Spec, Ra - Ahmedabad, India - BAXTER
Description
This is where you save and sustain lives
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 ontime filing of highquality 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 highquality submissions to regulatory authorities.
- Provide regulatory guidance to staff and interdisciplinary 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.
Reasonable Accommodations
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information.
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