Medical Device Regulatory Affairs Jobs in Mounds View, MN

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 - 21 days ago

Talent Software Services, Inc. - Fridley, Minnesota

of product compliance to sterilization, and microbiology requirements. Supports Regulatory Affairs and other departments by providing technical input on sterilization, and microbiology related content

from: resume-library.com - 7 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 - 7 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 - 5 days ago

Abbott Laboratories - Plymouth, Minnesota

; product-development/support; scientific affairs function. Preferred Qualifications 4+ years of related regulatory submission experience from medical device, pharmaceutical, or healthcare industry Advanced

from: resume-library.com - 5 days ago

Boston Scientific - Arden Hills, MN, US

in regulatory affairs or a combination of 3 years experience from a related field (R&D, Quality, Clinical, Medical Affairs, Biocompatibility) in the medical device industry Working knowledge of relevant US, EU

from: Boston Scientific - More than 30 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 - 23 days ago

Boston Scientific - Arden Hills, MN, US

and risk management, clinical trial safety and medical monitoring, post-market surveillance activities, assessment of device performance signals, and provision of general medical subject matter expertise

from: Boston Scientific - More than 30 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 - 6 days ago

Boston Scientific - Arden Hills, MN, US

their software development practices. Provide guidance on best practices, quality methodologies, and regulatory requirements. Facilitate training sessions for suppliers to enhance their understanding of medical

from: Boston Scientific - More than 30 days ago