Latest Medical Device Audit Senior jobs - JobisJob United States Mobile

11 Medical Device Audit Senior Jobs

Senior Quality Assurance Specialist X4 Life Sciences - New York, NY, United States and regulatory compliance of QMS medical devices. This position involves a range of responsibilities, including managing deviations, conducting internal audits, addressing nonconformities, implementing corrective 4 days ago
Senior Design and Quality Engineer Instrument Technology, Inc. - Westfield, MA, United States System (QMS). As the Senior Design & Quality Engineer you will lead and maintain our ISO 13485 certification, through audits, training, and other applicable compliance tasks. You will hold yourself 13 days ago
Director, Quality Assurance Varian Medical Systems - Austin, Texas preferred. 10-15 years of medical device experience. Minimum of 7 years management experience. Ability, competence, and confidence to lead people. Effective interpersonal skills. Experience with Class II 3 days ago
Senior Quality Engineer Facet Medical Technologies LLC - East Point, GA, United States 13485, CFR 820, and EU MDD/MDR regulations. Proficiency in process improvement methodologies, Statistical Process Control (SPC), and other statistical process methods is essential. Experience in medical 10 days ago
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IVD Auditor EPM Scientific - , CA, United States IVD Lead Auditor Job type: Permanent Location: Home Based (USA) A renowned and well-established Notified Body that are committed to ensuring the safety and efficacy of medical devices are looking 18 days ago
Sr. Operator - 1st Shift Abbott Laboratories - Plymouth, Minnesota of personnel, tooling, and equipment in assigned areas. Assemble, bond, coat, and process medical devices and related parts using microscopes and applicable tools. Assists in providing direct training to area 7 days ago
Clinical Research Manager Triton Medical Robotics - Burlingame, CA, United States quality by maintaining compliance, reviewing device complaints, reviewing audit reports and implementing corrective actions. Regularly communicates study status to senior management and represents 18 days ago
Senior Quality Manager Device Search Group - , CA, United States by regulatory bodies. If you have a proven track record in the medical device industry, enjoy working with small organizations and a passion for continuous improvement, we want to hear from you. Key 24 days ago
Computer Compliance Audit Manager GSK - Durham, NC supporting GxP activities. Entity external audits 3rd Party Service Suppliers Software as a Medical Device (SaMD) audits. For Cause audits based on identified risks or regulatory actions Progress audits 11 days ago
Regulatory Affairs Specialist, Selution (Irvine, CA) Cordis - Irvine, California /Biomedical/Pharmacy or equivalent professional experience. • 2+ years of experience in regulatory affairs in medical device/pharmaceutical industry, GLP, ISO 13485 environment • Experience in FDA / EU 15 days ago

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