Global Regulatory Affairs Specialist - Medical Devices
CMR Surgical
CMR Surgical is seeking a Regulatory Affairs professional to help prepare and manage submissions for EU MDR and FDA, ensuring compliance throughout product development. You will work with R&D, Quality and Manufacturing to embed regulatory requirements early in the lifecycle. The role emphasises strong communication, attention to detail and the ability to manage deadlines in a fast‑growing medical device environment. On‑site work in Cambridge, UK, with a competitive benefits package. #J-18808-Ljbffr
Vacancy posted 8 hours ago
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