Latest Internal Quality Audit Medical Device jobs in California

20 Internal Quality Audit Medical Device Jobs in California

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 Yesterday
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 6 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 2 days ago
Quality Engineer I/II Medical Instrument Development Laboratories, Inc. - San Leandro, CA, United States quality, ensuring compliance with standards, identifying issues, and recommending solutions. Lead and/or support internal and external audits, including supplier audits. Support manufacturing process 15 days ago
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Senior Quality Engineer Sonendo, Inc. - Laguna Hills, CA, United States Management activities, including the execution of supplier qualifications and supplier audits Ensure compliance with design control procedures Maintain compliance with Quality System procedures and company 15 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 14 days ago
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 3 days ago
Senior Quality Assurance Manager ACE Partners - , CA, United States feedback. Manage quality-related documentation and process improvement. Preferred Qualifications: Certification as a Quality Engineer and Auditor. Knowledge of Medical Device Risk management. Strong project 13 days ago
Sr. Quality Systems Specialist Katalyst Healthcares & Life Sciences - Carlsbad, California regulations, agency guidelines and internal policies to assure compliance. Lead process improvement projects and assessment of quality plans. Support Management during external/internal inspections 7 days ago
Quality Assurance Specialist Certified Laboratories, Inc. - Burbank, CA, United States regulated industry, preferably in pharmaceuticals, medical devices, or biotechnology. · Strong understanding of FDA regulations and guidelines, including cGMP, 21 CFR Part 11, and ICH guidelines. · Proven 29 days ago

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