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- Tasks: Lead the commissioning, qualification, and validation of a cutting-edge manufacturing facility.
- Company: Join Eblex Group, a leader in pharmaceutical engineering.
- Benefits: Competitive pay, career growth, and the chance to work on impactful projects.
- Other info: Fast-paced environment with opportunities for professional development.
- Why this job: Be part of a groundbreaking project that shapes the future of manufacturing.
- Qualifications: Experience in CQV within pharma or biotech environments is essential.
The predicted salary is between 40000 - 50000 £ 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.
Medical Engineer Full Time in England employer: Eblex Group
Contact Detail:
Eblex Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Engineer Full Time in England
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We can’t stress enough how important it is to make those personal connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their projects. We recommend practising common interview questions and tailoring your answers to highlight your CQV experience. Show them you’re not just a fit for the role, but also for their team culture!
✨Tip Number 3
Follow up after interviews! A simple thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from your conversation to remind them why you’re the perfect candidate for the CQV Engineer position.
✨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. Plus, we often have exclusive listings that you won’t find anywhere else, so keep an eye out for those!
We think you need these skills to ace Medical Engineer Full Time in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CQV Engineer role. Highlight your experience in commissioning, qualification, and validation, especially in pharmaceutical or biotech settings. We want to see how your background aligns with our needs!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to our greenfield CMO facility project. Keep it concise but impactful!
Showcase Relevant Experience: When detailing your experience, focus on specific projects where you’ve worked on clean utilities, HVAC systems, or GMP manufacturing. We love seeing concrete examples of your achievements and how they relate to the job!
Apply Through Our Website: Don’t forget to apply through our website for a smooth application process! It helps us keep track of your application and ensures you’re considered for this exciting opportunity with Eblex Group.
How to prepare for a job interview at Eblex Group
✨Know Your CQV Inside Out
Make sure you brush up on your knowledge of Commissioning, Qualification, and Validation processes. Be ready to discuss specific examples from your past experiences, especially in pharmaceutical or biotech settings. This will show that you’re not just familiar with the concepts but have practical experience applying them.
✨Familiarise Yourself with GMP Standards
Since this role involves ensuring compliance with GMP and regulatory requirements, it’s crucial to understand EU GMP guidelines, particularly Annex 1. Prepare to talk about how you've implemented these standards in previous projects, as this will demonstrate your capability to align with industry regulations.
✨Highlight Your Project Management Skills
Given the fast-paced project environment, be ready to showcase your ability to manage multiple tasks and meet key milestones. Share examples of how you’ve coordinated with engineering, quality, and project teams to achieve successful outcomes in your previous roles.
✨Prepare for Technical Questions
Expect technical questions related to clean utilities, HVAC systems, and validation lifecycle activities. Brush up on the specifics of these systems and be prepared to explain your approach to leading their qualification. This will help you stand out as a knowledgeable candidate who can hit the ground running.