<ul><li>Review analytical raw data, test reports, and chromatographic data to ensure accuracy and compliance with specifications.</li><li>Verify results from instruments such as HPLC, GC, UV, FTIR, and others to confirm they meet regulatory and internal quality standards.</li><li>Check calculations, method compliance, system suitability, and data integrity in all QC reports.</li><li>Review analytical method validation and verification reports as applicable.</li><li>Ensure timely review of stability study data, in-process, and finished product testing documentation.</li><li>Review logbooks, instrument calibration records, and ensure proper documentation practices are followed.</li><li>Support the investigation of OOS (Out of Specification), OOT (Out of Trend), and any laboratory deviations.</li><li>Ensure adherence to GMP, GLP, and GDP (Good Documentation Practices) throughout all review activities.</li></ul>

Officer/Sr. Officer-QC (Reviewer)