Latest Internal Quality Audit Medical Device jobs

88 Internal Quality Audit Medical Device Jobs

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 Yesterday
Quality Engineer - 226082 Medix™ - Plymouth, MN, United States quality records related to QMS and production activities. Participate in risk management activities and audits, including notified body, FDA, and internal audits. Support management review processes through 3 days ago
Sr. Design Quality Assurance Engineer - Marlborough, Massachusetts Boston Scientific - Marlborough, MA, US , NCEP’s, CAPA’s PIRs, Field Signals Evaluations and Field Actions. Support internal and external regulatory audits as required. Support collection and analysis of key quality trending information and data 12 days ago
Quality System Supervisor BostonGene - Waltham, MA, United States , deviation management, audit program, etc. ● Other duties as assigned. Qualifications ● BS Degree in the Sciences or other technical discipline, or 5+ years of QA experience in the medical device or diagnostic 7 days ago
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Quality Assurance Specialist ACE Partners - , NJ, United States accuracy and traceability. Quality Audits: Assist in conducting internal audits and assessments to identify areas for improvement and ensure adherence to quality standards and regulatory requirements 9 days ago
Sr. Auditor, External Supplier Quality AbbVie - North Chicago, Illinois products, medical devices, and regulated studies Independently plan and conduct internal system audits and external GxP supplier audits Maintain approved supplier list, global audit schedule and participate 2 days ago
Quality Engineer Eliassen Group - Marlborough, MA, United States and maintaining the quality management system, including corrective and preventive actions, calibration, preventive maintenance, and internal and external quality audits. MUST HAVES - QUALIFICATION SUMMARY 6 days ago
Senior Quality Engineer Lowell Inc. - Brooklyn Park, MN, United States , and lead a team of quality engineers to ensure compliance with ISO13485:2016, FDA CFR Title 21 Section 820, and other relevant standards and regulations for the medical devices. Lowell is the premier partner 6 days ago
Quality Engineer/ Sr. Quality Engineer Merz North America, Inc - Racine, WI experience in NCR/CAPA processes. * Audit Experience: Proven ability to perform internal and/or supplier audits. * Risk Management and Standards: Knowledge of Medical Device Risk Management regulation ISO 3 days ago
Senior Quality Assurance Specialist Avails Medical, Inc. - Menlo Park, CA, United States Quality Management System. Support internal and supplier audits and external regulatory inspections. Become an expert in the use and maintenance of the eQMS. Lead the NC/CAPA documentation and investigation 10 days ago

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