- 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 ... Technologists, Sonographers, and other Key Operators in the use of Fujifilm's Medical Informatics. The resource will assist with the development of international… 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 ... personnel. **Requirements** + High School diploma or GED or 0-2 years' in a medical device environment or equivalent experience in a similar work environment. +… more
- Medtronic (Minneapolis, MN)
- … principles is essential + Practical knowledge of project management. + Medical Device Industry experience. + Familiarity with these regulations: FDA ... of the Design Assurance team. Our purpose is to increase product development process rigor to ensure robust understanding of designs, documentation of compliance to… more
- Medtronic (Plymouth, MN)
- …Sigma / Lean Certification + Experience work in a highly regulated environment; medical device , pharmaceutical, aerospace, or similar + Working understanding of ... looking for a Senior Industrial Engineer to join the Process and Equipment Excellence Team. As a part of...medical device regulation including ISO-13485, US FDA… more
- Abbott (Plymouth, MN)
- …to travel approximately 15%, including internationally. **Preferred Qualifications** + Medical device experience is required Apply Now ... + Minimum 5 years manufacturing engineering experience. Prior manufacturing engineering or process development experience is required. + Strong analytical,… more
- Foth (Minneapolis, MN)
- **Foth** is a 100% member-owned science and engineering consulting firm headquartered in Wisconsin, with over 85 years of success. Our 700 members across 29 ... locations are dedicated to **solving our clients' toughest science and engineering challenges** . Consistently ranked by Engineering News Record in the top 150… more
- Abbott (Minneapolis, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...study execution. + Facilitate all aspects of the start-up process and site initiation visits + Understand regulatory and… more
- Philips (Plymouth, MN)
- … Engineering , or related technical discipline preferred + 5+ years of Supplier Quality Engineering experience in a medical device (Class II & III) or ... Supplier Quality Performance Monitoring. + Providing Quality oversight of product/ process change requests from suppliers, ensuring appropriate regulatory review and… more
- Abbott (Plymouth, MN)
- …in a regulated environment and clean room experience a plus. Hands-on 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 (St. Paul, MN)
- …of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971 + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more about our ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more