Job Description

Working at Freudenberg: We will wow your world!

Responsibilities:

  • You contribute to the further development of Regulatory Affairs and quality management systems in accordance with MDR and ISO 13485
  • You coordinate international approval and registration procedures for medical devices containing medicinal components
  • You prepare and maintain technical documentation and communicate with customers, suppliers, and authorities worldwide
  • You handle regulatory authority inquiries and research country-specific approval requirements
  • You support R&D, production, and logistics in matters of regulatory compliance and quality
  • You maintain change management processes and support design and process changes
  • You prepare and conduct audits, including communication with customers and authorities

    • Qualifications:

  • You hold a degree in natural sciences, biomedical engineering, or a comparable qualif...

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