Your profile:

• Completed studies in natural sciences or engineering, e.g., medical technology, biotechnology, industrial engineering, or comparable qualifications.
• 3-5 years of professional experience in Regulatory Affairs for medical devices
• Sound knowledge of the MDR and relevant standards (especially ISO 13485, ISO 14971)
• Experience in working with notified bodies and in preparing or accompanying audits.
• Good English and PC skills (MS Office, PDF editing programs, SAP)
• Strong teamwork and communication skills
• Structured, reliable and independent work style
• Analytical, solution-oriented thinking
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