Overview In this role you support general 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. Permanent position Hybrid work Prepare documentation required by pharmacovigilance legislation and periodic safety update reports Support audits/inspections and deliver training per plan Maintain PV database data quality, perform data extraction queries, and assist with database configuration 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 Knowledge sharing and training Regulatory/quality mindset MS Office SAP PV database management

📌 EHS Advisor (Pharma) (Barcelona)
🏢 Grifols
📍 Barcelona