Your responsibilities include but are not limited to:

• Supports the preparation and coordination of Annual Product Quality Review activities in accordance with Novartis procedures.
• Supports third-party management activities and related compliance processes.
• Contributes to the implementation and continuous improvement of Quality Systems.
• Participates in on-site health authority inspections and customer audits.
• Supports continuous improvement initiatives within the QA Compliance department.
• Supports CAPA tracking as well as the preparation, reporting, and review of QA department metrics, including Monthly Quality Reports and KPI reports.
• Collaborates with cross‑functional teams across Manufacturing and Quality Management.
• Ensures that all assigned activities and projects are performed in compliance with cGxP requirements, including data integrity principles.

Minimum requirements