• Review of Batch process record. • Handling of finished product release dispatch activity, Market Complaint, Return goods, Recall Material. • Preparation of APQR. • Handling of Change control and Deviation • Review of Master Documents. • Documentation Control. • Issuance of quality documents like BPR, Specification, Analytical method protocol formats, and labels. • Preparation of Quality Reports. • Preparation of Master documents. • Reviews of COA for Market release. • Checking documents of Failure, OOS/OOT investigation. • Plant Round , Line Clearance • Any work related to QA as & when required.
📌 Officer (India)
🏢 Cadila Pharmaceuticals
📍 India
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