Kenvue 目前正在招聘 a：
我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
法规事务副总监位置：
Asia Pacific, China, Shanghai, Shanghai工作地點：
完全現場你會做什麼
Ensures compliance with regulatory agency regulations and interpretations. Prepares responses to regulatory agencies' questions and other correspondence. Gathers and assembles information necessary for submissions in accordance with regulations and relevant guidelines. Involved with the preparation of necessary outlines, summaries, status reports, memos, graphs, charts, tables, and slides. Provides solutions to a variety of problems of moderate scope and complexity. Organizes and maintains reporting schedules for new drug application and investigational new drug applications.
Responsiblity
1. Be responsible for innovation projects’ notification and registration, closely monitoring registration status, and making sure regulatory milestone on-time delivery.
2. Actively collaborate with MKT/R&D, providing robust and innovative claims supported with sound science to drive competitive advantage.
3. Proactively finishing internal compliance tasks to meet internal process and requirements, maintain RA information in internal system.
4. Implementations by proactively partnering with business stakeholders in aligning, planning and developing regulatory strategies in line with the franchise priorities. effectively manage product registration and notification, claims assessment, AW/label approvals, dossiers preparation and on-time submission, monitoring the progress, status, and timelines.
如果您是殘障人士，請查看我們的 殘障人士援助頁面瞭解如何申請便利
