St
Posted:
March 02, 2026
Location:
Seoul, Seoul, South Korea
Job Description
Work Flexibility: HybridProduct Approval – to prepare tech file, submit and complete product registration to MFDS aligned with business plan in timely manner having with manager’s supervising. Change management of product registrations to perform modification process following by Corporate’s Change Notification process & MFDS requirements Processing new KGMP certification for MFDS product registration Data management after product registration at internal Stryker system Involve SKL’s QMS activities to maintain Stryker Korea’s QMS efficiently, which is complied with MDA(medical device act) observations, with ISO 13485 standards, and with Stryker standards. Those c...
Main objective / purpose of the role:
This role is to process MFDS product registrations w/ KGMP certification and post market surveillance of medical device in compliance with Regulatory & Corporate’s requirements.
Critical success factors / key deliverables:
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Job Type:
Full time
Location:
Seoul, South Korea
Posted:
March 02, 2026
Deadline:
April 11, 2026