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The Principal Mechanical Engineer will lead product development for infusion systems, create mechanical designs, perform thorough analysis, ensure compliance with safety standards, and oversee product transition to manufacturing, all aiming to enhance patient care.

As a Principal Systems Engineer at Baxter, you will lead the development of complex medical devices, ensuring they meet customer needs and regulatory standards. You will collaborate with cross-functional teams, manage system requirements, resolve interface issues, support risk analysis, and ensure compliance throughout the product lifecycle.

As a Quality Associate II, you will manage Quality System Records, conduct root cause investigations, identify and monitor process improvements, and provide training. You are responsible for overseeing the effectiveness of corrective actions and participating in audits to ensure compliance, all while maintaining a focus on quality and safety in products meant to enhance healthcare outcomes.