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For Companies At a Glance
- Tasks: Lead and support high-impact pharmaceutical projects ensuring compliance and excellence.
- Company: Join a leading pharmaceutical engineering consultancy with a hybrid work model.
- Benefits: Competitive salary, travel opportunities, and professional development in a dynamic field.
- Why this job: Make a real impact in the pharmaceutical industry while working on innovative projects.
- Qualifications: Relevant degree and experience in pharmaceutical CQV and validation required.
- Other info: Equal opportunities employer welcoming diverse applicants.
The predicted salary is between 36000 - 60000 £ per year.
ROLE OVERVIEW
We are currently looking for a CQV & Validation Engineer to join a leading pharmaceutical engineering consultancy based in a hybrid role with travel across the UK and Ireland. As the CQV & Validation Engineer, you will be responsible for delivering high-impact pharmaceutical projects, ensuring compliance and excellence in sterile, biologics, and ATMP facilities.
KEY DUTIES AND RESPONSIBILITIES
- Lead or support CQV project delivery, from protocol development and execution (IQ/OQ/PQ) to final reporting.
- Engage directly with client stakeholders in Engineering, QA, Validation, and MSAT to align on scope, risk, and compliance.
- Participate in Process Risk Assessments (PRAs) and contribute to integrated solutions across process, utilities, and equipment.
- Provide technical guidance on sterilisation, depyrogenation, SIP/CIP cycles, and thermal system mapping.
ROLE REQUIREMENTS
- Relevant degree in a related field.
- Proven industry experience in pharmaceutical CQV, validation, or sterile utilities.
- A working knowledge and practical experience with GMP environments, validation principles, and regulatory compliance (e.g., Annex 1 / FDA).
Key Words:
CQV / Validation Engineer / Pharmaceutical Engineering / Sterile Utilities / GMP Compliance / Annex 1 / FDA / Process Risk Assessment / SIP/CIP / Thermal System Mapping / Biologics
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career
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CQV Engineer employer: Hyper Recruitment Solutions LTD
Contact Detail:
Hyper Recruitment Solutions LTD Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CQV Engineer
✨Tip Number 1
Network like a pro! Reach out to professionals in the pharmaceutical engineering field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that CQV Engineer role.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and understanding of GMP compliance. We recommend practising common interview questions related to CQV and validation processes, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t just apply and wait! Follow up on your applications through our website. A quick email or message can show your enthusiasm and keep you on the radar of hiring managers.
✨Tip Number 4
Tailor your approach! When engaging with potential employers, highlight your experience with sterile utilities and regulatory compliance. We want you to stand out, so make sure your skills align with what they’re looking for!
We think you need these skills to ace CQV Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CQV Engineer role. Highlight your relevant experience in pharmaceutical engineering, especially any work with GMP environments and validation principles. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about CQV and how your background makes you a great fit for our team. Don’t forget to mention any specific projects or experiences that relate to sterile utilities or regulatory compliance.
Showcase Your Technical Skills: In your application, be sure to showcase your technical expertise, especially around sterilisation, depyrogenation, and thermal system mapping. We love seeing candidates who can demonstrate their knowledge of these areas, so don’t hold back!
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to upload all your documents in one go. Plus, it helps us keep track of your application better!
How to prepare for a job interview at Hyper Recruitment Solutions LTD
✨Know Your CQV Fundamentals
Make sure you brush up on your knowledge of CQV principles, especially around IQ/OQ/PQ protocols. Being able to discuss these confidently will show that you understand the core responsibilities of the role.
✨Familiarise Yourself with Regulatory Standards
Get to grips with GMP environments and relevant regulations like Annex 1 and FDA guidelines. This will not only help you answer questions but also demonstrate your commitment to compliance and excellence in pharmaceutical engineering.
✨Prepare for Technical Questions
Expect to be asked about sterilisation processes, SIP/CIP cycles, and thermal system mapping. Prepare specific examples from your past experience where you successfully applied these concepts to real-world projects.
✨Engage with Stakeholders
Think about how you would engage with client stakeholders in Engineering, QA, and Validation. Be ready to discuss how you would align on project scope and risk management, as this is crucial for the role.
