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- Tasks: Lead CQV activities for a cutting-edge manufacturing facility and ensure compliance with GMP standards.
- Company: Join Eblex Group, a leader in innovative pharmaceutical solutions.
- Benefits: Competitive pay, flexible working options, and opportunities for professional growth.
- Other info: Fast-paced environment with a chance to make a real impact on large-scale projects.
- Why this job: Be part of a groundbreaking project that shapes the future of manufacturing.
- Qualifications: Experience in CQV within pharma or biotech and strong knowledge of GMP regulations.
The predicted salary is between 50000 - 70000 £ per year.
Eblex Group is supporting a new greenfield CMO facility build in the UK and is seeking experienced CQV Engineers / Consultants to support the commissioning, qualification, and validation of a state-of-the-art manufacturing site. This is a high-impact contract opportunity to be involved from early-stage build through to facility readiness and GMP manufacturing, working on complex systems in a fast-paced project environment.
Scope of Work for the CQV Engineer:
- Execute Commissioning, Qualification, and Validation (CQV) activities across facility, utilities, and equipment
- Support development and execution of IQ/OQ/PQ protocols
- Lead qualification of clean utilities, HVAC systems, and process equipment
- Ensure all activities align with GMP and regulatory requirements
- Work closely with Engineering, Quality, and Project teams to meet key project milestones
- Support documentation, deviation management, and validation lifecycle activities
What We’re Looking For in a CQV Engineer:
- Proven experience in CQV within pharmaceutical, biotech, or CMO environments
- Strong background in greenfield or large-scale facility build projects
- Experience with clean utilities, HVAC, and GMP manufacturing equipment
- Strong understanding of EU GMP, Annex 1, and validation principles
- Ability to operate in a fast-paced, project-driven environment
- Excellent documentation and stakeholder coordination skills
This search is being conducted by Eblex Group. For confidential consideration, please apply directly or contact Eblex Group to learn more about the opportunity.
CQV Engineer in England employer: Eblex Group
Contact Detail:
Eblex Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CQV Engineer in England
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who have experience in CQV roles. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and project experiences. Be ready to discuss specific CQV activities you've led, especially in greenfield projects, as this will show you're the right fit for the fast-paced environment.
✨Tip Number 3
Showcase your documentation skills! Bring examples of your previous work, like IQ/OQ/PQ protocols or deviation management records, to demonstrate your attention to detail and compliance with GMP standards.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people at Eblex Group. Plus, it shows you’re proactive and serious about landing that CQV Engineer role.
We think you need these skills to ace CQV Engineer in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience in CQV, especially in pharmaceutical or biotech environments. We want to see how your background aligns with the specific requirements of the CQV Engineer role.
Showcase Relevant Projects: When writing your application, don’t forget to mention any greenfield or large-scale facility build projects you've worked on. We love seeing concrete examples of your experience with clean utilities and HVAC systems!
Highlight Compliance Knowledge: Since this role involves ensuring compliance with GMP and regulatory requirements, be sure to emphasise your understanding of EU GMP, Annex 1, and validation principles. This will show us you’re the right fit for the job.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It’s the best way for us to receive your application and get you one step closer to joining our team!
How to prepare for a job interview at Eblex Group
✨Know Your CQV Basics
Make sure you brush up on your knowledge of Commissioning, Qualification, and Validation processes. Be ready to discuss your experience with IQ/OQ/PQ protocols and how you've applied them in previous roles. This will show that you understand the core responsibilities of a CQV Engineer.
✨Familiarise Yourself with GMP Standards
Since this role involves working within GMP environments, it’s crucial to have a solid grasp of EU GMP guidelines, especially Annex 1. Prepare to talk about how you've ensured compliance in past projects and any challenges you faced while adhering to these standards.
✨Highlight Your Project Experience
Be prepared to share specific examples from your experience in greenfield or large-scale facility builds. Discuss the complexities you encountered and how you collaborated with engineering and quality teams to meet project milestones. This will demonstrate your ability to thrive in fast-paced environments.
✨Show Off Your Documentation Skills
Documentation is key in CQV roles, so be ready to discuss your approach to maintaining accurate records and managing deviations. Share examples of how your documentation practices have contributed to successful validation lifecycle activities, as this will highlight your attention to detail and organisational skills.