NextRaise Logo
JobsTrackerResumes
Job MatchATS
ResumesJobsProfile
Jobs
2 months ago
Apply with autofill
Apply with autofill
ZB
Zimmer Biomet·2 months ago
2 months ago

Regulatory Affairs Specialist (Contract)

Seoul, South KoreaMid · 2-5 years

Sign up free to see how well your resume matches this role.

About this role

Become part of our team as a Regulatory Affairs Specialist, supporting new product registration and maintaining existing product licences. You will ensure compliance with MFDS and corporate QA requirements, collaborating with global teams. Ideal for candidates with regulatory affairs experience and strong knowledge of medical device regulations.

Skills

  • mfds regulations
  • gmp compliance
  • product registration
  • license renewal
  • line extension registration
  • quality management systems
  • sop preparation
  • korean labeling documentation
  • gsp compliance
  • mda compliance
  • medical device regulations
  • regulatory documentation
  • project management
  • stakeholder management
  • english language proficiency
  • computer skills
H1B sponsor likely
AI tools
Apply faster with autofillThe NextRaise extension autofills your application in one click.Get the extension

Similar jobs

  • Sr. RA Specialist at abbvieSeoul, South Korea
  • Regulatory Affairs (Senior) Associate at gsknchSeoul, South Korea
  • [KOREA] Regulatory Affairs Specialist (NEW Position) at santenSeoul, South Korea
  • (Senior) Regulatory Affairs Specialist at iconSeoul, South Korea
  • Regulatory Affairs Manager at AmgenSeoul, South Korea
  • Regulatory Affairs Senior Specialist at AstraZenecaSeoul, South Korea