Teams at Structure Therapeutics

Leads and codes production AI systems across drug discovery, clinical development, manufacturing, and business operations. Builds generative AI applications, shared AI platforms, model and data pipelines, evaluation frameworks, MLOps processes, and secure regulated workflows. Leads engineers while remaining hands-on in architecture, coding, deployment, troubleshooting, vendor evaluation, and cross-functional collaboration with scientific, clinical, product, security, and business teams.

Leads global GCP quality assurance governance, compliance oversight, risk-based audits, inspection readiness, vendor oversight, CAPA management, and quality management system improvements across clinical programs. Provides expert guidance on global regulatory requirements, supports clinical and regulatory submissions, manages quality metrics and trends, and mentors QA staff, consultants, and auditors. Partners cross-functionally to protect patient safety, ensure data integrity, and drive continuous improvement.

Provides global GCP quality assurance oversight for clinical programs, vendors, audits, CAPAs, inspection readiness, and regulatory compliance. Leads study and vendor audits, evaluates risks, reviews clinical and regulatory documentation, supports QMS development, analyzes quality metrics, and drives continuous improvement. The role requires expertise in global GCP regulations, clinical trial quality systems, vendor oversight, regulatory inspections, data integrity, and patient safety.