Woven by Toyota is the mobility technology subsidiary of Toyota Motor Corporation. Our mission is to deliver safe, intelligent, human-centered mobility for all. Through our Arene mobility software platform, safety-first automated driving technology and Toyota Woven
ERM Japan was established in 1999 and has developed a strong presence and reputation in the provision of environmental and safety services over the past 25 years. Our fully staffed office of with over 100 bilingual
Woven by Toyota is the mobility technology subsidiary of Toyota Motor Corporation. Our mission is to deliver safe, intelligent, human-centered mobility for all. Through our Arene mobility software platform, safety-first automated driving technology and Toyota Woven
Overview We are currently seeking an Informatics Professional Service (IPS) Specialist who will provide high level consultation support to customers in the area of informatics, including Enterprise systems and chromatography data systems (CDS). Responsibilities Actively be
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
Job Description Job Description Menuma DMO Lead – Scope Summary: The Menuma Digital Manufacturing Operations (DMO) Lead is responsible for ensuring all DMO capabilities are effectively implemented, operationalized, and sustained in Menuma (Japan) manufacturing site. This
Job Description Summaryノバルティスの品質マニュアルとポリシーに基づき、現地規制の下、以下のことを達成する。 - 品質管理- 原料、製剤、最終製品の試験・検査を通じて製品の品質管理を行う。 - GMP/ GCTP（Good Gene, Cellular, and Tissue-based Products Manufacturing Practice：遺伝子・細胞・組織関連製品の適正製造規範）に基づき規制遵守を維持する。 - HSE- 日本の規制要件およびノバルティスのHSEポリシーに基づき、職場環境をモニターし、適切に維持する。 Job Description 主な役割責任 以下の業務が適切に行われていることを保証する。 原料、包装材料、原薬のサンプリングおよび受入試験 医薬品の最終製品の出荷試験 安定性モニタリング 環境モニタリング 品質管理記録の照査 品質管理部門の文書システムを管理する。 機器の校正、部門施設および機器のメンテナンスを適切に実施されていることを保証する。 試験室を維持する（文書、ガラス器具、試薬・試液、機器など）。 標準品（一次及び二次）が適切に取り扱われていることを保証にする。 すべてのチームメンバーに対して適切なトレーニングが実施されていることを保証する。 必須要件 薬学または化学の学士号以上をお持ちであること GMP規制、品質システム、品質保証、品質管理に関する深い知識 （医薬品医療機器等法、GMP、ICH品質ガイドライン、日本薬局方）
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
Location(s): Japan City/Cities: Tokyo Travel Required: Relocation Provided: Job Posting End Date: November 29, 2024 Shift: Job Description Summary: We aspire to achieve a balanced combination of global, regional and local brands that have the strongest
The Role Joining Moderna offers the unique opportunity to be part of a pioneering team thats revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee youll be
Title: Special Operations Physical Therapist (Yokota Air Base, Japan) Belong. Connect. Grow. with KBR! KBR is a company of innovators, thinkers, creators, explorers, volunteers, and dreamers; but we all share one goal: to improve the world
【Main Areas of Responsibilities and Key Activities】 ■Quality support: Act as QA in BJL-GMP organization and maintain local GMP warehouse for import pharma goods. Monitoring and understanding relevant laws and regulations related GMP/Quality management. Support / Lead
