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Senior Validation Engineer

Job in Aylesbury, Buckinghamshire, HP19, England, UK
Listing for: Orion Electrotech
Contract position
Listed on 2026-06-28
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering
  • Engineering
    Pharma Engineer, Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering
Salary/Wage Range or Industry Benchmark: 25 - 40 GBP Hourly GBP 25.00 40.00 HOUR
Job Description & How to Apply Below

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 delivery
Experience 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 site
Additional 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 validation
Role 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‑focused
Interview Process
  • CV review followed by Teams interview
  • Final on‑site interview
  • ASAP start required

INDMAN

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Position Requirements
10+ Years work experience
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