94 Internal Quality Audit Medical Device Jobs - page 4
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Quality Assurance Manager (Medical Device) EPM Scientific - Billerica, MA, United States inspection readiness for both internal and external audits Qualifications: Bachelors degree with approx. 8-10 years of Quality experience in medical device, combination product experience preferred Direct 4 days ago
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Research And Development Engineer TeDan Surgical Innovations - Sugar Land, TX, United States manufacturing process for manufacturability, quality requirements, design requirements, and state-of-the-art validations (IQ, OQ, PQ) Provide support of DHF reviews during internal, external, and customer audits 16 days ago
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Quality Management System Specialist II Enlitic - Fort Collins, United States initiation and management of NCRs and CAPAs including root cause analysis, action planning and verifying effectiveness of corrective actions and preventive actions. Provide support Internal External Quality $75,000 - $90,000 11 days ago
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Quality Coordinator (Manufacturing) HEF USA - Springfield, OH, United States include Automotive, Medical Devices, FireArms Develop and maintain internal standards, regulatory strategies, and plans Investigate complaints and non-compliance using Quality Tools Complete customer 2 days ago
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Quality Manager Eastman Kodak Company - Rochester, NY, United States . Graduate degree preferred but not required. • 10+ years’ related work experience preferred: • Experience in a FDA regulated environment: Medical Devices and/or Pharmaceuticals required. Knowledge of GMP 18 days ago
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Manufacturing _Quality Assurance Manager Midas Management and Research - Irwindale, California + years) in quality assurance within medical device manufacturing, with a strong understanding of FDA regulations and ISO 13485 standards. Proven experience in leading quality improvement initiatives 14 days ago
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Senior Quality Assurance Manager Top Quality Recruitment (TQR) - , NJ, United States and SOPs. Support Internal Audit program and regulatory audits. Preferred Skills Strong interpersonal and written/verbal communication skills Ability to handle multiple priorities daily while being flexible 7 days ago
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Senior Regulatory Affairs Specialist Barrington James - , CA, United States to post market. Support internal and external audits. Requirements: Proven experience in Regulatory Affairs within the medical device industry, with expertise in 510(k) submissions and MDR compliance 11 days ago
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Internal Quality Auditor Ursus, Inc. - Alameda, California and process improvements Performs other related duties and responsibilities, as assigned Qualifications: 4+ years of medical device (class II and III) industry experience 2+ years' experience in quality system Yesterday
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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 11 days ago
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