• Director, Medical Affairs

    J&J Family of Companies (Irvine, CA)
    …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical ... at https://www.jnj.com/medtech Johnson and Johnson is currently seeking a **Director, Medical Affairs , Electrophysiology** located **in Irvine, CA.** Atrial… more
    J&J Family of Companies (08/22/25)
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  • Sr Manager, Medical Affairs

    Gilead Sciences, Inc. (Parsippany, NJ)
    …BS/BAOR + 6+ Years with MS/MA or MBA **Preferred Qualifications** * 6+ years Medical Affairs ( medical device /pharmaceutical industry), managed care, and ... **Job Description** This role will have responsibility for leading the development of Medical Affairs (MA) strategies and Plans of Action (POA) within a… more
    Gilead Sciences, Inc. (08/01/25)
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  • Associate Director, Medical Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …compliance, product development, and clinical validation. **Key Responsibilities:** + Strategic Medical Leadership: Drive medical affairs activities ... support safety, efficiency, and clinical performance claims. + Global Medical Affairs Support: Ensure comprehensive Medical...+ At least 3 years of experience in the Medical Device /In Vitro Diagnostics industry. + Minimum… more
    BD (Becton, Dickinson and Company) (06/29/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Morristown, NJ)
    …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... team is part of the Global Regulatory Affairs , Regulatory CMC and Device ...closely with key stakeholders including clinical, medical affairs , Industrial Affairs ( Device Development,… more
    Sanofi Group (07/15/25)
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  • Clinical Affairs Manager, Interventional…

    Teleflex (Wayne, PA)
    …Cardiology environment. * Medical Device industry supporting Clinical and Medical Affairs , strongly preferred. * Proficient in Microsoft Word, Excel, and ... with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which… more
    Teleflex (08/13/25)
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  • Manager, Government Affairs

    Fujifilm (Washington, DC)
    …experts; issues to track may include healthcare policy, biopharmaceutical manufacturing, medical device , tax, trade, export controls, electronic materials, ... with federal government policy in focus areas of: life science, pharmaceutical, medical device industry, or electronic materials/semi-conductor chips OR 5+ years… more
    Fujifilm (07/15/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Tallahassee, FL)
    …**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, Device Clinical…

    Takeda Pharmaceuticals (Lexington, MA)
    …and device development teams + Serve as clinical liaison to Global Device Team, including engineering, regulatory affairs , quality, and commercial ... degree with 15+ years of experience** + Minimum 5 years of combination product, medical device , or pharmaceutical industry experience + Experience with both … more
    Takeda Pharmaceuticals (09/04/25)
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  • Orthotist and Prosthetist - Advanced Practitioner

    Veterans Affairs, Veterans Health Administration (Salt Lake City, UT)
    …Advanced Practitioner is a member of the Salt Lake City VA Medical Center, Prosthetics and Sensory Aids Department. This position is responsible for ... levels. Serves as an advisor to physicians, therapists and other medical professionals with regard to indications and contraindications of prosthetic and… more
    Veterans Affairs, Veterans Health Administration (08/10/25)
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  • Medical Affairs Associate Director

    IQVIA (Durham, NC)
    …role but may require onsite visits to clients. **Role and responsibilities** + Represent Medical Affairs on the content review committee as the lead Medical ... research design, methods, and outcome measures. + Advanced knowledge of pharmaceutical and medical device guidelines and regulations. + Experience on an approval… more
    IQVIA (08/12/25)
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