[ROLES & ​RESPONSIBILITIES] ​

지원자 ​역량 사항에 ​따라서 아래 업무 중 ​보직 ​결정

1. ​Preparation and/or first ​review of ​stability-related ​documents for ​engineering ​product.

​ 시생산 ​제품의 ​안정성시험 관리 및 ​문서 ​작성 ​및 1차 검토

2. ​Method validation, ​Process ​Validation test, ​and Cleaning ​validation ​Test, including preparation ​of protocol ​& report.

시험방법 밸리데이션, 공정 밸리데이션 시험 및 세척 밸리데이션 시험, 관련 계획서 보고서 작성

3. Technology transfer testing of analysis method & engineering product testing

시생산 제품 시험 및 시험방법 기술 이전 시험

4. Pharmaceutical Equivalence, Phosphate binding study, study the relevant new product project, etc.

의약품 동등성 시험, 인산결합 시험, 신제품 프로젝트 관련 스터디 등 

[QUALIFICATIONS]

1. People with practical experience in chemical analysis, scientific knowledge, analytical thinking, and problem-solving skills are preferred.

2. Prefer applicants with MS Office technology, analysis technology, chemical, and GMP knowledge, and the ability to use and manage analytical devices

- HPLC, GC, AA, UV, Dissolution, ICP/MS etc.

3. Preferential treatment for experienced pharmaceutical or chemical laboratories. (less than 15 years)

4. Preferential treatment for experienced global projects leading.  

5. A person who graduated with a bachelor's degree and majored in pharmacy, chemistry, biology, or similar fields.