Takeda Pharmaceuticals GQP品質保証担当者/Senior Specialist, GQP management in OSA, Japan









昇給・賞与: 昇給 原則年1回 賞与 年2回

勤務時間: 本社(大阪・東京) 9:00~17:30/工場(大阪・山口) 8:00~16:45 /研究所(神奈川)9:00~17:45


休暇: 年次有給休暇、特別有給休暇、リフレッシュ休暇、産前産後休暇、育児休暇、子の看護休暇、介護休暇、フィランソロピー休職制度










・品質保証業務にかかる英語力(TOEIC 800点以上を目安とするが、実務上のコミュニケーション能力を重視する)

【Objective and Accountabilities】

Quality Assurance as Marketing Authorisaion Holder in Japan

・management of QA system and its Continuous improvement

・management and communication with domestic and overseas manufacturers

・compliance to registration

Quality Assurance of exported products to ensure compliance of overseas regulation

【Employee Benefits】

Allowances: Commutation, Housing, Overtime Work etc.

Working Hours: Headquaters (Osaka/ Tokyo) 9:00-17:30, Production Sites (Osaka/ Yamaguchi) 8:00-16:45, Research Site (Kanagawa) 9:00-17:45

Holidays: Saturdays, Sundays, National Holidays, May Day, Year-End Holidays etc. (approx. 123 days in a year)

Paid Leaves: Annual Paid Leave, Special Paid Leave, Refresh Leave, Maternity Leave, Childcare Leave, Family Nursing Leave, Philanthropy Leav



【Experience:mandatory】QA as Marketing Authorisation Holder

【Experience:expected】business with overseas sites in English


・GMP experience, eg. manufacturing, QC/QA

・Computerised system

・Regulatory, Registration

・Continuous improvement, Project activities

・Business English in Quality (target TOEIC 800 , but more focused on practical communication capability)

Job: *Administration & Clerical

Title: GQP品質保証担当者/Senior Specialist, GQP management

Location: JP-OSA-Juso

Requisition ID: 1800250