Medical Device Regulatory Compliance Lead (MDR/ISO 13485)

Aurora Lifesciences is seeking an experienced Regulatory Compliance Specialist to join a medical device organisation and support regulatory compliance across the full product lifecycle. The role focuses on creating, reviewing and maintaining regulatory and technical documentation to ensure products remain compliant, audit-ready, and aligned with EU MDR and UK requirements.

You will collaborate with Quality, Engineering, NPD and Manufacturing teams on ongoing regulatory submissions and

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