CQV Engineer

About the Company

A pharmaceutical manufacturing site operating in a regulated environment, with a focus on commissioning, qualification and validation (CQV) activities.

Why This Role Matters

Your work will help ensure manufacturing equipment and systems are qualified and fit for purpose, supporting reliable pharmaceutical production.

The Role

Deliver hands-on CQV activities across the manufacturing site, including autoclave qualification. You will support projects from planning and execution through to documentation and close-out.

Key Responsibilities

• Plan and execute commissioning, qualification and validation activities for manufacturing equipment and systems.
• Carry out autoclave qualification and related testing, documenting results and addressing any issues identified.
• Prepare and review CQV protocols, reports and project documentation, supporting delivery through to completion.

Required Skills & Experience

• Proven CQV experience within pharmaceutical manufacturing.
• Demonstrable track record of delivering CQV projects.
• Hands-on experience with autoclaves and their qualification or validation.

What’s on Offer

• The opportunity to deliver CQV work at a pharmaceutical manufacturing site.
• A hands-on engineering role with involvement across the CQV project lifecycle.