• Global Regulatory Affairs

    Sanofi Group (Cambridge, MA)
    **Job title** : Global Regulatory Affairs Device Lead (Associate Director) **Location** : Morristown, NJ or Cambridge, MA or Framingham, MA **About the ... could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the… more
    Sanofi Group (10/23/25)
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  • GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting ... pathways. The team is accountable for developing and implementing global regulatory strategies for device ...team creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional… more
    Sanofi Group (09/20/25)
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  • Medical Device Regulatory

    Oracle (Boston, MA)
    …success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work in collaboration ... across global markets that impact to our businesses, regulatory affairs function, and quality/compliance programs. **Responsibilities** **Preferred… more
    Oracle (11/25/25)
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  • Senior Manager, CMC Global

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing ... variations) around small molecule drug substance, drug products and drug- device combination products. Ensure compliance with global ...local and/or global functional units [OPC CMC Global Regulatory Affairs , Global more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Regulatory Affairs Associate…

    GRAIL (Boston, MA)
    …with the FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such as PMAs, 510(k)s, post-approval ... and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For...IVD, medical device , or pharmaceutical industries. + Regulatory affairs and IVD device more
    GRAIL (12/03/25)
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  • Regulatory Affairs Manager

    Dentsply Sirona (Waltham, MA)
    …Years and Type of Experience: + 5(+) years of experience in regulatory affairs , preferably in the medical device industry. + Experience with leading ... care and deliver better and safer dentistry. Dentsply Sirona's global headquarters is located in Charlotte, North Carolina, USA....+ Manages day to day activities for less senior Regulatory Affairs professionals, including but not limited… more
    Dentsply Sirona (09/18/25)
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  • CMC Regulatory Affairs

    Parexel (Boston, MA)
    Exciting opportunity for an experienced and highly motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs ... device combination products are a plus) * Support regulatory leads in developing contingency plans for CMC-related scenarios... Affairs in cross-functional project meetings and provide regulatory guidance in collaboration with global more
    Parexel (10/11/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Boston, MA)
    …field or equivalent work experience, preferred + 2+ years' experience in Medical Device Regulatory Affairs /Quality experience preferred + Certification in ... **_What Regulatory Affairs contributes to Cardinal Health_**...medical devices + Supports all pertinent activities to ensure global product and regulatory requirements are accounted… more
    Cardinal Health (12/13/25)
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  • Principal Regulatory Affairs

    Philips (Cambridge, MA)
    …+ You've acquired a minimum of 7+ years' experience in Regulatory Affairs /Strategy within FDA regulated Medical Device environments. + You have proven ... The Principal Regulatory Affairs Specialist will develop and...projects across a spectrum of product lines. + Monitor global regulatory landscapes and guide cross-functional teams… more
    Philips (11/11/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Cambridge, MA)
    …more: careers.bms.com/working-with-us . **Position Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy ... background, PhD., MD, PharmD, MS + Significant experience in regulatory affairs and diagnostic-related development eg, >8-10...deep expertise in developing and executing global regulatory strategies across drug and device development.… more
    Bristol Myers Squibb (11/24/25)
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