Kenvue 目前正在招聘 a：
我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
我們是誰
我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
Senior Director interim leader for Regulatory, EMEA位置：
Europe/Middle East/Africa, United Kingdom, Reading, Berkshire工作地點：
混合你會做什麼
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
如果您是殘障人士，請查看我們的 殘障人士援助頁面瞭解如何申請便利
