12 Aug
|
Cadila Pharmaceuticals
|
Jammu
12 Aug
Cadila Pharmaceuticals
Jammu
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 Positive 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)
🏢 Cadila Pharmaceuticals
📍 Jammu