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 / Beneficios Benefits package

Permanent position

Hybrid work

Adaptable 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