Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
Senior Director interim leader for Regulatory, EMEA位置：
Europe/Middle East/Africa, United Kingdom, Reading, Berkshire工作地点：
混合你会做什么
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
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