Baxter

Senior System Verification Engineer needed in Bengaluru for medical device testing. Lead design verification for infusion pumps, executing test procedures and performance testing. Requires 6-10 years experience, including 3+ in system V&V, with a Bachelor's in Engineering. Benefits include profes...

Senior Specialist, Quality Assurance role in Minato, Tokyo, ensuring patient safety through GQP/GMP/QMS compliance. Requires 5+ years pharmaceutical QA experience, CMO management, and knowledge of PMD Act. Key duties include managing audits, inspections, and quality systems for drugs/medical devi...

Join Baxter’s Quality team in Round Lake, IL as a Quality Technician to ensure patient safety through sample management and weight loss analysis. You’ll maintain data integrity, support stability studies, and collaborate cross-functionally in a cGMP/FDA-regulated environment. Ideal for candidates...

Join Baxter’s Quality Assurance team in Ahmedabad, India, as a Sr Executive I, safeguarding patient safety through cGMP compliance. You’ll manage Document Control, review Batch Manufacturing Records (BMR/BPR), and ensure GDP standards. This role offers growth, professional development, paid time ...

Lead Quality Assurance operations in Cleveland as Manager II for Devices, ensuring FDA and ISO compliance. This role requires a Bachelor’s in a scientific field, 5+ years of experience, and leadership skills. Drive process improvements, manage audits, and analyze data to uphold product standards....

Qualified Person (QP) role in Dublin, Ireland, responsible for releasing Nutrition, Chemo, and Antibiotic sterile products. Ensure GMP compliance with Irish and European legislation in a clean room environment. Requires a Pharmacy degree, QP qualification, and aseptic manufacturing experience. Be...

Senior Regulatory Affairs Specialist sought by Baxter in Petaling Jaya, Malaysia. Leverage 6+ years of medical device regulatory expertise to shape regional strategies for Class II+ devices. Drive new registrations, renewals, and post-market compliance while navigating evolving regulations. Enjoy...

Join Baxter’s Quality team in Thetford, UK, as a Quality Assurance Associate and directly impact patient safety. You’ll ensure cGMP compliance, lead documentation reviews, and manage CAPAs in a regulated manufacturing environment. Ideal for detail-oriented professionals with GMP experience, stron...

As a Training Quality Manager at Baxter in Round Lake, IL, you will lead the strategy for cGMP-compliant training programs that directly impact patient safety. This role blends quality expertise with leadership, requiring 5+ years in a regulated environment and supervisory experience. You will ov...

Senior Section Lead, Market Complaint role in Ahmedabad, India, driving patient safety through quality compliance. You will oversee market complaint investigations, Field Actions, and regulatory notifications, ensuring adherence to global QMS standards. Ideal for a detail-oriented, collaborative ...

Baxter seeks a detail-oriented **Analyst, Tenders** in **Ciudad de México** to drive bid management for Mexico and Central America. Leverage your 2+ years of **tender experience** and knowledge of **government procurement portals** to identify opportunities, prepare offers, and manage critical do...

Seeking a **Specialist, Business Intelligence** in **Ciudad de México** to turn complex data into strategic insights. You will build **Power BI** and **Tableau dashboards**, perform predictive analytics, and automate reports for sales and finance. Requires 2-4+ years in BI, **SQL/Python** skills,...