C&Q Engineer

Join a cutting-edge pharmaceutical team where your precision and passion for engineering will help shape the future of life-saving medicines!

R&D Partners is seeking a CQ Validation Specialist to support key projects in a regulated manufacturing environment. This role involves ensuring that equipment, utilities, and systems meet required standards for quality and compliance. You will play a critical role in commissioning and qualification activities while adhering to GMP guidelines.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Test and validate laboratory systems, manufacturing equipment, and utilities.
• Assist with commissioning and qualification of clean utilities like purified water, WFI (water for injection), clean steam, and process gases.
• Support CAPEX projects by ensuring compliance with GMP regulations.
• Document and manage the qualification lifecycle activities.
• Collaborate with cross-functional teams to meet project milestones.

Key Skills and Requirements:

• A degree or equivalent qualification in Engineering, Life Sciences, or a related technical field.
• Hands-on experience in validation or engineering roles within pharmaceutical, biotechnology, or regulated manufacturing industries.
• Strong understanding of GMP (Good Manufacturing Practices) and qualification processes.
• Familiarity with laboratory systems, autoclave qualification, and clean utilities is an advantage.
• Flexibility to adapt working hours to meet project needs.

For more information, please contact Jack Keens.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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