VIRBAC

About the Company

Caring for animals together At Virbac, we are constantly exploring new ways to prevent, diagnose and treat the majority of animal pathologies. We develop care, hygiene and nutrition products to offer complete solutions to veterinarians, farmers and pet owners around the world. Our purpose: advancing the health of animals with those who care for them every day, so we can all live better together. - 1,397 MEUR sales (+7.5% at constant exchange rates and scope compared to 2023) - 62% of Virbac's sales 2024 come from companion animal sector and 38% from farm animals sector - More than 60% of sales outside Europe - 6,400 employees within the Group - Production sites in 12 countries - Sales subsidiaries in 35 countries - R&D centers on 5 continents Terms of use and moderation rules: https://corporate.virbac.com/home/linkedin-terms-of-use.html

Listed Jobs

Company Name

VIRBAC

Job Title

Chargé(e) de Pharmacovigilance Administrateur BDD . F/H

Job Description

**Job Title** Pharmacovigilance Officer & Database Administrator (F/M) **Role Summary** Lead the day‑to‑day management of adverse event data and oversee the administration of a pharmacovigilance database. Ensure accurate, timely reporting to regulatory agencies, partners and internal stakeholders while maintaining data integrity and regulatory compliance. **Expectations** - Handle adverse event reception, prioritisation and communication with agencies, subsidiaries and partners. - Enter and retrieve data from the European EVVET database for import into the corporate system. - Distribute events to relevant entities, guaranteeing regulatory, contractual and internal deadlines. - Contribute to regulatory compliance through audits, inspections, internal meetings and quality documentation. - Administer the database: product management, access controls and incident handling. - Support database upgrade projects and coordinate with IT, regulatory and medical teams. - Actively participate in cross‑functional, international collaboration and user support in English. **Key Responsibilities** 1. Receive, prioritise, and register adverse events. 2. Query and import data from European EVVET. 3. Distribute events and ensure compliance with time‑frames. 4. Maintain audit trail and quality documentation. 5. Manage database users, permissions and incidents. 6. Participate in system version upgrades and project management. 7. Collaborate with regulatory, medical, IT, and corporate teams. **Required Skills** - Expertise in pharmacovigilance processes and EU regulations. - Database administration (products, access, incident handling). - Strong analytical and data quality focus. - Project coordination experience (optional but advantageous). - Excellent written and verbal communication. - Fluent in English; ability to engage with international stakeholders. - Team orientation, organizational discipline and proactive spirit. **Required Education & Certifications** - Engineer/Master in Life Sciences, Biochemistry, or Pharmacy. - Prior professional experience in a comparable pharmacovigilance or data‑management role. - Knowledge of European pharmacovigilance regulation is essential.

Carros, France

Hybrid

03-11-2025