PV Specialist-PV QA Audit

This role supports the Global Head of Pharmacovigilance Quality Assurance in defining and establishing a robust, integrated Quality Management System (QMS) for the PV function. The position involves driving the development and implementation of quality aspects, ensuring regulatory compliance, and managing audit preparations and third-party audits. Key duties include overseeing CAPA processes, facilitating cross-functional collaboration, and maintaining a contemporary knowledge of global PV regulations and industry standards.