Job Positions and Qualifications
Common Qualifications
- Must be a foreign national eligible for a visa and employment in South Korea.
- Must hold a TOPIK (Test of Proficiency in Korean) Level 3 or higher.
- Scores obtained between March 9, 2023, and March 9, 2025, are recognized.
- Applicants without a language proficiency score must obtain and submit it by August 2025.
[Preferred Qualifications]
- At least 2 years of relevant work experience after obtaining a bachelor's degree.
- For those with (or expecting) a master's or doctoral degree, the study period is counted as work experience.
MSAT Process Technology
Key Responsibilities
- Technology transfer for biopharmaceutical cultivation/purification processes.
- Establishing technology transfer strategies and conducting process risk assessments.
- Preparing GMP documentation related to technology transfer.
- Monitoring production processes and investigating deviations.
- Collaborating with clients and responding to audits.
Required Qualifications
- Refer to Common Qualifications.
Preferred Qualifications
- Master’s or Ph.D. in Life Sciences, Chemical Engineering, or a related field.
- Experience in developing protein drug cultivation/purification processes.
- Experience in preparing GMP documentation (e.g., PCS, QRA, MBR, SOP) and responding to regulatory audits.
- Understanding of technology transfer and cGMP.
- Proficiency in business communication and documentation in English.
QC Quality Control
Key Responsibilities
- Technology transfer of physicochemical, biochemical, microbiological, and biosafety test methods.
- Lifecycle management of test methods.
- Laboratory management (routine walkthroughs, audit response, safety management, etc.).
- Preparing and managing GMP documents.
Required Qualifications
- Refer to Common Qualifications.
Preferred Qualifications
- Master’s or Ph.D. in Life Sciences, Chemical Engineering, or a related field.
- Experience in physicochemical, biochemical, microbiological, or biosafety testing.
- Experience in preparing GMP documents (e.g., SOP, NCR) and responding to regulatory audits.
- Understanding of quality systems and manufacturing processes in biopharmaceuticals.
- Proficiency in business communication and documentation in English.
CDO Process Development
Key Responsibilities
- Developing process technology for client projects.
- Developing antibody and gene-based process technology.
- Establishing analytical methods for product characterization.
- Supporting regulatory submission documents and client interactions.
Required Qualifications
- Refer to Common Qualifications.
Preferred Qualifications
- Master’s or Ph.D. in Chemistry, Chemical Engineering, Biology, Biotechnology, Pharmacy, or a related field.
- Experience in developing antibody and gene-based processes.
- Experience in preparing regulatory submission documents and establishing analytical methods.
- Understanding of technology transfer and drug approval processes.
- Proficiency in business communication and documentation in English.
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