•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
