I begin by understanding the context before proposing solutions.
This includes the product domain, users, constraints, and existing systems.
In complex or regulated environments, early clarity reduces downstream risk.
This phase typically includes:
Insights are translated into a clear experience structure that aligns user needs with business and technical realities.
Rather than expanding scope, this phase focuses on making complexity manageable and defining what truly matters.
This phase typically includes:
Design decisions are made with real-world implementation constraints in mind from the start.
With a front-end background, I prioritize clarity, scalability, and handoff readiness—reducing friction between design and engineering.
This phase typically includes:
Rather than treating delivery as an endpoint, I focus on early validation and refinement.
This helps ensure that designs hold up under real usage conditions and do not introduce unnecessary usability or implementation risk.
This phase typically includes:
I typically work closely with product, design, and engineering partners.
My role often sits at the intersection of design and implementation—helping teams align early and avoid costly rework later.
While I bring human-factors awareness and healthcare experience, I do not replace regulatory consultants or provide formal FDA/ISO documentation.
If a project continues beyond initial delivery, I support refinement through design iteration, clarification, and system-level adjustments—based on new information or feedback.
This ensures that products evolve without losing structural clarity or usability.
