Aurora Lifesciences seeks an experienced Regulatory Specialist to join a medical device organisation and manage regulatory documentation throughout the product lifecycle.
You will author, review and maintain Technical Files and regulatory records, support EU MDR and UK compliance, and drive regulatory submissions and post-market activities across Quality, Engineering, NPD and Manufacturing.
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Medical Devices Regulatory Affairs Specialist 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.
