About this role
Job Requirements
Key Responsibilities
• Own and prioritize requirements across the lifecycle (definition to decommissioning)
• Define platform requirements for native, on-prem, and cloud deployments
• Drive backlog prioritization based on value, risk, and dependencies
• Provide clear direction, context, and priorities to development teams
• Collaborate with internal and external stakeholders as the primary interface between business and engineering
• Ensure regulatory compliance, quality, and safety in product requirements
Focus Areas
• Healthcare domain knowledge and customer understanding
• Clinical workflows and Healthcare IT (Serviceability focus)
• Standards: DICOM, IHE
• Medical device software systems
• Regulatory basics: FDA 21 CFR 820, ISO 13485
• Agile methodology
• Data-driven decision-making and KPI tracking
• (Nice) Platform scalability, hybrid cloud, Kubernetes
Key Tasks
• Gather, prioritize, and communicate market, stakeholder, and system requirements
• Own backlog, define acceptance criteria, and ensure testability
• Guide teams, resolve conflicts, and enable execution clarity
• Manage Agile practices for requirements and product definition
• Use metrics and customer feedback to drive prioritization and releases
• Support rollout activities (training, presentations, workshops)
• Align feature development with platform strategy and reuse principles
Qualifications & Experience
• Bachelor’s/Master’s in Engineering, MCA, or equivalent
• 12–15 years experience
Skills & Background
• Strong ownership, accountability, and decision-making ability
• Self-driven with strong problem-solving skills
• Clear written and verbal communication
• Experience in software development and Agile methodologies
• Expertise in requirements engineering, product lifecycle management, and regulated environments
• Continuous learning mindset
Work Experience
Focus Areas
• Healthcare domain knowledge and customer understanding
• Clinical workflows and Healthcare IT (Serviceability focus)
• Standards: DICOM, IHE
• Medical device software systems
• Regulatory basics: FDA 21 CFR 820, ISO 13485
• Agile methodology
• Data-driven decision-making and KPI tracking
• (Nice) Platform scalability, hybrid cloud, Kubernetes