Analyst, Information Technology

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.  Your Role at Baxter: As a member of the Global IT Function, you as Business Analyst plays a critical role in identifying, designing, and delivering technology solutions that optimize business processes across Medical, Quality, Regulatory, Supply Chain functions within a medical device organization. This role bridges business strategy, data science and technology execution, ensuring technology initiatives are compliant, scalable and aligned with the company’s digital transformation roadmap and regulatory requirements Food and Drug Administration (FDA), ISO 13485, Good "X" Practice (GxP).  This individual partners closely with cross‑functional teams to translate complex business problems into a configurable solution, define data and process requirements, support solution development, manage validation needs and measure impact. What You'll Be Doing Partner with business leaders to identify high‑value improvement opportunities in areas such as regulatory affairs, patient safety, process optimization, product quality, complaint analytics and regulatory intelligence. Conduct feasibility assessments and prioritization of user stories. Stay current on emerging regulatory developments and industry best practices within regulated healthcare environments. Lead detailed discovery sessions to understand business workflows, data sources, constraints and pain points. Translate business needs into clear functional requirements for technical and vendor partners. Map current‑state and future‑state processes to identify automation and optimization opportunities. Review and analyze user requirements prior to submission and implementation; participate in validation activities as required. Ensure solutions comply with company Quality Management Systems (QMS) requirements, Good Automated Manufacturing Practice (GAMP 5), 21 Code of Federal Regulations (CFR) Part 11 regulations. Support the creation, review, and execution of validation deliverables, including Validation Plans, Risk Assessments, Risk Management Reports, Traceability Matrices, Validation Reports, User Acceptance Testing (UAT), and Regression Testing activities.