EU Regulatory Lead for Class III Medical Devices

Cure Talent is excited to announce a new opportunity for a Regulatory Affairs Manager in Witney, England. This pivotal role involves leading the EU regulatory strategy for a Class III medical device, ensuring compliance with MDR 2017/745, and interacting with global regulatory teams.

The successful candidate will possess extensive experience in Regulatory Affairs within medical devices, particularly for Class III products, and will demonstrate a depth of knowledge in EU regulations. This role offers significant long-term progression potential in a globally recognized organization.

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