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:
Responsibilities | Details |
---|---|
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. |
Meta Description:
Join Baxter as a Regulatory Affairs Specialist in Ahmedabad. Manage regulatory submissions and ensure compliance with global standards.