Operate & manage granulation, compression, coating, pelletization and capsule filling area. Operate and monitor pharmaceutical manufacturing equipment as per SOPs, BMRs, and GMP guidelines.
Responsible for the coordination of supportive equipment and process validation activities such as testing, calibration, scale-up, engineering and validation studies, and assurance that the necessary project documentation is complete, accurate and in compliance with cGMP regulations.
Execution of qualification / validation for equipment, utility and facility. Preparation & review of qualification protocols and handling change controls.
Experience in pharma industry for handling shift-related activities like work schedule, release of in-process and intermediate samples etc. Natco Pharma