QA Specialist CSV

Fidel Consulting KK • Chiyoda City, Tokyo • Posted July 12, 2026

About the Role

 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...