Global PV Policy & Compliance Lead - EU/QPPV Deputy

Elanco; Antwerpen; On-site; EUR 90,000 - 130,000; Full time

Job summary

Elanco in Belgium seeks a Senior Global PV Policy, Regulation and Compliance manager and deputy QPPV for the EU to support GPV and ensure compliance across PV systems, procedures, training, audits, and regulatory interfaces.

This role deputizes for EU/UK QPPV, leads GPV compliance, manages PVAs and regulatory interactions, and collaborates with Quality and external partners to drive continuous improvement in pharmacovigilance processes.

Qualifications

• Degree in Veterinary Medicine and at least 3 years experience in regulated industry, preferably in pharmacovigilance
• Knowledge of Veterinary Pharmacovigilance regulations and EU requirements
• EU residency or location in EU
• Good English language skills

Responsibilities

• Manage GPV procedures, training curricula, and onboarding/offboarding activities
• Support Pharmacovigilance Agreements 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 and handle regulatory authority interactions
• Provide strategic PV guidance and support benefit-risk monitoring activities
• Contribute to continuous improvement and compliance initiatives across Global Pharmacovigilance

Skills

Regulatory compliance

Pharmacovigilance

Stakeholder communication

Leadership

Education

Veterinary Medicine degree

3+ years regulated industry experience

Job description

Elanco in Belgium seeks a Senior Global PV Policy, Regulation and Compliance manager and deputy QPPV for the EU to support GPV and ensure compliance across PV systems, procedures, training, audits, and regulatory interfaces.

This role deputizes for EU/UK QPPV, leads GPV compliance, manages PVAs and regulatory interactions, and collaborates with Quality and external partners to drive continuous improvement in pharmacovigilance processes.