05 Oct
|
Cadila Pharmaceuticals
|
Ankleshwar
05 Oct
Cadila Pharmaceuticals
Ankleshwar
• 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 (Ankleshwar)
🏢 Cadila Pharmaceuticals
📍 Ankleshwar