At a Glance
- Tasks: Ensure regulatory compliance for iconic brands and manage product submissions.
- Company: Join Kenvue, a leader in everyday care with a rich heritage.
- Benefits: Hybrid work, competitive salary, and opportunities for personal growth.
- Other info: Be part of a passionate team dedicated to innovation and care.
- Why this job: Make a real impact on health and wellness products that people trust.
- Qualifications: Experience in regulatory affairs and strong understanding of compliance.
The predicted salary is between 36000 - 60000 £ per year.
Overview
What We Do
At Kenvue, we realize 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®. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact 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 Reports To
Regulatory Affairs Manager
Location
Europe/Middle East/Africa, United Kingdom, Reading, Berkshire
Work Location
Hybrid
What You Will Do
- The Senior Regulatory Affairs Specialist has an in-depth understanding of the regulatory environment within their geographical area of responsibility as well as requirements for regulatory submissions, approval pathways and compliance activities and the potential impact of these on business objectives.
- Ensures the success of new product registrations, line extensions and new indications and claims in alignment with the business plan.
- Manages the coordination, compilation, submission of new drug applications, cosmetics, medical devices, food supplements or any similar product to the regulatory agencies within their geographical and/or brand area of responsibility.
- Maintains compliance for all products with local regulations and quality system requirements.
Senior Regulatory Affairs Specialist employer: KENVUE
At Kenvue, we pride ourselves on being an exceptional employer, offering a vibrant workplace culture where every voice is valued and innovation thrives. Located in Reading, Berkshire, our hybrid work model provides flexibility while fostering collaboration among our global team of 22,000 passionate individuals. With a strong commitment to employee growth and development, we empower our staff to make a meaningful impact on the lives of millions through our iconic brands and science-driven approach.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Regulatory Affairs Specialist
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Kenvue 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 diving deep into Kenvue’s products and values. Show us that you’re not just another candidate; you’re genuinely excited about the impact our brands have on everyday care.
✨Tip Number 3
Practice your STAR technique for behavioural questions. We want to hear about your past experiences in regulatory affairs, so structure your answers to highlight your skills and achievements clearly.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the Kenvue family.
We think you need these skills to ace Senior Regulatory Affairs Specialist
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Regulatory Affairs Specialist role. Highlight your relevant experience and skills that align with the job description. We want to see how your background fits into our world of science and care!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you're passionate about regulatory affairs and how you can contribute to our mission at Kenvue. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements in previous roles. Quantify your successes where possible, as this helps us understand the impact you've made in your past positions. Numbers speak volumes!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our team at Kenvue!
How to prepare for a job interview at KENVUE
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulations and compliance requirements relevant to the role. Familiarise yourself with Kenvue's product lines and how they fit into the regulatory landscape. This will show that you're not just interested in the job, but that you understand the industry.
✨Showcase Your Experience
Prepare specific examples from your past work that demonstrate your expertise in regulatory submissions and compliance activities. Highlight any successful product registrations or approvals you've managed, as this will resonate well with the interviewers.
✨Emphasise Teamwork and Communication
Since the role involves coordination with various teams, be ready to discuss how you’ve effectively collaborated with cross-functional teams in the past. Share instances where your communication skills helped resolve issues or streamline processes.
✨Align with Kenvue’s Values
Research Kenvue’s mission and values, especially their focus on care and science. Be prepared to articulate how your personal values align with theirs and how you can contribute to their goal of impacting millions of people positively.
