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

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 language skills **What will give you a competitive edge (preferred qualifications):** - Capable of working independently and making decisions autonomously - Compliance oriented with a strong quality mindset, capable of working under pressure and with short timelines - Ability to coordinate/ lead complex compliance related projects - Experience with interactions with competent authorities in the EU - Experience in participating in audits and authority inspections and follow-up activities - Experience in working effectively in teams and in a multi-cultural environment - Ability to comprehend interrelations and submit proposals for solutions. - Personal accountability and a strong drive for execution Don’t meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job‑related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our [Elanco Workforce Privacy Notice.](https://assets-us-01.kc-usercontent.com/4b590e03-b18a-00d2-ed1a-0ad79db125c5/96361b9e-3b96-484f-adce-f598d5be5024/Elanco%20Workforce%20Privacy%20Notice.pdf) ### (1) [**Global Pharmacovigilance Policy, Regulation and Compliance Manager (Fixed duration - 2 years)**](https://elanco.wd5.myworkdayjobs.com/en-US/External_Career/job/PL---Warszawa/Senior-Associate-R-D_R0026556-1) locations11 Locations time typeFull time posted onPosted 10 Days Ago Loading #### Follow Us - [LinkedIn](https://www.linkedin.com/company/elanco "LinkedIn") - [X](https://twitter.com/Elanco/ "X") - [Facebook](https://www.facebook.com/elancoanimalhealth/ "Facebook") © 2026 Workday, Inc. All rights reserved.