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.
[Common 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.
Process Technology (MSAT)
Job Information and Responsibilities
- Optimize and continuously manage the client's biopharmaceutical process technology at Samsung Biologics to ensure the production of high-quality biopharmaceuticals (Manufacturing Science and Technology).
- Develop strategies for technology transfer of the client’s cell culture and purification processes.
- Provide on-site support at the client’s production facilities.
- Prepare and review GMP documents related to cell culture and purification process technology transfers.
- Conduct process risk assessments and reporting related to technology transfer.
- Investigate and support various deviations that occur during technology transfer.
Eligibility Criteria
- At least 2 years of experience in protein pharmaceuticals or cell culture/purification process development and technology transfer.
- Experience in preparing CAPA and GMP-related documents (PCS, QRA, MBR, SOP, etc.).
- Proficiency in English communication.
Preferred Qualifications
- Preferred majors: Biology, Chemical Engineering, Chemistry, or related fields.
- Knowledge of cGMP and BLA is a plus.
Sales Support (Project Management)
Job Information and Responsibilities
- Support sales activities after signing a contract for the development/production of potential clients' biopharmaceuticals at Samsung Biologics and manage the overall project.
- Lead communication with clients and coordinate with related departments such as process, distribution, and quality control to manage technology transfer and commercial production project timelines.
- Monitor progress based on contract terms and scope during project execution and resolve issues.
- Manage client distribution networks and oversee risk management throughout the project.
- Provide logistics administration support, including tracking the transport of client raw materials, ingredients, and samples.
- Respond flexibly to client requests and enhance client satisfaction.
Eligibility Criteria
- Native-level or equivalent English communication skills.
Preferred Qualifications
- Experience in the biopharmaceutical industry is preferred.
- Preferred majors: Biotechnology, Chemistry, Engineering, or related fields.
- PMP certification is a plus.
