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    Manager, GPRM Japan

    REQ-10057720
    7月 13, 2025
    Japan

    摘要

    製品レコード、進捗レポート、追加のレポート、変更、定期的な推奨事項を管理します。チーム戦略製品に関するアドバイスを提供し、証拠に基づいて規制当局に相談します。規制当局に連絡し、承認を迅速に行い、質問に答えるために交渉してください。製品ライフサイクル全体を通じて、プロジェクト チームの規制仲介者として機能します。新薬、バイオテクノロジー、医療機器の迅速かつタイムリーな認可と、販売可能な医薬品や医療機器の継続的な認可を確実に行います。マーケティングまたは研究グループおよび政府の規制当局の規制担当者として機能します。生産、ラインの拡張、技術マーク、規制および関連する解釈における開発および/またはマーケティングチームへのアドバイス。座標、通貨、および必要に応じて配信レポートを準備します。

    About the Role

    Major Accountabilities

    • Assist developing innovative and high quality regulatory strategies to facilitate regulatory processes in development and ensure registration with optimized labels that contribute to health and welfare of the Japanese nation.

    • Contribute to the regulatory activities in day-to-day operations for assigned TA area.

    • Lead cross functional communication for preparing and finalizing Japanese labeling for new drugs.

    • Take regulatory related actions to maintain post marketing products in Japan.

    • Establish goodrelationship with the Japanese HA in responsible projects

    • Contribute to the adherence to regulations, guidelines and global/internal procedures.

    • Ensure adequate reporting of adverse events / technical complaint / compliance issue in accordance with company procedures

    • 100% timely delivery of all training requirements including compliance

    Education:

    • Degree in pharmacy, medicines, science, agriculture and/or pharmaceutical engineering discipline required.  Advanced degree (Master Degree, PhD, etc.) prefered.

    • Pharmacist license preferred.

    Experience/Professional requirement:       

    • Demonstrate good presentation skills in delivering clear messages to audience and modifying language and style to meet the needs from audience.

    • Understand the drug development/maintenance processes, milestones in the assigned disease area and Novartis procedures for decision board review and approval.

    • Understand basic knowledge of Japan regulation

    • Possess basic knowledge of global regulatory environment, and contribute to elaborating the project specific  development/regulatory strategy and plan.

    • Report and summarize discussions in which RA plays an important role. Good in writing and reading English (e.g. exchange of scientific and technical information by e-mail and generation of scientific and technical documentation).

    • Proactively communicate issues and potential solutions.

    • Provide updates on current situation, and ensure that the same information is disseminated throughout the organization as needed. Network with others and share information.

    • Demonstrate cultural awareness and work in cross cultural environment.

    English Skill:

    Fluent English as business language.

    Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

    Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:   https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

    Accessibility and Accommodation:

    Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

     

    Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network. You can follow us via Novartis Recruitment WeChat Official Account and Novartis Recruitment WeChat Video Account.

    Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

    Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

    Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

    REQ-10057720

    Manager, GPRM Japan

    Apply to Job

    Source URL: https://m.leyunwang.com/careers/career-search/job/details/req-10057720-manager-gprm-japan-ja-jp

    List of links present in page
    1. https://www.novartis.com/about/strategy/people-and-culture
    2. https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf
    3. mailto:[email protected]
    4. https://talentnetwork.novartis.com/network
    5. https://www.novartis.com/about/strategy/people-and-culture
    6. https://talentnetwork.novartis.com/network
    7. https://www.novartis.com/careers/benefits-rewards
    8. https://novartis.wd3.myworkdayjobs.com/ja-JP/Novartis_Careers/job/Toranomon-NPKK-Head-Office/Manager--GPRM-Japan_REQ-10057720-6
    9. mailto:[email protected]
    10. https://novartis.wd3.myworkdayjobs.com/ja-JP/Novartis_Careers/job/Toranomon-NPKK-Head-Office/Manager--GPRM-Japan_REQ-10057720-6