Validation Engineer / Validation Lead (12 month contract)
A leading, global pharmaceutical manufacturing business is seeking an experienced Validation Engineer to support delivery of a major site validation and capital programme on a 12-month contract.
This is a high-impact role within a busy engineering environment, offering exposure across equipment, utilities, facilities, and laboratory systems, with a need for hands-on execution specialists. If this capability brings with it project lead experience, this will also be valued.
The Role
Working as part of the Engineering function, you will support delivery of a structured site-wide validation programme, alongside capital project activity.
Responsibilities will include:
- Supporting delivery of the Site Validation Master Plan (SVMP)
- Generating and reviewing validation / qualification documentation (IQ/OQ/PQ, FAT/SAT, etc.)
- Leading or supporting execution of validation activities across manufacturing, lab, and utility systems
- Working closely with internal stakeholders to ensure GMP and regulatory compliance
- Reviewing vendor documentation and supporting supplier-led validation activities
- Participating in FATs and site-based commissioning activities where required
- Managing or supporting third-party contractors and vendors
- Owning change controls, deviations, and CAPAs linked to validation activities
- Supporting requalification, new equipment introduction, and decommissioning activities
Project / Programme Exposure
In addition to core validation delivery, there is scope to contribute at a more strategic level:
- Supporting or leading capital project delivery (GxP and non-GxP)
- Defining project scope, timelines, and deliverables
- Managing project risks, budgets, and progress reporting
- Coordinating cross-functional stakeholders and teams
- Driving project governance, change management, and close-out activities
What We’re Looking For
We’re open to a range of profiles, from strong delivery-focused CQV engineers to more senior, project-led professionals:
- Experience in validation / CQV within GMP-regulated environments (pharma / biotech / related)
- Strong understanding of validation principles across equipment, utilities, or facilities
- Experience authoring and executing validation documentation
- Ability to work effectively across cross-functional teams and stakeholders
- Confidence operating in a fast-paced, project-driven environment
- Strong communication and problem-solving skills
Validation, commissioning, qualification, CQV, equipment, utilities, facilities, IQ, OQ, PQ, DQ, project, lead, FAT, SAT, engineer