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- Tasks: Ensure quality and compliance in critical facilities and equipment through validation activities.
- Company: Join CEVA Logistics, a leader in logistics with a focus on quality and compliance.
- Benefits: Competitive salary, life assurance, pension scheme, and professional development opportunities.
- Why this job: Make a real impact in a dynamic environment while growing your expertise in validation.
- Qualifications: Bachelor’s degree in science or engineering and experience in GMP facility validation.
- Other info: Collaborative team culture with pathways for career growth and learning.
The predicted salary is between 36000 - 60000 £ 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.
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.
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.
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.
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.
Validation Specialist in Ashby de la Zouch employer: CEVA Logistics
Contact Detail:
CEVA Logistics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Validation Specialist in Ashby de la Zouch
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend relevant events, and connect with professionals on LinkedIn. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and its values. Understand their approach to quality and compliance, especially in relation to GDP/GMP standards. This will help you tailor your answers and show you're genuinely interested.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to validation processes and regulatory compliance. Use the STAR method (Situation, Task, Action, Result) to structure your answers effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re keen on joining our team at CEVA Logistics and ready to contribute to our mission.
We think you need these skills to ace Validation Specialist in Ashby de la Zouch
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Validation Specialist role. Highlight your experience in GMP environments and any relevant qualifications to show us you’re the right fit.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you’re passionate about quality and compliance. Share specific examples of your past work in validation and how it aligns with our mission at CEVA Logistics.
Showcase Your Technical Writing Skills: Since strong technical writing is key for this role, include samples or mention experiences 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 from our team.
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 a Validation Specialist 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 role.
✨Be Ready for Scenario Questions
Expect questions about how you would handle deviations or perform GAP analyses. Think through some scenarios beforehand so you can articulate your problem-solving process and decision-making skills effectively.
✨Highlight Your Team Collaboration Experience
Since this role involves working closely with various teams, be prepared to discuss your experience in collaborative environments. Share specific examples of how you've successfully worked with internal teams, suppliers, or external partners in past projects.