Kenvueは現在、以下求人を募集しております。
Analista SR de Asuntos Regulatorios Cono Sur私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
GER ASSUN REGUL場所:
Latin America, Argentina, Buenos Aires, Capital Federal勤務地:
ハイブリッドあなたがすること
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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