Posted:2 days ago|
Platform:
Work from Office
Full Time
-To perform the manufacturing process of products and to fill all the quality records in shift as per GMP. (BMR/BPR/ECR/Log Books/etc.) Following the SOP.
-To give the requisition for Raw material/Packing material to Raw material store and verification of the same after receipt.
-To give requisition for any consumable items to engineering store and verification of the same after receipt.
-To give requisition for forms / formats and other quality related documents to QA and submission of the same to QA.
-To make sure that all production deviations, non-conformance & accidents are reported along with investigation report.
- To schedule training of plant personnel on SOPs, documentation and other cGMP compliances as per ICH Q7 and safety.
Mangalam Drugs & Organics
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