QA Specialist (1-year Contract)

Stryker · Seoul, South Korea · full time · On site · July 28, 2026

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Posted July 28, 2026 · Read from Stryker
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Work Flexibility: Hybrid

Education / work experience

  • BS in a science, engineering, business or related discipline.
  • 0+ years experience in manufacturing environment or equivalent.

Key areas of responsibility

  • Support post-market surveillance (PMS) activities, including complaint handling, product field actions, adverse event reporting, UDI reporting, and other activities in accordance with applicable local regulatory requirements.
  • Support Quality Management System (QMS) activities to ensure compliance with internal procedures and applicable regulatory requirements.
  • Support the maintenance and control of QMS documentation, including procedures, work instructions, forms, and quality records.
  • Support communications and document preparation for regulatory authorities and Notified Bodies, as applicable.
  • Assist with QMS improvement initiatives and process updates under the guidance of the QA team.
  • Assist with cross-functional QA projects and support QMS-related systems and documentation.
  • Perform other QA administrative and operational tasks as assigned.

Knowledge / competencies

  • Good command of written and spoken English.
  • Strong documentation skills with attention to detail.
  • Basic understanding of Quality Management System (QMS) and applicable regulatory requirements.
  • Proficiency in Microsoft Office applications (Excel, Word, and PowerPoint) and data management.
  • Strong communication and interpersonal skills with the ability to work effectively in a cross-functional environment.
  • Good organizational and problem-solving skills with the ability to manage multiple tasks.

Travel Percentage: None

Employer
Stryker
Location
Seoul, South Korea · On site
Contract
full time