Quality Management / Regulatory Affairs Employee (m/f/d)

Your future tasks will be:

• Further development of quality management in accordance with regulatory requirements
• Planning, coordination and creation of the technical documentation
• Conformity assessment procedures for CE marking
• Communication with authorities and notified bodies
• Coordination of the various departments

Our requirements for you:

• Technical or scientific university studies
• Enjoyment of analyzing complex interdisciplinary relationships
• Experience in quality management of medical devices
• High level of responsibility and quality awareness
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