| Job alert | Jobs 21 - 30 of 230 |
Mammography Technologist - Per Diem - Minnetonka, MN
Onsite Women's Health
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Minnetonka, MN
... Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate! Experience: Mammography: 2 years (Required) License: ... - Jun 05
Machine Operator
Manpower
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Independence, MN, 55599
... • Accurately complete all necessary production packaging paperwork (cleaning log, batch records, verify batch numbers, expiration and material numbers) and calculate amount of product accepted or rejected to comply with FDA regulations and to ensure ... - Jun 03
Machine Operator
Manpower
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Loretto, MN
... • Accurately complete all necessary production packaging paperwork (cleaning log, batch records, verify batch numbers, expiration and material numbers) and calculate amount of product accepted or rejected to comply with FDA regulations and to ensure ... - Jun 01
Maintenance Technician
Aerotek
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Minneapolis, MN
... **Work Environment** The work environment is a laboratory style setting, adhering to stringent FDA regulations. This includes wearing a full smock, hair/beard net, and boot covers. The facility houses a variety of machines that mix different ... - Jun 07
R&D Project Manager
VitalPath
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Crystal, MN, 55428
... This position is responsible for ensuring that all deliverables within the scope of the project are completed in accordance with VitalPath’s Quality Management System (QMS) and are compliant with FDA QSR (21 CFR 820), and applicable ISO 13485 ... - May 24
R&D Engineer II
VitalPath
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Crystal, MN, 55428
... strategy Excellent working knowledge of GD&T and Solidworks Working knowledge of Minitab Experience with design controls, FDA regulation, GMP, GDP, and QMS requirements Must be able to work with a microscope and sit/stand for an extended period of ... - Jun 03
Sr R&D Project Manager
VitalPath
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Crystal, MN, 55428
... This position is responsible for ensuring that all deliverables within the scope of the project are completed in accordance with VitalPath’s Quality Management System (QMS) and are compliant with FDA QSR (21 CFR 820), and applicable ISO 13485 ... - May 22
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
Principal Manufacturing Process Engineer
Schwan's
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Bloomington, MN, 55431
... - Experience with USDA, FDA, OSHA, EPA, requirements for manufacturing processes - Development of statistical models and data analytic tools using MS Excel, VB, SQL, Python are a plus. - Ability to travel 0 to 50% as required (dependent on location) ... - Jun 03