Job Description

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Your Responsibilities

Key Responsibilities:

+ Maintain, manage, and archive QM documents
+ Communicate with internal departments and international partners
+ Support monitoring and implementation of regulatory standards (e.g., ISO 13485, ISO 15189)
+ Participate in projects focused on process optimization in QM

Learning Opportunities:

+ Gain insights into regulatory and organizational requirements for medical devices
+ Understand the structure and operations of a company with ~500 employees
+ Contribute to ensuring quality and compliance within the organization

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Your profile

You are a registered student or are looking for a temporary job that offers you exciting practical experience You are available to work reliably for 20 hours a week for at least two semesters You are familiar with Microsoft Office (especially Word, PowerPoint, and Outlook) You have an organized and structured approach to work, enjoy attention to detail, and enjoy documentation work You communicate confidently in English and look forward to working with many international colleagues You are open-minded, motivated, and able to quickly familiarize yourself with new topics You are interested in regulatory requirements and quality management systems in the life sciences sector
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Why us?

Insights into the work of an international QM/RA department and plenty of room for further development Regular company events and health management with a free fitness area overlooking the city Lunch breaks and meetings on our roof terraces overlooking the Warnow river feel like a vacation Hourly Salary of 14€
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About us

With employees from over 50 nations, CENTOGENE is a truly international company with offices is in Rostock, Berlin, Delhi, Boston, Valencia, Belgrade, and São Paulo.


We were born to help diagnostic patients with rare disease and today we evolved to help patients of all clinical specialties to make bold progress with guided solutions for physicians, their patients and pharma partners.