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Strong employer brand, metro location, and product-owner visibility create moderate applicant competition.
Role requires regulated medical-device and safety-critical experience, making cross-industry transferability low.
Explicit senior experience bands and regulatory/safety-critical domain requirements make shortlisting highly strict.
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Lead end-to-end requirement engineering and backlog management for software products in regulated medical and vision care domains.
Drive product vision alignment, user experience design validation, and ensure delivery of scalable, secure, and regulatory-compliant solutions using Agile practices.
Manage stakeholder communication globally to maintain audit-ready documentation, compliance traceability, and incorporate AI-driven innovation opportunities.
10–12 years of software development/product engineering experience; minimum 3–5 years as Product Owner/Business Analyst/Technical Product Owner.
Bachelor’s or master’s degree in computer science engineering or related field.
Hands-on experience with Agile methodologies (Scrum, SAFe) and regulatory compliance standards such as IEC 62304, ISO 13485.
Experience in regulated or safety-critical medical device environments.
Experienced in managing complex product backlogs and requirement specifications in regulated healthcare or medical device software domains.
Able to bridge technical teams and global non-technical stakeholders, ensuring clear communication and alignment in Agile development environments.
Competent in integrating AI/ML capabilities into product roadmaps and leveraging data-driven decision-making to enhance product innovation and compliance.