design documents using internal standards and guidelines. The incumbent is responsible for leading the programming aspect of the project, both internally or CROs, for all programming deliverables and participates in the identification and development of programming standards and macro development to facilitate the creation of statistical deliverables from a single study through to regulatory approval, product launch, and annual reports. May be asked to oversee special projects / work with clinical task force. Meets statistical adhoc requests of senior management.</p><p><br><strong>As a Senior Manager, A typical day may include:</strong></p><p><br>• Independently coordinate and oversee the preparation, execution, reporting and documentation of project analysis programming within a therapeutic area using appropriate tools to track, allocate and summarize extent of work required, progress and completion of programming deliverables. Manage and coordinate programming and QC of analysis datasets and TFLs following Regeneron standard data models and/o integration of data across studies in support of CSS/CSE and esub deliverables.<br>• Implement and mentor others on the use of department standardization tools or therapeutic area standard analysis when programming clinical data or system application deliverables.<br>• Contribute to programming development and quality control of the programming deliverables utilizing Regeneron tools and methodologies.<br>• Programming representative within a therapeutic area in a multidisciplinary study team to ensure timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, programming representative for an application development to the user audience.<br>• Develop data models, programming standards and code, and training end users in the use of project standards to support programming deliverables that follow regulatory submission requirements.<br>• Mentor junior level staff in therapeutic area requirements. Develop collaborative work environment and be a positive role model.<br>• Advises all relevant employees about the procedures surrounding retention of data, records, and information for employees in their group.</p><p><strong>To be considered for this role, you must meet the following requirements</strong>:<br>Education<br>• Masters Degree<br>• SAS Certification desirable.</p><p>Experience<br>• 8 – 10 Years</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 08 Jan 2026 19:26:44 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director, Global Development Quality Assurance (GLP)]]></title>
    <date><![CDATA[Wed, 11 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45122]]></requisitionid>
    <referencenumber><![CDATA[R45122]]></referencenumber>
    <apijobid><![CDATA[r45122]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45122/senior-director-global-development-quality-assurance-glp/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Director, Global Development Quality Assurance (GDQA) you will provide leadership for an entire GLP function. You will lead all staff while developing and leading all aspects of the execution of functional/departmental mission and vision. You will create and oversee strategic partnerships and implement risk-based quality auditing activities internally and with external organizations. You are expect to apply your expert knowledge of the FDA and EU regulations and ICH guidance documents with other regulations affecting drug development. </p><p>You will manage Good Laboratory (GLP) audit function within GDQA. In addition, we partner with other members of the GDQA, identifying trends through metrics to diagnose and remediate systemic quality issues. We oversee the development, execution and reporting of the overall GxP Audit Program(s) for which they are responsible. </p><p>This position will be on-site 4 days/week at our Tarrytown, NY offices. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following</strong>: <br>• Developing and managing the overall strategic plan for the GLP audit functions. <br>• Represent the GDQA audit function by providing audit and compliance input in cross functional meetings and external meetings. <br>• Manage, hire and develop direct reports within GDQA and conducting Mid-year and End-of year performance assessments. <br>• Lead the identification of internal quality/compliance issues and act as a catalyst for process improvements to promote standardization and best practices. <br>• Represent GDQA on top priority teams, complex compliance projects and initiatives both within and across functional areas or other departments as applicable. <br>• Be responsible for policies, standards, and regulations, and evaluate potentially critical problems. <br>• Oversee the education and/or training of the GDQA organization and other Global Development departments as needed. <br>• Ensure succession planning and business continuity for GDQA department.</p><p><strong>This may be for you if you: </strong><br>• Can demonstrate success in leading a GLP Quality Assurance (GDQA) function. <br>• Self-motivated with the ability to work effectively in a dynamic environment with ambiguity <br>• Ability to effectively manage multiple priorities with a sense of urgency <br>• Strong people and project management, collaboration skills and negotiation of complex situations </p><p>To be considered a Bachelor’s degree (Master’s preferred) with 12+ years of relevant industry experience is required. We are seeking a minimum of 10 years’ experience working in GLP auditing and/or audit strategy and 6-8 years prior supervisory/leadership experience. Strong knowledge of FDA or other Regulatory Inspections of Investigator sites, Sponsors or CROs is necessary. Demonstrated experience in driving Quality into the Clinical Trial Operations processes. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$216,100.00 - $360,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 12 Feb 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Assoc Dir Health Economics & Outcomes Research, Solid Tumors]]></title>
    <date><![CDATA[Wed, 18 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45357]]></requisitionid>
    <referencenumber><![CDATA[R45357]]></referencenumber>
    <apijobid><![CDATA[r45357]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45357/assoc-dir-health-economics-outcomes-research-solid-tumors/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As an Associate Director you will develop HEOR strategies and plans, conduct HEOR and RWE studies and develop publications and deliverables. We work closely with Market Access, Medical Affairs, Clinical Development, Commercial, Regulatory and other groups to ensure evidence needs are identified and addressed to demonstrate the value with a focus on solid tumors.</p><p><br>This position is at our Sleepy Hollow, NY location and will require you to be onsite 4 days/week. We cannot offer a remote option. If eligible, we can offer relocation benefits. </p><p><strong>A typical day may include the following:</strong><br>• Develop and implement global HEOR strategies and programs for our portfolio throughout the product’s lifecycle, to inform and support clinical development and regulatory needs during early pipeline phase and ensuring optimal market access.<br>• Collaborate with business partners to develop and support compelling product value propositions with aim to optimize future patient access. <br>• Identify HEOR evidence requirements and gaps, and design, conduct, and deliver studies and tools to support relative value demonstration and product differentiation.<br>• Leverage RWD analytic tools and collaborate with HEOR RWDnA and Epidemiology teams generating insights to inform development programs and key business questions.<br>• Co-lead conduct of regulatory-grade real world evidence studies and provide education on emerging opportunities for employing RWE across the solid tumor portfolio.<br>• Collaborate on conduct and communication of epidemiology and pharmacoepidemiology analyses and studies. <br>• Provide relevant input into selection of patient population, comparators and endpoints within clinical trials to enable demonstration of robust incremental value over standard of care that can facilitate optimal future patient access.<br>• Develop and implement Clinical Outcomes Assessment (COA) measurement strategies and plans in support of product labeling, patient access and product differentiation. <br>• Develop and validate COA endpoints for integration in clinical studies. Produce COA evidence dossiers for regulatory submissions. <br>• Evaluate relevant payer and health technology assessment (HTA) decisions, collect feedback in advisory meetings and apply key learnings to pipeline products.<br>• Maintain an up-to-date awareness of regulatory (e.g. FDA, EMA) and payer/HTA considerations that may impact planning for and implementation of HEOR programs.<br>• Report, publish and disseminate HEOR data and study results in compliance with company, industry and regulatory requirements.</p><p><strong>This may be for you if you:</strong><br>• Want to have an impact on patient lives<br>• Enjoy working in a ‘rapid response’ environment<br>• Would like an opportunity to present to senior leaders<br>• Want to be part of a growing high performing team</p><p>To be considered it is required to have an Advanced graduate degree (Ph.D., MS, or MD, PharmD., B.Pharm with Master’s degree) in HEOR-related field (e.g. pharmacoepidemiology, epidemiology, healthcare/data analytics, health economics, health services research, public health). 4+ years with PhD or 6+ years with MS in HEOR; at least 3 years of life science company or healthcare consulting experience is a plus. Strong technical expertise required in design and conduct of HEOR studies and models. Solid understanding of regulatory (e.g. FDA, EMA) and HTA considerations. Experience in design and implementation of patient experience data in clinical trials, including experience in instrument selection, analysis and reporting of data. Experience with Oncology is preferred. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Feb 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager, Corporate Accounting]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45377]]></requisitionid>
    <referencenumber><![CDATA[R45377]]></referencenumber>
    <apijobid><![CDATA[r45377]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45377/associate-manager-corporate-accounting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Manager, Corporate Accounting is a key contributor within the accounting organization, responsible for overseeing core accounting activities. This role partners closely with Finance, Financial Reporting, IT, Facilities, and other business stakeholders to deliver accurate financial information, ensure compliance with accounting policies, and maintain effective internal controls. In addition, the Associate Manager plays an integral role in driving process improvements, enhancing operational efficiency, and helping scale accounting operations to support a growing organization.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><p>• Managing the timely and accurate completion of the monthly accounting cycle for areas of responsibility<br>• Reviewing and preparing journal entries, supporting schedules, account analyses, reconciliations and variance explanations<br>• Ensuring proper accounting and compliance with the Company’s accounting policies for capital expenditures, leases, prepaid expenses, and other areas of responsibility<br>• Presenting monthly financial results to Senior Management including the Corporate Controller and the CFO<br>• Ensuring accuracy of 10Q/K financial statement notes related to areas of responsibility <br>• Ensuring that (i) effective internal controls are in place and are adhered to and (ii) associated internal control documentation is prepared and/or updated on a timely basis<br>• Facilitating quarterly and annual requests from internal and external auditors and leading SOX walkthroughs<br>• Reviewing and updating the relevant Company accounting policies to reflect changes in the business or accounting guidance<br>• Assisting in supporting Oracle Fusion Cloud Financials ERP implementation project<br>o Performing user acceptance testing, and ensuring workpapers and process documentation is updated as appropriate<br>• Managing and participating in continuous improvement initiatives and special projects as necessary</p><p><br><strong>The Role Might be for You If You:</strong></p><ul><li>Possess in-depth accounting knowledge gained through a mix of public accounting and hands-on corporate accounting experience</li><li>Can effectively communicate across all levels of the organization and build rapport with stakeholders</li><li>Are coachable and dependable with a willingness to learn and determination to drive tasks to completion</li><li>Have experience leading, coaching and developing team members</li></ul><p>To be considered for this role, you must have 5+ years of accounting experience and 1+ year(s) in a people management role. Strong analytical skills and attention to detail are critical. Must be able to operate in a fast-paced environment and handle multiple priorities.</p><p>Big 4 Accounting experience and CPA or CPA track are preferred. High proficiency with Microsoft applications is required, specifically Microsoft Excel. Experience with Oracle GL, Smartview, and Oracle Fixed Asset Module a plus. ERP implementation experience a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 08:56:53 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Biotech Production Specialist]]></title>
    <date><![CDATA[Mon, 23 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45600]]></requisitionid>
    <referencenumber><![CDATA[R45600]]></referencenumber>
    <apijobid><![CDATA[r45600]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45600/associate-biotech-production-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Within this role you will be working as part of the Manufacturing Team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors.<br> </p><p><strong>As an Associate Biotech Production Specialist, a typical shift might include, but is not limited to, the following:</strong></p><ul><li><p>Working as part of the Manufacturing team to carry out tasks in line with the production schedule as directed by Team Leads and Supervisors</p></li><li><p>Monitoring production processes</p></li><li><p>Participating in equipment start-up, commissioning, and validation activities</p></li><li><p>Assisting with troubleshooting in case of equipment failure</p></li><li><p>Performing manufacturing level maintenance on equipment</p></li><li><p>Adhering to safety and GMP (Good Manufacturing Practice) requirements at all times when carrying out tasks</p></li><li><p>Performing equipment cleaning, preparation and execution as well as completing associated documentation</p></li><li><p>Performing various tests and in-process sampling</p></li><li><p>Reviewing, editing and revising completed batch records, logbooks, and SOPs in accordance with cGMP standards</p></li><li><p>Maintaining housekeeping in designated area and adhering to the clean standards of the facility</p></li></ul><p><br><strong>This role might be for you if:</strong></p><ul><li><p>You possess excellent verbal and written communication skills</p></li><li><p>You enjoy problem solving</p></li><li><p>You demonstrate a can-do attitude</p></li><li><p>You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook</p></li><li><p>You demonstrate an ability to work within a successful team</p></li><li><p>You can adapt to a changing environment and have the ability to adhere to a schedule</p></li></ul><p><br>To be considered for this opportunity you should have a BS/BA in Life Sciences or a related field. Relevant experience may be substituted in lieu of the educational requirement.</p><p>Our site operates on a 24/7 basis, and we offer a number of different shift working patterns that could fit with your lifestyle</p><p><strong>What is on offer?</strong> </p><p>You will be supported through a comprehensive onboarding programme which will include formal classroom learning along with on-the-job training all within an encouraging environment. </p><p>Ensuring the health and well-being of our people is just as meaningful to us as the patients our life-transforming medicines serve. That's because we know caring for people around the globe should start with supporting our employees through our comprehensive compensation and benefits offering that includes:</p><ul><li><p>Competitive Salary</p></li><li><p>Shift Premiums</p></li><li><p>Annual Bonus</p></li><li><p>Stock Schemes</p></li><li><p>Employer Pension Contributions </p></li><li><p>Education Assistance</p></li><li><p>Generous Annual & Flexible Leave Programs </p></li><li><p>Competitive Private Medical, Dental & Vision Plans</p></li><li><p>Career & Personal Development</p></li><li><p>Wellness Programs - Onsite Gyms & Fitness Classes </p></li><li><p>Concierge Services – Onsite Beauty Therapist / Barber / Car Valet</p></li><li><p>Community Volunteering</p></li><li><p>Employee Interest Groups / Employee Teams & Clubs</p></li><li><p>Employee & Family Events</p></li></ul><p>#LI-Onsite #JOBSIEST #REGNIELSM #IRELIM</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 24 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, SDLC, Testing & Release Management]]></title>
    <date><![CDATA[Mon, 09 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44112]]></requisitionid>
    <referencenumber><![CDATA[R44112]]></referencenumber>
    <apijobid><![CDATA[r44112]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44112/director-sdlc-testing-release-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director of SDLC, Testing & Release Management will own, develop, and execute the strategic vision for SDLC, CI/CD, testing, release management, and AI‑augmented automation across the enterprise to accelerate digital transformation that includes deployment and upgrades of several GMP IT solutions.</p><p>As a Director, a typical day might include the following:</p><ul><li>Establish and govern standardized SDLC processes ensuring consistency, efficiency, speed and compliance.</li><li>Build, train and guide internal IT SDLC team on SDLC and CSA processes and requirements, development of effective and efficient test plans, compliant documentation ready for QA approval. Serve as the organizational authority for Computer Software Assurance (CSA).</li><li>Develop test automation frameworks including LLM‑ and AI‑driven testing. Enhance release management processes for reliability and continuity.</li><li>Lead and mentor a cross‑functional organization, partner with QA, Compliance, and Regulatory teams to accelerate new system implementations and system changes.</li><li>Define and improve quality metrics and KPIs including AI‑enabled indicators.</li><li>Drive adoption of modern testing methodologies and AI‑assisted validation, establish robust test data management practices. Oversee risk evaluation of emerging technologies including LLMs.</li><li>Ensure compliance with CSA, CSV, Part 11, Annex 11, GAMP 5. Enforce documentation standards, including automated draft content generation.</li><li>Serve as the primary escalation point. Represent test and release functions at executive forums.</li></ul><p>This role may be for you if you have:</p><ul><li>CI/CD: Jenkins, GitLab CI, GitHub Actions.</li><li>Testing: Selenium, JUnit, TestNG, Cypress, Playwright.</li><li>AI/LLM: testing tools, prompt engineering, model governance.</li><li>IaC: Terraform, Ansible.</li><li>Cloud & Containers: Docker, Kubernetes.</li><li>Monitoring: Prometheus, Grafana, ELK.</li><li>Version Control: Git, SVN.</li><li>Work Management: Jira, Confluence, Azure DevOps.</li><li>Validation Systems: electronic validation platforms.</li><li>Change‑management leadership with strong decision‑making, risk‑management skills and budget/resource planning.</li><li>Compliance leadership including AI‑enabled systems.</li></ul><p>In order to be considered for this position, you must hold a BS/BA degree in Information Technology or related field and</p><ul><li>Associate Director: 10 + years industry experience in Information Systems and Technology with 8+ years of managing employees and budgets, 7+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment plus experience with IT Compliance guidelines as per GAMP 5.</li><li>Director: 12+ years working in Information Systems and Technology with 10+ years of managing employees and budgets, 10+ years working in a GMP manufacturing environment and experience in a biotech/pharma environment plus experience with IT Compliance guidelines as per GAMP 5.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$147,800.00 - $286,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Mar 2026 14:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Development Strategy Planning & Operations, Hematology]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44886]]></requisitionid>
    <referencenumber><![CDATA[R44886]]></referencenumber>
    <apijobid><![CDATA[r44886]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44886/associate-director-clinical-development-strategy-planning-operations-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Clinical Sciences Strategy and Planning, will partner with the Executive Director, Clinical Science Strategy and Excellence, to support the strategic and operational advancement of the assigned CDU(s) portfolio. This role will serve as a key operational partner, driving execution of critical initiatives while performing Chief of Staff functions for the department. The position requires close collaboration with the CDU leadership team, Clinical Scientist leadership, and cross-functional stakeholders to ensure alignment of priorities, effective communication, and operational excellence across Clinical Sciences.</p><p>This role is both strategic and tactical, requiring a nimble thinker with strong interpersonal skills, drug development and operational acumen, and the ability to pivot quickly as new data and priorities emerge. The ideal candidate will demonstrate the ability to translate strategic vision into operational execution while fostering cross-organizational collaboration.</p><p><strong>A typical day in the life of an Associate Director, Clinical Sciences Strategy and Planning may include the following responsibilities: </strong></p><ul><li>Partners with the Executive Director and CDU leadership team to drive and optimize critical Clinical Sciences initiatives, ensuring focus on the most impactful items for business success.</li><li>Supports the execution of key projects and initiatives within the portfolio, tracking progress and ensuring alignment with Regeneron's strategic goals and objectives.</li><li>Creates and maintains content for CDU communication platforms (e.g., intranet, SharePoint sites) to drive awareness and clarity about the Clinical Sciences strategy, organization, portfolio, and work activities.</li><li>Develops agendas for key internal meetings, facilitates effective discussions, documents clear action items, and drives communication and accountability within the Clinical Sciences organization.</li><li>Assists in driving pipeline planning activities for the CDU portfolio, working with the CDU Leadership Team and other key stakeholders to ensure continuity of corporate planning and execution.</li><li>Responsible for supporting cross-CDU resource and planning activities, including workforce/headcount planning, space planning, and quarterly/annual planning and budgeting processes.</li><li>Supports the Executive Director clinical trial excellence initiatives, implementation of next-generation technologies, and enterprise-wide initiatives by coordinating cross-functional workstreams and tracking deliverables.</li><li>Identifies and regularly reports on key performance metrics, providing insights and recommendations for enhancing team effectiveness and cross-organizational collaboration.</li><li>Supports the preparation of board meetings, executive team meetings, and other senior management meetings, including development of presentation materials and briefing documents.</li></ul><p>This role may be for you if you have the following:</p><ul><li>Advanced Degree in a scientific or business field preferred; MD, PhD, MBA, or PharmD strongly preferred.</li><li>Minimum of 7 years of relevant experience in clinical research, drug development, and/or pharmaceutical operations.</li><li>Proven ability to manage complex projects and drive operational excellence in a matrixed environment.</li><li>Excellent communication and interpersonal skills, with the ability to build strong relationships at all levels of the organization.</li><li>Strong analytical and problem-solving skills, with the ability to synthesize information and make informed recommendations.</li><li>Demonstrated experience in fostering cross-organizational collaboration and managing multiple priorities simultaneously.</li><li>Scientific acumen with the ability to understand and communicate complex clinical and scientific concepts.</li><li>Experience with strategic planning, portfolio management, or Chief of Staff functions preferred.</li><li>High level of integrity and professionalism, with the ability to handle sensitive information with discretion.</li><li>Proficiency in creating executive-level presentations and communications.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 14:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director of IT Operations (Infrastructure Architecture)]]></title>
    <date><![CDATA[Tue, 24 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45562]]></requisitionid>
    <referencenumber><![CDATA[R45562]]></referencenumber>
    <apijobid><![CDATA[r45562]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45562/associate-director-of-it-operations-infrastructure-architecture/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director of IT Operations (Infrastructure Architecture) ensures the reliable operation, delivery, and management of IT/Operational Technology (IT/OT) infrastructure and services, with a focus on supporting a highly regulated GxP environment. This role provides strategic direction, operational management, and administrative oversight for the daily IT operational activities, including hardware, communications & WiFi infrastructure, and service delivery. The position also ensures integration and alignment with corporate IT systems and infrastructure while maintaining robust compliance, security, and service standards.</p><p>As an Associate Director of IT Operations (Infrastructure Architecture), a typical day might include the following:</p><ul><li>Ensure the reliable operation of IT/OT infrastructure, including but not limited to servers, hardware, communications and desktop support, plus oversight of daily operational activities.</li><li>Define, implement, and lead IT/OT infrastructure architecture, with a focus on hyper-converged systems, advanced networking, and wireless technologies, to ensure robust connectivity and security.</li><li>Build scalable and secure wireless networks to support industrial and enterprise needs.</li><li>Provide operational management for data centre operations, network services, telecom, asset management, and security plus ensure systems and procedures are in place for effective monitoring and reporting.</li><li>Maintain compliance with industry standards, including experience with automation systems such as DeltaV/Emerson and Rockwell/Allen-Bradley.</li><li>Manage service providers to ensure high-quality service delivery and alignment to service level agreements (SLAs) and act as the escalation point for major incidents.</li><li>Ensure compliance with relevant regulations and standards, including GxP, FDA and other global regulatory requirements.</li><li>Maintain robust security measures to protect IT/OT infrastructure, including data integrity and disaster recovery planning.</li><li>Lead and mentor a diverse technical team and run recruitment, training, performance evaluations, and target setting for the IT Operations team.</li><li>Collaborate with partners to ensure seamless integration between IT and OT systems.</li><li>Provide regular management reporting on service performance and IT operations.</li></ul><p>​​​</p><p>This role may be for you if you:</p><ul><li>Have management and delivery experience including management of a diverse technical team, including Helpdesk, Desktop, Server and Network staff, with experience managing vendors and managed services.</li><li>Have experience in developing and deploying SLAs, Metrics and other best practices, as well as having successfully implemented ITIL practices into an organisation.</li><li>Have experience with Business Continuity and Disaster Recovery planning.</li><li>Have a strong background in Microsoft OS, in particular Server and GPO elements.</li><li>Have a strong understanding of Data Integrity and associated tools.</li><li>Possess hands-on experience designing and documenting infrastructure architecture across networking, compute, and security domains.</li><li>Have demonstrated experience with security frameworks (NIST CSF, IEC 62443, or ISO 27001) and applying them within regulated environments.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology or related field along with</p><ul><li>Senior Manager: 8+ years of progressively more responsible experience, including 8+ years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment.</li><li>Associate Director: 10 years of progressively more responsible experience, including 10 years of management experience and a minimum of 3 years’ experience in an FDA or similarly regulated environment.</li><li>May consider equivalent combination of education and experience. Level is determined based on qualifications relevant to the role.</li><li>Preferred knowledge of understanding of IT compliance guidelines, including PICS, CFR21 Part 11, Annex 11, and GAMP.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$126,300.00 - $241,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Marketing - HCP+DTC (Dermatology)]]></title>
    <date><![CDATA[Thu, 19 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45693]]></requisitionid>
    <referencenumber><![CDATA[R45693]]></referencenumber>
    <apijobid><![CDATA[r45693]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45693/director-marketing-hcpplusdtc-dermatology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director of Marketing (DTC + HCP), US Dermatology is responsible for leading, developing and completing comprehensive US digital marketing strategies to reach, educate, and activate consumers and HCPs across the omnichannel ecosystem, including web, social media, influencer, paid media, and CRM, carried out in collaboration with the Dermatology alliance team. The Director formulates and fosters innovation to provide optimal patient and customer experience. This role requires a strategic and creative problem solver with a deep understanding of bio/pharmaceutical brand marketing, digital and omnichannel marketing trends, and online consumer/HCP behavior. This role will report to the Senior Director of Dermatology Consumer Marketing.</p><h3><strong>A Typical Day Might Look Like this:</strong></h3><ul><li>Lead the development of the Dermatology Omnichannel Marketing strategy (DTC and HCP) within the overall brand strategy across all current and future Dermatology indications</li><li>Plan, develop, and help execute branded, unbranded, and multi-cultural digital consumer and NPP marketing initiatives across various online channels, including but not limited to web, social media, display, SEM, CRM, email. Includes supporting and sponsoring materials through joint medical, regulatory, and legal review committees </li><li>Own end-to-end social media strategy and activation for DTC, architecting a first-in-class influencer model and scaling integrated paid and owned programs to accelerate patient demand and optimize ROI</li><li>Lead and mentor consumer and HCP digital marketing/NPP professional(s), fostering a collaborative and innovative work environment</li><li>Demonstrated leadership experience managing direct report(s), fostering a collaborative working environment</li><li>Partner with alliance media to develop efficient and effective media mix strategies</li></ul><h3><strong>This Position Might Be for You if:</strong></h3><ul><li>You bring Strategic, scientific, and analytical competence focused on delivering results</li><li>You can demonstrate leadership and experience managing direct report(s).</li><li>You bring brand marketing experience, with expertise in DTC/HCP media and ROI analysis </li><li>You can demonstrate competency and tenured experience in social media marketing channels (influencer activation a plus)</li><li>You can focus on execution and manage multiple projects in a fast-paced environment.</li><li>You have organizational agility and the capability to reprioritize based on external or internal changes.</li><li>You can manage external partners like agencies.</li></ul><p>To be considered you must have a bachelor’s degree is required; an MBA is a plus. 12+ years of “progressive” industry/relevant professional experience in strategic roles. 8+ years of experience in pharmaceutical/biotech marketing or a related industry, including consumer/HCP brand marketing/franchise management and omnichannel strategy, with strong understanding of digital marketing trends and innovations. Experience navigating and managing alliance partnerships is preferred. Must be willing to travel 20% of the time, including weekend travel as needed. Willingness to work in a hybrid environment with a minimum of 4 days on-site at Sleepy Hollow, NY</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 20 Mar 2026 15:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Scientist, Flow Cytometry]]></title>
    <date><![CDATA[Wed, 11 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44331]]></requisitionid>
    <referencenumber><![CDATA[R44331]]></referencenumber>
