• Quality Technician II

    Abbott (Minnetonka, MN)
    …skills, as well as attention to detail **Preferred** + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (08/08/25)
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  • Global Supplier Quality Engineer - Systems…

    Danaher Corporation (Chaska, MN)
    …need It would be a plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Familiarity with ISO13485, 21 ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Systems and Innovation for Beckman Coulter… more
    Danaher Corporation (08/19/25)
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  • Global Supplier Quality Engineer…

    Danaher Corporation (Chaska, MN)
    …needs It would be a plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Certifications such as CQE, ... System (http://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Global Supplier Quality Engineer - Electronics for Beckman Coulter Diagnostics will… more
    Danaher Corporation (08/19/25)
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  • Product Performance Sr. Analyst

    Abbott (Plymouth, MN)
    …types of product complaints + Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (08/22/25)
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  • Manufacturing Quality Technician

    ManpowerGroup (St. Michael, MN)
    Manpower Engineering is partnering with a leader in the Medical Device industry for a Manufacturing Quality Technician. **Job Title: Manufacturing Quality ... to and providing guidance regarding interpreting ISO 13485 & FDA standards in link with the Manufacturing Quality...in 2D and 3D CAD (Solidworks) **Benefits:** * Comprehensive Medical , Dental, and Vision plans. * PTO/Vacation * Dedicated… more
    ManpowerGroup (06/14/25)
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  • Global Supplier Quality Engineer - Plastics

    Danaher Corporation (Chaska, MN)
    …needs. It would be a plus if you also possess : + Experience in FDA -regulated or medical device manufacturing environments. + Certifications such as CQE, ... diagnostic tools that address the world's biggest health challenges. The Global Supplier Quality Engineer - Plastics for Beckman Coulter Diagnostics will serve as a… more
    Danaher Corporation (07/02/25)
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  • Principal Regulatory Affairs Specialist

    Philips (Plymouth, MN)
    …+ You have a minimum of 8+ years' Regulatory Affairs experience within FDA regulated Medical Device /HealthTech product environments. Experience with Software ... as Medical Device (SaMD) and Ultrasound Imaging Devices highly desired. + You have strong knowledge of US FDA , China NMPA, CE Marking, EU MDD/MDR, JPAL,… more
    Philips (07/23/25)
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  • Senior Supplier Quality Engineer

    Philips (Plymouth, MN)
    …discipline preferred + 5+ years of Supplier Quality Engineering experience in a medical device (Class II & III) or similar environment with manufacturing or ... that drive selection of the best suppliers based on all technical, quality and business (including cost) requirements throughout the product lifecycle. **Your… more
    Philips (08/13/25)
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  • Principal Product Security Engineer

    Medtronic (Mounds View, MN)
    …plays a critical role in ensuring the security of Medtronic Surgical Operating Unit medical device solutions. Reporting to the Director of Product Security, this ... impact by exploring a career with the world's leading Medical Device company, striving "to alleviate pain,...ability to implement secure architecture in embedded and connected device ecosystems + Familiarity with FDA and… more
    Medtronic (08/28/25)
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  • Quality Inspector

    Steris Corporation (Cottage Grove, MN)
    …ensure the proper documentation and disposition. They may also review other related Quality documentation such as device history or calibration records. Duties + ... and service solutions around the globe. Position Summary The Quality Inspector is responsible for assisting in administration of...to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other… more
    Steris Corporation (08/17/25)
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