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Computer Validation and Control Engineer

AstraZeneca

UK - Liverpool permanent

Posted: February 24, 2026

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Quick Summary

Collaborate with equipment and process owners to establish and improve process control systems to meet asset, manufacturing, and quality requirements.

Job Description

Job Title: Computer Validation and Control Engineer

Location: Liverpool, UK

Introduction to role:

Are you ready to make a positive impact in a team where it means more? At AstraZeneca, we are driven by our commitment to deliver accelerated growth and improve people's lives. We are seeking a Computer Validation and Control Specialist to join our dynamic team at our Liverpool manufacturing site. This role offers the opportunity to collaborate closely with equipment and process owners, ensuring the establishment, control, and improvement of process control systems to meet asset, manufacturing, and compliance demands. Located near the vibrant city center of Liverpool, you'll enjoy a rich cultural scene, excellent shopping, and world-class museums. Are you ready to step up and lead in an environment that thrives on innovation and collaboration?
 

Accountabilities:

In this role, you will use a risk-based framework for validation criticality and performance to establish, sustain, and enhance process control systems performance. You will represent the validation department on cross-functional teams delivering process, system, and equipment improvements. Additionally, you'll provide subject matter expertise support to the validation manager regarding validation requirements for change control proposals.
 

Essential Skills/Experience:

• Science degree or equivalent in Biochemistry, Chemistry, Microbiology, Virology or Biochemical Engineering
• A proven experience in establishing, maintaining, and optimising process control systems within a regulated manufacturing environment, applying risk-based validation methodologies to ensure compliance and operational excellence
• 3–5 years’ demonstrable experience within a manufacturing operations environment
• Strong technical report writing skills with a high level of attention to detail with ability to identify errors during documentation review
• Expert level knowledge of Computer Validation requirements & current GAMP standards
• Experience in the configuration of computer systems utilising the GAMP5 methodologies, current data integrity standards and 21 CFR Part 11 including all applicable regulatory guidelines
• Excellent verbal and written communication skills

At AstraZeneca, you'll be part of an inclusive network of diverse and high-performing teams. We support each other on our journeys with a shared drive and passion for impacting people's lives. With opportunities for global careers and great rewards, you'll experience a sense of belonging like no other. Our commitment to sustainable practices ensures we manage our environmental impact across all activities and products. Join us as we lead the way in delivering Lean processes that drive efficiency and speed.
 

Ready to take action? Apply now and be part of a team that's transforming the future of medicine!

Where can you find more?

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Date Posted

24-Feb-2026

Closing Date

19-Mar-2026

Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

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