Analista SR de Asuntos Regulatorios Cono Sur

我們做什麼

在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。

我們是誰

我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.

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你會做什麼

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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