Biomapas
11 months ago
Sr. QPPV Office (QPO) Specialist
Sign up to save this job, get alerts, and apply with an optimized CV.
Company information
- Company
- Biomapas
- Location
- Polska Poland
- Posted
- 11 months ago
Job description
Join our global Pharmacovigilance team as a Sr. QPPV Office (QPO) Specialist. Sr. QPPV Office (QPO) Specialist is responsible for the development of pharmacovigilance systems, and the oversight of end-to-end pharmacovigilance activities and projects’ compliance with Quality Management System as well as the reporting and exchanging of safety and pharmacovigilance information for medicinal products. Position is in any EU country. Responsibilities: Manage full Pharmacovigilance systems and projects; Ensure compliance with Quality Management System; Develop and maintain pharmacovigilance systems; Oversee end-to-end pharmacovigilance activities and projects; Report and exchange safety and pharmacovigilance information for medicinal products.
Required skills
Interested in this position?
Create your free account and tailor your CV to match this job.