Validation & Quality Engineers - UK & Ireland, Cambridge

Criterion International are currently working with an innovative international Medical Device company. We are now looking to employ Validation & Quality Engineers to work for our client. The roles will be long-term, based in various locations across the UK & Ireland. Responsibilities: * Develop, specify and validate new automated equipment. * Carry out IQ, OQ and PQs. * Author, review and execute validation protocols. * Working with automated handling and equipment including execution of software and hardware validation. * Ensure regulatory compliance with European and US software validation requirements. * Ensure computerised system validation procedure(s) is (are) kept up to date and maintained. * Ensure best practice is always carried out Qualifications & Experience: * Degree qualified in Engineering or Science. * 2+ years of Manufacturing engineering experience within the medical device or similar FDA regulated industry. * Experience with equipment development / validation of new automated equipment. * Experience with IQ/OQ/PQ is preferred. Salary and Benefits * Salary ? To be negotiated * Healthcare Cover and Screening * Life Assurance * Pension Contribution * Training & Education Please apply with your up to date CV or call Alex on (phone number removed)