Accomplished Scientist with over 8 years of experience in pharmaceutical science research and process development, including 2 years at ReCode Therapeutics. Expertise in parenteral drug delivery technologies, including the development and scale-up of LNP-based drug products for Primary ciliary dyskinesia (PCD) and cystic fibrosis (CF), advancing candidates into clinical trials. Proven track record in applying Critical Quality Attribute (CQA) studies, optimizing manufacturing processes, and managing cross-functional teams to deliver innovative, scalable solutions for complex drug formulations.
Formulation & Process Development
Parenteral Drug Delivery
Advanced Characterization Techniques (HPLC, SEC/AF4-MALS, UV, dRI, SLS, DLS, TEM)
Critical Quality Attributes (CQAs) and Process Optimization
Cross-Functional Team Leadership
Clinical Trial Support and Scale-Up
Scientific Writing
Research design
Data Collection