Senior Director, Regulatory Affairs - Tokyo

登録メンバーのみ Tokyo, 日本

1ヶ月前

Default job background
フルタイム
When our values align, there's no limit to what we can achieve. ·   · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by someth ...
Lorem ipsum dolor sit amet
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.

Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.

Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
フルアクセスを取得

すべての上級職にアクセスして、理想の仕事を手に入れましょう。



似たような仕事

  • 会社で働く

    Regulatory Affairs Expert

    登録メンバーのみ

    メルクと一緒に、あなたの力を発揮しよう · 冒険、限界への挑戦、そして発見に焦がれるあなたへ。あなたの大志を、メルクで羽ばたかせましょう · ...

    Tokyo

    3週間前

  • 会社で働く

    Regulatory Affairs Expert

    登録メンバーのみ

    Life Science Regulatory Management、レギュラリースペシャリストとして業務を行う。東京勤務、週2日在宅ワーク可。 · ...

    Tokyo フルタイム

    1ヶ月前

  • 会社で働く

    Specialist, Regulatory Affairs

    登録メンバーのみ

    当社のライフサイエンス※製品に関する薬事業務全般をご担当いただきます。具体的には以下の業務を担っていただきます。 · ...

    Minato

    1ヶ月前

  • 会社で働く

    Senior Regulatory Affairs

    登録メンバーのみ

    当社は革新的な医療技術を通じて医療現場の課題解決に貢献するグローバルメドテック企業です。 · 本ポジションでは医療機器のISO13485に基づく品質マネジメントシステム(QMS)の運用および改善を担当いただきます。QMS文書を作成・改訂し続続的なプロセス改善を行うことができます。また手順書を作り規制対応を行い、および輸送管理安全管理(Vigilance)まで幅広い領域で仕事をすることができます。 · ...

    Chiyoda

    4週間前

  • 会社で働く

    Manager, Regulatory Affairs

    登録メンバーのみ

    BDは、ヘルスケア分野における多様なニーズに応える医療技術、デバイス、実験機器を開発する世界をリードする医療技術企業です。感染症の撲滅と治癒を目指す戦いにおいて最先端の研究を提供し国内外の人々に画期的な医療・バイオテクノロジーサービスへのアクセスを向上させるという私たちの使命で、私たちが求めています。 · ...

    Minato

    1ヶ月前

  • 会社で働く

    Regulatory Affairs

    登録メンバーのみ

    The Regulatory Affairs Manager is responsible for overseeing the preparation of regulatory submissions required to market new or modified devices in both domestic and international markets including all relevant maintenance activities. This position will also oversee the preparat ...

    Tokyo

    1ヶ月前

  • 会社で働く

    Regulatory Affairs

    登録メンバーのみ

    The Regulatory Affairs Manager is responsible for overseeing the preparation of regulatory submissions required to market new or modified devices in both domestic and international markets including all relevant maintenance activities. This position will also oversee the preparat ...

    Tokyo, Japan

    1週間前

  • 会社で働く

    Regulatory Affairs Associate

    登録メンバーのみ

    A life sciences organisation is seeking a Regulatory Affairs Associate to provide hands-on administrative and documentation support to the Regulatory Affairs function in Japan. This role plays a key supporting role in regulatory project coordination, documentation quality, and su ...

    Tokyo, Tokyo

    3週間前

  • 会社で働く

    Head of Regulatory Affairs

    登録メンバーのみ

    Lead regulatory affairs in Japan for pharmaceutical products. · ...

    Greater Tokyo Area

    1ヶ月前

  • 会社で働く

    Regulatory Affairs Manager

    登録メンバーのみ

    We are seeking a highly motivated Regulatory Affairs Manager to lead regulatory strategies and ensure compliance for pharmaceutical and medical device products. This role plays a critical part in supporting product launches, ...

    Tokyo, Tokyo

    1ヶ月前

  • 会社で働く

    Regulatory Affairs Expert

    登録メンバーのみ

    We are seeking a Regulatory Affairs Expert to join our team at Merck. · Maintain regulatory approvals for In Vitro Diagnostics (IVD) and Medical Devices, · Acting as an agent for Foreign Manufacturer Accreditation, · Preparation of DMF for APIs and excipients, · API Import licens ...

    Tokyo, Tokyo

    1ヶ月前

  • 会社で働く

    Regulatory Affairs Manager

    登録メンバーのみ

    This position offers a unique opportunity for growth with an international cosmetics manufacturer expanding into Japan. · The role involves managing compliance systems for pharmaceuticals , quasi-drugs ,and cosmetics . · ...

    Greater Tokyo Area

    1ヶ月前

  • 会社で働く

    Manager, Regulatory Affairs

    登録メンバーのみ

    +We are now looking for in-country regulatory professionals to join our growing global regulatory team. · ...

    Tokyo

    1週間前

  • 会社で働く

    Regulatory Affairs Manager

    登録メンバーのみ

    Support Associate Director Regulatory Affairs EMEA/Japan to ensure compliance with regulations and statutes concerning development, manufacturing, distribution, marketing and sales of Hill's products in Japan. · ...

    Japan

    1週間前

  • 会社で働く

    Regulatory Affairs Manager

    登録メンバーのみ

    Ceva Animal Health busca a un Regulatory Affairs Manager para liderar la estrategia regulatoria de productos veterinarios en Japón. Se requiere experiencia en gestión de sumisiones regulatorias, conocimientos de regulaciones veterinarias y habilidades para comunicarse con autorid ...

    Japan

    1日前

  • 会社で働く

    Regulatory Affairs Expert

    登録メンバーのみ

    Merck is seeking a Regulatory Affairs Expert to perform tasks such as preparation and submission of DMF for APIs and excipients. · ...

    Tokyo フルタイム

    1ヶ月前

  • 会社で働く

    Japan Regulatory Affairs Lead

    登録メンバーのみ

    We are supporting a global life sciences organization in identifying an experienced Japan Regulatory Affairs Lead (CMC-focused) to define and execute Japan-specific CMC regulatory strategies. · 10–15+ years of experience in Japan Regulatory Affairs (Pharmaceuticals). · ...

    Tokyo

    1ヶ月前

  • 会社で働く

    Senior Manager, Regulatory Affairs

    登録メンバーのみ

    +Job summary · Create Japanese Package Inserts (JPIs) of new drugs and manage revisions of JPIs of post approval products to be in line with CCDS.ResponsibilitiesCreate Japanese Package Inserts (JPIs) of new drugs and manage revisions of JPIs of post approval products to be in li ...

    Tokyo

    3週間前

  • 会社で働く

    Japan Regulatory Affairs Lead

    登録メンバーのみ

    We are supporting a global life sciences organization in identifying an experienced Japan Regulatory Affairs Lead (CMC-focused). This role is responsible for defining and executing Japan-specific CMC regulatory strategies ensuring compliance with Japanese regulations. · ...

    Tokyo フルタイム

    3日前

  • 会社で働く

    Regulatory Affairs Expert

    登録メンバーのみ

    We are looking for a Regulatory Affairs Expert to join our team at Merck. · Maintenance of regulatory approvals for In Vitro Diagnostics (IVD) and Medical Devices. · ...

    Japan

    1週間前

  • 会社で働く

    Principal Specialist, Regulatory Affairs

    登録メンバーのみ

    This role involves working as a specialist in regulatory affairs. · ...

    Tokyo, Tokyo

    1ヶ月前