C&Q Engineer (Commissioning & Qualification) – 12 Month Contract
The Role
As a C&Q Engineer, you will support commissioning and qualification activities across critical GMP systems, ensuring readiness for handover and operational start-up. Roles are available across varying experience levels.
Key Responsibilities
• Support commissioning and qualification execution across equipment, utilities and facility systems.
• Author and execute C&Q documentation including protocols, test scripts, traceability matrices and turnover packs.
• Drive system walkdowns, punch-list management, vendor interaction and field verification activities.
• Ensure all work is completed to cGMP standards with strong quality and documentation practices.
Requirements
• Degree in Engineering, Science or a related discipline (or equivalent experience).
• Experience in CQV / commissioning / qualification within pharma, biotech or medical device environments.
• Strong understanding of GMP systems and project delivery in fast-paced builds.