Medical Device Compliance Engineer — Regulatory Submissions
Listed on 2026-10-10
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Engineering
Medical Device Industry
Aurora Life Sciences is seeking an experienced Compliance Engineer to join our medical device team and ensure regulatory compliance across the full product lifecycle. You will create, review and maintain technical documentation, support EU MDR, UK regulations, and post-market activities while collaborating with Quality, Engineering and Manufacturing.
The role offers exposure to regulatory submissions, Notified Bodies and continual process improvement.
We would love to welcome a new Medical Device Compliance Engineer — Regulatory Submissions to our group in Doncaster, England, United Kingdom.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
The position is based in Doncaster, England, United Kingdom.
This opportunity is part of our work in Legal, Engineering.
The advertised compensation is 42.000 - 64.000.
We aim to respond to suitable candidates as soon as possible.
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