Une candidature sur mesure pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.
Eno Health in Brussels is building an AI-powered platform to support clinicians and patients with regulated, runtime-validated interfaces across web, mobile, and API layers.
This full-time hybrid role collaborates with clinical leadership, focusing on feature work, API design, accessibility, and performance, ensuring compliance with EU MDR and IEC 62304.
You will implement a design-system, ship data-dense interfaces, and uphold strict data-safety practices in a regulated environment.
Eno Health is an AI-powered platform designed to be the ultimate decision-support system for healthcare providers seeking to facilitate personalised care and long-term wellness for patients. We are building a compliant, secure, and European-sovereign biomedical AI solution for personalised healthcare. The platform streamlines practitioners' workflows and patient data processing, enabling faster, more precise clinical decisions.
Role Description
You will build the products and product surfaces where clinicians and patients meet the platform: a practitioner console, an API, a patient dashboard, and a mobile environment. These are health-data interfaces in a regulated product. Therefore, types are load-bearing: every API boundary is validated at runtime, because a silently miscast lab value is a patient-safety issue, not a bug ticket. Copy is regulated: what the interface may claim is controlled vocabulary, served from configuration, so corrections never wait on an app store release. If you have ever been frustrated that front-end work is treated as the soft part of the system, this role is the opposite of that.
You will work across the mobile app, web surfaces, and the API layer, with a designer-quality brand system to build on and direct access to the clinical team when an interface question is actually a clinical question. Expect a mix of feature work, API design, accessibility and performance work, and writing, because every release needs to be traceable and reviewed, and because our software lifecycle feeds into a medical-device technical file (EU MDR, IEC 62304).
This is a full-time hybrid role based in the Brussels Metropolitan Area, with flexibility for remote work.
Qualifications
What We Offer