GMP Validation Engineer – Cleanrooms, HVAC & Autoclaves

Cypartners

Cambridge

Remote

GBP 52,000 - 74,000

Full time

2 days ago
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Job summary

CY Partners is recruiting a GMP Validation Engineer to join a specialist consultancy serving pharmaceutical, laboratory and healthcare environments across the UK.

The role covers validation and commissioning of HVAC systems, cleanrooms and critical equipment, with hands-on qualification activities, technical documentation, and risk assessments. Regular UK-wide travel is required, with a home-based setup and flexible working to support clients.

Qualifications

  • Hands-on GMP facilities validation and HVAC qualification experience.
  • Experience with cleanroom validation and pharmaceutical equipment qualification.
  • Ability to develop and execute validation protocols and technical documentation.
  • Knowledge of GMP, QA, and regulatory guidelines.

Responsibilities

  • Lead and execute qualification activities for HVAC systems, cleanrooms, autoclaves, sterilisation equipment and critical GMP utilities.
  • Undertake cleanroom qualification, including environmental monitoring, airflow, pressure differentials, HEPA filter integrity and contamination control assessments.
  • Develop and execute validation documentation, including URS, VMP, DQ, IQ, OQ and Validation Summary Reports.
  • Review facility designs, engineering specifications and technical documentation.
  • Conduct quality risk assessments and support cross-contamination control strategies.
  • Support projects from design and commissioning through to qualification and handover.
  • Work with clients, designers, contractors and multidisciplinary engineering teams to ensure successful project delivery.
  • Ensure compliance with cGMP, MHRA guidance and relevant regulatory requirements.

Skills

GMP validation
HVAC qualification
Cleanroom validation
Pharma equipment qualification
Project management
Communication skills
Stakeholder engagement

Job description

CY Partners is recruiting a GMP Validation Engineer to join a specialist consultancy serving pharmaceutical, laboratory and healthcare environments across the UK.

The role covers validation and commissioning of HVAC systems, cleanrooms and critical equipment, with hands-on qualification activities, technical documentation, and risk assessments. Regular UK-wide travel is required, with a home-based setup and flexible working to support clients.

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