GMP Validation Engineer – Cleanrooms, HVAC & Autoclaves
Location: Home-based, Southern UK Territory
Working Arrangements: Flexible working, with regular UK-wide travel
CY Partners is recruiting a GMP Validation Engineer on behalf of a specialist consultancy providing validation and technical support to pharmaceutical, laboratory, aseptic and healthcare environments.
This is an excellent opportunity for an experienced validation, CQV or commissioning professional with expertise in facilities, HVAC systems, cleanrooms and critical equipment qualification to work on a varied portfolio of projects across the life sciences and healthcare sectors.
Working with clients including NHS organisations, universities and leading research institutions, you will support projects from design and specification through to commissioning, qualification and final handover.
The Role
You will provide technical validation and qualification expertise across GMP-regulated facilities, systems, utilities and equipment.
Key responsibilities include:
- Leading and executing qualification activities for HVAC systems, cleanrooms, autoclaves, sterilisation equipment and critical GMP utilities.
- Undertaking cleanroom qualification, including environmental monitoring, airflow, pressure differentials, HEPA filter integrity and contamination control assessments.
- Developing and executing validation documentation, including URS, VMP, DQ, IQ, OQ and Validation Summary Reports.
- Reviewing facility designs, engineering specifications and technical documentation.
- Conducting quality risk assessments and supporting cross-contamination control strategies.
- Supporting projects from design and commissioning through to qualification and handover.
- Working with clients, designers, contractors and multidisciplinary engineering teams to ensure successful project delivery.
- Ensuring compliance with cGMP, MHRA guidance and relevant regulatory requirements.
About You
We are particularly interested in candidates with hands-on experience in GMP facilities validation, HVAC qualification, cleanroom validation or pharmaceutical equipment qualification.
Ideally, you will have:
- Practical experience qualifying HVAC systems, cleanrooms, utilities or critical pharmaceutical equipment.
- Knowledge of autoclaves, sterilisation systems, temperature mapping and equipment qualification.
- Understanding of cleanroom design, HEPA filtration, airflow, pressure cascades and contamination control.
- Experience preparing and executing validation protocols and technical documentation.
- Knowledge of GMP, quality risk management and relevant regulatory guidance.
- Strong project management, communication and stakeholder engagement skills.
- Willingness to travel regularly across the UK, including occasional overnight stays.
Experience with RIBA design stages, process gas qualification, AI technologies or coaching colleagues would also be advantageous.
Additional Information
This is a home-based role covering a Southern UK territory, with regular travel to client sites across the UK. Flexible working is available, with some flexibility around working hours to accommodate client commitments.
Interested?
If you have experience in GMP validation, cleanroom qualification, HVAC systems, autoclaves or pharmaceutical facilities and equipment, we would love to hear from you.
Whether your background is in validation, CQV, commissioning or pharmaceutical engineering, this is an opportunity to apply your expertise across a diverse range of specialist projects.
We look forward receiving your application!