Regulatory & Quality Manager

🕒 il y a 2 mois

🇩🇪 Allemagne – Télétravail

⏰ Temps Plein

🟡 Intermédiaire

🟠 Senior

🚔 Conformité

🗣️🇺🇸🇬🇧 Anglais requis

🗣️🇩🇪 Allemand requis

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Floy

51 - 200 employés

Fondée en 2021

🏥 Santé

💼 Conseil

🤖 Intelligence artificielle

Healthcare • Consulting • Artificial Intelligence

Floy développe des logiciels basés sur l'intelligence artificielle qui assistent les radiologues dans la détection de maladies complexes et difficiles à identifier. La collaboration entre Floy-AI et les radiologues garantit des résultats optimaux pour les patients en permettant la détection précoce et donc le traitement anticipé des maladies.

Description

• Own and continuously improve Floy's ISO 13485-certified Quality Management System • Lead MDR conformity assessments and interactions with the Notified Body • Prepare technical documentation for AI-powered medical devices • Act as the regulatory partner for interdisciplinary product teams • Support audits, risk management, and continuous improvement activities • Collaborate with Product, AI, Engineering, and Marketing to integrate quality, regulatory compliance, and clinical value throughout the product lifecycle

🎯 Exigences

• Bachelor's or Master's degree in Life Sciences, Medical Technology, Biomedical Engineering, Regulatory Affairs, or a related field • Professional proficiency in English and German, written and spoken • Experience in Regulatory Affairs for medical devices, ideally under the EU MDR • Strong written communication skills and ability to prepare clear, structured documentation • Analytical thinking and a pragmatic, solution-oriented mindset • Ability to work independently while collaborating effectively across interdisciplinary teams • Enthusiasm for digital health, AI, and innovative medical technologies

🏖️ Avantages

• Regular feedback • Weekly 1:1s • Meaningful, challenging work • Autonomy • Flexibility • Flexible, remote-friendly team culture • Regular company retreats • Fair compensation

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