Prolaio Offices

Support production quality activities including supplier qualification, in-process and finished goods inspections and release, environmental monitoring, complaint investigations, and transfer of products/processes from Design to Production. Report quality metrics to management and support regulatory compliance (ISO 13485, CFR Part 820).

Own end-to-end product design for clinical cardiology products from discovery through production. Lead product vision and strategy, solve complex ambiguous problems, and deliver information architecture, high-fidelity mockups, and interactive prototypes. Collaborate with Product, Engineering, clinical, regulatory, and legal teams, run workshops, conduct user research, and provide clear design specifications for development handoff.

Design and govern Prolaio's regulated healthcare data platform: define architectures, models, pipelines, and lifecycle management for clinical, device, claims, and patient-generated data; apply healthcare terminologies and common data models; enable secure, interoperable, AI-ready datasets for analytics, research, clinical operations, and regulated workflows.