    <apijobid><![CDATA[r44331]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44331/associate-scientist-flow-cytometry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking a highly motivated<strong> Associate</strong> Scientist – Flow Cytometry to join our Research Flow Cytometry Core (RFCC). The RFCC facility provides sorting, analysis and maintenance services to all of Regeneron’s Research Departments. In this exciting role, you will perform sorting experiments for the research staff. You will also maintain analytical instruments that are located in the various buildings on Regeneron’s campus, as well as data analysis using various flow cytometric software programs.</p><p><strong>As an Associate Scientist – Flow Cytometry, A Typical Day Might Include:</strong></p><ul><li><p>Ensuring proper maintenance, alignment, and calibration of cell sorting equipment</p></li><li><p>Analyzing flow cytometric data</p></li><li><p>Maintaining and organizing schedules for cell sorting equipment</p></li><li><p>Maintaining adequate inventory of flow cytometry supplies and reagents</p></li><li><p>Supporting maintenance of flow cytometry equipment, such as LSRFortessa X-20, FACSymphony A3/A5, FACSDiscovery A8, Aurora, CytoFLEX (LX), IntelliCyt iOue, and Amnis ImageStreamX MkII cytometers</p></li><li><p>Operating a Sony MA900, FACSFusion, FACSymphony S6, and FACSDiscovery S8 high-speed cell sorters</p></li></ul><p><strong>This Role Might Be For You If:</strong></p><ul><li><p>You are able to critically analyze and troubleshoot scientific problems</p></li><li><p>You have a customer-centric viewpoint</p></li><li><p>You have good scientific initiative and ability to multi-task, prioritize work and balance multiple projects</p></li><li><p>You can work independently but also within a collaborative team environment and have flexibility to work on changing priorities</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS in a scientific field and 1-3 years of relevant experience using cytometric instrumentation. Experimental laboratory work and cytometry sorting is strongly preferred. Must be flexible and willing to perform flow cytometric duties that expedite and support scientific staff's flow cytometric goals and objectives. Experiences with cell sorting, tissue culture, cytometry staining, assay development, and data analysis is advantageous. Additionally, we need someone with analytical problem-solving experience. Cover letter is encouraged.</p><p><strong>#regncyto</strong></p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$70,300.00 - $110,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 25 Mar 2026 14:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Fill/Finish Associate (Internal Fill/Finish MFG)]]></title>
    <date><![CDATA[Wed, 01 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46367]]></requisitionid>
    <referencenumber><![CDATA[R46367]]></referencenumber>
    <apijobid><![CDATA[r46367]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46367/fillfinish-associate-internal-fillfinish-mfg/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Fill/Finish Associate. The Fill/Finish Associate performs all duties related to the production and support of drug product manufacturing. Works individually, and as part of a team, to support and perform operations to maintain formulation, filling, assembly, labeling and cartoning/packing equipment for parenteral biological products. Seeks to understand and develops proficiency in processes or procedures of increasing complexity.<br><br>As a Fill/Finish Associate, a typical day might include the following:</p><ul><li><p>Produces life-saving therapeutics for various indications developed from a dynamic internal pipeline</p></li><li><p>Works with a team that is accountable for production activities ranging from formulation of drug product to packaging of final drug product, which may include the following process-related responsibilities:</p></li><li><p>Operates highly automated equipment to fill drug product into vials or syringes within isolators or other aseptic environments</p></li><li><p>Assembles filled drug product into syringes and autoinjectors</p></li><li><p>Operates state of the art packaging lines to place assembled and labeled drug product into packaging configurations for distribution</p></li><li><p>Monitors production line for proper operation through process controls including pneumatics, robotics, manual and PLC feedback loop systems</p></li><li><p>Cleans, handles, and installs interchangeable parts for various systems and equipment</p></li><li><p>Collaborates to create and maintain operating procedures to perform routine activities that adhere to regulatory expectations</p></li><li><p>Ensures working spaces and equipment are clean, safe, and ready for processing activities</p></li><li><p>Maintains gowning qualification and adheres to clean room behaviors wherever required</p></li><li><p>Performs environmental sampling using various methods where applicable</p></li><li><p>Records GMP data that is accurate, legible, attributable, and contemporaneous and completes review on those records</p></li><li><p>Maintains and ensures proper documentation of all training</p></li><li><p>Navigates and utilizes electronic systems to support manufacturing operations</p></li><li><p>Travel (domestic and international) may be required.</p></li><li><p>Ensures compliance with applicable procedures while executing activities and escalates any non-conformities during operations</p></li><li><p>Performs reconciliation of product and controlled materials where applicable</p></li></ul><p>This role might be for you if:</p><ul><li><p>Ability to perform basic algebra and geometry</p></li><li><p>Reading/writing skills</p></li><li><p>Must be able to stand for extended periods of time and lift, push and pull at least 50lbs.</p></li><li><p>Knowledge of cGMP and FDA regulated (preferred) manufacturing environment and familiarity with cGMP filling, assembly or packaging processes preferred.</p></li><li><p>Necessary to have keen attention to detail and demonstrate from previous work experiences.</p></li><li><p>Preferred experience with aseptic technique and operating filling equipment or with assembly or packaging of parenteral products in vials, syringes and cartridges using both manual and automated equipment preferred.</p></li><li><p>Basic understanding of Microsoft Office Suite.</p></li><li><p>Demonstrates strong interpersonal, cross-cultural, communication, negotiation and has a high emotional IQ.</p></li><li><p>Exhibits confidence and strong problem-solving skills and demonstrates ingenuity, creativity and resourcefulness.</p></li><li><p>Gains understanding from provided instructions and works towards established goals.</p></li><li><p>Understands and listens to team members and stakeholders’ needs while supporting a positive team environment.</p></li><li><p>Possess a strong and effective communication style among peers and with management team</p></li><li><p>Values and acts with integrity</p></li></ul><p>Shift Requirements: Physical</p><ul><li><p>Ability to perform physical requirements for entirety of shift (up to 10 hours):</p></li><li><p>Some physical requirements can include but not limited to: bending, climbing, crawling, kneeling, reaching, reaching overhead, sitting, squatting, walking, standing, driving, hand manipulation and ability to lift/push/pull up to 50lbs</p></li></ul><p>Gowning and Environment</p><ul><li><p>Full cleanroom attire (Examples may include: including laundered undergarments, gown, facemask, hairnet, safety glasses, safety shoes and booties, latex gloves and the use of sanitizing agents during gowning process including IPA)</p></li><li><p>Ability to remove jewelry, make-up and nail adornments when wearing cleanroom attire</p></li></ul><p><br>To be considered for the Fill/Finish Associate you must have a GED/High School diploma and previous work experience.</p><p><em>Level is figured out based on qualifications relevant to the role. </em></p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$16.44 - $39.13]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 01 Apr 2026 15:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Affairs Strategy - Immunology & Inflammation]]></title>
    <date><![CDATA[Fri, 03 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46317]]></requisitionid>
    <referencenumber><![CDATA[R46317]]></referencenumber>
    <apijobid><![CDATA[r46317]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46317/manager-regulatory-affairs-strategy-immunology-inflammation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development and the policies/procedures required to ensure compliance with regulations. </p><p><strong>A typical day might include the following:</strong> </p><ul><li><p>Coordinate the preparation, submission, management and maintenance of global regulatory submissions related to clinical and nonclinical aspects of product development, including, but not limited to, the following: INDs/CTAs, amendments and information requests, Orphan drug applications, Annual Reports and Investigator’s Brochure </p></li><li><p>Assist in coordination and preparation for Agency meetings and associated briefing document preparation </p></li><li><p>Leads and tracks queries and commitments with regulatory agencies, collaborates with subject matter experts to provide written responses to queries, provides periodic status updates regarding conditions/commitments </p></li><li><p>Provide representation for study-level regulatory activities and participate in cross-functional departmental team projects and product development activities/meetings </p></li></ul><p><strong>This role might be for you:</strong> </p><ul><li><p>If you bring good understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and industry standard practices. </p></li><li><p>If you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred </p></li><li><p>If you have a high attention to detail; ability to coordinate and prioritize assigned projects according to company goals </p></li><li><p>You bring strong interpersonal skills both written and verbally </p></li></ul><p><strong>To be considered for this opportunity</strong>, we expect you must have a MD, PhD or PharmD degree along with 2+ years of regulatory experience. We expect to see individuals have worked on filings, helped with developing regulatory related documents and engaged with external partners and authorities. </p><p>#GDRAJobs</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 03 Apr 2026 15:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, ERP Product Testing and Release Management Lead (Oracle)]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44209]]></requisitionid>
    <referencenumber><![CDATA[R44209]]></referencenumber>
    <apijobid><![CDATA[r44209]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44209/director-erp-product-testing-and-release-management-lead-oracle/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Oracle Fusion ERP Product Testing and Release Management Lead governs testing and release activities for the Oracle Fusion Cloud implementation. The role focuses on quarterly Oracle patch impact analysis, regression testing, controlled release cycles, and system stability across phased deployments. This position works closely with the Testing (MTS) team, SI partners, GPOs, Product Leads, QA/CSV, and Oracle to ensure consistent testing standards, effective use of automated testing tools, robust test documentation in Jira, and compliance with Regeneron’s validation, SOX, and data integrity requirements.</p><p><strong>A typical day:</strong></p><ul><li><p>Partner with the Testing (MTS) team to plan, coordinate, and execute regression testing—including preparation and maintenance of test scripts, test scenarios, regression libraries, and automation for quarterly Oracle updates.</p></li><li><p>Use enterprise automation tools (e.g., Tosca or equivalent) to build and maintain automated regression test suites across Oracle ERP Cloud and integrations with boundary applications.</p></li><li><p>Oversee the use of Jira for managing test scripts, test scenarios, execution tracking, defect logging, triage, and reporting.</p></li><li><p>Lead testing governance across Regression, Integration SIT, UAT, and release readiness cycles.</p></li><li><p>Review Oracle quarterly patch release notes, perform impact assessment, and identify functional or technical areas requiring testing or remediation.</p></li><li><p>Maintain a risk-based regression testing strategy aligned with Oracle’s patch cadence and program release cycles.</p></li><li><p>Coordinate with SI partners to ensure all testing deliverables (scripts, scenarios, data, traceability matrices) meet Regeneron’s standards and are updated in Jira.</p></li><li><p>Collaborate with GPOs, Product Leads, and SMEs to ensure comprehensive cross-functional end-to-end test coverage.</p></li></ul><p><strong>This role may be for you, if you:</strong></p><ul><li><p>Expertise in analyzing Oracle Fusion Cloud quarterly updates and identifying system impacts.</p></li><li><p>Ability to interpret release notes and convert them into actionable testing scope.</p></li><li><p>Experience with automated testing tools such as Tosca, Selenium, or similar, especially for Oracle Cloud regression automation.</p></li><li><p>Strong understanding of ERP testing processes across Regression, SIT, UAT, and validation cycles.</p></li><li><p>Proficiency with Jira for managing test scripts, test scenarios, execution cycles, and defect tracking.</p></li><li><p>Solid grounding in SOX, GxP, data integrity, validation, and audit readiness.</p></li></ul><br><p><strong>To be considered:</strong></p><ul><li><p>Bachelor’s degree in Computer Science, Information Systems, Engineering, or a related field.</p></li><li><p>15+ years of experience in Oracle ERP applications testing, quality assurance, or release management.</p></li><li><p>10+ years of experience specifically with Oracle Fusion Cloud testing and release management.</p></li><li><p>Experience with Oracle Fusion Cloud or Oracle EBS release cycles and quarterly update impact analysis.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 09:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist II - Ophthalmology -  Naples, Miami, Ft. Myers]]></title>
    <date><![CDATA[Tue, 07 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45442]]></requisitionid>
    <referencenumber><![CDATA[R45442]]></referencenumber>
    <apijobid><![CDATA[r45442]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45442/medical-specialist-ii-ophthalmology-naples-miami-ft-myers/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Fort Myers]]></city>
    <state><![CDATA[Florida]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Territory: South Florida</strong> (Miami, West Palm Beach, Ft Lauderdale, Naples, Ft Myers, Sarasota, and other surrounding cities)</p><p>Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron markets several medicines, including for eye diseases, and has product candidates in development in other areas of high unmet medical need.</p><p><strong>A typical day might include the following:</strong><br>The Medical Specialist II will report to the Regional Director and will be responsible for daily development and management of relationships with Retina Specialists and other customer accounts in the assigned territory to grow revenues and consistently deliver product goals. The primary focus on this role will be the approved indications suffered by patients as it relates to conditions of the eye. The Medical Specialist II will provide technical and clinical product knowledge and support and will effectively utilize Regeneron marketing and operations resources to enhance productivity and provide optimal customer satisfaction.</p><p><strong>This role may be for you if you:</strong><br>• Have experience in biologics and buy and bill products<br>• Can demonstrate history of high sales performance<br>• Experience with reimbursement programs, government programs, managed care, formulary and contract negotiation</p><p>To be considered for this opportunity, you must have a BA/BS in science or business (master’s degree a plus). A minimum of 5 years’ specialty sales experience in the Pharmaceutical or Biotechnology industry. Ophthalmology and/or Buy & Bill with relevant retina experience is preferred. Residency in the territory is required. Overnight travel may be necessary.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 07 Apr 2026 09:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Country Manager Immunology DACH (f/m/d)]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46508]]></requisitionid>
    <referencenumber><![CDATA[R46508]]></referencenumber>
    <apijobid><![CDATA[r46508]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46508/country-manager-immunology-dach-fmd/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we’re driven by a passion for innovation and making a difference in patients’ lives. As our Country Manager Immunology (f/m/d) for the DACH region, you’ll play a pivotal role in shaping the success of our immunology portfolio. This role includes leading the commercial execution and co-promotion of immunology therapies across multiple indications, driving strategic initiatives, and leading a high-performing team in Germany, Switzerland, and Austria.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Leading and managing the commercial execution and co-promotion of the immunology portfolio for multiple indications</p></li><li><p>Developing and implementing strategic and annual business plans for the DACH region in collaboration with alliance partners</p></li><li><p>Overseeing operational responsibilities, including financial performance, budget and oversight of broad commercial functions including primarily sales force, commercial operations, training, sales force analytics, commercialization and in total a team of ~150 FTEs</p></li><li><p>Preparing for potential future launches of Regeneron’s immunology pipeline</p></li><li><p>Attracting, developing, and retaining a high-performing multidisciplinary team</p></li><li><p>Providing input into strategies for marketing, market access, pricing, and reimbursement led by alliance partners</p></li><li><p>Advocating Regeneron’s vision and mission to medical, patient, and business communities</p></li><li><p>Promoting the company’s profile and ensuring productive and legally compliant relations with business partners, customers, patients, and country authorities</p></li><li><p>Acting as a core member of Regeneron’s international leadership team, contributing to strategies across major markets outside the U.S.</p></li></ul><ul><li><p>Assuming full accountability for the DACH immunology commercial operations including:</p><ul><li><p>Ensuring that the operating objectives and standards of performance are understood and owned by the management team and employees</p></li><li><p>Ensuring consistency between local and global policies and SOPs including adherence to all relevant compliance principles</p></li></ul></li><li><p>Driving affiliate implementation and adherence to the Regeneron mission and values</p></li><li><p>Developing effective relationships with Regeneron’s collaboration partner</p></li></ul><p><strong>This Role May Be For You, If You:</strong></p><ul><li><p>Bring clear patient focus and passion to make a difference in patients’ lives</p></li><li><p>Have demonstrated strategic thinking</p></li><li><p>Champion fact-based, analytical decision making</p></li><li><p>Have the ability to establish goals to guide action and objectively measure performance</p></li><li><p>Have problem solving abilities and critical thinking</p></li><li><p>Demonstrate superior ability to communicate in a multicultural environment in proficient German and English</p></li><li><p>Are results and performance driven</p></li><li><p>Are an excellent team player and collaborator inter- and intra-organizationally</p></li><li><p>Have inspiring leadership presence and a positive mindset</p></li><li><p>Act with transparency and integrity</p></li><li><p>Are ready to travel ~20% of the time</p></li><li><p>Bring international cultural awareness and sensitivity</p></li></ul><p><strong>To Be Considered:</strong></p><p>You’ll need a minimum of 15 years of progressive management experience in the pharmaceutical or biotech sector, with significant experience in sales leadership. An advanced degree in science and/or business is required with an MBA preferred. Proven expertise in leading successful product launches, particularly in immunology or biologics, is highly valued. You bring demonstrated experience driving significant results in a high-performance, rapid-growth innovative enterprise. You have a proven track record of achieving short and long-term objectives and results through the implementation of highly-collaborative, cross-functional teams and infrastructure. Outstanding knowledge of the pharmaceutical specialty market in DACH and experience with co-promoted products with significant aptitude for managing intercompany relationships in alliance structures will set you apart.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager,  Accounting Operations]]></title>
    <date><![CDATA[Sun, 12 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43569]]></requisitionid>
    <referencenumber><![CDATA[R43569]]></referencenumber>
    <apijobid><![CDATA[r43569]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43569/associate-manager-accounting-operations/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron's Accounting Operations Team, located in Sleepy Hollow, NY, is seeking a dynamic and diligent Associate Manager. In this exciting role, you will have an opportunity to collaborate with various teams within the organization, streamline accounting processes, and maintain strong relationships across different business functions. You will ensure accuracy in financial data, optimize accounting workflows, and manage a team of accounting professionals to achieve organizational goals. In addition, you will be responsible for tracking departmental indicators to support the organization’s objectives. If you have a solid understanding of accounting principles, exceptional analytical skills, and excellent organizational abilities this position is perfect for you.</p><p><strong>This is an on-site role that will require 4 days in the office per week.</strong></p><h3><strong>A Typical Day Might Include the Following:</strong></h3><ul><li>Lead and collaborate with cross-functional teams to identify and implement process improvements, standardization, and automation initiatives</li><li>Develop and present arguments, process models, and workflow diagrams to support decision-making.</li><li>Empower the Accounting Operations team, providing guidance, support, and fostering a positive work environment</li><li>Use important metrics to track the department's performance, identify areas for improvement, and ensure the department effectively supports key financial goals</li><li>Support a team of individuals that conducts data analysis to identify trends, patterns, and insights that inform strategic decisions.</li><li>Prepare and deliver clear and concise reports, dashboards, and presentations to Accounting leadership.</li><li>Work with Accounting Operations management to prioritize projects/tasks, allocate resources, and plan weekly and monthly goals.</li><li>Enhance partnerships with offshore teams to ensure accurate and timely completion of accounting close deliverables</li><li>Supervise and evaluate the efficiency of implemented solutions and provide ongoing support.</li><li>Participate in special projects or initiatives as assigned by management</li></ul><h3><strong>This Role Might Be for You If:</strong></h3><ul><li>You are a proactive and analytical problem solver with the ability to think innovatively and be adept at evaluating opportunities for efficiencies across Accounting in a global multinational company.</li><li>You have demonstrated a track record of learning and implementing process improvements in the financials landscape and work in a collaborative and fast paced environment.</li><li>You can handle dynamic priorities, manage multiple projects and resources, and have a drive to succeed.</li><li>You are highly energetic and self-motivated.</li></ul><p>This role requires a BS/BA in Accounting and 6-8+ years of experience in an Accounting function. A strong understanding of Sarbanes-Oxley Technology (SOX) controls and expertise in business process design and documentation. Proven understanding large scale ERP system is a plus. Six Sigma certification preferred.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 13 Apr 2026 14:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager, Regulatory Submission Project Management (RSPM)]]></title>
    <date><![CDATA[Thu, 09 Apr 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44752]]></requisitionid>
    <referencenumber><![CDATA[R44752]]></referencenumber>
    <apijobid><![CDATA[r44752]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44752/manager-regulatory-submission-project-management-rspm/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced and detail-oriented Manager, Regulatory Submission Project Management (RSPM) to join our dynamic team. This pivotal role offers the opportunity to lead the planning, execution, and review of regulatory operations activities, ensuring the successful submission of regulatory documents and data to health authorities. If you thrive in a collaborative environment and are passionate about driving regulatory milestones, this position could be your next career step.</p><p><strong>A Typical Day:</strong></p><ul><li>Collaborating with cross-functional teams to create submission timelines and responsibility matrices.</li><li>Guiding teams and resolving issues related to submission documents to maintain quality and timelines.</li><li>Managing submission deliverables and coordinating with Regulatory Publishing and vendors on document status.</li><li>Reviewing submission content plans and validating documents for compliance with health authority guidelines.</li><li>Supporting PMDA consultations, Clinical Trial Notifications, PCAs, MCNs, and NDAs through operational excellence.</li><li>Maintaining submission templates and obtaining literature references to support submissions.</li><li>Ensuring consistency and standardization across regulatory submissions.</li><li>Tracking and managing metadata within the electronic data management system (EDMS).</li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li>You have a strong knowledge of Regulatory Agency regulations, guidelines, and specifications (e.g., PMDA, FDA, EMA, and ICH).</li><li>You excel in project management and timeline management for regulatory submissions.</li><li>You enjoy working with submission processes and systems such as Veeva Vault RIM or docuBridge.</li><li>You are adept at eCTD preparation and validation processes.</li><li>You thrive in fast-paced environments and can adapt quickly to changing priorities.</li><li>You have strong proficiency with MS Office applications and Adobe Acrobat.</li><li>You value collaboration and have exceptional attention to detail.</li><li>You are driven by the opportunity to make meaningful contributions to regulatory milestones.</li></ul><p><strong>To Be Considered:</strong><br>To excel in this role, you must have a Bachelor's Degree and at least six years of pharmaceutical industry or relevant experience. Strong knowledge of submission processes, eCTD guidelines, and regulatory tools is essential. Proficiency with systems like Veeva Vault RIM and docuBridge is highly desirable. Native level fluency in Japanese and business level English is required.</p><p>This is your chance to be part of a team that drives impactful regulatory submissions while fostering innovation and collaboration. Apply now to make a difference in regulatory excellence!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 09 Apr 2026 04:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director Resource Management]]></title>
    <date><![CDATA[Wed, 15 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46443]]></requisitionid>
    <referencenumber><![CDATA[R46443]]></referencenumber>
    <apijobid><![CDATA[r46443]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46443/director-resource-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Director, Resource Management (DRM) is a key liaison across multiple functions in Research and Preclinical Development (RpD) providing comprehensive resource management and strategic resource planning for RpD functions with respect to current programs as well as planning for the future development portfolio. The DRM will supervise and coach two resource managers on the team. To be successful, the DRM will need to have an in-depth understanding of pharmaceutical discovery, pre-clinical development, research and early development functional roles, responsibilities and work effort. The DRM will be an expert in industry standard resource management tools and respective reporting tools to provide key insights regarding capacity, resource planning and forecasting. The DRM will be confident in the design of effective insight driven dashboards and collaborate closely with the IT function to enable development, implementation, and support. The DRM will promote the adherence to RM best practices, processes and the delivery of high-quality resource planning, capacity management, tracking, and forecasting of functional resources.</p><h3><strong>As a Director, a typical day may include the following:</strong></h3><ul><li><p>Serves as the key interface and point of contact with R&pD for the review and assessment of functional resource strategies including the assessment of available resources against requirements and confirmation of resource plans with functional leadership</p></li><li><p>Works with partners to ensure that Target, Project, and Program assumptions are current and resource utilization is optimized</p></li><li><p>Partners with applicable functions to design, develop, implement, and update algorithms in the RM tool used in resource demand forecasts</p></li><li><p>Directs other RMs assigned to additional functional areas to ensure cross-functional consistency for resource and headcount management</p></li><li><p>Assists partner functions with capacity management providing support for annual headcount planning and ensuring data quality for the quarterly budget reforecast activities</p></li><li><p>Deliver regular and ad-hoc resource reports, including forecasted resource demand, capacity, gap analyses, and FTE planned vs. actuals that provide clear insights needed for decision making</p></li><li><p>Is viewed as Subject Matter Expert (SME) in Resource Management for targets, assets, programs, and studies</p></li><li><p>Provides leadership and operational support for resource management processes including active resource management, capacity planning, and strategic workforce planning</p></li><li><p>Liaises with the Data Analytics (DA) team to design reports to help identify trends and develop metrics and analytics around resourcing and to develop functional and portfolio resourcing benchmarks and metrics</p></li><li><p>Conducts portfolio and program level scenario analyses. Models impact of changes in assumptions on resource estimates</p></li><li><p>Proactively identifies and communicates resource-related gaps, issues and risks to partner functions based on analysis of resource data. Supports review and discussion to resolve resource and/or capacity conflicts</p></li></ul><h3><strong>This role may be for you if:</strong></h3><ul><li><p>Adept at managing a limited supply of resources against constantly changing portfolio</p></li><li><p>Excellent analytical, budgeting, and resource balancing skills</p></li><li><p>Problem solving abilities, troubleshooting, conflict resolution, and resourcefulness</p></li><li><p>Effective communication (clear and concise written and verbal skills), influencing, negotiating, and selling</p></li><li><p>Excellent interpersonal and leadership skills, ability to build relationships internally and externally (e.g. with supervisors, peers, partners and stakeholders)</p></li><li><p>Detail oriented and capable of working independently in ambiguous situations</p></li><li><p>Ability to manage multiple tasks and tight deadlines with confidence</p></li><li><p>Ability to prioritize and organize workload across multiple groups</p></li><li><p>Experience with supervising, coaching, and mentoring direct reports</p></li><li><p>Proficiency in Microsoft Office Suite</p></li></ul><p>To be considered for this role, you must have a Bachelor’s Degree required and 12+ years’ experience in Biotech/Pharmaceutical/CRO, including, but not limited to, Research, Early and Late Development functional areas. Master’s Degree (MS/MBA) and 10+ years of relevant experience may be considered. A solid understanding of the drug discovery and development process with particular emphasis on preclinical development, translational medicine, and early development for biological molecules. Expert with Planisware for project planning and resource forecasting including the design, development, and implementation of algorithms. We are seeking extensive experience with reporting for business facing resource management in research and development. This opportunity requires the ability to travel up to 20%.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 16 Apr 2026 09:56:15 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Supply Analyst - Kinaxis Maestro]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43446]]></requisitionid>
    <referencenumber><![CDATA[R43446]]></referencenumber>
    <apijobid><![CDATA[r43446]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43446/principal-supply-analyst-kinaxis-maestro/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal Supply Analyst - Kinaxis Maestro will drive innovation in supply chain planning and execution. In this role, you’ll design, implement, and optimize solutions using the Kinaxis Maestro platform, helping deliver life-saving products to patients worldwide.</p><div><p>As a Principal Supply Analyst, a typical day might include the following:</p><ul><li>Design and configure Maestro solutions for campaign management, lifecycle planning, and inventory optimization.</li><li>Develop worksheets, dashboards, and analytics to support planning and execution.</li><li>Build custom templates, algorithms, and scripts to enhance functionality. Integrate Maestro with ERP systems (e.g., Oracle, SAP) and life sciences platforms.</li><li>Ensure compliance with FDA, EMA, GMP, and other regulatory standards.</li><li>Train end-users on Maestro functionalities and best practices.</li><li>Maintain detailed documentation for workflows and configurations.</li><li>Monitor system performance and identify improvement opportunities.</li><li>Resolve issues related to data integrity and system integrations.</li><li>Work cross-functionally with operations, logistics, planning, manufacturing, and finance teams.</li></ul></div><p>This role may be for you if you have:</p><ul><li>Strong understanding of demand planning, clinical trial supply chains, SIOP and regulatory compliance.</li><li>Experience integrating ERP and life sciences-specific software, preferably Oracle.</li><li>Good understanding of Kinaxis Maestro data model, control table, and data management.</li><li>Excellent problem-solving and communication abilities.</li><li>Proficiency in Agile methodologies (e.g., Scrum) and programming skills (Python, SQL) are a plus.</li></ul><p>In order to be considered for this position, you must hold a Bachelor’s degree in supply chain management, Computer Science, Engineering, or related field and</p><ul><li>Senior Supply Analyst: 5+ in Supply Chain Planning solutions, 3+ years Hands-on experience with Kinaxis Maestro, preferably in life sciences.</li><li>Principal Supply Analyst: 8+ in Supply Chain Planning solutions, 5+ years Hands-on experience with Kinaxis Maestro, preferably in life science.</li><li>Kinaxis Maestro Author or Administrator certifications, Level 2 or higher preferred.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Patient Journey Data & Analytics]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46284]]></requisitionid>
    <referencenumber><![CDATA[R46284]]></referencenumber>
