At Divis Laboratories Ltd., I developed and optimized pharmaceutical processes and designed API synthesis techniques to support high yield and purity.
I carried out process validation in line with GMP, FDA, and ICH guidelines, and used root cause analysis and corrective and preventive actions to address deviations.
I developed and revised SOPs and contributed to workflow improvements. Lean and Kaizen methodologies helped increase process efficiency by 20%, while new synthesis techniques reduced production time by 15%.
I currently work as an Executive at MSN laboratories. I hold a B.Sc. in Chemistry (Hons.) and have training in GMP, process validation, and quality control.
