Job Description
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...
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Submit ApplicationJob Details
- Location Chiyoda City, Tokyo
- Job Type Full-time
- Category Computer Occupations
- Posted Date July 05, 2026
- Application Deadline August 14, 2026