Scientist II, Quality Control

Role: Scientist II in Quality Control supporting analytical method validation, transfer, and testing of raw materials, in-process samples, finished drug substances, and drug products for biopharma applications. Responsibilities: lead and coordinate analytical projects, perform method development and optimization (LCMS, HPLC/UPHPLC, GC, FTIR, UV/Vis, KF), prepare technical documentation, mentor junior staff, and interpret data related to API and drug product stability. Requirements: MS in Chemistry with 5+ years or BS with 8+ years laboratory experience; proficiency in analytical techniques, cGMP, ICH, and CDER standards; strong attention to detail and independent work capability. High-Value: biopharma QC, analytical validation, multiple sophisticated techniques, experience supporting API and drug product release, team leadership, and technical coordination. WorkSetup: not specified.