Senior Global PV Policy, Regulation and Compliance manager, Deputy QPPV (EU)

At Elanco (NYSE: ELAN) – it all starts with animals!

As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.

At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.

At Elanco, we pride ourselves on fostering a diverse and inclusive work environment.

We believe that diversity is the driving force behind innovation, creativity, and overall business success.

Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.

Making animals’ lives better makes life better – join our team today!

The Senior Global PV Policy, Regulation and Compliance manager and deputy QPPV for the EU supports the Global Pharmacovigilance (GPV) organization and the Qualified Person for Pharmacovigilance (QPPV) to maintain and advance the global PV system concerning procedure, training, audit/inspection, PV agreements/contracts, compliance management related tasks, and regulatory requirements (e.g.

Pharmacovigilance System Master File (PSMF)) and communication.

The Senior Global PV Policy, Regulation and Compliance manager and deputy QPPV (EU) coordinates or performs the activities within the department and is in contact with the described interfaces of other departments.

By executing the tasks described, the Senior Global PV Policy, Regulation and Compliance manager and deputy QPPV (EU) is continuously challenging the existing processes and defined workflows and is seeking creative, new solutions to improve compliance, efficiency and effectiveness.

Deputizes for the EU and UK QPPV, in its absence, for EU related QPPV responsibilities.

 

Your responsibilities:


* 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

What You Need to Succeed (minimum qualifications):


* Degree in Veterinary Medicine and at least 3-years experience in regulated industry, preferably in the area of pharmacovigilance


* Knowledge of the processes and regulatory requirements in Veterinary Pharmacovigilance, particularly for the EU


* Located in the EU


* Good English languag...