Validation Specialist

Validation Specialist

Speke, Liverpool

Do you feel passionate about the possibilities of applying science to changing lives? Do you have experience working within the validation and qualification of biopharmaceutical and pharmaceutical equipment and utilities? If so, this may be the role for you.

Here at AstraZeneca, you will have the opportunity to make a difference in people’s lives every single day. As one of the world’s premier biotechnology companies our mission is centred on delivering life-changing products, advance world health and helping to fight and cure disease. AstraZeneca has a dynamic environment that champions collaboration and innovation. We attract top minds and we cultivate and build top talent.

Located at AstraZeneca’s Fluenz manufacturing Liverpool site you will be only a short distance from the exciting city centre of Liverpool. Rich in history, as well being a creative hub, Liverpool offers an attractive cost of living along with a great quality of life. The city has something for everyone; live music, an exciting food and restaurant scene, nationally famous art galleries, excellent shopping and world-class museums.

We are looking for a Validation Specialist to join us on a permanent basis.

Duties & responsibilities:

• To liaise with the equipment or process owners in the co-ordination and execution of all validation related activities, including equipment qualification and revalidation, analytical, process, cleaning, local computer systems , utilities and facilities validations
• Maintain compliance with the validation and revalidation schedule for temperature controlled units, process and cleaning validation requirements and associated periodic reviews using a risk based framework for validation criticality and performance
• Represent the validation department on cross functional teams delivering process, system and equipment improvements
• Provide subject matter expertise support to the validation manager associated with validation requirements for change control proposals

Skills & Experience:

• Science degree or equivalent in Biochemistry, Chemistry, Microbiology, Virology or Biochemical Engineering
• Excellent verbal and written communication skills,
• Strong technical report writing skills with a high level of attention to detail with ability to identify errors during documentation review
• Extensive experience with thermal mapping of refrigerators, freezers, incubators, autoclaves
• Substantial knowledge of cGMP standards, in particular manufacturing, laboratory areas
• Experience in the validation of computer systems utilising the GAMP5 methodologies, current data integrity standards and 21 CFR Part 11 including all applicable regulatory guidelines

At AstraZeneca, our work is important and valued. We are proactive, science-based, and solutions-oriented, always striving to make a significant impact on patients' lives. Our inclusive and friendly community fosters collaboration and innovation, ensuring that each voice matters. With a focus on growth and innovation, there are always exciting opportunities to quality assure new products as we go to market around the world.

Ready to make a difference? Apply now to join our team!

Date Posted

11-Sept-2025

Closing Date

25-Sept-2025

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.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.