| Job alert | Jobs 11 - 20 of 387 |
Supplier Quality Engineer
LanceSoft, Inc.
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Minneapolis, MN
... for US FDA • Knowledge of product design and medical device manufacturing processes injection molding, assembly, extrusion, braiding, • Works closely with internal and external project team to execute m to medium complexity project-based tasks. ... - May 31
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
Software Verification Engineer
Blue Star Partners LLC
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Saint Paul, MN
... Role, Responsibilities, and Deliverables: Work independently and as a team member to plan, write, and execute test cases according to company practices, FDA regulatory, and ISO standard procedures. Design new test suites for new features and ... - Jun 08
Machine Operator
Manpower
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Minnetonka, MN, 55305
... • 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 08
Regulatory Specialist
Bell International Laboratories
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Saint Paul, MN, 55130
... 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 files. ... - May 23
Facilities Engineer
The Davis Companies
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Saint Paul, MN, 55130
... Familiarity with regulatory requirements governing pharmaceutical manufacturing facilities, such as FDA regulations (cGMP, GxP), is typically essential. Proficiency in relevant engineering software and tools is preferred. This may include CAD ... - May 21
School Nutrition Business Support Specialist - Management Analyst 2
State of Minnesota
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Minneapolis, MN, 55405
... **Minimum Qualifications** 2 years of experience with data analysis work experience in nutrition, health, foodservice, USDA or FDA Nutrition Programs OR A bachelor's degree and 1 year of experience with data analysis work experience in nutrition, ... - May 31
Senior Manufacturing Quality Engineer
Anteris
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Osseo, MN, 55369
... of complex problems (technically) associated with the manufacturing process Revise / analyze if the current products and processes (including taken actions or decisions) comply with the regulations, such as FDA CFR 820, ISO 13485, 14971, etc. ... - Jun 05
Senior Scientist
Planet Pharma
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Minneapolis, MN
... Preference of someone with experience with implantable devices, class III, others class II Good knowledge of FDA guidances and applications of these standards. Biochemistry background ideal Required Knowledge and Experience: Requires Bachelor’s ... - Jun 02