Regulatory Affairs Specialist
Há 5 dias
About the Role
Kenvue, a global leader in consumer healthcare, is seeking an experienced Regulatory Affairs Specialist to join its team. As a key member of our regulatory function, you will play a critical role in ensuring compliance with local regulations and quality system requirements for our medicinal products.
Key Responsibilities:
- Assists in the coordination, compilation & submission of new drug applications, cosmetics, medical devices, food supplements or any similar product to the regulatory agencies within their geographical and/or brand area of responsibility.
- Collects and organizes information on regulatory requirements for quality, preclinical and clinical data to meet applicable regulations.
- Prioritizes, plans and monitors allocated projects against defined timelines.
- Develops and maintains a thorough understanding of the regulatory environment and supporting data requirements.
Requirements:
- Knowledge of consumer healthcare environment and product development.
- Understanding of processes and departments within a healthcare company.
- Effective time and organization management.
- Proficiency in English.
About Kenvue
We are a global house of iconic brands that put people first, care fiercely, earn trust with science and solve with courage. Our diverse and brilliant team of 22,000 people is passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact the lives of millions of people every day.
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