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Analytical method development of finished dosage forms. Stability studies of finished dosage forms. Analytical method validation Analytical method transfer.

Seeking a highly motivated and results-driven Production In-charge to oversee the manufacturing operations for our range of high-quality DNA/RNA Extraction Kits and Lateral Flow Kits

Strong knowledge of country-specific labeling regulations and guidelines across the US, EU, Canada, Australia, and Switzerland, combined with hands-on experience in label development, including CCDS, USPI, and packaging components. 

Personnel monitoring. Trend analysis and reporting. Sample handling. EM monitoring in aseptic process area including Grade A,B,C and D

Qualification of equipment & Documentation, IPQA, QMS-Ohange Control CAPA, Deviation, Process Validation, Cleaning Validation, APQR, Audit Compliance.

Operation of Blister machines. Troubleshooting, BQS Cartonator: Operation of Cartoning machines. Troubleshooting

Aurobindo Pharma Limited is an Indian multinational pharmaceutical manufacturing company headquartered in HITEC City, Hyderabad, India.

Clearance for visual inspection. Supervision of visual inspection activity. Visual inspection batch record closure. Post line clearance for visual inspection.

Coordination with quality control department & quality assurance department for getting analytical data with respect to , process optimization batches & validation batches.