) Review and document analytical data in compliance with cGMP and data integrity principles Investigate OOS/OOT results and support deviation and CAPA activities Ensure compliance with FDA, cGMP, and GLP requirements Prepare and review analytical reports, protocols, and SOPs Participate in method transfer, verification, and validation activities Support regulatory and internal audits Strong knowledge of FDA regulations, cGMP, and data integrity Analytical troubleshooting and problem-solving skil…