Regulatory Compliance Assistant

Our vision is a new category of habit-forming healthcare globally; one that is patient-centred, predictive, and intrinsically scalable. We’re a digital-native healthcare provider, using personalised video streams to deliver treatment pathways at population scale, with transformative economics. By personalising each patient’s interaction in real-time, we deliver world-class medical treatment in an engaging consumer experience.Regulatory Compliance AssistantEngineeringFull-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.### The RoleFlok 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. No prior experience of medical device development is required, as long as you’re willing to learn. 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. You’ll need:* Strong organisational and time management skills* Good communication skills with the ability to build effective working relationships* And excellent attention to detail**Your key responsibilities will be:*** Supporting the administration and ongoing maintenance of the QMS* Assisting colleagues with documenting and recording quality-related actions in line with agreed timelines* Supporting periodic internal/external audits and reviews* Supporting the tracking and reporting of QMS training across the organisation* Running day-to-day regulatory affairs work, including change-request meetings, documenting supplier evaluations, facilitating risk analysis sessions, etc.And the potential to develop into a QARA lead, helping us to improve our overall approach to regulatory compliance in multiple countries.### What We Offer* Interesting and challenging work* In-person working from a beautiful work space in the Cambridgeshire countryside* An onsite gym* A digital health subscription of your choice* Early stage equity with employee-friendly terms (via an EMI scheme)* Comprehensive medical coverage (including dental and optical) and life insurance* Optional remote working on Wednesdays, with an annual allowance of 10 extra remote days* Desk setup allowance for your favourite keyboard / mouse / whatever!* Regular pulse-checks to help us build a culture we’re proud of* Monthly team BBQs and desserts on Flok* A fast paced work environment geared towards excellence and professional growth (with annual training budget)* Top notch specialty tea and coffee* A chance to have a big impact in a small early stage team making a difference to the lives of people across the UK!#J-18808-Ljbffr…