Senior Validation Engineer Aylesbury, Buckinghamshire Orion Electrotech £25 – 40 – Hour 1 hour ago

# Senior Validation Engineer#### Aylesbury, Buckinghamshire## Orion ElectrotechView Profile#### Contact Orion ElectrotechApply on company site## Share:#### Stay Safe”Only access Gumtree from gumtree.com and do not follow links sent by other users””Share photos and ask lots of questions about the items you are buying and selling””If an ad or reply sounds too good to be true, it probably is””Use the ‘Reply to ad’ button for your safety and privacy””Don’t reply to email addresses hidden in text and pictures””Beware of fake Gumtree, eBay or escrow sites and invoices”1 of 6Read all safety tipsHours: Full TimePosted: 2 hours agoSalary: £25 – 40 – HourRecruiter: Orion ElectrotechCloses: 25 Aug 2026Course: NoRecruiter Type: Direct Employer## DescriptionSenior 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 “Thank you for your application. xjnqpsq Due to the volume of applications we receive, unfortunately we are not able to respond to every application personally, therefore, if you have not heard back from us within 5 working days please assume your application has been unsuccessful. To see our other available vacancies please visit our website#J-18808-Ljbffr…