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- Tasks: Join a dynamic team to ensure quality in pharmaceutical manufacturing through commissioning and validation.
- Company: NGAGE Smart4Sciences is a leader in the pharmaceutical sector, driving innovation and quality.
- Benefits: Enjoy flexible working arrangements and competitive pay without IR35 restrictions.
- Why this job: Be part of a crucial project that impacts healthcare while developing your engineering skills.
- Qualifications: Experience in Commissioning, Qualification & Validation, especially in GMP environments is essential.
- Other info: This is a contract role based in Cheshire, perfect for those seeking hands-on experience.
The predicted salary is between 43200 - 72000 £ per year.
Proactive CQV Engineers required for ongoing Capital Investment project for expansion of Pharmaceutical GMP manufacturing.
Well versed background across Commissioning, Qualification & Validation including Cleaning & CSV.
Please contact Simon Fowler at NGAGE Smart4Sciences.
CQV Engineer employer: Smart4Sciences
Contact Detail:
Smart4Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CQV Engineer
✨Tip Number 1
Network with professionals in the pharmaceutical industry, especially those who have experience in CQV roles. Attend industry events or join relevant online forums to connect with potential colleagues and learn about job openings.
✨Tip Number 2
Familiarise yourself with the latest regulations and standards in GMP manufacturing. Being knowledgeable about current practices will not only boost your confidence but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Prepare to discuss specific projects you've worked on that relate to commissioning, qualification, and validation. Highlighting your hands-on experience will make you stand out as a candidate who can hit the ground running.
✨Tip Number 4
Research StudySmarter and our values before applying. Understanding our mission and how your skills align with our goals will help you articulate why you're a great fit for the CQV Engineer position.
We think you need these skills to ace CQV Engineer
Some tips for your application 🫡
Understand the Role: Familiarise yourself with the specific responsibilities of a CQV Engineer in the pharmaceutical industry. Highlight your experience in Commissioning, Qualification, and Validation, especially in GMP environments.
Tailor Your CV: Make sure your CV reflects relevant experience in CQV processes. Include specific projects you've worked on that demonstrate your expertise in Cleaning and CSV, as these are crucial for the role.
Craft a Compelling Cover Letter: Write a cover letter that connects your skills and experiences directly to the job description. Mention your proactive approach and how it aligns with the ongoing Capital Investment project.
Proofread Your Application: Before submitting, carefully proofread your application materials. Check for any spelling or grammatical errors, and ensure that all information is clear and concise.
How to prepare for a job interview at Smart4Sciences
✨Know Your CQV Fundamentals
Make sure you have a solid understanding of Commissioning, Qualification, and Validation processes. Be prepared to discuss specific methodologies you've used in past projects, especially in the pharmaceutical sector.
✨Showcase Your Experience with GMP
Highlight your experience in Good Manufacturing Practices (GMP) during the interview. Be ready to provide examples of how you've ensured compliance and quality in previous roles.
✨Prepare for Technical Questions
Expect technical questions related to cleaning validation and computer system validation (CSV). Brush up on relevant regulations and standards to demonstrate your expertise.
✨Demonstrate Problem-Solving Skills
Be prepared to discuss challenges you've faced in previous CQV roles and how you overcame them. This will show your ability to think critically and adapt in a fast-paced environment.
