
Pharmacovigilance QA Specialist
- Sant Cugat del Vallès, Barcelona
- Permanente
- Tiempo completo
- You will conduct audits according to plan established to support compliance with good pharmacovigilance practices (GVP).
- You will work with Global Pharmacovigilance (GPV) Staff to resolve audit findings and offer suggestions for improvement.
- You will manage deviations and CAPAs.
- You will support and advise the Pharmacovigilance staff regarding compliance issues within the area of expertise.
- You will support the review of SOPs and documentation generated by GPV.
- You have a Bachelor's degree in Health Sciences. Specialization in pharmacovigilance and/or audits is a plus.
- You have 3 to 5 years of experience in pharmacovigilance and/or audits within a pharmaceutical company
- You have advanced English proficiency (C1.1)
- You are proactive, a team player and have strong written and oral communication skills.
- You are rigorous and analytical.