Europe/Middle East/Africa, Spain, Community of Madrid, Madrid
勤務地:
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The Regulatory affairs Intern will participate to the coordination, compilation,
submission of new drug applications, cosmetics, medical devices, food supplements or any similar product to the regulatory agencies in Spain. In their role, they will cooperate with Commercial/Marketing teams.
Essential duties and responsibilities
Medicines Regulatory activities
- New marketing authorization activities
- Maintenance activities of existing licenses: preparations of administrative, quality regulatory packages and safety related variations for their submission to Healthcare Authorities (H.A.)
Artwork review and approval with the help of the Regulatory Specialist.Internal Aws tool user.
- Review of promotional materials direct to Healthcare Professionals and consumers.
- New legislation monitoring, impact analysis and communication to business partners.
- H.A. tools: Fraccionamiento (Breaking‑up of SPCs and PILs).RAEFAR, LABOFAR
Specific requirements
Cosmetic Regulatory activities:
- Artwork review and approval. Internal Aws tool user.
- Review of the promotional material for Healthcare Professionals, consumers and internal departments
- Scientific advice for promotional materials with the support of the Regulatory contact in the Regional Team
- Product information advice for Consumer affairs and consumer service
- Ensure completion of databases.
- New legislation mo
📌 Regulatory Affairs Intern (Madrid)
🏢 Kenvue
📍 Madrid
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