We use cookies to enhance your experience, analyze traffic, and serve personalized content. By clicking “Accept”, you agree to the use of cookies.
English
Čeština
Deutsch
Ελληνικά
Español
Français
Magyar
Italiano
日本語
한국어
简体中文
Nederlands
Polski
Português
Română
Русский
Svenska
Türkçe
Українська
Tiếng Việt
Countries
?
This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Join a dynamic team in Gurgaon as an Apprentice in Post Market Surveillance. You will manage complaints and vigilance reports, ensuring regulatory compliance (MDRs) and timely closure. Ideal for candidates with strong English communication skills and proficiency in MS Office, ready to thrive in a...
Seeking a **Sr Analyst, Procurement Indirect Systems** in **Bengaluru, India** to drive global P2P excellence at Baxter. You will support Asia-Pacific users, resolve system queries, and administer platforms like **Coupa** and **SAP**. Ideal candidates possess strong **AP/Procure to Pay** experien...
Senior Regulatory Affairs Specialist sought for Baxter’s Ahmedabad, India office. You will implement global regulatory strategies, secure marketing authorizations, and manage compliance risks for medical device/pharma products. Requires a Bachelor’s in science, 2+ years regulatory experience, pro...
Seeking a Specialist, RA in Ahmedabad, India, to manage Aggregate Safety Reports (PSUR/PBRER/PADER) and support post-approval activities. Key duties include RFI evaluation, authoring support, RMP/CO/NCO development, and signal management. Requires expertise in regulatory submissions, XEVMPD maint...
Seeking a Specialist, RA in Ahmedabad, India, to manage aggregate safety reports (PSUR/PBRER/PADER) and regulatory submissions. Key duties include RFI evaluation, authoring support, and coordinating RMP, CO/NCO activities with global teams. Ideal for experts in pharmacovigilance and regulatory af...
Senior Manager IT – MDM leads global Master Data Management initiatives at Baxter in Bengaluru, India. This role requires 10+ years delivering complex MDM programs ($2M+), expertise in Syndigo/Riversand and JD Edwards, and Agile/Waterfall proficiency. Drive data modeling, quality, and integration...
Senior Regulatory Specialist (Grade 16) sought in Ahmedabad, India. You will implement global regulatory strategies and secure marketing authorizations for Baxter’s medical device portfolio. Requires 2+ years of regulatory experience, a scientific degree, and strong project management skills. Joi...
Join Baxter in Bengaluru as an MDM Data Quality Analyst, a pivotal role supporting global data governance. You'll ensure high-quality data across domains, manage compliance, and resolve issues using DB inquiry tools. Ideal for experts with MDM experience and strong business acumen. Enjoy benefits...
Baxter seeks a strategic **Sr. Manager, IT – MDM** in **Bengaluru, India** to lead global **Master Data Management** programs. You will drive large-scale initiatives using **Syndigo (Riversand)** and **JD Edwards**, focusing on data modeling, quality, and integration. This role demands 10+ years ...
Senior Manager IT – MDM leads global Master Data Management initiatives at Baxter in Bengaluru, India. Requires 10+ years delivering complex MDM programs ($2M+), expertise in Syndigo/Riversand, JD Edwards, and Agile/Waterfall. Drive data modeling, quality, integration, and change management acros...
Senior Regulatory Specialist (Gr 16) sought in Ahmedabad, India. Leverage your scientific degree and 2+ years of pharmaceutical/medical device regulatory experience to manage project plans, ensure compliance, and interface with authorities. Requires strong project management, negotiation, and tec...