Job Description

Senior Validation Engineer / Validation Manager (Quality)

Aylesbury Monday–Friday, On-Site (flexibility for 1 day WFH)

6-Month Contract (Potential to Go Permanent) £25-£40 per hour

We’re supporting a growing manufacturing business in a regulated environment with the appointment of a Senior Validation Engineer / Validation Manager to support a significant pipeline of validation activity on site.

This is a hands-on role focused on delivering validation across new and existing equipment, with an immediate requirement to bring structure, complete documentation, and ensure validation processes are audit-ready.

Key Responsibilities

Deliver end-to-end validation across equipment and processes (IQ/OQ/PQ)

Lead process validation activities across manufacturing lines, including new and existing equipment

Complete and improve validation documentation, ensuring full compliance and audit readiness

Support validation of new machinery coming into the site, including re-validation of existing equipment 

Carry out cleaning validation across both new and current production equipment

Support implementation of a structured Quality Risk Management (QRM) system

Contribute to analytical validation activity across new equipment (desirable but not essential)

Work closely with quality, hygiene, production, and project teams to ensure aligned deliveryExperience Required (Must-Haves)

Strong background in validation within a regulated environment (pharma, medical device preferred – open to other transferable industries)

Proven experience delivering full lifecycle validation (URS, protocols, reports)

Hands-on experience with IQ/OQ/PQ across manufacturing or processing equipment

Solid experience in process validation (start to finish)

Strong documentation skills and ability to bring structure to existing processes

Good understanding of regulatory standards such as cGMP, FDA, ISO (9001 / 22716 advantageous) or similar 

Ability to operate as a standalone validation specialist on siteAdditional Experience (Desirable)

Exposure to analytical or lab-based validation

Experience supporting audits or working in audit-ready environments

Experience implementing or working with QRM systems

Experience with cleaning validationRole Overview

Immediate focus on closing validation gaps across existing equipment

Significant involvement in validation of new machinery coming onto site

50/50 split between revalidation work and new equipment validation

Operating as the primary validation lead, supported by wider teams (no direct reports)

Fast-paced environment with a strong need for someone organised, practical, and delivery-focusedInterview Process

CV review followed by Teams interview

Final on-site interview

ASAP start required 

INDMAN

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