Regulatory & Quality Manager
Indexed description
Your Responsibilities
- Own and continuously improve our ISO 13485-certified Quality Management System.
- Lead MDR conformity assessments and interactions with our Notified Body.
- Prepare technical documentation for AI-powered medical devices.
- Act as the regulatory partner for our interdisciplinary product teams.
- Support audits, risk management, and continuous improvement activities.
- 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 the 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.
- We support your growth through regular feedback, weekly 1:1s, and meaningful, challenging work.
- We offer autonomy, flexibility, and the chance to work alongside thoughtful, capable colleagues.
- We have a flexible, remote-friendly team culture, regular company retreats, and fair compensation.
Floy was founded in June 2021 and raised 12m€ total funding from Europe’s leading investors. Over the last months, the team grew to 60 exceptional people. Our pace only accelerates from here.
Create a free Caio profile to unlock more results and save your role and location preferences.
Unlock free search