Medical Device Regulatory Affairs Jobs in Minneapolis, MN

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

from: Usajobs.gov - 12 days ago

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

from: Pharmadiversityjobboard.com - 15 days ago

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

from: linkedin.com - 6 days ago

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

from: linkedin.com - 8 days ago

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

from: resume-library.com - 3 days ago

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

from: linkedin.com - 17 days ago

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

from: linkedin.com - 5 days ago

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

from: resume-library.com - 3 days ago

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

from: resume-library.com - 3 days ago

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

from: Boston Scientific - 16 days ago