Neko Health AB seeks a regulatory affairs engineer to own the clinical regulatory work for our devices, drafting clinical evaluation plans and reports and supporting submissions to the FDA, EU and UK.
The role spans hardware and software, collaborating with engineering, clinical and quality teams, and emphasizes ISO 14155, IEC standards, and post-market surveillance throughout product development.
#J-18808-Ljbffr
Full job description from WhatJobs. Apply for this role →
Cambridge
We're looking for a Regulatory Affairs Engineer for a contract role with a medical device manufacturer.
Explore: Clinical Research Associate jobs in London Clinical Research Associate jobs in the UK Engineering recruitment Specialist jobs in London
Worked with Verifera as a candidate or employer? Your honest review helps the next person trust verified hiring.