[향남공장] Quality Control Team Specialist
마감기한
2025년 10월 10일, 14:59
부문
QC
직군
QC
경력사항
경력 5년 이상
고용형태
정규직
근무지
알보젠코리아대한민국 경기도 화성시 향남읍 제약공단2길 36, 화성시

[Roles & ​Responsibilities]

1.분석기기 ​관리 ​및 운영담당자 ​Analytical Instrument Management & ​Operation

​ -      ​분석기기 구매 및 ​도입 지원 ​(Support ​analytical instrument ​purchase ​and ​introduction)

-      ​기기 ​적격성평가(IQ/OQ/PQ) 수행 및 ​문서화 ​(Perform ​and document qualification ​(IQ/OQ/PQ) of ​instruments)

​ -      ​분석기기 유지보수 ​및 ​교정 관리 (Conduct ​regular maintenance, ​calibration, and GMP documentation)

-      분석기기 트러블슈팅 및 기술 지원 (Troubleshoot equipment issues and provide technical support)

-      영어 문서 작성 가능자 (Ability to write technical documents in English)


2.제품, 원료 시험방법서 제ㆍ개정 (Establishment and Revision of Test Methods for Products and Raw Materials)


3.시험방법 밸리데이션, 공정 밸리데이션 시험 및 세척 밸리데이션 시험, 관련 계획서 보고서 작성 (Method validation, Process Validation test, and Cleaning validation Test, including preparation of protocol & report. )


4. 시생산 제품 시험 및 시험방법 기술 이전 시험 (Technology transfer testing of analysis method & engineering product testing)


5. 의약품 동등성 시험, 인산결합 시험, 신제품 프로젝트 관련 스터디 등.  (Pharmaceutical Equivalence, Phosphate

binding study, study the relevant new product project, etc. )



[Qualfiations]

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. More than 5 years of experience in the pharmaceutical field.

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.

공유하기
[향남공장] Quality Control Team Specialist

[Roles & ​Responsibilities]

1.분석기기 ​관리 ​및 운영담당자 ​Analytical Instrument Management & ​Operation

​ -      ​분석기기 구매 및 ​도입 지원 ​(Support ​analytical instrument ​purchase ​and ​introduction)

-      ​기기 ​적격성평가(IQ/OQ/PQ) 수행 및 ​문서화 ​(Perform ​and document qualification ​(IQ/OQ/PQ) of ​instruments)

​ -      ​분석기기 유지보수 ​및 ​교정 관리 (Conduct ​regular maintenance, ​calibration, and GMP documentation)

-      분석기기 트러블슈팅 및 기술 지원 (Troubleshoot equipment issues and provide technical support)

-      영어 문서 작성 가능자 (Ability to write technical documents in English)


2.제품, 원료 시험방법서 제ㆍ개정 (Establishment and Revision of Test Methods for Products and Raw Materials)


3.시험방법 밸리데이션, 공정 밸리데이션 시험 및 세척 밸리데이션 시험, 관련 계획서 보고서 작성 (Method validation, Process Validation test, and Cleaning validation Test, including preparation of protocol & report. )


4. 시생산 제품 시험 및 시험방법 기술 이전 시험 (Technology transfer testing of analysis method & engineering product testing)


5. 의약품 동등성 시험, 인산결합 시험, 신제품 프로젝트 관련 스터디 등.  (Pharmaceutical Equivalence, Phosphate

binding study, study the relevant new product project, etc. )



[Qualfiations]

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. More than 5 years of experience in the pharmaceutical field.

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.