• Medical Devices Regulatory

    Meta (Burlingame, CA)
    …combination of AI with great form factors can do. We are seeking an experienced medical devices regulatory affairs professional to help us execute ... device products with distribution into many worldwide markets. **Required Skills:** Medical Devices Regulatory Affairs Strategy Specialist Responsibilities:… more
    Meta (07/10/25)
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  • Director of Regulatory & Medical

    System One (Malvern, PA)
    Job Title: Director of Regulatory and Medical Affairs Location: Malvern, PA Type: Direct Hire Essential Duties/Responsibilities: + Manage Regulatory and ... in life sciences related field. + RAC certification. + 15+ years Regulatory Affairs in medical device field with management responsibilities. + Strong… more
    System One (05/16/25)
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  • Medical Director, Global Medical

    Otsuka America Pharmaceutical Inc. (San Juan, PR)
    …in translational medicine (T0 - T1) or early development (phase 1) assets either within Medical Affairs , Regulatory Affairs , or Clinical Development is ... Medical Director of CNS Early Assets, Global Medical Affairs , responsible for certain assets within...evidence, US and global commercial teams, market access, and regulatory affairs , to ensure integrated global strategies… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Senior Specialist, Regulatory

    West Pharmaceutical Services (Exton, PA)
    Senior Specialist, Regulatory Affairs - Medical Device Requisition ID: 69746 Date: Jul 10, 2025 Location: Exton, Pennsylvania, US Department: Regulatory ... planet through our sustainability efforts. **Job Summary** The Sr. Specialist, Regulatory Affairs , Medical is responsible for influencing department … more
    West Pharmaceutical Services (05/14/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Irvine, CA)
    …experience + Or advanced degree with a minimum of 2 years of experience in medical device regulatory affairs **This is not a remote position** **Nice ... To Have** + 4 years of experience in medical device regulatory affairs + Excellent technical knowledge of medical products and understanding of relevant… more
    Medtronic (06/10/25)
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  • Sr. Lead Specialist, Regulatory

    GE HealthCare (Madison, WI)
    Regulatory Affairs Certification (RAC) issued by the Regulatory Affairs Professionals Society (RAPS). + Experience in medical device regulatory ... pulse oximetry. You will work within a team of Regulatory Affairs professionals to ensure GE HealthCare...labeling compliance, etc. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is… more
    GE HealthCare (07/10/25)
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  • Principal Regulatory Affairs

    Abbott (Plymouth, MN)
    …+ Minimum of 5 years' experience working with Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) is a plus. + ... get on with their lives. **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist** to join Abbott's Electrophysiology Division on-site in… more
    Abbott (05/22/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Boston, MA)
    …+ Bachelors in related field, preferred + 2+ years' experience in Medical Device Regulatory Affairs /Quality experience preferred + Certification ... **_What Regulatory Affairs contributes to Cardinal Health_**... and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory more
    Cardinal Health (07/09/25)
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  • Senior Regulatory Affairs

    Stryker (Weston, FL)
    …years of experience in an FDA regulated industry + 2+ years of experience in medical device regulatory affairs + Thorough understanding of FDA, Europe, and ... Weston, FL. **What you will do** As the **Senior Regulatory Affairs Specialist** , you will support...certification or Advanced Degree (Masters in Regulatory Affairs ) + Previous experience with Class II/III medical more
    Stryker (06/01/25)
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  • Regulatory Affairs Specialist

    Astrix Technology (Fort Worth, TX)
    …EC Certificates (MDD /MDR) and associated documentation. **Key Requirements:** + 4+ years in medical device regulatory affairs + Experience with European MDR ... ** Regulatory Affairs Specialist** Clinical Fort Worth,...Supporting EU MDR compliance and lifecycle change management for medical devices. + Works closely with site regulatory more
    Astrix Technology (06/02/25)
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