Company Profile:
We have an outstanding opportunity for a CQV Engineer to join our world renowned client on an initial 12-month contract. The site prides itself on being on the forefront of cutting‑edge multi-product capabilities and has seen sizeable investment recently. The company consistently ranks high in Great Place to Work and top workplace lists across the pharma and healthcare sector and promotes a positive and inclusive environment.
If interested, don't hesitate to reach out today for more info.
Job Summary:
The person be expected to work independently or as part of a cross-functional CQV team to author and execute qualification protocols, manage deviations, and support system handover for GMP operations. It would involved Commissioning & Qualification of equipment and utilities in a drug substance manufacturing environment.
Key Responsibilities:
• Deliver end-to-end CQV lifecycle documentation: URS, DQs, FAT/SAT, IQ, OQ, and support for PQ where applicable.
• Perform equipment and system commissioning, including verification of installation, utilities integration, control functionality, and safety systems.
• Lead CQV efforts on systems including (but not limited to):
- Bioreactors and single-use technologies
- Chromatography Columns
- Clean-in-place (CIP) and steam-in-place (SIP) systems
- WFI, clean steam, and process gases
- Process tanks, skids, and associated piping
• Conduct impact assessments, risk assessments (e.g. ASTM E2500), and define appropriate qualification strategies.
• Liaise with vendors, automation, engineering, and quality functions to coordinate execution and resolve issues.
• Support and lead the resolution of deviations, non-conformances, and change controls related to CQV scope.
• Maintain up-to-date and compliant documentation in line with GMP and data integrity requirements.
• Provide progress updates and contribute to system readiness reviews and handover milestones.
Required Experience & Qualifications:
• Bachelor’s degree in Engineering, Life Sciences, or related technical field.
• Minimum 5 years’ CQV experience in a GMP-regulated drug substance or biologics manufacturing environment.
• Demonstrated hands-on experience with commissioning and qualification of:
- Large-scale bioprocess equipment
- Utility systems (WFI, HVAC, compressed gases, clean steam)
- Automation-integrated equipment (DeltaV)
• Deep understanding of CQV best practices, ISPE Baseline Guides, GAMP 5, and ASTM E2500.
• Experience working on capital projects, preferably from construction to handover.
• Ability to work independently on protocol development, execution, and resolution management.
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