Operate & manage granulation, compression, coating, pelletization and capsule filling area. Operate and monitor pharmaceutical manufacturing equipment as per SOPs, BMRs, and GMP guidelines.
This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.
Execution of qualification / validation for equipment, utility and facility. Preparation & review of qualification protocols and handling change controls.
Unichem Laboratories Ltd., is looking for dynamic individuals with ambitious career aspiration at our pharmaceutical and R&D facilities in Pilerne, Goa. Apprentices or freshers in pharmaceutical Production, QC, Analytical Development, Engineering and IT