Our client are looking for a QA/RA Officer on a permanent basis to support in implementing and maintaining quality systems whilst also supporting regulatory compliance across the product lifecycle. Activities include: Assisting in the development, implementation, and upkeep of quality management systems in accordance with relevant regulations and standards. Conducting internal audits to verify adherence to quality processes and identify areas for enhancement. Supporting establishing and maintaining Key Performance Indicators (KPIs) to monitor the performance of the Quality Management System (QMS). Supporting manufacturing and supply chain teams in managing nonconforming material, acceptance procedures, part qualification, and process validation. Assisting the QA/RA team in Corrective and Preventive Action (CAPA) activities as assigned. Facilitating the commercialisation of medical devices by obtaining and maintaining product registrations. Assisting in developing technical files to ensure ongoing global compliance with applicable product requirements. Providing advice on regulatory changes impacting product and business regulations.