Regulatory Affairs and Quality Assurance Assistant - Cambridge
This role involves supporting quality assurance and regulatory affairs activities within a medical devices R&D environment, ensuring compliance with ISO 13485, FDA 510(k), and 21 CFR Part 820 standards. The assistant will collaborate closely with R&D teams, providing guidance on regulatory requirements during product development and improvement. The position plays a key part in maintaining quality management systems and enabling the delivery of innovative, life-improving medical technologies.