Quality Specialist

What you will do:

• Perform production release activities as a Quality Assurance representative in accordance with company policies, procedures, and compliance requirements
• Perform destructive analysis on returned complaint samples to support complaint investigations
• Perform outlier analysis to identify abnormal data points and distinguish between common cause and special cause variations
• Support Quality Assurance activities including audits and documentation control (Change Control, Deviation handling, Complaint investigation, CAPA, Risk Assessment, Calibration, Validation, etc.) in accordance with the Quality Management System (Veeva)Perform production release as a Quality Assurance in accordance with Company compliance and procedure

Who you are:

• Minimum, bachelor’s degree from an accredited University or College, preferably in Biological Science and/or Microbiology  
• 3 or more years of related Quality Assurance or Quality Engineering experience
• Agreeable personality, able to communicate effectively at all levels both internal and external to Cytiva
• Comprehensive understanding of ISO 9001, GMP, and GDP requirements
• Strong analytical- and problem-solving skills.

Travel, Motor Vehicle Record & Physical/Language/ Environment Requirements:

• Fluent level of English & Korean in written and verbal communications 한국어 및 영어로의 서면 및 구두 의사소통능력이 뛰어난 분
• Ability to travel abroad upon business needs 해외여행에 결격 사유가 없으신 분
• Must have a valid driver’s license with an acceptable driving record within territory or locations 운전을 하여 담당하는 국내 고객사에 방문할 수 있는 분
• If foreign national, legal work permit is required to pursue employment contract by Korean immigration law 대한민국에서의 근무가 가능한 비자가 있는 분
• Ability and resilience to manage required chemical materials to pursue task in healthy and safe condition 업무 수행이 필요한 화학 물질을 건강하고 안전한 조건에서 다룰 수 있는 분
• Ability to lift, move or carry equipment, any other physical requirements
• 들어 올리거나 이동하거나 운반할 수 있는 능력, 기타 물리적 요구 사항

It would be a plus if you also possess previous experience in:

• Desirable: 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

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. 

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.