Job Positions and Qualifications
Common Eligibility Criteria
- Foreign nationals with no disqualifications for obtaining a visa or working in Korea
- Holders of TOPIK (Test of Proficiency in Korean) Level 3 or above
※ Scores obtained between September 3, 2022, and September 3, 2024, are accepted.
※ Those without a language score can submit their results by January 2025.
[Preferred Qualifications]
- At least two years of relevant work experience after obtaining a bachelor's degree
※ The duration of study will be recognized as work experience for those who have obtained or are expected to obtain a master's or doctoral degree.
Purification Process Development
Job Information and NotesKey Responsibilities
- Develop purification processes for biosimilar antibodies and novel antibodies (including bispecific antibodies and antibody-drug conjugates).
- Design and conduct purification experiments for microorganisms and proteins by size (e.g., virus filters, UF/DF membranes).
- Optimize large-scale purification processes.
- Develop purification processes for drug substances and conduct quality equivalence testing.
- Develop purification processes using UF/DF and column chromatography.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Biology/Chemistry (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
Clinical Bioanalysis
Job Information and NotesKey Responsibilities
- Develop pharmacokinetics (PK) and pharmacodynamics (PD) analytical methods for biopharmaceuticals.
- Develop immunogenicity analytical methods for biopharmaceuticals.
- Prepare standard operating procedures (SOPs) for analytical methods and validate these methods.
- Manage risks associated with biopharmaceutical analysis.
- Conduct quality analysis and equivalence verification for developing products.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Biology/Pharmacology (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
Physicochemical Analysis
Job Information and NotesKey Responsibilities
- Develop and troubleshoot analytical methods for linker-payload in antibody-drug conjugates (ADCs).
- Conduct physicochemical analysis (LC, CE, icIEF) and primary/secondary structural analysis (mass spectrometry).
- Analyze and review characteristics of linker-payload in ADCs.
- Prepare Common Technical Documents (CTD) related to linker-payload analysis in ADCs.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Chemistry (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
Device Development
Job Information and NotesKey Responsibilities
- Develop devices for each product (e.g., autoinjectors) and verify developed devices.
- Establish and verify production processes for devices.
- Evaluate the functionality of materials, assess material variability under different environmental conditions (temperature, pressure), and implement improvements.
- Perform comparative analysis and evaluation of devices, and conduct defect analysis.
- Monitor and manage risks associated with Contract Manufacturing Organizations (CMOs) and respond as needed.
- Prepare regulatory documents and respond to regulatory authorities.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Materials/Mechanical Engineering (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
Formulation Development
Job Information and NotesKey Responsibilities
- Develop and analyze formulations for the efficient delivery of antibody drugs.
- Develop and analyze customized formulations for next-generation antibody drugs (bispecific antibodies and ADCs).
- Develop, optimize, and transfer freeze-drying processes.
- Analyze and report on protein aggregation (aggregation path).
- Develop formulation processes and establish application processes.
- Monitor and manage risks associated with contract manufacturing in formulation processes and respond as needed.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Biology/Chemistry (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
Drug Product (DP) Process Development
Job Information and NotesKey Responsibilities
- Develop manufacturing processes for drug products.
- Conduct risk assessments and support risk management for drug product manufacturing processes.
- Prepare and revise technical reports and related regulatory submissions.
- Model mixing/buffering processes using computational fluid dynamics (CFD).
- Optimize formulation process modeling through simulation.
- Evaluate and analyze extractables and leachables in drug products.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Biology/Chemistry (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
Package Design Development
Job Information and NotesKey Responsibilities
- Develop pharmaceutical package designs.
- Manage changes and version control for pharmaceutical artwork.
- Develop package designs based on regulatory approvals and launch plans in different countries.
- Work on developing the structure of pharmaceutical packages.
- Research and analyze trends in pharmaceutical packaging.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Visual Design/Industrial Design (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
DP Manufacturing
Job Information and NotesKey Responsibilities
- Develop and strategize drug product manufacturing processes.
- Characterize and validate drug product manufacturing processes.
- Transfer, manage, and manufacture GMP processes with CMOs.
- Develop and manage automated foreign particle inspection processes in drug products.
- Manage the chemical, manufacturing, quality safety, and regulatory compliance of drug products.
Eligibility Criteria
- Refer to the Common Eligibility Criteria.
Preferred Qualifications
- Majors in Biology/Chemistry (Master's/PhD preferred).
- Experience related to the role (projects, papers, patents, competitions, etc.).
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