Location
barcelona, cataluña, Spain
Posted
July 06, 2026
Job Description
Summary
In this role you will lead, support and report independent GCP/PV audits and approve follow-up corrective and preventive activities according to the Novartis Quality Systems and Standards, Good Clinical Practice(GCP)/Good Pharmacovigilance Practice(GPvP) and the current GCP/PV regulations. You will provide GCP/PV related quality guidance and assist in the identification and implementation of quality assurance training needs for Global GxP Audit and other business partners.
The audits performed on behalf of General GxP Audit include all audit types across GCP and PV disciplines including internal and external targets.
About the Role
In this role you will be required to travel up to 60% of time.
Major accountabilities
- Plan, lead, conduct, document, report and follow-up of GCP/PV audits according to the requirements specified in the respective Novartis procedures as well as applicable regulations, standards, quality agreem...