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Job Function

Regulatory Affairs Group

Job Sub Function

Regulatory Affairs

Job Category

Professional

All Job Posting Locations:

Mexico City, Mexico

Job Description

OVERALL RESPONSIBILITIES:





Responsible for executing the submission process of product approval documents within the filing requirements. Expedites approval processing by addressing issues and ensuring compliance with government regulations and interpretations

Position Duties & Responsibilities

Develops appropriate plans for the submission of product approval documents to ensure rapid and timely approval on medical devices and continued approved status of marketed medical devices.
Resolves moderately complex problems.
Provides regulatory support and expertise for moderately complex projects across all functional areas involved in projects.
Compiles moderately complex product approval packages.

Functional And Technical Competencies

Leverages a working knowledge of the regulatory environment, including compliance, current and proposed laws, regulations and guidance, to prepare compliant Regulatory strategies that are aligned with R&D; and business objectives of the company, including con

📌 Analyst Reg Aff (Ciudad de México)
🏢 Johnson & Johnson MedTech
📍 Ciudad de México