Regulatory Affairs Engineer, Manufacturing Lifecycle

Neko Health · Stockholm

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Company
Neko Health
Location
Stockholm
Employment type
Full-time
Posted
September 24, 2026

About this job

ABOUT THE ROLE We are looking for a regulatory affairs or quality engineer to work on design transfer and on the regulatory compliance of manufacturing and distribution at Neko. This role sits at the point where a finished design becomes a manufactured device. Day to day you will work on the transfer of products from engineering into production, on the good manufacturing practice requirements that apply once a device is being built, and on the documentation that has to be in place before a device can be released and shipped to the markets where we operate. The work is hands-on and close to the factory floor: with the production team, in the records created when a device is built, and in the paperwork that has to be right before a shipment leaves.…

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