Senior Product Registration Specialist

Há 4 dias

Barueri, São Paulo, Brasil beBeeCompliance Tempo inteiro R$104.000 - R$141.000

Our team focuses on ensuring that our products meet regulatory and quality standards in Brazil. As a key member of the Agilent Global Regulatory Team, you will provide critical support to business teams for IVD registrations in Latin America.

Key Responsibilities
  • Register IVD and CDx submissions with local authorities.
  • Coordinate preparation of product documentation necessary for obtaining Brazil regulatory permits, licenses, and registrations.
  • Maintain alignment between Brazil QMS and Agilent QMS.
  • Monitor new regulations to ensure compliance.
  • Maintain and track product compliance documentation for regulated products.

We seek a highly skilled, motivated, and customer-focused professional to join our Brazil team. A Bachelor's degree in Pharmaceutical Sciences is required, along with at least 8 years of relevant experience in a regulated environment.

This role involves working closely with cross-functional teams to achieve seamless IVD registrations in Latin America. It demands strong organizational skills, attention to detail, and excellent communication skills to effectively coordinate with stakeholders.

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