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CSV Consultant

About the Company

A specialist pharmaceutical consultancy delivering validation, compliance and quality services to regulated life sciences organisations. The team works with clients to ensure systems meet the highest regulatory standards.

Why This Role Matters

Your expertise will help ensure computerised systems are compliant, reliable and fit for purpose, supporting the safe manufacture of life-changing medicines.

The Role

You'll deliver Computer System Validation activities across pharmaceutical client projects, working with quality, engineering and IT teams to ensure compliance with industry regulations.

Key Responsibilities

  • Prepare and execute CSV documentation in accordance with GMP and GAMP guidance.
  • Support the validation of new and existing computerised systems within regulated pharmaceutical environments.
  • Collaborate with client teams to identify compliance risks and deliver practical validation solutions.

Required Skills & Experience

  • Proven experience delivering Computer System Validation (CSV) projects.
  • Strong understanding of GMP regulations and GAMP guidance.
  • Excellent communication skills with experience working in a consultancy or client-facing environment.

What’s on Offer

  • Competitive salary with hybrid working and flexible project exposure.
  • The opportunity to work with leading pharmaceutical organisations on diverse validation projects.


Location: | Salary: £45000 - £65000 per | Job type: Permanent | Posted: 07/10/2026

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