- 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...performance, scalability, and security + Independently design, code, and test major features, as well as work jointly with… more
- Medtronic (Minneapolis, MN)
- …maintenance. * Experience creating test plans, verification and validation reports for medical device or non- medical device product releases * ... to the highest quality possible. * Drive continuous product test coverage maturity across the portfolio helping identify and...tools * 5+ years experience testing applications for multiple device form factors and screen resolutions * 5+ years… more
- 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
- Actalent (Maple Grove, MN)
- …engineers to advance R&D department technical ability and core competencies. Essential Skills + Medical device work history with 5+ years of experience. + Strong ... Senior R&D Engineer Job Description Design and develop new devices...Knowledge of project management, documentation, design control methodology, and medical device regulations. + Understanding of clinical… more
- Abbott (Plymouth, MN)
- …+ Writes and submits intellectual property. + Ensure quality system compliance for medical device development. + Champions design for manufacturability as part ... serve people in more than 160 countries. **Senior R&D Engineer - Electrophysiology Plymouth, MN** **Working at Abbott** At...Engineering + Required minimum years of work experience in medical device R&D - 5+ years with… 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...to verify and validate manufacturing equipment and processes. Implement Test Method Validation (TMV) to ensure the reliability of… more
- J&J Family of Companies (New Brighton, MN)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson & Johnson is hiring for a **Principal R&D Engineer (Reducer Catheter) - Shockwave Medical ** to...of 10 years' experience in engineering preferably in the medical device industry. + 3+ years of… 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
- Actalent (Brooklyn Park, MN)
- …action may be taken. Essential Skills + 3+ years of experience in medical device manufacturing, specifically with ISO13485 standards. + Experience in ... Manufacturing Engineer Job Description We are seeking a skilled...support the manufacturing of both commercial and non-commercial finished medical devices. The primary responsibility for this role will… more
- Southern Glazer's Wine and Spirits (Minneapolis, MN)
- …Analysts, Test /QA Engineers, and Product Managers, the Staff Software Engineer is instrumental in driving the achievement of key business objectives. **Duties ... from a wide-ranging menu of our Top Shelf Benefits, including comprehensive medical and prescription drug coverage, dental and vision plans, tax-saving Flexible… more