Req # 205903 Location Bengaluru, Karnataka, India Job Category Regulatory Affairs Date posted 07/17/2026
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 productive 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.
Job Summary
As a Global Regulatory Affairs - Associate, you are responsible for providing regulatory support for change assessments,
submission preparation for product registrations and submitting regulatory dossiers using various publishing tools for drugs, biologics & medical devices. Supporting various phases of product life cycle, generate capability towards fundamental global regulatory requirements and different regulatory pathways. Collaborating with cross-functional teams within the organization, including R&D;, quality assurance and manufacturing departments. Ability to take ownership of tasks and deliver without supervision while using their expertise to seek help when necessary.
What you'll be doing
- Engage with Global and Regional regulatory teams located across the globe to ensure regulatory activities are aligned to business needs for various drugs, biologics & medical devices submissions.
- Supporting stakeholders in managing product registrations and ensuring high quality submissions to Regulatory Authorities.
- Responsible for Regulatory Product Life Cycle Management Activities.
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📌 RA Associate (Bengaluru)
🏢 BAXTER
📍 Bengaluru
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