Description
The role develops, optimizes, and validates analytical methods for new chemical entities and generic compounds using HPLC-UV, GC, LC-MS/MS, and ICP-MS; performs preclinical dose verification and Certificates of Analysis for IND submissions; calibrates and maintains laboratory equipment; manages GLP/GMP-compliant raw data and documentation; and supports laboratory operations and cross-functional projects. The position requires a master's degree in chemistry, pharmaceutical sciences, or a related discipline, 3–4 years of relevant analytical laboratory experience, and expertise in regulatory compliance and method development.
