Latest Medical Device Regulatory Affairs jobs in Saint Paul, MN

13 Medical Device Regulatory Affairs Jobs in Saint Paul, MN

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 24 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 24 days ago
Global Medical Director - AFS & CRMDx Boston Scientific - Arden Hills, MN, US trial safety and medical monitoring, post-market surveillance activities, assessment of device performance signals, and provision of general medical subject matter expertise. Supported teams include 4 days ago
Medical Device - 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 11 days ago
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Director of Quality & Regulatory Lumicity - Minneapolis, MN, United States **Director of Quality and Regulatory Affairs (Medical Devices)** **Position Overview:** As the Director of Quality and Regulatory Affairs in the medical device industry, you will be responsible 16 days ago
Senior Regulatory Affairs Specialist - Cardiac Surgery (hybrid) Medtronic - Mounds View, MN profile. Bachelor's degree required Minimum of 4 years of experience in regulatory affairs in the medical device industry Or advanced degree with a minimum of 2 years of experience in regulatory affairs 16 days ago
Director of Clinical ACE Partners - Minneapolis, MN, United States Director of Clinical Research Minnesota Medical Device The Director of Clinical Research is responsible for all clinical aspects through the product life cycle. You will be working closely 8 days ago
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 10 days ago
Regulatory Affairs Specialist II Boston Scientific - Maple Grove, MN, US certification(s) preferred · Minimum of 3 years related experience, medical industry experience preferred; some regulatory affairs experience required Preferred qualifications: · Thorough understanding of FDA 9 days ago
Principal Regulatory Affairs Specialist - Cardiac Surgery (Hybrid) Medtronic - Mounds View, MN are evident in your applicant profile. Bachelor's degree required Minimum of 7 years of experience in regulatory affairs in the medical device industry Or minimum 5 years of medical device regulatory experience 19 days ago

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