27 Quality Control Medical Devices Jobs in Santa Clara, CA
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New Product Development Engineer Kelly - Santa Clara, CA, United States development. Experience in medical device industry or other highly regulated field. Experience with medical electrical-mechanical systems. Knowledge of FDA requirements for design control of medical devices 8 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 30 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 26 days ago
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NPI Sr Test Engineer Johnson & Johnson - Santa Clara, CA with DFM, DFT. Produce high quality documentation that is clearly understandable by internal and external personnel. Preferred: Experience in Medical Device industry, Robotics, Manufacturing. Experience USD 105,000.00 per year 16 days ago
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Regulatory Specialist II The Fountain Group LLC - Santa Clara, California Skills: Knowledge of regulations and standards affecting IVDs and/or biologics/Medical device Education: BS preferred in a technical discipline like biology, chemistry, microbiology, immunology, medical 21 days ago
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Robotics Head of Hardware (Ottava) - Johnson & Johnson MedTech Johnson & Johnson - Santa Clara, CA , and release Interface with Quality and Regulatory teams to support medical device documentation and submissions for approved clinical use Work with Service and Manufacturing teams to develop solutions USD 273,000.00 - 370,000.00 per year 28 days ago
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Staff Software Product Security Engineer Johnson & Johnson - Santa Clara, CA to integrate with mechanical, electrical, and distributed computing systems. Document designs and specifications per design control processes and conform to Industry Standards for Medical Device Software (IEC USD 139,000.00 - 224,000.00 per year 27 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 7 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 5 days ago
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Senior Quality Engineer - Hybrid CyberCoders - Sunnyvale, CA of and experience with eQMS systems, medical device regulations, and 21 CFR 820, ISO 13485, and ISO 14971. Additionally, knowledge of EU MDR, Master Control, Testing, Risk Analysis, Process Validation, CAPA, and NCR 122,000.00 - $160,000.00 8 days ago
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