    <apijobid><![CDATA[r46284]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46284/associate-director-patient-journey-data-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Director, Patient Journey Data & Analytics will report into Director, Patient and Channel Data Management within the Commercial Strategy and Insights and Analytics (CSI&A) department. </p><p><strong>In this role, a typical day might include:</strong></p><p>The Associate Director, Patient and Channel Data management is responsible for the curation, governance, quality and operationalization of patient/specialty data assets that power commercial decision making across therapeutic areas. The ideal candidate brings deep expertise in specialty pharmaceutical data ecosystems, strong problem-solving capabilities, and the ability to influence and drive alignment across a broad set of cross-functional partners.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><ul><li><p>Serve as the subject matter expert and strategic owner for channel and patient support services data assets; develop and maintain data management frameworks, SOPs, data dictionaries, and data maps across all relevant data domains</p></li><li><p>Establish and monitor data quality metrics to ensure accuracy, completeness, and integrity; drive root cause analysis and resolution of data quality issues, including SP/SD/patient-level data reconciliation</p></li></ul><p><em>Develop</em></p><ul><li><p>Support integration of specialty data into commercial reporting, forecasting, and analytics platforms; maintain alignment with enterprise data governance principles in partnership with governance teams</p></li><li><p>Contribute to launch readiness by building data infrastructure and reporting frameworks ahead of new product or indication launches; represent the data management function in commercial operations working groups and leadership reviews</p></li></ul><p><em>Partnership and Collaboration</em></p><ul><li><p>Provide accurate channel-level data inputs to support gross-to-net and revenue deductions modeling in partnership with Trade and Market Access teams</p></li><li><p>Manage relationships with data aggregators, specialty distributors, SP data providers, and PSS vendors, including contract scope, data delivery SLAs, issue escalation, and regular business reviews</p></li><li><p>Serve as a key data management partner across internal stakeholders (PSS, Trade, CIT, I&A Market Access, Advanced Analytics), translating complex data concepts into clear business context for non-technical audiences</p></li></ul><p><em>Execute</em></p><ul><li><p>Manage end-to-end data flows from specialty distributors and specialty pharmacies, including SD 867/852 transaction data, SP inventory and dispense, chargeback, and ex-factory shipment data</p></li><li><p>Build, manage and govern PSS data assets across the full patient journey (patient intake, BI/BV, eBV, PA/ePA, copay enrollment/claims, free goods/PAP/IAP) in strict compliance with HIPAA, PHI requirements, and Regeneron data governance and tokenization standards</p></li><li><p>Maintain working knowledge of and leverage industry-standard commercial datasets (IQVIA LAAD, APLD, Symphony Health, Precision, MMIT); apply data tokenization methodologies to link patient-level data across sources while maintaining PHI compliance</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>BA/BS with 10+ years (or MBA/MS with 7+ years) of experience in commercial data management, analytics, or operations within the pharmaceutical or biotechnology industry</p></li><li><p>Deep expertise in patient/specialty pharmaceutical data ecosystems, including: Deep expertise in specialty pharmaceutical data ecosystems, including channel/trade data (SD 867/852, SP inventory/dispense, chargeback, ex-factory), SP/SD reconciliation and audit controls, and PSS data (patient intake, BI/BV, eBV, PA/ePA, copay enrollment/claims, free goods, IAP/PAP)</p></li><li><p>Strong working knowledge of industry-standard datasets including IQVIA LAAD, APLD, Symphony Health, Precision, and MMIT</p></li><li><p>Experience with data tokenization, PHI handling, and HIPAA compliance requirements</p></li><li><p>Proficiency with data management and analytics tools (e.g., SQL, Snowflake, Databricks, or equivalent)</p></li><li><p>Proven experience managing external data vendors and holding partners accountable to SLAs</p></li><li><p>Demonstrated ability to influence without authority and drive alignment across cross-functional teams</p></li><li><p>Demonstrated flexibility, leadership presence, and emotional intelligence when navigating complex stakeholder environments and competing priorities</p></li><li><p>Strong problem-solving skills with a structured, analytical approach to identifying and resolving data issues</p></li><li><p>Excellent written and verbal communication skills; ability to translate complex data concepts for diverse audiences</p></li><li><p>Experience supporting an ophthalmology, retina, or other specialty/rare disease commercial franchise (Preferred)</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 21 Apr 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialist II-Oncology-Las Vegas, NV]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46212]]></requisitionid>
    <referencenumber><![CDATA[R46212]]></referencenumber>
    <apijobid><![CDATA[r46212]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46212/medical-account-specialist-ii-oncology-las-vegas-nv/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Las Vegas]]></city>
    <state><![CDATA[Nevada]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Las Vegas, NV</strong></p><p>The Oncology Account Specialist will engage HCPs who treat NSCLC/NMSC patients within specific accounts - including academic centers, large group practices, IDN’s, and community accounts. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Key Account Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Engage Oncology Specialists (NSCLC/NMSC) and other key experts within assigned account alignment and deliver clinical messages to grow brand share and revenue.</p></li><li><p>Facilitate partnership with multiple collaboration partners; Regional Director, Territory-based Oncology Account Specialists, OKALs (Oncology Key Account Leaders), Reimbursement Specialists to proactively resolve customer needs, identify market dynamics and trends, and develop strategies which support brand and corporate objectives in assigned territory</p></li><li><p>Develop strong working relationships with aligned designated accounts and specialists</p></li><li><p>Execute market profiling activities to ensure a deep understanding of regional and local health care delivery, influencers and payer systems.</p></li><li><p>Proactively identify business opportunities with assigned accounts and leads appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if:</strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum 3 years successful experience in Oncology sales (NSCLC and/or NMSC experience Preferred). Buy and bill experience with biologics required. Minimum of (3) years of experience working with key NSCLC/NMSC thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Oncology NSCLC/NMSC therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 16:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Data Enablement]]></title>
    <date><![CDATA[Sun, 26 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46265]]></requisitionid>
    <referencenumber><![CDATA[R46265]]></referencenumber>
    <apijobid><![CDATA[r46265]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46265/director-data-enablement/]]></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>Director, Data Enablement (Armonk, NY)</strong></p><p>Regeneron Pharmaceuticals, Inc. seeks a Director, Data Enablement (Armonk, NY) to drive strategic partnerships with GD-IT Business Solution Partners, DA&DS, Data Platform Services, and GD-IT Operations Resources to ensure that business technology solutions projects are aligned with organizational goals and objectives. Lead collaboration with GD-IT Solution Architecture and Enterprise teams to identify and implement cutting-edge technologies that are vital to meet the intended business outcomes, overseeing creation and execution of end-to-end projects. Provide executive oversight for implementation plans – guiding Portfolio Managers, Project Managers, and Business Analyst resources. Lead the definition and optimization of implementation processes and standards, engaging business and team members to confirm requirements details and to ensure that design meets business needs communicated in improvement requests and defects, while crafting and maintaining solution roadmaps and demand management processes in consultation with GD-IT Business Solution Partners, Functional Area Implementation Leads, and Enterprise partners. Serve as a senior expert in implementation and adoption of Master Data Management solutions, overseeing implementation of multiple workstreams and ensuring the MDM program is completed on schedule, on budget, and to quality. Identify data integration needs and collaborate with Strategic Data Enablement and Enterprise teams to implement required integrations, overseeing system validation process and execution activities, and partnering with the GD-IT Quality Management Lead and Enterprise Quality Assurance and Validation teams. Oversee project execution for all project management lifecycle activities. Act as a key liaison with senior leadership, providing regular updates on project status, risks, and opportunities. Represent the data enablement function at internal and external forums, conferences, and industry events. Local telecommuting permitted up to 2 days per week. 20% domestic travel required to other Regeneron sites as well as to attend conferences, and 10% international travel required. Lead and mentor a team, including 2 Direct Reports in the positions of Associate Director – Data Enablement (Harmonization and Enhancement).</p><p>SALARY RANGE: $261,248.00 - $305,200.00 per year</p><p><strong>Job Requirements</strong><strong>:</strong></p><p>Requires a Bachelor’s degree in Computer Engineering, Computer Science, or related field with 5 years of implementation and support of Master Data Management (MDM) programs experience. Must have experience with: MDM implementation using Informatica IDMC platform; Data Quality, Data Governance, Information Architecture, and Technology Implementation; Design, Build / Implementation as well as Postproduction Adoption of MDM solutions; MDM best practices and processes; IDMC Customer360, Product 360, Reference360, CDGC, Data Quality, and Data marketplace microservices; Working with business and providing recommendations on match/merge rules; Crafting and maintaining solution roadmap and demand management processes; and Leading and managing cross-functional teams, with experience in strategic planning, project management, and process optimization.</p><p>Apply at <a href="https://careers.regeneron.com">https://careers.regeneron.com</a>. Reference code: R46265.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 27 Apr 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Validation Specialist (Fill Finish)]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46783]]></requisitionid>
    <referencenumber><![CDATA[R46783]]></referencenumber>
    <apijobid><![CDATA[r46783]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46783/principal-qa-validation-specialist-fill-finish/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is currently seeking a Principal QA Validation Specialist to join our Quality Assurance department. They will lead the utilities and EMPQ team for 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>As a Principal QA Validation Specialist, a typical day might include the following:</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: WFI (Water for Injection), 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></ul><p>This role might be for you if you:</p><ul><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><li>Have proven ability to lead teams in a fast-paced, dynamic environment</li><li>Are able to gown and work in manufacturing areas as required</li></ul><p>Gowning and Environment </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>To be considered for the Principal QA Validation Specialist you must be willing and able to work Monday-Friday, 8am-4:30pm. You must hold a BS/BA in Engineering, Chemistry, or Life Sciences and 8+ years of relevant experience. Experience in utility and facility qualification/validation is required. Level is determined based on qualifications relevant to the role. </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$92,200.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 12:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Scientist, Oncology (Histology and Immunohistochemistry)]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46021]]></requisitionid>
    <referencenumber><![CDATA[R46021]]></referencenumber>
    <apijobid><![CDATA[r46021]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46021/scientist-oncology-histology-and-immunohistochemistry/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Histology team is seeking a highly motivated Senior Associate Scientist/Scientist to join the Oncology/Immuno-Oncology department at Regeneron Pharmaceuticals, as we make transformational advances in harnessing the power of the immune system to fight cancer. The position will involve executing complex histological studies to reveal potential target expression and investigate the mechanism of action of novel immuno-oncology therapeutics. This role will be deeply involved in the development of cutting-edge therapeutics including bispecific antibodies, antibody-drug conjugates, and CAR-T cells. You will work closely with other team members and collaborators to advance programs spanning from initial target discovery to support of ongoing clinical-stage therapeutics.<br><br><strong>As a Scientist, a typical day may include the following:</strong><br> </p><ul><li><p>Independent execution of immunohistochemistry (IHC) assays, including the use of high-throughput Ventana and Biocare autostainer platforms</p></li><li><p> RNA in-situ hybridization (ISH) based assays using modern platforms such as RNAscope.</p></li><li><p>Histological tissue processing, microtomy, cryosectioning, and H&E staining of human and non-human tissues</p></li><li><p>Development and characterization of novel antibodies and probes for IHC and ISH assays</p></li><li><p>Scanning of slides and assembly of images in PowerPoint and other formats for presentation</p></li><li><p>Basic analysis of images and frequent collaboration with members of the Pathology department</p></li></ul><p><strong>This role may be for you if:</strong><br> </p><ul><li><p>You have proven basic histology skills and a desire to further expand and develop your skill set and knowledge of the immuno-oncology drug development process.</p></li><li><p>You are enthusiastic to learn new skill sets, including multiplex IHC, complex image analysis, and performing cell culture </p></li><li><p>You are detail-oriented, have strong time management skills, and appreciate an opportunity for growth as a scientist.</p></li><li><p>You possess the drive and desire to learn how to troubleshoot and think outside the box to solve complex problems.</p></li><li><p>You have excellent written and verbal communication skills, and the ability to work as part of a diverse team.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><p>A BS with 7 years or MS with + 5+ years of laboratory experience (in academia or industry) in a relevant scientific discipline (Immunology, Oncology, Molecular/Cell Biology) and direct hands-on experience executing histology and immunohistochemistry techniques. Experience with autostainer platforms (e.g., Ventana or Biocare) is a plus. Experience in the research and development of targeted cancer therapeutics, including antibodies and CAR-T cells, is an advantage. The ideal candidate will possess strong organizational skills including the ability to manage and record details of several complex projects simultaneously. A demonstrated ability to communicate seamlessly and work across diverse groups to achieve a common goal is also desired.<br><br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:26:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager,  Research Program Management]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46243]]></requisitionid>
    <referencenumber><![CDATA[R46243]]></referencenumber>
    <apijobid><![CDATA[r46243]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46243/associate-manager-research-program-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Associate Manager in Research Program Management plays a key role in executing Regeneron’s programs through the drug discovery pipeline. The Associate Manager drives projects with a moderate to high level of complexity and coordinates with cross functional groups including the Therapeutic Focus Area, Technology centers, and the broader Research team to achieve portfolio and program goals. </p><p><strong>As an Associate Manager, a typical day may include: </strong></p><ul><li><p>Executes programs with guidance; manages projects and tasks independently and with awareness of internal/external interdependencies.</p></li><li><p>Can identify and may champion resolution of critical gaps, risks, or issues, as related to assigned programs, projects, and tasks.</p></li><li><p>May be aware of strategic goals related to programs and projects. </p></li><li><p>With guidance, can prioritize projects and programs and allocate team resources. Manager's input is needed to align with organizational strategic objectives. </p></li></ul><p><strong>Communication and Team Management </strong></p><ul><li><p>With minimal guidance, drives and contributes to decision making amongst cross functional program teams. </p></li><li><p>With minimal guidance, distills complex information and identifies the most pertinent key information; effectively captures rationale for decision-making.</p></li><li><p>With minimal guidance, facilitates collaboration between functional areas to ensure effective, accurate, and timely scientific / technical and program-related communication. </p></li><li><p>With minimal guidance, can tailor communications based on audience.</p></li><li><p>Has strong relationships with project leaders, managers and individuals within each project team and key cross-functional partners.</p></li></ul><p><strong>This role might be for you if you: </strong></p><ul><li><p>Identifies and collates key data and functions needed to drive discussion and decision making for moving projects/programs through discovery and drug development process.</p></li><li><p>May provide technical and/or operational guidance to project teams and/or other RPM members for their assigned programs. </p></li></ul><ul><li><p>Has technical expertise in existing processes that relate to and support projects and programs.</p></li><li><p>Independently analyzes and identifies areas of minimal complexity for process improvement.</p></li><li><p>Contributes to process improvement initiatives</p></li><li><p>Creates new processes as needed with guidance, leads the development and gains alignment on process improvement solutions, informed by knowledge of technical/scientific challenges faced by the project teams.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Minimum of BS/MS/PHD. </p></li><li><p>Knowledge of molecular biology, protein structure-function, and assay development concepts is required</p></li><li><p>Prior experience in drug development is required</p></li><li><p>Regularly utilizes strategic thinking around complex scientific principles</p></li><li><p>Ability to organize complicated workflows/operations</p></li><li><p>Prior project/program management experience is desirable</p></li><li><p>Excels in team building and communication</p></li><li><p>Excellent written, verbal, organizational, and interpersonal communication skills.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$98,100.00 - $160,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 22:26:30 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Global Procurement - Commercial]]></title>
    <date><![CDATA[Sun, 26 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43833]]></requisitionid>
    <referencenumber><![CDATA[R43833]]></referencenumber>
    <apijobid><![CDATA[r43833]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43833/executive-director-global-procurement-commercial/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Executive Director, Global Procurement – Commercial Procurement will provide strategic leadership and direction with a focus on Commercial Communications Procurement. The role focuses on a very exciting part of Commercial Procurement which includes Advertising, Media, Corporate Affairs/Public Relations, and Promotional Medical Communications. This role will be critical to driving performance across the Commercial Communications categories including alignment with stakeholder goals, driving towards competitive advantages (strategic and financial), optimizing supplier relationships, including small and diverse suppliers. This role works in close collaboration with Commercial Stakeholders to enable company revenue targets and the new product pipeline.<br><br>This individual will report to the Vice President of Commercial Procurement and serve as a member of the Global Procurement Extended Leadership Team, contributing to a continual path towards excellence in Procurement. The role will be accountable for managing direct reports to drive short-term priorities and the long-term vision to support stakeholder and Global Procurement priorities. They will lead the development, retention, and recruiting of talent to enable the company’s Commercial Procurement team. This includes collaborating with the VP of Commercial Procurement on performance goals, coaching and mentoring, and fostering a collaborative and inclusive work environment that encourages innovation and continuous learning.<br><br><strong><em>The role is based at our HQ campus in Sleepy Hollow, NY and is hybrid / onsite 4 days per week - it is not eligible for remote work. </em></strong></p><p><strong>A Typical Day May Include</strong></p><ul><li>Lead the composition, development and execution of category strategies in Commercial Communications;</li><li>Translate category strategies into achievable and meaningful sourcing projects that deliver value to Regeneron and its patients;</li><li>Partner with Commercial Procurement Leadership colleagues to ensure strategies evolve as Regeneron and its pipeline evolves;</li><li>Implement category strategies to meet objectives, including meeting our ESG objectives (sustainability, supplier diversity);</li><li>Collaborate with other parts of Global Procurement to best manage cross-category suppliers;</li><li>Anticipate needs and plan strategies to optimize achievement of corporate goals;</li><li>Collaborate and execute a best in class partner management program;</li><li>Implement and manage technology solutions to drive value via efficiency and effectiveness</li><li>Build and manage a team that provides all Commercial Communications Procurement support globally;</li><li>Continually enhance capability and capacity through ongoing talent development; establishing/communicating criteria for evaluating staff performance; managing direct reports, implementation of consistent work processes; and</li><li>Drive process excellence with a focus on stakeholder experience</li></ul><p><strong>This Role May Be For You If You </strong></p><ul><li>Believe that value can be driven through strategic partnerships and efficient ways of working.</li><li>Embrace challenging the status quo.</li><li>Are curious about how to deliver value to Commercial Communications stakeholders in a changing biopharma landscape.</li><li>Enjoy tracking global v local trends.</li><li>Can tap into strong in-depth knowledge of efficient global procurement organizations and processes within the biopharmaceutical industry to support the growth and evolution of a Global Procurement organization.</li><li>Enjoy successfully leading global categories or global teams, processes, and suppliers within a multi-national organization.</li><li>Serve as role-model leader consistently exhibiting behaviors across an organization of direct reports to create clarity, provide a clear and understandable vision with transparency and trust both within and outside of the organization.</li><li>Operate with integrity, focus, clarity, and sound judgement in an environment of ambiguity.</li><li>Can influence and partner with senior executives and peer functions to drive strategic change and efficiency.</li></ul><p><strong>To Be Considered For This Position You Should Possess </strong></p><ul><li>Experience managing Associate Director+ level professionals required with previous success driving results within a multi-national Global Procurement team.</li><li>~15 years or more experience in relevant functions or industries, demonstrating growth in experience, scale, and development throughout.</li><li>In-depth knowledge of marketing and sales procurement categories including but not limited to media, content, production, and medical communications.</li><li>Ability to identify root causes and develop solutions to address complex problems.</li><li>Problem solving, risk management, program rollouts, and ability to put together forecasts for volume and savings.</li><li>Negotiation and contract management skills.</li><li>Ability to adapt in fast paces and ever-evolving space.<br> </li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 27 Apr 2026 10:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-Dermatology-Los Angeles North, CA (San Fernando Valley, Santa Barbara, Santa Maria)]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47241]]></requisitionid>
    <referencenumber><![CDATA[R47241]]></referencenumber>
    <apijobid><![CDATA[r47241]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47241/medical-specialist-i-dermatology-los-angeles-north-ca-san-fernando-valley-santa-barbara-santa-maria/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Los Angeles]]></city>
    <state><![CDATA[California]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Geography: Los Angeles North, CA (San Fernando Valley, Santa Barbara, Santa Maria)</strong></p><p>Our Medical Specialists are at the forefront of engaging Dermatologists and other key customers. We need someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. Our ideal candidate must be driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p><strong>As a Medical Specialist, a typical day may include the following:</strong></p><ul><li><p>Developing strategy and executing tactics within key accounts in the Dermatology therapeutic area</p></li><li><p>Establishing and fostering strong working relationships with health care professionals, including nurses, office staff key patient advocacy support groups</p></li><li><p>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</p></li><li><p>Analyzing market dynamics and trends to develop strategies which support brand and corporate objectives</p></li><li><p>Engaging in initiatives to promote sales success such as industry related congresses, local and regional meetings and medical conferences</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are confident in demonstrating strong and consistent sales performance that exceeds expectations related to product goals</p></li><li><p>You are innately guided by core values of ethics and compliance and always act in a manner consistent with those values</p></li><li><p>You have a competitive spirit and harness your “grit” to power your approach to sales</p></li><li><p>You collaborate effectively with internal and external partners</p></li><li><p>You share a passion and learning aptitude for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><li><p>You are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</p></li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree. A Master’s degree or other advanced education/certifications are a plus. We expect that a successful candidate will have specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience. Having a minimum of 2 years selling in the Immunology market or a similar subcutaneous self-injectable biologic specialty market is also a requirement for this role, dermatology experience preferred. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments. This role requires the ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sample Management Associate]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45879]]></requisitionid>
    <referencenumber><![CDATA[R45879]]></referencenumber>
    <apijobid><![CDATA[r45879]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45879/sample-management-associate/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A Sample Management Associate supports biobanking operations efficiently and effectively while beginning to independently lead sample data processes. Possesses a thorough knowledge and understanding of clinical/non-clinical study protocols and associated documentation. Is fully capable of multi-tasking across assignments. Works with clients directly in a team environment. The incumbent may help in assessing and investigating new opportunities that will lead to increased efficiencies and improved productivity with regards to biobanking operations.</p><p><strong>As a Sample Management Associate, a typical day may include:</strong></p><ul><li><p>Trains on clinical/non-clinical study protocols and associated study documentation to build knowledge of study conduct as it pertains to biospecimen management. Executes study reference file creation by interpreting protocols and other applicable data inputs with guidance.</p></li><li><p>Performs the accessioning and receipt of non-clinical/clinical samples by assessing and verifying data, both manually and with automated platforms such as Microsoft VBA and Streamlit. May identify and communicate issues with automated platforms to drive resolution.</p></li><li><p>Has an in-depth knowledge of Microsoft Excel and can analyze discrepancies in sample metadata using complex formulas with limited guidance.</p></li><li><p>Drives necessary operations in applicable software systems (e.g., LIMS, ELN, etc.) to perform specimen and data management. Has the ability to identify and troubleshoot routine challenges.</p></li><li><p>Fulfills clinical/non-clinical sample requests to support bioanalysis deliverables as well as company-wide research initiatives.</p></li><li><p>Facilitates the completion and review sample transfer documentation, as applicable.</p></li><li><p>Responsible for assigning and coordinating sample management activities for assigned programs under limited guidance.</p></li><li><p>Under supervision, executes the reconciliation and data cleaning of biospecimens to drive deliverables forward.</p></li><li><p>May be responsible for the review of study documents to support study start up and protocol amendments.</p></li><li><p>Ensures a state of audit readiness. Assists in the preparation of supporting documents for Quality Audits, as applicable. May participate in study audit activities.</p></li><li><p>Provides cross-functional support to other sample management teams, as needed.</p></li><li><p>May assist with the training of other laboratory staff.</p></li><li><p>Participates in sub-group meetings and may shares results or progress of work with others.</p></li><li><p>Responsible for his/her own safety in the laboratory, as well as for the safety of co-workers and visitors.</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Ensure compliance and proper documentation in accordance with SOPs, and applicable regulations.</p></li><li><p>Handle high priority and multiple tasks within the appropriate timeframe while maintaining accuracy. Adapts to changing priorities. Is capable of multi-tasking across assignments.</p></li><li><p>Capable of identifying and troubleshooting problems pertaining to clinical/non-clinical protocols and associated documents as well as routine sample management processes and/or procedures.</p></li><li><p>Collaborates and maintains effective verbal and written communication with internal and/or external stakeholders to facilitate data discrepancy resolution. Communicates with CRO’s and third-party vendors to support biospecimen operations.</p></li><li><p>Communicates optimally with their manager and actively seeks out feedback to deepen self-development.</p></li></ul><h3>To be considered for this role, you must meet the following:</h3><ul><li><p>Bachelor’s degree</p></li><li><p>Typically, 2-4 years of relevant post-degree laboratory experience for Bachelor’s degree</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$66,300.00 - $98,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 21:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temporary Clinical Trial Recruitment and Retention Implementation Manager]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46737]]></requisitionid>
    <referencenumber><![CDATA[R46737]]></referencenumber>
    <apijobid><![CDATA[r46737]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46737/temporary-clinical-trial-recruitment-and-retention-implementation-manager/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[[Unknown]]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for an experienced Recruitment & Retention Manager to support the delivery of patient-focused clinical trials at Regeneron. In this role, you will help bring recruitment and retention strategies to life across global studies by collaborating closely with internal teams, CROs, and specialist vendors. Your work will directly influence patient identification, engagement, and participation, ensuring solutions are compliant, data-driven, and ready ahead of key study milestones. This role offers the opportunity to shape operational excellence while contributing to meaningful progress in clinical development. This is a 12-month contract.</p><h3>A Typical Day:</h3><ul><li><p>Overseeing trial-level recruitment and retention tactics across assigned studies</p></li><li><p>Collaborating with study teams to deliver compliant recruitment plans before FPFV</p></li><li><p>Coordinating with Clinical Trial Management on milestones and country allocations</p></li><li><p>Managing specialist vendors, tracking KPIs, compliance, and contractual delivery</p></li><li><p>Reviewing and improving recruitment materials, content, and design elements</p></li><li><p>Monitoring performance metrics and pivoting strategies based on emerging data</p></li><li><p>Maintaining tracking systems, checklists, and recruitment process documentation</p></li></ul><h3>This Role May Be For You:</h3><ul><li><p>Prefer structured work that balances planning, execution, and follow-through</p></li><li><p>Are comfortable using data and metrics to guide operational decisions</p></li><li><p>Care about delivering patient-focused solutions that meet regulatory standards</p></li><li><p>Value clear documentation, consistency, and continuous process improvement</p></li><li><p>Are motivated by contributing to successful study delivery behind the scenes</p></li></ul><h3>To Be Considered</h3><p>You must hold a Bachelor’s degree and bring 7 or more years of relevant experience in clinical trial recruitment, retention, or related clinical operations, with advanced degrees considered in lieu of years of experience. Experience across the clinical drug development lifecycle—including enrollment tracking and recruitment strategy execution—is required, along with hands-on vendor management. Applicants should demonstrate solid understanding of ICH/GCP, EUCTR, and IVDR guidelines, and show technical proficiency with CTMS, TMF systems, AI-supported document tools, and core MS applications. This role may require up to 5-10% travel.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 04:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Field Medical Affairs, South Center]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46696]]></requisitionid>
