• 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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  • 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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  • 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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  • Regulatory Affairs Business Specialist

    Philips (Plymouth, MN)
    …**You're the right fit if:** + Experience in regulatory affairs, quality compliance , product development or equivalent in the medical device industry ... Devices business by coordinating regulatory activities and ensuring products meet relevant medical device standards and requirements. **Your role:** + Assists in… more
    Philips (08/01/25)
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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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  • Development Quality Engineer I

    Abbott (St. Paul, MN)
    …and demonstrated use of Quality tools/methodologies, statistical/data analysis + Prior medical device experience preferred + Working knowledge of FDA 21 CFR ... location in St. Paul, MN in the Structural Heart Medical Device division. Our business purpose is...new or modified products conform to requirements and establish compliance with the quality system. This position… more
    Abbott (08/01/25)
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  • Senior Program Manager-Design Quality

    Philips (Plymouth, MN)
    …and execution to drive continuous quality improvements in the design of Medical Device products and systems to world-class levels, in close, cross-functional ... -in-design tools, technologies, processes and techniques, with a specific focus on medical device -product/systems design to arrive at first time right, safe,… more
    Philips (07/01/25)
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  • Senior Quality Engineer (Onsite)

    Olympus Corporation of the Americas (Brooklyn Park, MN)
    …and sub-assemblies to ensure compliance with company policies and procedures and medical device regulations. The Product Quality Engineer will partner ... years of experience in Quality Engineering within an FDA regulated medical device manufacturing environment. + Strong working knowledge of technical problem… more
    Olympus Corporation of the Americas (07/24/25)
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