• Technical Program Manager, Hardware…

    Meta (Sunnyvale, CA)
    …radios & signal emissions, industry certifications, product marking, product safety, and medical devices . Your technical expertise and program management skills ... **Summary:** As a Hardware Regulatory Readiness and Compliance Technical Program Manager at...standards, and overall skills to interpret regulations for hardware devices and schedule impact 16. Track record of implementing… more
    Meta (08/01/25)
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  • Assistant General Counsel, Regulatory

    Cardinal Health (Sacramento, CA)
    …regulation) preferred * Experience in private practice strongly preferred * Familiarly with medical device and pharmaceutical regulation * Active license in good ... **_What Regulatory contributes to Cardinal Health_** Legal provides the...regulations; and other product-specific environmental / sustainability drug and device lifecycle obligations and stewardship programs. This role will… more
    Cardinal Health (06/18/25)
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  • Director of Product Management (Apps and Services)…

    Abbott (Alameda, CA)
    …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... fully at every stage of life. Our life-changing technologies span diagnostics, medical devices , nutrition, and branded generic medicines. With 115,000 colleagues… more
    Abbott (07/16/25)
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  • Associate Director, Interventional Glaucoma…

    AbbVie (Irvine, CA)
    …marketing plans to deliver strong business performance for AbbVie's only eye care medical device . This person's key responsibilities are to lead the strategic ... from concept review to final approval, via close collaboration with legal, compliance, regulatory and medical . + Represent the US commercial strategy as a… more
    AbbVie (06/05/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (San Carlos, CA)
    regulatory strategies for projects and issues affecting development of new products or medical devices or new indications for existing products + Provides ... submissions. + May supervise staff + May have responsibility for maintaining a compliant medical device quality system for R&D and informing project teams of… more
    Grifols Shared Services North America, Inc (08/01/25)
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  • Chief Compliance Officer

    Medtronic (Los Angeles, CA)
    medical device , biotech, or pharmaceutical company. + Deep knowledge of medical device regulatory environments (FDA, EU MDR, etc.). + Experience with ... the global compliance and privacy functions for Medtronic Diabetes - a $2.8 billion medical device business that has recently announced that it will be spinning… more
    Medtronic (07/30/25)
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  • Principal Systems Engineer

    Abbott (Pleasanton, CA)
    …integrate information from varied disciplines including Clinical Medicine, Engineering, Marketing and Regulatory Affairs required. + Medical device industry ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
    Abbott (07/18/25)
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  • Senior Quality Systems Specialist

    Danaher Corporation (Sunnyvale, CA)
    …Union In Vitro Diagnostic Regulation (IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) ... Certification + ISO 9001:2015 process and assessment certification activities + Regulatory Intelligence program + Technical Writing Cepheid, a Danaher operating… more
    Danaher Corporation (05/17/25)
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  • Regulatory Affairs Process Specialist

    Kelly Services (Sunnyvale, CA)
    Kelly(R) Science & Clinical is seeking a Regulatory Affairs Process Specialist for a 6-month contract opportunity with a leading molecular diagnostics company based ... in the biotechnology realm. **Workplace:** Remote US **Position Title:** Regulatory Affairs Process Specialist **Position Type:** 6-month contract **Pay rate:**… more
    Kelly Services (07/24/25)
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  • Senior Technical Writer

    Actalent (Santa Clara, CA)
    …oversight on proper documentation for regulatory submissions. Essential Skills + Medical device experience and understanding of an ISO13485 environment. + ... clear documentation for internal and external use in a medical device environment. Responsibilities + Distill technical...Proficiency in technical writing, specifically within medical devices . + Experience with DHF, firmware,… more
    Actalent (07/24/25)
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