Technical Supervisor

Cadila Pharmaceuticals LimitedJammu, Jammu and KashmirOn-siteFull-timeStaff, 8–12 yearsListed 1 week ago

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About this role

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 Manufacturing 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.