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
Overview: Microsoft Cloud Operations + Innovation (CO+I) is the team behind the cloud. CO+I is responsible for delivering over 200 Microsoft web portals, Live and Online Services around the world including infrastructure, security and compliance, operations,
Job Description: Employer: DWS Group Title: Portfolio Analyst Location: Japan Job Code: #LI-ZL1 #LI-01 About DWS: Today, markets face a whole new set of pressures – but also a whole lot of opportunity too. Opportunity to
【Job Responsibility】 Highly skilled and high potential leader with a proven track record of delivering results in progressive roles to join our team. Have the opportunity to shape and drive a sustainable and high-performing financial accounting
Description Kenvue is currently recruiting for: Legal Entity Controller - Japan/South East A sian Countries The Legal Entity Controller role primarily oversees the legal entit ies (LE) financial close process , financial reporting process, ensuring the integrity
Description Kenvue is currently recruiting for: Legal Entity Controller - Japan/South East A sian Countries The Legal Entity Controller role primarily oversees the legal entit ies (LE) financial close process , financial reporting process, ensuring the integrity
Head of Japanese Accounting & Finance About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases
Enterprise Technology Services - Application Support Specialist (E-trading and Regulatory) - Tokyo Location Tokyo Business Area Sales and Client Service Ref # 10039588 Description & Requirements Bloomberg delivers critical information in a world where information matters. We
At Tetra Pak we commit to making food safe and available, everywhere; and we protect whats good – protecting food, protecting people, and protecting the planet. By doing so we touch millions of peoples lives every
Are you passionate about process optimization and lean manufacturing? Do you have a knack for driving change and influencing stakeholders? If so, you might be the cLEAN (Current LEAN) Partner we are looking for at our
Main duties and responsibilities Airport stakeholders’ relationship management Build and maintain positive and effective relationships with Airport management, Customs and all relevant stakeholders Lead key negotiations with airport, customs, agents and related stakeholders make contracts with
The Apex Group was established in Bermuda in 2003 and is now one of the world’s largest fund administration and middle office solutions providers. Our business is unique in its ability to reach globally, service locally
Controllers, Operations, Regulatory Reporting - Portfolio Level, Senior Analyst, Tokyo ABOUT GOLDMAN SACHS At Goldman Sachs, we connect people, capital and ideas to help solve problems for our clients. We are a leading global financial services firm providing
This role is responsible for managing and leading a team to deliver effective Distribution & Logistics Operations in areas for Warehousing, Planning, Inventory Control, Logistics, Transportation, 3PL Management , Imports / Exports, Operations Compliance, Project Management,
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JOB TITLE: SR. CLINICAL RESEARCH SPECIALIST DEPARTMENT: クリニカル・メディカルアフェアーズ 臨床試験信頼性保証 REPORTING TO: SR. CLINICAL RESEARCH MANAGER - 背景 臨床開発本部は、日本国内外の臨床試験（治験）を通じて新しい医療機器の有効性と安全性を評価・検証し、厚生労働省（医薬品医療機器総合機構）へ承認申請を行い医療機器として製造販売承認を取得する業務を担います。そして製造販売承認を取得した新医療機器等に対しては、日常の診療において機器を使用したときの医療機器の品質、有効性及び安全性等に関する情報の収集、検出、確認又は検証のために行う調査又は試験を実施し、臨床試験（治験）では得られなかった医療機器の適正な使用 についての情報、安全性情報などを集める業務も担います。また、市販後臨床研究などを通じて、Medtronic製品の更なる臨床的な有用性を探るためのエビデンス構築を担います。 Medtronicで実施される臨床試験（治験）は、臨床開発本部、Medical Clinical Regulatory Solutions（MCRS）及びCorporate Clinical Quality Compliance(CCQC)の３部門体制にて実施され、MCRSは主にモニタリング、安全性情報管理を、CCQCは監査を担います。 臨床開発本部に所属するCVG/DIB Clinical担当は、循環器領域および糖尿病関連の医療機器を担当製品とし、国内外の関連部門と連携を取りながらプロジェクトの中心的な役割を担います。 - 要約 海外で実施された臨床試験（国際共同試験を含む）の資料（以下、海外臨床試験資料）を製造販売承認申請の審査資料（以下、申請資料）として利用する際の準備、適合性書面調査及びGCP実地調査に対応する。製品領域は、循環器領域から脳神経疾患領域など多岐に渡る。海外の臨床試験チーム、社内の臨床試験チーム及び薬事部などの関連部署と協働すると共に、業務の進行を担う。 - 業務内容 業務運営 本担当は日本法人内の薬事部門、臨床開発部門、海外臨床試験チームと協働し、これらをとりまとめ主導し、下記の業務を遂行する。 適合性調査に係る情報の共有 本邦の信頼性基準、GCPに対する懸念に対する対応 2.
Job Description AirAsia X is seeking dynamic and competent Station Manager - Haneda (HND) to be part of the best airline team in the sky! The overall purpose of the job is to ensure effective and
Major Accountabilities: Lead the management of product system requirements throughout the development lifecycle, ensuring completeness, correctness, and traceability. Establish and maintain effective processes and tools for capturing, analyzing, documenting, and managing requirements. Collaborate with stakeholders to
Be in charge of finance reporting between HQ (Japan) and oversea subsidiaries for a historic Japanese pharmaceuticals company in an international working environment | Career path, international mobility opportunities, WFH and flex time available. Client Details This
Number 1 position in Japan to lead finance operations and collaborate closely with the global teams | WFH, flex time available Client Details A longstanding leader in the medical device field, this company has grown its
