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The QMS Manager - Deviation/CAPA at Esperion Therapeutics is responsible for overseeing the Deviation and Corrective and Preventive Actions (CAPA) processes within the Quality Management System (QMS). This role involves managing the end-to-end deviation process, ensuring timely closure and effective corrective actions, and collaborating with cross-functional teams to maintain compliance with regulatory standards. The ideal candidate will have a strong background in quality management, root cause analysis, and risk assessment, along with experience in computer systems validation.