• Program Manager - EU…

    Medtronic (North Haven, CT)
    …Surgical product portfolio achieves initial European Union Medical Device Regulation ( EU MDR ) and UK Conformity Assessed (UKCA). This Program Manager ... of interdependent information to create recommendations for action and program success. + Cultivate a broad understanding of Medtronic's...+ PMP or PgMP certification + Strong knowledge of EU MDR and UKCA regulations + Experience… more
    Medtronic (07/24/25)
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  • Quality Engineering Manager , Post-Market…

    Medtronic (North Haven, CT)
    …and writing for compliance. * Knowledge and expertise in FDA 21 CFR 820 & 806, EU MDR (Regulation ( EU ) 2017/745), ISO 14971, ISO 24971, IEC 60812, and ... world. A Day in the Life of a Post-Market Risk, Quality Engineering Manager - reporting to Director of Post-Market Risk, Surgical Operating Unit. Responsibilities… more
    Medtronic (07/02/25)
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  • Sr Quality Engineering Manager…

    Medtronic (North Haven, CT)
    …and writing for compliance. * Knowledge and expertise in FDA 21 CFR 820 & 806, EU MDR (Regulation ( EU ) 2017/745), ISO 14971, ISO 24971, IEC 60812, and ... one (department, function, geography typically comprised of other People or Program managers and / or supervisors and experienced professionals. Recommends… more
    Medtronic (07/29/25)
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  • Principal Quality Engineer - Post-Market Risk

    Medtronic (North Haven, CT)
    …and writing for compliance. * Knowledge and expertise in FDA 21 CFR 820 & 806, EU MDR (Regulation ( EU ) 2017/745), ISO 14971, ISO 24971, IEC 60812, and ... latitude in determining deliverables of assignments, with limited oversight from manager . Coaches, reviews and delegates work to lower level specialists.… more
    Medtronic (07/24/25)
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