
Analytical scientist with experience in method development, LC-MS/MS, HPLC, and regulated bioanalytical workflows supporting drug development. Background includes method qualification, troubleshooting, stability testing, and supporting technology transfer activities. Strong documentation skills with experience in GMP-aligned environments, QC laboratory operations, and cross-functional collaboration with R&D, QA, and external partners. Interested in nanoparticle formulation, analytical control strategies, and bridging R&D methods into GMP readiness.