• Principal Software and Security Compliance

    Medtronic (Minneapolis, MN)
    …embedded security of regulated or safety critical devices. + Experience in Quality / Compliance and/or Audit with medical device requirements (eg, MDSAP, ... Compliance Audit Specialist focus will be primarily medical device software, product security, and risk...Bachelor's degree with 7+ years of work experience in Quality or regulated industry OR Advanced degree with 5+… more
    Medtronic (07/29/25)
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  • Senior R&D Engineer

    Abbott (Plymouth, MN)
    …activities + Writes and submits intellectual property. + Ensure quality system compliance for medical device development. + Champions design for ... Mechanical / Chemical / Biomedical Engineering + Required minimum years of work experience in medical device R&D - 5+ years with BS, 3+ years with MS or 1+ year… more
    Abbott (07/22/25)
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  • Engineer - Medical Device Electrical…

    Intertek (Fridley, MN)
    Engineer - Medical Device Electrical Safety, Fridley, MN Interested in future career opportunities in the product testing industry? Intertek, a leading provider ... and Certification) Services, is looking for an Engineer - Medical Device Electrical Safety to join our...and efficiently help clients meet safety, performance, environmental and quality requirements for every market. Spanning a wide range… more
    Intertek (08/08/25)
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  • Software Quality Engineer (Cloud And Med…

    Actalent (Golden Valley, MN)
    …best practices. + experience with Cloud tools (azure, aws) + Conduct detailed quality reviews of documents for clarity and compliance . + Ensure documents ... Job Title: Software Quality Engineer Job Description We are seeking a...to submission. The role requires ensuring clarity of content, compliance with procedures, and providing objective evidence with a… more
    Actalent (08/08/25)
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  • Regulatory Operations Compliance Manager…

    Abbott (Maple Grove, MN)
    …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...to manage implementation projects for emerging regulations and lead/drive quality compliance metrics for the Regulatory shared… more
    Abbott (06/19/25)
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  • Quality Sys Compliance Specialist II

    Patterson Companies, Inc. (St. Paul, MN)
    …work experience + 2-4 years' experience with quality management systems and regulatory compliance in the medical device or related regulated field + ... responsible for maintaining and managing the daily operations of the Patterson Quality Management System. Manages compliance activities with responsibility for… more
    Patterson Companies, Inc. (08/08/25)
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  • Senior Regulatory Quality Specialist…

    Abbott (Maple Grove, MN)
    …Registration support + Ad and Promotional Material - Regulatory Review + EU and US medical device compliance + Project management skills - organize and host ... for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more… more
    Abbott (06/19/25)
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  • Senior Product Compliance Analyst

    Xylem (Chaska, MN)
    …and approval of risk activities as well as other deliverables as related to medical device projects * Review and approve all Labeling (product, advertising and ... Product Compliance Analyst** is focused on product compliance to regulatory requirements for medical devices...field, or equivalent work experience * 5+ years of Medical Device Regulatory Affairs experience, domestic and… more
    Xylem (07/09/25)
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  • Senior Quality Systems Engineer

    3M (Maplewood, MN)
    …Here, you will make an impact by: + Leading the development and implementation of global Medical Device Quality Processes for 3M + Leading Global Quality ... military environment + Two (2) years of experience in Quality System in Medical Device ...Quality Management systems ( ie Enovia PLM, Trackwise, Compliance Quest) + Working knowledge of root cause analysis… more
    3M (07/12/25)
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  • Principal Quality Engineer

    Medtronic (Minneapolis, MN)
    …of work experience in Engineering and/or Quality **Nice to Have** + Medical device , pharma, or drug- device combination products preferred. + Experience ... following and other duties may be assigned. + Develop, characterize, and validate medical device manufacturing processes. + Provide guidance and knowledge on… more
    Medtronic (08/08/25)
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