• Global Medical Affairs Director…

    Sanofi Group (Morristown, NJ)
    **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown, NJ **About the job** **About us:** In order to pursue ... miracles of science to improve people's lives", Specialty Care Medical Affairs have a vision to be...engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs … more
    Sanofi Group (10/02/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Trenton, NJ)
    …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... The Senior Counsel, reporting to the Division General Counsel, Medical Devices , will be an experienced commercial...Counsel and senior business management on general legal and regulatory risks affecting the Medical Device… more
    Fujifilm (09/04/25)
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  • Program Manager, Real-World Evidence (Remote)

    Stryker (Trenton, NJ)
    …of RWE studies in close collaboration with internal stakeholders from Clinical Strategy, Medical Affairs , Regulatory , HEOR, and Commercial + Ensure ... and/or other health data partners to identifyadditionalreal-world data sources for medical device evidence generation. + Ensure quality and performance… more
    Stryker (11/07/25)
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  • Associate Director, Program Manager

    Organon & Co. (Jersey City, NJ)
    …years of industry experience​ in R&D functions (eg, Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs , etc.) + ... leading the development or life-cycle management of drugs or devices which improve human health. The program manager may...plan, paid vacation and holiday time, paid caregiver/parental and medical leave, and health benefits including medical ,… more
    Organon & Co. (11/04/25)
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  • GRA Device Associate

    Sanofi Group (Morristown, NJ)
    …strategic partner within Sanofi's regulatory framework, providing expert guidance on medical device regulatory requirements across the product lifecycle. ... critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team...teams. + Contribute to and execute innovative and sustainable medical device regulatory strategies covering… more
    Sanofi Group (09/20/25)
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  • Hemoglobinopathies Strategy Lead

    Novo Nordisk (Plainsboro, NJ)
    …closely with cross-functional teams, including sales, marketing, medical affairs , market access and policy/advocacy (MAPA), regulatory affairs ... Nordisk's Rare Disease portfolio. The Rare Disease portfolio includes medical treatments, customer solutions, and devices across...drive market share and revenue growth. Partner with legal, regulatory , and medical affairs for… more
    Novo Nordisk (10/28/25)
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  • Sr Medical Science Liaison

    Terumo Medical Corporation (Somerset, NJ)
    …product and scientific support for the organization that includes Medical Affairs , Clinical Operations, Sales, Marketing, Regulatory Affairs , to ensure ... therapeutic area, provide support in the following ways: + Medical affairs strategy: + Contribute to the...+ Regulatory activities partnership: + Work with regulatory affairs to ensure that all written… more
    Terumo Medical Corporation (10/01/25)
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  • Project Manager, Med Device , R&D PMO,…

    Eliassen Group (Trenton, NJ)
    …http://careers.eliassen.com/iXUiCO + Description + Recommended Jobs **Description:** Our Fortune 500 Medical Device client is seeking a Project Manager to ... risk management, and communication across all stakeholders. * Coordinate with Regulatory Affairs to ensure documentation and submission readiness for… more
    Eliassen Group (10/25/25)
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  • Senior RA Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …Bioengineering, Biology, Chemistry). + Minimum of 5 years of Regulatory Affairs experience in medical devices , preferably sterile single-use disposable ... **Job Description Summary** The Senior Regulatory Affairs (RA) Specialist will represent...Q-Sub), EU technical documentation under MDR, and other global regulatory filings. + Evaluate medical device… more
    BD (Becton, Dickinson and Company) (11/14/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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