Operator, API Manufacturing, Hikari Site/ 光工場製薬部原薬製造担当者① at Takeda Pharmaceutical Company Limited USA

Hikari, , Japan -

Full Time

Start Date

Immediate

Expiry Date

10 May, 26

Salary

0.0

Posted On

09 Feb, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP Knowledge, Microsoft Office, Sampling, Equipment Management, Record Keeping, Communication, Problem Solving, Teamwork, Attention to Detail, Compliance, Continuous Improvement

Industry

Pharmaceutical Manufacturing

Description

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, Japan Worker Type Employee Worker Sub-Type Regular Time Type Full time Takeda is an industry-leading, global pharmaceutical company with an unwavering dedication to putting patients at the center of everything we do. We live our values of Takeda-ism – Integrity, Fairness, Honesty, and Perseverance – and are united by our mission to strive towards Better Health and a Brighter Future for people worldwide through leading innovation in medicine. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. At Takeda, you will make an impact on people’s lives – including your own. Takeda is an equal opportunity employer. For applicants of U.S and Puerto Rico positions: Click here to learn about our commitment to Equal Employment Opportunity (EEO). If you are limited in the ability to use our job application tool, or otherwise require a reasonable accommodation for a disability please click here.

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Responsibilities

The role involves general manufacturing tasks related to active pharmaceutical ingredients, including sampling, equipment inspection, and maintaining cleanliness in the manufacturing area. It also requires effective communication with the Function Leader and adherence to compliance and quality requirements.