Validation & Quality Engineers - UK & Ireland

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)

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