This position is for an 8–12 week full-time, on-site internship to be conducted in Summer 2027 (June–September 2027). *Minimum 12 weeks internship is required for all international hires (who require JP visa support).* *Target Candidates: Students graduating
This position is for an 8–12 week full-time, on-site internship to be conducted in Summer 2027 (June–September 2027). *Minimum 12 weeks internship is required for all international hires (who require JP visa support).* *Target Candidates: Students graduating
About the OpportunityJob Type: Permanent Application Deadline: 30 September 2026 Job Description Title Associate Director, Product Development and Management Department Product Development and Management, Japan Location Tokyo, Japan Reports To Co-Head of Product Development & Management Level Grade 7
Job ID 515115 Posted since 24-Jul-2026 Organization Smart Infrastructure Field of work Sales Company Siemens K.K. Experience level Experienced Professional Job type Full-time Work mode Office/Site only Employment type Permanent Location(s) Tokyo - Tokyo - Japan
This role owns the channel sales strategy, and growth execution for Ring products across Japans off-Amazon retail channels. The Channel Sales Development Manager will work cross-functionally with local account managers, field sales, channel marketing managers and international stakeholders,
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１．主な職務における成果責任/ Description of Primary Role & Responsibility Summary ■ 日本における医薬品の承認申請業務（非臨床3パート：薬理、動態、毒性） ■ 薬事関連資料（IB, CTDなど）の作成及び当局からの照会事項、対面相談の対応等 ■ Global部門の開発戦略に基づいた、日本での非臨床研究開発戦略の立案と実行 ■ 非臨床研究開発の専門分野における日本における情報発信 ■ 日本のサイエンスの現状を調査・情報収集し、Global非臨床研究開発部門にOpen Innovationとして紹介、共同研究の機会の構築 Responsibilities ■ 日本における医薬品の承認申請業務（非臨床3パート：薬理、動態、毒性） 日本の開発プロジェクトチームに非臨床(3パート)の専門家として参画し、プロジェクトにおける専門的科学知識やノウハウを提供 開発ターゲットにおける科学的知識、競合や規制ガイドラインの情報を把握 プロジェクトの進捗状況、可能性のある障害等を把握、チームに発信する Globalで実施されている非臨床試験の進捗をモニターし、チームに情報を提供する 非臨床関連の規制ガイドラインに関する専門家としてファイザーDJ（研究開発部門）およびファイザーJapanに対して、貢献する プロジェクトに関わる規制当局（PMDA等）との会議にDSRDの代表として参加する ■ 薬事関連資料（IB, CTDなど）の作成及び当局からの照会事項、対面相談の対応等 非臨床に関連する規制文書（PMDA相談、CTPN,CTDなど）を作成しGlobal担当者と協力してPMDAの質問に対応する グローバル規制文書に、日本での規制を適応させ包括的な非臨床評価を行う 文書のレビュー等を含めて、非臨床分野の規制文書の作成をタイムラインに合わせて実施する Globalの担当者と協力して、日本の基準に基づいた規制文書のコンテンツ、フォーマットに責任を持つ