Operator, API Manufacturing, Hikari Site/ 光工場 製薬部原薬製造担当者①
Hikari, YamaguchiOn the Global Manufacturing and Supply (GMS) team at Takeda, you’ll be part of a rapidly transforming industry that’s applying technology and data in new ways. Within our agile, innovative, people-centric organization, your work will matter every day as you use your skills to help us manufacture therapies for patients on our four platforms:
- Small Molecules
- Biologics
- Plasma
As part of the GMS team, you'll have the opportunity to pursue unique experiences and build new skills, and you'll know that the work you do every day makes an impact — on our patients, our people, our planet, and on yourself.
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
募集部門の紹介
光工場製薬部は、高血圧症治療剤、消化性潰瘍治療剤、抗がん剤等、タケダが誇る医薬品の原薬を生産しています。それらは、様々な化学反応工程や精製工程をコンピュータシステムで制御するなど、高度な製薬技術を駆使して、厳密な工程管理のもとに生産しています。
職務内容
原薬に関する製造作業全般
- サンプラー 原薬製造に関するサンプリング
- 原薬製造に関わる設備点検、部品交換、定期検査などの設備管理
- 原薬製造に関する製造記録の記入(DCS、MES操作含む)
- 原薬製造エリアの設備機器の清浄度維持管理
- 原薬製造における諸問題の是正措置の設定と解決
- Function Leaderとの積極的、効果的なコミュニケーション
- 全てのcGMP, コンプライアンス、規制、品質要求事項の遵守
- AGILE活動を通した継続的改善の実践におけるリード、あるいは関与や補助
- 応募要件
・手順を遵守し、丁寧に作業ができる方。
・交代勤務に対応できる方。
学歴
高校卒業以上
- 実務経験
・原薬製造の業務経験は問いません。
(医薬品製造業経験者(特に原薬製造技術やプロセス分野における基礎知識)が望ましい)
スキル
GMPに関する知識
Microsoft Office(Word, Excelなど)の基本スキル
- 資格
危険物取扱者が望ましい
その他
変形労働時間制および交替勤務を適用することがあります
求める人物像
- 仕事に対して意欲的、積極的な姿勢で取り組み、協調性がありチームワークを大切にするかた
- 仕事のやりがい
- 原薬の製造を通じて光工場から世界の患者さんの健康に貢献できます。
- 本職務で身につくスキル・経験
- GMPを遵守した低分子医薬品原薬の製造スキル
Takeda Compensation and Benefits Summary:
Allowances: Commutation, Housing, Overtime Work etc.
Salary Increase: Annually, Bonus Payment: Twice a year
Working Hours: Headquarters (Osaka/ Tokyo) 9:00-17:30, Production Sites (Osaka/ Yamaguchi) 8:00-16:45, (Narita) 8:30-17:15, 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, Sick Leave, Family Support Leave, Maternity Leave, Childcare Leave, Family Nursing Leave.
Flexible Work Styles: Flextime, Telework
Benefits: Social Insurance, Retirement and Corporate Pension, Employee Stock Ownership Program, etc.
Important Notice concerning working conditions:
It is possible the job scope may change at the company’s discretion.
It is possible the department and workplace may change at the company’s discretion.
Locations
Hikari, JapanWorker Type
EmployeeWorker Sub-Type
RegularTime Type
Full timeWorking at Takeda
-
Inclusion
Here, you will feel welcomed, respected, and valued as a vital contributor to our global team. -
Collaboration
A strong, borderless team, we strive together towards our priorities and inspiring mission. -
Innovation
Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients. -
Great Place to Work
Recognized for our culture and ways of working, we’re proud to be Certified as a Great Place to Work® in 25 countries and regions. -
Work-Life
Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family. -
Empowerment
Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.
We're Steadfast In Our Commitment to Four Key Imperatives
Patient
Responsibly translate science into highly innovative medicines and accelerate access to improve lives worldwide.
People
Create an exceptional people experience.
Planet
Protect our planet.
Data & Digital
Transform Takeda into the most trusted, data-driven, outcomes-based biopharmaceutical company.
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