16 results for Regulatory Affairs Manager Jobs in Tokyo, JP

Job Description SummaryProvides regulatory strategy and direction to the business regarding healthcare industry regulatory requirements for product launch, premarket submissions/registrations and postmarket compliance, working closely with healthcare regulatory bodies globally. In-depth understandin...

🔎 Title: Regulatory Affairs Contractor – PMDA Submissions 📍 Location: Onsite / Tokyo, Japan ⌛ Contract length: Minimum 9 months ✉️ Contact: [email protected]🔸 The company A global medical device company is seeking to strengthen its regulatory capabilities in Japan. This company is a well-establishe...

Job TitleRegulatory Affairs ManagerJob DescriptionJob title:Regulatory Affairs ManagerPhilips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better...

About INovaiNova is a different kind of health company. We are leading the way to better health by delivering innovative, patient-centric products that improve the lives of people around the world. Our diverse portfolio of iconic, market-leading consumer health brands and prescription medicines are ...

Job DescriptionMajor accountabilities: 複数のBSプロジェクトの進捗に貢献する 他のメンバーが担当するBSプロジェクトをサポートする BSのPMDA相談の成功及び承認取得のための薬事戦略案を策定し、Global teamに提示し、Global teamの計画と統合する BSのGlobal team及びSKK関係者をリードし、PMDA相談や国内承認申請（一変を含む）の準備を進め実施する 薬事関連業務について、Global 及び 国内の社内関係者をリードして業務を取りまとめ、業務目標を達成する 規制当局（PMDA、MHLW等）との交渉をリードする 外部委託先...

Position: Regulatory Affairs Manager, JapanReports to: General ManagerLocation: Tokyo, JapanPurposeThis role, reporting to the General Manager, is responsible for defining and executing the regulatory strategy for Japan. It involves overseeing product registrations and maintenance, supporting regula...

Site Name: Japan - Tokyo - AkasakaPosted Date: Mar 13 2025職務の目的規制当局及び社内関連部署と良好な関係を築き、規制当局との窓口業務を適切に遂行し、主に市販製品のライフサイクルマネジメントを確実に行う。主な業務内容市販製品の品質関連の変更に伴う薬事手続き市販製品に係る薬機法等の薬事規制に関する社内コンサルタント業務国内で発出される各種薬事規制の収集・分析・社内への適用推進業務業界団体・学術団体等を通じた薬制に関する規制調和の推進承認前GMP適合性調査（新薬申請時・一部変更承認申請時）・定期GMP適合性調査の管理外国製造業者認定の管理業態...

Let’s Talk About The Team And YouThe RA Global team is located at various offices around the world and is responsible for compliance with multiple regulatory frameworks as it relates to design, development and manufacture of products as well as services which meet our customer’s requirements.Based i...

Job Description SummaryWho We AreBD is a leading global medical technology company that creates medical technology, devices and laboratory equipment for a variety of needs across the healthcare sector. At BD, we are looking for candidates who possess passion, innovative solutions and a commitment to...

Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discover...