Legend Biotech Benefits Overview

Supports and conducts GxP audits across GCP, GLP, and GVP; coordinates regulatory inspection readiness; manages audit observations, CAPA follow-up, quality documentation, vendor oversight, deviations, investigations, metrics, and data integrity reviews. Advises clinical and preclinical stakeholders, develops SOPs, delivers training, and supports continuous quality improvement. The role is remote with up to 25% domestic and international travel.