Regulatory and Medical Affairs Intern

Kenvue is currently recruiting for a: Regulatory and Medical Affairs Intern What we do At  Kenvue , we realize the extraordinary power of everyday care.

Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love.

Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated.

We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day.

We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours.

For more information , click here . Role reports to: Senior Regulatory Affairs Manager Location: Europe/Middle East/Africa, Turkey, Istanbul, Istanbul Work Location: Hybrid What you will do Kenvue Türkiye is looking for a Regulatory and Medical Affairs Intern to join our team for a 1-year fixed-term contract.

This internship offers hands-on exposure to the daily operations of a global FMCG business, assisting Regulatory Affairs department operational activities.

Key Responsibilities: • Daily check the Health Authority website and related Government pages to inform the department about new announcements, laws, guidelines etc.

• Weekly the check status of cosmetic product notification on the HA portal, inform the departmant, keeps record. • Involves to regular weekly check of Health Authority Letters from portal with Regulatory Affairs Specialist and inform the department..

• Sets monthly regulatory intelligence assessment meeting and joins the assessment meeting for tracking announcements, guidelines, or laws with regulatory affairs colleagues.

• Prepares product notification dossier by collecting artworks, pictures, and required information. • Supports regulatory department activities like documentation, archiving etc.

• Provides keeping cabinet indexes up to date. • Weekly uploads Health Authority Letters, Product Submission dossier and product notification dossier to the CEDMS system.

Requirements: • 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 take full responsibility for assigned projects from start to finish • Proactive and outgoing; comfortable reaching out to different stakeholders and following up independently • Eager to learn regulatory department processes, including variation applications and compliance tracking • Detail-oriented, with the ability to support risk assessment preparation and follow up on sample/lab-related processes • Interest in gaining hands-on exposure across both pharmaceutical and cosmetic product categories • Available to work 4 days/week, with 2–3 days at office.

If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.