Senior Executive-QC

• Perform analysis of finished products, in-process, intermediate, miscellaneous, and stability samples as per pharmacopoeial, in-house, and customer specifications.

• Operate and perform routine calibration of LC-MS, HPLC, GC, analytical balances, and other QC laboratory instruments as per approved SOPs and procedures.

• Conduct wet analysis and routine chemical testing of finished product samples using approved analytical methods.

• Ensure accurate and timely recording, review, and maintenance of analytical data, worksheets, logbooks, and other QC documentation in compliance with cGMP requirements.

• Ensure adherence to SOPs, analytical methods, specifications, pharmacopoeial standards, and applicable quality requirements during all testing activities.

• Identify and promptly report abnormal observations, deviations, OOS/OOT results, and other analytical discrepancies to the concerned authority.

• Follow all applicable laboratory safety procedures, cGMP practices, and EHS requirements during analytical activities.

• Ensure proper handling, cleaning, and upkeep of laboratory instruments and equipment to maintain reliable analytical performance.

• Take responsibility for reporting and coordination activities in the absence of the reporting authority, as required.

• Support the QC team in ensuring timely completion of testing, documentation, and reporting.

• Perform other quality control-related activities and responsibilities as assigned by seniors.