Senior Systems & Regulatory Software Engineer Medical Devices | High Salary or High-Rate Contract | Kent | Remote

We are seeking an experienced Technical Expert to join our global team, working with active medical devices under MDR 2017/745 and ISO 13485 standards Electrionics device and audit experience is recognised.

This is a fully remote role , offering the flexibility to work from anywhere, while engaging with international clients and supporting the certification of a diverse portfolio of medical device manufacturers.

What You’ll Be Doing Reviewing technical documentation for active medical devices and assessing compliance with EU MDR 2017/745 Evaluating Quality Management Systems (QMS) in line with ISO 13485 Managing certification activities for an international portfolio of medical device manufacturers Collaborating with teams and clients across multiple regions to ensure consistent, high-quality compliance

What We’re Looking For Bachelor’s or postgraduate degree in biomedical engineering, biotechnology, biology, chemistry, pharmacy, bioengineering, or equivale...