Tech Stack

Description

You will lead a team of regulatory consultants, develop regulatory strategies for client projects, and manage high-quality submissions to health authorities in Mexico. You'll coordinate cross-functional teams, monitor regulatory standards, and ensure compliance to support product lifecycle management.

Requirements

• 5+ years in regulatory affairs
• Formal college or higher education in science-related discipline
• Fluency in English and local language
• Good understanding of local regulations for OTC, cosmetics, and medical devices
• Strong working knowledge of Microsoft Word, Excel, PowerPoint

Responsibilities

• Create regulatory strategies with clients to secure Ministry of Health approval
• Lead a team of consultants to meet project objectives
• Prepare and coordinate high-quality regulatory submissions for product launches and updates
• Support CMC dossier preparation and review
• Manage regulatory action items and project implementation plans