Process validation Technology transfer from one manufacturing location to other Transfer from development lab/pilot plant to commercial locations Handling changes like batch size, Equipment, Alternate Vendors, Material Vendors, specifications etc Preparation of master batch documents, validation protocols and reports Trouble shooting Process improvements, cycle time reduction Quality improvement Data collection, review & analysis of data Desired Skills: 2 - 8 years of experience in Process development/Tech transfer areas. Having good knowledge and hands of experience on the equipment, process and materials of Oral dosage forms. Additional exposure in other dosage forms is desirable. Knowledge on Formulation development, GMP & regulatory requirements will be an added advantage.