Summary:
We are seeking proactive and detail-oriented CQV Engineers to join our client’s biotechnology facility in North East England. Ideal candidates will bring hands-on experience with KNEAT software, strong knowledge of CQV principles, and a proven track record in coordinating complex commissioning activities across multiple vendors.
Responsibilities:
* Prepare, review, and approve CQV documentation using KNEAT in compliance with GMP and project requirements.
* Execute commissioning and qualification activities, including SAT coordination, vendor management, and punch closure.
* Support walkdowns, system turnovers, and alignment with project schedules and validation strategies.
* Ensure safety-first practices in all field activities and support safe system energization and equipment livening.
* Collaborate effectively within a large, cross-functional team to resolve issues and drive progress.
* Identify potential challenges early and contribute solution-focused ideas to ensure smooth project delivery.
Qualifications & Experience:
* Bachelor’s degree in Engineering or Science discipline
* Prior experience using KNEAT for CQV documentation lifecycle.
* Solid understanding of Commissioning, Qualification & Validation (CQV) methodologies and regulatory compliance.
* Demonstrated experience coordinating multi-vendor commissioning activities, especially during SAT phases.
* Strong attention to detail and ability to thrive in a fast-paced, start-up environment.
* Safety-conscious mindset with a proactive approach to risk identification and mitigation.
* Excellent communication and teamwork skills, capable of working within large professional teams.
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