QPPV

We’re looking for an experienced QPPV to lead and oversee our Pharmacovigilance (PV) system and ensure the highest standards of patient safety and regulatory compliance. In this pivotal role, you will be the key expert responsible for the safety of our marketed products and the integrity of our global PV operations. What You’ll Do Serve as the designated QPPV for EU/UK market authorisations Maintain full oversight of the PV system and PSMF, ensuring inspection readiness Monitor product safety profiles, lead signal management, and guide benefit–risk decisions Oversee AE case management, compliance metrics, PSURs, RMPs, and safety deliverables Act as the main contact for health authorities and internal/external partners Support audits, inspections, and continuous improvement of PV processes Provide leadership to PV teams and ensure robust PV training across the organisation

What You Bring Degree in Life Sciences, Pharmacy, or Medicine 5+ years in PV, ideally with QPPV or Deputy QPPV experience Deep knowledge of EU GVP, ICH guidelines, and global PV regulations Strong communication, leadership, and decision-making skills Ability to manage complex safety issues with clarity and scientific rigor Fluency in English; additional European languages are a plus

Why This Role High-impact leadership position at the core of patient safety Opportunity to shape a global PV system within a collaborative, science-driven environment Competitive package and long-term growth potential