Quality Control Executive

Detail-oriented Pharmaceutical Quality Control Professional with experience in chemical and instrumental analysis of Raw material, In-process sample, and finished products. And Reviewer with strong expertise in review of analytical data, laboratory documentation and compliance with GMP, GLP, and regulatory guidelines.Review of analytical worksheets, Raw data, chromatograms, and laboratory notebooks.Preparation and Verification of Certification of Analysis (COA)Management of Stability, FP and GLP system for receipts, and TestingReview of STP, SOP, Validation & Investigation ProtocolsEvaluation of OOS, OOT, Deviation & Investigation,In case of any lab deviation with respect to procedure. It is investigated and documented.Checked instrument usage logs, Calibration records, and maintenance logs.Ensured data integrity compliance (ALCOA+)Review Stability study data and reports and summary.Operated and troubleshot HPLC, GC, UV, FTIR, Dissolution ApparatusEnsure high precision, accuracy, and data integrity in all laboratory testing and documentation processes.Trained and guided junior analystsEnsure compliance with GMP, GLP, WHO, and ICH guidelines.

Work arrangement
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