We are looking for an experienced QC Analytical professional (6–12 years) with strong exposure to analytical testing, data review, and GMP-compliant quality systems in a biopharmaceutical environment. Key Responsibilities: • Review analytical data for DS, DP, stability, method validation, and method transfer samples. • Perform and review chromatographic and plate-based analytical techniques. • Manage reference standards, laboratory documentation, calibration activities, and inventory. • Handle investigations related to Deviations, OOS, OOT, CAPA, and Change Controls. • Support equipment qualification (IQ/OQ/PQ), analyst qualification, and training activities. • Ensure compliance with GMP, GLP, and GDP requirements. Technical Expertise Required: • CEX-HPLC, SE-HPLC, RP-HPLC • ELISA, RT-PCR • Capillary Electrophoresis (Maurice System) • Analytical data review and laboratory documentation Qualification: M.Sc., M.Pharm, M.Tech (Biotech), or relevant Master's degree. Experience: 6–12 years ...