About this role
Senior Scientist Analytical Development & Quality Control at Protagonist Therapeutics. Location: Newark, California, United States. Role: developing methods, managing CDMOs, authoring filings Requirements: PhD or MS in analytical chemistry or related field with 5+ years supporting CMC development; UHPLC and advanced MS expertise; peptide or complex molecule analytical method development; cGMP/GLP and CDMO experience; strong communication and leadership. Category: Research and Development (R&D) Seniority: Senior Level Tools: UHPLC, UV, PDA, MALS, CAD, MS, conductivity, fluorescence Commitment: Full Time Workplace: Onsite Languages: English