99 Internal Quality Audit Medical Device Jobs - page 9
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Supervisor, Quality Operations pennsylvania and processes. Job Qualifications Required: : Minimum of 5 years of quality operations experience within medical device manufacturing, service or distribution environment, with strong concentration in compliance Competitive More than 30 days ago
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Quality Lab Supervisor - Chemistry (3rd Shift) Baxter - Round Lake, IL know operating and troubleshooting procedures for lab equipment, and quality and regulatory requirements pertinent to pharmaceutical and medical device manufacturing labs. Must possess excellent 18 days ago
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GCP QA Auditor Medpace, Inc. - Cincinnati, Ohio and medical devices. Develop audit management plans and audit strategy with clients for ongoing clinical trials. Coordinate and conduct internal system audits and external investigative site/vendor audits 22 days ago
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Quality Engineer Medcura - Riverdale, Maryland functional teams to execute direction for the company’s Quality compliance requirements on new and existing devices. This position is responsible for the day-to-day execution of all Quality System requirements 20 days ago
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Associate Director, Clinical Monitoring Oversight Clinical Dynamix, Inc. - Cambridge, MA, US and review, management of clinical systems, oversight of clinical metrics tracking and reporting), inspection readiness efforts and audit-ready Trial Master Files reviews (internal and at CRO). Travel required 22 days ago
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Quality (QC) Inspector Design West Technologies, Inc. - Tustin, CA 92780, USA environment. Requirements: High school diploma or equivalent Minimum 2-5 years' experience in quality assurance or inspection, preferably in an aerospace, defense, automotive, medical devices, or manufacturing $26 - $33 per hour 26 days ago
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Quality Specialist Thermo Fisher Scientific - Incheon, Korea, Republic of records management Monitor internal quality compliance level, as well as daily quality performance Management of customer facing quality processes to provide timely and professional reply to customer 26 days ago
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Sr. Supplier Quality Engineer CyberCoders - Oldsmar, FL coming out of medical device manufacturing to manage our business relationships with suppliers with a focus on improvement of product quality. What You Will Be Doing Maintain & improve our quality 90,000.00 - $120,000.00 26 days ago
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Sr. Regulatory Specialist-CT/AMI Philips - Orange, OH, US such as FDA, 3rd party external regulatory agencies like SFDA, KFDA, JPAL, etc. and notified body audits. Implements internal or external quality system audits. Reporting to the Director of Regulatory Affairs More than 30 days ago
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Principal Regulatory Affairs Specialist Philips - Bothell, WA, US to optimize clinical study approvals and review of clinical study protocols. Representing Philips in internal and external audits with regulatory agencies or Notified Bodies as needed. Mentor and coach Philips More than 30 days ago
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