Regulatory Affairs Industrial Placement

Kenvue Inc.; Reading; Hybrid; GBP 20,000 - 22,000; Full time

Benefits offered by this job

Competitive benefit package

Paid company holidays

Paid vacation

Volunteer time & more

Learning & development opportunities

Kenvuer Impact Networks

Job summary

Kenvue is recruiting for Regulatory Affairs Industrial Placements in the UK, based at Reading HQ. This 12-month, full-time placement (37 hours/week) reports to the Director, Regulatory Affairs, Self Care Lead, with the UK/EMEA RA team. 2nd-year students enrolled in a degree program are invited to apply.

The role emphasizes leadership, technical and communication skills through training, coaching and mentorship, with projects across RA. Hybrid work is offered.

Qualifications

• Legally authorized to work in the UK for the duration of the internship.
• Enrolled at an accredited university for a 12-month placement.
• Commit to 12 months, 37 hours per week (Mon–Fri).
• Working toward a 2:1 degree.
• Proficient in Windows Office applications.

Responsibilities

• Provide regulatory input and guidance on local regulatory requirements to product teams.
• Collaborate with EMEA RA Head on cross-country projects.
• Deliver regulatory-submission content and ensure compliance of documentation.
• Monitor regulatory review progress and maintain communications with Health Authorities.
• Prepare and submit regulatory submissions per guidelines.
• Stay updated on current regulatory legislation and policy.
• Deliver regulatory policy and advocacy work under EMEA RA lead guidance.

Skills

Regulatory mindset

Cross-team collaboration

Analytical skills

Communication

Time management

Problem solving

Work authorization UK

Willingness to learn

Education

Bachelor/Master/PhD enrollment

2:1 degree requirement

Fields: Pharmacist/Medical/Science

Tools

Excel

PowerPoint

Word

Outlook

Job description

Kenvueは現在、以下求人を募集しております。

Regulatory Affairs Industrial Placement

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:

Senior Director interim leader for Regulatory, EMEA

場所:

Europe/Middle East/Africa, United Kingdom, Reading, Berkshire

勤務地:

ハイブリッド

あなたがすること

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

障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。