| Job alert | Jobs 1 - 10 of 305 |
Regulatory Affairs Manager
Custom Search, Inc.
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Minnetonka, MN, 55345
... Support inspections by FDA, notified body, and other regulatory agencies. Desired Profile: Bachelor’s Degree with at least 5-8 years of related Regulatory experience, mostly in medical devices. 1+ years’ experience in a Regulatory Affairs management ... - Apr 26
Medical Device Sr Manufacturing Engineer
Master compliance
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Plymouth, MN, 55441
... Work experience with the following: FDA Quality System Regulations, current Good Manufacturing Practices (cGMP), ISO 13485, ISO 9001 standards or equivalent. - Apr 26
Research & Development Engineer
VitalPath
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Crystal, MN, 55428
... Working directly with the customer and cross-functional team to develop a catheter design that meets customer’s expectations of budget, schedule, design functionality while ensuring full compliance to FDA QSR (21 CFR 820), and applicable ISO 13485 ... - May 01
Quality Assurance Manager
Bell International Laboratories
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Minneapolis, MN
... Utilize expertise in regulatory compliance to successfully register products, ensuring compliance with FTC/FDA rules and regulations. Collaborate with cross-functional teams to address quality issues, implement corrective actions, and ensure that ... - May 03
Quality Systems Engineer - Training
Inspire Medical Systems I
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Saint Louis Park, MN, 55416
... We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Our focus on patient outcomes is at the core of everything we do, and ... - May 01
Clinical Data Specialist
Inspire Medical Systems I
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Saint Louis Park, MN, 55416
... We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Our focus on patient outcomes is at the core of everything we do, and ... - Apr 23
Assembler
CathX
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Fort Snelling, MN, 55111
... This role complies to FDA QSR (21 CFR 820), ISO 13485 requirements and adheres to the Quality Management System (QMS). ESSENTIAL FUNCTIONS: Reads work orders, follows production drawings and sample assemblies, or receives verbal instructions ... - Apr 12
Sr. Quality Systems Specialist
Redbock - an NES Fircroft company
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Mounds View, MN
... Duties: Provide continuous and rigorous assessment of quality system to assure compliance with Medtronic internal policies in general and specific to quality system processes, FDA part 820.30 regulations (Design Controls, specifically Design Changes ... - May 02
RN - Medical Policy/Utilization Management
Javen Technologies
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Eagan, MN, 55122
... Research issues on an ad hoc basis to determine coverage status of other health plans, FDA approval status; this may also require limited research of evidence-based literature. Lead work groups as needed. Lead projects that support Medical Policy ... - Apr 20
Sanitation Technician
Rise Baking Company
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Minneapolis, MN, 55406
... is responsible for supporting the Company’s sanitation food safety program by focusing on proper cleaning and sanitizing of plant equipment and building in a manner that meets and complies with all food safety policies, FDA and OSHA regulations. ... - May 02