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Working Student (m/f/d) Documentation / QM

Düsseldorf, Germany



   Your tasks

  • Assist the head of our quality management and  medical device approval in the day-to-day business in  the regulated environment of medical device  manufacturing (ISO 13475, MDR).  

  • You support the formal documentation in quality  management and / or the medical device file. This  includes technical and formal reviews, spell checks in  German and English, release processes and proper  archiving of documents. 

  • Ideally, you will take on tasks and processes in quality  assurance, such as the creation and training of work  instructions, as well as the verification of the  corresponding work results in the form of document  review and softaware testing. 

  •  In addition, literature research and its textual  preparation or the validation of medical requirements  could be part of your work


You are ideally enrolled in a medical/life  sciences or natural sciences university and have  experience and enjoy creating and reviewing documents.

Experience & Know-How

Confident handling of IT-supported text and  data processing (e.g. MS Office, Jira, Confluence) is  desirable. Ideally, you have gained initial experience  through comparable activities.


We require very good German and good English  skills, both written and spoken.

Personality and way of working

You are a team player with  strong communication skills and a precise, independent,  proactive and reliable way of working. You enjoy word  processing and working in a regulated manner.

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