Job Description
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
1. Bachelor’s or postgraduate degree in biomedical engineering, biotechnology, biology, chemistry, pharmacy, bioengineering, or equivale...