As Manager, Quality Engineering, this role ensures compliance with United States Pharmacopeia and Food and Drug Administration (FDA) standards, managing quality processes, validation protocols, and investigations with robust Corrective and Preventive Actions (CAPAs). Through cross-functional collaboration and training on Current Good Manufacturing Practice (cGMP) and data integrity, it strengthens team capabilities, manages risks, and ensures audit readiness to support Empower’s mission of delivering accessible, innovative healthcare solutions.
While performing the responsibilities of the job, the employee is required to talk and hear. The employee is often required to remain in a stationary position for a significant amount of the workday and frequently use their hands and fingers to handle or feel in order to access, input, and retrieve information from the computer and other office productivity devices. The employee is regularly required to move about the office and around the corporate campus. The employee is regularly required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch or crawl.
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Additional Voluntary Benefits
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