• Medical Device Regulatory

    Oracle (Concord, NH)
    …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
    Oracle (11/25/25)
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  • Senior Manager, CMC Global Regulatory

    Otsuka America Pharmaceutical Inc. (Concord, NH)
    **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global ... relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs , Global Regulatory Strategy, Manufacturing facilities,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Principal Regulatory Affairs

    Bausch + Lomb (Concord, NH)
    …+ Minimum of 8 years in recent experience in strategic pharmacuetical Regulatory Affairs . This position does not work with medical device , cosmetics or ... and ability to see the business drivers outside of Regulatory Affairs + Ability to take innovative...**We offer competitive salary & excellent benefits including:** + Medical , Dental, Eye Health, Disability and Life Insurance begins… more
    Bausch + Lomb (09/06/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Concord, NH)
    …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare… more
    Fujifilm (09/04/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Concord, NH)
    …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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  • Biocompatibility & Toxicology Senior Scientist

    DEKA Research & Development (Manchester, NH)
    …time to market + Insure the organization stays up to date on global regulatory changes to medical device biocompatibility standards and requirements through ... Toxicology Senior Scientist to join our team focused on medical device and combination product development. The...this role will work directly with Research & Development, Regulatory & Clinical Affairs and Quality Engineering… more
    DEKA Research & Development (10/17/25)
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  • Field Clinical Specialist, North MA…

    Edwards Lifesciences (Manchester, NH)
    …surgery or interventional cardiology are strongly preferred; candidates with other relevant medical device clinical sales support experience will be considered + ... Director and will collaborate with multiple departments including Sales, Clinical Affairs , Marketing, Quality, Regulatory , and Education. After extensive… more
    Edwards Lifesciences (11/19/25)
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