1 to 1 of 1 ISO 13485 Jobs in Suffolk

to the technical file for regulatory submission of the medical products. Managing project timelines and project team workloads. Generating project documentation in line with ISO 13485 and other medical device regulatory requirements. Working closely with the customer to gather relevant concept information. Work closely with the design team …/or training will be provided to assist carrying out these responsibilities. As a medical device manufacturer, our design and development processes comply with ISO 13485 requirements. This position will require organisational and communication skills (verbal and written), problem solving skills, cross-functional teamwork and the ability to more »