Job Summary

• Lead and manage global compendial monitoring programs for clinical and commercial pharmaceutical products.
• Ensure ongoing compliance with international pharmacopoeia standards and analyze regulatory changes.
• Provide strategic insights, maintain regulatory readiness, and support product quality and compliance across multiple regions.

Matching Summary

Skills & Requirements

Key Requirements

• Requires GxP regulatory intelligence experience
• Requires experience with international pharmacopoeias
• Requires ability to assess impact of compendial updates
• Requires experience expanding monitoring programs

Work Rights