| Job alert | Jobs 31 - 40 of 244 |
Quality Specialist Details STERIS
Steris
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Eden Prairie, MN
... Position Summary At STERIS, the Quality Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory ... - Jun 05
Quality Specialist Details STERIS
Steris
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Eden Prairie, MN
... Position Summary At STERIS, the Quality Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory ... - Jun 05
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. ... - Jun 04
Engineering Project Manager
GForce Life Sciences
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Plymouth, MN, 55447
... (design verification and qualification timing, etc) Knowledge of regulatory requirements for US FDA Knowledge of product desing and medical device manufacturing processes (swiss machine, injection molding, assembly, extrusion, braiding, etc.) - May 31
Account Manager
Harland Medical Systems
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Eden Prairie, MN, 55344
... Personnel engaged in manufacturing shall obtain training required by ISO 13485, FDA 21 CFR part 820, FDA 21 CFR part 210 & 211, and Harland Medical System’s internal procedures, where deemed appropriate per assigned job functions. - May 23
Director of Quality & Regulatory
Lumicity
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Minneapolis, MN
... **Key Responsibilities:** - **Regulatory Compliance:** Oversee all aspects of regulatory compliance for medical device products, ensuring adherence to FDA regulations, ISO standards, and other applicable requirements. - **Quality Management Systems ... - May 25
Regulatory Compliance Specialist
Bell International Laboratories
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Eagan, MN, 55122
... * Coordinate and prepare routine submissions for FDA and other regulatory entities. * Monitor applicable regulatory requirements to assure compliance with domestic and foreign regulatory standards. * Maintain regulatory approvals and associated ... - May 23
IT Director
Electromed Inc.
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New Prague, MN, 56071
... Knowledge and experience with ISO & FDA Quality System requirements. Experience with QAD, Brightree, Microsoft Dynamics CRM, PowerBI, and/or Snowflake preferred. Be You. Our people celebrate diverse individuals, backgrounds, and thinking. As an ... - Jun 04
Medical Device - Senior Regulatory Affairs Associate
Elucent Medical, Inc.
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Eden Prairie, MN, 55344
... Experience preparing & defending regulatory submissions to the FDA (510(k) Knowledge of global regulatory requirements including EU, Canada and Asia. Demonstrated experience of basic engineering principles; electrical, mechanical and software Proven ... - May 30
Whole Foods Inventory Manager
Whole Foods Market
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Shorewood, MN, 55331
... Exposure to FDA approved cleaning chemicals. Exposure to temperatures: <32 degrees Fahrenheit (freezing), 32-40 degrees Fahrenheit (refrigerators), >90 degrees Fahrenheit. Ability to work in wet and dry conditions. Ability to work a flexible ... - Jun 04