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- Tasks: Support regulatory intelligence and policy development for self-care products.
- Company: Join Kenvue, a leader in everyday care with iconic brands.
- Benefits: Enjoy competitive pay, paid holidays, volunteer time, and summer Fridays.
- Other info: Hybrid work model with opportunities for learning and growth.
- Why this job: Make a real impact on health and wellness through regulatory expertise.
- Qualifications: 5+ years in EU regulatory frameworks; strong communication skills required.
The predicted salary is between 55000 - 65000 ÂŁ per year.
Kenvue is currently recruiting for a Senior Regulatory Specialist - Self Care.
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!
Role Overview
As a Senior Regulatory Affairs Specialist – Self-Care, you will be part of the EMEA Regulatory Science & Advocacy team and you will support regulatory intelligence, policy development, external engagement, and cross‑functional alignment. You provide clear regulatory insights to help guide strategic decisions in the evolving EU self‑care environment.
Key Responsibilities:
- Regulatory Intelligence & Foresight: Monitor regulatory developments from EMA, HMA, CMDh, the European Commission, and national competent authorities. Track topics such as EU pharmaceutical legislation revision, Rx‑to‑OTC switches, labelling and packaging rules, pharmacovigilance, benefit‑risk considerations, and quality standards. Identify potential impacts on products, portfolios, processes, and strategic plans. Provide concise analyses to support business preparedness.
- Regulatory Policy Contribution: Contribute to company positions on EU regulatory and policy initiatives affecting the self‑care landscape. Coordinate internal inputs to public consultations, draft guidelines, and legislative proposals. Ensure EMEA‑specific insights are reflected in global regulatory and policy discussions. Support development of advocacy materials and briefing documents.
- External Advocacy & Representation: Participate in industry association working groups and relevant regulatory or policy platforms. Support interactions with regulators, policymakers, and institutional stakeholders. Contribute scientific and regulatory expertise to help shape proportionate, consumer‑centric, and innovation‑friendly frameworks for OTC medicines.
- Internal Leadership & Alignment: Collaborate with Regulatory Affairs, Medical, Quality, Legal, Government Affairs, R&D, and Commercial teams. Communicate regulatory changes clearly and pragmatically. Provide regulatory assessments to support decision‑making and internal governance processes. Help ensure organizational readiness for evolving regulatory expectations.
Qualifications:
- Relevant bachelor’s degree or higher in Regulatory Affairs, Life Sciences, Pharmacy, Law, Public Policy, or related field.
- Minimum 5 years of experience with EU regulatory frameworks for self‑care and OTC products.
- Strong understanding of EU regulatory processes and interactions with competent authorities.
- Proven ability to interpret complex regulatory texts and translate them into actionable guidance.
- Excellent communication, synthesis, and stakeholder engagement skills.
- Fluency in English.
What’s in it for you?
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
- Extensive Learning & Development Opportunities
- Employee Resource Groups
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
Senior Regulatory Specialist - Self Care in Sonning employer: KENVUE
Contact Detail:
KENVUE Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Specialist - Self Care in Sonning
✨Tip Number 1
Network like a pro! Reach out to current or former Kenvue employees on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing Kenvue's brands and values inside out. Show how your experience aligns with their mission of delivering extraordinary care and innovation in self-care products.
✨Tip Number 3
Practice common interview questions but also be ready for situational ones. Think about how you've handled regulatory challenges in the past and be ready to share those stories!
✨Tip Number 4
After the interview, don’t forget to send a thank-you email! It’s a nice touch that shows your enthusiasm for the role and keeps you fresh in their minds. And remember, apply through our website for the best chance!
We think you need these skills to ace Senior Regulatory Specialist - Self Care in Sonning
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Senior Regulatory Specialist role. Highlight your experience with EU regulatory frameworks and how it aligns with Kenvue's mission of delivering exceptional self-care products.
Showcase Your Passion: Let your enthusiasm for regulatory affairs shine through! Share examples of how you've contributed to regulatory intelligence or policy development in your previous roles, showing us that you care about making a difference.
Be Clear and Concise: When writing your application, keep it straightforward. Use clear language to explain your qualifications and experiences, making it easy for us to see why you're a great fit for the team.
Apply Through Our Website: We encourage you to submit your application directly through our website. This way, you can ensure that all your details are captured correctly and we can easily track your application!
How to prepare for a job interview at KENVUE
✨Know Your Regulatory Stuff
Make sure you brush up on the latest EU regulatory frameworks, especially those related to self-care and OTC products. Familiarise yourself with recent changes and how they might impact Kenvue's brands. This will show that you're not just knowledgeable but also genuinely interested in the role.
✨Showcase Your Communication Skills
As a Senior Regulatory Specialist, you'll need to communicate complex regulatory information clearly. Prepare examples of how you've successfully communicated regulatory changes or policies in the past. This will demonstrate your ability to engage with various stakeholders effectively.
✨Prepare for Scenario Questions
Expect questions that ask how you'd handle specific regulatory challenges or changes. Think about potential scenarios related to EU pharmaceutical legislation or labelling rules, and be ready to discuss your approach. This will highlight your problem-solving skills and strategic thinking.
✨Align with Kenvue’s Values
Kenvue values care, trust, and innovation. Be prepared to discuss how your personal values align with theirs. Share experiences where you've put people first or contributed to innovative solutions in your previous roles. This will help you connect with the interviewers on a deeper level.