RBW Consulting
Validation Engineer
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Validation Engineer
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
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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
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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
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