About this role
Department: Quality Control Location: Ankleshwar Qualification: B.Sc./M.Sc. – Chemistry Experience: 2–5 years in Pharmaceutical QC
Key Responsibilities
Perform analysis and testing of In-Process (IP) and Finished Products (FP) as per approved specifications and SOPs. Handle analytical instruments such as HPLC, GC, UV, Dissolution, KF, pH meter, etc. Review analytical results, calculations and QC documentation. Ensure compliance with GMP, GLP and ALCOA+ principles. Investigate OOS/OOT results and support laboratory investigations. Maintain laboratory records, logbooks and analytical worksheets. Coordinate with Production and QA for IP/FP testing and release. Ensure timely completion of testing as per production requirements.