R&D Pharmacist ü Working following cGMP regulations with corporation with all departments. ü Formulation Development for new products. ü Preparing trials and pilot batches & follow up their stability testing results. ü Preparing & arranging documents for registration in compliance with SFDA & GCC requirements. ü Preparing CTD(common technical document). ü Analyzing dissolution profiles data. ü Supervising scale up batches Trouble shooting. ü Supervising and sampling process validation batches for US & MENA markets. ü Preparing process validation batches documents and reports for US & MENA markets. ü Prepare & check qualification protocols & reports for new machines in R&D department.