Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
JobTailor Logo

See all jobs on JobTailor

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Zoetis

PV Medical Manager – Deputy QPPV

Zoetis

Contribute to global pharmacovigilance operations at Zoetis, focusing on regulatory compliance and data analysis. Collaborate with teams on trending reports and safety evaluations for veterinary pharmaceuticals.

Posted 6/24/2026full-timeRemote • 🇪🇸 SpainMid-LevelSeniorWebsite

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
pharmacovigilancedata analysisreportingregulatory submissiontrending reportssignal managementpolicy designadverse drug event reporting
Soft Skills
interpersonal skillsability to work under pressurecollaborationcommunication
Tools & Technologies
pharmacovigilance electronic systemdatabase software
Certifications & Qualifications
Veterinary Medicine (DVM, VMD)
Industry Keywords
Veterinary Pharmaceutical IndustryEuropean Union regulationsFDAUSDA

About the role

Key responsibilities & impact
  • Contributor to a Global Team with collective responsibility for regulatory activities associated with global pharmacovigilance
  • Collaborate with signal management team regarding validation activities for assigned products
  • 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
  • Function as Pharmacovigilance subject matter expert for assigned product group(s)
  • Provide pharmacovigilance input for advertising and promotional material

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
  • 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
  • Strong interpersonal skills
  • Ability to work under pressure and in a highly matrix environment is essential
  • Experience with database software and pharmacovigilance systems is desirable

Benefits

Comp & perks
  • Competitive healthcare and retirement savings benefits
  • Array of benefits, policies, and programs to support employee well-being