Overview

In this role you support global pharmacovigilance for Grifols investigational and marketed products, ensuring high-quality safety deliverables within regulatory timelines. You will manage safety data, support audits and inspections, and maintain the PV database to ensure data integrity. You work closely with cross-functional teams to uphold compliance and training. This position offers exposure to a leading pharma group with a strong commitment to diversity and professional development.

Compensaciones / Incentivos

- Benefits package
- Permanent position
- Hybrid work
- Flexible schedule
- Career development opportunities

Responsabilidades

- Process adverse event case reports for marketed products, including follow-up with reporters
- Prepare documentation required by pharmacovigilance legislation and periodic safety update reports




- Review weekly literature and regulatory updates; ensure archiving and document control
- Support audits/inspections and deliver training per plan
- Maintain PV database data quality, perform data extraction queries, and assist with database configuration updates
- Assist in SOP and working practice updates
- Ensure legal/regulatory compliance of pharmacovigilance tasks

Requisitos principales

- Bachelor in Health Sciences (Pharmacy, Biology, Chemistry)
- 1–2 years of experience in pharma (CRO or pharmaceutical company)
- knowledge of MS Office and SAP
- advanced level of English

- Attention to detail
- Knowledge sharing and training
- Regulatory/quality mindset
- MS Office
- SAP
- PV database management

📌 Drug Safety Officer (Barcelona)
🏢 Grifols
📍 Barcelona