Comply with laboratory safety rules and applicable regulatory requirements
Prepare,revise,and review GMP and GLP test methods,worksheets,and procedures
Maintain,archive,and manage GMP and GLP documentation properly
What they want
Hold a bachelor's degree in chemistry,life sciences,or related engineering fields
Understand cGMP for QC laboratories and compendial standards such as USP and EP
Demonstrate strong interpersonal communication and collaboration skills
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Nice to have
Bring prior experience working in the pharmaceutical industry
Bring prior experience working in a quality control department
Apply quality control testing,documentation,compliance,and continuous improvement skills
Seoulstart's read
Visa tier (likely)
E-7 specialty / professional (likely)
Korean language
Korean not required
English friendliness
High: JD in English, foreign-friendly signals
Context
Incheon site QC at a global pharma manufacturer; expect strict GMP,audits,and local regulatory alignment.
This is Seoulstart's analysis of the public job description, not the employer's stated policy. Verify visa sponsorship, language requirements, and remote allowances directly with the recruiter.