Description

• 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.

📌 Senior Officer (India)
🏢 Cadila Pharmaceuticals
📍 India