As a Regulatory Affairs Specialist at Baxter, you’ll manage regulatory submissions, ensure compliance, and provide strategic guidance across multiple functions. Join us to contribute to life-saving innovations and enhance patient outcomes.

Job Overview

Position: Regulatory Affairs Specialist

Company Profile: Baxter is committed to delivering innovative solutions that improve patient outcomes and enhance quality of life. Join us in our mission to advance healthcare.

Detailed Job Description

As a Regulatory Affairs Specialist at Baxter, you’ll manage regulatory submissions, ensure compliance, and provide strategic guidance across multiple functions. Join us to contribute to life-saving innovations and enhance patient outcomes.

Key Responsibilities

• Submission Management: Ensure timely and high-quality regulatory submissions.
• Dossier Preparation: Assist in maintaining and controlling regulatory dossiers.
• Cross-Functional Interaction: Collaborate with Compliance, Marketing, R&D, Engineering, Manufacturing, and QA/QC teams.
• Regulatory Guidance: Provide strategic regulatory advice to teams and interact with regulatory agencies.
• Quality Standards: Develop and maintain quality standards and procedures for Regulatory Affairs.
• Product Launch: Facilitate product development and launch activities for respective markets.

How to Apply

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