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.
📌 Executive Jammu (India)
🏢 Cadila Pharmaceuticals
📍 India
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