Key Responsibilities:Develop and validate analytical methods for drug substances and drug productsHandle techniques like HPLC, GC, UV, IR, Dissolution, etc.Perform method transfer to QC/plant locationsPrepare protocols, reports, and documentation as per regulatory guidelinesSupport stability studies and impurity profilingEnsure compliance with GLP, c GMP, and data integrity normsTroubleshoot analytical issues during development and commercial stagesWork closely with R&D, QA, and manufacturing teams