Job 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 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.