PV Medical Manager – Deputy QPPV

This is a fully remote position, open to applicants in Spain.

📋 Description

• Member of a Global Team sharing responsibility for regulatory tasks related to global pharmacovigilance.

• Work in conjunction with the signal management team on validation activities for designated products.

• Generate trending reports for assigned marketed products to pharmacovigilance stakeholders.

• Offer insights during negotiations with regulatory bodies concerning the submission of ADE reports.

• Support the development of pharmacovigilance policies as required.

• Aid in the upkeep of a pharmacovigilance electronic system.

• Act as the pharmacovigilance subject matter expert for designated product group(s).

• Contribute pharmacovigilance insights for advertising and promotional materials.

⛳️ Requirements

• A minimum qualification of a Veterinary Medicine degree (DVM, VMD).

• At least 5 years of experience in the Veterinary Pharmaceutical Industry, including veterinary pharmacovigilance within the European Union.

• Essential ability to review and analyze pharmacovigilance data for the development of trending reports.

• Knowledge of FDA/USDA and international regulations regarding Adverse Drug Event (ADE) reporting is advantageous.

• Excellent interpersonal skills.

• Capability to perform under pressure and thrive in a highly matrixed environment is crucial.

• Experience with database software and pharmacovigilance systems is preferred.

🏝️ Benefits

• Competitive healthcare and retirement savings benefits.

• A wide range of benefits, policies, and programs aimed at supporting employee well-being.