Medical Device Regulatory Affairs Jobs in Minnetonka, MN

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 - 11 days ago

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

from: linkedin.com - 16 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 - 10 days ago

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

from: linkedin.com - 8 days ago

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

from: linkedin.com - 24 days ago

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

from: Boston Scientific - 9 days ago

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

from: linkedin.com - 24 days ago

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

from: Boston Scientific - 4 days ago

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

from: Dice.com - 16 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 - 12 days ago