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Product Owner (DICOM, Medical Devices)
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Product Owner (DICOM, Medical Devices)
SiemensEarly Applicant
- Posted 15 hours ago
- Be among the first 10 applicants
Job Description
Job Requirements
Key Responsibilities
Focus Areas
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
- 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
- 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
- Bachelor's/Master's in Engineering, MCA, or equivalent
- 12–15 years experience
- 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
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
More Info
Key Skills
FDA 21 CFR 820
Data-driven decision-making
medical device software systems
KPI tracking
About Company
Skills:
supplier risk management , Iso 13485, Root Cause Analysis, Process Validation, Design Controls, Contract Manufacturing, Medical Devices, Supplier Quality Auditing, Regulatory Inspections, FDA Quality System Requirements, Capa, Supplier Qualification, SCAPA, EU IVDR, Cqa, EU MDR, Qms, cqe, Approved Supplier List, Quality Agreements, Pfmea, Supplier Quality Engineering, QTA
Skills:
value realization , Iso 13485, Digital Connected-Device Enablement, FDA 21 CFR, Design Thinking, operating model design, Agile Delivery, Regulatory Pathways, Product Development, Roadmap Development, Scaled Agile Frameworks, EU MDR, Quality Systems, Process Re-engineering, IVDR