Latest Medical Device Regulatory Affairs jobs in Minneapolis, MN

14 Medical Device Regulatory Affairs Jobs in Minneapolis, MN

Consumer Safety Officer Food and Drug Administration - Minneapolis, Minnesota (FDA), Office of Regulatory Affairs (ORA), Office of Medical Product and Tobacco Operations (OMPTO), Office of Medical Device and Radiological Health Operations (OMDRHO). The incumbent provides advice 13 days ago
Senior C++ Embedded Software Engineer (Medical Devices) Minneapolis, MN product design and engineering, preclinical and clinical development, data management, market access, regulatory affairs and quality assurance, Veranex enables accelerated speed to market, controlled 16 days ago
Senior Regulatory Affairs Associate Elucent Medical, Inc. - Eden Prairie, MN, United States 5 years of medical device Regulatory Affairs Proven track record with regulatory submissions. Experience preparing & defending regulatory submissions to the FDA (510(k) Knowledge of global regulatory 7 days ago
Senior Regulatory Affairs Specialist Laborie - Plymouth, MN, United States , Engineering, or other relevant discipline and 4+ years’ experience in Regulatory Affairs in the medical device industry. Working knowledge of quality system regulations and guidelines. Great communication 9 days ago
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Regulatory Affairs Specialist III Katalyst Healthcares & Life Sciences - Maple Grove, Minnesota degree or an equivalent combination of education and work experience 3+ years of experience in Regulatory Affairs or related discipline in medical devices (R&D, Quality, Clinical, Biocompatibility 4 days ago
Regulatory Affairs Manager Custom Search, Inc. - Minnetonka, MN, United States Our mid sized medical device client is adding a Manager Regulatory Affairs to the team. The Manager ensures compliance with applicable laws and regulations in the development, manufacturing 18 days ago
Product Development Manager Fasikl - Bloomington, MN, United States requirements and market demands. Responsibilities: · Support the development of new medical devices, from prototype through the design control process, to regulatory approval and commercialization. · Collaborate 6 days ago
Senior Project Manager, Clinical Evaluation Abbott Laboratories - Maple Grove, Minnesota understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU 4 days ago
Regulatory Affairs Manager - Electrophysiology Abbott Laboratories - Plymouth, Minnesota or MBA. A Ph.D. in a technical area or law is helpful. Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) Previous experience with 510k / PMA submissions. Prior 4 days ago
Principal Reg Affairs Specialist - Electrophysiology Boston Scientific - Arden Hills, MN, US regulatory requirements for medical devices including Quality Systems standards and clinical investigations Able to work independently with minimal supervision Solid understanding and knowledge of product 17 days ago

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