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GxP Computerised Systems Validation Consultant

Role overview

Summary

This role focuses on validating software used in drug development to ensure compliance with GxP standards during technology due diligence for clients in the life sciences sector. You will collaborate with a pharma specialist and technology due diligence lead at Intelance to assess and report on the reliability of platforms that generate clinical trial outputs.

Qualifications

  • At least five years of computerised system validation in a GxP setting.
  • Hands on use of GAMP 5, 21 CFR Part 11 and EU GMP Annex 11.
  • Experience validating or auditing systems that produce clinical trial or regulatory submission outputs.
  • Working knowledge of CDISC data standards.
  • Preferred: Experience validating systems that use machine learning or AI is a strong plus.

Responsibilities

  • Review the validation approach, records and evidence for platforms that produce clinical trial and real world evidence outputs.
  • Check audit trails, access controls, electronic records and change control against 21 CFR Part 11 and EU GMP Annex 11.
  • Judge whether the validation is proportionate to risk, using GAMP 5 and Computer Software Assurance thinking.
  • Check that outputs follow the expected data standards, such as CDISC SDTM and ADaM.

Key facts

Hard skills

Other skills

  • Problem Solving

About the company

Intelance logo

Intelance

  • 11–50
Intelance provides digital enablement advisory & implementation services that help organisations achieve their growth ambitions through the use of cloud solutions. Our extensive partner network, knowledge of the ever-changing technology landscape, and pool of highly experienced digital transformation experts enable us to provide you with unique, practical, and industry-specific insights. We kick off every new client relationship with an in-depth discovery meeting between you and one of our industry experts to give us a better understanding of your current infrastructure, identifying the inefficiencies in your core business processes, how these inefficiencies are affecting the goals you have set out to achieve, along with a proposed implementation plan and delivery team for our solution recommendations. All our solutions are supported by validated proof of concepts, methodologies and cloud platforms that can be tailored to suit your specific needs. We make use of pre-built industry assets to reduce the time required for deployment and implementation into your environments providing you with significant cost savings, guaranteed alignment to your relevant departments/functional areas, scope for continuous improvements based on feedback from your users, and the ability to track tangible returns on investment that contribute to your overall bottom line. For more information, visit https://www.intelance.co.uk.

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Job description

About Intelance

Intelance is an independent technology, AI and cyber assurance firm based in the UK. We help organisations check, govern and improve their technology through enterprise architecture, AI governance, cyber assurance and data governance work. We are building a small panel of senior associates to deliver technology and AI due diligence on company sales and investments.

The role

You will check whether software used in drug development is validated to GxP standards, as part of technology due diligence for clients who are selling, buying or investing in life sciences technology companies. Pharmaceutical buyers want proof that a platform producing trial and regulatory outputs works reliably, keeps a full audit trail and would stand up to an inspection.

You report to an Intelance engagement partner and work alongside our pharma specialist and technology due diligence lead, who bring your findings into the final report.

What you will do

  • Review the validation approach, records and evidence for platforms that produce clinical trial and real world evidence outputs.

  • Check audit trails, access controls, electronic records and change control against 21 CFR Part 11 and EU GMP Annex 11.

  • Judge whether the validation is proportionate to risk, using GAMP 5 and Computer Software Assurance thinking.

  • Check how validation is kept current when AI workflows and machine learning models change.

  • Check that outputs follow the expected data standards, such as CDISC SDTM and ADaM.

  • Rate each finding by how it could affect the deal, and write clear, practical fixes.

What you will bring

  • At least five years of computerised system validation in a GxP setting.

  • Hands on use of GAMP 5, 21 CFR Part 11 and EU GMP Annex 11.

  • Experience validating or auditing systems that produce clinical trial or regulatory submission outputs.

  • Working knowledge of CDISC data standards.

  • Clear, plain writing that founders, buyers and lawyers can follow.

  • Experience validating systems that use machine learning or AI is a strong plus.

How the work is set up

  • Remote within the UK, with occasional meetings in London.

  • Around 3 to 5 days between late November 2026 and the end of January 2027, with further engagements as the practice grows.

  • Freelance, or through your own limited company, at £550 to £700 a day depending on experience. Reasonable travel costs for client meetings are covered.

  • A panel agreement, NDA and statement of work are signed before any client details are shared.

  • You work from an Intelance mailbox and use our evidence log and report templates, so every report meets the same standard.

How to apply

Send your CV and answer the short screening questions. They take about two minutes. We aim to reply to every shortlisted candidate within five working days.

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