Boston, Massachusetts, United States
I was actively involved in analyzing and processing data derived from Drug Substances (DS), Drug Products (DP) samples, and process intermediates utilizing analytical chromatographic techniques and reporting chromatographic data to ensure final product quality and regulatory compliance. Oversaw routine testing of GMP and non-GMP samples containing mRNA and lipid components for their integrity and utilized findings to steer advanced downstream processes. I conducted plate-based assays to ascertain residual protein concentration in plasmid DNA, contributing to patient safety and upholding quality standards within pharmaceutical manufacturing.