Analista SR de Asuntos Regulatorios Cono Sur

Analista SR de Asuntos Regulatorios Cono Sur

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:

GER ASSUN REGUL

Ubicación:

Latin America, Argentina, Buenos Aires, Capital Federal

Lugar de trabajo:

Híbrido

What will you

What you will do

The Regulatory Affairs Coordinator is responsible for defining and implementing the regulatory strategy of Kenvue’s brands across the LAS region, ensuring product launches, compliance with internal policies, and adherence to national health regulations. This role oversees the regulatory portfolio, coordinates submissions, renewals, and approvals, and supports innovation projects to guarantee timely market access and regulatory excellence.

Key Responsibilities:

• Ensure compliance with national regulatory requirements, internal procedures, and company ethics and compliance principles in all assigned markets.
• Plan and execute regulatory processes, submissions, notifications, and other requirements from local health authorities.
• Provide timely and clear information on regulatory requirements that could impact current and future business plans, promoting internal alignment and process adaptation.
• Implement robust regulatory strategies to enable agile product approvals, claims, and promotional materials while mitigating potential risks and adding business value.
• Coordinate and execute local and regional strategies to optimize product development, registration, and lifecycle management in alignment with evolving regulations.
• Support the development and review of product artworks to ensure compliance with country-specific requirements.
• Develop regulatory timelines and monitor progress, taking proactive actions to anticipate challenges and minimize delays.
• Serve as a strategic partner, connecting with cross-functional teams locally and regionally to achieve common objectives.
• Actively participate in local forums, cross-functional teams, and industry associations, providing regulatory guidance and updates on validated strategies and potential business impacts.
• Guarantee adherence to operational procedures and regulations applicable to cosmetics, food, medical devices, and pharmaceutical products.
• Analyze the impact of new or updated regulations on the business and propose appropriate actions.

Qualifications

• Education level required: Bachelor’s degree in Pharmacy.
• Years of experience: Minimum of 5 years of regulatory affairs experience.
• Language: Intermediate Business English (Portuguese desirable).
• Technical skills: Advanced technical knowledge in consumer health or pharmaceutical products (cosmetics, medicines, hygiene, and health products); experience managing submissions and regulatory processes before health authorities; project management skills; strategic and creative thinking focused on delivering results; teamwork and communication skills.

Si usted es una persona con una discapacidad, consulte nuestra página de Disability Assistance para obtener información sobre cómo solicitar una adaptación.