Associate RA
Published date: 2026/11/07
- Location: Ahmedabad, Gujarat, India
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
Ensure the on-time filing of high-quality regulatory labeling submissions for US, Canada and Europe Market
To assist in the preparation, maintenance, and control of regulatory Dossiers (Module-1, labeling part) for US, Canada and Europe Market
Interact with all levels in the organization, and across several functions particularly Compliance, Marketing, R&D, engineering (packaging), 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 for US, Canada and Europe Market
Oversee the preparation and filing of high-quality labeling 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 for US, Canada and Europe Market
Facilitate product labeling development/Launch activities for respective Markets.
SPL preparation and Drug listing activity for USA products.
Maintain query/variation labeling database for US, Canada and Europe Market
Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
Ensure the on-time filing of high-quality regulatory labeling submissions for US, Canada and Europe Market
To assist in the preparation, maintenance, and control of regulatory Dossiers (Module-1, labeling part) for US, Canada and Europe Market
Interact with all levels in the organization, and across several functions particularly Compliance, Marketing, R&D, engineering (packaging), 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 for US, Canada and Europe Market
Oversee the preparation and filing of high-quality labeling 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 for US, Canada and Europe Market
Facilitate product labeling development/Launch activities for respective Markets.
SPL preparation and Drug listing activity for USA products.
Maintain query/variation labeling database for US, Canada and Europe Market
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