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 Xencors Qualified Person (QP) service providers, including preparation and maintenance of QP Declarations (QPDs) and support of batch certification activities for EU/UK clinical. Develop and deliver new hire and ongoing GMP/GxP training content: annual GMP refresher, data integrity, deviation/CAPA and root cause analysis, change control, documentation practices, and topic-specific training driven by CAPA or regulatory change; ensure training is completed and documented prior to independent performance of GMP activities.