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Abbott is seeking a Supervisor for Quality Assurance in Yongin-si, South Korea, with a focus on managing QC testing schedules, deviation management, and supporting project-related testing. The ideal candidate should have extensive experience in GMP QA or QC within the biotechnology or pharmaceutical sectors, along with strong English communication skills.
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Job Summary
The role involves managing QC testing schedules, project timelines, and reviewing approval certificates for quality control.
Candidates must handle deviation investigations, OOS reviews, and execute corrective actions to ensure regulatory compliance.
This position requires leading a three-shift FQC team while supporting projects and preparing for internal and external audits.
Matching Summary
Match Score: 75
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Abbott is seeking a Supervisor for Quality Assurance in Yongin-si, South Korea, with a focus on managing QC testing schedules, deviation management, and supporting project-related testing. The ideal candidate should have extensive experience in GMP QA or QC within the biotechnology or pharmaceutical sectors, along with strong English communication skills.
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Skills & Requirements
Must-have
QC test schedule management
Deviation and CAPA review
OOS investigation and resolution
Audit preparation and response
FQC organization management
Business English proficiency
Nice-to-have
Inspection/Audit experience
Background in life sciences
Chemistry or biochemistry degree
Clinical pathology background
MS Excel and Word skills
Key Requirements
Bachelor's degree or higher
13-15 years of GMP QA/QC experience
Experience with in vitro diagnostics or pharmaceuticals