Regulatory Affairs Intern Opportunity at Kenvue | Apply Now
Regulatory Affairs Intern opportunities at Kenvue offer an excellent career start for students and recent graduates in life sciences, biology, and biomedical engineering. If you are looking for Kenvue careers or an internship in Italy, this six-month hybrid internship in Rome provides hands-on regulatory affairs experience, professional development, and the opportunity to work with globally recognized healthcare brands.
Job Details
- Job Position: Regulatory Affairs Intern
- Location: Rome, Lazio, Italy
- Monthly reimbursement: 800 euros
About Kenvue
Regulatory Affairs Internship candidates will join Kenvue, a global consumer health company built on more than a century of heritage and rooted in science. Kenvue is home to iconic brands including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S®, and BAND-AID®. The company has approximately 22,000 employees worldwide and fosters an inclusive workplace where innovation, scientific excellence, and customer care remain at the forefront.
Regulatory Affairs Intern Description
The Regulatory Affairs Intern will provide 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. This role is crucial for maintaining regulatory standards and ensuring product safety.
Eligibility Criteria
- Master’s degree or currently enrolled in a scientific university course such as Biomedical Engineering or Biology.
- Proficiency in the Italian language.
- Fluency in English.
- Strong proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Ability to interact in a multi-department and dynamic environment.
- Good skills in archiving, ownership, and accountability.
Regulatory Affairs Intern – Key Responsibilities
- Preparation of registration applications and variations for medicinal products according to national, mutual recognition, and decentralized procedures.
- Monitoring of the Italian Official Journal and updates in Italian and European legislation.
- Preparation and finalization of advertising submissions to health authorities for medicinal products (OTC/SOP) and medical devices.
- Maintaining administrative compliance of Italian products in the company database.
- Labelling management and artworks changes check.
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