This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.
- Ensure the on-time filing of high-quality regulatory submissions, and to assist in the preparation, maintenance, and control of regulatory Dossiers.
- Interact with all levels in the organization, and across several functions particularly Compliance, Marketing, R&D;, engineering, manufacturing, and QA/QC.




- Participate in discussions to provide strategic regulatory guidance to team members in India and other Region operations.
- Interact with regulatory agency on regulatory submissions and follow ups of drug products.
- Oversee the preparation and filing of high-quality submissions to regulatory authorities.
- Ensure that all applications are filed in accordance with regulations and requirements.
- Provide regulatory guidance to staff and inter-disciplinary project teams.
- Be a proactive member of the Regulatory team to ensure Baxter’s continuing compliance with regulatory authorities.
- Continue to develop quality standards and procedures for RA.
- Facilitate product development/Launch activities for respective Markets

Equal Employment Opportunity

Baxter is an equal chance employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexu

📌 Spec, RA (Ahmedabad)
🏢 BAXTER
📍 Ahmedabad