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Baxter Logo Baxter · IT - Software Development

Principal Product Owner

India, Bengaluru · Job Posted June 09, 2026
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Job Description

This is where new knowledge is discovered. Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally. From Scientists to Engineers, your work creates the products that save and sustain lives.

Job Responsibility

  • Define and own the product vision and development strategy for the Digital Platform supporting multiple medical device categories and clinical workflows
  • Translate business, clinical, and device‑specific needs into a cohesive platform roadmap aligned with portfolio strategy
  • Drive platform evolution with a long‑term architectural view including compute layer strategy, connectivity, cybersecurity, interoperability, and data services
  • Serve as Product Owner within an Agile/Scrum team, ensuring a prioritized, clear, and well‑groomed backlog
  • Collaboratively develop feature definitions, user stories, acceptance criteria, and boundary conditions that enable scalable platform features
  • Partner closely with engineering, UX/UI, architecture teams, and test organizations to ensure successful feature delivery
  • Act as the customer proxy, managing stories for complex Software systems/modules ensuring delivery of quality & completeness with the scrum team
  • Ensures effective change management within the systems/modules
  • Is an integral part of the PI/Sprint planning process, prioritizes features & facilitates meeting the sprint objectives
  • Engage continuously with device R&D teams to extract platform needs across ECG, patient monitoring, respiratory therapy, ophthalmology, and BP monitoring domains
  • Align with portfolio management, marketing, and commercial teams to understand business use cases, service scenarios, data workflows, and customer value propositions
  • Facilitate cross‑team architecture discussions to ensure integration feasibility, requirements clarity, and platform reusability
  • Inculcate a deep understanding of customer/therapy needs, usability & clinical workflows, UX design and use these to effectively make design/architecture decisions related to the Software system
  • Apply Model-Based Systems Engineering (MBSE) methodologies to define system behavior, interfaces, constraints, and verification approaches
  • Lead structured system decomposition and requirements flow‑down across compute, connectivity, and application layers
  • Support the creation of robust architecture models and platform definition artefacts, ensuring consistency across product lines
  • Apply analytical skills to resolve complex issues by applying due diligence and structured problem solving techniques
  • Identify and manage technical risks across the platform lifecycle, including architecture, dependencies, cybersecurity, and interoperability risks
  • Collaborate with Quality & Regulatory teams to ensure platform features and documentation support compliance (e.g., IEC 62304, ISO 13485, IEC 60601, cybersecurity standards)

Requirements

  • Experience in Requirement analysis, flow down, risk assessment, system thinking
  • Develop or refine user/product requirements and work with developers for their implementation and testing
  • Demonstrated experience with MBSE, system modeling tools (e.g., SysML, Cameo, Rhapsody), and structured requirements management
  • Hands-on experience in the system and medical risk management activities for our products and ensuring the safety of the product for patients and caregivers
  • Resolve systems-related technical issues by applying problem-solving tools such as cause and effect diagrams, 5 Whys, Pareto charts, etc
  • Ability to generate alternative solutions to problems or processes
  • Simulate therapy algorithms using modeling & simulation software like Matlab/Simulink
  • Ability to apply engineering concepts to electro-mechanical systems with software, their functionality, connectivity, and usability aspects
  • Strong interpersonal skills with the ability to work collaboratively with others in a team environment
  • Previous exposure with Medical Devices, FDA Regulations or other applicable regulatory requirements
  • Working knowledge of UL/IEC 60601-1, ISO13485, ISO14971, IEC81001-5-1
  • Demonstrated experience in accomplishing objectives
  • Able to deliver on multiple projects simultaneously
  • Self-motivated with good interpersonal skills
  • Bachelor's or Master's degree in Computer Science, Electronics Engineering, Biomedical Engineering, or related technical field
  • 10+ years of experience in software development, systems engineering, or technical product ownership within medical devices or regulated healthcare technology
  • Strong understanding of embedded systems, cloud/digital architectures, connectivity (BLE, Wi-Fi, cloud sync), and medical device software frameworks
  • Experience working with multi‑device product ecosystems or digital health platforms
  • CE/UL certification is a plus

What we offer

  • Support for Parents
  • Continuing Education/ Professional Development
  • Employee Heath & Well-Being Benefits
  • Paid Time Off
  • 2 Days a Year to Volunteer
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