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
Work Schedule Other Environmental Conditions Office Job Description バイオサイエンス事業部 製品の商業利用に関連する事業開発マネージャーをお任せします。 1. バイオサイエンス事業部製品カテゴリー PCA (Protein and Cell Analysis) タンパク・抗体・細胞分析用試薬等 PCA_1, PCA_2 Molecular biology 分子生物学研究用試薬 Molecular biology_1 Moldcular biology_2 Sample Prep サンプル精製用試薬 Sample Prep Cell biology 細胞生物学研究用試薬 Cellbiology 業務内容
職種 正社員 職務明細 At PlayEveryWare (プレイエブリウェア), no two projects are exactly alike. We bring games to previous and current generation consoles and work on cutting edge technology. Each project brings exciting new technical challenges and opportunities
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
We are Reckitt そのチカラを自由に使え。 今の自分を超えていけ。 FREE YOUR POWER. PROGRESS YOURSELF. Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Take lead in quality activities to ensure effective compliance. Manage QMS and other quality claims. Client Details * Global pharmaceutical company specializing in innovative treatment for oncology, urology, and auto-immune areas. * Rich development pipeline for new
Lead in GQP QA operational activities for the business for company products. Ensure effective compliance, continuous improvement activities, and overall quality processes. Client Details * Global Pharmaceutical company specializing in generics, biosimiilars, APIs, and new products for unmet
Reporting to the Hinseki and lead in handling and handling QMS as well as other quality activities. Ensure effective compliance for companys products Client Details * Global medical device company specializing in the oncology area * International
Position Details The client is looking for an experienced team lead who has a passion for working on complex/large systems and understands the importance of maintaining and supporting one. You will be joining a team of diversely
JOB SUMMARY On the basis of Sanofi quality policy and Japanese regulations, make available to customers high quality products and services through promoting Quality Assurance activities strongly and leading / supporting Japanese Contract Manufacturing Organization in
Are you ready to unleash your full potential? We’re looking for people who are passionate about payments to chart Worldpay’s path to being the largest and most-loved payments company in the world. About the team Enterprise
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
General Summary / 職務概要 シニアマネージャーの指示のもと,Repack/Relabeling 業務(現在2 拠点)の運用/PLAN をコスト面含めて契約社員をリードしながら全般的にマネージする。 具体的には契約を含めた業務委託先との各種交渉,生産計画から包装加工作業•倉庫搬入に至るまでのOperation の構築•Performance 管理,会社の戦略•顧客ニーズに合わせた包装加工を実現するための資材開発•手配を行う。 また改善においてはOperation だけでなく,エンジニアやIT,グローバルサプライチェーンチームと協働しシステム•機械設備の要件洗い出しを行い,導入から運用まで全般をLead する。 機械設備に関してはテクサポチームと連携をとりながら予防保全を計画から実行までをサポートする。薬機法の順守及び品質の高いオペレーションを提供し,当該加工に関わる問い合わせおよび苦情に対し,常に迅速かつ適切に対応する任務も担う。また場合によってはLPG 業務(在庫管理•BO Management)のサポート業も行う。 Duties & Responsibilities / 職務および職責 シュリンク/KIT/リパック加工業務 #1 外部製造業者 オペレーション管理 #2 新製品発売時など,マーケティング,セールス,バックオフィス部門と協働してプロセスの構築 #3 マーケティング部門の要望とオペレーション上の制約条件のすり合わせ #4 スケジュールの枠組みと必要なタスクの構築 #5 工程設計,工数設計ができ,システムRFP を作成 #6 設備導入が必要な場合,ﾃｸﾆｶﾙｻﾎﾟｰﾄと仕様,費用,日程の取り決め
職務内容 須賀川工場において,主に Quality Engineering ,及び須賀川 Leadership Team Member として下記の業務を行う。 • 須賀川工場内プロセスの構築,分析,改善 • 製造元へのプロセス改善の提案,実現化 • バリデーション責任者として,バリデーション関連業務の遂行 • 須賀川 Leadership Team Member として組織運営 • 須賀川工場戦略的優先課題プロジェクトチームのリード • 須賀川 EHS IOSS 活動のリード • 短期的,中長期的な部門戦略•目標設定,及び進捗管理 APAC Supply Chain Quality 内諸活動等への参画,連携 職務経験
Position Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials and/or overseeing a Clinical Research Organization responsible for
Position Summary: Responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials and/or overseeing a Clinical Research Organization responsible for
