Production - Chemist /Officer

Mangalam Drugs & Organics; Valsad District; On-site; INR 300,000 - 420,000; Full time

Job summary

Mangalam Drugs & Organics in Gujarat is seeking a production role to perform manufacturing processes and fill quality records during shifts in line with GMP practices. You will ensure compliance with BMR, BPR, ECR, log books and SOPs.

You will coordinate requisitions for raw materials, packing materials, and consumables, verify receipts, and submit quality documents to QA. You will help report deviations and participate in training on cGMP and safety.

Responsibilities

• 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.

Job description

Role & responsibilities

-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.