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(link is external)

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(link is external)

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 diversityandincl.china@novartis.com 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(link is external). You can follow us via Novartis Recruitment WeChat Official Account and Novartis Recruitment WeChat Video Account.

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All our current job openings are displayed here(link is external). If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information.

偽の求人広告や採用オファーにご注意ください

ノバルティスでは、当社名や幹部の名前を不正に使用して求職者をだます「採用詐欺」が発生していることを認識しています。

ノバルティスでは、面接なしに採用オファーを出すことはなく、候補者に金銭を要求することも決してありません。

現在の求人情報はすべてこちら(link is external)に掲載されています。詐欺の可能性がある求人広告や採用オファーに遭遇した場合は、返信したり、金銭や個人情報を送ったりしないよう強くおすすめします。

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(link is external)

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(link is external)

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(link is external)

Development
Universal Hierarchy Node
Japan
Toranomon (NPKK Head Office)
Research & Development
Full time
Regular
No

利便性と合理的配慮

ノバルティス は 障害 を 持 つ 個人 と 協力 し、 合理的配慮 を 提供 することをお 約束 します。健康状態 や 障害 を 理由 に 採用 プロセス のいかなる 部分 においても、あるいは 職務 の 必須事項 を 果 たすた めに 合理的配慮 が 必要 な 場合 は midcareer-r.japan@novartis.com 宛 てに 電子 メール をお 送 りください。その 際 ご 依頼内容、 ご 連絡先、求人票 の 番号 を 明 してください。

A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10057720

Manager, GPRM Japan

Apply to Job(link is external)