企業情報 · 世界中の人々の健康と生活の質を向上させることを使命とするグローバル製薬企業。革新的な医薬品開発に注力し、品質と安全性を最優先に取り組んでいます。ハイブリッド勤務制度 · グローバルプロジェクトへの参画機会 · ...

APAC地域を対象としたGCP監査に携わり · 柔軟な働き方とキャリアアップの機会が豊富 · BС/バ学位または同等の資格 · 製薬企業またはCROでのGCP監査経験(5年以上) · ...

+ Job summary · As a Customer Quality Specialist at Johnson & Johnson, you will be responsible for ensuring the quality of our products and services. You will work closely with internal departments and external stakeholders to resolve customer complaints and improve product quali ...

The QAQC Assistant Manager is responsible for leading non-conformance management and customer complaint investigation. They will assist the Quality manager with implementing overall quality system plans and coordinating activities. · ...

+Highly motivated Reward Specialist required to join our team at TÜV SÝ Japan Ltd.We are seeking an experienced reward specialist who will assist with compensation management (salary administration), welfare system management (benefits) entry/exit leave management contract manage ...

At TÜV SÜD we are passionate about technology. Innovations impact our daily lives in countless ways, and we are dedicated to being a part of that progress. We test, we audit, we inspect, we advise. We never stop challenging ourselves for the safety of society and its people. We b ...

This role includes two main tasks: Quality Assurance providing daily support to the team and stakeholders by acting as Quality Assurance QA and an Editor ensuring effective execution to improve performance with high quality service delivery for Clients. · Client Support will ensu ...

The Data & Analytics Manager will lead the rollout and ongoing evolution of the global data platform in Japan. · They will ensure data quality and effective stakeholder communication while driving adoption of global/regional reports that support commercial, finance, and supply ch ...

Financial Controller, Investment Banking/Capital Markets position at a leading global investment banking and capital markets firm in Tokyo office. · ...

The main responsibility of this role is to lead the work for product homologation for trucks buses & engines. · ...

Job Description · 弊社の品質保証(QA)は、製品開発ライフサイクルの各重要な段階、承認後のマーケティングを含む、において品質に焦点を当てる独立した組織であり、高品質で安全かつ効果的な製品を確保し、世界中の人々の生活を改善し命を救うという会社の使命に貢献しています。 · ...

R&D部門に所属し、APACチームをリードするポジションです。グローバル組織で戦略的に活躍します。監査計画立案・実行、国際規制当局への対応、チーム牽引などを行います。 · ...

We are seeking an experienced M&E Project Manager to join our team at Linesight. As a key member of our project management team, you will be responsible for managing large-scale construction projects from start to finish. ...

+ Legal & Compliance Counsel Job Summary The Legal & Compliance Counsel provides legal support to Cardinal Health Japan including commercial division and manufacturing site. · Provide proactive legal and compliance advice · Draft negotiate and review contracts · Anticipate regula ...

Sr.QA Auditor (Monitoring対応)です。これは、私たちIQVIATHATですがヒューマンデータサイエンスの先駆的な企業として、医療・ヘルスケアの進歩に取り組む皆さんを支援することで、「誰もが健康であれば自分らしく生きられる社会」の実現に向けています世界最大規模を持つ医療・ヘルスケア関連データを基盤にして人・データ・サイエンスを融合させた視点から未だ満たされていない治療ニーズに対応し、新しい薬や医療機器の開発と販売、その厳格化する規制への対応などすべての人々にとってより良い将来を見据えながら医学研究を行う力となります。 · ​ ...

Principal Safety Evaluation is responsible for ensuring the safety of products and patients throughout the product lifecycle. This includes conducting cross-functional activities to support the development of GSK Japan's projects, designing and implementing safety plans for clini ...

At Medtronic you can begin a life-long career of exploration and innovation while helping champion healthcare access and equity for all. · p苦情担当スペシャリスト · tough punishment specialist · safety management department member performing following duties: kakujou shori: customer complai ...

体外診断用医薬品及び医療機器の薬事業務をお任せします。製品の承認申請、臨床評価、品質マネジメントシステムの維持管理、販売業管理、変更・更新業務などに携わっていただきます。将来的に、製造販売業の総括、品責、安責、卸売販売業の管理薬剤師としての役割も視野に入れた業務をお任せします。 · ...

An exciting opportunity to join Medtronic's Diabetes business unit as an Administrative Assistant I (DIAB @ Tokyo). This role involves supporting various administrative tasks related to product quality assurance. · ...

We are seeking a Quality Control Lead to join our Saitama Site leadership team. As a key member of our site leadership team, you will oversee the quality control department to ensure product quality from incoming materials to outgoing products based on GMP and Japan Pharmacopeia ...

We're in an unbelievably exciting area of tech and are fundamentally reshaping the data storage industry. Here, you lead with innovative thinking, grow along with us, and join the smartest team in the industry. · This type of work—work that changes the world—is what the tech indu ...