    <referencenumber><![CDATA[R46696]]></referencenumber>
    <apijobid><![CDATA[r46696]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46696/senior-manager-field-medical-affairs-south-center/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an experienced Field Medical Affairs professional specializing in Hematology to join our team in Spain. In this pivotal role, you will serve as a scientific and clinical resource, engaging with key opinion leaders, healthcare professionals, and internal stakeholders to advance disease awareness and support innovative research initiatives. By collaborating across Medical Affairs, Clinical Development, Market Access and Commercial, you’ll help drive impactful strategies that shape the future of hematological care. This is your chance to create a meaningful difference in patient outcomes while growing your expertise in a dynamic, matrix-driven environment.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Building and nurturing peer relationships with leading experts in Hematological Malignancies.</p></li></ul><ul><li><p>Presenting scientific and clinical data to healthcare professionals and investigators.</p></li></ul><ul><li><p>Supporting and managing clinical trials by identifying investigators and trial sites.</p></li></ul><ul><li><p>Collaborating with internal teams and cross-functional partners to align strategies.</p></li></ul><ul><li><p>Responding to requests for information about disease states and Regeneron’s products.</p></li></ul><ul><li><p>Ensuring compliance with company policies and regulatory guidelines.</p></li></ul><ul><li><p>Assisting with the development of abstracts, posters, and manuscripts for scientific communication.</p></li></ul><ul><li><p>Providing support to the commercial team.</p></li></ul><p><strong>This Role May Be For You, if you:</strong></p><ul><li><p>Thrive in a collaborative, matrix environment and enjoy cross-functional teamwork</p></li><li><p>Value building and maintaining positive relationships with healthcare professionals and investigators.</p></li></ul><ul><li><p>Are committed to scientific integrity and professional communication at all times.</p></li></ul><ul><li><p>Excel at organizing, planning, and balancing multiple priorities, both independently and as part of a team.</p></li></ul><ul><li><p>Are passionate about advancing hematological research and supporting innovative clinical initiatives.</p></li></ul><p><strong>To Be Considered</strong></p><p>Applicants must hold a Bachelors degree, with preferably 5+ proven experience, including at least 3 years in a Field Medical or Medical Manager role within the biotech or pharmaceutical industry, focusing on Oncology or Hematology. Expertise in the Hematology therapeutic area is required, with experience in lymphoma and/or multiple myeloma strongly preferred. Established relationships with key opinion leaders in malignant hematology and familiarity with institutions specializing in Hematologic Malignancies are advantageous. Drug launch experience, knowledge of treatment guidelines, clinical research processes, EU and pharma regulations, and strong communication skills are essential. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 20:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Account Specialists  - Hematology]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47428]]></requisitionid>
    <referencenumber><![CDATA[R47428]]></referencenumber>
    <apijobid><![CDATA[r47428]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47428/medical-account-specialists-hematology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Arizona]]></city>
    <state><![CDATA[Arizona]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Hematology Oncology Account Specialist is responsible for engaging Oncology specialists and other key Oncology customers within a geographical universe and settings, including academic centers, large group practices, IDNs, and community accounts in support of the launch of our Multiple Myeloma product. This key role will focus on presenting clinically focused selling messages to build and grow revenue and to consistently deliver product goals. To achieve goals, you will demonstrate initiative, drive, and independence; take ownership by demonstrating outstanding account management-based selling skills. This will be accomplished by leading performance and delivering results in a compliant manner with integrity rigorously following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical / biological products in the US. We seek a true collaborative partner to working closely with Reimbursement and Access Specialists, Regional Science Managers to efficiently and effectively address customer needs.</p><p><strong>A typical day may include the following:</strong></p><ul><li><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 appropriate coordination of effort by the Regeneron Oncology account team, e.g. supports contracting pull-through with accounts.</p></li><li><p>Develop a breadth of relationships within each account to ensure an understanding of each account’s objectives, goals, and challenges and identifies approved Regeneron Oncology resources that are aligned to the customer’s needs.</p></li><li><p>Demonstrates dedication to compliance through understanding of regulations and policies that govern customer interactions and consistent focus on ensuring compliance with them.</p></li></ul><p><strong>This role might be for you if: </strong></p><ul><li><p>You have proven advanced clinically based and account-based selling skills</p></li><li><p>You have shown success and positive consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>You are results oriented with a track record of success with product launches</p></li><li><p>You are a strong account manager with analytical, problem-solving and planning skills</p></li></ul><p>To be considered for this opportunity you will have the following:</p><p>A Bachelors degree; Master’s degree or additional advanced education/certifications a plus and a minimum of 5 years successful experience in Oncology sales, Hematology Oncology preferred. Buy and bill experience with biologics required. Minimum of 3 years of experience working with key thought leaders or high influence customers in group practices, academic hospitals, key institutions. Current account management experience in calling on large Oncology group practices and/or integrated delivery networks. You must possess a strong understanding of the Hematology Oncology therapeutic area and the current Oncology marketplace. You represent your peers as a leader, with the ability to collaborate with and coordinate activity among individuals in different reporting structures within the organization. We seek an individual with passion and a learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends. Must have ability to travel and cover large geography territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$154,600.00 - $198,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 15:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs (MSL) - Oncology - Ile-de-France]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47534]]></requisitionid>
    <referencenumber><![CDATA[R47534]]></referencenumber>
    <apijobid><![CDATA[r47534]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47534/senior-manager-field-medical-affairs-msl-oncology-ile-de-france/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[France]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization.</p><p>We are seeking an experienced Field Medical Affairs professional specializing in Immuno-Oncology to join <strong>our team in France</strong>. In this pivotal role, you will serve as a scientific and clinical resource, engaging with key opinion leaders, healthcare professionals, and internal stakeholders to advance disease awareness and support innovative research initiatives. By collaborating across Medical Affairs, Clinical Development, Market Access and Commercial, you’ll help drive impactful strategies that shape the future of Oncology care. This is your chance to create a meaningful difference in patient outcomes while growing your expertise in a dynamic, matrix-driven environment.</p><p><strong>Senior Manager, Field Medical Affairs (MSL) - Oncology</strong></p><p>Ile de France, Paris - France</p><p><strong>A Typical Day:</strong></p><ul><li>Building and nurturing peer relationships with leading experts in Immuno-Oncology</li><li>Presenting scientific and clinical data to healthcare professionals and investigators.</li><li>Supporting and managing clinical trials by identifying investigators and trial sites.</li><li>Collaborating with internal teams and cross-functional partners to align strategies.</li><li>Responding to requests for information about disease states and Regeneron’s products.</li><li>Ensuring compliance with company policies and regulatory guidelines.</li><li>Assisting with the development of abstracts, posters, and manuscripts for scientific communication.</li><li>Providing support to the commercial team.</li></ul><p><strong>This Role may be for you, if you:</strong></p><ul><li>Thrive in a collaborative, matrix environment and enjoy cross-functional teamwork.</li><li>Value building and maintaining positive relationships with healthcare professionals and investigators.</li><li>Are committed to scientific integrity and professional communication at all times.</li><li>Excel at organizing, planning, and balancing multiple priorities, both independently and as part of a team.</li><li>Are passionate about advancing oncology research and supporting innovative clinical initiatives.</li></ul><p><strong>To Be Considered</strong></p><p>Applicants must hold a PhD, or PharmD, with preferably 5+ proven experience, including at least 3 years in a Field Medical or Medical Manager role within the biotech or pharmaceutical industry, focusing on Oncology or Onco-Immunology. Expertise in the Oncology therapeutic area is required, with experience in lymphoma and/or multiple myeloma strongly preferred. Established relationships with key opinion leaders and familiarity with institutions specializing in Immuno-Oncology are advantageous. Drug launch experience, knowledge of treatment guidelines, clinical research processes, EU and pharma regulations, and strong communication skills are essential.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 03:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Specialist I-(Gastro)-Omaha, NE]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47495]]></requisitionid>
    <referencenumber><![CDATA[R47495]]></referencenumber>
    <apijobid><![CDATA[r47495]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47495/medical-specialist-i-gastro-omaha-ne/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Omaha]]></city>
    <state><![CDATA[Nebraska]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Medical Specialist, Gastroenterology (MS) - Omaha, NE</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>A typical day may include the following:</strong></p><p>A core responsibility of the MS will be to collaborate with their district colleagues, alliance counterparts, as well as other field-based and home office personnel teams to proactively address customer needs, market dynamics and trends and develop strategies which support brand and corporate objectives within their assigned geography. The MS will participate and help lead initiatives to support sales success as assigned (e.g. participate in industry related congresses, local and regional meetings and medical conferences).</p><p><strong>This role may be for you if:</strong></p><ul><li><p>Demonstrate advanced clinically-based selling skills</p></li><li><p>Proven success and positive track record of consistent sales performance in complex markets with diverse customer segments operating with a high degree of integrity within compliance guidelines</p></li><li><p>Proven success navigating and demonstrating positive impact with large groups, institutional settings, and Ambulatory Surgery Centers</p></li><li><p>Results oriented with a proven track record of success with product launches</p></li><li><p>Demonstrate a passion and learning aptitude for science and is proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</p></li><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>To be considered you must possess a Bachelor’s degree required; Master’s degree or other advanced education/certifications a plus. Specialty pharmaceutical/biopharmaceutical experience with a minimum of 5 years pharmaceutical sales experience including a minimum of 2 years selling in the Gastroenterology market and/or a similar subcutaneous self-injectable biologic specialty market. Ability to travel and cover large geographic territories.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$143,500.00 - $187,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Manager R2R]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47437]]></requisitionid>
    <referencenumber><![CDATA[R47437]]></referencenumber>
    <apijobid><![CDATA[r47437]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47437/associate-manager-r2r/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization is dedicated to inventing, developing, and commercializing medicines that change lives for people with serious diseases. As we continue to expand our global footprint, our finance shared services play a critical role in supporting accurate reporting, strong governance, and scalable operations.</p><p>As an Associate Manager – Finance Service Delivery, you will support Regeneron’s global finance and payroll operations within a Shared Services / Global Capability Center environment. You will oversee day‑to‑day finance service delivery activities, support payroll and accounting processes, ensure adherence to controls, and partner closely with global stakeholders to maintain high service standards.</p><p><strong>A Typical Day May Include the Following:</strong></p><ul><li><p>Act as a point of contact for daily finance service delivery activities and stakeholder queries</p></li><li><p>Support end‑to‑end finance and payroll service delivery across multiple countries</p></li><li><p>Review reconciliations between finance systems, payroll vendor outputs, and accounting records</p></li><li><p>Support monthly and quarterly close activities, including review of supporting schedules and templates</p></li><li><p>Monitor Actuals vs Expected figures and highlight variances with clear observations</p></li><li><p>Partner with Accounting teams to validate financial data and ensure completeness and accuracy</p></li><li><p>Support international payroll accounting activities, including validations and reconciliations</p></li><li><p>Ensure adherence to governance requirements, internal controls, and CFO policies</p></li><li><p>Prepare and provide documentation, data, and explanations for internal and external audits</p></li><li><p>Maintain and update standard operating procedures, templates, and process documentation</p></li><li><p>Identify opportunities for process improvement, efficiency, and automation across finance operations</p></li><li><p>Support workload planning, task prioritization, and smooth execution of finance activities</p></li></ul><div></div><p><strong>This Job May Be for You If You Have:</strong></p><ul><li><p>Experience supporting finance operations, payroll finance, accounting, or shared services delivery</p></li><li><p>Working knowledge of reconciliations, financial controls, and compliance requirements</p></li><li><p>Comfort handling large datasets and working across multiple finance systems</p></li><li><p>A structured, detail‑oriented approach with strong follow‑through</p></li><li><p>Ability to manage multiple priorities in a fast‑paced environment</p></li><li><p>Clear written and verbal communication skills</p></li><li><p>Experience working with global or cross‑functional stakeholders.</p></li></ul><p><strong>To be considered for this role:</strong></p><div><ul><li><p>8+ years of relevant experience in Finance, Accounting, or Finance Shared Services, preferably within a multinational, Shared Services, or Global Capability Center environment</p></li><li><p>Relevant undergraduate degree, with a Bachelor’s or Master’s degree in Accounting or Finance (such as B.Com, BBM, M.Com, or MBA)</p></li><li><p>Professional qualifications are preferred</p></li><li><p>Proficiency in English</p></li><li><p>Experience working with global teams and stakeholders</p></li></ul></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 07:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Temp QC Technical Resources Specialist]]></title>
    <date><![CDATA[Fri, 08 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45771]]></requisitionid>
    <referencenumber><![CDATA[R45771]]></referencenumber>
    <apijobid><![CDATA[r45771]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45771/temp-qc-technical-resources-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>Within this role you will support lifecycle management within the QC Technical Resources group. You will participate (Perform, Review, Co-ordinate) in assay development, characterization, optimization, transfer, validation and investigation for QC group. You may provide technical support, guidance and supervision for release, stability, and in-process testing and assay development as a subject matter expert (SME).</div><div></div></div><div><div><div><div><div><div><div><div><div><p>This is a 12-month contract.</p><p><strong>As a Temp QC Technical Resources Specialist, a typical day might include, but is not limited to, the following:</strong> </p><ul><li><p>Collaborating with Analytical Sciences (AS) to integrate methods into QC Commercial evaluating and selecting suitable methods prior to process validation</p></li><li><p>Monitoring and analyze daily method performance in the QC lab, coordinating with subject matter experts for problem resolution as needed</p></li><li><p>Liaising with Regulatory Sciences and External Manufacturing to manage timelines for method validation and transfers, communicating updates to management</p></li><li><p>Monitoring method updates, performance, and quality metrics, ensuring consistent harmonization and performance evaluations across multiple sites</p></li><li><p>Coordinating post-transfer investigations and multi-site trending, escalating issues to management when necessary</p></li><li><p>Driving process improvements and support investigational analysis, performing and coordinating assay qualifications and transfers</p></li><li><p>Developing and drafting new test procedures and assays, authoring technical documents like Analytical Development and Validation Reports</p></li><li><p>Participating in training programs for QC personnel, ensuring all activities align with project timelines and deliverables<br> </p></li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li><p>The ability to work independently or as part of a team</p></li><li><p>Strong skills in planning, critical thinking and problem-solving, ability to follow directions and perform well-defined tasks</p></li><li><p>Excellent written and oral communication skills</p></li><li><p>The ability to develop strategy and create metrics to measure effectiveness of strategy</p></li></ul><p>To be considered for this opportunity you should have a BS/BA in a life sciences field and 2 years of experience or equivalent combination of education and experience.</p><p><strong>Education and Experience:</strong></p><ul><li>Scientist level minimum 2 years of experience</li><li>Sr Scientist level minimum 5+ years of experience</li></ul><p><br>#LI-Onsite #JOBSIEST #IRELIM</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 08 May 2026 08:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Director Clinical Data Management]]></title>
    <date><![CDATA[Thu, 14 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45840]]></requisitionid>
    <referencenumber><![CDATA[R45840]]></referencenumber>
    <apijobid><![CDATA[r45840]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45840/senior-director-clinical-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health.</p><p>As a Senior Director, Clinical Data Management - India, you will be part of the Clinical Data Management Leadership Team and plays a key role in shaping the global operational vision, strategy, and direction for Data Management in support of the clinical pipeline. This Includes the establishment of a highly performing Data Management group in the region.</p><p>The incumbent will bring deep technical and operational expertise to strengthen internal clinical data management capabilities across clinical data reporting, clinical data review, medical coding, local lab data processing and delivery, database build and testing, and external data acquisition. The focus is on improving database quality, streamlining data flow, and enabling faster, more reliable clinical insights through modern platforms, automation, and scalable processes.</p><p>This role partners closely with Clinical Data Management Central Services, Clinical Data Operations, External Data Acquisition and Delivery teams, as well as internal collaborators and external vendors, to ensure data management activities are delivered with quality, compliance, and operational efficiency from study start-up through archival across key development programs.</p><p>This position is office-based and will be on site at <strong>Regeneron’s Hyderabad office.</strong></p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Build and lead a strong regional Clinical Data Management organization to expand internal capabilities across clinical data reporting, data review, coding, laboratory data processing, database build and testing, and external data delivery.</p></li><li><p>Define and supervise functional metrics, KPIs, and KQIs to supervise quality, compliance, and timely delivery.</p></li><li><p>Be responsible for the delivery of high-quality laboratory data, coded terminology, and external data to support statistical analysis across the portfolio.</p></li><li><p>Provide effective oversight of FSPs and external data vendors.</p></li><li><p>Identify operational risks early and implement practical solutions to support critical study turning points globally.</p></li><li><p>Evaluate resource needs and allocation to maintain strong productivity and delivery against functional goals.</p></li><li><p>Shape organization design, hire top talent, and support performance and development across the team.</p></li><li><p>Lead cross-functional initiatives that improve efficiency, strengthen operations, and support inspection readiness.</p></li><li><p>Advance the use of automation and AI/GenAI solutions to reduce manual effort, improve data quality, and enable faster data access.</p></li><li><p>Build strong partnerships across internal teams and external collaborators to support collaboration throughout the drug development process.</p></li><li><p>Chip in to the development of global SOPs, WIs, BPTs, and training curricula for Clinical Data Management.</p></li><li><p>Model company values through collaboration, innovation, accountability, respect, and sound leadership.</p></li><li><p>Stay current on emerging trends, technologies, and standard methodologies in Clinical Data Management, and represent Regeneron in industry forums and professional associations.</p></li></ul><p><strong>This job may be for you if you have:</strong></p><ul><li><p>Leadership experience in Clinical Data Management or a related field, including leading medium to large teams (50–150) supporting global data management functions.</p></li><li><p>Strong expertise in clinical data management processes, industry procedures, and key clinical systems such as EDC, eSource, eCOA, IRT, Clinical Data Repositories, medical coding platforms, and laboratory normal range repositories.</p></li><li><p>Experience assessing cases, running proof-of-concept initiatives, and scaling effective technical solutions to address operational challenges.</p></li><li><p>Sophisticated knowledge of clinical data management principles, technologies, regulations, and standards, including 21 CFR Part 11, ICH-GCP, GxP, and GDPR.</p></li><li><p>Strong discernment and a broad understanding of the pharmaceutical or biotech industry.</p></li><li><p>A track record of solving complex business problems, leading transformation, and navigating change such as new operating models, acquisitions, or portfolio shifts.</p></li><li><p>The ability to influence and build trusted relationships with senior collaborators across functions and levels.</p></li><li><p>Success in building high-performing teams focused on innovation, transformation, and operational excellence.</p></li><li><p>Strong communication and collaborator leadership skills.</p></li><li><p>The ability to operate efficiently in a fast-paced environment.</p></li><li><p>Willingness to travel up to 25%.</p></li></ul><p><strong>To be considered for this role you must have</strong></p><ul><li><p>15+ years of clinical data management experience in a pharmaceutical or biotech setting.</p></li><li><p>10+ years of functional leadership experience.</p></li><li><p>8+ years of people management, leadership, and mentoring experience.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 02:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Pharmacology (Oncology)]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47422]]></requisitionid>
    <referencenumber><![CDATA[R47422]]></referencenumber>
    <apijobid><![CDATA[r47422]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47422/associate-director-clinical-pharmacology-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>We are looking for an Associate Director for our Clinical Pharmacology group. The incumbent will provide strategic and scientific expertise, as well as represent Clinical Pharmacology at relevant meetings. This position will provide Clinical Pharmacology subject matter support to new and on-going clinical programs primarily in the Oncology area.</p><p><strong>This role is onsite 4-days per week at either our Tarrytown, NY, Warren, NJ or Cambridge, MA location. </strong></p><p><strong>A day in the life of an Associate Director may look like:</strong></p><ul><li><p>Proactively-identify and provide significant PMx contributes 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.</p></li><li><p>Is regarded as an expert in the field; as such is able to contribute to the overall strategic program development and is able to communicate complex PMx strategies and results in an influential manner to the development team.</p></li><li><p>Independently designs and conducts or otherwise oversees the development of PMx analysis plans and applies standardized or advanced scientific techniques to conduct PK, PD, and/or other types of quantitative analyses. Informs PMx management of results and issues in a timely manner.</p></li><li><p>Advanced knowable of the field and know willingness to provide mentorship, is regarded as a scientific leader in PMx.</p></li><li><p>Responsible for the preparation and timely delivery of accurate and well-articulated nonclinical or clinical study reports and regulatory submission documents as appropriate.</p></li></ul><p><strong>This may be the right role for you if you:</strong></p><ul><li><p>Want the ability to make a significant impact on the organization and external groups and can influence and effect change.</p></li><li><p>Enjoy making contributions to multi-disciplinary meetings by sharing cross-functional skills and knowledge.</p></li><li><p>Want to work in cross-functional teams with forward-thinking, passionate, and driven teammates</p></li></ul><p><strong>In Order to be considered qualified for this role you must have:</strong></p><p>A PhD in Biology, Pharmacology, Engineering, Pharmacy (Pharm.D.) or Medicine (MD) with at least 6+ years of relevant Clinical Pharmacology experience. Oncology experience is strongly preferred, but not required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 21:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Tumor Lead Marketing Skin]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47469]]></requisitionid>
    <referencenumber><![CDATA[R47469]]></referencenumber>
    <apijobid><![CDATA[r47469]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47469/regional-tumor-lead-marketing-skin/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Regional Tumor Lead Marketing Skin to play a pivotal role within our Regional Marketing Team in International Oncology. In this position, you’ll act as the bridge between global and local, ensuring that insights from countries build meaningful, actionable plans while supporting excellent execution and agility in markets. You’ll collaborate closely with regional and global stakeholders to align priorities, guide brand strategy, and drive performance across markets—offering an outstanding opportunity to create impact on scale.</p><h3>A Typical Day:</h3><ul><li></li><li><p>Leading country insight collection and prioritization to inform global brand strategy</p></li><li><p>Ensuring alignment of local priorities with global strategic direction</p></li><li><p>Developing the regional tactical plan, including budget alignment</p></li><li><p>Facilitating regional tumor marketing meetings to drive execution against plan</p></li><li><p>Reviewing country brand plans and sharing insights to improve execution quality</p></li><li><p>Collaborating with global and local teams on content needs, adaptations, and co-creation, while streamlining material development processes</p></li><li><p>Driving regional launch planning and optimization, supporting excellence in country</p></li></ul><h3>This Role May Be For You:</h3><ul><li><p>Energized by working with, leveraging and developing talents in countries</p></li><li><p>Enjoy connecting global strategy with local market realities</p></li><li><p>Comfortable prioritizing across countries and balancing trade-offs</p></li><li><p>Energized by guiding brand planning and execution at regional level</p></li><li><p>Enjoys shaping content strategies across multiple markets</p></li><li><p>Confident leading discussions and aligning diverse stakeholders</p></li><li><p>Motivated by improving execution through insights and performance data</p></li><li><p>Open to regular travel and engaging with teams across geographies</p></li></ul><p>To be considered, you should hold a bachelor’s degree (preferably in a science-related field) and bring at least 10 years of experience in biotech or pharmaceutical brand marketing, including a minimum of 2 years in a leadership role. You should demonstrate experience managing agencies and suppliers, as well as a proven understanding of healthcare compliance requirements across different countries. Strong planning, prioritization, communication, and presentation skills are essential, along with experience working across complex, evolving environments. Experience in oncology marketing and product launches is preferred, along with a willingness to travel regularly (approximately 50%) to support regional activities and collaboration</p><div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Finance]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47681]]></requisitionid>
    <referencenumber><![CDATA[R47681]]></referencenumber>
    <apijobid><![CDATA[r47681]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47681/senior-manager-finance/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Hyderabad]]></city>
    <state><![CDATA[Telangāna]]></state>
    <country><![CDATA[India]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is founded on the belief that the right idea, combined with the right team, can lead to meaningful progress. Our growing global organization focuses on inventing, developing, and commercializing medicines that help people with serious diseases. As we continue to expand globally, our finance organization plays a critical role in supporting business decision-making through analysis, insights, and strong financial planning.</p><p>As a Senior Manager – Finance, you will support global financial planning, analysis, and forecasting activities. You will partner with cross-functional teams across geographies to provide insights into financial performance, support business decisions, and drive planning processes. This role focuses on financial analysis and business partnering and does not involve direct accounting entries or transaction processing.</p><p><strong>A Typical Day May Include the Following</strong></p><ul><li>Support preparation of budgets and forecasts across international markets</li><li>Perform analysis of actual financial results and provide insights against plan</li><li>Partner with global Commercial, Medical Affairs, and other functions to support decision-making</li><li>Support consolidated international P&L analysis, particularly for Oncology business</li><li>Maintain product and brand-level P&L models</li><li>Work closely with country finance teams to:<ul><li>Track revenue across markets (units, local currency, USD)</li><li>Monitor operating expenses across functions</li><li>Prepare dashboards and performance reports</li></ul></li><li>Prepare materials for monthly business reviews and leadership reporting</li><li>Support preparation of monthly sales reports and performance summaries</li><li>Calculate accruals and prepayments and share inputs with Accounting teams</li><li>Support Gross-to-Net analysis across markets</li><li>Perform constant currency analysis for financial comparisons</li><li>Support financial modelling for rebates, claw-backs, and pricing agreements</li><li>Provide analysis for tenders and pricing/volume decisions</li><li>Prepare FTE cost and rate calculations</li><li>Support regulatory reporting such as HCP spend tracking</li><li>Load and manage data in budgeting and forecasting systems</li><li>Coordinate quarterly revenue landing and forecast updates</li><li>Deliver ad-hoc analysis and respond to business queries</li></ul><p><strong>This Job May Be for You If You Have</strong></p><ul><li>Strong experience in financial planning & analysis (FP&A) or commercial finance</li><li>Expertise in P&L management, forecasting, and financial modelling</li><li>Ability to interpret financial data and translate it into business insights</li><li>Experience working with global teams and cross-functional stakeholders</li><li>Strong analytical thinking and problem-solving skills</li><li>Ability to work in ambiguous and evolving business environments</li><li>Good communication skills with the ability to explain complex financial concepts</li><li>High attention to detail with a structured approach to analysis</li></ul><p><strong>To Be Considered for This Role</strong></p><ul><li>6+ years of relevant post-qualification experience in Finance or FP&A</li><li>Bachelor’s degree in Finance, Accounting, or related field; MBA or equivalent preferred</li><li>Professional qualifications such as ACA, ACCA, CMA, CIMA, CPA, or similar</li><li>Experience in biotech/pharma industry or Shared Services environment is an advantage</li><li>Fluent in English; additional language skills are beneficial</li><li>Experience supporting international or multi-country finance environments</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Northeast]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47570]]></requisitionid>
