OverviewIn this role you will support general 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 / Beneficiosbenefits package
hybrid work arrangement
temporary contract
flexible start times
schedule: Mon-Thu and Fri hours
ResponsabilidadesProcess 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 principalesBachelor 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 (España)
🏢 Grifols
📍 España