• Senior Regulatory Quality Specialist…

    Abbott (Maple Grove, MN)
    …managing projects related to harmonized regulatory activities in the Abbott's medical device division. As an individual contributor, the function of a ... medical products, nutritionals). 2-3 years of experience in regulatory preferred but may consider quality assurance,...- Regulatory Review + EU and US medical device compliance + Project management skills… more
    Abbott (06/19/25)
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  • Product Stewardship & Regulatory Expert…

    Chemours (St. Paul, MN)
    …Engineering, Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw ... outside lawyers, consultants, industry associations, and local agencies on specific medical regulatory topics. + Coordinate and review customer… more
    Chemours (06/19/25)
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  • Regulatory Operations Compliance Manager…

    Abbott (Maple Grove, MN)
    …managing projects related to harmonized regulatory activities in the Abbott's medical device division. As an individual contributor, the function of a ... (eg, medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support,… more
    Abbott (06/19/25)
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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 ... scientific affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical,… more
    Abbott (05/19/25)
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  • Regulatory Affairs Specialist -Peripheral…

    Medtronic (Minneapolis, MN)
    …applicant profile._ + Bachelor's degree required + Minimum of 2 years of experience in regulatory affairs in the medical device industry + Or advanced degree ... with a minimum of 0 years of experience in regulatory affairs in the medical device... Device Regulation (MDR), and/or other global regulatory requirements and quality standards. + Effective… more
    Medtronic (07/25/25)
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  • Regulatory Affairs Business Specialist

    Philips (Plymouth, MN)
    …business by coordinating regulatory activities and ensuring products meet relevant medical device standards and requirements. **Your role:** + Assists in ... and less complex projects. + Demonstrates basic understanding of Regulatory 's role in the Quality System with...quality compliance, product development or equivalent in the medical device industry strongly preferred. + Your… more
    Philips (08/01/25)
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  • Principal Regulatory Affairs Specialist…

    Medtronic (Minneapolis, MN)
    …profile._ + Bachelor's degree in a technical discipline + Minimum 7 Years of medical device regulatory experience with Bachelor's degree + Or minimum ... 5 Years of medical device regulatory experience with...13485, and other global regulatory requirements and quality standards + History of successful device more
    Medtronic (07/17/25)
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  • Principal Regulatory Affairs Specialist…

    Abbott (Plymouth, MN)
    …submissions. + Must be familiar with relevant regulatory requirements for medical devices including Quality Systems standards and clinical investigations. + ... necessary detail. + Maintains ongoing surveillance and analysis of all pertinent medical device regulations to ensure submission requirements worldwide are… more
    Abbott (05/22/25)
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  • Regulatory Operations Specialist I

    Abbott (St. Paul, MN)
    …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives… more
    Abbott (08/01/25)
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  • Sr. Regulatory Affairs Specialist

    Medtronic (Minneapolis, MN)
    …MDR, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards + Experience with Class III medical devices (PMA) + History ... 5-8 years industry experience + At least 2-3 years regulatory , clinical, quality experience + Advanced degree...and working with cross-functional project teams. + 4+ years medical device industry experience + In depth… more
    Medtronic (07/29/25)
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