 This role is in Sanford, NC.POSITION RESPONSIBILITIES:Review and approve QA documentation including validation protocols, method transfers, and compendial assessments.Provide final QA approval for change controls, CAPAs, deviations, and lab investigations (OOS/OOT/OOE)Support electronic record reviews and compendial change documentation.Make real-time quality decisions in compliance with cGMP and regulatory standards.Collaborate cross-functionally to resolve technical and quality issues.Contribute to start-up activities and performed additional QA duties as needed.
