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 global scale within a leading pharmaceutical company.
Compensaciones / Ventajas • 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 (Barcelona)
🏢 Grifols
📍 Barcelona