Latest Quality Control Medical Devices jobs in Morgan Hill, CA

7 Quality Control Medical Devices Jobs in Morgan Hill, CA

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 20 days ago
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 22 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
Staff Quality Engineer (Software) HealthCare Recruiters International - San Jose, CA, United States programs. Minimum of 8 years of Quality Engineering work experience in the medical device field with complex medical devices, i.e. devices that include capital hardware, disposable hardware, and software 23 days ago
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Staff Quality Engineer (EE or ME) HealthCare Recruiters International - San Jose, CA, United States , Mechanical, Industrial, Electrical, Life Sciences, etc. Minimum of 8 years of Engineering work experience in the medical device field with complex medical devices, i.e. devices that include capital hardware 23 days ago
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 15 days ago
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 23 days ago

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