Lead Validation Engineer — Medical Devices & Regulatory

A leading medical device company in the UK seeks a skilled Validation Engineer to join the operations team in Suffolk. In this role, you will develop and document validation protocols for manufacturing processes, ensuring compliance with regulatory standards such as ISO 13485 and FDA. You will collaborate with cross-functional teams to enhance process quality and participate in audit preparations. The ideal candidate holds a Bachelor’s degree in engineering or life sciences with at least three years of experience in the medical device field.
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