Work Flexibility: Hybrid

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:

Product 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 requirementsProcessing new KGMP certification for MFDS product registrationData management after product registration at internal Stryker systemInvolve 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 can be such as quality documentation, internal audit, training, participation in internal or external audits, etc.Collaborate with business franchise partner, Stryker Design division RAQA, and regulatory agencies and draw out the effective communications and resolutions on any issues that may arise on workActively participate in MFDS or external meetings as a professional mannerParticipate in various RA projects internally and externallyDo every work in compliance with regulatory requirements and Stryker corporate requirements

Knowledge / Skills / Attributes

Academic qualifications / degree & relevant prior experience:

Key strengths / personal attributes for the role:

BA in science, engineering, medical, law, etc.Min 4yr of RA experience in healthcare industryBetter to have relevant experience of Government officialsBetter if fluent in EnglishWell-organized and logical thinkingPassionate and a great sense of responsibilityCommitted to punctuality, discipline & detailedProfessional communication skillsStrategic and planning skills

Travel Percentage: 10%