Regulatory Engineering Lead, Medical Devices & Clinical Eval
Listed on 2026-10-03
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Engineering
Medical Device Industry, Biomedical Engineer
Neko Health AB seeks a regulatory affairs engineer to own the clinical side of regulatory work. You will author clinical evaluation plans and reports, and manage submissions to FDA, EU and UK, drawing on the company’s own clinical evidence.
You’ll plan and support clinical studies under ISO 14155, appraise literature and clinical data, and keep evaluations current as devices evolve, collaborating with hardware and software teams.
Our group is growing, and we are hiring a Regulatory Engineering Lead, Medical Devices & Clinical Eval in England, United Kingdom.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Regulatory Engineering Lead, Medical Devices & Clinical Eval role in the description above.
We appreciate your interest in this position.
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