Job Requirements Job Description: Key Responsibilities: • Own, manage and prioritize requirements in the product life cycle from definition to phase-out. • Define requirements for native, on-premises, and cloud deployments. • Provide clear direction, context, and priorities to development teams. • Collaborate closely with key internal stakeholders and engage with external stakeholders. Focus Areas: • Must - Basic understanding of DICOM, IHE, Legal regulations and standards applicable for medical devices, affecting safety aspects (i.e.
FDA 21CFR820QSR, ISO 13485) • Must - Knowhow of Containers, Kubernetes, Dockers and other Containerization technologies. • Must - Knowledge on serviceability, Infrastructure, and product deployment technologies. • Must - Good programming skills & should have worked for a majority of time in software programming roles. • Must - Agile Methodologies, Product Lifecycle Management & Software development cycle experience for Medical Devices • Must- Experience in Requirements Engineering, Usability Engineering and feature definition activities. Nice to have - knowledge of Clinical workflows What are my tasks? • Gather, prioritize, create & communicate stakeholder and market requirements & S/W specifications • Guide and support development teams,



resolving conflicts and answering questions • Manage all the Agile methodology practices related to requirements engineering and product definition • Provide input to project management and support rollout activities such as training, presentations, and workshops What do I need to know to qualify for this job? Qualification: A Bachelors / Masters degree in engineering and / or MCA or equivalent. Work Experience: 12 to 15 years Desired Knowledge & Experience: • Self-driven & problem-solving behavior, explicit written and spoken communication skills. • Willingness to constantly learn & un-learn to improve self. • A strong background in software development, ideally with hands-on programming experience and agile methodologies is required. • The role demands experience in requirements engineering, product lifecycle management, and IT integration in regulated environments. Work Experience • Must - Basic understanding of DICOM, IHE, Legal regulations and standards applicable for medical devices, affecting safety aspects (i.e.
FDA 21CFR820QSR, ISO 13485) • Must - Knowhow of Containers, Kubernetes, Dockers and other Containerization technologies. • Must - Knowledge on serviceability, Infrastructure, and product deployment technologies. • Must - Good programming skills & should have worked for a majority of time in software programming roles. • Must - Agile Methodologies, Product Lifecycle Management & Software development cycle experience for Medical Devices • Must- Experience in Requirements Engineering, Usability Engineering and feature definition activities. Nice to have - knowledge of Clinical workflows

📌 Product Owner (Serviceability, Product deployment) (India)
🏢 Siemens Healthineers
📍 India