Global Pharmacovigilance Specialist - Data & Safety

Grifols; Barcelona; On-site; EUR 45,000 - 65,000; Full time

Job summary

Grifols in Barcelona, Spain, is hiring a Technical Drug Safety Officer to join our global pharmacovigilance team. You will support safety data collection, processing and reporting for Grifols investigational and marketed products, ensuring high quality deliverables and regulatory timelines.

The ideal candidate holds a Bachelor’s in Health Sciences (Pharmacy/Biology/Chemistry), with 1–2 years in pharma, and strong English plus proficiency in MS Office and SAP.

Qualifications

• Bachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry) and ideally a Master or Postgraduate in pharma/PV.
• 1–2 years of experience in a similar pharma role (CRO or company) is highly valued.
• Knowledge of MS Office and SAP; advanced English.

Responsibilities

• Participate in safety data collection, review, processing, evaluation and compilation.
• Process adverse event reports for marketed products and conduct follow-up with reporters.
• Prepare documentation for PV legislation and regulatory reporting timelines.
• Review weekly literature and PV legislation updates; ensure archiving compliance.
• Prepare periodic safety update reports; ensure data quality and database integrity.
• Support audits and inspections and provide PV training as needed.

Skills

Advanced English

PV knowledge

Education

Bachelor’s in Health Sciences

Master in pharmaceutical sector

Tools

MS Office

SAP

Job description

Grifols in Barcelona, Spain, is hiring a Technical Drug Safety Officer to join our global pharmacovigilance team. You will support safety data collection, processing and reporting for Grifols investigational and marketed products, ensuring high quality deliverables and regulatory timelines.

The ideal candidate holds a Bachelor’s in Health Sciences (Pharmacy/Biology/Chemistry), with 1–2 years in pharma, and strong English plus proficiency in MS Office and SAP.