Regulatory Affairs Engineer, Post-Market Surveillance

Mission

Neko is redefining what prevention means, from treating illness when it arrives, to sustaining health before it's ever at risk. Our mission: make data-driven, preventative care accessible to more people, before symptoms appear.

In a single, non-invasive visit under an hour, proprietary technology and direct clinical care combine to deliver personalised, actionable insights. It's a team that thinks in 10x, not 10%. Every role here plays a part in building a world where prevention is the norm, and where your work genuinely helps people live longer, healthier lives.

About the role

We are looking for a regulatory affairs engineer to strengthen how Neko runs post-market surveillance across its device portfolio.

This cross-programme role reports to the RA Engineering Lead. Neko already has a post-market surveillance system in place, and you will be responsible for operating it, ensuring it is applied consistently across all devices, and driving its continuous improvement. Your duties will include implementing the PMS SOP, producing periodic reports, and transforming an established process into one that is increasingly systematic and efficient as the portfolio expands. While the RA Engineering Lead provides overall direction and supports regulatory decisions, you will have autonomy in determining how the work i