Kenvueは現在、以下求人を募集しております。
Manager Regulatory Affairs - SelfCare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:
Global Ingredient Management Director場所:
Europe/Middle East/Africa, France, Haute-de-Seine, Issy Les Moulineaux勤務地:
ハイブリッドあなたがすること
Kenvue is currently recruiting for a:
Regulatory Affairs Manager – Self-Care
This position can be based at Issy-les-Moulineaux, France or Reading, United Kingdom. This position is reporting to EMEA Regulatory Science & Advocacy Director.
Who We Are
At Kenvue, we realise the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.
Role Overview
As Regulatory Affairs Manager – Self-Care, you will be part of the EMEA Regulatory Science & Advocacy team, you will lead regulatory intelligence, shape regional policy positions, engage across the self-care ecosystem, and ensure internal alignment. You provide clear, actionable insights to support strategic decisions in an evolving regulatory landscape for self-care products
Key Responsibilities
1. Regulatory Intelligence & Foresight
- Monitor regulatory and scientific developments from EMA, HMA, CMDh, the European Commission, and national competent authorities.
- Identify emerging changes related to EU pharmaceutical legislation revision, ingredients, switches, labeling, pharmacovigilance, digital health, advertising and claims initiatives impacting self-care products.
- Anticipate regulatory trends, identify risks and opportunities, and provide actionable regulatory insights to internal stakeholders.
2. Regulatory Policy Strategy & Development
- Build regional regulatory positions on emerging self-care regulations and contribute to company-wide policies and advocacy priorities.
- Coordinate internal input to consultations, industry discussions, and legislative initiatives.
- Support the development of science-based positions and pragmatic regulatory approaches.
- Collaborate with global and regional teams to ensure consistency and alignment of regulatory strategies.
3. External Advocacy & Representation
- Participate in trade associations, technical committees, and expert forums.
- Build constructive relationships with regulatory authorities, scientific committees, and institutional stakeholders.
- Promote science‑based and pragmatic regulatory approaches.
4. Internal Leadership & Alignment
- Serve as a key regulatory partner for R&D, Medical, Safety, Quality, Marketing, Legal, Sustainability, and Commercial teams.
- Communicate complex regulatory changes clearly and pragmatically to support decision-making.
- Provide impact assessments and strategic recommendations to strengthen organizational readiness and compliance.
- Drive alignment across functions and support capability building on evolving self-care regulations.
Qualifications
- Relevant bachelor’s degree or higher in Regulatory Affairs, Life Sciences, Pharmacy, Law, Public Policy, or related field.
- Minimum 10 years of experience in regulatory affairs within the pharmaceutical, OTC, or self-care industry.
- Strong understanding of EU regulatory processes and interactions with competent authorities.
- Experience engaging with trade associations, health authorities, or industry working groups.
- Strong communication, stakeholder management, and cross-functional leadership skills.
- Fluency in English.
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