Posted:5 days ago|
Platform:
Work from Office
Full Time
Role & responsibilities Conduct chemical and physical analysis of raw materials, intermediates, and finished products using analytical instruments (HPLC, GC, UV, FTIR, Dissolution, etc.). Prepare and review analytical reports, Certificates of Analysis (CoAs), and maintain accurate laboratory records. Perform routine and non-routine analysis in compliance with pharmacopeias (USP, BP, IP, EP) and internal specifications. Ensure timely calibration, maintenance, and qualification of laboratory instruments. Conduct stability studies and support product shelf-life monitoring. Participate in investigations of OOS (Out-of-Specification), OOT (Out-of-Trend), and deviations, and assist in implementing CAPAs. Maintain compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Support regulatory inspections and audits (USFDA, MHRA, WHO-GMP, etc.). Coordinate with QA, Production, and R&D teams for quality-related issues. le
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