- Philips (Plymouth, MN)
- …if:** + You have a minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of ... The Staff Design Assurance Engineer will play a critical role in support...to Design/Process Controls. + You have strong understanding of Medical Device QSR regulations/standards including ISO 13485,… more
- Medtronic (Mounds View, MN)
- …minimum of 2 years of relevant experience **Preferred Qualifications** + Knowledge of Medical device software development, IEC-62304 and FDA guidance in a ... of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. Medtronic is seeking a motivated and detail-oriented Sr.… more
- Medtronic (Minneapolis, MN)
- …of various government and industry regulations to include FDA QSR 21 CFR 820, EU Medical Device Directive (EU MDD 93/42 EEC), ISO 13485, ISO 9001, and ISO ... close on - 20 Oct 2025 Position Description: Sr. Supplier Quality Engineer for Medtronic, Inc. located in Minneapolis, MN. Responsible for communicating technical… more
- Medtronic (Mounds View, MN)
- …of 5 years of relevant experience **Preferred Qualifications** + Extensive experience in medical device or highly regulated industries. + Expertise in advanced ... culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. As a Principal Electrical Engineer , you will… more
- Medtronic (Plymouth, MN)
- …Good Manufacturing Practices (GMP) standards and navigate the complexity of government and medical device industry regulations including FDA 21 CFR Part 820, ISO ... opening will close on - 9 Sep 2025 **Position Description:** Sr. Quality Engineer for Covidien, LP, (a Medtronic company) located in Plymouth, MN. Responsible for… more
- Medtronic (Fridley, MN)
- …with a minimum of 5 years of relevant experience. **Nice to Have:** Medical device experience **Physical Job Requirements** The above statements are intended ... professional growth and cross-functional collaboration as we work together to engineer the extraordinary. Responsibilities may include the following and other duties… more
- Philips (Plymouth, MN)
- …requirements to devise and deliver optimal design solutions for sophisticated medical device components, showcasing advanced technical expertise, working under ... requirements to devise and deliver optimal design solutions for sophisticated medical device components, demonstrating advanced technical expertise and strategic… more
- NTT America, Inc. (St. Paul, MN)
- …+ Reports to the Director of Americas Region for Global Solutions & Sales Engineering and works closely with NTT Data GDC Sales Representatives ... in a timely manner. + Drives innovation within the Global Solutions & Sales Engineering team, staying up-to-date with the latest hyperscale industry trends and… more
- Insight Global (St. Paul, MN)
- …Global is seeking a Senior Electrical Engineer for one of our rapidly growing Medical Device clients in the Minneapolis area. This person will be joining the ... client's R&D organization and will work closely with the sales team as they capture a variety of projects...of projects from their respective partners. The Senior Electrical Engineer will design microchips as a part of the… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... **Position Overview** The Lead Project Engineer (PE) oversees all technical aspects of Synapse...must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical… more