- TE Connectivity (Plymouth, MN)
- …Molding, Tool and Model Shop, Quality Engineering , Purchasing, and Sales Engineering , to launch medical products. + Properly document and internally ... + 2 or more years of related electro-mechanical product design and development engineering experience with a BS degree + Medical product development experience… 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 ... ensure thorough identification and evaluation of manufacturing risks. Coordinate Process Verification and Validation activities by conducting Installation Qualification… more
- Abbott (Minnetonka, MN)
- …reporting gaps in manufacturing personnel training and knowledge Make sure all medical device operators are certified prior to performing manufacturing processes ... a high degree of independent action and initiative Assist with interviewing of medical device candidates **Education** High School Diploma / GED an equivalent… more
- Insight Global (Arden Hills, MN)
- … or biomedical -5+ years of experience with design assurance, sustaining or R&D engineering - Medical Device Background - IEC 60601 experience -Experience ... post market quality CAPA's (corrective and preventative action) -Experience in design engineering , process development and continuation engineering null We… more
- Abbott (Plymouth, MN)
- …+ Knowledge of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971 + Prior medical device experience preferred. **What We Offer** At Abbott, you can have a ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Medtronic (Minneapolis, MN)
- …+ Knowledge and apply this knowledge to post market surveillance of products. + Medical device experience; or experience in a regulated environment + Experience ... to regulations and expectations of Regulatory Bodies. This is a scientific ( engineering , technical, medical ) writing position. This individual will partner with… more
- Medtronic (Fridley, MN)
- …+ 10 years of experience in a highly regulated environment, preferably within the medical device industry is desired. + 5 years of experience in Instrument ... at both the inception and conclusion of the NPI process , ensuring long-term product viability is considered at every...or Quality. + 5+ years of hands-on experience in medical device product development is desired. +… more
- Delta Air Lines, Inc. (Minneapolis, MN)
- …a broad spectrum of EUC technologies, including desktop virtualization, device management, security, application delivery, and end-user support, ensuring optimal ... intervention. + **Security and Compliance:** Implement and enforce policies for device and data security, ensuring compliance with organizational standards and… more
- Abbott (Minnetonka, MN)
- …follow-up skills, as well as attention to detail **Preferred Qualifications** + Prior medical device experience preferred + Experience working in a broader ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… 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 ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...+ Provides feedback to Customers, Sales, Field Service, Marketing, Engineering , and Product line management on equipment issues and… more