    <referencenumber><![CDATA[R47570]]></referencenumber>
    <apijobid><![CDATA[r47570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47570/regional-director-neurology-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - New York]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Build our future together: </strong> </p><p>The Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Northeast Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Northeast (New York, Pennsylvania, Massachusetts, Vermont)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Regional Director-Neurology-Mountain West]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47571]]></requisitionid>
    <referencenumber><![CDATA[R47571]]></referencenumber>
    <apijobid><![CDATA[r47571]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47571/regional-director-neurology-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 Regional Director (RD), Rare Neurology will report to the Executive Director, Strategic Customer Engagement, Rare Neurology and be responsible for recruiting, leading, developing and retaining the Rare Neurology Medical Specialist team in the Mountain West Region. The RD is responsible for ensuring strong and consistent sales performance that exceeds forecast and expectations relating to product goals and driving accountability for all results throughout the Region assigned allowing Regeneron to have a major presence in the Rare Neurology market. The RD will work closely with their counterpart(s) to insure full cooperation and transparency within the region. The RD will work closely with Training and Development to insure appropriate development of personnel within the region designed to continue to facilitate growth in the commercial organization. The RD will accomplish this in a compliant manner with a high degree of integrity strictly following all Regeneron policies and in compliance with all policies and procedures governing the promotion of pharmaceutical and biologic products in the US.</p><p><strong>When & where: </strong> </p><ul><li><p>Remote role </p></li></ul><ul><li><p>Location: Mountain West (Minnesota, Iowa, Missouri, Kansas, Idaho, Colorado, New Mexico and Arizona)</p></li></ul><p><strong>Discover your role:</strong> </p><p>• Build and develop a high performing, high integrity, high quality sales team and provide overall leadership to the team.</p><p>• Responsible for meeting and/or exceeding assigned sales objectives and ensuring actions plans are aligned to the strategic initiatives of the brand.</p><p>• Lead regional sales force activities including hiring, training, performance evaluation and development while ensuring compliance to corporate policies.</p><p>• Ensure each employee is trained on and effectively implementing customer education.</p><p>• Communicate most current knowledge of the industry and competitor products to regional teams.</p><p>• Ensure participation in industry related trade shows, meetings, conferences, etc.</p><p>• Analyze sales and customer data to ensure appropriate resources are deployed in the region.</p><p>• Allocate and manage the region's budget and utilization of promotional resources</p><p>• Ensure strong, consistent performance that consistently meet or exceed brand objectives and product sales goals while consistently demonstrating accountability for all results.</p><p>• Build the Company’s credibility and relationships with key customers (e.g. Regional, local clinical experts, advocacy groups etc.) and their staffs in the field of Rare Neurology.</p><p>• Ensure the Rare Neurology Medical Specialists are viewed by their customers as clinical experts in the field of Rare Neurology.</p><p>• Develop and execute an Incentive Compensation plan for field team in accordance with corporate objectives and within guidelines in a compliant manner.</p><p>• Partner with multiple internal stakeholders to proactively analyze and address market dynamics and trends that support brand and collaboration objectives.</p><p>• Demonstrate strong understanding of Payer environment, reimbursement and challenges within payer markets including: government programs, managed health care and evolving health care systems.</p><p><strong>This role requires:</strong> </p><p>• Bachelor’s degree mandatory, Master’s degree or other advanced education / certification is a plus (Focused degree in science or clinical experience is a plus).</p><p>• Minimum of 10 years of pharmaceutical/biopharmaceutical experience with 5 years of sales leadership/management of which 3 years must be at the Regional Director/District Manager in the field of Rare Neurology</p><p>• Experience in complex therapies (REMS, Biologics, specialty pharmacy) in the Rare Disease or Neurology field highly preferred ie. Myasthenia Gravis, Multiple Sclerosis, Parkinson's, and Epilepsy.</p><p>• Proven success and positive track record of performance with a high degree of integrity as a Regional Director/District Manager in complex markets within complex systems required.</p><p>• Successful record of hiring, coaching, developing, promoting, and retaining top talent within span of control.</p><p>• Proven ability and success in developing physician/customer clinical experts in a Regional scope required.</p><p>• Excellent leadership and interpersonal skills; should be an effective team player who can engender credibility and confidence.</p><p>• Strong ability to partner and collaborate with other internal field teams and alliance partners.</p><p>• Ability to travel extensively with local and regional influence.</p><p>• Demonstrated history of leading high performance sales team.</p><p>• Ability to manage and drive a region's objectives and goals.</p><p>• • Product launch experience is a plus.</p><p>• Experience with selling to diverse customer segments.</p><p>• Understanding reimbursement challenges and opportunities of a buy and bill product required or other relevant Rare Neurology experience considered.</p><p>• Ability to analyze sales and other relevant market data.</p><p>• Strategic thinker who will challenge status quo to improve performance.</p><p>• Leadership skills that include motivating, mentoring and the ability to provide professional development to his/her team.</p><p>• Candidates must reside within the assigned territory.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$210,800.00 - $266,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 18:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Statistical Programmer]]></title>
    <date><![CDATA[Fri, 06 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44896]]></requisitionid>
    <referencenumber><![CDATA[R44896]]></referencenumber>
    <apijobid><![CDATA[r44896]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44896/principal-statistical-programmer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>A principal statistical programmer provides timely support to the study team on all programming matters according to the project strategies.</p><p><strong>In this role, a typical day might include:</strong> ​</p><p>As an integral part of a study, the incumbent provides project leadership and programming support for processing data from clinical studies. Requirements will be identified according to a Statistical Analysis Plan and programming specifications using internal standards and guidelines. The incumbent assists in providing guidance in implementing and executing the programming and project standards. The evaluation and development of study requirements and validation plan are also in the scope of this position. Works independently to design and test program logic, coding programs, program documentation and preparation of programs. Oversees projects designed to support ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical adhoc requests of senior management. Provides documentation and consistent maintenance of code, logs, and output in a regulated environment.</p><p><strong>This role might be for you if can:</strong> ​</p><ul><li>Support and/or lead programmer for programming and QC of analysis datasets, TFLs or standard tools following Regeneron standard data models or user requirements. Assist in the coordination of activities and communicate shifting timelines and milestones. </li><li>Integration of data across studies in support of CSS/CSE. Create, manage and maintain the programming specifications for the analysis datasets utilizing Regeneron tools and methodologies. </li><li>Support creation and validation of submission requirements (i.e. annotated CRF, data export files, define documents).</li><li>Work in a multidisciplinary study team to provide timely and quality support for analysis and reporting of clinical trials up to regulatory approval, product launch and annual reports. If applicable, develop and provide department training for applications and standard tools developed by the department functions group.</li><li>Provide programming support for simple presentations and basic statistical ad-hoc requests. Assist in the more complex data presentations.</li><li>Participate in department working groups; provide input in development of tools and improvement of processes.</li></ul><p><br><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li>Masters Degree</li><li>SAS, (Base, Stat, Macro, graph). </li><li>3 + Years experience</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$109,900.00 - $179,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 06 Feb 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sales Specialist - South West England]]></title>
    <date><![CDATA[Thu, 05 Feb 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45109]]></requisitionid>
    <referencenumber><![CDATA[R45109]]></referencenumber>
    <apijobid><![CDATA[r45109]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45109/sales-specialist-south-west-england/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Sales Specialists at Regeneron are at the forefront of engaging key professionals and customers. We are looking for someone who is highly proficient in presenting clinically-focused sales messaging that resonates and compels potential and existing customers to take action. We are driven by the highest degree of integrity and appreciation for always doing what is right – aligned with our core beliefs and values. We see this as an outstanding opportunity to join a fast-paced, results-oriented, customer-focused team if you are up for the challenge.</p><p>This role is focused on the maintenance and growth of key accounts within the South West England territory.</p><p><strong>As a Sales Specialist, a typical day may include the following:</strong></p><ul><li>Developing, implementing and supervising territory account plans based on market insights. Ensure continuous and timely updates to the plan in response to changing market dynamics.</li><li>Outstanding account management and operational excellence applying key data sources to strategically develop a territory account plan. And to supervise and progress activity and sales metrics.</li><li>Working closely with alliance partners to develop innovative solutions whilst adhering to SOP’s, regulatory, legal compliance guidelines and ABPI Code</li><li>Collaborating with regional colleagues, as well as other field-based and home office personnel teams to proactively address customer needs</li><li>Ability to work across multiple indications in a specialist therapeutic area.</li><li>Leading with the Science and put the patient front and centre of all we do. Ensure patient access through partnering with key customer stakeholders</li></ul><h3>This role may be for you if:</h3><ul><li>You are confident in demonstrating strong and consistent sales performance that goes above and beyond related to product goals</li><li>Innately guided by core values of ethics and compliance and always act in a manner consistent with those values</li><li>Have a competitive spirit and harness your “grit” to power your approach to sales, collaborating effectively with internal and external partners</li><li>Share a passion for science and are proactive in strengthening knowledge related to disease-state, treatment options and healthcare trends</li><li>Are able to effectively connect your work to the overarching brand strategy and shift focus dynamically as needed</li></ul><p>To be considered you must possess a minimum of a Bachelor’s degree and, at least, 5 years' pharmaceutical sales experience. Previous respiratory or specialist medicine experience desired but not essential. We need someone with shown success and consistent sales performance in complex markets across diverse customer segments.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 05 Feb 2026 06:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Director, Oracle ERP Business Program Lead]]></title>
    <date><![CDATA[Mon, 09 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44473]]></requisitionid>
    <referencenumber><![CDATA[R44473]]></referencenumber>
    <apijobid><![CDATA[r44473]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44473/executive-director-oracle-erp-business-program-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Business Program Lead is responsible for the overall management, execution, and delivery of Regeneron’s ERP Modernization Program and reports to the Program Sponsors. This role provides strategic leadership, governance, and oversight across all workstreams, ensuring alignment with business objectives and adherence to guiding principles. The Program Lead drives oversight of program planning, execution, risk management, and stakeholder engagement, while championing business-led change and adoption. Operating in a matrix environment, this role partners with Program Managers, Global Process Owners, IT leadership, System Integrators, and functional teams to deliver measurable business outcomes.</p><div></div><p><strong>A typical day in this role might look like: </strong></p><ul><li>Accountable for the integrated program plan, scope, schedule, dependencies, budget as well as alignment to the business case.</li><li>Lead governance forums (SteerCo, Design Review Board) and enforce guiding principles and key design decision (template-first, clean core).</li><li>Accountable for the execution of program deliverables; monitor progress, risks, and issues; implement mitigation plans.</li><li>Serve as primary liaison to executive sponsors; prepare and present status updates and decision requests.</li><li>Oversee vendor and SI performance; ensure deliverables meet scope, timeline, and quality standards.</li><li>Champion change management and readiness; oversee communications, training, and adoption strategies.</li><li>Ensure compliance with SOX, GxP, and audit requirements in all program activities.</li><li>Define and track success metrics; ensure benefit realization and continuous enhancements post-go-live.</li></ul><div></div><p><strong>This role might be for you if: </strong></p><ul><li>Bachelor’s degree in Business, Finance, Engineering, or related field; MBA preferred.</li><li>15+ years of experience in large-scale ERP or business transformation programs; 10+ years in program leadership.</li><li>Proven ability to manage complex, multi-year global programs with cross-functional teams and vendors.</li><li>Strong knowledge of ERP systems (Oracle Fusion preferred) and end-to-end life science business processes.</li><li>Expertise in program governance, risk management, and change leadership.</li><li>PMP or PgMP certification preferred; Iterative methodology delivery experience a plus.</li><li>Exceptional communication, stakeholder management, and leadership skills.</li><li>Willingness to travel up to 25%.</li></ul><div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$255,000.00 - $424,900.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 10 Feb 2026 10:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Clinical Data Reporting]]></title>
    <date><![CDATA[Mon, 16 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45331]]></requisitionid>
    <referencenumber><![CDATA[R45331]]></referencenumber>
    <apijobid><![CDATA[r45331]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45331/associate-director-clinical-data-reporting/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div>The Associated Director of Clinical Data Management Reporting will provide strategic leadership for clinical and external data reporting across clinical development unit (CDU) programs. This role focuses on the creation, standardization, and delivery of clinical data programming, external data reconciliation, and reporting deliverables across portfolio, ensuring alignment with study data review plans (DRP), study milestone needs, operational metrics, and regulatory requirements. The incumbent will be accountable for the oversight and execution of all data management programming deliverables at the portfolio level. Responsibilities include quality and timely delivery of programming outputs such as data review plan listings, exception listings, external data reconciliation reports, operational metrics, and other reports supporting clinical trial quality and risk management. The Director will manage internal teams and external vendors, ensuring study milestones are met while safeguarding data quality, integrity, and compliance with global regulatory standards. The position emphasizes cross-functional collaboration, deep expertise in clinical data programming, external data handling and reconciliation, industry standards, programming methodologies, and clinical data management systems. </div><div><div><div><div><p><strong>As a Associate Director, Clinical Data Reporting, a typical day may include:</strong></p><ul><li><p>Drive strategic leadership with full accountability for the planning, execution, and delivery of high-quality clinical data management programming deliverables across the portfolio of clinical development units. </p></li><li><p>Provide comprehensive oversight of clinical programming and visualization outputs that reveal key insights to support clinical data review, including data review listings, exception listings, external data reconciliation, operational metrics, and other quality reports and ensure accuracy, reliability, and integrity of data supporting clinical studies across the portfolio.</p></li><li><p>Advance operational excellence by establishing robust data reporting standards, implementing scalable programming strategies, optimizing workflows incorporating automation, and ensuring consistent delivery of high-quality outputs in accordance with defined user requirement specifications.</p></li><li><p>Provide subject matter expertise in advanced clinical data programming, data extraction and transformation, visualization, and emerging technologies to enhance and advance internal data reporting capabilities. </p></li><li><p>Collaborate with clinical data management teams, functional line management, and cross-functional teams to align priorities, streamline workflows, optimize resource allocation, and drive successful delivery of clinical data management programming objectives. </p></li><li><p>Apply quality-by-design principles to all clinical data management programming and reporting deliverables ensuring that high-quality outputs are aligned and consistent with risk-based strategies, and inspection readiness.</p></li><li><p>Lead continuous improvement initiatives to modernize clinical data reporting workflows through standardization, process optimization, and automation to improve programming efficiency and scalability. </p></li><li><p>Proactively identify potential risks to data quality, integrity, and delivery timelines and implement mitigation strategies to ensure continuity, compliance, and successful delivery of programming objectives.</p></li><li><p>Ensure inspection readiness and regulatory compliance of programming documentation; contribute to internal audits and health authority inquiries.</p></li><li><p>Establish and monitor KPIs to track performance, conformance with programming standards, and identify opportunities to enhance and/or optimize reporting capabilities.</p></li><li><p>Responsible for line management and performance of Clinical Data Management Reporting staff, development of competencies and assessment of annual performance.</p></li><li><p>Provide leadership and mentorship to programming teams, fostering skill development, knowledge sharing, and operational excellence. </p></li><li><p>Author and contribute to the development of clinical data management programming and reporting SOPs, WIs and departmental training needs.</p></li></ul><p><strong>To be considered for this role, you must meet the following requirements:</strong></p><ul><li><p>Demonstrated ability to oversee the development, validation, and delivery of clinical data management programming and visualization outputs to cross-functional teams across drug development programs.</p></li><li><p>Experience in transforming raw clinical data, external data handling, processing, validation, and reconciliation outputs into actionable insights to ensure data accuracy and quality in compliance with industry standards.</p></li><li><p>Demonstrated ability to function as a clinical data management programming and reporting SME in solving complex issues and guiding internal teams and external vendors for successful outcomes. </p></li><li><p>Demonstrated ability to build relationships and collaborate across diverse business units including Clinical Data Management, Clinical Development, Precision Medicine, Imaging, and GDIT.</p></li><li><p>Expertise in managing and reconciling clinical eCRF and external data types including PK, ADA, Biomarker, Imaging, ECG, etc., to ensure data accuracy, integrity, and regulatory compliance. </p></li><li><p>Proven experience in clinical data operations, clinical data management, reporting, and analytics within a pharmaceutical, biotech, or clinical research organization.</p></li><li><p>Knowledge of clinical data management principles, technologies, data extraction, transformation, and integration, programming methods and techniques, regulations and best practices, including 21 CFR Part 11, ICH-GCP, and CDISC standards -- related to data acquisition, processing, handling, and reporting. </p></li><li><p>Knowledge and expertise in industry standard reporting and data visualization tools including SAS, R, JReview, Spotfire, Tableau, Power BI, and R Shiny to drive operational excellence for clinical data management reporting. </p></li><li><p>Excellent interpersonal, oral, and written communication skills.</p></li><li><p>Ability to adjust in a fast-paced environment.</p></li><li><p>May require up to 25% travel.</p></li><li><p>BS/MS </p></li><li><p>10+ years of clinical data management experience in a pharmaceutical or biotech</p></li><li><p>5+ years of people management, leadership, and mentoring experience.</p></li></ul></div></div></div></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 17 Feb 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Commercial Operations Lead]]></title>
    <date><![CDATA[Thu, 12 Feb 2026 18:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45302]]></requisitionid>
    <referencenumber><![CDATA[R45302]]></referencenumber>
    <apijobid><![CDATA[r45302]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45302/director-commercial-operations-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Munich]]></city>
    <state><![CDATA[Bavaria]]></state>
    <country><![CDATA[Germany]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We’re looking for a Commercial Operations Lead to join our team in Munich, supporting our commercial business across the Germany<strong>.</strong> This is an impactful role focused on translating strategic commercial plans into flawless local execution. You’ll partner closely with sales, marketing, and training teams to drive operational perfection, while helping ensure alignment with regulatory standards and evolving business priorities.</p><p>You'll be joining a dynamic global team, with the opportunity to craft how we deliver commercial support to field-based teams in a fast-paced and highly collaborative environment.</p><h3><strong>A Typical Day:</strong></h3><ul><li><p>Providing strategic and operational leadership to Commercial Operations teams.</p></li><li><p>Translating global commercial strategies into locally relevant, tactical plans.</p></li><li><p>Supervising performance analytics and reporting to advise business decisions.</p></li><li><p>Handling key Sales Operations activities such as field sizing, onboarding, communications, and incentive tracking.</p></li><li><p>Partnering with Commercial Training to coordinate development for field-based staff.</p></li><li><p>Supporting the localization of promotional materials with Marketing and IT.</p></li><li><p>Collaborating with Compliance and Internal Audit teams to maintain adherence to internal policies and external regulations.</p></li><li><p>Building strong relationships with field managers to proactively identify and resolve operational issues.</p></li><li><p>Coordinating contracts and logistics for Speaker Programs and Advisory Boards.</p></li><li><p>Ensuring oncology meetings, sponsorships, and events align with business needs.</p></li></ul><h3><strong>This Role May Be For You:</strong></h3><ul><li><p>You enjoy redefining big-picture strategy into practical local execution.</p></li><li><p>You’re comfortable collaborating across departments and geographies.</p></li><li><p>You bring structure and accountability to multi-stakeholder projects.</p></li><li><p>You thrive in complex environments where priorities shift and evolve.</p></li><li><p>You value accuracy and clarity in communications, especially when supporting external teams.</p></li><li><p>You take pride in mentoring others and encouraging team growth.</p></li><li><p>You’re motivated by solving operational challenges that support patient-impacting work.</p></li></ul><p><strong>To be considered</strong></p><p>You’ll need to bring significant leadership experience in Commercial Operations within the German biopharmaceutical industry. A strong grasp of market dynamics, local laws, and reporting requirements is important. You should be confident navigating analytics, experienced with tools like PowerPoint, Excel, Veeva, and WORD, and able to communicate fluently in English. Prior experience supporting field sales in a pharma setting is desirable, along with a Bachelor’s degree and at least 7 years of industry experience, including 5 years in global commercial operations.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 13 Feb 2026 11:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr Assoc Scientist- Biomolecular Interactions/Kinetics]]></title>
    <date><![CDATA[Mon, 30 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R41252]]></requisitionid>
    <referencenumber><![CDATA[R41252]]></referencenumber>
    <apijobid><![CDATA[r41252]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r41252/sr-assoc-scientist-biomolecular-interactionskinetics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>We are seeking a motivated Sr Assoc Scientist to join the High Throughput Antibody Screening and Biomolecular Interaction Group within the Therapeutic Proteins team.</strong> You will support Therapeutics Protein activities by implementing methods to characterize protein interaction kinetics and biochemical properties using SPR, BLI, ITC, and other analytical technologies in support of our VelocImmune fully-human antibody pipeline.</p><p><strong>As a Sr Assoc Scientist, a typical day might include:</strong></p><ul><li><p>Conducting experiments including antibody characterization, method development, and analytical support for biologics development using biochemical and biophysical methods</p></li><li><p>Troubleshooting established test methods used in development and release testing of screening reagents</p></li><li><p>Tabulating results and writing summary reports of assay development</p></li><li><p>Presenting findings at group and interdepartmental meetings</p></li><li><p>Maintaining lab supplies and equipment</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Can work independently, show initiative to design and carry out experiments based on protocols</p></li><li><p>Manage and organize data independently, as well as have decision-making capabilities but know when to reach out for support</p></li><li><p>Can troubleshoot methodological and technical issues</p></li><li><p>Enjoy working in a fast-paced and deadline driven team environment and are capable of multi-tasking across assignments</p></li><li><p>Have excellent communication skills</p></li></ul><p><strong>In order to be considered for this role,</strong> you must have at least a BS/MS with 4+ years of relevant lab experience. We need someone with a foundational knowledge in structural biology, biophysics, or chemical biology. Must have experience in protein chemistry techniques (HPLC, FLPC, ion-exchange, affinity, size exclusion chromatography, and protein conjugation chemistry) and protein analysis (SDS-PAGE, Western-blot, ELISA). Knowledge and experience in using biophysical methodologies such as Biacore, Octet, or ITC to study protein/small molecule or protein/protein interactions and binding kinetics is required.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$79,100.00 - $129,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 31 Mar 2026 09:26:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Automation System Specialist]]></title>
    <date><![CDATA[Wed, 18 Mar 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R43990]]></requisitionid>
    <referencenumber><![CDATA[R43990]]></referencenumber>
    <apijobid><![CDATA[r43990]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r43990/senior-automation-system-specialist/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Menands]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Automation System Specialist (Administrator), you will be embedded in a tight-knit team responsible for administration of automated/computerized system software and firmware to meet cGMP and policy requirements. In this critical role our team specifies and maintains software configuration for biopharmaceutical process, monitoring, and testing systems. This involves evaluation of new software for functional equivalence, validation activities to demonstrate suitability of software/process and maintaining the qualified state of systems throughout their lifecycle through change control.</p><p>In this role, a typical day might include:</p><ul><li><p>Administering system applications including user control access; adding, modifying, and removing users; defining user types, user groups and security settings.</p></li><li><p>Monitoring data backup or archival to ensure systems can meet defined RTO (Recovery Time Objective) and RPO (Recovery Point Objective).</p></li><li><p>Utilizing configuration management and recipe/method management.</p></li><li><p>Authoring documents such as impact statements, Configuration Specifications, risk assessments, Standard Operating Procedures, Work Instructions, Policies, and corrective/prevention action plans.</p></li><li><p>Supporting system SAT (Site Acceptance Testing) / FAT (Factory Acceptance Testing), validation and qualification efforts.</p></li><li><p>Conducting system integration with existing systems (e.g. LIMS, Historian).</p></li><li><p>Ensuring systems remain in a compliant state by processing change control requests for system configuration, including requirement and/or design specifications, test plans, technical evaluation, and quality risk assessments.</p></li><li><p>Providing end-user support including system functionality training, solving problems at the application level and hardware troubleshooting (includes working with vendors to resolve issues).</p></li><li><p>Participating in, leading, or authoring investigations and root cause analysis for issues of non-compliance.</p></li><li><p>Leading aspects of the work for contractors and providing guidance as applicable.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Have experience with a combination of the following: Ignition, MQTT brokers, HiveMQ, HighByte, or other similar platforms.</p></li><li><p>Have interest in manufacturing process within a regulated technical environment.</p></li><li><p>Have a solid understanding of System Design Lifecycle and Quality Risk Management.</p></li><li><p>Enjoy designing and implementing sustainable technical\procedural solutions in a complex environment.</p></li><li><p>Understand process control systems and product release testing systems.</p></li><li><p>Are familiar with regulatory and quality policies, procedures, documentation methods.</p></li><li><p>Enjoy working independently as part of a broader team with a proven focus on customer service and maintaining compliance.</p></li><li><p>Enjoy project management and have strong organizational skills.</p></li><li><p>Are motivated to participate in continuous process improvement.</p></li></ul><p>Applicants ideally should have a BS/BA in Science, Engineering or related field and the following minimum relevant experience for each level:</p><ul><li><p>Senior Automation System Specialist (Administrator): 5+ years</p></li><li><p>Principal Automation System Specialist (Administrator): 8+ years</p></li></ul><p>Equivalent combination of education and experience may be considered. Level will be determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$78,700.00 - $150,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 19 Mar 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Global Patient Safety]]></title>
    <date><![CDATA[Thu, 16 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45330]]></requisitionid>
    <referencenumber><![CDATA[R45330]]></referencenumber>
    <apijobid><![CDATA[r45330]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45330/senior-manager-global-patient-safety/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Minato-Ku]]></city>
    <state><![CDATA[Tokyo]]></state>
