Your Responsibilities:
* Support in the planning, coordination, and follow-up of international registrations for medical devices
* Assist in ensuring compliance with regulatory requirements according to MDR, MDSAP, and ISO 13485
* Contribute to the preparation and maintenance of technical documentation for global registrations
* Help compile and organize documentation for license renewals, updates, and new submissions
* Communicate with international partners, authorities, and internal departments in alignment with the Regulatory Affairs team
Your Profile:
* Completed degree in medical engineering, life sciences, or a comparable field Initial practical experience or internships in the field of Regulatory Affairs is an advantage
* Basic understanding of relevant regulatory frameworks (e.g., MDR 2017/745, ISO 13485, MDSAP) is a plus
* Structured, detail-oriented, and eager to learn
* Excellent written and spoken German and English skills
Job Types: Full-time, Permanent
Education:
* Bachelor's (Preferred)
Language:
* German (Required)