Senior Pharmacovigilance Specialist – Belgium & Luxembourg

About the role

Join the Pharmacovigilance Department in Brussels to support PV activities for Belgium and Luxembourg. You will manage adverse event cases, local agreements and risk‑minimisation measures while collaborating with cross‑functional teams.

Key responsibilities

• Develop and maintain local PV procedures in line with regional standards.
• Manage day‑to‑day adverse event case processing and reporting.
• Negotiate and oversee local PV agreements and due‑diligence activities.
• Support audits, inspections and readiness activities, acting as contact for health authorities when required.

Required profile

• Master’s or bachelor’s degree in health, life science, medical science, regulatory affairs or equivalent.
• Minimum two years of industry experience in pharmacovigilance or regulatory affairs.
• Knowledge of PV regulations in Belgium and Luxembourg and experience interacting with auditors/inspectors.
• Fluency in French or Dutch (Dutch preferred) and working knowledge of the second language.

Required skills

• MS‑Office proficiency.
• Experience with IT applications used for PV data management.

What we offer

• Competitive salary and incentive bonus plan.
• 32 vacation days per year.
• Health insurance, excellent pension scheme and eco‑cheques.
• Hybrid working arrangement and various training modules for personal development.