This role is responsible for resourcing, and performance of four connected quality programs: (1) GMP/GLP supplier quality management, including qualification, periodic review, and disqualification; (2) the internal audit program; (3) the GMP training program, including onboarding and role-based curriculum/training assignment; and (4) quality support for Xencor's Qualified Person (QP) service providers, including preparation and maintenance of QP Declarations (QPDs) and support of batch certification activities for EU/UK clinical. Maintain the Approved Supplier List (ASL) and ensure qualification status is accurate, current, and inspection-ready in Veeva Vault, Xencor's quality management system of record (Vault QMS / QualityDocs).Apply risk-based supplier categorization consistent with ICH Q9, ICH Q10, EU GMP Chapter 7 (Outsourced Activities), EU GMP Chapter 5 (starting-material supply chain controls), and 21 CFR 210/211 and 21 CFR 58 expectations.