다케다제약은 1781년 설립되어, 올해 창립 232주년을 맞는 일본 오사카에 본사를 둔 글로벌 제약회사입니다. 일본 내 1위, 아시아에서는 18조원의 매출을 기록하며 업계 1위를 자랑하는 다케다제약은 ‘공정’’정직’’불굴’의 기본가치를 바탕으로 삼아 성실(Integrity)이라는 경영철학을 실천하기 위해 노력하고 있습니다. 2만명 이상의 직원이 전 세계 여러 국가에서 일하고 있으며, 한국에서는 2010년 8월에 법인설립을 시작으로 한국제약시장의 중추적인 역할을 하기 위한 첫발을 내디뎠습니다.
기업형태
중소기업(300명이하)
고용형태
정규직
근무지
서울
최종학력
대학교(4년)
모집기간
2019년 04월 19일 ~ 2019년 04월 30일
등록일
2019-04-26
학력
경력
연령
성별
채용인원
우대조건
대학교(4년)
2년이상
무관
무관
0명
해당없음
모집정보
채용분야
BT(바이오)/NT(나노)/GT(그린) - 생산관리/품질관리/품질보증
고용형태
정규직
업무내용/자격요건
모집분야 및 자격요건
모집분야 및 자격요건
담당업무
자격요건
모집인원
Job Description
The main responsibilities of the Wholesale/Import managing Pharmacist is to control the release of the Products in compliant with local regulations. Pharmacist license registration is required to represent Takeda Pharmaceuticals Korea Co., Ltd. ensuring high quality and timely conduct of monitoring and managing Product release.
KEY ACCOUNTABILITIES AND RESPONSIBILITIES
- To Register the pharmacist license onTakeda Pharmaceuticals Korea Co., Ltd. as drug wholesaler and importer
- To manage product incoming process and product release process
- To inspect and manage the documentation for returned/damaged products
- Overall supervising for the re-dressing operation Overall control QA requirements at warehouse
- To coordinate the training of TPK product handling for the warehouse employees
- To coordinate and support the local SOPs development on drug wholesaler and importer
- To documentation and maintain the KGSP and KGMP related QA documents as required by local regulation and SOPs
- To support the archive of up-to-dated importation documentation
- To prepare and report of self audit documents to Seoul regional KFDA/ public health center
- To manage the retention samples in warehouse
Job Description
- Plan, set-up, monitor and coordinate clinical studies to the required standards of GCP, KGCP, and the company
- Manage the CRO for outsourced clinical studies or PMS and track the progress of study to ensure it is conducted, recorded, and reported in accordance with the protocol, SOPs, ICH GCP, KGCP, applicable regulatory requirements and within the given budget and timeline
- Responsible for the management of designated clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation and organizing Ethics Committee submissions
- Ensure procedures are in place for appropriate optimization of patients into theclinical trial
- Track and ensure timeline completion of trials and ensure trials are completed in accordance with local regulations and guidance
- Support Investigator Initiated Sponsored Research (IISR) in terms of drug management and contract related activities
Job Description
[Main Responsibilities]
- Marketing Planning: To develop the operating plan/POAs for designated product(s) for promotional campaigns in line with the marketing strategy.
- Forecasting: To use modeling or forecasting tools with the help of the team leader to forecast future trends and business needs.
- Implementation of Plans: To ensure effective implementation of designated promotional plans to achieve desired business outcomes.
- Monitoring and Control: To monitor progress against designated promotional plans to ensure corrective action can be taken if deviations occur
Essential responsibilities
- To register the pharmacist license according to the local requirements