[스카우트 채용공고]

Quality Assurance GMP Compliance

바이엘코리아

http://www.bayer.co.k..

관심기업

업종	의료/제약/건강	자본금
기업형태	외국기업	매출현황
대표자		사원수
회사주소	서울 동작구 신대방동 395-62 삼성보라매 옴니타워

직종	생산관리·품질관리·품질보증, 제약·의약
근무형태	계약직	채용직급	-
모집인원	0 명	나이	제한없음
경력	경력	급여조건	당사규정
학력	대졸 이상	접수기간	접수기간이 지났습니다

[홈페이지접수]

접수기간이 지났습니다

상세요강
상세지원요약

* 담당업무 상세조건	●업무개요 ○ Tracks deviation related issues and makes final deviation documents and follows up its corrective & preventive actions if required. And controls deviation related documents(deviation report, related SOPs, guidelines) ○ Plans annual audit schedule and proceeds audits according to the schedule. And prepares audit reports and follows up the findings. And based on audit report and quality data, prepares supplier evaluation documents. ○ Plans annual training schedule for the production div. and performs basic GMP trainings for all production div. staffs. Checks training status of each department and controls training related documents ○ Review production batch records and QC testing records for final product release and coordinate batch release procedure. And review that QC testing worksheets including data spread sheets are prepared according to valid product license and QS/TS ○ Prepares annual product review reports based on the batch records review data, deviations and changes implemented and checks all the data which required annual product review ○ Prepares related documents which requested to submit to authorities and coordinates authority inspections including update of site master files. ○ Initiates and coordinates a stability program according to the respective SOPs and review stability test data. ○ Checks and confirms that the goods are controlled properly according to KGSP and premises and equipment in Yongma warehouse are in a good and hygienic condition ●응시자격 ○ University graduate and majored in Chemistry ○ Preferably a Pharmacist ○ At least 3 year- experience in QA, especially for GMP & auditor training with understanding of GMP, Customer complaint handling, F/U Deviation report, prepare & review of SOP, etc. ○ Cooperative attitude, reliability and inter-personal skill ○ Good in communication and organizing tasks ○ Sense of interdepartmental and interdisciplinary cooperation ○ Analytical thinking ○ Excellence in MS office program+Hangul ○ English communication in written & verbal (if possible) ○근무지: 경기도 안성시 미양면 제2공단1길 92 ●지원방법 ○당사 홈페이지 지원

* 담당업무
상세조건

●업무개요

○ Tracks deviation related issues and makes final deviation documents and follows up its corrective &
preventive actions if required. And controls deviation related documents(deviation report, related SOPs, guidelines)

○ Plans annual audit schedule and proceeds audits according to the schedule. And prepares audit reports
and follows up the findings. And based on audit report and quality data, prepares supplier evaluation documents.

○ Plans annual training schedule for the production div. and performs basic GMP trainings for all production div.
staffs. Checks training status of each department and controls training related documents

○ Review production batch records and QC testing records for final product release and coordinate batch
release procedure. And review that QC testing worksheets including data spread sheets are prepared
according to valid product license and QS/TS

○ Prepares annual product review reports based on the batch records review data, deviations and
changes implemented and checks all the data which required annual product review

○ Prepares related documents which requested to submit to authorities and coordinates authority inspections
including update of site master files.

○ Initiates and coordinates a stability program according to the respective SOPs and review stability test data.

○ Checks and confirms that the goods are controlled properly according to KGSP and premises and equipment
in Yongma warehouse are in a good and hygienic condition

●응시자격

○ University graduate and majored in Chemistry

○ Preferably a Pharmacist

○ At least 3 year- experience in QA, especially for GMP & auditor training with understanding of GMP,
Customer complaint handling, F/U Deviation report, prepare & review of SOP, etc.

○ Cooperative attitude, reliability and inter-personal skill

○ Good in communication and organizing tasks

○ Sense of interdepartmental and interdisciplinary cooperation

○ Analytical thinking

○ Excellence in MS office program+Hangul

○ English communication in written & verbal (if possible)

○근무지: 경기도 안성시 미양면 제2공단1길 92

●지원방법

○당사 홈페이지 지원

* 입사지원 시 중요사항을 꼭 체크하세요!

* 근무환경	근무지역 : 경기 급여조건 : 당사규정
* 접수개요	오늘마감 접수기간이 지났습니다 ■ 접수기간 ■ 오늘 ■ 마감 2014. 09 일 월 화 수 목 금 토 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 [홈페이지접수]
* 담당자 정보
모집기간이 지난 채용정보의 경우 담당정보는 공개되지 않습니다.

등록 : 2014년 9월 12일 (금) 10:36 최종수정 : 2014년 9월 12일 (금) 10:36

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