Product Owner (Serviceability, Product deployment)

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, clear 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

Work arrangement
No