Cadila Pharma

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.

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