Latest Medical Device Regulatory Affairs jobs in Arden Hills, MN

13 Medical Device Regulatory Affairs Jobs in Arden Hills, MN

Sr. Regulatory Affairs Specialist - Cardiac Diagnostics CDx Boston Scientific - Arden Hills, MN, US or related discipline (R&D, Quality, Clinical, Medical Affairs, Biocompatibility) in medical devices, pharmaceutical, or health care industry Working knowledge of relevant US/EU and/or International regulatory More than 30 days ago
Regulatory Specialist II - Electrophysiology Pulsed Field Ablation 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 More than 30 days ago
Laboratory Technician Collabera - Minneapolis, MN, United States procedures and regulatory requirements. Complete FDA Medical Device Reporting (MDR) submissions and other regulatory reports for competent authorities. Collaborate cross-functionally with other departments 3 days ago
Software Supplier Quality Engineer III 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 More than 30 days ago
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Principal Regulatory Affairs Specialist - Electrophysiology Boston Scientific - Arden Hills, MN, US degree (Masters or PhD) Demonstrated proficiency with relevant US/EU regulatory requirements for medical devices including Quality Systems standards and clinical investigations Able to work independently More than 30 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 9 days ago
Quality Systems Analyst- St. Paul, MN MGC Diagnostics - St Paul, MN, United States , Scientific, or Engineering discipline 5-7 years of experience in Quality Assurance, Regulatory Affairs, or other Quality Systems role, preferably in medical device or other regulated industry. Knowledge of ISO 5 days ago
Senior Clinical Scientist/Project Manager Clinical Evaluation (on-site) Abbott Laboratories - Maple Grove, Minnesota team member will combine understanding of scientific and research methodology, medical device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical 4 days ago
Regulatory Affairs Analyst- St. Paul, MN MGC Diagnostics - St Paul, MN, United States in medical device or other regulated industry. Knowledge of ISO 13485, MDSAP, EU MDR, UK MDR and other global regulatory requirements. Process-oriented problem solver and strong documentation creation 5 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 25 days ago

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