Your tasks
- Assist the Head of Quality Management and Medical Device Authorisation in the day-to-day business in the regulated environment of medical device manufacturing (ISO 13485, MDR).
- You will maintain the medical device file and create the necessary formal documentation. This task also includes technical and formal reviews, monitoring the approval process and the proper archiving of documents.
- Your tasks may also include scientific literature research and the preparation of results as part of the validation of medical efficacy.
- Furthermore, you will accompany the entire product life cycle of our medical device and support the creation of the required documents.
Your strengths
Ideally, you are enrolled in a medical/life sciences or natural sciences degree programme.
Know how:
Confident handling of IT-supported text and data processing (e.g. MS Office, Jira, Confluence) is desirable. Knowledge in the field of scientific work such as literature searches in medical databases is also an advantage. Ideally, you have already gained initial experience through comparable activities.
Language:
Very good German and good written and spoken English skills.
Personality and ways 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 organised working methods. You enjoy regulated work processes and the clean creation and organisation of documents.