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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
• 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 xqbhyrx

Responsabilidades
• 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

Requisitos principales
• Benefits package
• Permanent position
• Hybrid work
• Flexible schedule
• Career development opportunities

📌 Drug Safety Officer (San Cugat del Vallés)
🏢 Grifols
📍 San Cugat del Vallés