Responsible for day-to-day activities of Quality assurance, prepare and maintain documentation, BMR, BPR, SOPs as per cGMP norms. Line clearance, IPQA
Coordinate with other depart for smooth running of plant
Capable of handling external Audits°Min Exp 2 to 10 years in Quality department of a reputed pharmaceutical Company
Knowledge of working in GMP Co. MS Office (MS Word & MS Excel) / ERP software.
and good time management skills°Performance linked incentive & annual bonus extra