Overview In this role you will support integral pharmacovigilance for Grifols’ investigational and marketed products, ensuring high-quality safety deliverables and timely regulatory reporting. You will manage safety data in the worldwide PV database and contribute to audits, training, and SOP updates. You will work with cross-functional teams to review literature and keep PV practices compliant. This is an opportunity to impact patient safety at a global scale within a leading pharmaceutical company. Compensaciones / Beneficios * benefits package * hybrid work arrangement * temporary contract * flexible start times * schedule: Mon-Thu and Fri hours Responsabilidades * Process adverse event reports for Grifols marketed products,



including follow-up with reporters * Compile and reconcile information for pharmacovigilance documentation to meet regulatory requirements * Review weekly literature and updates in PV legislation * Ensure archiving of deliverables and documents * Prepare and contribute to periodic safety update reports * Support audits and inspections; provide training per plan * Assist in updates to SOPs and working practices * Operate PV databases, including data extraction and ensuring data integrity and configuration updates Requisitos principales * Bachelor in Health Sciences * 1-2 years of experience in a similar pharma role (CRO or company) * Knowledge of MS Office and SAP * Advanced level of English * Attention to detail * Training/educational delivery * Team collaboration * MS Office * SAP * Pharmacovigilance databases

📌 Technical Drug Safety Officer (San Cugat del Vallés)
🏢 Grifols
📍 San Cugat del Vallés