Latest Quality Control Medical Devices jobs in Hayward, CA

24 Quality Control Medical Devices Jobs in Hayward, CA

Project Manager Scientific II DivIHN Integration Inc - Hayward, CA, US , EU MDR guidelines, GXP regulations and quality management systems for both medical devices and biologics manufacturing; ISO 13485, 1CFR Parts, 11, 210, 211 and 820 (at minimum). 4. Experience More than 30 days ago
Quality Engineer I/II Medical Instrument Development Laboratories, Inc. - San Leandro, CA, United States device industry, specifically 21 CFR 820, ISO 13485:2016, and EU MDD/MDR. At least 2-5 years of medical device experience, with exposure to Change Control, CAPA, Supplier Controls, NCMRs, and/or Complaint 11 days ago
Director of Manufacturing Engineering The Mullings Group - Menlo Park, CA, United States companies/product lines Demonstrated knowledge of FDA regulations for Class II IVD products and proficiency in ISO 13485 medical devices quality management systems Proven track record of managing cost Yesterday
Quality Manager Jobot - Hayward, CA Assist in training company employees on the principles of Quality and other Quality System elements Support regulatory and agency inspections, audits, investigations, and inquiries regarding the control $100,000 - $125,000/Year 15 days ago
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Operations Manager, Electrical and Capital Equipment Galvanize Therapeutics, Inc. - Redwood City, CA, United States working knowledge of medical device design controls and quality systems Strong CAD skills with experience in device design (SolidWorks preferred) Experience commercializing medical devices and/or medical 20 days ago
Senior Quality Technician Randstad Life Sciences US - Menlo Park, CA, United States in accordance with our medical device and clinical laboratory quality management system requirements. This person works closely with Supply Chain, Manufacturing Science & Technology (MSAT), Quality Control (QC 23 days ago
Project Manager, QARA Thermo Fisher Scientific - Fremont, California, United States of America working in an FDA regulated environment with a solid understanding of design control quality standards and regulatory compliance requirements for medical device or diagnostics (ex. 510K submissions 2 days ago
Staff Instrument Software Engineer Ruby Robotics - San Mateo, CA, United States OpenCV for camera sensing / computer vision applications ● Experience at an early stage medical startup ● Experience developing medical devices within FDA requirements and guidelines including risk 21 days ago
Sr. R&D Engineer Aulea Medical Inc. - Pleasanton, CA, United States and develop product(s) in full compliance with the company’s Design Control requirements and consistent with FDA QS Regulations, ISO 13485, MDD 2007/47/EC, and Canadian Medical Devices Regulations 29 days ago
Medical Device Quality Engineer I Anatomage, Inc. - Santa Clara, California We Look For Experience with Medical Device Software and Hardware Experience with QMS/eQMS Knowledge of ISO 13485 / MDSAP Global regulatory affairs experience (FDA, MDD/CE/MDR, UKCA, etc.) Document Control 12 days ago

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