Your Responsibilities:

• Support the Regulatory Affairs team with international registration processes for medical devices
• Assist in creating and maintaining technical documentation
• Research regulatory requirements for different target markets (e.g., EU, USA, Canada, Japan)
• Help prepare applications for product registrations, renewals, and updates
• Collaborate with internal departments and occasionally communicate with international partners

Your Profile:

• Currently enrolled in a degree program in medical engineering, life sciences, or a related field
  Strong interest in regulatory topics and international regulations
• Initial experience with MDR, ISO 13485, or MDSAP is a plus (e.g., through an internship or academic projects)
• Independent and structured working style, with a team-oriented mindset
• Excellent verbal and written communication skills in German and English

Interested? Then we look forward to receiving your application. Send your documents by e-mail to: career@vsybiotechnology.com