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Hellerup, Capital Region of Denmark, Denmark permanent
LeadershipComplianceRegulatory AffairsPatient SafetyGlobal Project ExecutionCommunicationQuality AssuranceRisk ManagementVendor CoordinationStrategic Planning

Are you passionate about leading Affiliate PV activities, quality processes and patient safety? Do you have experience with incorporating local PV needs into global systems, close involvement with mul...

March 24, 2026 View Details

QPPV Specialist

Eva Pharma

Riyadh, Riyadh Province, Saudi Arabia permanent
PharmacovigilanceSignal DetectionAudit ParticipationICSR ProcessingMedDRA CodingRMPPSMFKSA PV RegulationsCAPA Planning

Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are com...

December 18, 2025 View Details
Spain - Barcelona permanent
Pharmaceutical industry experienceRegulatory Project ManagementPhysical InspectionsContinuous improvementProject managementPV legislationPV system governance

The Senior director QPPV deputises for the EU Qualified Person for Pharmacovigilance (QPPV), assuming QPPV responsibilities during their absence. Execute EU QPPV responsibilities for a portfolio of as...

February 27, 2026 View Details
3 Locations permanent
Regulatory CompliancePFEP ManagementAudits and InspectionsRegulatory UpdatesDocumentation SystemsTime ManagementPharmacovigilance RegulationsQPPV OversightEUQPPV CollaborationPV Inspection Readiness

Position Purpose The QPPV Compliance Director supports the activities of European Union Qualified Person for Pharmacovigilance (EUQPPV) and the European Safety Office and guarantees the oversight of ...

February 25, 2026 View Details
Belgrade, , Serbia Hybrid permanent
PharmacovigilanceComplianceSOP DevelopmentICSR ManagementLiterature ReviewSafety ReportingAudit ManagementRegulatory Change ManagementRisk Management

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable imp...

February 13, 2026 View Details
Poland Remote permanent
Pharmacovigilance SystemsQuality Management SystemRegulatory ComplianceRisk ManagementPSURsRisk MinimizationSurveying RegulationsTrainingCommunication with AuthoritiesMedical WritingComputer LiteracyMS Office

Join our global Pharmacovigilance team as a Sr. QPPV Office (QPO) Specialist. Sr. QPPV Office (QPO) Specialist is responsible for the development of pharmacovigilance systems, and the oversight of end...

January 19, 2026 View Details
Czechia Remote permanent
PharmacovigilanceRegulatory ComplianceQuality Management SystemsSafety Information ExchangeDatabase OperationsRisk MinimizationLiterature ReviewTraining DeliveryAttention to DetailTechnological Adaptation

Join our global Pharmacovigilance team as a Junior QPPV Office (QPO) Specialist . Junior QPPV Office (QPO) Specialist supports the QPPV Office and Pharmacovigilance (PV) department by ensuring complia...

January 19, 2026 View Details