Responsible for formulation and development of Oral solid dosage form for Europe and USA Market.Support to regulatory affairs department for deficiency responses within stipulated timelines.Prepare master documents during formulation development,scale up protocol,Batch Manufacturing Report and Product development Report.Responsible for timely availability of required resources and logistics during formulation development.Effective co-ordination and follow-up with cross functional departments for duly project tracking and ensuring smooth progress of projects.