Are you an experienced CAPEX Project Manager looking to make a meaningful impact in a highly regulated, fast‑growing biopharmaceutical environment? Our client, a world-leading organisation dedicated to improving the lives of patients with rare and serious diseases, is expanding their capital project team and seeking a skilled professional to drive critical site developments.

About the Role

As CAPEX Project Manager, you will take the lead on the planning, execution, and coordination of major capital investment projects across a complex, GMP-regulated manufacturing site. You will manage all project-related activities from concept through to completion, collaborating closely with cross-functional stakeholders to ensure delivery on time, within budget, and in alignment with quality and regulatory expectations.

This position is central to enabling future capacity, enhancing operational efficiency, and ensuring compliance across a highly controlled environment.

Key Responsibilities

• Lead the end-to-end management of CAPEX projects, ensuring alignment to scope, schedule, cost, and quality requirements.
• Coordinate and collaborate with cross-functional teams including Engineering, Operations, Quality, Procurement, EHS, and external partners.
• Ensure all project deliverables are developed, reviewed, approved, and executed in accordance with internal standards and regulatory requirements (GMP).
• Serve as the primary point of contact for all internal and external stakeholders, ensuring clear communication, efficient decision-making, and strong risk management throughout project lifecycle.
• Oversee vendor selection, contract management, and performance monitoring.
• Manage project documentation, reporting, budget control, and change management activities.
• Ensure projects are delivered safely and compliantly, particularly within capacity-constrained and highly regulated environments.

About You

You will thrive in this role if you bring:

• Proven experience managing CAPEX projects in pharmaceutical, biotechnology, or other GMP-regulated manufacturing settings.
• Strong leadership skills with the ability to coordinate diverse stakeholder groups.
• Excellent organisational and communication capabilities, with a proactive approach to managing complexity and change.
• Deep understanding of GMP, engineering standards, and regulatory compliance requirements.
• Experience working within capacity‑constrained environments is a strong advantage.

Why Join?

• Opportunity to influence large-scale, business-critical projects in a globally recognised biopharmaceutical organisation.
• Work in an innovative environment where high standards and patient impact drive every decision.
• Engage with diverse teams and stakeholders, shaping the future of a rapidly expanding site.

If you are motivated by technical challenge, meaningful work, and the opportunity to deliver high-impact capital projects, we would love to hear from you.

Apply today or contact me directly for a confidential conversation.