The Estée Lauder Companies
Regulatory Affairs Intern
Skills
9 days ago
Share this opportunity
Share this opportunity to other talents of your network:
✓ Offer them a visibility boost with clients.
✓ Help your contacts find their next job.
Important information
Contract type:
Internship
Location:
Petersfield, UK
Work mode:
Onsite
Published on:
17 October 2026
What they need
Description
The Estée Lauder Companies (ELC) Global Product Stewardship, Regulatory Affairs team has an opening for a 13-month internship as Associate Regulatory Affairs Scientist – Intern. This role will be based at Whitman Laboratories in Petersfield, UK.
The Regulatory Affairs team manages local compliance requirements as well as providing expertise and technical background to global corporate functions on cosmetic ingredients and legislation relevant to ELC products within the EU and other areas of the world.
The Associate Regulatory Affairs Scientist – Intern will be responsible for ensuring the timely submission of EU and UK Cosmetic Notifications for appointed brands, ensuring key business timelines are met. In addition, the successful candidate will support the Consumer Care department with relevant consumer queries and support the EU Regulatory team with key projects where required.
The successful candidate will work closely with the wider EMEA Regulatory team as well as our product safety function.
Key Responsibilities:
- Coordinating the notification of cosmetic products in the EU and UK, through CPNP (Cosmetic Product Notification Portal) and SCPN (Submit Cosmetic Product Notification) respectively.
- Management of notification timelines to align with product launch dates.
- Contribute to special projects relating to EU and UK Cosmetic Notification.
- Review requests for confirmation of notification compliance from supply chain functions to support stock transfer.
- Facilitate responses to consumer regulatory related queries through consumer care function.
- Support regulatory projects within the EMEA regulatory team which may include tasks such as review of regulatory texts, supporting authority queries, reviewing compliance documentation and updating regulatory databases.
Qualifications
- Must be studying towards or already have a degree in Biochemistry, Chemistry, Biology, Toxicology or any similar scientific discipline. Should be on course to achieve at least a 2:1.
- Strong time management and organisational skills with the ability to meet deadlines and work independently.
- Highly competent computer skills and an aptitude for learning how to use new systems. Full training on internal systems will be provided.
- Team player, able to build strong relationships with cross-functional teams and leverage those relationships to manage complex/novel requests.
- A passion for learning and an inquisitive mind.
Other offers great for you!
These companies are also looking for great profiles
Cherrypick
Chef de projet MOE Supply Chain
570
Freelance
92320 Châtillon, France
Hybrid, Onsite
Skills
20 hours ago
Quick apply
YUNIKO
Business Analyst ERP Dynamics 365 (H/F)
35k€ - 40k€
Permanent contract
67340 Ingwiller, France
Onsite
Skills
18 hours ago
Quick apply
YUNIKO
Consultant·e AI Engineer & Data Scientist – Agents IA (H/F)
50k€ - 70k€ + variable annuel max. 10k€
Permanent contract
Paris, France
Onsite, Hybrid
Skills
18 hours ago
Quick apply
No company information available.