1 of 1 Permanent ISO 13485 Jobs in Cardiff

team environment. Key Duties and Responsibilities:- Regulatory To carry out engineering activities in accordance with company QA procedures and to meet regulatory regimes such as Medical Device Regulation (EU), ISO13485 (Int), FDA CFR820 (USA) and appropriate standards including IEC 60601, IEC 62304, ISO 14971 Software management Assignment and management of appropriate resources providing motivation, supervision and guidance of software More ❯