Senior Global PV Policy, Regulation and Compliance manager, Deputy QPPV (EU)
Quick Summary
Manage GPV procedures, training curricula,
Requirements
~2 min read- 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
- 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!
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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.
Responsibilities
~1 min read- →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
Location & Eligibility
Listing Details
- First seen
- August 22, 2026
- Last seen
- August 22, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 49%
- Scored at
- August 22, 2026
Signal breakdown
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