Quality Control Specialist

About the job Quality Control Specialist Key Responsibilities

• Support daily QC activities across production areas such as assembly, pouching, labeling, 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 organized 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.

• Bachelors degree in Biology, Chemistry, or a related scientific/engineering field (preferred).
• 05 years of experience in Quality Control or Quality Assurance within a GMP-regulated manufacturing environment.
• Experience in medical device, pharmaceutical, or diagnostics industry preferred.
• Bilingual in English and Korean preferred.
• Working knowledge of ISO 13485, GMP, and FDA quality regulations is a plus.
• Strong attention to detail and documentation accuracy.
• Ability to work independently and as part of a team in a fast-paced environment.
• Excellent time management and problem-solving skills.
• Proficiency in Microsoft Office (Word, Excel).