Qc Analyst

Job description

Role & responsibilities • Perform testing of raw materials, packaging materials, in-process samples, and finished products as per specifications and test methods. • Operate analytical instruments including HPLC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, and pH Meter. • Handle laboratory software such as Empower, Lab Solutions, CDS Software, LIMS, and Microsoft Excel for data acquisition, analysis, and reporting. • Prepare standard and sample solutions and perform assay, related substances, dissolution, and content uniformity testing. • Review chromatograms, analytical results, and laboratory records to ensure data accuracy and integrity. • Maintain instrument calibration, qualification, and preventive maintenance records. • Investigate OOS, OOT, and laboratory deviations in compliance with SOPs and GMP requirements. • Ensure compliance with GLP, GMP, data integrity, and regulatory guidelines. • Support method validation, method transfer, stability studies, and audit activities. • Coordinate with QA and Production for timely release of raw materials and finished products. Preferred candidate profile • B.Pharm, M.Pharm, B.Sc., or M.Sc. in Chemistry or a related field. • 26 years of experience in Pharmaceutical Quality Control. • Hands-on experience in HPLC operation, troubleshooting, and data review. • Strong knowledge of GMP, GLP, pharmacopoeial requirements, and laboratory documentation.