    <country><![CDATA[Japan]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Join Us in Ensuring Patient Safety Globally!</strong></p><p>At our company, we are committed to safeguarding patient health worldwide through innovative pharmacovigilance practices. We are seeking a <strong>Senior Manager, Global Pharmacovigilance (GVP)</strong> to be based in Japan. Reporting directly to the Safety Management Officer, you will play a pivotal role in overseeing critical pharmacovigilance activities, including individual case safety reports (ICSRs), research reports (RRs), foreign safety measures (FSMTs), and aggregate reporting. If you thrive in a collaborative environment and are passionate about advancing global patient safety, this is your opportunity to make a meaningful impact.</p><p><strong>A Typical Day:</strong></p><ul><li><p>Oversee and evaluate Japan ICSR, RR, and FSMT reports for accuracy and compliance.</p></li><li><p>Manage vendor activities related to pharmacovigilance, ensuring adherence to contracts and performance standards.</p></li><li><p>Author and update working instructions while conducting related training sessions.</p></li><li><p>Contribute to the development and implementation of Japan Risk Management Plans (J-RMPs) and ensure compliance with the associated activities.</p></li><li><p>Collaborate with cross-functional teams, including Medical Affairs, Regulatory Affairs, and external partners, to deliver key pharmacovigilance deliverables.</p></li><li><p>Support the preparation of safety sections for Japan New Drug Applications (J-NDAs) and address inquiries from the Pharmaceuticals and Medical Devices Agency (PMDA).</p></li><li><p>Lead process improvement initiatives to enhance quality and compliance in pharmacovigilance operations.</p></li></ul><p><strong>This Role May Be For You If:</strong></p><ul><li><p>You have over seven years of experience in pharmacovigilance or drug safety within the pharmaceutical or biotech industry.</p></li><li><p>You are well-versed in PMDA/MHLW and ICH guidelines and regulations governing pharmacovigilance activities.</p></li><li><p>You excel at managing complex projects, such as safety database implementations or license succession involving data migration.</p></li><li><p>You thrive in cross-functional collaborations and have experience working with teams like Medical Affairs and Regulatory Affairs.</p></li><li><p>You have successfully supported or led regulatory inspections, including PMDA Re-examinations and GCP Reliability Inspections.</p></li><li><p>You possess strong analytical and organizational skills, enabling you to oversee multiple projects simultaneously.</p></li></ul><p><strong>To Be Considered:</strong><br>Candidates must have a Bachelor's degree or higher and at least seven years of experience in pharmacovigilance and post-marketing surveillance operations. Familiarity with contracting and managing external service providers is essential, along with prior global pharmacovigilance experience. Preferred candidates will have demonstrated success in regulatory authority inspections and cross-functional collaborations.</p><p><strong>Why Join Us?</strong><br>This is more than just a job—it’s an opportunity to contribute to a mission that directly impacts global patient safety. We offer a collaborative environment where innovation is encouraged, and your expertise will be valued and recognized.</p><p>Take the next step in your career and apply to join our dedicated team today!</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 17 Apr 2026 02:26:11 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Sr QA Material Supplier Specialist (Qualification)]]></title>
    <date><![CDATA[Sun, 12 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46600]]></requisitionid>
    <referencenumber><![CDATA[R46600]]></referencenumber>
    <apijobid><![CDATA[r46600]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46600/sr-qa-material-supplier-specialist-qualification/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The QA Material Supplier Specialist - Qualification implements activities within the material qualification program to support the utilization of raw materials in Drug Substance and Drug Product Manufacturing.</p><div><p>In this role, a typical day might include the following:</p><ul><li><p>Performing activities associated with qualification of raw materials such as, development of sampling and testing protocols, review of test data, drafting summary reports, etc.; execution of sampling activities may be on the floor</p></li><li><p>Representing Quality Assurance in support of deviations, change controls, CAPAs, etc. including active participation in investigation, evaluation, and problem resolution</p></li><li><p>Provides guidance internally and externally to ensure quality and regulatory expectations are met in relation to material quality standards</p></li><li><p>Support and/or approval of SCARs (Supplier Corrective Action Requests)</p></li><li><p>Working with Suppliers to obtain documentation to support closure of SCARFs (Supplier Corrective Action Request Follow-Ups)</p></li><li><p>Reviews/approves Drug Product Component Supplier-specific documentation such as Approved Supplier Approvals and TSE/BSE Assessments</p></li><li><p>Provides support to relevant departments in the utilization of Drug Product Test Components</p></li><li><p>Establishing, reviewing, and editing Regeneron controlled documents</p></li><li><p>Continually evaluating Regeneron processes and procedures with an eye toward continuous improvement; identify gaps in systems and develop feasible plans for correction</p></li></ul><p>This role may be for you if you:</p><ul><li><p>Excel in a quality driven organization</p></li><li><p>Are an organized individual with attention to detail</p></li><li><p>Have good written, verbal, and interpersonal communication skills and the ability to effectively interact cross functionally</p></li><li><p>Can navigate changing priorities</p></li><li><p>Are able to learn and use computerized systems for daily performance of tasks</p></li><li><p>Can prioritize, manage multiple tasks, and meet deadlines</p></li><li><p>Are able to lift up to 25 lbs</p></li><li><p>Are comfortable working in a warehouse environment 20% of the time</p></li></ul><p>​To be considered for this role you must hold a Bachelor’s degree and the following minimum amounts of relevant experience for each level: </p><ul><li><p>QA Material Supplier Specialist – 3+ years </p></li><li><p>Senior QA Material Supplier Specialist – 5+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p></div><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$67,400.00 - $128,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 13 Apr 2026 16:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Development Engineer II - Analytics]]></title>
    <date><![CDATA[Mon, 13 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46534]]></requisitionid>
    <referencenumber><![CDATA[R46534]]></referencenumber>
    <apijobid><![CDATA[r46534]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46534/process-development-engineer-ii-analytics/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Process Development Analytics group with PMPD (Preclinical Manufacturing Process Development) core mission is to analyze samples received by PMPD subgroups and provide quality and impurity data, and to characterize and optimize assay robustness, precision, and accuracy. Tech development and automation is also prioritized to further optimize assays and resources. The group is seeking a laboratory Scientist or Engineer interested in the analytical characterization of biopharmaceuticals. In this role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced, high-throughput laboratory setting.</p><h3>A Typical Day in the Role of Engineer II Might Look Like:</h3><ul><li>Conduct high throughput biophysical/biochemical analysis of samples generated during manufacturing process development and research projects.</li><li>Conduct experiments to further statistical understanding of assay performance and interpret the results in collaboration with multi-functional groups.</li><li>Deliver written or oral communications as a representative of the PMPD Analytics group at a wide variety of internal projects.</li><li>Collaborate with team members and supervisor to develop novel analytical assays and investigate new analytical technologies.</li><li>Contributes to continuous improvement efforts for increasing efficiency and throughput within the PMPD Analytics group.</li></ul><h3>This Role Might Be For You if You Have:</h3><ul><li>A working knowledge of modern methods of protein research, such as liquid chromatography, capillary electrophoresis, and immunoassays.</li><li>An interest in high throughput analytical methodologies, and their use in biopharmaceutical manufacturing process development.</li><li>An interest in joining a collaborative team with a focus on continuous improvement.</li></ul><p>This role requires a B.Sc., with 5+, or M.Sc. with 3+ years of biochemistry/ chemical/biochemical engineering or a related field. A good understanding of the principles and practice in one or more fields of analytical methodology such as size and charge variant based analysis, Reversed Phase or Mixed Mode chromatography. Knowledge of statistical analyses and statistical design of experiments is a plus.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$93,900.00 - $153,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 14 Apr 2026 16:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Project Engineer]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45461]]></requisitionid>
    <referencenumber><![CDATA[R45461]]></referencenumber>
    <apijobid><![CDATA[r45461]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45461/associate-project-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are seeking an Associate Project Engineer who will design, specify and commission new and renovated biopharmaceutical process equipment. This role will provide engineering support and assist with problem solving for existing equipment and manufacturing processes.</p><p><strong>As an Associate Project Engineer, a typical day might include the following: </strong></p><ul><li>Designing and specifying cGMP process equipment, piping, and/or controls</li><li>Managing small projects related to process equipment and manufacturing</li><li>Assisting in the design review, site acceptance and installation of equipment</li><li>Preparing process and instrument drawings and other related drawings</li><li>Developing Process Flow Diagrams for manufacturing processes</li><li>Supporting validation department by preparation of design documents and assists in protocol execution</li><li>Assisting in investigations of process equipment and control system anomalies</li><li>Implementing corrective/preventative actions for existing equipment and manufacturing processes</li><li>Preparing engineering evaluations for and executing modification change control documentation</li><li>May supervise mechanical, electrical, and automation contractors</li></ul><p><strong>This role might be for you if you:</strong></p><ul><li>Are a self-starter with high initiative and possess a data-driven approach to problem-solving</li><li>Have demonstrated strong interpersonal skills</li><li>Are able to prioritize, re-prioritize as needed and adapt to change</li><li>Have strong analytical and organizational skills</li><li>Have demonstrated adaptability and flexibility to working in different environments, teams etc.</li></ul><p>To be considered for this position you should have a BEng or higher in Chemical, Process or Mechanical Engineering.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 10:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Thought Leader Liaison - Northeast]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46776]]></requisitionid>
    <referencenumber><![CDATA[R46776]]></referencenumber>
    <apijobid><![CDATA[r46776]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46776/associate-director-thought-leader-liaison-northeast/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Remote - Maine]]></city>
    <state><![CDATA[Maine]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<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 Senior 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, 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>The typical day may include the following:</h3><ul><li><p>The Oncology TLL will engage in meaningful and strategic discussions to gather insights & share clinical information with assigned key thought leaders in the geography</p></li><li><p>Conduct substantive business discussions related to on-label product information, disease state, and general corporate overviews</p></li><li><p>Embrace a customer-centric, needs-based approach to drive strategic thought leader engagements</p></li><li><p>Coordinate thought leader engagements for senior executives at local/regional/national conferences and/or during day-to-day business</p></li><li><p>Develop/maintain list of key thought leaders in the assigned geography</p></li><li><p>Assist with thought leader development</p></li><li><p>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</p></li><li><p>Share with Marketing and other functional groups the insights gleaned from interactions with thought leaders</p></li><li><p>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</p></li><li><p>Ensure all interactions and activities with thought leaders adhere to company policies, industry regulations, and compliance guidelines</p></li></ul><h3>This role may be for you if:</h3><ul><li><p>You possess a strong science background with deep knowledge of Oncology</p></li><li><p>You can comprehend complex information/ideas and effectively distill them down to a simpler form to effectively deliver concise presentations with impact</p></li><li><p>You can successfully collaborate with and provide input/feedback to all functions within the project team</p></li><li><p>You can balance/lead multiple projects simultaneously</p></li><li><p>You possess strong analytical and communication skills and are comfortable engaging with individuals at all levels of the organization and across different functional teams</p></li></ul><p>To be considered for this opportunity, we expect you to have a bachelor’s degree required; Master’s degree or other advanced education/certification is a plus. Along with specialty pharmaceutical/biopharmaceutical experience, with a minimum of 8 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. You also have expertise in marketing strategies within the pharmaceutical industry. Ideally, you would have launch experience. You must be able to travel 60%-80% of time </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 14:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[HVAC Technician, Wednesday-Saturday 2nd shift]]></title>
    <date><![CDATA[Tue, 21 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46908]]></requisitionid>
    <referencenumber><![CDATA[R46908]]></referencenumber>
    <apijobid><![CDATA[r46908]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46908/hvac-technician-wednesday-saturday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<div><div>We are currently looking to add a HVAC Technician to our growing team, working a Wednesday-Saturday 14:00pm–12:30am shift. Our HVAC Technicians are responsible for start-up, normal operation, monitoring and shutdown of HVAC and equipment; troubleshooting, preventative maintenance, calibration, and repair work for all mechanical related systems.</div></div><div><div><div><div><div><div><div><div><div><p><strong>Please note training will take place Monday-Friday 7:00am-3:30pm for approximately 6 months. Working hours thereafter will be Wednesday-Saturday 14:00pm-12:30am. Employees working premium shifts receive incentive pay, such as shift differential and/or weekend pay.</strong></p><p>As a HVAC Technician, a typical day might include the following:</p><ul><li><p>Maintaining coolers and freezers including Ultra Low temperature Freezer</p></li><li><p>Maintaining Centrifugal and Reciprocating refrigeration chillers</p></li><li><p>Maintaining Chilled water systems including distribution and condenser pumps</p></li><li><p>Maintaining Air Compressors</p></li><li><p>Electrical power systems and stand-by power generation equipment</p></li><li><p>Following current good manufacturing practices (cGMPs) and good business practices (G)</p></li><li><p>Participating in rotational on-call for site emergency work</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment with strict adherence to SOP's, cGMP's, GDP’s and quality standards</p></li><li><p>Becoming fully gown qualified to work within Production areas</p></li><li><p>Communicating and coordinating with each department and within Facilities Management when planned and unplanned work events occur</p></li><li><p>May plan and schedule outside contractors/vendors to perform scheduled and/or non-scheduled Preventative Maintenance or general work</p></li></ul><h3>This role might be for you if you:</h3><ul><li><p>Demonstrate basic problem-solving skills</p></li><li><p>Are able to learn and follow routine procedures independently as well as part of a team</p></li><li><p>Are comfortable and have the flexibility to work in a changing environment</p></li><li><p>Can lift, push, and pull at least 50lbs</p></li><li><p>Seek to build and maintain positive working relationships with the business</p></li><li><p>Possess strong written and verbal communication skills</p></li><li><p>Maintain effective time management skills to allow deadlines to be met in a timely manner</p></li><li><p>Have knowledge of Microsoft Office Suite and overall comfort and general familiarity with computer systems</p></li></ul><p>To be considered for the HVAC Technician position you must be willing and able to work a Wednesday-Saturday 14:00pm–12:30am schedule. Applicants ideally should have technical school training with field experience in AC, Heating, Chilled Water Systems, Building Automation Controls, and Maintenance and the following minimum amounts of experience for each level:</p><ul><li><p>HVAC Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li><li><p>HVAC III: 5+ years of related experience or HSD/GED with 8+ years of related experience</p></li><li><p>HVAC IV: 8+ years of related experience or HSD/GED with 8+ years of related experience</p></li></ul><p>Level will be determined based on qualifications relevant to the role. Will substitute relevant work experience in lieu of education. Electronic, PLC, mechanical and building automation systems experience in Pharmaceutical Industry preferred. EPA certified for refrigeration gases.</p></div></div></div></div></div></div></div></div></div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 22 Apr 2026 10:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Statistical Programming]]></title>
    <date><![CDATA[Wed, 22 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46205]]></requisitionid>
    <referencenumber><![CDATA[R46205]]></referencenumber>
    <apijobid><![CDATA[r46205]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46205/senior-manager-statistical-programming/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager Statistical Programming provides technical leadership and support to the project teams on all statistical programming matters according to the project strategies within therapeutic area(s). The incumbent manages the programming aspect of a project in collaboration with partnering functions, stakeholders, and external functional service providers for all programming deliverables from the single study through to regulatory approval, product launch, data monitoring boards, regulatory safety reports, and other requests. Oversees documentation and ensures consistent maintenance of code, logs, and output within a regulated environment. The incumbent will lead or participate in process and methodology development for department goals and SME topics. Maybe responsible for goal setting and performance management.</p><p><strong>In this role, a typical day might include: ​</strong></p><ul><li><p>Manage and lead programming support within multiple studies/projects in various study activities to ensures timely and high-quality programming deliverables in assigned projects and areas. Lead and coordinate programming documentation including specifications, as appropriate, for multiple studies following programming standards and processes</p></li><li><p>Demonstrate company values and act as a role model by demonstrating excellence, competence, collaboration, innovation, respect, ownership, and accountability</p></li><li><p>Ensure the commitment and reinforcement of the roles and responsibilities of the statistical programming function</p></li><li><p>Proactive communication with study and project teams to clarify requirements and specifications, guide direct reports or support programmers on assignment status</p></li><li><p>Lead and support global regulatory authority submissions including preparing programming deliverable for submission and working closely with partnering functions to address health authority requests.</p></li><li><p>Lead and manage department goals and SME topics</p></li><li><p>May oversee development of direct reports by setting goals, managing performance, evaluating, and monitoring training needs, supporting development plans, mentoring, and coaching</p></li><li><p>May participate in screening and interviewing candidates for contractor and permanent positions.</p></li></ul><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>MS (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline with 10+ (12+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry, including some project and people management experience.</p></li><li><p>Advanced SAS programming skills in a clinical data environment with expertise in at least one, preferably multiple, therapeutic areas. Knowledge of other programming languages such as R, Python etc. is a plus.</p></li><li><p>Understanding of pharmaceutical clinical development across multiple therapeutic areas (i.e. understanding of statistical concepts, techniques and clinical trial principles) and good knowledge of regulatory submissions and requirements</p></li><li><p>Ability to work on global interdisciplinary teams. Good organizational, interpersonal, communication, and leadership skills. Establish and maintain effective working relationships with coworkers, managers, and clients</p></li><li><p>Ability to effectively manage multiple tasks and projects</p></li><li><p>Problem solving and innovative skills that demonstrate initiative and motivation</p></li><li><p>Ability to influence others, mentor, and coach junior programmers to achieve results</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 23 Apr 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal IT Lab Integration Developer]]></title>
    <date><![CDATA[Thu, 23 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45570]]></requisitionid>
    <referencenumber><![CDATA[R45570]]></referencenumber>
    <apijobid><![CDATA[r45570]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45570/principal-it-lab-integration-developer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Principal IT Lab Integration Developer is responsible for designing, developing, validating, and supporting integrations between laboratory systems, analytical instruments, enterprise platforms (LIMS), and data platforms within a regulated pharmaceutical environment. This role combines application development, system integration, data management, and regulatory compliance within a GMP-regulated laboratory environment.</p><p>As a Principal IT Lab Integration Developer, a typical day might include the following:</p><ul><li>Support the design and implementation of the QC Lab Orchestration Layer, enabling workflow coordination across all Laboratory instruments and middleware.</li><li>Define integration patterns (APIs, event-driven, message queues, file-based where needed).</li><li>Ensure scalability, resilience, and performance of lab integrations.</li><li>Translate QC business processes into orchestrated digital workflows.</li><li>Design and develop integrations between instruments and the Orchestration Layer.</li><li>Build and support API-based, file-based, and message-based integrations (REST, SOAP, SFTP, JSON, XML).</li><li>Provide level 2/3 support for QC Lab Systems.</li><li>Partner with QC Analysts, QA, IT infrastructure and external vendors.</li><li>Develop instrument data capture and automation workflows.</li><li>Configure and support middleware and integration platforms.</li><li>Ensure all integrations comply with GxP, 21 CFR Part 11, and data integrity (ALCOA+) requirements.</li><li>Participate in Computer System Validation (CSV/CSA) activities (IQ/OQ/PQ documentation).</li><li>Perform impact assessments and change control documentation.</li><li>Monitor and troubleshoot integration issues in production environments.</li><li>Collaborate with QC, R&D, Manufacturing, and QA teams.</li><li>Support audits and regulatory inspections.</li></ul><p>This role may be for you if you have:</p><ul><li>Skill in connecting various lab instruments (e.g., liquid handlers, analyzers) to central platforms like LIMS or ELNs to automate data capture and reduce manual transcription.</li><li>Knowledge of RESTful APIs, web services, and middleware tools used to bridge communication between the orchestration engine and disparate lab hardware.</li><li>Proficiency in languages such as Python or VBA for customizing automated workflows and data parsing.</li><li>Ability to understand data formats across different systems, ensure consistent values/naming conventions, and providing the correct data to the authorized locations.</li></ul><p>In order to be considered for this position, you must hold a BS/BA in Information Technology, Math or related field and </p><ul><li>Senior: 5 years of relevant experience or equivalent combination of education and experience.</li><li>Principal: 8 years of relevant experience or equivalent combination of education and experience.</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$88,300.00 - $168,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 24 Apr 2026 09:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, Customer Master & CRM Data Management]]></title>
    <date><![CDATA[Wed, 29 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47203]]></requisitionid>
    <referencenumber><![CDATA[R47203]]></referencenumber>
    <apijobid><![CDATA[r47203]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47203/director-customer-master-crm-data-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron is seeking a Director, Customer Master & CRM Data Management to join our Commercial Organization! <br> </p><p><strong>In this role, a typical day might include:</strong></p><p>The Director, Customer Master & CRM Data Management will report into the Executive Director, Commercial Data Management within the Commercial Strategy, Insights & Analytics (CSI&A) organization at Regeneron Pharmaceuticals, Inc. This role serves as the Commercial Customer Data Owner accountable for the integrity, quality, governance, and strategic evolution of Regeneron’s commercial customer master data spanning HCP, HCO, address, affiliation, and hierarchy domains. The Director will also oversee overall commercial business needs related to a next-generation master data management (MDM) platform, as well as the insights and analytics (I&A) needs for Regeneron’s next-generation customer relationship management (CRM) platform, while also ensuring continuity and excellence of data quality on the current platforms. The ideal candidate brings deep expertise in pharmaceutical customer data management, MDM & CRM platforms, and cross-functional stakeholder engagement, with the leadership presence to chair the Customer Master Data Council and drive commercial-wide alignment.</p><p><strong>This role might be for you if you can/have:</strong></p><p><em>Lead</em></p><p>1) Serve as the strategic Customer Data Owner for the commercial customer master, as well as the business owner of the MDM platform, setting the vision, standards, and roadmap for HCP, HCO, address, affiliation, and hierarchy data across all therapeutic areas and commercial systems (CRM, commercial data warehouse [CDW], and downstream platforms)</p><p>2) Chair the Customer Master Data Council; establish governance cadences, decision rights, and RACI frameworks across CSI&A, Commercial IT (CIT), and business stakeholders in alignment with the data governance operating model</p><p>3) As the business owner, in collaboration with CIT, define and drive the Commercial team’s MDM platform transition through requirements definition, phased implementation, UAT, and go-live; own the ongoing customer master capability roadmap from a Commercial business perspective, including near-real-time CM-CRM-CDW synchronization, canonical data feeds, and next-gen identity resolution frameworks</p><p><em>Develop</em></p><p>4) Build and formalize the Customer Master Data Governance program, including data dictionaries, Critical Data Element (CDE) catalogs, data quality (DQ) rule catalogs, and controlled field and intake channel standardization; establish and continuously improve data quality KPIs, SLA frameworks, and closed-loop remediation processes with dashboards providing transparent DQ and data change request (DCR) metrics to all stakeholders</p><p>5) Lead organizational change management associated with the MDM platform transition, including stakeholder communication, training, and adoption planning for internal teams and downstream system owners</p><p><em>Partnership and Collaboration</em></p><p>6) Partner closely with CIT & Commercial platform leads (e.g., CRM, CDW), CRM product owners, CDW owners, and 3rd-party data vendors (IQVIA, MedPro) to ensure customer data flows correctly and consistently across all commercial systems</p><p>7) Manage external data vendor relationships including contract oversight, SLA enforcement, data delivery quality reviews, and issue escalation for customer master data sources</p><p>8) Oversee and mentor a team of data stewards (Lead Business Data Steward and TA/Brand-level stewards); foster a culture of data ownership, accountability, and continuous improvement in data quality practices</p><p><em>Execute</em></p><p>9) Oversee day-to-day DCR governance, ensuring single intake, search-before-create enforcement, auto-approval thresholds, and timely SLA compliance</p><p>10) Perform and direct data analytics to troubleshoot customer master issues, quality-check system changes, validate affiliation and hierarchy integrity, and respond to ad hoc stakeholder questions</p><p>11) Document, maintain, and update all standard operating procedures (SOPs) and workflows related to customer master data management; ensure proper version control and cross-functional accessibility</p><p><strong>To be considered for this opportunity, you must have the following:</strong></p><ul><li><p>BA/BS required; advanced degree (MBA, MS) preferred</p></li><li><p>12+ years of progressive experience in commercial data management within pharmaceutical or biotechnology (or 10+ years with MBA/MS); at least 3 years in a director-level or senior leadership role</p></li><li><p>Deep expertise in pharmaceutical customer master data including HCP/HCO identity, affiliation management, hierarchy maintenance, address validation, and DCR governance processes</p></li><li><p>Demonstrated experience leading or serving as business lead for an MDM platform implementation or major system transition (e.g., Reltio, Veeva Network, IQVIA OCE, Informatica MDM, or equivalent)</p></li><li><p>Strong working knowledge of commercial customer data vendors and sources including IQVIA OneKey and MedPro, and their integration into commercial customer master platforms</p></li><li><p>Experience establishing and operating data governance frameworks including data quality KPIs, SLA management, DQ rule catalogs, CDEs, and stewardship programs</p></li><li><p>Proficiency with data management and analytics tools (SQL, Snowflake, Databricks, or equivalent); ability to perform analytics to diagnose and resolve data quality issues</p></li><li><p>Proven ability to translate complex business requirements into technical specifications and manage cross-functional delivery with IT partners</p></li><li><p>Strong executive communication and presentation skills; demonstrated experience influencing senior stakeholders and chairing governance forums</p></li><li><p>Demonstrated ability to lead, develop, and mentor a team; experience building stewardship programs and driving adoption of data governance practices</p></li><li><p>Familiarity with privacy and compliance requirements applicable to commercial customer data (HIPAA, state-level HCP data regulations, aggregate spend reporting)</p></li></ul><p>Preferred Skills</p><ul><li><p>Experience with mainstream biotech commercial platforms (CRM, CDW) </p></li><li><p>Background in commercial operations roles (field force data, sales operations, analytics) providing appreciation for the downstream impact of customer master data quality</p></li><li><p>Familiarity with IQVIA LAAD/APLD or other secondary HCP-level datasets and their relationship to customer master identity resolution</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$183,100.00 - $305,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 30 Apr 2026 13:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Market Access Analytics - Neurology]]></title>
    <date><![CDATA[Mon, 20 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46822]]></requisitionid>
    <referencenumber><![CDATA[R46822]]></referencenumber>
    <apijobid><![CDATA[r46822]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46822/associate-director-market-access-analytics-neurology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Regeneron Pharmaceuticals is seeking an Associate Director, Market Access Analytics, Neurology to join our organization supporting both launch and in-line brands.</p><p><strong>In this role, a typical day might include:</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><strong>This role might be for you if you can/have:</strong></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>To be considered for this opportunity, you must have the following:</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><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$157,200.00 - $256,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 10:56:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Director, AI Engineering (Global Development)]]></title>
    <date><![CDATA[Tue, 28 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R44760]]></requisitionid>
    <referencenumber><![CDATA[R44760]]></referencenumber>
