- Abbott (Plymouth, MN)
- …primarily in R&D or clinical engineering. **Preferred Qualifications** + Medical device experience. + Master's Degree in Biomedical, Mechanical , or Systems ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Medtronic (Minneapolis, MN)
- …responsibility for the validation of design verification test methods for complex electro- mechanical medical devices . Medtronic's Coronary and Renal ... Methods for a new Product Development project for complex electro- mechanical medical devices . Candidate should...is essential + Practical knowledge of project management. + Medical Device Industry experience. + Familiarity with… more
- Medtronic (Fridley, MN)
- …organization in the definition, design, development, and testing of complex medical device systems within the Neuromodulation Operating Unit. Neuromodulation ... Change Lives** In this role as a **Principal Systems Engineer ** , you will have responsibility for developing new...system verification and validation strategy and testing. + Previous medical device experience with a history of… more
- Abbott (Plymouth, MN)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... + Writes and submits intellectual property. + Ensure quality system compliance for medical device development. + Champions design for manufacturability as part… 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 ... Engineer Job Description Design and develop new devices or elements of new devices with...Knowledge of project management, documentation, design control methodology, and medical device regulations. + Understanding of clinical… 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 ... 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… 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 **Sr R&D Engineer - Shockwave Medical ** to join our...experience in developing catheters, access delivery systems, and/or implantable devices + Experience in catheter and/or implantable device… 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
- Actalent (Minneapolis, MN)
- R&D Engineer Job Description This position supports the design... devices . The role requires expertise in medical device design, focusing on Class II ... sustaining engineering projects. + Lead new product development initiatives for disposable medical devices . + Ensure compliance with FDA Design Controls and… 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 ... experience. + Minimum of 10 years' experience in engineering preferably in the medical device industry. + 3+ years of experience in leading cross-functional… more