Develop, oversee and implement production procedure according to GMP Modify and review batch production documentation. Batch production records initial review. Develop and implement SOP. Assist to provide training to operators. Take part in EHS and calibration related activities.
Requirements:
University graduate, with major in Pharmaceutical is preferred With experiences in pharmaceutical manufacturing company is preferred Solid online quality control experience Good knowledge of GMP Good skill of computer (Office software) Good at reading and writing in English