scarlet is seeking a Device Specialist in London to drive regulatory assessments of medical devices. You will join a multidisciplinary team, audit management systems, and review technical documentation while helping build internal tools for scaling assessments.
The role requires 4+ years in medical device design/verification, strong regulatory analysis skills, and the ability to work independently on complex projects. Equity is offered alongside a competitive Β£75K-Β£85K salary.
#J-18808-LjbffrDevice Compliance Specialist β QA, Regulatory Docs (London) employer: Scarlet
At Scarlet, we are dedicated to transforming healthcare accessibility through innovative technology, making us an exceptional employer for those passionate about quality in medical devices. Our remote work culture fosters flexibility and autonomy, while our commitment to employee growth ensures that you will have ample opportunities to develop your skills in a supportive environment. Join us in shaping the future of healthtech, where your contributions directly impact patient care and safety.