Manager Quality & Regulatory Affairs - Medical AI (w/d/m | 50-100%)
Full time
Your responsibilities as Quality & Regulatory Affairs Manager
- Your main task on the quality side is to maintain and develop the eQMS in accordance with current requirements and steer our audits
- Your main tasks on the regulatory side are to advise our leadership on regulatory changes and their impact on our business, steer our country-specific consultants and update the technical file for our product
- You are great in your job when your colleagues follow your processes and guidelines, because they understand it makes their life easier in the long run
What we are looking for
Your must-haves
- Master’s degree in science, engineering or health
- First applied experience in medical devices
- The unique combination of critical thinking and a positive can-do-attitude
- Excellent English + German for writing short & precise
Your nice-to-haves
- Experience in precision medicine, medical AI or digital health
- Experience in dealing with medical authorities like FDA, EMA or NBs
- Great communication skills to take the team with you on your journey
What we offer
- Direct impact on improving quality of life for patients & providers
- Full responsibility for your area & team, enabling fast personal growth
- Flexible working hours, remote work & central office in Munich’s startup hub
- Compensation package, startup culture & an international rock star team
How to apply
Reach out to us via email with information about your availability, salary expectation and a link to your conclusive profile (LinkedIn, CV). We do not require a motivation letter, but if you like please share with us in 2-3 sentences why you want to help us in preventing blindness with AI.
deepeye Medical
Our mission is to prevent vision loss and ultimately blindness by developing AI software that assists eye doctors in therapy planning for their pat...