INTERNSHIP DETAILS

Regulatory Affairs Export

CompanyRecordati
LocationPuteaux
Work ModeOn Site
PostedMarch 15, 2026
Internship Information
Core Responsibilities
The role involves supporting the International Regulatory Affairs team in daily activities, including maintaining export marketing authorizations and preparing pharmaceutical product registration files. Additional tasks include legal mention creation, packaging article validation, and updating tracking tables.
Internship Type
full time
Company Size
4224
Visa Sponsorship
No
Language
French
Working Hours
40 hours
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About The Company
Recordati has been at the forefront of life-enhancing and life-changing medicines for 100 years. With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical force, listed on the Italian stock exchange, with over 4,500 employees. We are a group of like-minded, passionate individuals who go to extraordinary lengths for our partners, customers, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries. At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest – we want to give people the opportunity to be the best version of themselves. This drive will never stop. Together, we will always be reimagining tomorrow – with new ideas, new technologies and new innovations to fight diseases. Recordati. Unlocking the full potential of life.
About the Role

Job Purpose

Vous accompagnerez l'équipe Affaires Réglementaires Internationales dans la gestion quotidienne des activités du service, notamment :
•    Le maintien du portefeuille des AMM export : préparation des dossiers de variations et de renouvellement auprès des autorités de santé pour les médicaments, 
•    La création/modification des mentions légales en anglais,
•    La relecture et validation des articles de conditionnement,
•    La demande de Certificats du Médicament et/ou Certificats de Libre Vente auprès de la Chambre de Commerce,
•    La préparation des dossiers d'enregistrement des produits pharmaceutiques, à l'Export,
•    La relecture d'éléments promotionnels et de formation,
•    La mise à jour de tableaux de suivi.
Zone géographique couverte : Europe, Afrique, Asie, Maghreb, Moyen Orient, Russie etc.

Key Responsibilities

Required Education

Etudiant(e) en pharmacie orienté(e) Affaires Réglementaires, vous avez idéalement de bonnes connaissances en Affaires Réglementaires et vous recherchez un stage afin de mettre en pratique vos connaissances acquises. 
Vous maîtrisez les logiciels du pack Office. Force de proposition, Rigoureux(se), organisé(e) et dynamique, vous êtes reconnu(e) pour votre esprit d'équipe ainsi que pour vos qualités relationnelles et d’adaptation

Required Skills and Experience

Technical Competencies

Required Behaviours and Competencies

Required Languages

Vous êtes à l'aise avec l'anglais

Travel required in %

Key Skills
Regulatory AffairsPharmacyOffice SoftwareTeamworkCommunicationAdaptabilityOrganizationAttention to Detail
Categories
HealthcareScience & ResearchConsulting