:

To assure Quality and cGMP compliance of the products being manufactured and Packed for Penicillin Block.

- To review MMD-I / BPR and release of the batches for further processing stage like Granulation, compression, coating, inspection, filling and packing.
- To ensure IPQA functions and periodical verification of in- process parameter as per batch record and SOP.
- To review & impact assessment of break down intimation slip (BDIS) and to advise precautions to be taken before, during and after attending BDIS & Closure of BDIS.
- Ensure timely review of executed batch processing record and stage clearance for further activity.
- Review and approval of Master MMD-I & Batch packing record • To deliver the training for IPQA/Shop floor Team as per schedule and as when required.




- To participate in Regulatory/Internal Audit and cGMP review meeting and facilitate its compliance.
- Preparation, review and approval of SOP and ensure proper implementation at shop floor.
- Intermediate & final Release of Finished Product in SAP.
- To assess the impact of Incident, Deviation, Change Control and CAPA.
- To participate in investigation of cGMP non conformances, Deviation, Market complaints and Incident for identification of root cause and implementation of identified CAPA.
- To ensure that batch must be manufactured and checked in compliance with laws in forced in that member state and in accordance with requirement of marketing authorization, registration dossier (ND).
- Any other job assigned time to time by HOD.

📌 Executive (Dholka)
🏢 DigiCAD
📍 Dholka