Jobs at Baxter International Inc.

The Director leads Baxter's incentive compensation programs, partnering with various departments to ensure strategic alignment, operational excellence, and compliance in incentive plan execution.

The Senior Human Factors Engineer will analyze, design, and refine products and systems, ensuring compliance with regulations and enhancing safety and performance.

Own and grow territory revenue for HST OR capital equipment by managing key accounts, building relationships with KOLs and hospital stakeholders, driving proposals and pipeline in CRM, coordinating demos/installations with cross‑functional teams, ensuring compliance, and delivering market feedback and territory development.

Sell the Carnation Ambulatory Monitor (CAM) Patch to primary care offices in Northern New Jersey. Prospect, qualify, and close opportunities, support full sales cycle, schedule demos, use Salesforce for reporting, and collaborate with account executives, regional managers, and technical teams. Travel up to 20% and perform administrative tasks.

Investigate and analyze medical device complaints and service data, determine root causes and risk levels, identify trends and systemic issues, lead corrective and preventive actions (CAPA), ensure GMP compliance, and drive continuous improvement of quality systems for marketed products.

Sell the Carnation Ambulatory Monitor (CAM) Patch to primary care offices and clinics in the Greater Houston area. Manage full sales cycle including prospecting, lead qualification, forecasting, demo scheduling, and admin in Salesforce.com. Partner with account executives, regional managers, and technical teams to deliver solutions. Use sales analysis tools to track activity and grow revenue; travel up to 20%.

Lead design and deployment of production-grade ML and Agentic AI solutions for financial forecasting, variance analysis, and process optimization. Build forecasting and RAG/LLM pipelines, establish data governance, present insights to senior leadership, mentor team members, and partner with Finance/IT to drive measurable ROI.

Provide bilingual (English/French) technical support and troubleshooting for Baxter medical devices via phone and email; document incidents in approved systems; manage service part orders and returns; support field/service/sales with technical input; read schematics and travel within U.S. and Canada for training.

Support cross-functional teams on new product development and sustaining engineering projects in a regulated medical device environment. Maintain project plans, track milestones, risks, and actions; participate in Agile/Scrum ceremonies; support design change implementation, status reporting, and issue/change management to meet quality, cost, and schedule objectives.

Contribute to design and development of electro-mechanical medical devices from concept through verification/validation. Define and decompose requirements, perform risk management (ISO 14971), support usability engineering (IEC 62366), collaborate with software/hardware teams, and develop high-quality technical documentation and verification test plans to meet regulatory and business constraints.

Drive awareness, adoption and secondary sales for Hemostat and Adhesion Prevention portfolio across assigned territory. Plan and execute account-level activations, forecast sales, manage product supply, track complaints, map competition, train paramedical staff, and meet monthly revenue targets while collaborating with sales, marketing and corporate accounts.

The Associate Marketing Manager will develop market models, conduct competitive intelligence analysis, and collaborate with teams to provide insights that shape strategic decisions in the infusion therapies market.

Lead systems and electronics engineering for medical device products: define requirements, perform system design and verification, manage risk, produce technical documentation, use simulation and PCB tools, troubleshoot electromechanical systems, and support regulatory/quality practices to ensure safe, compliant products.

Perform accurate organization, scanning, labeling, and data entry of CAM and MCT products into systems, maintain records, handle disposal per policy, communicate errors and follow up, and provide occasional customer service.

Define customer needs and system requirements, manage requirements with DOORS/POLARION, perform risk management per EN ISO 14971, support usability per IEC 62366, collaborate with hardware/software teams, produce technical documentation, and support verification/validation and integration for electro-mechanical medical devices under FDA/MDR design controls.

Lead technical cost-out and supplier development projects to deliver material/component cost reductions, supply resilience, and margin improvement. Perform should-cost, clean-sheet, teardown analyses; drive specification changes, trials, validations, and cross-functional execution with Procurement, R&D, Quality, and Operations. Track initiatives end-to-end and ensure regulatory compliance and handover to operations.

Design and develop electro-mechanical medical devices ensuring compliance with regulatory codes and standards (IEC, ISO, FDA, MDR). Manage requirements (DOORS), carry out risk management (EN ISO 14971), lead integration and compliance testing, support notified body audits, create technical files (MDD/STED/MDR), and collaborate with QA/RA on global registrations and product certifications.

Lead systems and electronics engineering for medical device products: define requirements, perform system-level design and risk management, develop and verify electromechanical and embedded hardware, produce documentation and DFx/DFMEA outputs, collaborate with project teams, and ensure compliance with medical/device standards and quality processes.

The Technical Lead is responsible for identifying cost reduction opportunities, leading cross-functional teams in project execution, and collaborating with suppliers to achieve cost optimization while ensuring product performance and compliance.

As a Technical Lead, you will analyze and optimize costs, manage cross-functional projects, engage suppliers, and ensure regulatory compliance to deliver cost savings while maintaining product performance.