Regulatory Affairs Industrial Placement

Kenvue Is Currently Recruiting For A: Regulatory Affairs Industrial Placement 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® that you already know and love. Science is our passion; care is our talent. Who We Are Role Reports To: Senior Director interim leader for Regulatory, EMEA Location: Europe/Middle East/Africa, United Kingdom, Reading, Berkshire Work Location: Hybrid What You Will Do Kenvue is currently recruiting for 3x: Regulatory Affairs Industrial Placements This position reports into the Director, Regulatory Affairs, Self Care Lead, and is based at Kenvue UK HQ in Reading, UK. What You Will Do The Regulatory Affairs industrial Placement is a 12 month experience (starting June 2027) designed to help university students develop leadership, technical, and communication skills through practical business experience and ongoing training, development, coaching and mentorship. This role will enable the student to have real-life work application of concepts and theories learned in the classroom. This is a full-time (37 hours per week) assignment. The intern will be assigned to the UK or EMEA Regulatory Affairs department and will work with a range of projects for the duration of the term. We are looking for 2nd year students who are already enrolled in a course that allows them to undertake a 12 month industry placement. Key Responsibilities

• Works to provide regulatory input and technical guidance on local regulatory requirements to product development teams
• Collaborate with EMEA RA Head on cross countries projects/presentations
• Deliver superior and differentiated claims
• Assesses the acceptability of quality, preclinical and clinical documentation for submission filing to comply with applicable local Health Authority requirements, where relevant.
• Provides regulatory assessment and guidance for proposed product claims/labelling, ensuring that the provided clinical and non clinical data are consistent with the local regulatory requirements and support the proposed product classification and claims.
• Prepares and submits regulatory submissions according to applicable regulatory requirements and guidelines.
• Monitors the progress of the regulatory authority review process through appropriate communication with the Health Authority.
• Familiarizes and understands the current regulatory legislation to keep the legislative knowledge up to date at local
• Deliver regulatory policy and advocacy work under EMEA RA head guidance What We Are Looking For
• Required Qualifications
• Candidates must be legally authorized to work in the UK
• Actively enrolled in an accredited university through the duration of the internship pursuing a Bachelor's, Master's or PhD degree
• Ability to commit to 12-month, 37 hours per week (Monday – Friday) for the length of the assignment
• Working towards a 2:1 Degree
• Proficient in Windows software applications (Excel, PowerPoint, Word, Outlook)
• Ability to provide their own transportation between home and work office location
• Desired Qualifications
• Degree focused in: Pharmacist, Medical or Science (Biology, Molecular Biology, Chemistry, Personal Care, Microbiology, Neuroscience, Consumer & Sensory Science, Food Science, Pharmacy, etc.)
• Strong analytical, organizational and communication skills
• Passionate or interested in the consumer industry
• Displays willingness to learn, strong problem-solving skills and capable of working in a fast-paced environment What's In It For You
• Competitive Benefit Package*
• Paid Company Holidays, Paid Vacation, Volunteer Time & More!
• Learning & Development Opportunities
• Kenvuer Impact Networks If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.