Manager Regulatory Affairs - SelfCare

Manager Regulatory Affairs - SelfCare

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

Global Ingredient Management Director

Lieu :

Europe/Middle East/Africa, France, Haute-de-Seine, Issy Les Moulineaux

Lieu de travail :

Hybride

Ce que tu vas faire

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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