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To perform calibration of the analytical instruments as per calibration schedule Follow the standard practices cGLP during lab experiments Operation of HPLC, GC, Dissolution, FTIR, UV-Spectrophotometer, KF (Karl Fischer) Auto Titrator and Auto Titrator. Cleaning verification method development API method evaluation and verification API solubility study assessment Method Development for drug product formulation Routine analysis of development samples and lab stability samples Method verification of different analytical methods Reporting of analytical data and submit for review and release. Follow GxP (GMP, GDP, GLP) for all processes. Preparation of test procedures for routine development analysis
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