メディカル・医療/完全週休2日制の転職求人一覧

- Engage with policy stakeholders to shape high-level policies and regulations across therapeutic areas.- Plan, execute, and/or support rule-making projects both independently and crossfunctionally, in alignment with corporate strategy and crosstherapeutic/ brand strategy from a life-cycle management (LCM) perspective.- Monitor and analyze government policies, providing insights to the senior management, capability clusters, and enabling functions, as well as the global Public and Governmental Affairs (PGA) community to continuously update XXX on high-level government policies and access issues.- Liaise with the central government for XXX to mitigate political and policy risks for XXX’s business, including crisis communication with authorities in collaboration with relevant capability clusters and enabling functions.- Attend trade association meetings to shape industry-level and collective policy recommendations favorable to XXX’s innovation

当社基幹工場の設備部門にて、点眼液生産工場にある生産設備の安定稼働や製造環境の維持管理のための設備や機器の保全業務を担う。【詳細】・設備の定期点検・設備のトラブル対応・設備の改善(安全、3M など)・保全業務に必要な予算の立案と執行・新規設備導入などの仕様検討や工事などの支援※建設業務は含みません【能登工場について】能登工場は、世界最大レベルの点眼液生産工場で、病院向けの医療用や市販の OTC 製品の製造を行っています。また、製品は日本国内だけではなく海外へも輸出しています。