

Assistant manager in pharmaceutical manufacturing with practical command of upstream and downstream unit operations, including reactors, dryers, centrifuges, ANFD, and sparkler filters. Drives cGMP work with QA, QC, and regulatory teams, supports equipment qualification, and prepares PFDs, material and energy balances, and equipment mapping. Strengthens plant performance through OOS/OOT investigations, debottlenecking, yield improvement, and solvent recovery optimization.
Process simulation
Pfd preparation
Material and energy balance
Equipment qualification
OOS investigation
Cleaning validation
Process validation
Project management
Process optimization
Technology transfer
Troubleshooting
Yield improvement
Process scale-up
Solvent recovery optimization
Plant de-bottlenecking
cGMP compliance
Pharma regulatory compliance
Validation documentation
Equipment mapping
Root cause analysis
Batch record review
Deviation management