About the RoleWe are seeking a detail-oriented and proactive Pharmacovigilance (PV) professional to support day-to-day safety operations within a global pharmaceutical environment. This is a hands-on, operational role focused on ensuring the quality and compliance of outsourced case processing activities. The successful candidate will join a collaborative team and contribute to maintaining high standards in patient safety reporting.Key ResponsibilitiesPerform quality reviews of Individual Case Safety Reports (ICSRs) processed by external vendorsSupport literature screening activities and ensure accurate documentationMaintain compliance with global pharmacovigilance regulations and internal SOPsCollaborate with cross-functional teams to ensure timely and accurate safety data handlingAssist in audit readiness and regulatory inspectionsContribute to continuous improvement initiatives within PV operationsRequirementsBachelor’s degree in Life Sciences or a related field1–3 years of experience in pharmacovigilance (PV), ideally in a case processing capacitySolid understanding of adverse event reporting and PV regulationsHands-on experience with Argus Safety DatabaseStrong attention to detail and organizational skillsAbility to work independently and manage multiple prioritiesExcellent communication skills in English; French is a cultural asset