Job summary
This senior role supports global pharmacovigilance operations by managing policies, regulatory compliance, training, and audits within animal health. The position serves as deputy Qualified Person for Pharmacovigilance (QPPV) for the EU, contributing to continuous improvement and regulatory oversight. A veterinary degree and experience with veterinary pharmacovigilance regulations in the EU are required. The role is based in the EU and involves collaboration across departments and with external authorities, primarily conducted in English.
Location and work setup
- Location
- Norway
- Work setup
- On-site
Responsibilities
Oversee and update global pharmacovigilance procedures and training programs, coordinate onboarding and offboarding within the department. Manage pharmacovigilance agreements lifecycle and compliance tracking. Lead compliance reporting and communication with stakeholders. Support audits, inspections, corrective actions, and maintenance of the Pharmacovigilance System Master File. Act as liaison between pharmacovigilance, quality teams, and external partners. Serve as deputy EU/UK QPPV, including liaising with regulatory authorities and providing strategic pharmacovigilance guidance. Drive continuous compliance improvement initiatives across global pharmacovigilance.
Qualifications
Veterinary Medicine degree with minimum three years' experience in a regulated industry, preferably in veterinary pharmacovigilance within the EU. Solid knowledge of EU veterinary pharmacovigilance regulations and processes. Fluent in English with strong decision-making skills. Experience managing compliance projects, interacting with regulatory authorities, and handling audits and inspections is desirable. Ability to work independently, under pressure, and coordinate complex projects in a multicultural team environment.