Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
GER ASSUN REGUL位置：
Latin America, Argentina, Buenos Aires, Capital Federal工作地点：
混合你会做什么
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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