• Sr Quality Compliance Manager

    Abbott (Pleasanton, CA)
    …Eight (8) years of Quality Systems, Quality Assurance and/or Regulatory Compliance/ Affairs experience in medical device manufacturing or other similarly ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (06/19/25)
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  • 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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  • Senior Counsel ( Medical Device )

    Fujifilm (Sacramento, CA)
    …**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 (08/08/25)
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  • Biomedical Engineer

    Veterans Affairs, Veterans Health Administration (Long Beach, CA)
    …Report: Not required Preferred Experience: Specialized expertise in areas such as Medical Device Isolation Architecture (MDIA) and Specialized Device ... basis with limited oversight by senior biomedical engineers. They participate in medical device hazard investigations, to assure compliance with patient safety… more
    Veterans Affairs, Veterans Health Administration (08/23/25)
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  • Registered Nurse (Chief Nurse - Sterile Processing…

    Veterans Affairs, Veterans Health Administration (Palo Alto, CA)
    …Veterans Integrated Services Network Advisory Board, Clinical Product Review, Reusable Medical Device , Environment of Care Rounds, and Enterprise Equipment ... outcomes. Provides health system-wide leadership for critical and semi-critical Reusable Medical Device (RDM), including sterile storage, reprocessing, standard… more
    Veterans Affairs, Veterans Health Administration (08/08/25)
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  • Project Manager, Device Engineering

    Gilead Sciences, Inc. (Foster City, CA)
    …goals, and results to team members across functions and departments, including device development, packaging, quality, regulatory affairs and manufacturing. ... + Experience in the pharmaceutical or biotechnology industry is preferred + Medical device or combination product experience is preferred + PMP certification is… more
    Gilead Sciences, Inc. (08/29/25)
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  • Associate Regulatory Operations Specialist

    J&J Family of Companies (Santa Clara, CA)
    medical fields is preferred + 0 - 1 years' experience in medical device , life science, pharma industry Experience in regulatory affairs is preferred + ... health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** ...aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease… more
    J&J Family of Companies (08/29/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (San Carlos, CA)
    …submissions. + May supervise staff + May have responsibility for maintaining a compliant medical device quality system for R&D and informing project teams of ... projects and issues affecting development of new products or medical devices or new indications for existing products +...years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the… more
    Grifols Shared Services North America, Inc (08/01/25)
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  • Sr. Medical Sciences Specialist - Shockwave…

    J&J Family of Companies (Santa Clara, CA)
    …reports, and regulatory submissions. + As needed, assist in the Medical Affairs review of advertising/promotional/education material. + Support the Clinical ... and scientific information while adhering to legal, compliance and regulatory requirements. The Sr. Medical Sciences Specialist...minimum of 3 years of relevant Medical Affairs experience in the Medical Device more
    J&J Family of Companies (09/03/25)
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  • Senior Specialist, Medical Writing

    Edwards Lifesciences (Irvine, CA)
    …portfolio of products across TMTT. The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment to ... in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory ...field with 6 years of related experience working in medical affairs , clinical affairs and/or… more
    Edwards Lifesciences (06/11/25)
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