Back
Metro location and common product title increase candidate density, but regulated medical-device requirement reduces competition.
Strong regulatory and medical-device experience requirement limits cross-industry transferability.
Explicit seniority and regulated medical-device experience requirements make shortlisting highly selective.
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Own end-to-end requirement engineering and backlog management ensuring clear, testable, and traceable requirements aligned with business, clinical, and regulatory needs.
Lead UX/product design validation and collaborate closely with UX/UI and development teams to deliver scalable, secure, user-centric solutions.
Manage stakeholder communication and Agile delivery practices, including risk management, regulatory compliance, and integration of AI-driven product features.
10–12 years in software development/product engineering, with minimum 3–5 years as Product Owner or equivalent role.
Bachelor’s or Master’s degree in computer science engineering or related field.
Hands-on experience with Agile methodologies (Scrum/SAFe) and strong requirement engineering and documentation skills.
Experience in regulated or safety-critical environments with knowledge of IEC 62304, ISO 13485, ISO 14971, FDA/MDR regulations.
Experienced in technical product ownership within regulated, safety-critical industries, preferably medical devices or digital health solutions.
Strong ability to translate complex and legacy system requirements into clear, actionable user stories and maintain traceability across artifacts.
Skilled in stakeholder management and cross-functional collaboration across global teams, driving alignment in Agile environments with focus on compliance and innovation.