Developing and validating new methods for drug products and drug substances by using UPLC, HPLC and UV-Visible Spectrophotometer.Reviewing documents and giving support for audit like USFDA and WHO.Coordinating between the different teams which are involved in developing new analytical methods for different formulation dosage forms.Involved on Analytical method transfer between different formulation manufacturing facilities in India and in USA Preparation of Standard Operating Procedure for the Instruments.Calibration of Instruments like HPLC, Dissolution, UV-Visible Spectrophotometer and reviewing of final STP’s.Coordinating between research teams of different units based in US, UK, Brazil, China and UK on active projectsFormulizing budget and R&D requirements and cost cutting measures.Scheduling and liaising the research results review with senior scientists and management.