● Led CAPA-Complaint projects, developed GMP SOP’s and meticulously documented 15,000+ samples, ensuring regulatory adherence, data integrity and helped design innovative protocols.● Optimized laboratory processes for vaccine trials, cutting project timelines by 50% and managing budgets effectively.● Conducted comprehensive and detailed investigations for quality deviations (DRs) and assessed their impact on Critical Incident Notifications/Alerts.● Successfully isolated H1N1 protein for vaccine development, showcasing expertise in microbiology techniques.● Developed literature review strategies and produced detailed reports, translating research into actionable insights.● Developed GMP-compliant SOPs, experimental concepts, and quality documents, boosting productivity by 25%.

●Performed various molecular biology techniques, such as DNA extraction, PCR, gel electrophoresis, and Western blotting, to contribute to data generation and analysis.● Conducted cell culture experiments, including cell line maintenance, viability assays, and drug treatments, to investigate cellular responses in oncology and immunology studies. ● Collaborated with research team members to troubleshoot experimental issues and optimize protocols for improved efficiency and accuracy.

● Led cross-functional teams to streamline logistics processes, improve operational efficiency, and reduce lead times. ● Established strong relationships with vendors and negotiated favorable contracts to drive cost savings and ensure reliable supply chain operations