23 Quality Control Medical Devices Jobs in Pleasanton, CA
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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 10 days ago
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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 7 days ago
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Quality Engineer Abbvie - Dublin, CA information about AbbVie, please visit us at Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Key Responsibilities Support the development of medical devices and/or device USD 104,728.00 - 118,500.00 per year 17 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 26 days ago
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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 17 days ago
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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 18 days ago
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Regulatory Affairs Specialist GForce Life Sciences - Santa Clara, CA, United States Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2 Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry 26 days ago
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Senior Quality Assurance Manager Connect Life Science - San Jose, CA, United States leader in the field of Medical Devices, equipped with an engineering background and a proactive approach, to spearhead a team of 5 direct reports through the development phase of a new product, working 28 days ago
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Senior Technical Writer Amick Brown - Santa Clara, CA and technical bulletins) for medical device systems. Complete documentation control steps to release final documentation. This includes Change Orders in the documentation control system. Informs and adheres Depends on Experience 21 days ago
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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 29 days ago
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