Cadila Pharma

•	Preparation of Certificate of Analysis (COA) according to released activity completed every month as per dispatched plan
•	Prepare inspection plan as per specification in SAP.
•	Prepare COA as per Specification/RA and Customer requirement and also enter data in SAP.
•	Responsible for releasing or rejecting of finished drug substance in SAP.
•	Regular follow-up with QC personnel and coordination to ensure of Release activity.
•	Plant Rounds.
•	Issuance of documents to all departments.
•	General documentation & co-ordination with other departments for cGMP compliance.
•	Internal and external audit related works
•	Preparation of finished products label
•	Preparation of release label and released the material during material dispatch
•	Purchase order verification
•	Release of finished goods in SAP
•	Preparation of certificate of analysis of finished goods
•	Review of filled batch process records
•	Review of filled batch process records of intermediate and SRP.
•	Review of filled batch process records of finished product.
•	Review of master batch process record of intermediates and SRP.
•	Monitoring of finished product packing and labelling.

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