Cadila Pharma

Production:
•	Supervision of production & Maintenance activities of respective shift.
•	To ensure that every raw material used is of right quality (approved from QC, having reference number) and quantity (verifying the weights, if required by reweighing) in every batch.
•	To ensure 100% implementation of process conditions for batch as per BPRs.
•	To do SAP transaction related to production module
Documentation:
•	To ensure to have online completion of documents with respect to his shift
•	To check critical operation with respect to BPR and to verify the related documents
•	Authorize for cGMP Document signatory in absence of Factory Manager & Dy. Factory Manager
Quality:
•	To ensure that instructions in BPRs are followed judiciously’
•	To ensure Intermediates/ FP produced is as per quality specification
cGMP:
•	To ensure proper calibrations of pH meters & weighing balances as per SOP
•	To ensure timely updating of equipment status boards
•	Ensure BPRs of ongoing batches are available at specified places near equipment and are online with production
Safety:
•	To ensure the operators are aware / trained in usage of PPEs.
•	To coordinate with EHS for HAZOP, JSA & PSSR.
•	To Coordinate with EHS for various safety permits.
•	Wastage avoidance/ Reduction:
To coordinate with QA department for Good Documentation Practices
•	To coordinate with QC department for getting analysis report

Job Details

Skills Required

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