General
Full-time, Cambridge (UK)
If this sounds like something you'd enjoy, email join@flok.health with your CV & a cover letter, or apply via our contact form. Please confirm that you know it is an in-person role in Cambridge, and that you either already live nearby or you're willing to relocate.
Apply nowFlok Health has built the world's first AI physiotherapy clinic, working with the NHS and treating patients across the UK. Our patients get access to high-quality personalised care, without sitting on a waiting list or needing to leave their home. Part of our work involves building and maintaining a (Class IIa) software Medical Device, which includes an ISO 13485 compliant Quality Management System (QMS) in accordance with EU & UK regulations.
We’re looking for a Compliance Assistant to help us in the day-to-day operation of our QMS. If you’ve previously worked in a compliance role or in medical device development, that would be beneficial, but it’s not required, as long as you’re willing to learn.
You’ll need:
This is a varied role working across quality/regulatory, software, and operations, supporting multiple teams across the business, and you'll be working in an innovative regulated technical environment.
Your key responsibilities will be:
And the potential to develop into a QARA lead, helping us to improve our overall approach to regulatory compliance in multiple countries.
More than a billion people a year suffer unnecessarily from conditions like MSK pain, where the right treatment approach is well-established but undeliverable at scale. We're changing that. Our team has deep expertise across clinical, engineering, and regulated AI, has a track record of healthtech innovation, and is backed by top VCs and multiple unicorn founder angels.
If you like:
Then you'll fit right in!