    <apijobid><![CDATA[r44760]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r44760/director-ai-engineering-global-development/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Our Global Development (GD) team is seeking a Director, AI Engineering to embark on a digital transformation incorporating AI, machine learning, and automation. The goal is to help us reduce cycle times, improve quality, and allow us to focus on more meaningful work. You will play a key role in developing platforms, processes and technologies across GD. </p><p><strong>A typical day may include the following: </strong><br>• Provide strategic direction and technical leadership to an eventual team of engineers to design, implement, and refine novel algorithms and scalable AI /ML solutions. These will be tailored to applications such as clinical trial design, regulatory intelligence, patient identification and stratification. Oversee the deployment of these solutions into production environments, employing hands-on technical expertise to ensure excellence in execution.<br>• Architect and refine data engineering and data architecture strategies to integrate and optimize diverse data sources. <br>• Partner with the Digital Transformation AI lead and leaders across Global Development to evaluate and implement use cases for implementing AI in the enterprise, including automating manual processes such as protocol review, monitoring, and adverse event review<br>• Provide strategic leadership to initiatives with Global Development IT and enterprise IT to building infrastructure (software and hardware) to support advanced analytics, including vendor evaluation<br>• Collaborate with senior leaders to identify high-value opportunities for AI/ML integration and lead the execution of innovative solutions that address critical business challenges.<br>• Empower colleagues to leverage AI/ML effectively by providing guidance that bridges technical expertise with strategic insights, fostering a culture of innovation and continuous learning.<br>• Establish robust validation frameworks for AI models, ensuring reliability and efficiency<br>• Stay at the forefront of AI/ML advancements, evaluating emerging technologies and methodologies for potential adoption within Regeneron.<br>• Lead initiatives to continuously improve the organization's AI capabilities, fostering a competitive edge. </p><p><strong>This may be for you if you: </strong><br>• Want to be a part of scaling AI in a growing multi-national organization. <br>• Can demonstrate managing cross functional teams. <br>• Demonstrated success bringing transformative change. <br>• Want to have an impact on patient lives</p><p>To be considered you are to have a PhD in Computer Science, Data Science, AI/ML, Engineering, or related with 10-12 years experience or a Master or Bachelor’s with 12–15+ years experience in AI?ML or software engineering. Your experience must include a deep understanding of generative AI, machine learning, natural language processing, and statistical modeling. Expertise in programming (Python, R, etc.), with a focus on applying advanced technical skills to data analysis, automation, and software development is required. Expertise in database platforms and cloud computing infrastructure. Experience managing and analyzing large-scale clinical datasets Excellent communication skills, including experience presenting to senior leadership, both technical and non-technical. Experience managing multiple projects in parallel. Experience working in and managing cross-functional teams. Have track record of model development, implementation to scale, maintenance, and evaluation in a healthcare of life sciences setting<br> May require travel up to 20%. <br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$205,000.00 - $341,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 29 Apr 2026 09:26:22 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Reimbursement Business Manager-Dermatology-Columbus, OH]]></title>
    <date><![CDATA[Mon, 27 Apr 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R45962]]></requisitionid>
    <referencenumber><![CDATA[R45962]]></referencenumber>
    <apijobid><![CDATA[r45962]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r45962/reimbursement-business-manager-dermatology-columbus-oh/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Columbus]]></city>
    <state><![CDATA[Ohio]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p><strong>Field Reimbursement Manager - Dermatology (Columbus, OH)</strong></p><p>The Reimbursement Business Manager (RBM) is a critical front-line member of the Regeneron Commercial and Field Reimbursement Management team. We are seeking someone to support HCP offices in acquiring appropriate access to Regeneron products for patients. Ensuring efficient access, effective pull-through, and understanding of access services and program support as it relates to the Regeneron Alliance product portfolio. You will drive and support the company and divisional reimbursement strategy for Regeneron products within various payer segments. The RBM position requires the ability to successfully navigate and across multiple internal stakeholders, sales teams, Payer teams, and Alliance partners.</p><p><strong>A typical day may include the following:</strong></p><ul><li><p>Work cross-functionally and collaboratively with Regeneron and Alliance sales organizations (Sales Directors and Medical Specialists) to act as a process and payer subject matter expert, in efforts to support the healthcare provider segment.</p></li><li><p>Build and execute a Strategic tactical plan for the execution of Alliance products access and reimbursement initiatives relevant to the defined needs of each respective product and account within the defined customer market</p></li><li><p>Provide appropriate process, payer and specialty pharmacy support services/activities in concert with District Managers/Medical Specialists (field sales), to educate physician offices regarding coverage of alliance products (Dupixent).</p></li><li><p>Establish and maintain knowledge on the local and national payer landscape, including Specialty Pharmacy and Utilization Management criteria for assigned products</p></li><li><p>Establish relationships within targeted healthcare provider offices to assist healthcare professionals in resolving payer coverage issues that may be barriers to Alliance product access in a manner that aligns with Regeneron policies, processes, and standard operating procedures</p></li><li><p>Ensure individual training and knowledge is maintained to the level required to guarantee that personnel are seen as the most knowledgeable team in the industry as it pertains to access and reimbursement across Alliance therapeutic areas as well as future product markets</p></li></ul><p><strong>This role may be for you if:</strong></p><ul><li><p>You are patient focused, and have expertise in supporting healthcare provider offices with medical coding, claims/billing processes</p></li><li><p>You are an ethical, standout colleague and have can grow in a cross-functional team environment - contributing creative ideas and positive energy to the group.</p></li><li><p>You possess excellent organizational, project management, and communication skills.</p></li><li><p>Experience working with products delivered through a Specialty Pharmacy network is essential.</p></li><li><p>Collaboration and proactive communication skills.</p></li><li><p>Background in leadership and effective cross functional partnership a plus.</p></li><li><p>Established ability to work within an Account Management based structure.</p></li></ul><p>To be considered for this opportunity, you will possess the following:</p><p>A bachelors' degree and Minimum 5 years’ experience in pharmaceuticals and/or sub-cutaneous self-injectable biologics working in a matrix environment – with 2 years Reimbursement experience. Knowledge of Commercial Insurers, Managed Care, Government, and Federal payer sectors. Knowledge of Integrated Delivery Network/Integrated Health Systems. Knowledge of CMS policies and expertise in Part D.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$165,600.00 - $209,600.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Commercial]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 28 Apr 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Automation]]></title>
    <date><![CDATA[Mon, 04 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47040]]></requisitionid>
    <referencenumber><![CDATA[R47040]]></referencenumber>
    <apijobid><![CDATA[r47040]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47040/senior-manager-automation/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are looking for a Senior Manager Automation to supervise a team responsible for cGMP automation quality systems, software change control, and automation related corrective actions. The Senior Manager Automation develops procedures and methods for executing automation projects and support activities, while coaching and developing Automation professionals. This group ensures manufacturing systems are operating as expected and provides time-sensitive fixes to keep manufacturing running. This is a dynamic role that focuses on providing impeccable customer service, while developing direct reports to ensure their continued success and growth.</p><p>As a Senior Manager Automation, a typical day might include the following:</p><ul><li>Managing the performance, training, development, and results of the team</li><li>Providing technical and automation support to manufacturing</li><li>Overseeing activities related to the configuration and support of manufacturing process equipment and the maintenance of cGMP software administration program</li><li>Managing periodic evaluation reports for automated systems used in commercial manufacturing</li><li>Overseeing the investigation of manufacturing deviations and anomalies related to automation and software</li><li>Managing projects related to corrective action or equipment performance improvement.</li><li>Implementing modification/change control procedures and protocols.</li><li>Supporting Validation with initial design review, software testing and protocol review</li></ul><p>This job might be for you if you:</p><ul><li><p>Have the demonstrated ability to mentor and empower a team of automation professionals to deliver results under demanding timelines and situations</p></li><li>Can organize and present technical overviews to engineering staff, multi-functional departments, and management independently while influencing desired courses of action</li><li>Possess a unique blend of business and technical savvy</li><li>Are able to communicate across all levels and capable of effectively meeting and exceeding customer expectations</li><li>Have the skills to balance changing priorities by making timely decisions and delegating tasks</li><li>Possess an understanding of bioprocessing and testing software, cGMP software quality system principles, and data integrity regulations</li><li>Consistently maintain professionalism in communication, maintaining composure in high-pressure situations</li><li>Strive for compliance with regulatory, corporate, and site-specific policies and procedures</li></ul><p>To be considered for this position, you should have a BS/BA in engineering, software programming or related field and the following experience:</p><ul><li>Manager: 7+ years of experience with automated equipment used in pharmaceutical or biopharmaceutical industry</li><li>Senior Manager: 8+ years of experience with automated equipment used in pharmaceutical or biopharmaceutical industry</li><li>3+ years of leadership/supervisory experience</li><li>1+ year of direct experience in design, installation, maintenance, and or trouble shooting of automated control systems</li></ul><p>Level will be determined based on qualifications relevant to the role</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$121,100.00 - $231,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 04 May 2026 08:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director, Finance & Administration - Canada]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46239]]></requisitionid>
    <referencenumber><![CDATA[R46239]]></referencenumber>
    <apijobid><![CDATA[r46239]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46239/associate-director-finance-administration-canada/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Mississauga]]></city>
    <state><![CDATA[Ontario]]></state>
    <country><![CDATA[Canada]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are hiring an Associate Director, Finance & Administration to partner closely with country leadership and commercial teams, supporting high‑impact business decisions through financial insight, forecasting, and analysis. This role sits at the centre of the country organisation, working across Finance, Accounting, Tax, Treasury, and global CFO functions to shape commercial performance, governance, and long‑term planning.</p><p>If you enjoy combining critical thinking with hands‑on delivery—and value visible ownership at country level—this is a role where your expertise will genuinely influence outcomes.</p><h3>What You’ll Be Doing:</h3><ul><li><p>Partnering with country leadership on budgeting, forecasting, and financial planning</p></li><li><p>Preparing and presenting forecasts, including actuals versus forecast analysis</p></li><li><p>Managing resource planning, including FTE utilisation across cost centres</p></li><li><p>Supporting commercial teams with P&L ownership and profitability insights</p></li><li><p>Translating epidemiology and commercial data into financial forecasts</p></li><li><p>Coordinating with Accounting on revenue accuracy, accruals, and reporting</p></li><li><p>Acting as a local finance liaison across Tax, Treasury, and CFO functions</p></li><li><p>Ensuring compliance with internal policies and external regulations</p></li></ul><h3>This Role May Be For You If:</h3><ul><li><p>You enjoy working closely with senior collaborators to support sound decisions</p></li><li><p>You like roles that balance strategic perspective with practical execution</p></li><li><p>You are comfortable partnering across commercial, medical, and G&A teams</p></li><li><p>You value clear country ownership and accountability</p></li><li><p>You enjoy collaborating with global and local finance colleagues</p></li><li><p>You are motivated by improving processes and strengthening governance</p></li></ul><h3>To Be Considered:</h3><p>You will have a relevant undergraduate degree, along with a postgraduate qualification (such as an MBA) and/or a recognised professional finance qualification. You will bring at least five years of post‑qualification finance experience, primarily within the biotech or pharmaceutical industry, including experience supporting commercial P&Ls. Fluency in English and the local country language is required. International experience and additional language skills are an advantage.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 04:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager Vendor Relationship Management]]></title>
    <date><![CDATA[Tue, 12 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47550]]></requisitionid>
    <referencenumber><![CDATA[R47550]]></referencenumber>
    <apijobid><![CDATA[r47550]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47550/senior-manager-vendor-relationship-management/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Warren]]></city>
    <state><![CDATA[New Jersey]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Senior Manager, Vendor Management</strong>, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical trial execution. This role ensures that vendors meet the necessary qualifications and compliance standards, manage relationships, and oversee delivery to time, cost, and quality. This position is capable of leadership and oversight of vendor segments, and of the technical aspects such as quality, compliance, business continuity, and inspection readiness.</p><p><em>***Please note that this role is based in either Warren, NJ or Armonk, and is NOT eligible remote.</em></p><p><strong>A typical day in this role looks like:</strong></p><p>This position is expected to have the ability to execute a variety of roles to meet the expectations of effective relationship management and driving compliance and high-quality delivery. </p><p>Relationship Management</p><ul><li>Oversee the performance and health of vendors within assigned segment to ensure deliver to plan – time, budget quality.</li><li>Develop/enhance vendor performance scorecards that drives identification of mitigations/contingencies against performance risks/issues</li><li>Build and maintain strong relationships with key vendors.</li><li>Act as the primary point of contact for relationship level vendor-related issues and escalations. </li><li>Assess portfolio resource demand and shortfall/mitigations for current and potential future portfolio with key vendors</li><li>Lead the integration of new vendors into Regeneron strategy and operating model(s) to create stronger probability of success with new collaborations</li></ul><p>Leadership</p><ul><li>Mentor and develop team members, fostering a culture of continuous improvement.</li><li>Collaborate with cross-functional teams to ensure cohesive vendor management practices.</li><li>Engage with DSOE’s Change Mgmt function to facilitate process change, stakeholder readiness and communication strategy as required.</li><li>May have direct supervision over support staff. </li></ul><p>Quality and Compliance Oversight:</p><ul><li>Ensure vendors comply with regulatory requirements and organizational standards, including proper documentation of partnerships is developed and maintained.</li><li>Conduct regular quality and compliance assessments of vendors.</li><li>Develop and implement corrective action plans for any identified issues.</li><li>Lead relevant governance meetings on behalf of Regeneron including agendas, minutes, and timely follow-up of action items</li></ul><p>Vendor Qualification and Business Continuity:</p><ul><li>Develop and/or manage against business continuity plans involving vendors.</li><li>Conduct regular reviews and updates of business continuity plans.</li><li>Ensure minimal disruption in clinical trial operations through effective continuity planning.</li><li>Contribute to the Qualification process, with a steady focus on continuous improvement and stakeholder management</li></ul><p>Inspection Readiness and Support:</p><ul><li>Ensure vendors are prepared for regulatory inspections and applicable audits.</li><li>Coordinate and support inspection activities, including pre-inspection preparation and post-inspection follow-up.</li><li>Maintain inspection readiness documentation and records.</li></ul><p>Vendor Management Operations, where applicable:</p><ul><li>Lead and facilitate the conduct of the internal governance bodies related to sourcing strategy and operating models </li><li>Accountable for continuous assessment of capacity management for external resources </li><li>Lead the integration of new processes and/or changes to process across applicable vendors</li><li>Oversee Vendor training curriculum assignments and training compliance</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Strong knowledge of GCP, FDA, EMA, and other relevant regulatory requirements.</li><li>Highly collaborative with strong written and verbal communication skills; effective customer focus; ability to interact with all levels of employees and maintain confidentiality.</li><li>High aptitude and competency with Microsoft Office along with new/emerging technical solutions. </li><li>Excellent organizational and project management skills.</li><li>Strong communication and interpersonal skills.</li><li>Ability to work independently and as part of a team.</li><li>Self starter who takes initiative, and can handle risk and uncertainty.</li><li>Ability to work in a fast-paced environment and manage multiple priorities</li><li>Able to exercise sound judgement and decision making. </li><li>May require up to 25% travel</li></ul><p><strong>In order to be considered qualified for this role, a minimum of Bachelors degree is required. </strong></p><ul><li>Minimum of 10 years of experience and success in a clinical project/ trial management role within biotech/pharmaceutical industry</li><li>7+ years in pharma industry, specifically in operations and/or vendor management discipline.</li><li>Strong knowledge of GCP, FDA, EMA, and other relevant</li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 13 May 2026 08:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Executive Assistant - Law Department]]></title>
    <date><![CDATA[Tue, 05 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47226]]></requisitionid>
    <referencenumber><![CDATA[R47226]]></referencenumber>
    <apijobid><![CDATA[r47226]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47226/executive-assistant-law-department/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Sleepy Hollow]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>At Regeneron, we pair science with technology to accelerate the discovery and delivery of life‑changing medicines. We are searching for an Executive Assistant to support Law Department executives who oversee and interact with multiple functional teams, including Privacy, Trade Controls, and Industrial Operations Law — as well as the attorneys and professionals within those teams. This role requires advanced understanding of the Law Department and its business clients, including key relationships. We're looking for someone who brings strategic thinking, technological fluency, and genuine curiosity to the work of a fast-moving, high-impact legal team. The Executive Assistant will exercise considerable judgment and initiative, with the ability to influence stakeholders and understand key relationships.</p><p><strong>In this role, a typical day might include:</strong></p><ul><li><p>Managing complex calendars, expenses, and time commitments for executives.</p></li><li><p>Anticipating the needs of leaders and teams before they arise; resolving scheduling conflicts with minimal direction.</p></li><li><p>Triaging incoming requests and inquiries, escalating time-sensitive or significant matters with good judgment and discretion.</p></li><li><p>Identifying, developing, and implementing process improvements, bringing new tools or approaches to the team proactively, while maintaining highly organized and efficient administrative workflows and independently executing solutions.</p></li><li><p>Leveraging AI tools (such as Microsoft CoPilot) to draft communications, summarize information, and streamline administrative workflows.</p></li><li><p>Planning, managing and executing internal and external meetings end‑to‑end, including team meetings, large offsites, live trainings, and cross-functional gatherings, with attention to gathering agendas, logistics, coordination with stakeholders, catering decisions, materials and follow up.</p></li><li><p>Building polished PowerPoint presentations by synthesizing inputs from multiple contributors into organized, executive-ready decks.</p></li><li><p>Submitting requisitions, tracking of deadlines, monitoring purchase orders and renewals.</p></li><li><p>Collaborating cross‑functionally and serving as a trusted partner to peers.</p></li><li><p>Communicating effectively across all levels while maintaining confidentiality.</p></li><li><p>Demonstrating organizational knowledge and understanding leader priorities, including support for increasingly complex responsibilities.</p></li><li><p>Handling travel arrangements and expense reports for executives including managing complex international travel (typically VP+), visas and expense reporting.</p></li><li><p>Maintaining departmental SharePoint, Teams and Intranet sites, keeping them current, organized and useful as working resources.</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Are highly collaborative and adept at coordinating across teams to develop and implement solutions and operate under minimal guidance.</p></li><li><p>Exhibit discretion, independence, and sound judgment.</p></li><li><p>Adapt well to change, ambiguity, and shifting priorities, and can embrace AI and modern productivity tools as a part of how you work.</p></li><li><p>Work comfortably with senior leaders and understand how they think and what they expect.</p></li><li><p>Possess advanced knowledge or ability to readily learn company and Law Department policies, practices, and resources and act as a point person for supported leaders and departments.</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>Associate or bachelor’s degree preferred.</p></li><li><p>8 or more years of administrative experience required, with at least 4 years supporting senior leaders in a business or legal environment.</p></li><li><p>Advanced proficiency in Microsoft 365 (Outlook, PowerPoint, Excel, Word, Teams), SharePoint, Concur, and collaboration platforms; ability to troubleshoot and train others.</p></li><li><p>Proven ability to manage complex calendars, orchestrate senior‑level meetings and events, and coordinate domestic/international travel with precision.</p></li><li><p>Exceptional organization, prioritization, and follow‑through; positive, can‑do attitude and respect for colleagues at all levels.</p></li><li><p>Flexibility to support after‑hours needs tied to executive travel, global time zones, and critical events.</p></li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$38.61 - $63.03]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 05 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs-Neurology (mid-Atlantic states)]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46427]]></requisitionid>
    <referencenumber><![CDATA[R46427]]></referencenumber>
    <apijobid><![CDATA[r46427]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46427/senior-manager-field-medical-affairs-neurology-mid-atlantic-states/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>As a Senior Manager, you will play a pivotal role as a field-base/Medical Science Liaison providing scientific and Neurology therapeutic area expertise. The Senior Manager will become a scientific expert communicating accurate and applicable science to medical and health care professionals, and payers. In addition, you will support our strategic medical objectives by developing and maintaining professional relationships through facilitating collaboration opportunities. </p><p><strong>Territory: </strong>Eastern PA, DE, NJ, MD, VA, Washington DC & Metro</p><p>A typical day may include the following:<br>• Develop and maintain peer–to–peer collaborations and relationships with medical and scientific experts, and population health decision makers. <br>• Participate on committees or project teams supporting field medical strategies and tactics. <br>• Respond to unsolicited medical information requests, handle questions and liaise with headquarters personnel ensuring proper responses has been provided and data is fair and balanced. <br>• Develop an understanding of the regional landscape including specialties involved in care of patients in that area & other landscape mapping activities. <br>• Identify and bring actionable information & insights that enhance the value and appropriate use of our products back to appropriate internal collaborators. <br>• Build and cultivate important working relationships across field partners to ensure an integrated approach when working with HCP’s or experts. <br>• Collaborate with physicians on medical affairs initiatives including publications, Company– sponsored research (CSR), regional advisory boards, regional medical education opportunities, training and speaker development programs. <br>• Develop and sustain expertise in product/molecule data, disease state management, emerging therapies, and the competitive landscape. <br>• Respond to HCP inquiries with integrity, compliance, and adherence to legal, regulatory, and our guidelines, policies & procedures ensuring focused and balanced clinical and scientific information. <br>• Support clinical research activities throughout the life cycle (phase 1-4), as well as Investigator Initiated Studies, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ experts and sites in alignment with Medical Affairs objectives</p><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) along with a minimum of 3-5 years related work experience preferred (clinical, managed care, or industry experience) including experience as a Medical Science Liaison. Recent experience in Neurology is preferred. Experience communicating and disseminating scientific and clinical data in required. Travel withing the assigned territory and attendance at industry conference is required. </p><p>#msl #medicalscienceliaison<br> </p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 09:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Manager, Field Medical Affairs- Houston/Dallas (Neurology)]]></title>
    <date><![CDATA[Sat, 09 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46423]]></requisitionid>
    <referencenumber><![CDATA[R46423]]></referencenumber>
    <apijobid><![CDATA[r46423]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46423/senior-manager-field-medical-affairs-houstondallas-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>As a Senior Manager, you will play a pivotal role as a field-based/Medical Science Liaison providing scientific and Neurology therapeutic area expertise. The Senior Manager will become a scientific expert communicating accurate and applicable science to medical and health care professionals, and payers. In addition, you will support our strategic medical objectives by developing and maintaining professional relationships through facilitating collaboration opportunities. </p><p>Territory: TX (Houston & Dallas), OK, AR, LA, MS</p><p><strong>A typical day may include the following: </strong></p><ul><li><p>Develop and maintain peer–to–peer collaborations and relationships with medical and scientific experts, and population health decision makers. </p></li><li><p>Participate on committees or project teams supporting field medical strategies and tactics. </p></li><li><p>Respond to unsolicited medical information requests, handle questions and liaise with headquarters personnel ensuring proper responses have been provided and data is fair and balanced. </p></li><li><p>Develop an understanding of the regional landscape including specialties involved in care of patients in that area & other landscape mapping activities. </p></li><li><p>Identify and bring actionable information & insights that enhance the value and appropriate use of our products back to appropriate internal collaborators. </p></li><li><p>Build and cultivate important working relationships across field partners to ensure an integrated approach when working with HCP’s or experts. </p></li><li><p>Collaborate with physicians on medical affairs initiatives including publications, Company– sponsored research (CSR), regional advisory boards, regional medical education opportunities, training and speaker development programs. Develop and sustain expertise in product/molecule data, disease state management, emerging therapies, and the competitive landscape. </p></li><li><p>Respond to HCP inquiries with integrity, compliance, and adherence to legal, regulatory, and our guidelines, policies & procedures ensuring focused and balanced clinical and scientific information.</p></li><li><p>Support clinical research activities throughout the life cycle (phase 1-4), as well as Investigator Initiated Studies, focusing on identification of pre-clinical, clinical and post-marketing study investigators/ experts and sites in alignment with Medical Affairs objectives </p></li></ul><p>To be considered a Clinical/Science doctorate Degree required (MD, PharmD, PhD, DNP, DVM) along with a minimum of 3-5 years related work experience preferred (clinical, managed care, or industry experience) including experience as a Medical Science Liaison. Recent experience in Neurology is preferred. Established relationships with KOLs in neuromuscular centers is preferred. Experience communicating and disseminating scientific and clinical data required. Travel within the assigned territory and attendance at industry conferences is required. </p><p>#msl #medicalscienceliaison</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$150,500.00 - $245,500.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Sun, 10 May 2026 19:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Process Technician, Wednesday-Saturday 2nd shift]]></title>
    <date><![CDATA[Sun, 10 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47301]]></requisitionid>
    <referencenumber><![CDATA[R47301]]></referencenumber>
    <apijobid><![CDATA[r47301]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47301/process-technician-wednesday-saturday-2nd-shift/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[East Greenbush]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are currently looking to fill a Process Technician position with a Wednesday-Saturday 2:00pm-12:30am schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Process Technicians play a vital role in supporting our manufacturing operations. They provide operational, maintenance, and troubleshooting support for manufacturing process area maintenance through strict compliance with Standard Operating Procedures (SOPs) and cGMPs.</p><p><strong>Please note training will take place Monday-Friday 1st shift 6:00am-2:30pm for several weeks. Working hours thereafter will be Wednesday-Saturday 2:00pm-12:30am.</strong></p><p>As a Process Technician, a typical day might include the following:</p><ul><li><p>Performing daily operations, maintenance and repairs on utility systems, manufacturing equipment and building systems in a cGMP environment</p></li><li><p>Ensuring safe and efficient hands-on maintenance of all plant manufacturing equipment and related support equipment</p></li><li><p>Identifying any off-nominal conditions with mechanical equipment and mechanical troubleshooting of manufacturing/utility equipment in a clean room environment</p></li><li><p>Performing daily Work Orders (WOs) and PMs and efficiently coordinating the workflow and documentation of PMs and WOs</p></li><li><p>Troubleshooting electrical equipment during off-nominal conditions; locating the source of trouble and arranging for/performing all necessary repairs</p></li><li><p>Coordinating with each impacted department and within Facilities Management when planned and unplanned work events occur</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Can interpret P&IDs, equipment/system layouts, wiring diagrams and specifications in planning and performing maintenance and repairs</p></li><li><p>Have prior experience in equipment maintenance or a related position requiring mechanical skills and abilities</p></li><li><p>Are safety-minded while looking for opportunities to continuously improve</p></li><li><p>Strive for compliance with regulatory, corporate, and site-specific policies and procedures</p></li><li><p>Can fully gown as required when entering and working on production floor</p></li><li><p>Are able to support a rotational on-call schedule</p></li></ul><p>To be considered for this position you must be willing and able to work Wednesday-Saturday 2:00pm-12:30am. Applicants should have an AAS degree, preferably in an Engineering or Construction Technologies related field, and the following minimum amounts of proven experience for each level:</p><ul><li><p>Process Technician II: 2+ years of related experience or HSD/GED with 5+ years of related experience</p></li></ul><p>#REGENTOSK</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (hourly)</strong></strong></p>$24.76 - $38.70]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Mon, 11 May 2026 16:56:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Staff GMP Data Integrity Business Partner]]></title>
