Regulatory Affairs Specialist - Medical Devices - Cambridge
This role involves providing regulatory guidance across the full product development lifecycle, supporting multidisciplinary teams in a technology-driven environment. You will interpret global regulations including ISO 13485, ISO 9001, and FDA 21 CFR 820, ensuring compliance while enabling innovation. The position is embedded in project work, offering real-time input on regulatory strategy and contributing to quality management systems across medical and non-medical sectors.