Location
stein
Job Type
Full-time
Posted
July 07, 2026
Job Description
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.