Analista SR de Asuntos Regulatorios Cono Sur

Analista SR de Asuntos Regulatorios Cono Sur

O que fazemos

At Kenvue, percebemos o extraordinário poder do cuidado diário. Construída com base em mais de um século de herança e enraizada na ciência, somos a casa de marcas icônicas - incluindo NEUTROGENA®, AVEENO®, TYLENOL,® LISTERINE,® JOHNSON'S® e BAND-AID® que você já conhece e ama. A ciência é a nossa paixão; O cuidado é o nosso talento.

Quem somos

Nossa equipe global é de ~ 22.000 pessoas brilhantes com uma cultura no local de trabalho onde cada voz é importante e cada contribuição é apreciada. Somos apaixonados por insights, inovação e comprometidos em entregar os melhores produtos aos nossos clientes. Com experiência e empatia, ser um Kenvuer significa ter o poder de impactar milhões de pessoas todos os dias. Colocamos as pessoas em primeiro lugar, nos importamos ferozmente, ganhamos confiança com a ciência e resolvemos com coragem - e temos oportunidades brilhantes esperando por você! Junte-se a nós para moldar nosso futuro - e o seu. Para obter mais informações, clique em aqui.

Role reporta para:

GER ASSUN REGUL

Localização:

Latin America, Argentina, Buenos Aires, Capital Federal

Local de trabalho:

Híbrido

O que você fará

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.

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