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 / Incentivos

- 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 (Barcelona)
🏢 Grifols
📍 Barcelona