Formulation Scientist & Analytical Expert with 8+ years developing innovative drug delivery systems
Ph.D. pharmaceutical scientist specializing in formulation development, LNP characterization, and analytical method development for both small molecules and biologics. Proven track record advancing drug candidates from preclinical through Phase II clinical stages with expertise in:
Core Expertise:
LNP Development & Purification: Lipid nanoparticles, extracellular vesicles, liposomes
Formulation Development: Small molecules, biologics, extended-release systems, parenteral products
Analytical Development: HPLC/UPLC, LC-MS, dissolution testing (USP I-IV), method validation
Drug Product Development: Injectable formulations, oral solids, QbD optimization, scale-up manufacturing
Characterization: DLS, FTIR, DSC, PXRD, TEM, SEM, particle size analysis, stability studies
Key Achievements:
Led pilot scale-up manufacturing for both small molecules and monoclonal antibodies
Developed extended-release formulations for Phase I clinical evaluation (HIV prevention/contraception)
Successfully transferred technology to industry (Chebulinic acid formulation licensed 2019)
Published 20+ peer-reviewed articles in top-tier journals (ACS Applied Materials & Interfaces, Biomaterials Science)
Secured research funding as Principal Investigator (Magee Women's Research Institute Pilot Grant 2024)
Industry Experience: Bristol Myers Squibb | Cross-functional collaboration with CMC, Clinical, PK teams
Education: Ph.D. Pharmaceutics & Pharmacokinetics | CSIR-Central Drug Research Institute
Currently seeking opportunities in Formulation Development, Analytical Sciences, or Drug Product Development roles.