PV Medical Manager – Deputy QPPV

Zoetis

Contributor to global pharmacovigilance activities involving ADE reporting and regulatory compliance at Zoetis. Requires veterinary degree and experience in veterinary pharmaceutical industry.

Posted 6/24/2026full-time🇪🇸 SpainMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

Contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance
Good understanding of the ADE reporting regulations (US and EU)
Collaborate with signal management team regarding validation activities for assigned products (including signal detection)
Prepare trending reports of assigned marketed products to the pharmacovigilance stakeholders
Provide input for negotiations with regulatory agencies regarding submission of ADE reports
Assist in the design pharmacovigilance policies as needed
Assist in the maintenance of a pharmacovigilance electronic system from a data capture, trend analysis and regulatory submission perspective
Function as Pharmacovigilance subject matter expert for assigned product group(s)
Provide pharmacovigilance input for advertising and promotional material upon request
Risk Mitigation in support of Global Manufacturing and Quality and Regulatory label defense activities
Complete PV Data requests and Health Hazard Assessments for assigned products upon request
Act as Deputy EU/UK QPPV

Requirements

What you’ll need

Minimum requirement of a Veterinary Medicine (DVM, VMD)
5 or more years of experience in Veterinary Pharmaceutical Industry including veterinary pharmacovigilance in the European Union
Additional graduate degree or diploma in animal science and/or epidemiology or related experience is a plus
Ability to review and analyze pharmacovigilance data to develop trending reports is essential
Knowledge of the FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting is a benefit
Experience with database software and pharmacovigilance systems is desirable.

Benefits

Comp & perks

No bonuses or specific perks mentioned in the job announcement.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

pharmacovigilanceADE reportingsignal detectiondata analysistrending reportsrisk mitigationHealth Hazard Assessmentsregulatory submissionpharmacovigilance policiessubject matter expert

Soft Skills

collaborationcommunicationnegotiationorganizational skillsattention to detail

Certifications

DVMVMD