Regulatory Affairs Intern

Kenvue Is Currently Recruiting For A:

Regulatory 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:

Regulatory Affairs Specialist

Location:

Europe/Middle East/Africa, Italy, Lazio, Rome

Work Location:

Hybrid

What You Will Do

Kenvue is currently recruiting for:

Regulatory Affairs Internship

This position reports to Regulatory Affairs Specialist and is based at Rome.

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.

What You Will Do

The Regulatory Affairs Intern is responsible for providing support in daily regulatory activities to ensure compliance with the lifecycle of medicinal products, medical devices, food supplements, and cosmetics in accordance with national and European legislation.

Key Responsibilities

• preparation of registration applications and variations for medicinal products according to national, mutual recognition and decentralized procedures;
• Monitor of the Italian Official Journal and updates in Italian and European legislation;
• Preparation/Finalization of advertising submissions to HA for medicinal products (OTC/SOP) and medical devices;
• maintain administrative compliance of Italian products in Company database;
• Labelling management/Artworks changes check.

Required Qualifications

What we are looking for

• Master's degree or be undergraduates in a scientific university course such as Biomedical Engineering, CTF, Pharmacy, Biology, or Chemistry;
• Proficiency in Italian language;
• Fluent in English.
• Strong proficiency in Microsoft Office (Word, Excel, PowerPoint);
• Ability to interact in a multi-department and dynamic environment;
• Good skills of archiving, ownership and accountability.
• What’s in it for you
• Competitive Total Rewards Package
• Learning & Development Opportunities
• Inclusive and collaborative work environment
• 6 months internship contract
• Monthly reimbursement: 800 euros