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

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