Experienced bioanalytical and quality scientist with over a decade of success in LC-MS/MS method development, stability program support, and translational pharmacology. Proven expertise in managing QC documentation, stability studies, and regulated bioanalysis under FDA and ICH guidelines. Skilled in interpreting chromatographic data, leading assay validations, and collaborating with CDMOs/CTLs. Demonstrated capability in maintaining critical reagents, authoring regulatory reports, and supporting clinical-stage programs for biologics and small molecules.
American Society for Clinical Pathology
Opportunity Grant Awardee, Philippine-American Educational Foundation (Fulbright), U.S. Department of State – Education USA, 2010
Citizenship: U.S. Citizen