About the Role
The Quality Control Specialist will support production and testing activities in compliance with GMP and ISO 13485 standards.
Key Activities
Support daily QC activities across production areas such as assembly, pouching, labelling, and packaging.
Perform and verify line clearance, equipment checks, and in-process inspections.
Record and review production and QC testing data in Device History Records (DHRs) in real time.
Conduct AQL inspections and sampling on finished products as required.
Identify and report non-conformances, assist in root cause analysis, and ensure proper documentation.
Maintain organised records and ensure data archiving in accordance with SOPs.
Assist in training new QC personnel and support cross-functional communication with production teams.
Communicate effectively in both English and Korean to support collaboration across departments.
Preferred Skills
Experience in the medical device, pharmaceutical, or diagnostics industry preferred.
Bilingual in English and Korean preferred.
Education and Experience
Bachelor’s degree in Biology, Chemistry, or a related scientific/engineering field (preferred).
0–5 years of experience in Quality Control or Quality Assurance within a GMP-regulated manufacturing environment.
About Us
Finding a great opportunity that fosters growth, a great culture, and leadership opportunities can be difficult. Top Quality Recruitment (TQR) connects professionals with leadership opportunities across the Packaging, Food and Beverage, Medical Devices, and Biotechnology industries. With 50+ years of experience, we believe in one-to-one communication and finding the best candidate/employer match possible.
TQR is an equal-opportunity employer that encourages diversity. We will consider all applications.
Accommodation for applicants with disabilities is available upon request.
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