Senior Regulatory Affairs Professional

Siemens Healthineers

SEL SD
Onsite
Regulatory strategies development
Kgmp/iso 13485 compliance
High-risk medical device experience
Join us in pioneering breakthroughs in healthcare for everyone, everywhere, sustainably

Job Summary

  • Join us in pioneering breakthroughs in healthcare for everyone, everywhere, sustainably.
  • You will develop regulatory strategies and manage hands-on preparation and submission of dossiers for new registrations.
  • We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries.

Matching Summary

Join us in pioneering breakthroughs in healthcare for everyone, everywhere, sustainably.

Skills & Requirements

Must-have

  • regulatory strategies development
  • KGMP/ISO 13485 compliance
  • high-risk medical device experience

Nice-to-have

  • familiarity with Digital Medical Products Act
  • proactive risk identification
  • collaborative team environment

Key Requirements

  • Korean native or native level Korean
  • bachelor’s degree or equivalent
  • 5 years of relevant experience

Work Rights

Not specified

Tailored Resume

Cover Letter