Login

Quality, compliance, clinical and regulatory affairs

Quality, compliance, clinical and regulatory affairs are at the heart of Corin with teams working across the world ensuring that we are fully compliant with the country specific requirements and standards.

These areas cover all the relevant post market surveillance, clinical trials, quality documentation, validation, verification, C-markings, packaging and labelling requirements etc and work closely with all divisions within Corin.

Experience within a medical devices business is highly desirable in these areas, in particular working with Class 3 devices.

Compliant, Regulated, Process Driven and Organised are key skills.