- Actalent (St. Paul, MN)
- …on sustaining engineering. The team is responsible for managing changes to medical devices after commercialization, ensuring that any changes in raw materials do ... standards. Responsibilities + Manage and sustain engineering changes for commercialized medical devices. + Ensure product integrity amidst changes in raw materials.… more
- Fujifilm (St. Paul, MN)
- …activities. + Keep abreast of new legislation and enforcement matters relevant to the medical device industry as well as industry and compliance best practices. ... Degree. + 2 to 3 years of corporate compliance experience in the medical device and/or pharmaceutical industry and working knowledge of healthcare related… more
- Abbott (Plymouth, MN)
- …of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly ... scientific affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical,… more
- Abbott (Plymouth, MN)
- …changes for compliance with applicable regulations. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Supports all ... ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
- Abbott (St. Paul, MN)
- …in a broader enterprise/cross-division business unit model. + Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
- Medtronic (Minneapolis, MN)
- …profile._ + Bachelor's degree in a technical discipline + Minimum 7 Years of medical device regulatory experience with Bachelor's degree + Or minimum ... or familiarity with software regulations and requirements. The **Principal Regulatory Affairs Specialist ** develops strategies for worldwide...5 Years of medical device regulatory experience with… more
- Abbott (Plymouth, MN)
- …necessary detail. + Maintains ongoing surveillance and analysis of all pertinent medical device regulations to ensure submission requirements worldwide are ... their lives. **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Electrophysiology...device regulations, or with EU and other international medical device regulations and submissions. + Must… more
- Abbott (St. Paul, MN)
- …to various international affiliates. * Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are ... heart disease. The Opportunity - We are seeking a Regulatory Operations Specialist I for our St....of education and work experience + Some experience with medical device industry preferred. + Experience working… more
- Medtronic (Mounds View, MN)
- …2+ years of experience in regulatory affairs **Nice to Have** + 4+ years of medical device regulatory affairs experience + Local to CO and willing to ... Day in the Life** We are seeking a Senior Regulatory Affairs Specialist to join our team...Quality Management Systems (QMS) + Technical Writing + International medical device regulatory submission/approval experience,… more
- Abbott (St. Paul, MN)
- …for the treatment of structural heart disease. The Opportunity We are recruiting for a Regulatory Affairs Specialist I to join our team on-site in St. Paul, MN. ... of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000...As an individual contributor, the function of a Regulatory Affairs Specialist I is to provide… more