Associate Scientist
➢ Worked as a study director in the GLP lab.➢ Interacted with clients for study design, Execution, support for operational challenges,and interpretation of results.➢ Performed Adventitious and Retrovirus studies for pharmaceutical products as per regulatory guidelines.➢ Designed virus clearance study in accordance with guidelines (EMA and ICH Q5A).➢ Produced and purified virus-like particles (VLPs).➢ Propagated and purified Viruses.➢ Developed and validated methods for cell-based assays and qPCR.➢ Developed and optimized the virus purification platform to enrich virus titer and stock purity using Ultracentrifugation.➢ Reviewed and interpreted raw data to produce high-quality reports and data sets suitable for inspection by regulatory agencies as per ALCOA+.➢ Prepared and implemented standard operating procedures (SOPs).➢ Managed research budgets and resources efficiently, improving project outcomes and minimizing waste.➢ Mentored junior scientists, provided training, and enhanced laboratory practices through quality control measures.➢ Managed multiple projects simultaneously, ensuring timely completion and high-quality deliverables.➢ Led a team of researchers efficiently, providing guidance and support to maximize productivity and achieve project goals.➢ Maintained a safe and organized laboratory environment by adhering to best practices for chemical handling and waste disposal.➢ Implemented quality control measures throughout the experimentation process to ensure the integrity of study outcomes.➢ Simultaneously managed several complex projects, meeting all pertinent milestones.