Product Owner (DICOM, Medical Devices)

Siemens Healthineers AG

Bengaluru

On-site

INR 4,000,000 - 6,500,000

Full time

3 days ago
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Job summary

Siemens Healthineers AG in Bengaluru, India, is seeking an experienced Senior Product Owner/Manager to lead requirements engineering for healthcare platform products. You will own backlog, define acceptance criteria, and align features with platform strategy across native, on-prem, and cloud deployments.

You'll collaborate with business and engineering stakeholders, ensure regulatory compliance, and drive data-driven decision making, KPI tracking, and agile delivery in a highly regulated medical

Qualifications

  • Bachelor’s/Master’s in Engineering, MCA, or equivalent.
  • 12–15 years experience in product or requirements roles.
  • Experience in software development and Agile environments.
  • Regulated healthcare industry exposure is a plus.

Responsibilities

  • 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 and align features with platform strategy.

Skills

Ownership
Agile methods
Requirements engineering
Stakeholder management
Communication

Education

Bachelor’s/Master’s in Engineering
MCA or equivalent

Job description

  • 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
Job Requirements
  • 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
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