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Baxter Regulatory Affairs Specialist

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Regulatory Affairs Specialist

Company: Baxter
Location: Ahmedabad, Gujarat
Experience Required: 1 to 2 Years
Qualification: B.Pharm, M.Pharm, MSc, BSc, Ph.D
Salary: Not disclosed


Role Overview:

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:

ResponsibilitiesDetails
Submission ManagementEnsure timely and high-quality regulatory submissions.
Dossier PreparationAssist in maintaining and controlling regulatory dossiers.
Cross-Functional InteractionCollaborate with Compliance, Marketing, R&D, Engineering, Manufacturing, and QA/QC teams.
Regulatory GuidanceProvide strategic regulatory advice to teams and interact with regulatory agencies.
Quality StandardsDevelop and maintain quality standards and procedures for Regulatory Affairs.
Product LaunchFacilitate product development and launch activities for respective markets.

Meta Description:

Join Baxter as a Regulatory Affairs Specialist in Ahmedabad. Manage regulatory submissions and ensure compliance with global standards.


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