• Sr. Regulatory Affairs Specialist - ACM

    Medtronic (Lafayette, CO)
    …This position is most suited for individuals with a broad background covering the total regulatory life cycle of medical devices and strong working knowledge ... and experience with reviewing advertising and promotional materials for medical devices . The initial project scope for this employee will be related to … more
    Medtronic (07/01/25)
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  • Sr. Lead Specialist, Regulatory Affairs

    GE HealthCare (Madison, WI)
    …by the Regulatory Affairs Professionals Society (RAPS). + Experience in medical device regulatory affairs + Demonstrated life-long learner; eagerness ... **Job Description Summary** A trusted regulatory subject matter expert to provide guidance to...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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  • Director, Cybersecurity Regulatory Affairs

    IQVIA (Washington, DC)
    …guidelines, and apply these to services provided. * Stay current on US medical device regulatory requirements. Qualifications: * Bachelor's degree required; ... marketing applications. * Conduct risk management and vulnerability analyses on medical devices and support manufacturer's cybersecurity strategy development,… more
    IQVIA (07/10/25)
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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 ... leader dedicated to helping people see brilliantly. The largest device company in the world - with complementary businesses...compliance and lifecycle change management for medical devices . + Works closely with site regulatory more
    Astrix Technology (06/02/25)
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  • Director, US Regulatory Affairs…

    Sanofi Group (Cambridge, MA)
    …responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge,...+ Dealt effectively with cross-functional groups, which may include Medical , Legal, Marketing, etc. + Experience managing others is… more
    Sanofi Group (05/22/25)
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  • Regulatory Affairs Specialist - Post Market

    Canon USA & Affiliates (Lansing, MI)
    …Good PC skills, including MS Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device industry required + Minimum ... ** Regulatory Affairs Specialist - Post Market - req1434**...$72,000 to max $116,100 (annual equivalency) **_About us!_** _Canon Medical Systems USA, Inc., a world leader in diagnostic… more
    Canon USA & Affiliates (06/07/25)
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  • Regulatory Affairs Training Specialist

    Insight Global (Cincinnati, OH)
    …Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ . Skills and Requirements 3+ years of regulatory experience within the medical device or ... Job Description An employer is seeking a Regulatory Affairs Training Specialist for a long-term contract...the family of MS Products. Prior experience withing the regulatory space is required as is strong attention to… more
    Insight Global (07/18/25)
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  • Associate Director, Medical Events Group

    Abbott (Alameda, CA)
    …+ Minimum of 5 years of experience in Quality Systems, Quality Assurance and/or Regulatory Affairs + Medical device industry or other regulated environment ... of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines....products. Manage staff whose team is responsible for filing Medical Device Reports to the FDA (US),… more
    Abbott (05/23/25)
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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 ... to internal regulatory processes and procedures for medical devices and combination products. + Engage...regulatory experience. At least 5 years of relevant medical device and/or combination product regulatory more
    Sanofi Group (07/15/25)
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  • Systems Engineer - Medical Device

    Lilly (Indianapolis, IN)
    …+ Experience in Systems Engineering in a regulated industry, or experience working on medical devices + 2+ years of work experience, relevant internships will be ... technical disciplines (Software, Electrical, Mechanical, Materials, etc.) as well as Medical , Marketing, Regulatory , Quality, Manufacturing, and Global Patient… more
    Lilly (07/10/25)
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