Experteer Overview
In this role you will support Global Pharmacovigilance (GPV) and deputize the EU QPPV, ensuring the PV system aligns with regulatory requirements. You will manage procedures, training, and onboarding/offboarding, and oversee PVAs, PSMF, audits, and CAPA activities. You’ll act as a key interface between GPV, Quality, and external partners, driving continuous improvement and compliant operations. The role offers the chance to shape pharmacovigilance processes at a global level while maintaining strong regulatory relationships in the EU. This is a chance to contribute to safer animal health products and robust compliance culture.

Compensaciones / Ventajas
• Manage GPV procedures, training curricula, and onboarding/offboarding activities
• Support Pharmacovigilance Agreements (PVAs) lifecycle management and compliance oversight
• Coordinate GPV compliance reporting, metrics, and stakeholder communication




• Support GPV audits, inspections, CAPA management, and PSMF maintenance
• Act as a key interface between GPV, Quality, and external partners
• Deputize for the EU/UK QPPV when required, including regulatory authority interactions and PV oversight
• Provide strategic PV guidance and support benefit-risk monitoring activities
• Contribute to continuous improvement and compliance initiatives across Global Pharmacovigilance

Responsabilidades
• Degree in Veterinary Medicine
• at least 3-years experience in regulated industry
• Knowledge of processes and regulatory requirements in Veterinary Pharmacovigilance, EU focus
• Located in the EU
• Good English language skills

Requisitos principales
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📌 Senior Global PV Policy, Regulation and Compliance manager, Deputy QPPV (EU) (Madrid)
🏢 Elanco
📍 Madrid