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Validation technician

Liverpool (Merseyside)
Adepto Technical Recruitment Ltd
Technician
£30,000 - £35,000 a year
Posted: 16 February
Offer description

Validation Technician - Pharmacetuicals - Permanent - Merseyside - upto £35,000 DOE

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

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Supporting process qualification, validation, and revalidation activities

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Assisting with preparation and execution of validation protocols

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Collecting and reviewing operational data to confirm ongoing compliance

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Supporting deviation investigations and CAPA activities

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Assisting with Change Control and SOP updates

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Working closely with Production, Quality, and Engineering teams

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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:

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Structured exposure to validation processes within a regulated pharmaceutical setting

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Cross-functional experience working with multiple site departments

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Autonomy in your responsibilities, with support from experienced validation professionals

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Real, practical learning where you can see the impact of your work

What We’re Looking For

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Scientific qualification or relevant GMP manufacturing experience

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Exposure to a regulated environment (pharmaceutical preferred)

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Understanding of GMP, quality systems, or regulatory standards

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Strong attention to detail and problem-solving ability

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Organised, proactive, and comfortable working across teams

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