• Senior Manager Quality System Job Details…

    STERIS (Plymouth, MN)
    Senior Manager Quality System Req ID: 46132 Job Category: Quality Plymouth, MN, US, 55447 Description: At STERIS, we help our Customers create a healthier and safer ... solutions around the globe. Position Summary The Senior Quality Manager is responsible for leading quality improvement for complex...9001, ISO 13485, MDSAP and CFR Part 820/211, EU MDR , and other applicable standards. This role leads the… more
    STERIS (09/21/24)
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  • Senior Manager , Toxicology

    Abbott (St. Paul, MN)
    …Regulations (EU MDR ) and ISO 10993 series. This is a manager and senior-level technical contributor responsible for serving as a leader in biocompatibility, ... and maintenance of biocompatibility deliverables to support EU Medical Device Regulations ( MDR ) technical files + Assess biological safety and toxicology on products… more
    Abbott (09/07/24)
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  • Program Manager - Neuro Science

    Medtronic (Minneapolis, MN)
    …connected, compassionate world. **A Day in the Life** Seeking a dynamic Program Manager to drive cross-functional programs as part of the Neuromodulation (NM) and ... Pelvic Health (PH) operations product lifecycle management team. This team manages complex projects and programs in the released product space, including regulatory… more
    Medtronic (09/05/24)
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  • Product Manager , End User Support…

    Ensono (St. Paul, MN)
    Product Manager , End User Support & Security ServicesRemote - United States106 At Ensono, our **Purpose is to be a relentless ally, disrupting the status quo and ... the role and what you'll be doing:** The Product Manager , End User Support & Security Services is responsible...product definition & design in collaboration with Sales, Finance, Operations & other Product leaders. including but not limited… more
    Ensono (09/21/24)
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  • Clinical Research Specialist - Peripheral Vascular

    Medtronic (Plymouth, MN)
    …and prepares status reports. + May be responsible for clinical supply operations , site and vendor selection. + People working within region/country may also ... sites with proven results in study execution + Experience in clinical operations + Experience developing clinical strategies and study design + Experience in… more
    Medtronic (08/28/24)
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  • Senior Principal Regulatory Affairs Specialist…

    Medtronic (Minneapolis, MN)
    …not limited to Regulatory Affairs, Research and Development, Clinical, Quality, Operations , Global Supply Chain and Marketing and externally with regulatory bodies ... business functions. This position reports to the Senior Regulatory Affairs Manager . **Role And** **Responsibilities:** + Develop and support global regulatory… more
    Medtronic (09/17/24)
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