Requirements Engineer – Digital Health

🕒 il y a 8 mois

🇩🇪 Allemagne – Télétravail

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

👷🏻‍♀️ Ingénieur

🗣️🇺🇸🇬🇧 Anglais requis

🗣️🇩🇪 Allemand requis

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imito AG

11 - 50 employés

Fondée en 2016

🏥 Santé

💼 Conseil

☁️ SaaS

Healthcare • Consulting • SaaS

imito AG est une entreprise de logiciels de santé qui fournit des applications cliniques mobiles et web pour la photographie médicale sécurisée, la documentation des plaies et la mesure des plaies assistée par IA. Leurs produits (imitoCam, imitoWound/WoundGenius, imitoScan) permettent aux cliniciens de capturer, mesurer, documenter et intégrer des images et des documents de patients avec des systèmes EMR, DMS et PACS utilisant des normes telles que FHIR, HL7 et DICOM. La plateforme est conforme au RGPD, cliniquement validée par la recherche, et déployée dans des hôpitaux et des centres de soins pour rationaliser les flux de travail cliniques et permettre une documentation collaborative et prête pour l'audit.

Description

• Translate complex clinical workflows and stakeholder needs into clear, actionable technical specifications and user stories for our developers. • Elicit, analyze, document, and manage requirements throughout the product lifecycle. • Ensure all documentation complies with Medical Device Regulation (MDR) and ISO 13485 standards. • Define requirements for system integrations, leveraging knowledge of healthcare standards (HL7, FHIR, DICOM). • Participate in risk analysis and ensure safety-critical requirements are identified and tested. • Work closely with Product Management, UX/UI designers, and the development team to refine the product vision.

🎯 Exigences

• Professional experience in requirements engineering, business analysis, or product ownership, ideally within the Healthcare/MedTech sector. • A degree in Medical Informatics, Computer Science, Biomedical Engineering, or a comparable field. • Familiarity with interoperability standards (FHIR, HL7, DICOM) is a strong plus. • Experience with tools like Jira and Confluence is desired. • Experience with Medical Device Regulation (MDR) or FDA requirements is highly valued. • Excellent communication skills in English and German (required to support our DACH customer base). French is a plus.

🏖️ Avantages

• Flexible working hours and location (remote work available within Germany) • A value-driven corporate culture with direct communication, flat hierarchies, and strong team cohesion. • Work on a product that directly improves patient care and simplifies the work of medical staff. • Permanent contract with an established and growing company.

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