CMR Surgical in Cambridge, United Kingdom, is seeking a Regulatory Affairs Specialist to ensure that our medical devices comply with EU MDR, FDA and global regulatory requirements.
You will support regulatory submissions (510(k)s, Q-Submissions and IDEs), assess changes for impact on submissions, and collaborate with R&D, Quality, Clinical and Manufacturing to embed regulatory requirements early in product development.
#J-18808-LjbffrRegulatory Affairs Specialist, Medical Devices EU/FDA in Cambourne employer: Cmr Surgical
CMR Surgical is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Cambridge. Employees benefit from flexible hybrid working arrangements, competitive compensation, and opportunities for professional growth within a pioneering company dedicated to advancing minimal access surgery. Join us to be part of a mission-driven team where your contributions directly impact healthcare outcomes.
