Regulatory and Medical Affairs Intern

About the role

Kenvue Türkiye is looking for a Regulatory and Medical Affairs Intern to join the team on a 1‑year fixed‑term basis. The internship provides hands‑on exposure to the daily operations of a global FMCG business while supporting the Regulatory Affairs department.

Key responsibilities

• Daily monitor Health Authority websites and government pages for new announcements, laws, and guidelines.
• Weekly check the status of cosmetic product notifications on the HA portal and keep records.
• Regularly review Health Authority letters with the Regulatory Affairs Specialist and inform the department.
• Organise and attend monthly regulatory intelligence assessment meetings to track announcements, guidelines, or laws.
• Prepare product notification dossiers by collecting artworks, pictures, and required information.
• Support documentation, archiving, and maintain cabinet indexes up to date.
• Upload Health Authority letters, product submission dossiers, and notification dossiers to the CEDMS system on a weekly basis.

Required profile

• Currently enrolled in Pharmacy (5th year) or Chemical Engineering (3rd–4th year, based on course load).
• Strong analytical mindset with a sense of ownership, able to manage projects from start to finish.
• Proactive, outgoing, and comfortable reaching out to different stakeholders independently.
• Eager to learn regulatory processes, including variation applications and compliance tracking.
• Detail‑oriented with the ability to support risk‑assessment preparation and follow‑up on sample/lab processes.
• Interest in gaining hands‑on exposure across pharmaceutical and cosmetic product categories.
• Available to work four days per week, with 2–3 days on‑site in the office.