Experteer Overview In this role you will support global 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 general scale within a leading pharmaceutical company. Compensaciones / Beneficios
• 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 Responsabilidades
• 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 Requisitos principales
• benefits package
• hybrid work arrangement
• temporary contract
• flexible start times
• schedule: Mon-Thu and Fri hours

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