Director Of Validation

Director of CQV

Introduction

Join a global leader in pharmaceutical manufacturing during a time of rapid growth and investment. We are currently seeking an experienced CQV Director to lead and deliver large-scale commissioning, qualification, and validation (CQV) initiatives, with a strong focus on capital projects , regulatory compliance, and GMP readiness.

This is a high-impact leadership role critical to ensuring operational excellence and regulatory compliance during facility builds, expansions, and major equipment installations.

This Role Will Offer You

• Leadership of CQV strategy across multi-million-dollar capital projects
• A collaborative, cross-functional team environment spanning Quality, Engineering, and Manufacturing
• Influence over GMP site readiness and long-term validation frameworks
• Competitive salary, bonus structure, and a comprehensive benefits package
• A chance to shape CQV standards at a growing, innovation-driven organization

You Will Be Responsible For

You Will Bring the Following

Please feel free to Email me at devon.nzepuome@biotalent.com

BioTalent Ltd are acting as an employment agency in relation to this opportunity.