Role Objective:- 1. Ensure the cGMP compliance of QC area Key Responsibilities: • Follow up of Standard operating procedure for testing and analysis RM/FG etc. • Follow up of Current Good Laboratories Practices. • Completion of Online Documents. • Ensure for calibration of equipments. • To ensure the delivery of product as per the production schedule. • To ensure the work discipline and cleanliness in production area. • To prepare Standard Operating Procedure. • Handling of deviation, initiation of change control and CAPA. • To impart training. • To follow safety norms in daily routine. • Monitoring and recording of Environmental condition of tablet compression / Bin-charging area as per defined frequency.
