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 / Ventajas 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