• Regulatory Affairs experience within the Healthcare & Life Sciences industry
• Advanced/Fluent English

Sobre nosso cliente

A global leader in the dental and medical devices industry, recognized for its innovation, high-quality standards, and strong expertise in highly regulated environments.

With a well-established international presence, the company operates in a truly global structure, connecting teams across Latin America and Europe and contributing to solutions that positively impact patients worldwide.

Descrição

• Act as the regulatory representative in cross-functional product development teams
• Ensure compliance of product documentation, including requirements, verification and validation activities, labeling, and instructions for use
• Develop and implement regulatory strategies for global product registration
• Prepare and maintain technical documentation for CE marking and ens...