Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Head of RA & MA Japan位置：
Asia Pacific, Japan, Tokyo-To, Chiyoda工作地点：
混合你会做什么
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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