Working Student (m/f/d) - Quality Assurance
Area of responsibility
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 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.
Education: Ideally, you are enrolled in a medical/life sciences or natural sciences degree program.
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 skills: Very good German and good written and spoken English skills.
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 a regulated way of working. You enjoy regulated work processes and the clean creation and organization of documents.