Are you a Computer System Validation Engineer with experience of the automation industry? Are you able to Able to develop and write high quality validation documents? Are you looking to join one of the UK's best Automation companies who operate in an open and honest way with Core values and Behaviours being the basis of all their hires? Are you based within commutable distance of the Warrington OR Middlesbrough areas or are willing to relocate here? If the answers are yes, my client an organisation who look to offer a a genuine one-stop-shop for all forms of industrial computing and control are looking for a full time Computer Systems Validation Engineer to join their team.Check below to see if you have what's needed for this opportunity, and if so, make an application asap.Essential Requirements: You'll have working knowledge in Validation in one or more of the following areas (Computer System/Process/Project/Equipment/Cleaning etc.) within the Biotech/Med Device/ Pharmaceutical (FDA/MHRA regulated industries) You will have a suitable qualification (preferably degree level) Regulatory knowledge within: cGMP and GxP, GAMP, FDA 21 CFR Part 11, Annex 11, Data Integrity would be hugely desirable You will fit within our clients CORE values which are: Accountability, Communication, Entrepreneurial, Inspiring and Team Player This is an absolute essential if you are to be successful What you get in return: A Competitive starting salary dependant upon your background and experience Health Insurance Laptop Workplace Pension Flexible working hours with early finish on Fridays The Role Delivery of Project Work from yourself and the customer's team of Engineers in line with agreed timescales Ensure that Customer experiences a proactive approach to solving their problems Assist PM in developing the relationships within the customer's site to help build business with them Ensure that all tasks are carried out within budget Technical: Modify, review and create Validation Documents, Quality Plans, Specifications, Test Specifications, Validation Reports Carry out Assessments of computerised systems to ensure that specifications and current regulations are met.Keep abreast of current Computer Validation related regulations Carry out system testing against specifications, record test results and review test results in line with current validation regulations.Work within the regulations required for Pharmaceutical projects and manufacturing, e.g.GMP, GAMP.The Company Our Client are a specialist Systems Integrator that provides high quality, project-based system solutions to Customers in several industry sectors around the world.They truly believe that their people are key to our success and as such, they will always try hard to demonstrate their company values every day.That means they need great people who want to be part of a growing business, widening their customer base and enhancing their customers experience and their expectations of them, by solving their problems on a daily basis.Cordant Group is an equal opportunities employer