Job Description
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.
Contact Detail:
Tandem Project Management Ltd. Recruiting Team