2 of 2 ISO 13485 Jobs in West London

using cutting-edge additive manufacturing. This is a hands-on Quality Engineer role where youll play a key part in maintaining and improving an ISO 13485 QMS while supporting product development, validation, and regulatory activities ahead of major commercial launches. What youll be doing: Own and maintain … ISO 13485) Manage document control, CAPAs, and change control Support NPD, validation, and testing activities Conduct internal audits and support external/regulatory audits Work closely with engineering and clinical teams What were looking for: 2+ years in medical device quality Strong knowledge of ISO 13485 ...

embed a culture of quality across the business. QA Specialist key responsibilities: Own and maintain the document management system, ensuring all quality documents meet ISO 9001:2015 requirements. Design and deliver staff training on QMS processes, keeping training records accurate and up to date. Administer the Non-conformance … working closely with the H&S competent person and relevant duty owners. QA Specialist requirements: Hands-on experience working within a Quality Management System (ISO 9001:2015 and 13485:2016), ideally in the Life Sciences or Medical Devices sector. Practical involvement in internal and external audits. Confident with ...