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- Tasks: Ensure quality and compliance in critical facilities and equipment through validation activities.
- Company: CEVA Logistics, a leader in logistics with a focus on quality and compliance.
- Benefits: Competitive salary, supportive team culture, life assurance, pension scheme, and professional development.
- Other info: Dynamic environment with opportunities for career growth and learning.
- Why this job: Play a key role in developing and validating essential facilities while growing your expertise.
- Qualifications: Bachelor’s degree in science or engineering and experience in GMP facility validation.
The predicted salary is between 40000 - 50000 £ per year.
Are you passionate about quality, compliance, and ensuring that critical facilities and equipment operate to the highest standards? At CEVA Logistics, we are looking for a QA Validation Engineer to support the commissioning and qualification of new GDP/GMP facilities, including ISO 7 and ISO 8 cleanrooms.
This role is essential to ensuring our systems, equipment, and environments operate safely, effectively, and in full compliance with all regulatory expectations. You will collaborate with internal teams, suppliers, and external partners to deliver robust validation activities across new and existing facilities.
What are you going to do?
In this role, you will carry out validation and qualification activities for new GDP/GMP facilities, equipment, cleanrooms, and systems. You will review and approve validation protocols (IQ/OQ/PQ), assess vendor documentation, manage deviations, and ensure all validation activities meet internal standards and regulatory requirements.
You will perform GAP analyses, support risk and impact assessments, monitor changes to validated systems, and guide decisions on revalidation needs. You will also contribute to SOP updates, environmental monitoring support, and process improvement initiatives.
Working closely with project teams, you will help plan, schedule, and deliver validation tasks on time, including supporting the validation of automation systems and warehouse management systems.
What are we looking for?
We are seeking a detail driven, analytical QA professional with experience in facilities and equipment validation within a GMP environment. You will bring strong knowledge of cleanroom qualification, commissioning processes, and validation standards across manufacturing and GDP facilities.
You should have a solid understanding of MHRA and FDA regulations, strong technical writing capabilities, and the ability to communicate effectively across diverse teams. You’ll be someone who thrives under pressure, uses sound judgement to solve problems, and contributes positively to project environments.
A Bachelor’s degree in science or engineering is required, along with experience in facility/equipment qualification and validation. Experience in commissioning new facilities, automation validation, and quality systems is highly desirable.
What do we have to offer?
We offer a competitive benefits package, a supportive team culture, and the opportunity to play a key role in the development and validation of critical facilities across our network. You’ll work in a dynamic, compliance‑driven environment with opportunities to grow your expertise in validation, quality systems, and regulated operations.
You will also benefit from our rewards platform, life assurance, pension scheme, and professional development pathways designed to support your long‑term success.
About tomorrow
We invest in your future. With numerous opportunities across our global operation and a strong commitment to professional development, we offer a pathway for you to grow, learn, and lead within CEVA Logistics. Join CEVA for a challenging and rewarding career.
Lab Specialist Quality in Leicester employer: CEVA Logistics
Contact Detail:
CEVA Logistics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lab Specialist Quality in Leicester
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Understand their values, recent projects, and challenges they face. This will help you tailor your answers and show that you're genuinely interested in joining their team.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or use online platforms to get comfortable with common questions. The more you practice, the more confident you'll feel when it’s your turn to shine.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Lab Specialist Quality in Leicester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Lab Specialist Quality role. Highlight your experience in GMP environments and any relevant qualifications to show us you’re the right fit.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality and compliance, and how your background aligns with our needs at CEVA Logistics. Keep it engaging and personal!
Showcase Your Technical Writing Skills: Since strong technical writing is key for this role, include examples of your previous work or projects where you’ve created validation protocols or SOPs. This will help us see your capabilities in action.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates during the process!
How to prepare for a job interview at CEVA Logistics
✨Know Your Regulations
Make sure you brush up on MHRA and FDA regulations before the interview. Being able to discuss these in detail will show that you understand the compliance landscape and are ready to tackle the challenges of the role.
✨Showcase Your Technical Writing Skills
Prepare examples of your technical writing, especially related to validation protocols like IQ/OQ/PQ. This will demonstrate your ability to communicate complex information clearly, which is crucial for the QA Validation Engineer position.
✨Be Ready to Discuss Problem-Solving
Think of specific instances where you've had to solve problems under pressure. Highlight your analytical skills and how you used sound judgement to navigate challenges in previous roles, particularly in a GMP environment.
✨Collaborate and Communicate
Since this role involves working with diverse teams, be prepared to discuss your experience in collaboration. Share examples of how you've effectively communicated with internal teams, suppliers, and external partners to achieve project goals.