Latest Internal Quality Audit Medical Device jobs in Santa Clara, CA

8 Internal Quality Audit Medical Device Jobs in Santa Clara, CA

Quality Assurance Manager SN&N Electronics, Inc. - Morgan Hill, CA, United States management reviews Responsible for any additional quality activities as assigned by management Qualifications: 5+ years experience in medical device quality 2+ years experience in design assurance 2+ years 5 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 5 days ago
Senior Quality Engineer - Hybrid CyberCoders - Sunnyvale, CA investigations would be a major plus. Key Responsibilities: Develop and implement quality control systems to ensure compliance with applicable product standards Perform internal audits to ensure compliance 122,000.00 - $160,000.00 6 days ago
Lead Analyst GForce Life Sciences - Fremont, CA, United States initiatives. Prepares for and leads internal and external audits, manages recertification projects, and drives compliance efforts in collaboration with stakeholders. Contributes to process improvements 10 days ago
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Senior Quality Assurance Manager Sheathing Technologies, Inc - Morgan Hill, CA, United States you will be responsible for: · Maintaining the company’s Quality Management System (QMS) · Enforce compliance with global regulatory requirements, including 21 CFR Part 820, ISO 13485, ISO 14971, UK Medical Device 7 days ago
Quality Ops Analyst TopTalentFetch - Hayward, CA, US /External Quality Audit activities and other key quality initiatives, as appropriate Administers and maintains Quality System records Minimum Qualifications 1-3 years of experience in medical device Quality 2 days ago
Quality Engineer IV AbbVie - Dublin, California through the implementation of inspection criteria, procedures, and training. Perform duties in compliance with FDA’s Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations Yesterday
Design Quality Engineer II Nevro Corp. - Redwood City, California Design and Configuration management Support risk management processes and initiatives. Support internal and external regulatory audits, and other quality assurance functions. Define or identify potential 19 days ago

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