Summary: We are seeking proactive and detail-oriented CQV Engineers to join our clients 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: Bachelors 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.