Latest Quality Control Medical Devices jobs in Rosemount, MN

21 Quality Control Medical Devices Jobs in Rosemount, MN

Director of Quality Assurance and Regulatory Affairs Interrad Medical - Plymouth, MN, United States regulations and standards across the globe Guide the company’s regulatory strategy Manage regulatory audits and inspections from preparation to responses Includes Medical Device Single Audit Program (MDSAP 10 days ago
Senior Design Assurance Engineer Cypress HCM - Minneapolis, MN, United States Experience in investigating and implementing Corrective and Preventive Actions Experience in design controls, and test method and process validation Experience with European Medical Device Regulations, FDA 21 21 days ago
Senior Design Assurance Engineer Tactile Medical - Saint Paul, Minnesota : Education & Experience 5+ years of experience as a Quality Engineer within the medical device industry Bachelor level degree in Engineering (Mechanical, Material Science or Biomedical) or related Science 3 days ago
Quality Engineer III Integer Holdings Corporation - Brooklyn Park, MN, United States of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc. Provides support to other quality engineers. Performs other functions 24 days ago
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Manufacturing Quality Engineer Cypress HCM - Brooklyn Park, MN, United States investigations, MRB, CAPA, ECO implementation and process performance. Support and ensure to Develop process documentation and complete PFMEAs and Quality Control Plans. Define operation specifications related 25 days ago
Labelling Consultant Katalyst Healthcares & Life Sciences - Arden Hills, Minnesota improvement and innovation. Requirements: BS degree minimum. 5+ years of Medical Device industry experience as a Labelling expert Strong hands-on experience developing product labelling and literature. Strong 2 days ago
Principal Design Assurance Engineer Accordance Search Group - Plymouth, MN, United States and ultrasound physics · Experience with verification and validation testing, risk management, design control, and Quality Management Systems · Experience with medical device software development life cycle 28 days ago
Director, Quality Phillips-Medisize - Minneapolis, MN (multiple products/multiple customers) * Knowledge of FDA and international regulations and ISO standards related to medical device design and manufacturing (e.g. MDR, 21 CFR 11, 820, 211 and ISO 13485, 14971 5 days ago
Manufacturing Engineer I Boston Scientific - Arden Hills, MN, US Science Prior experience in regulated industry, preferably medical device manufacturing Experience with manufacturing quality traceability systems & document control Experience with Minitab or other 4 days ago
Design Assurance Engineer III Boston Scientific - Maple Grove, MN, US development, or related medical device / regulated industry experience Preferred Qualifications: ISO 13485, ISO 14971 and FDA Quality System Regulations understanding with a focus on Design Controls and Risk 3 days ago

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