2 ISO 13485 Jobs in Scotland with Remote Work Options

will feed into your constantly evolving test procedure designs. We would love to hear from people who are familiar with industry standards such as ISO 13485, IATF 16949 and you can expect to liaise with the Quality team in terms of compliance and continuous improvement. As a detailed more »

accountable for maintaining compliance of the Quality Management System, input into the management of complaints and post-market activities ensuring that the requirements of ISO 13485:2016, CFR 21 Part 820 IVDD/IVDR are adhered to. The successful candidate shall be responsible for carrying out day-to … timely completion of post market and vigilance related activities Support and input to internal/external audits Essential Knowledge and experience of working to ISO13485, FDA 21 CFR Part 820 Experience of working on post launch IVD or medical device activities in a quality role To find out more about more »