Position Summary : Lead Engineering and C&Q (Commissioning and Qualification) Team at Fuji Site in alignment with/and implementing global guidelines , in following areas: - Engineering and Project Management, - Commissioning and Qualification plan and execution,
Take lead in diverse range of RA projects to support clients in obtaining regulatory approval. Provide expertise in RA strategy/development. Client Details * One of the largest global CROs in the industry * Partnering with small to
This is Adyen Adyen provides payments, data, and financial products in a single solution for customers like Meta, Uber, H&M, and Microsoft - making us the financial technology platform of choice. At Adyen, everything we do
Job Overview The Sr Specimen Management Associate is responsible for various activities associated with receipt, storage, and shipment of clinical specimens. Responsible for equipment maintenance. Guides entry level staff on routine procedures. Essential Functions • Responsible
職務概要 Position Summary: Ø 正しい手順で時間通りに検査,製造する作業のオペレーション業務をリードし,正しい品質の製品を継続的に製造する。 Execute operations of inspection/production lines complying with the proper procedures on a timely manner and produce good quality products continuously Ø 法規制の順守に関する責任 Regulatory Compliance Responsibilities: Ø 全ての従業員はコンプライアンスの順守を最優先に行う。 All employees must concern compliance
Location: Minato City,Tokyo,Japan Accountant & Finance Manager (Hybrid; English Fluency Req.) Location: Minato-ku, Tokyo, Japan Salary: ¥5,658,326.98 - ¥10,147,297.75 per annum Benefits: Mobile and Travel Allowance, PTO Job Type: Full-Time Typical Hours: 40 hours/week, partially remote Start
Company Description Wise is a global technology company, building the best way to move and manage the world’s money. Min fees. Max ease. Full speed. Whether people and businesses are sending money to another country, spending
企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
Company Description AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives
企業概要 シーカは、建築分野や自動車産業における接着、シーリング、制振、補強、保護のための革新的なシステムや製品の開発・生産で世界をリードする特殊化学品会社として、世界的に認知されています。世界103カ国に子会社を持ち、400以上の工場を持つシーカは、全世界で33,000人以上の従業員を擁し、2023年度の売上高は110億スイスフランでした。日本では、シーカは長い歴史を持ち、1,000人以上の専門家からなる献身的なチームを擁しています。 求人内容 労働安全衛生(EHS)マネージャーとして、弊社のEHSプログラムを開発、整備、管理、維持し、事故や負傷の件数を最小限に抑え、その重症度を低減しながら、企業の効率性と従業員、顧客、およびコミュニティの健康を維持していただきます。 EHS関連の法律と法規の遵守を監視し、変更があればいち早く把握し、これらの変更の影 響を必要な関連部署等に通知し、必要な提案を行う。 EHSトレーニングプログラムを開発し、整備し、管理し、モニタリングを行う。 月次、四半期、年次のトレーニングプログラムを実施する。 EH&Sパフォーマンス指標のタイムリーな報告を行う。分析を実施し、トレンドを監視し、改善案を作成する。 現地オペレーションへ専門知識とアドバイスを提供する。 各工場・オフィスのチームと協力して、新しいまたは変更されたプロセス・装置が人間工学の基準に準拠し、規制要件を満たしていることを確認する。 メモ、報告指標、安全ニュースレター、現地会議、関連する出版物の配布を通じて安全に関連する問題の伝達を行う。 法的に必要なEHSレポートの作成・提出を行う。 すべてのEHS関連の内部要件および国内/地方の規制およびルールを法的に遵守するためのプログラムの管理を行う。 ニアミス、および事故調査の原因分析を主導する。再発防止のための是正措置の実施を監視する。 事故予防と費用管理の長期目標を設定します。 Develop, organize, administer, and maintain the Company’s Environmental Health & Safety Program. Minimize the number and reduce the severity of accidents
Job Description Responsible for all activities of Japan regulatory operations as a lead of regulatory operation in collaboration with Global RA, Japan R&D, and other functional areas within Biogen. Manage and maintain regulatory operational activities in drug development, NDA
企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
Company Description Jobs for Humanity is collaborating with FIS Global to build an inclusive and just employment ecosystem. We support individuals coming from all walks of life. Company Name: FIS Global Job Description Position Type :
企業概要 AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across
Location： Global Innovation Center Division： Development Acceleration Center Job level： Staff Report to： Group Manager Contract type： Full time Roles & Responsibilities 製品・サービスの価値の最大化や強い訴求の実現に向け、有用性業務の企画を立案し、中心となって 実行する。 ・各国規制・薬事を理解したうえでの、製品の魅力を体現するための有用性試験計画立案 ・有用性試験外部委託業務（試験機関調整、サンプル手配、結果の解析など） ・他社動向・トレンドを踏まえた新規有用性試験法の調査・開拓 For maximization of product value and achievement of attractive claims,
Are you experienced in CMC regulatory affairs or in generating high-quality documentation related to drug manufacturing and marketing approval/maintenance? Do you have a strong understanding of CMC requirements in Japan? We are seeking a CMC Expert to
* Lead double-hatted product controllers covering investment banking and global markets division * Ensure accuracy of books and records and monitor deal pipeline (deal status tracking), in coordination with business units, global counterparts and business partners
Job Description Job Summary: To ensure that clinical supplies are stored and distributed in accordance with Fisher Clinical Services (FCS) approved procedures and policies, cGMP, cGDP, and regulatory requirements. Maintain the FCS Japan Quality System in compliance
Job Description Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue over $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer.
