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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。
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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：
Head of RA & MA Japan位置：
Asia Pacific, Japan, Tokyo-To, Chiyoda工作地點：
混合你會做什麼
The Senior Regulatory Affairs Associate is responsible for managing regulatory submissions and ensuring compliance with applicable laws and guidelines. You will collaborate with cross-functional teams to support product approvals and maintain regulatory documentation:
**Key Responsibilities**
• Pioneer the development and implementation of cutting-edge regulatory strategies that streamline product approvals while ensuring full compliance with global standards.
• Collaborate cross-functionally with R&D and marketing teams to translate complex regulatory requirements into innovative product labeling and communication strategies.
• Lead the creation of dynamic regulatory intelligence reports that anticipate industry shifts and proactively adapt company policies.
• Design and execute interactive training modules to elevate regulatory awareness and agility across the organization.
• Champion the integration of emerging digital tools and AI-driven analytics to enhance regulatory submission accuracy and efficiency.
What we are looking for
**Required Qualifications**
• Bachelor's degree in a relevant scientific or regulatory field
• Minimum of 3 years experience in regulatory affairs or related domain
• Strong understanding of regulatory guidelines and compliance requirements
• Experience in regulatory affairs for OTC pharmaceutical products
• Proven ability to interpret and synthesize scientific data
• Effective communication skills for preparing regulatory documentation
• Work experience using English in Multinational company or domestic company (TOEIC 700 or more)
**Desired Qualifications**
• Pharmacist or master degrees in a relevant science
• Work experience in Consumer industry (OTC drugs, Quasi-drugs, Cosmetics, Medical devices for consumer use, food, etc)
• Expertise in navigating complex regulatory landscapes with innovative problem-solving
• Experience in crafting persuasive regulatory narratives and stakeholder presentations
• Proficiency in leveraging technology and data analytics for regulatory process improvement
• Strategic foresight in regulatory affairs and compliance monitoring
• Proactive approach with a commitment to continuous learning and pioneering novel regulatory methods
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