Perform new analytical method development, method validation & method verification for pharmaceutical raw materials and finished products. Perform OOS, OOT, GLP, GDP for analytical instruments like HPLC, GC, Ion Chromatography, ICP-MS. Review laboratory deviations such as gap analysis, CAPA. Create & review protocols for stability testing and method validation; write & review SOPs, reports for method validation & verification, and Stability testing protocols.