Regulatory and Medical Affairs Intern
- Función del trabajo:
- Fecha de publicación:
- Fecha de finalización:
- ID:
- 2607047907W
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Kenvue está reclutando actualmente para a:
Lo que hacemos
En Kenvue, nos damos cuenta del extraordinario poder del cuidado diario. Sobre la base de más de un siglo de herencia y arraigados en la ciencia, somos el hogar de marcas icónicas, incluidas NEUTROGENA®, AVEENO,® TYLENOL,® LISTERINE,® JOHNSON'S® y BAND-AID® que ya conoces y amas. La ciencia es nuestra pasión; El cuidado es nuestro talento.
Quiénes somos
Nuestro equipo global está formado por ~ 22.000 personas brillantes con una cultura laboral en la que cada voz importa y cada contribución es apreciada. Nos apasionan las ideas, innovación y comprometidos con la entrega de los mejores productos a nuestros clientes. Con experiencia y empatía, ser un Kenvuer significa tener el poder de impactar a millones de personas todos los días. Ponemos a las personas en primer lugar, nos preocupamos ferozmente, nos ganamos la confianza de la ciencia y resolvemos con coraje, ¡y tenemos oportunidades brillantes esperándote! Únase a nosotros para dar forma a nuestro futuro y al suyo. Para obtener más información, haga clic en aquí.
Role reports to:
Senior Regulatory Affairs ManagerUbicación:
Europe/Middle East/Africa, Turkey, Istanbul, IstanbulLugar de trabajo:
HíbridoWhat will you
Kenvue Türkiye is looking for a Regulatory and Medical Affairs Intern to join our team for a 1-year fixed-term contract. This internship offers hands-on exposure to the daily operations of a global FMCG business, assisting Regulatory Affairs department operational activities.
Key Responsibilities:
Daily check the Health Authority website and related Government pages to inform the department about new announcements, laws, guidelines etc.
Weekly the check status of cosmetic product notification on the HA portal, inform the departmant, keeps record.
Involves to regular weekly check of Health Authority Letters from portal with Regulatory Affairs Specialist and inform the department..
Sets monthly regulatory intelligence assessment meeting and joins the assessment meeting for tracking announcements, guidelines, or laws with regulatory affairs colleagues.
Prepares product notification dossier by collecting artworks, pictures, and required information.
Supports regulatory department activities like documentation, archiving etc.
Provides keeping cabinet indexes up to date.
Weekly uploads Health Authority Letters, Product Submission dossier and product notification dossier to the CEDMS system.
Requirements:
Currently enrolled in Pharmacy (5th year) or Chemical Engineering (3rd–4th year, based on course load)
Strong analytical mindset with a sense of ownership — able to take full responsibility for assigned projects from start to finish
Proactive and outgoing; comfortable reaching out to different stakeholders and following up independently
Eager to learn regulatory department processes, including variation applications and compliance tracking
Detail-oriented, with the ability to support risk assessment preparation and follow up on sample/lab-related processes
Interest in gaining hands-on exposure across both pharmaceutical and cosmetic product categories
Available to work 4 days/week, with 2–3 days at office.
Si usted es una persona con una discapacidad, consulte nuestra página de Disability Assistance para obtener información sobre cómo solicitar una adaptación.
