Regulatory & Quality Manager

Floy

Check country restrictionsPublished on Aug 11, 2026Confirmed active on Nov 15, 2026
Full-timeHealthcare

Job briefing

Read from the posting and checked against our job index

Apply from
Not stated
Work model
Fully remote
Full posting text checked
Salary
Not stated
Roles in the same field in our index: median €5,000 per month, middle range €4,122 to €6,250 (114 postings).
Level and language
Lead · English, German

Tech stack

  • ISO 13485
  • EU MDR

Good to know

Listed with us since
August 11, 2026
Employer
1 more open role at Floy in our index. It is fully remote. See remote jobs at Floy
Benefits in the posting
Regular feedback, Weekly 1:1s, Meaningful, challenging work, Autonomy, Flexibility, Regular company retreats

Generated automatically by nomado24 from the posting and our index. Not an employer statement. The original posting is authoritative.

Job description

Your mission

At Floy, Regulatory & Quality is a key enabler of innovation. Your mission is to transform complex regulatory requirements into practical, scalable solutions that support the development and successful certification of AI medical devices. As part of the Medical Excellence team, you will collaborate closely with Product, AI, Engineering, and Marketing to ensure that quality, regulatory compliance, and clinical value are integrated throughout the entire product lifecycle.

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.

What are we looking for?

  • 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.

Why us

Pioneer medical AI to maximize human health. Become part of an ambitious team valuing individuals, dedication and a joyful work experience. Solve novel challenges with life-saving implications.

  • 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.
Medicalpermanent

This role is provided by an external source. Applications are handled on the source website.

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