Your advantages:

• Support throughout the entire application process
• Support during the ongoing project by our team

Your tasks:

• Supporting the team in the area of ​​Regulatory Affairs with a focus on medical devices
• Support in creating technical documentation
• Creating PSURs and PMCF reports
• Updating usability analyses
• Assistance in the creation and revision of documents relevant to licensing.
• Support in adapting our quality management system (QM system) to new legal requirements

Your qualifications:

• A completed degree in a natural science field, such as medical technology, medicine, biology, or biotechnology.
• Initial knowledge in the field of regulatory affairs for medical devices, ideally in the creation of technical documentation.
• High quality standards and a careful and structured working method
• Strong teamwork and communication skills