Descrizione dell'offerta
Kenvueは現在、以下求人を募集しております。
Regulatory Affairs Intern Regulatory Affairs Internship based at Rome, reporting to a Regulatory Affairs Specialist. Hybrid work arrangement in Italy, Lazio, Rome.
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. Join us in shaping our future and yours.
Location Europe/Middle East/Africa, Italy, Lazio, Rome
Work arrangement Hybrid
What you will do The Regulatory Affairs Intern provides 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 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 the Company database.
Labelling management and artwork changes check.
Required Qualifications
Master’s degree or undergraduate studies in a scientific university course such as Biomedical Engineering, CTF, Pharmacy, Biology, or Chemistry.
Proficiency in the 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 in archiving, ownership, and accountability.
What’s in it for you
Competitive Total Rewards Package
Learning & Development Opportunities
Inclusive and collaborative work environment
6‑month internship contract
Monthly reimbursement: 800 euros
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。
#J-18808-Ljbffr
Regulatory Affairs Intern Regulatory Affairs Internship based at Rome, reporting to a Regulatory Affairs Specialist. Hybrid work arrangement in Italy, Lazio, Rome.
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. Join us in shaping our future and yours.
Location Europe/Middle East/Africa, Italy, Lazio, Rome
Work arrangement Hybrid
What you will do The Regulatory Affairs Intern provides 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 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 the Company database.
Labelling management and artwork changes check.
Required Qualifications
Master’s degree or undergraduate studies in a scientific university course such as Biomedical Engineering, CTF, Pharmacy, Biology, or Chemistry.
Proficiency in the 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 in archiving, ownership, and accountability.
What’s in it for you
Competitive Total Rewards Package
Learning & Development Opportunities
Inclusive and collaborative work environment
6‑month internship contract
Monthly reimbursement: 800 euros
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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