Hiring foreign experienced employees in the R&D field

Job Description

[Cell Line Development] - Development of high-expression production cell lines - MCB/WCB characterization and manufacturing - Host cell improvement (gene editing, directed evolution, etc.) [Culture Process Development] - Development of biosimilar and novel drug antibody culture processes - Scale-up process development [Purification Process Development] - Development of biosimilar and novel drug antibody purification processes - Data analysis and development of purification prediction models [Bioassay] - Development of cell-based assays for activity measurement and development of standard operating procedures (SOPs) - Development of binding assays and development of SOPs - Preparation and review of bioassay-related regulatory documentation - Comparability assessment of originator and biosimilar drugs [Clinical Bioanalysis] - Development and validation of clinical sample analysis methods for pharmacokinetics, pharmacodynamics, and immunogenicity - Transfer and follow-up management of assays to clinical sample analysis CROs (assay validation and sample analysis) - Preparation of regulatory documentation related to clinical sample analysis methods and review [Physical and Chemical Analysis] - Analytical method development and troubleshooting - Physicochemical analysis (LC, CE, icIEF) and primary/secondary structure analysis (Mass spectrometry) [Analytical Method Technology Transfer] - Technology and process transfer for chemical and biological analytical methods - Establishment of a validation strategy for pharmaceutical analytical methods and preparation and review of related documentation - Preparation and review of analytical method-related approval documents - Stability data evaluation, reporting, and documentation [Formulation Development] - Formulation development and analysis for efficient material delivery of antibody drugs - Establishment of formulation process development and application process - Monitoring, management, and response to contract manufacturing risks for formulation processes - In-house process validation [Finished Drug Product Manufacturing Process Technology Transfer] - Drug Product process development, strategy development, and risk factor assessment and management - Drug Product process characterization and validation - Process technology transfer to a DP CMO [FDP Process Development] - Development of a FDP (Finished Drug Product) manufacturing process - Raw drug substances and key components required for FDP process development Material supply/delivery management - Product approval and supplementary response support [AI Tech Engineering] - Development and operation of a state-of-the-art LLM system - Application of AI in new drug development - AI infrastructure and operations management

Qualifications

- Applicants with at least two years of relevant experience. ※ For those who have (or are expected to have) a master's or doctoral degree, the period of study will be recognized as work experience. - Applicants who are foreign nationals and do not have any disqualifications for visa acquisition or domestic employment. - Applicants who have a TOPIK (Test of Proficiency in Korean) score of Level 3 or higher. ※ Scores from March 9, 2024, to March 9, 2026, will be accepted. However, applicants without language proficiency scores may submit their scores by August 2026.

Preferred

※ Check the recruitment notice for details

Etc

- Only those who pass the document screening will be required to submit supporting documents (separate information will be provided). ㆍOne copy each of Graduation Certificate (original), Transcript (original), and Career Certificate (original) ㆍTOPIK Score Report / Other Certificates and Confirmations

Preferred Visas

Benefits

Cover Letter

Required