About BLR WORLD BLR WORLD is an award-winning talent consultancy for the culture, entertainment, and events sectors, enabling organisations to plan, staff, and operate unique permanent and temporary visitor experiences with the very best people. About
Job Description SummaryResponsible for dedicated product. Achieve sales targets for the products you are responsible for, formulate and execute marketing strategies and plans for that purpose, and conduct market analysis on the products you are responsible.
Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including
Company Description Overview: The Assistant Finance Manager is responsible for assisting the Finance Manager (‘FM”) in managing all aspects of financial matters for Hong Kong and Macau. This role requires a person who is willing to
We are looking for a Implementation Consultant to join our Intellectual Property Lifecycle Management (IPLM) Product & Onboarding Services Team in Japan. The IPLM Implementation Consultant is responsible for ensuring the world-class delivery of Clarivate’s IPLM
企業概要 Santenは、眼科医療に特化した130年の歴史を持つ製薬企業です。日本発のグローバル企業として60カ国以上に拠点を持ち、目の健康のために様々な革新的な治療法とデジタルソリューションを提供し、世界中の人々の視覚に関わる社会問題に取り組んでいます。 求人内容 ・CEO室傘下、基本理念・サステナビリティ本部において、各種プロジェクトの業務を遂行。 ・サステナビリティは外部からの要請に応えて実践＆開示していく必要性が高まっている。 IFRS財団を中心としたグローバルなサステナビリティ開示の法制化、CSRD（欧州のサステナビリティ開示指令）など欧州を中心とした規制は全て事業運営に直結しており、上場企業にとっては対応が必須となっている。 ・「サステナビリティ経営」自体が新しい概念であり、Santenの中においてその推進体制の強化が急がれている。 Under the CEO’s office, CORE PRINCIPLE & Sustainability promotes related projects. Sustainability is increasingly necessary to meet external demands through practice and disclosure. The legalization of global sustainability disclosure,
Reporting lines Report to Head of IT Onsite service Japan Main responsibilities The OnSite Service Engineer is the key member to maintain Network/Server & Endpoint devices at Japan OnSite Service Organization. This position will play a
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Since our founding, IDEMIA has been on a mission to unlock the world and make it safer through our cutting-edge identity technologies. Our technology leadership makes us the partner of choice for hundreds of governments and
SmartNews is a global leader in redefining information and news discovery, committed to providing users with accurate, timely information and supporting quality journalism. We combine the power of our unique machine-learning technology with the expertise of
Company Description PSI is a leading Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Originating from Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical
JOB SUMMARY Functions as the leader of the property’s sales department for properties with bookings over 300 peak rooms and significant local catering revenue. Manages the propertys reactive and proactive sales efforts. Provides day to day
JOB SUMMARY Accountable for overall success of the daily kitchen operations. Exhibits culinary talents by personally performing tasks while leading the staff and managing all food related functions. Works to continually improve guest and employee satisfaction
Company Description We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North
■主な業務内容: 英製薬大手AstraZenecaの一員として、Japan Market Company におけるGMP/GDP Quality Leadを務め、GMPおよびGDPの実施及び遵守状況を確認し、AZ-Globalの要件を満たすための更新・改善を行う。 主な担当予定業務: ・グローバル品質マニュアル、cGxPおよび国内規制に従い、グローバルGxP組織と連携し、日本市場におけるQuality Leadとして、品質システムの構築と維持管理および改善を行う。 ・医薬品品質システム（CAPA, Change Control, Deviation, Self-Inspection, Training, Complaint, Documentationなど）や供給業者管理の運用および継続的な改善を行う。 ・グローバルGxP組織がリードするプロジェクトに参画し、GMP/GDP関連分野のイニシアチブを取る。 ・部門横断的なGxPに関連する重要課題、実施部門単独では解決困難な課題について、施策立案、実行および主導を行う。 ・発出される品質関連法規等への対応を行う。 経験 Experience ■必須 Mandatory ・医療用医薬品又は医療機器業界での品質保証の経験(工場QAとしてのGMP及びGDP経験：少なくとも２～３年以上)、 医薬品品質システム(PQS)の責任者として運用管理・改善等の経験 ■歓迎 Nice to have ・医療用医薬品に関するGMP及びGDP経験：５年以上 ・医薬品品質システム(PQS)の責任者として運用管理・改善等の経験 ・GMP又はGQPのQAでのマネジャー経験 ・海外での業務経験 資格
Job Description About This Role This role is serving as IT focal point for Japan R&D, acting as IT Business Analyst, affiliate level of IT project manager and supporting Japan R&D members for any kinds of
Legal, AWM Public Legal, Vice President, Tokyo ABOUT GOLDMAN SACHS The Goldman Sachs Group, Inc. is a leading global investment banking, securities and investment management firm that provides a wide range of financial services to a
Are you interested in contributing to keeping JP Morgan Chase strong and resilient? If you are keen to be part of the Credit Risk team to help the firm grow its business in a responsible way
At EY, you’ll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture and technology to become the best version of you. And we’re counting on your
The Role This position will be supporting all aspects of compliance within the Group, and ensure that its employees are complying with regulatory requirements and internal policies and procedures. Job Responsibilities Ensure that employees understand and adhere
