Senior Scientist, Analytical Development and Quality Control

Role: Senior Scientist in Analytical Development and Quality Control supporting drug product formulation for Nurix's oncology and inflammation programs. Responsibilities: lead analytical method development, validation, and lifecycle management for drug formulations including amorphous solid dispersions and lipid-based systems; support late-phase tech transfer, regulatory submissions (IND/IMPD/NDA), and commercialization; oversee external CDMO testing, author technical reports, and contribute to investigations and stability studies; collaborate cross-functionally across R&D, Quality, Regulatory, and Manufacturing. Requirements: PhD in Chemistry, Pharmaceutics, or related field; 8+ years industrial CMC experience; expertise in chromatographic and dissolution methods, stability, validation, and control strategies; experience with amorphous solid dispersions/lipid systems, CDMO oversight, and regulatory filings; strong technical writing and data review skills; knowledge of cGMP, ICH guidelines. Preferred: experience supporting global filings, and working in fast-paced environments. HighValue: drug product analytical development, validation, regulatory submission support, amorphous solid dispersions/lipid formulations, cGMP compliance, cross-functional collaboration. WorkSetup: onsite in Brisbane, CA; travel up to 5%.