PV Medical Manager – Deputy QPPV
Zoetis
full-time
Posted on:
Location Type: Remote
Location: Portugal
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About the role
- 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
- 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
- Knowledge of the FDA/USDA and international regulations on Adverse Drug Event (ADE) reporting
- Strong interpersonal skills
- Ability to work under pressure and in a highly matrix environment
- Experience with database software and pharmacovigilance systems
Benefits
- Health insurance
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
pharmacovigilancedata analysisreportingregulatory submissionsignal managementtrending reportspolicy designadverse drug event reporting
Soft Skills
interpersonal skillsability to work under pressurecollaborationcommunication
Certifications
Veterinary Medicine (DVM, VMD)