Description:
- 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 Valuable 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.