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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Medical Device Regulatory Compliance Lead (MDR/ISO 13485) employer: Aurora Lifesciences
As an Operations Director at our regulated manufacturing site, you will be part of a dynamic and supportive work culture that prioritises safety, quality, and continuous improvement. We offer exceptional employee growth opportunities, including leadership development and the chance to shape the future of our operations while working in a collaborative environment. Join us to make a meaningful impact in a role that combines strategic oversight with hands-on leadership in a thriving industry.
