Working at Freudenberg: We will wow your world!
Responsibilities:
1. You contribute to the further development of Regulatory Affairs and quality management systems in accordance with MDR and ISO 13485
2. You coordinate international approval and registration procedures for medical devices containing medicinal components
3. You prepare and maintain technical documentation and communicate with customers, suppliers, and authorities worldwide
4. You handle regulatory authority inquiries and research country-specific approval requirements
5. You support R&D, production, and logistics in matters of regulatory compliance and quality
6. You maintain change management processes and support design and process changes
7. You prepare and conduct audits, including communication with customers and authorities
Qualifications:
8. You hold a degree in natural sciences, biomedical engineering, or a comparable qualification
9. You have experience in the medical device industry, ideally also in the validation of sterilization processes (ETO)
10. You are familiar with regulatory requirements for medical devices in the EU (EU MDR, ISO standards, MPDG); knowledge of pharmaceutical regulations (AMG, GMP) and international standards (US FDA) is an advantage
11. You have a good understanding of medical devices and functional pharmaceutical coatings
12. You work independently, in a structured manner, and as part of a team
13. You are proficient in MS Office, Adobe Acrobat, and quality management systems according to EN ISO 13485
14. You have excellent written and spoken German and English skills