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Danaher Corporation Logo Danaher Corporation · IT - Administration

Qc Lab Technician

Korea, Republic of, Incheon · Job Posted June 01, 2026
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Job Description

The QC Lab Technician for Cytiva Korea is responsible for Filtration Product Quality Control tests as reporting to the Senior Quality Manager to ensure compliant execution, monitoring, and continuous improvement of QMS and Quality Control in line with certification requirements and customer expectations. This position is part of the Quality and Regulatory Affairs team located in Song-do, Incheon, South Korea and will be on-site. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

Job Responsibility

  • Perform Quality Control test for production release
  • Maintain laboratory condition for QC test(Chemical, Consumables, Cell paste, and equipment related to QC test)
  • Support QA duties as required including Audits, Documentation Control (Change Control, Deviation handling, Complaint investigation, CAPA, Risk assessment, Calibration, Validation, etc.)
  • Maintain the Quality Management System in accordance with Corporate, BU and Regulatory Requirements and set up and maintenance of LIMS in new site
  • Implement continuous improvement practices in new plant site, including supporting kaizen events for relevant Quality processes

Requirements

  • Bachelor’s degree from an accredited University or College, preferably in Biological Science and/or Microbiology
  • Related quality experience would be a plus
  • Agreeable personality, able to communicate effectively at all levels both internal and external to Cytiva
  • Understanding of ISO 9001, GMP, and GDP requirements
  • Strong analytical- and problem-solving skills
  • Good level of English & Korean in written and verbal communications
  • Ability to travel abroad upon business needs
  • If foreign national, legal work permit is required to pursue employment contract by Korean immigration law
  • Ability and resilience to manage required chemical materials to pursue task in healthy and safe condition
  • Ability to lift, move or carry equipment, any other physical requirement

Nice to have

  • Knowledge of Lean tools (like DBS) and understanding of Cytiva products
  • Internal Audit against applicable ISO 9001 and GMP standards
  • Quality Assurance/Laboratory experience desirable in Pharmaceutical Industry
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