Conducted literature search on APIs, Formulation, Patent search, Selection of Excipients, Technologies for the development of Solid oral dosage forms (Immediate Release, Extended release), developing robust formula and manufacturing process., Carry out pre-formulation studies: formulation and excipient screening/ compatibility studies, selection of Excipients and feasibility trials for process selection and comparative evaluation with respect to the pre-development studies., Stability data compilation., Perform day to day lab trial activities like balance daily calibration, area monitoring, temperature and RH monitoring, maintaining lab raw material store., Updating trial details online in the laboratory note book., Involved in execution of trouble shooting trials conducted at lab level., Co-ordination with cross functional teams for smooth execution of development projects., Preparation of documentation like: BOM, SOPs, Compilation, Master Formula Record, Stability protocols, DEC study protocols etc., Review of documentation like: BMR, analytical reports, etc., Routine and Stability analytical data compilations., LNB, Test & import License.