副研究員/研究員

• Work hands-on in the laboratory to develop, optimize, qualify, transfer, and validate analytical test methods for both drug substance and drug product, from preclinical nomination through late-phase clinical development; • Conduct in-house stability studies and interpret stability data to justify material use periods; • Build kinetic stability models for formulation screening and packaging selection; • Author high-quality documentation, including methods, protocols, and technical reports; • Coordinate and oversee method validation and testing at contract laboratories and manufacturers; • Collaborate with others scientists on CMC teams to meet program goals; • Act as an exemplary and data-driven scientist with critical thinking and innovative problem solving skills in a fast‑paced, can-do environment.