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Job Description:
Please note this job requires business level Japanese in speaking, writing, and reading.
タケダの紹介:
タケダは「世界中の人々の健康と輝かしい未来に貢献する」ことを企業の存在意義(パーパス)としています。そして目指す未来を共有しながら、一人ひとりが自分の可能性を引き出し、お互いの個性を認め合う、多様性にあふれた先進的な組織作りに取り組んでいます。私たちと一緒に、世界中の人々のいのちに貢献し、さらなる成長と活躍を目指しませんか。
タケダはグローバルな研究開発型のバイオ医薬品のリーディングカンパニーです。従業員は創業時から受け継いできたタケダの価値観であるタケダイズム(誠実=公正・正直・不屈)を道しるべとしながら、患者さんに寄り添い(Patient)人々と信頼関係を築き(Trust)社会的評価を向上させ(Reputation)持続可能な事業を発展させる(Business)を日々の行動指針としています。
"Better Health for People, Brighter Future for the World" is the purpose of a company. We aim to create a diverse and inclusive organization where people can thrive, grow and realize their own potential while enabling our purpose. We continue to innovate and drive changes that will transform the lives of patients. We're looking for like-minded professionals to join us.
Takeda is a global values-based, R&D-driven biopharmaceutical leader. We are guided by our values of Takeda-ism, which has been passed down since the company's founding. Takeda-ism incorporates
Integrity, Fairness, Honesty,
and
Perseverance,
with Integrity at the core. They are brought to life through actions based on Patient-Trust-Reputation-Business, in this order.
募集部門の紹介:
成田工場は主に血漿由来の治療薬を製造しています。患者の命を救い、信頼できる血漿由来の治療薬を製造することを、最大の使命として、社会貢献する高い役割を担っています。成田工場では原薬(血漿分画)製造工程、製剤製造工程、検査包装工程と、血漿から製剤までの一貫した製造工程を持ち、幅広い製造技術や知識を所有しています。「命」に直結する製剤が主力製品であるため、責任の重さは重大であり、「命」を守る仕事のやりがいと尊さは、何事にも代えがたいものがあります。高い専門性と製造技術を誇る成田工場で、さらなる成長と活躍をご一緒に経験しましょう。
検査包装グループではバイアルの目視検査、印字、包装工程を担当しています。認定された目視検査員が1本1本バイアルの目視検査を行い、包装工程では各種包装機を操作しながら医薬品の包装作業を行い患者さんへ製品を届けています。
職務内容:
- 目視検査員はトレーニング期間と認定試験を経て目視検査員となり、検査作業に従事して頂きます。
- 包装工程では各包装機に資材の供給及び操作を行い包装し、包装済み品の目視検査及び梱包作業を行います。
- 包装作業の前後では包装作業に必要となる資材の準備や出納管理、在庫管理を行います。
- 生産作業記録を正確に記録し、問題発生時には上長へ報告を行います。
- 生産スケジュールに従い原資材の出庫及び保管管理を行う。
- 工程異常時に上長や品質保証部門へ報告する。
- 製造間接業務(SAP操作、変更管理起案、逸脱起票、是正処置予防処置実行、製造指図記録書改訂、SOP改訂、バリデーション実行等)のタスクを実行する。
- 新人作業員への教育とフォローを行う。
- 5S活動、改善活動による品質、生産性に寄与する。
応募要件:
<学歴>
高卒以上
<実務経験>
【必須要件】
- 製造オペレーターの経験もしくはそれに類する社会人経験
【望ましい要件】
- 医薬品・化学・食品・化粧品・半導体業界などでの製造経験
- 生産トラブル対応、保全経験
- 改善活動による品質、生産性、効率性の改善経験
- 製造に係る間接業務(変更管理、逸脱処理、是正処置予防措置対応、各種手順書作成、製造指図記録書改訂、バリデーション)経験
- 医薬品の包装経験
- 注射剤の目視検査経験
<スキル・資格>
- Word/Excelの基本スキル
- 製造管理システムや教育管理システムなどの基幹システムを習得し操作できる能力
求める人物像:
医薬品製造という観点で、手順を遵守し丁寧に作業できる人材を求めます。
またチームでの活動が多いことから、コミュニーション能力や協調性も重視いたします。
目視検査作業は集中力が必要なため、集中して作業する能力が求められます。
仕事のやりがい:
最終工程を担う責任感と、医薬品を必要としている患者さんへ届けられる達成感を得ることができます。
本職務で身につくスキル・経験:
- 最新のGMPに基づく医薬品製造知識・経験を積むことができます
- 包装関連全般の知識は医薬品製造以外の業界でも通用する知識が得られます
- 改善活動が身につきます。
- 特殊技能である注射剤の目視検査技術が身に付きます
- 当局査察、内部監査の対応知識が身に付きます
Takeda Compensation and Benefits Summary:
- Allowances Commutation, Housing, Overtime Work etc.
- Salary Increase Annually, Bonus Payment Twice a year
- Working Hours Headquarters (Osaka/ Tokyo , Production Sites (Osaka/ Yamaguchi , (Narita , Research Site (Kanagawa
- 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:
JPN - Chiba - Narita Plant
Worker Type:
Employee
Worker Sub-Type:
Regular
Time Type:
Full time
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