• Developed innovative antibody purification operations following principals of quality by design, design of experiments, and multivariate analysis, for the clinical and commercial production of drug product
• Authored development reports formally summarizing scientific development methodology
• Functioned as a group lead for the evaluation and implementation of an electronic lab notebook solution, involving drafting a project charter outlining goals, interfacing with IT, gathering and prioritizing user requirements, and planning for a successful roll out
• Participated in a cross-functional tech transfer team, whose job is to transfer a manufacturing process from development to a GMP facility and developed and implemented a new systematic approach to risk assessment based off of FMEA
• Coded multiple laboratory tools in Excel VBA with simple user interfaces to increase productivity of group by 30%
• Lead a cross-functional team to develop a comprehensive, Excel-based model of manufacturing processes for improved process development, tech transfer, and cost of goods analysis