    <date><![CDATA[Wed, 06 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46942]]></requisitionid>
    <referencenumber><![CDATA[R46942]]></referencenumber>
    <apijobid><![CDATA[r46942]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46942/staff-gmp-data-integrity-business-partner/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Troy]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Staff GMP Data Integrity Business Partner role implements the data governance standards, policies, and procedures into business operations. This position serves as a site resource and subject matter authority on good data governance and integrity (DGI) practices and ensures business groups are aligned to Regeneron Manufacturing's Data Governance Program. </p><p>In this role, a typical day might include the following:</p><ul><li><p>Implementation of standards, policies, and procedures and engage with the allocated business unit on DGI priorities, action plans.</p></li><li><p>Assess business unit’s current policies and processes and be responsible for the achievement of local DGI significant metrics.</p></li><li><p>Conduct regular data audits and assessments to identify DGI issues and work to prepare for DGI auditing and inspections.</p></li><li><p>See opportunities to improve data-related processes, systems and tools within allocated business area that are aligned with the business’s evolving needs and industry standard processes.</p></li><li><p>Work in partnership with other DGI Business Partners, Technical Experts & ECM Experts to deliver on the plan and feedback themes to allow CI & evolution of the DGI approach.</p></li><li><p>Feedback themes to Data Governance Leadership team to allow CI & evolution of the data governance approach.</p></li></ul><p>This role might be for you if you:</p><ul><li><p>Stay updated on latest industry trends, regulatory changes and enforcement actions within the biopharma industry and assessing the impact of these within Regeneron.</p></li><li><p>Can foster a culture of quality & DGI within the organization.</p></li><li><p>Encourage CI by actively seeking feedback and supporting initiatives designed to enhance data quality and governance.</p></li><li><p>Have knowledge of applicable federal, state, and local regulations (e.g. GDPR), rules, policies, and procedures such as FDA Guidance on Data Integrity, EMA Data Integrity Guide, and WHO Guide to Data Integrity.</p></li><li><p>Have expert knowledge of cGMP & GDP.</p></li><li><p>Can translate complex regulatory and technical requirements into clear guidance for cross-functional teams.</p></li><li><p>Possess strong stakeholder management and influencing skills.</p></li></ul><p>To be considered for this role you must hold a Bachelor’s degree and the following amount of relevant experience for each level:</p><ul><li><p>Principal: 8+ years</p></li><li><p>Staff: 10+ years</p></li><li><p>Senior Staff: 12+ years</p></li></ul><p>May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$92,200.00 - $206,100.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Wed, 06 May 2026 10:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal QA Specialist - IT]]></title>
    <date><![CDATA[Mon, 11 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46510]]></requisitionid>
    <referencenumber><![CDATA[R46510]]></referencenumber>
    <apijobid><![CDATA[r46510]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46510/principal-qa-specialist-it/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Co. Limerick]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>Working within the Quality Assurance organization this position is responsible for ensuring IT systems, programs and quality events are robust and compliant. The position will liaise with the IT and broader QA organizations to ensure all aspects of IT related programs are in compliance with regulatory agency expectations and internal company policies and procedures.</p><p><strong>As a Principal QA Specialist, a typical day might include the following:</strong></p><ul><li><p>Supporting IT related change controls, CAPAs, data integrity initiatives, deviations, internal and external audits and other verticals to ensure a robust, compliant state of programs</p></li><li><p>Engaging with Corporate and IOPS IT ensuring IT processes and procedures meet Regeneron’s Quality System requirements</p></li><li><p>Reviewing, editing and approving SOPs, deviation notifications, deviation investigations, and corrective actions</p></li><li><p>Responsible for compliance monitoring of area operations, including trending of failures and evaluating efficiency of corrective actions</p></li><li><p>Collaborating, investigating and troubleshooting to determine solutions or recommendations for changes and/or improvements</p></li><li><p>Participating and supporting the Quality Risk Management (QRM) principles in the formal and informal risk assessment initiatives</p></li><li><p>Supporting the development, review and approval of Quality Assurance Agreements (QAA), along with the Approved Supplier List (ASL) process</p></li><li><p>Contributing information reflecting best practices, industry trends and recommendations for strategic plans to drives changes and improvements</p></li><li><p>Communicating project and program status and metrics to Senior Management</p></li></ul><p><strong>This role might be for you if you:</strong></p><ul><li><p>Demonstrate strong interpersonal skills and can collaborate effectively</p></li><li><p>Can balance changing priorities with a growing workload by communicating timely decisions</p></li><li><p>Demonstrate knowledge of 21CFR11 and Annex 11 as well MHRA, FDA and WHO data integrity guidelines</p></li><li><p>Have an understanding of the interdependencies of change management, deviation and continuous improvement</p></li><li><p>Can work in a dynamic organization where innovative solutions are required to ensure a high-level of quality is achieved with aggressive timelines</p></li></ul><p>To be considered for this position you should have a BSc/BA/BEng in IT/Automation/Analytics or related field and 5-7 years of experience or equivalent combination of education and experience. Recent experience in a data integrity role is preferred; however, it is not required. </p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Industrial Operations & Product Supply]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Tue, 12 May 2026 09:56:09 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior Paralegal - R&D and Regulatory]]></title>
    <date><![CDATA[Thu, 07 May 2026 00:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47214]]></requisitionid>
    <referencenumber><![CDATA[R47214]]></referencenumber>
    <apijobid><![CDATA[r47214]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47214/senior-paralegal-rd-and-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>Regeneron’s R&D Regulatory law group is seeking a <strong>Senior Paralegal </strong>to join our legal team. The Senior Paralegal will play an important role in various R&D and regulatory-related activities. The ideal candidate will possess excellent organizational skills and be motivated to learn about drug development regulations. </p><p>This role functions as a senior manager-level individual contributor, providing sustained ownership of complex R&D regulatory contract processes and exercising independent judgment in a high-risk, highly regulated environment, without people management responsibilities.</p><p><strong>In this role, a typical day might include the following:</strong> </p><ul><li><p>Support maintenance of contract playbooks, templates, and internal clinical research documents</p></li><li><p>Work with R&D attorneys to review contracts and other regulatory forms</p></li><li><p>Partner with R&D attorneys to formulate and communicate compliant and practical solutions that meet business objectives</p></li><li><p>Assist with fact-gathering to support legal advice</p></li></ul><p><strong> </strong></p><p><strong>This role might be for you if have experience with :</strong></p><ul><li><p>Strong organizational skills; able to effectively manage projects and responsibilities by applying prioritization skillset and sound judgment</p></li><li><p>Demonstrated ability to work accurately and effectively</p></li></ul><p><strong>To be considered for this role, you must have:</strong></p><ul><li><p>BA/BS required</p></li><li><p>8 or more years of progressive paralegal work experience</p></li><li><p>Previous experience in a pharmaceutical company or biotech and knowledge of issues related to clinical research a plus</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Corporate Functions]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 07 May 2026 18:26:06 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Field Medical oncology]]></title>
    <date><![CDATA[Wed, 13 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46734]]></requisitionid>
    <referencenumber><![CDATA[R46734]]></referencenumber>
    <apijobid><![CDATA[r46734]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46734/field-medical-oncology/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Spain]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>We are excited to welcome a passionate Field Medical Affairs professional to our Oncology team in Spain. In this impactful role, you’ll serve as a scientific and medical resource, collaborating closely with internal and external stakeholders to advance Regeneron’s Oncology portfolio. By engaging with leading experts and supporting clinical and research initiatives, you’ll help build the future of cancer care. Join us and make a meaningful difference for patients while growing your expertise in a collaborative, innovative environment.</p><h3><strong>A Typical Day:</strong></h3><ul><li><p>Engaging with key opinion leaders to foster scientific exchange and build positive relationships.</p></li><li><p>Presenting clinical and scientific data to healthcare professionals and research collaborators.</p></li><li><p>Supporting the development and management of company-sponsored and investigator-initiated studies.</p></li><li><p>Identifying and assisting with the selection of investigators and trial sites for Oncology research.</p></li><li><p>Participating in cross-functional collaborations with Medical Affairs, Clinical Development, and Market Access teams.</p></li><li><p>Gathering and sharing relevant clinical and competitive intelligence from medical conferences.</p></li><li><p>Acting as the primary resource for disease state and product information within your territory.</p></li><li><p>Ensuring compliance with company policies while maintaining integrity in all interactions.</p></li></ul><h3><strong>This Role May Be For You, if you:</strong></h3><ul><li><p>Thrive in collaborative, matrixed environments and enjoy working across diverse teams.</p></li><li><p>You are motivated by building and nurturing relationships with healthcare professionals and scientific leaders.</p></li><li><p>Communicate complex scientific information with clarity and confidence.</p></li><li><p>Adapt seamlessly to changing priorities and field-based challenges.</p></li><li><p>Balance independent work with team-based projects, demonstrating initiative and accountability.</p></li><li><p>Value integrity and professionalism in all aspects of your work.</p></li></ul><p>To be considered, you must hold a bachelor’s degree, with at least 5 years of relevant experience—including 3 or more years in a Field Medical or Medical Manager role within the biotech or pharmaceutical industry, specifically in Oncology. Experience in lymphoma and/or multiple myeloma is preferred, alongside established relationships with key opinion leaders in malignant Oncology. Drug launch experience, knowledge of treatment guidelines, clinical research processes, EU and pharma regulations, and strong communication skills are essential. Proficiency in strategic conversation and adaptability. Experience working in a matrix environment and familiarity with commercial operations are preferred.</p><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Thu, 14 May 2026 07:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Senior  Manager Clinical Data Management Study Lead]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R46045]]></requisitionid>
    <referencenumber><![CDATA[R46045]]></referencenumber>
    <apijobid><![CDATA[r46045]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r46045/senior-manager-clinical-data-management-study-lead/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Uxbridge]]></city>
    <state><![CDATA[Middlesex]]></state>
    <country><![CDATA[United Kingdom]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Senior Manager, Clinical Data Management provides oversight of lead Data Manager(s) on assigned clinical data management projects in multiple therapeutic areas to assure proper planning and execution for data management results that meet Regeneron standards and within timelines.</p><h3><strong>A typical day might include the following:</strong></h3><ul><li><p>Serves as primary DM contact for assigned therapeutic areas to interact with clinical counterparts for overall project planning and issue resolution. Projects, allocates and prioritizes DM resources within the assigned therapeutic projects.</p></li><li><p>Supervises direct DM reports for planning and managing all relevant DM activities within the assigned therapeutic areas for timely and quality results and within the budget. Mentor junior data managers for skills advancement. If required, leads and performs clinical data management tasks for studies.</p></li><li><p>Supervises and ensures all databases are developed, validated and ready for transfer and/or analysis according to policies and procedures, SOP’s and work instructions in compliance with applicable regulations.</p></li><li><p>Reviews and approves for final archival of project documentation, including, but not limited to, Data Management Manual, CRF Completion Guidelines and validation specifications, and work instructions for assigned projects. Designs and modifies CRF.</p></li></ul><h3>This role might be for you if:</h3><ul><li><p>Supervises DM direct reports for the initiation and approval of the building, and validation of clinical databases, subsequent changes in clinical databases and data validation activities. Coordinates with clinical project team for issue resolution.</p></li><li><p>Contributes to development of Regeneron DM outsourcing strategies and long-term relationships with outsourcing partners with objective of ensuring data quality and efficiencies through data and process standardization.</p></li><li><p>Ensures adequate management of CROs and vendors in the therapeutic projects and coordinates all data management functions.</p></li><li><p>Establishes goals, expectations and accountabilities for direct reports. Regularly reviews DM performance in respect to quality and timeliness standards according to Regeneron SOPs and working procedures. Responsible for coaching, handling training and leading the direct reports.</p></li></ul><h3>To be considered</h3><ul><li><p>Bachelor’s degree in mathematics, Science or a related field, along with at least 8-10 or more years of clinical data management experience in biotech, pharmaceutical or health related industry. Previous oncology and/or ophthalmology experience a plus. Previous managerial experience is preferred</p></li><li><p>Directed and comfortable working in teams with the ability to work and operate independently within a tight time line environment. High degree of creativity, latitude and attention to detail required.</p></li><li><p>Knowledge of all applicable regulations including; CFR, GCP, and ICH Guidelines. Strong communication, leadership and business development skills required.</p></li><li><p>Proficient with appropriate EDC applications and Microsoft Office applications. Software proficiency with CDMS required. Experience with JMP and SAS a plus.</p></li></ul><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$134,400.00 - $219,200.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Fully remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 08:56:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Medical Director, Clinical Development, MASH/Metabolism (Regeneron Genetics Medicine)]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47478]]></requisitionid>
    <referencenumber><![CDATA[R47478]]></referencenumber>
    <apijobid><![CDATA[r47478]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47478/medical-director-clinical-development-mashmetabolism-regeneron-genetics-medicine/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Medical Director, Clinical Sciences, MASH/Metabolism works with their supervisor and other members of the cross-functional study team to author protocols and facilitate execution of study activities and data summarization. The Medical Director leads collaborations with discovery scientists and translational colleagues to understand current and emerging genetic targets across a variety of therapeutic areas and disease states including but not limited to MASH and metabolism, rare diseases, and others; provides input on potential disease areas/indications; and crafts clinical experiments that corroborate or inform the biology for decision-making purposes and enable clinical development programs within the Regeneron Genetics Medicine Clinical Development Unit. This Medical Director will report into the VP Therapeutic Area Lead.</p><p><strong>As a Medical Director, a typical day might include the following:</strong></p><p>• Leads the cross-functional study team to craft novel clinical development strategy for genetic medicines, including First in Human (FIH), Phase 2, and Phase 3 clinical trials</p><p>• Responsible for the relevance and accuracy of medical science underpinning of clinical study based on detailed scientific review and consultation</p><p>• Authors, reviews, and finalizes the medical and scientific portions of study strategies and clinical study protocols and amendments</p><p>• Authors, reviews, and edits documents related to trials, such as monitoring plans, SAPs, amendments, IRB/IEC submissions and regulatory submissions</p><p>• Accountable for timely clinical trial execution, reviewing adverse events, monitoring patient health, and quality of results</p><p>• Analyzes the benefits and risk aspects of an assigned therapeutic candidate</p><p>• Ensures clinical team compliance with FDA, EMEA, ICH and GCP guidelines as well as SOPs regarding safety</p><p>• Authors clinical sections of communications/documentation for regulatory agencies and may participate in meetings as needed</p><p>• Conducts detailed literature reviews and analysis of development opportunities from mechanistic, pharmacological and clinical development perspectives</p><p><strong>This role may be for you if: </strong></p><p>• You want to make an impact delivering genetic medicines for patients with serious diseases</p><p>• You have specialist postgraduate clinical training and practice, and/or scientific research training and with a track record of success</p><p>• You demonstrate critical, science-to-medicine translational thinking skills and sound decision making</p><p>• You have the ability to work productively in a fast-paced collaborative working environment</p><p>To be considered for this role, you must have an M.D. Degree (M.D./Ph.D. Degree or prior research experience preferred). Board Certification/Eligibility in a relevant therapeutic area (Hepatology, Gastroenterology, Endocrinology, or Nephrology preferred. A minimum of 2-3 years of clinical practice or industry experience is preferred. This role requires a minimum of four days on-site weekly in Tarrytown, NY.</p><p>#MDJOBS, #MDJOBSCD</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$284,900.00 - $385,700.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 11:26:08 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Associate Director Imaging]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47703]]></requisitionid>
    <referencenumber><![CDATA[R47703]]></referencenumber>
    <apijobid><![CDATA[r47703]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47703/associate-director-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>Regeneron Imaging Sciences is seeking a multidisciplinary <strong>Associate Director Imaging</strong> to lead a core team of highly talented scientists and subject matter experts providing collaborative partnerships and services in the fields of in vivo imaging, microscopy, histology, and computational image analysis. A unique state-of -the-art core facility, Imaging Sciences supports Regeneron’s research programs with multimodality and multiscale imaging and compelling modality-agnostic image data analysis across therapeutic focus areas and various stages of preclinical drug discovery and development.</p><p>The successful candidate will be an independent imaging scientific leader among cross-functional teams at Regeneron including preclinical and clinical colleagues. This position provides excellent opportunities to champion the deployment of appropriate imaging tools to bridge research gaps and further drug development by contributing to a better appreciation of disease biology from the sub-cellular to the systems-level, and a deeper understanding of the workings of our drugs from the nano- to the macro-scale.</p><p><strong>A Typical Day in the Role Might Look Like:</strong></p><ul><li><p>Periodic surveillance and understanding of imaging needs across the Regeneron research organization and relay such information to the team.</p></li><li><p>Co-strategize with team leads and subject matter experts to identify how and where imaging or image analysis tools can provide meaningful insights and/or effective solutions.</p></li><li><p>Organize outreach efforts with the core team leaders to raise awareness and advocate for the use of in-house imaging capabilities to support Regeneron research efforts.</p></li><li><p>Facilitate the team to formulate and pitch solutions and partnerships towards achieving a common goal through effective and successful collaborations.</p></li><li><p>Work closely with stakeholders to forecast outcomes, build contingency plans, troubleshoot unanticipated roadblocks to collective progress in a multi-team effort.</p></li><li><p>Lead the team to prepare and make effective presentations to senior leadership on topics ranging from vision and goals to impactful scientific progress and updates.</p></li><li><p>Serve as a two-way conduit between departmental as well as research-wide scientific leadership and the imaging core for allocation of effort in alignment with company needs and priorities whilst communicating the team’s needs and accomplishments upwards.</p></li></ul><p><strong>This Role Might Be for You if You:</strong></p><ul><li><p>Deep understanding of disease biology, drug mechanism(s) of action, in vitro, in vivo, and ex vivo models and imaging assays across modalities that can be leveraged to best answer research questions at hand.</p></li><li><p>Familiarity with the utility of computational image analysis tools to extract powerful quantitative information including but not limited to study endpoints, imaging biomarkers, measures of pharmacodynamic effects, and radiomic features etc., from imaging data.</p></li><li><p>Demonstrated ability to collaborate and lead cross-functional team efforts implementing imaging assays for providing meaningful insights and/or solutions to move research programs forward.</p></li><li><p>Excellent communication and organizational skills – adept at influencing across functions and levels.</p></li></ul><p><strong>To be considered for this position</strong>, you must have a PhD with 10+ years of broad multimodal preclinical imaging experience – with at least 7 years of industry experience. Experience in drug discovery for disease indications in oncology/immune-oncology, cardiovascular and renal diseases, infectious diseases, obesity, musculoskeletal and metabolic disorders, neurosciences, and genetic diseases.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$176,100.00 - $287,300.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 12:26:07 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Manager GD Training Systems]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47406]]></requisitionid>
    <referencenumber><![CDATA[R47406]]></referencenumber>
    <apijobid><![CDATA[r47406]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47406/manager-gd-training-systems/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Dublin]]></city>
    <state><![CDATA[]]></state>
    <country><![CDATA[Ireland]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The <strong>Manager, Learning Center of Excellence, Systems</strong> (Mgr LCoE Systems) is responsible for providing design, development, delivery, evaluation, logistical support and content management support for system application training. The Mgr LCoE Systems will work closely with the Dir LCoE Systems and AD LCoE Systems to continually improve the scale, depth, and quality of system application training that aligns with strategic objectives within Global Development.</p><p><strong>A typical day in this role looks like:</strong></p><p>This position is expected to have the ability to execute a variety of roles to meet the expectations of effective relationship management and driving compliance and high-quality delivery. </p><p><strong>Strategic Alignment:</strong></p><ul><li>Understand the business and associated roles within Global Development. </li><li>Understand the business needs and technical challenges experienced by Global Development associates and collaborate with Dir and AD LCoE Systems to determine strategy for designing and delivering systems training at scale.</li></ul><p><strong>Relationship Management </strong></p><ul><li>Use knowledge of business and customer base in order to identify SMEs and potential departmental trainers that could be leveraged for system application training delivery.</li><li>Consult with Training Business Partners, Global Dev IT and System Owners/SMEs to design and deliver learning solutions, in a wide range of multimedia formats.</li><li>Interact with LCoE C3 team to ensure accurate assignment and compliance oversight.</li><li>Support</li><li>Maintain and continue to develop a robust and accurate end-to-end knowledge of business processes and applicable procedures for Global Development</li><li>Participate in system and business process training related activities, such as performing UAT on training materials and auditing face to face/virtual instructor led system/business process training sessions.</li><li>With Dir and AD LCoE Systems, establish method for system training curriculum creation and oversight, ensure management input at designated timepoints</li><li>Work with functional SMEs and Dir and AD LCoE Systems to establish role based curriculum or training matrices to match system requirements</li><li>Support Dir and AD LCoE Systems in creating/executing/maintaining detailed training plan for all supported systems, create all deliverables and work closely with support teams (System Owners, SMEs, Facilitator/ Trainer, Super Users).</li><li>As needed, conduct system training sessions as well as plan and facilitate workstream sessions related to the implementation of systems supported by GDT.</li><li>Dir and AD LCoE Systems may require Systems Training Manager to develop subject-matter expertise in the target application to help facilitate the design and development of learning solutions, in cases where functional SMEs require additional support.</li></ul><p><strong>Effectiveness tracking </strong></p><ul><li>Evaluate continuous feedback from surveys, help desk queries, Super User/Trainer qualitative feedback regarding existing systems and make recommendations for improvement to training.</li><li>Track trends and monitor training compliance; prepare routine progress reports on job specific training programs for management.</li><li>Implement plan for improving compliance across supported stakeholder groups.</li></ul><p><strong>This role may be for you if you have:</strong></p><ul><li>Instructional Design: Creating quick reference guides, video tutorials, Instructor Led Training guides</li><li>Facilitiation skills – Comfortable facilitating in a face to face and virtual environment </li><li>Time Management - Ability to manage multiple projects with overlapping deadlines</li></ul><p><strong>In order to be considered qualified for this role</strong>, a minimum of Bachelors degree is required. and</p><p>ideally 2+ years Clinical, Pharmaceutical or Medical Device experience with understanding of GxP guidelines;</p><ul><li>At least 2 years’ experience designing and delivering system application training *incorporating system and business process* </li><li>Ideally 3+ years instructional design experience.</li></ul><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p>]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Global Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 14:56:10 GMT]]></lastactivitydate>
  </job>
  <job>
    <title><![CDATA[Principal Cloud DevSecOps Engineer]]></title>
    <date><![CDATA[Thu, 14 May 2026 19:00:00 GMT]]></date>
    <requisitionid><![CDATA[R47382]]></requisitionid>
    <referencenumber><![CDATA[R47382]]></referencenumber>
    <apijobid><![CDATA[r47382]]></apijobid>
    <url><![CDATA[https://careers.regeneron.com/en/jobs/r47382/principal-cloud-devsecops-engineer/]]></url>
    <company><![CDATA[Regeneron]]></company>
    <city><![CDATA[Tarrytown]]></city>
    <state><![CDATA[New York]]></state>
    <country><![CDATA[United States of America]]></country>
    <postalcode><![CDATA[]]></postalcode>
    <description><![CDATA[<p>The Regeneron Genetics Center (RGC) IT team is looking for a passionate Principal Cloud DevSecOps Engineer with strong technical ability, communication, and collaboration skills. As the Principal Cloud DevSecOps Engineer, you will be responsible for the design and implementation of cloud infrastructure, automation, security controls, and compliance processes on AWS, supporting data, HPC, AI, and microservice platforms used by research scientists and bioinformaticians. You will work hands-on to build and implement cloud DevSecOps solutions, embed security into system design, and provide technical support and guidance to end users and internal teams. You will also provide technical mentorship for Lead and Senior DevSecOps engineers and coordinate with InfoSec, Privacy, and internal IT teams to ensure security, scalability, and reliability of the RGC cloud platform.</p><p><strong>In this role, a typical day might include the following:</strong></p><ul><li><p>Design and implement infrastructure-as-code, automation scripts, and CI/CD pipelines supporting data, HPC, AI, and microservice platforms on AWS</p></li><li><p>Embed security controls into system design and implementation — including IAM policies, network segmentation, secrets management, and compliance validation pipelines</p></li><li><p>Design and implement tools to automate operational processes across RGC’s cloud and systems engineering platforms</p></li><li><p>Support all audit related activities including providing evidence and remediation of findings for RGC’s cloud platform</p></li><li><p>Develop and implement continuous delivery systems and CI/CD methodologies for RGC’s systems engineering platforms using both AWS services and GitHub Actions, ARC self-hosted runners on EKS, and SAST/DAST integration.</p></li><li><p>Recommend and deploy monitoring, metrics, and logging systems on RGC’s cloud engineering platforms</p></li><li><p>Identify and implement opportunities to build systems that are highly available, scalable, and self-healing</p></li><li><p>Develop SOPs and configure cloud services to support compliance validation</p></li><li><p>Provide technical support, training, and documentation to end users and research teams using RGC’s data, HPC, AI, and microservice platforms</p></li><li><p>Serve as a technical point of contact for user-facing issues related to cloud platform, DevOps pipelines, security services, and solving problems in collaboration with internal IT teams</p></li><li><p>Stay on top of the latest advances in cloud platforms and related security & compliance controls</p></li><li><p>Provide technical guidance and mentorship for Lead and Senior DevSecOps engineers</p></li><li><p>Interact with InfoSec and Privacy teams to define and iterate on security requirements, and implement them across the platform</p></li></ul><p><strong>This job might be for you if:</strong></p><ul><li><p>You have an eye for detail and pride yourself on the quality of your work. Operational excellence and secure-by-design thinking matter more than just finishing the tasks.</p></li><li><p>You thrive in a fast-paced environment working across data, HPC, AI, and microservice platforms, and enjoy being a technical resource for the teams that depend on them.</p></li><li><p>You work on current problems while thinking of future solutions, and take satisfaction in both building the right thing and supporting the people who use it.</p></li></ul><p><strong>To be considered for the Principal Cloud DevSecOps Engineer, you must have: </strong> </p><ul><li><p>Bachelor's Degree in Computer Science, or related field.</p></li><li><p>8+ years of in-depth AWS services experience and relevant security certifications.</p></li><li><p>Hands-on experience designing and implementing cloud infrastructure automation, CI/CD pipelines, infrastructure-as-code, and security controls. </p></li><li><p>Solid understanding of cloud security posture including IAM, network segmentation, secrets management, compliance validation, and security-by-design principles. </p></li><li><p>Experience supporting data, HPC, AI, or microservice platforms in a technical or user-facing capacity. Knowledge of core AWS services EC2, EBS, S3, ELB, RDS, EKS, and IAM. Tangible experience with Linux administration and automation of security controls and compliance validation. </p></li><li><p>Experience with monitoring tools like Splunk, Grafana, Prometheus. AWS and other related certifications are a plus.</p></li></ul><p><strong>Level commensurate on experience and qualifications.</strong> Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.</p><div><div><div><div><div><div><div><p>Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.<br>Please be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on-site policy and expectations for your role and your location.<br> </p><p>Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.</p><p>For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.</p><p>Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.</p><p><strong><strong>Salary Range (annually)</strong></strong></p></div></div></div></div></div></div></div>$128,600.00 - $210,000.00]]></description>
    <jobtype><![CDATA[Full_time]]></jobtype>
    <category><![CDATA[Research & Preclinical Development]]></category>
    <sourcename><![CDATA[Regeneron Pharmaceuticals Inc.]]></sourcename>
    <remotetype><![CDATA[Hybrid remote]]></remotetype>
    <lastactivitydate><![CDATA[Fri, 15 May 2026 15:26:09 GMT]]></lastactivitydate>
  </job>
</source>