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PV Medical Manager – Deputy QPPV
ZoetisDeputy QPPV in global pharmacovigilance team at Zoetis focusing on regulatory activities and product safety. Collaborating on signal management, preparing reports, and ensuring regulatory compliance.
About the role
Key responsibilities & impact- Contribute to regulatory activities associated with global pharmacovigilance
- Collaborate with signal management team regarding validation activities
- Prepare trending reports of assigned marketed products
- Provide input for negotiations with regulatory agencies
- Assist in the design of pharmacovigilance policies
- Maintain pharmacovigilance electronic systems
- Function as subject matter expert for assigned product group(s)
Requirements
What you’ll need- Minimum requirement of a Veterinary Medicine (DVM, VMD)
- 5+ years of experience in Veterinary Pharmaceutical Industry
- Knowledge of FDA/USDA regulations on ADE reporting
- Strong understanding of ADE reporting regulations (US and EU)
- Experience with database software and pharmacovigilance systems
- Ability to review and analyze pharmacovigilance data
Benefits
Comp & perks- Global team collaboration
- Professional development opportunities
- Flexible work environment
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
pharmacovigilanceADE reportingdata analysisregulatory compliancesignal managementtrending reportspolicy designdatabase softwarepharmacovigilance systems
Soft Skills
collaborationnegotiationsubject matter expertise
Certifications
Veterinary Medicine (DVM, VMD)