CQV Engineer in London

CQV Engineer in London

London Freelance 45000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • 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 contract rates, dynamic work environment, and the chance to shape a new facility.
  • Other info: Fast-paced environment with opportunities for professional growth and development.
  • Why this job: Be part of a high-impact project from the ground up and make a real difference.
  • Qualifications: Experience in CQV within pharma or biotech, with strong knowledge of GMP regulations.

The predicted salary is between 45000 - 60000 £ 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 London employer: Eblex Group

Eblex Group is an exceptional employer, offering CQV Engineers the chance to play a pivotal role in the development of a cutting-edge greenfield CMO facility in the UK. With a strong emphasis on collaboration and innovation, employees benefit from a dynamic work culture that fosters professional growth and provides opportunities to engage in high-impact projects within the pharmaceutical sector. The company's commitment to excellence and adherence to GMP standards ensures that team members are part of a meaningful journey towards advancing manufacturing capabilities.
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Contact Detail:

Eblex Group Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CQV Engineer in London

✨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 personal connections can lead to job opportunities.

✨Tip Number 2

Prepare for interviews by researching the company and understanding their projects. We recommend practising common CQV-related questions and having examples ready that showcase your experience in greenfield projects and GMP compliance.

✨Tip Number 3

Showcase your skills through a portfolio or case studies of past projects. We love seeing tangible evidence of your work, especially in complex systems and fast-paced environments. It sets you apart from the crowd!

✨Tip Number 4

Don’t forget to apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate CQV Engineers who are ready to make an impact.

We think you need these skills to ace CQV Engineer in London

Commissioning
Qualification
Validation
GMP Compliance
Clean Utilities
HVAC Systems
IQ/OQ/PQ Protocols
Documentation Skills
Stakeholder Coordination
Regulatory Requirements
Project Management
Fast-Paced Environment Adaptability
EU GMP Knowledge
Deviation Management

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 settings. 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 projects you've worked on. We love seeing concrete examples of your work that demonstrate your expertise in commissioning and validation.

Be Clear and Concise: Keep your application clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and experiences. We appreciate straightforward communication!

Apply Through Our Website: For the best chance of getting noticed, apply directly through our website. This helps us keep track of your application and ensures it reaches the right people quickly. We can’t wait to hear from you!

How to prepare for a job interview at Eblex Group

✨Know Your CQV Fundamentals

Make sure you brush up on your knowledge of Commissioning, Qualification, and Validation principles. Be ready to discuss your experience with IQ/OQ/PQ protocols and how you've applied them in past projects. This will show that you’re not just familiar with the terms but can also implement them effectively.

✨Showcase Your Project Experience

Prepare to talk about specific greenfield or large-scale facility build projects you've worked on. Highlight your role in these projects, especially regarding clean utilities and HVAC systems. Use concrete examples to demonstrate your ability to meet key project milestones and work in a fast-paced environment.

✨Understand GMP and Regulatory Requirements

Familiarise yourself with EU GMP guidelines, particularly Annex 1. Be prepared to discuss how you ensure compliance in your CQV activities. This will show that you understand the importance of regulatory requirements and can navigate them effectively in your work.

✨Emphasise Team Collaboration Skills

Since the role involves working closely with Engineering, Quality, and Project teams, be ready to share examples of how you've successfully collaborated with different stakeholders. Highlight your documentation skills and how you manage deviations, as this is crucial for maintaining project integrity.

CQV Engineer in London
Eblex Group
Location: London

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