More jobs:
Validation Technician
Job in
Liverpool, Merseyside, L1, England, UK
Listed on 2026-02-16
Listing for:
Adepto Technical Recruitment Ltd
Full Time
position Listed on 2026-02-16
Job specializations:
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Quality Assurance - QA/QC
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Pharmaceutical
Pharmaceutical Manufacturing
Job Description & How to Apply Below
Start Your Career in Validation
A growing secondary pharmaceutical manufacturer is looking for a Validation Technician to join its site-based Quality & Technical team.
This is an excellent opportunity for someone early in their validation or GMP career who wants hands-on experience in a regulated pharmaceutical environment, with clear development pathways.
You’ll play an important role in supporting validation activities across manufacturing processes and equipment, helping ensure the site remains compliant, inspection-ready, and operating to the highest quality standards.
What You’ll Be Doing
* Supporting process qualification, validation, and revalidation activities
* Assisting with preparation and execution of validation protocols
* Collecting and reviewing operational data to confirm ongoing compliance
* Supporting deviation investigations and CAPA activities
* Assisting with Change Control and SOP updates
* Working closely with Production, Quality, and Engineering teams
* Supporting audit readiness and validation documentation
This is a hands-on, practical role where you’ll develop a strong understanding of GMP validation in a live manufacturing environment.
Why This Role is a Great Career Move
This position is designed to build your technical foundation and set you up for progression.
You’ll benefit from:
* Structured exposure to validation processes within a regulated pharmaceutical setting
* Cross-functional experience working with multiple site departments
* Autonomy in your responsibilities, with support from experienced validation professionals
* Real, practical learning where you can see the impact of your work
What We’re Looking For
* Scientific qualification or relevant GMP manufacturing experience
* Exposure to a regulated environment (pharmaceutical preferred)
* Understanding of GMP, quality systems, or regulatory standards
* Strong attention to detail and problem-solving ability
* Organised, proactive, and comfortable working across teams
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