Quality in preclinical development is a matter of operational resilience as much as regulatory mandate. This role serves as a GLP Auditor within our Research & Development Quality audit program, responsible for executing the global audit plan to ensure the accuracy of non-clinical safety/toxicology studies trial data and compliance with legal and corporate standards. By conducting audits of our external vendors (GLRP, GLP and GcLP) and internal trial management processes, you identify the findin