Appealing Points:

• Lead Quality & Compliance in Global Pharma IT – Ensure GxP compliance, computer system validation, and data integrity across complex global IT systems and regulated processes.


• Drive Regulatory Excellence – Lead validation oversight, audit readiness, and quality governance while ensuring compliance with 21 CFR Part 11 and global pharmaceutical standards.


• Influence Enterprise-Wide Quality Initiatives – Partner with cross-functional global teams to improve validation processes, q...