Job Positions and Eligibility Requirements
Common Eligibility Requirements
- Foreign nationals who are eligible for visa acquisition and employment in South Korea
- Holders of TOPIK (Test of Proficiency in Korean) Level 3 or higher
- Valid scores from March 9, 2023, to March 9, 2025, are accepted.
- Those without language test scores must submit results by August 2025.
[Preferred Qualifications]
- Individuals with 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 recognized as work experience.
Antibody-Drug Conjugate (ADC) Technology Development and Analysis
Job Description
Key Responsibilities
- Design, synthesis, exploration, SAR, and molecular modeling of synthetic compounds
- Design, synthesis, and exploration of ADC-oriented Linkers and Payloads
- ADC Linker-Payload conjugation with antibodies
- Development of physicochemical/bioanalytical methods for compound analysis and structural analysis
- Process optimization to improve yield and purity of compound synthesis
Eligibility Requirements
- Refer to Common Eligibility Requirements
Preferred Qualifications
- Majors in Biology/Chemistry (Master’s/PhD preferred)
- Relevant experience (projects, publications, patents, competitions, etc.)
Downstream Process Development
Job Description
Key Responsibilities
- Development of downstream processes for biosimilar antibodies and new drug antibodies (bispecific antibodies, ADCs)
- Design and execution of purification experiments by microbial size and protein size (Virus filters, UF/DF membranes)
- Optimization of large-scale production purification processes
- Development of API (Active Pharmaceutical Ingredient) purification processes and equivalence testing
- Development of purification processes using UF/DF and column chromatography
Eligibility Requirements
- Refer to Common Eligibility Requirements
Preferred Qualifications
- Majors in Biology/Chemistry (Master’s/PhD preferred)
- Relevant experience (projects, publications, patents, competitions, etc.)
Bioassay
Job Description
Key Responsibilities
- Development of Cell-based Assays and creation of Standard Operating Procedures (SOPs)
- Development of Binding Assays and creation of Standard Operating Procedures (SOPs)
- Preparation and review of regulatory documents related to biological assays
- Equivalence evaluation between originator drugs and biosimilars
- Review and management of biological analysis data
- Quality analysis and equivalence verification of developmental products
Eligibility Requirements
- Refer to Common Eligibility Requirements
Preferred Qualifications
- Majors in Biology/Pharmaceutical Sciences (Master’s/PhD preferred)
- Relevant experience (projects, publications, patents, competitions, etc.)
Device Development
Job Description
Key Responsibilities
- Development and validation of devices for each product (e.g., Autoinjectors)
- Establishment and validation of production processes for devices
- Functional evaluation of materials, environmental variability assessment (temperature, pressure), and improvement
- Comparative analysis and evaluation between devices, defect analysis
- Risk monitoring, management, and response for Contract Manufacturing Organizations (CMOs)
- Preparation of regulatory documents and correspondence with regulatory authorities
Eligibility Requirements
- Refer to Common Eligibility Requirements
Preferred Qualifications
- Majors in Materials/Mechanical Engineering (Master’s/PhD preferred)
- Relevant experience (projects, publications, patents, competitions, etc.)
Formulation Development
Job Description
Key Responsibilities
- Formulation development and analysis for efficient delivery of antibody drugs
- Customized formulation development and analysis for next-generation antibodies (bispecific antibodies and ADCs)
- Development, optimization, and technology transfer of lyophilization processes
- Analysis and reporting related to protein aggregation (Aggregation Path)
- Development of formulation processes and establishment of application processes
- Risk monitoring and management for outsourced formulation processes
Eligibility Requirements
- Refer to Common Eligibility Requirements
Preferred Qualifications
- Majors in Biology/Chemistry (Master’s/PhD preferred)
- Relevant experience (projects, publications, patents, competitions, etc.)
Drug Product (DP) Process Development
Job Description
Key Responsibilities
- Development of manufacturing processes for Drug Products
- Risk assessment and management support for Drug Product manufacturing processes
- Preparation and improvement of technical reports and related regulatory submission materials
- Modeling for mixing/buffering processes using Computational Fluid Dynamics (CFD)
- Simulation for optimizing formulation process modeling
- Evaluation and analysis of extractables and leachables in Drug Products
Eligibility Requirements
- Refer to Common Eligibility Requirements
Preferred Qualifications
- Majors in Biology/Chemistry (Master’s/PhD preferred)
- Relevant experience (projects, publications, patents, competitions, etc.)
.png)
.png)
.png)