A leading medical device company is seeking a Senior QA Auditor in California, responsible for planning, executing, and documenting audits, focusing on ISO 13485 compliance. The role requires extensive experience in the medical device or pharmaceutical industry and strong skills in quality systems and communication. The position involves developing audit plans, ensuring compliance with regulations, and managing corrective actions. Ideal candidates will have a bachelor's degree and ISO 13485 Lead Auditor certification, alongside a history of managing audits with regulatory bodies. #J-18808-Ljbffr
Senior QA Auditor - ISO Lead, Medical Devices • California, MO, United States
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