- Medtronic (Fridley, MN)
- …requirements development, traceability, and system-level verification and validation. + Extensive medical device experience from concept through market release, ... bold thinking and collaboration, we bring together the right expertise to engineer groundbreaking therapies and technologies that transform patient care. Join a… more
- Medtronic (Brooklyn Park, MN)
- …with 0 years of experience. **Nice to Have** + Experience in a ** medical device ** manufacturing environment, specifically within **high-volume production** . + ... fast-paced environment. + Experience supporting **perfusion systems** or other **Class II/III medical devices ** . + Green Belt certification; formal **DMAIC** or… more
- Medtronic (Mounds View, MN)
- …+ Experience in Systems Engineering including defining systems architecture within medical device product development + Experience with the application ... growth and cross-functional collaboration as we work together to engineer the extraordinary. As a Senior Systems Engineer...of Design Controls for medical devices + Demonstrated ability to create… more
- Medtronic (Plymouth, MN)
- …Sigma / Lean Certification + Experience work in a highly regulated environment; medical device , pharmaceutical, aerospace, or similar + Working understanding of ... lasting impact. We are looking for a Senior Industrial Engineer to join the Process and Equipment Excellence Team....medical device regulation including ISO-13485, US FDA… more
- Medtronic (Mounds View, MN)
- …deliver meaningful innovations. Cardiac Rhythm Management (CRM) Senior Software Verification Engineer develops the next generation medical technologies that ... compassionate world. **A Day in the Life** Senior Software Verification Engineer Careers That Change Lives Transforming Patient Management with Smart Technology!… more
- Medtronic (Minneapolis, MN)
- …controls. Utilize GMP (Good Manufacturing Practices) for Class II and Class III medical devices to ensure quality products and outcomes. Navigate the ... regulations to include FDA QSR 21 CFR 820, EU Medical Device Directive (EU MDD 93/42 EEC),...product controls; GMP for Class II and Class III medical devices ; FDA QSR 21 CFR 820,… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …expertise in applying FDA design control requirements (21 CFR ) as applied to medical device software and medical device regulation (IEC-62304) ... **Job Description** We're looking for a Principal Software Engineer to join our growing team and lead...developers in the delivery of products, both in an R&D and Commercial setting + Estimate engineering effort, plan… 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 ... on - 9 Sep 2025 **Position Description:** Sr. Quality Engineer for Covidien, LP, (a Medtronic company) located in...of the manufacturing processes for a variety of vascular devices including embolic coils, stents, catheters, balloons, aspiration … more
- Medtronic (Minneapolis, MN)
- …clinical specialist or a sales/service/engineering position in the Cardiac Rhythm or Implantable Medical Device Industry. Must possess a minimum of two (2) years ... opening will close on - 8 Oct 2025 Position Description: Technical Field Engineer II for Medtronic, Inc., Minneapolis, MN. Responsible for regional education and… more
- Medtronic (Mounds View, MN)
- …more connected, compassionate world. **A Day in the Life** Software Cloud Engineer II Careers that Change Lives Transforming Patient Management with Smart ... work. Our Cardiac Rhythm Management (CRM) Software organization develops next-generation medical technologies that alleviate pain, restore health, and extend life… more