Stability Coordinator/Manager

Role: Manage and coordinate drug substance and drug product stability programs for Viking Therapeutics' pipeline, supporting early-stage development through late-stage clinical and pre-commercial phases. Responsibilities: design and oversee ICH-compliant stability protocols, manage sample inventory, trend and interpret stability data, lead investigations for OOS/OOT events, contribute stability data to regulatory filings, and ensure compliance with ICH guidelines and cGMP standards. Collaborate closely with Analytical Development, Drug Substance, Drug Product, Quality, Regulatory Affairs, and external CROs/CMOs. Provide stability program updates to stakeholders. Requirements: B.S. in Chemistry, Pharmaceutical Sciences, Biochemistry, or related; 2+ to 4+ years of experience in stability or analytical operations within biopharma; hands-on experience managing stability studies, ICH guidelines, and working with external testing labs. Preferred: experience with peptide or GLP-1/GIP products, stability data systems (LIMS), and data integrity practices. High-Value: focus on small molecules and peptides, stability testing from early to late development, regulatory documentation contributions, cGMP compliance. Work setup: not specified.