• Medical Device Regulatory

    Oracle (St. Paul, MN)
    …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
    Oracle (12/22/25)
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  • Senior Regulatory Affairs

    Medtronic (Mounds View, MN)
    …profile._ + Bachelor's degree required with a + Minimum of 4 years of experience in medical device regulatory affairs experience + Or Advanced degree ... approval with the agencies. The Sr Regulatory Affairs Specialist is responsible for assessment of device...heart valve products + Experience with Software as a Medical Device + RAC Medical more
    Medtronic (12/12/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (St. Paul, MN)
    …in related field or equivalent work experience, preferred + 2+ years' experience in Medical Device Regulatory Affairs /Quality experience preferred + ... **_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 (12/13/25)
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  • Regulatory Affairs Associate…

    GRAIL (St. Paul, MN)
    …, development, clinical affairs , quality, or program management within the IVD, medical device , or pharmaceutical industries is required. + Regulatory ... FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such...and international regulatory frameworks and processes for medical device development and approvals is required.… more
    GRAIL (12/03/25)
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  • Senior Regulatory Affairs Specialist…

    Abbott (Plymouth, MN)
    …of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly ... affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical, or… more
    Abbott (12/27/25)
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  • Sr Regulatory Affairs Spec…

    Medtronic (Minneapolis, MN)
    …in the medical device industry, particularly with Class III medical devices (PMA). + ** Regulatory Submission Expertise:** Proven experience preparing and ... connected, compassionate world. **A Day in the Life** **SENIOR REGULATORY AFFAIRS SPECIALIST** In collaboration with leading...**To Be Successful in This Role** + ** Medical Device Experience:** Direct experience… more
    Medtronic (12/11/25)
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  • Regulatory Affairs Specialist II…

    Abbott (Plymouth, MN)
    …etc.), math, engineering, or medical fields. + Master's degree in Regulatory Affairs . + Regulatory experience with capital equipment including ... on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced ** Regulatory Affairs Specialist II** to join our team on-site in Plymouth,… more
    Abbott (11/22/25)
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  • Senior Manager, CMC Global Regulatory

    Otsuka America Pharmaceutical Inc. (St. Paul, MN)
    **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global ... relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs , Global Regulatory Strategy, Manufacturing facilities,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Regulatory Affairs Coordinator

    ManpowerGroup (Maplewood, MN)
    …with Microsoft Office tools. + Some regulatory experience with drug and/or medical device products is preferred. + Ability to navigate a matrix environment ... organization in the healthcare industry_ , is seeking a ** Regulatory Affairs Coordinator** to join their team,...Declarations of Conformity. + Assist with state licensing for medical devices and drug products by reviewing requirements and… more
    ManpowerGroup (12/17/25)
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  • Advanced Regulatory Affairs

    Bio-Techne (Minneapolis, MN)
    …disease worldwide.** Pay Range: $62,300.00 - $102,350.00 **POSITION SUMMARY** Responsible for regulatory affairs activities to assist in regulatory ... submission, annual reports, registrations, and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance, and standards.… more
    Bio-Techne (11/21/25)
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