Kenvueは現在、以下求人を募集しております。
Senior Regulatory Affairs Associate私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
Head of RA & MA Japan場所:
Asia Pacific, Japan, Tokyo-To, Chiyoda勤務地:
ハイブリッドあなたがすること
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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