- Abbott (Plymouth, MN)
- …and water optimization (eg ASHRAE BEAP, AEE, CEM, LEED, etc.) desirable. + Medical device manufacturing experience preferred. Clean room experience a plus. + ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Abbott (Plymouth, MN)
- …+ Knowledge of FDA, GMP, ISO 13485, and ISO 14971 + Prior medical device experience Apply Now (https://www.jobs.abbott/us/en) **Learn more about our health ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Actalent (Brooklyn Park, MN)
- …+ Expertise in NCMR's and CAPA's investigation. + Working knowledge of medical device regulations (FDA 21CFR820, ISO). + Experience in process ... or associated fields. + 5+ years' experience in the medical device industry. + Working knowledge of...industry. + Working knowledge of new product design and development in medical devices. + Application of… more
- Actalent (Mounds View, MN)
- …Skills + Bachelor's degree in Electrical Engineering. + 1+ years of experience in medical device product development or equivalent. + Proven hands-on ... Job Title: Electrical EngineerJob Description We are seeking a skilled Electrical Engineer to join our team. This role involves working on electronic and mechanical… more
- Philips (Plymouth, MN)
- …with full working knowledge of 21 CFR 820, ISO 13485 and ISO14971 medical device /safety requirements. Strong knowledge/experience with CAPAs, NCRs and product ... We're looking for a highly qualified Senior Design Assurance Engineer (sustaining) to join our San Diego team. **Your role:** + Provide quality engineering support… more
- Philips (Plymouth, MN)
- **Sr. Design Quality Engineer ** **In this role you** Serve as a...**You're the right fit if:** + Good understanding of Medical Device QSR, ISO 13485 and ISO ... member completing relevant Design Assurance activities on new product development projects that help ensure our overall project and...HHAs, etc. Familiarity with ISO 14971, Risk Management for medical devices. + Knowledge of how to apply Design… 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 ... Synapse product implementation, fromsolution validation phases through product go-live. The Project Engineer (PE) must have wellrounded knowledge in all areas of … more
- Abbott (Plymouth, MN)
- …machine and process set-ups preferred. + Manufacturing engineering experience required. Previous medical device experience preferred. + Experience working in a ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Spectrum Plastics Master (Minneapolis, MN)
- …Bachelor's degree (BS) in Engineering with 1-5 years injection molding experience. + Medical device industry and validation experience is preferred. + Strong ... JOB PURPOSE: The Project Engineer position is responsible for two main functions....the sales close to transfer to production. Support business development and the commercial team with technical expertise in… more
- Danaher Corporation (Chaska, MN)
- …lines originally designed and manufactured in other locations + Working within the medical device or other regulated industry (particularly supporting testers & ... tools that address the world's biggest health challenges. The Sr. Test Engineer for Beckman Coulter is responsible for developing, implementing, and maintaining a… more