Medical Device Regulatory Affairs Jobs in Minneapolis, MN

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Senior C++ Embedded Software Engineer (Medical Devices)  

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

Product Development Manager  

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

Senior Project Manager, Clinical Evaluation  

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

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from: resume-library.com - 5 days ago

Senior Regulatory Affairs Specialist - Electrophysiology  

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

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from: resume-library.com - 5 days ago

Principal Reg Affairs Specialist  

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

Sr Microbiologist-Steriliz  

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

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from: resume-library.com - 7 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

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from: resume-library.com - 23 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

from: Boston Scientific - More than 30 days ago

Packaging Engineer  

Judge Group, Inc. - Maple Grove, MN

, Regulatory Affairs, Quality Assurance, and Operations, to ensure alignment and integration of packaging requirements throughout the product lifecycle. Regulatory Compliance: Stay abreast of regulatory

from: Dice.com - 27 days ago

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Global Medical Director - Atrial Fibrillation Solutions & Cardiac Rhythm Management/Diagnostics  

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


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