Recruitment Jobs and Qualifications
Common Qualifications
- Must be a foreign national legally eligible to obtain a visa and work in Korea with no disqualifications
- Must hold TOPIK Level 3 or higher
※ Valid scores are recognized from September 22, 2023 to September 22, 2025.
Applicants without a valid language score must submit one by February 2026.
MSAT Process Technology
Responsibilities
- Technology transfer of biopharmaceutical upstream/downstream processes
- Establishment of technology transfer strategies and process risk assessments
- Preparation of GMP-related documents for technology transfer
- Process monitoring during production and investigation of deviations
- Customer and regulatory inspection support
Qualifications
- Minimum of 2 years of relevant experience
※ Master’s/Ph.D. degree holders (including candidates) may have their study period recognized as work experience.
Preferred Qualifications
- Master’s/Ph.D. degree in Life Sciences, Chemical Engineering, or a related field
- Experience in upstream/downstream process development for protein therapeutics
- Experience preparing GMP-related documents (PCS, QRA, MBR, SOP, etc.) and responding to regulatory inspections
- Understanding of technology transfer and cGMP regulations
- Proficiency in business-level English (spoken and written)
CDO Process Development
Responsibilities
- Process development for client projects
- Development of antibody- and gene-based process technologies
- Establishment of analytical methods for product characterization
- Support in preparing regulatory submission documents and client communication
Qualifications
- Minimum of 2 years of relevant experience
※ Master’s/Ph.D. degree holders (including candidates) may have their study period recognized as work experience.
Preferred Qualifications
- Master’s/Ph.D. degree in Chemistry, Chemical Engineering, Biology, Biotechnology, Pharmacy, or a related field
- Experience in antibody- and gene-based process development
- Experience in regulatory documentation and analytical method establishment
- Understanding of technology transfer and regulatory approval for pharmaceuticals
- Proficiency in business-level English (spoken and written)
Required Documents
- Documents must be submitted only by those who pass the application screening stage (further instructions will be provided).
ㆍOriginal graduation certificate / transcript / career certificate (1 copy each)
ㆍTOPIK score report / other certificates and confirmations