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Manager Regulatory Affairs - Swiftwater, PA

Swiftwater, Pennsylvania



Sanofi, a global healthcare leader, discovers, develops and distributes therapeutic solutions focused on patients' needs. Our Sanofi Pasteur Swiftwater, PA site, where we both research and manufacture vaccines since 1897, has had a tremendous impact on global health and the quality of human life. Nestled among the Pocono Mountains in Swiftwater, Pennsylvania, Sanofi Pasteur is home to state-of-the-industry facilities—and a rich and unique history. Our Swiftwater campus is more than 500 acres, housing 44 buildings and encompassing more than one million square feet of building space. Many of our facilities, while bright and modern, still retain the rustic charm of the original stonework.

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  • Health & Wellness

    Comprehensive coverage including medical, dental, vision, and health and wellness programs.

  • Financial

    Sanofi wants to ensure employees are equipped for financial health, Sanofi provides a competitive 401K Match program and Financial Wel-Being Tools and Programs.

  • Culture

    At Sanofi, we demonstrate our commitment to inclusion and diversity through Culture groups and programs. There are many ways to make a difference and connect with other Sanofi employees: including ERG groups and 2 PAID days off to Volunteer.

  • Work/Life Balance

    Sanofi provides significant Work/Life benefits to help you excel beyond the workday. Including Workplace Flexibility through part‑time, remote work, flex‑time and job share options.

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"I give thanks to my powerhouse team for reminding me that I have a support system behind me, pushing me forward."

Bob Shustack Head of Global Support Functions Finance, North America



  • Collaborates on CMC regulatory strategies and risk assessments; and is comfortable providing regulatory advice internally, as well as in a team environment.
  • Author, review, approve and/or contribute to submission-grade documents for projects and regulatory files (INDs, CTAs, BLAs, CTDs, etc.) . Can be associated with US, Canada, and/or International filings.
  • Responsible for accurate tracking and management of Health Authority requests, this includes educated follow-ups with regional regulatory affairs and/or affiliates as necessary.
  • Is able to clearly communicate status updates to respective global regulatory affairs colleagues, so that dissemination of information at project team level is accurate and clear.  Projects may consist of any product phase (Pre-IND through Phase III; post-approval.)  Will also assist in CMC working groups as required.
  • Uses time management skills to successfully meet deliverables.  Anticipates delays in pre-defined submissions and either sets up corrective actions plan or proposes alternative solutions for discussion. 
  • Provide support to GMP inspections and preparation as requested.
  • Is aware of on-going Health Authorities activities / negotiations where CMC related issues/topics are concerned. This may also entail communication with internal functions i.e. industrial affairs, and project teams to seek updates and/or information for health authority responses and/or meeting.  This role may / may not participate in Health Authority contact activities.
  • Sets up necessary meetings internally among cross-functional parties and is able to negotiate issues between parties as needed / requested.
  • Provides input and resources towards the development and implementation of new regulatory systems, procedures, and/or tools.
  • Responsible for staying up-to-date on regulatory guidances and technical/scientific developments.


Basic Qualifications:

  • Bachelor’s degree with 2+ years Regulatory Affairs experience OR Master’s degree in Regulatory Affairs
  • Requires in depth knowledge and understanding of CMC topics, as well as North American, European and International regulations/guidelines.   
  • Ability to manage multiple priorities efficiently.
  • Ability to communicate effectively on complex topics.
  • Effective writing abilities
  • Experience working on project teams and/or cross-functionally within a professional environment.

Preferred Qualifications:

  • Degree in a scientific field (Biology or Life Sciences)
  • Demonstrated knowledge in microbiology, immunology, virology, or bacteriology. 
  • Minimum of 2 years prior Manufacturing or Quality Assurance experience in the pharmaceutical / biotech industry.
  • Previous Regulatory Affairs CMC Authoring

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.


At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.

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