FEATURED JOBExecutive
Cadila Pharmaceuticals Ltd
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Posted: 11 Aug 26
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.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2939243
Job Category Quality Control
Locality Address
State Jammu & Kashmir
Country India
About Company
Cadila Pharmaceuticals Ltd
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