Jobs at Cala Health

Own end-to-end UI/UX design for Cala’s web, mobile, and connected-device experiences. Create user flows, wireframes, high-fidelity interfaces, dashboards, design systems, documentation, and engineering handoffs. Conduct user research and usability testing, lead design reviews, ensure accessibility, and support regulated medical-device development. Collaborate with Product, Engineering, and QA while scaling Cala’s visual and interaction language across platforms.

Owns firmware for clinical studies, including development, testing, documentation, release management, logging, and field support. Builds rapid prototypes for sensing, stimulation, and algorithm concepts; performs hardware and firmware debugging; supports clinical teams; and transfers research technology to commercial development. The role also requires AI-assisted development, collaboration across engineering and clinical teams, and adaptability in a small R&D environment.

Own inventory accounting, COGS, standard costing, margin analysis, month-end close, reserves, accruals, inventory controls, audit compliance, and manufacturing variance analysis. Partner with Operations, Engineering, and R&D on cost reduction and new product introduction modeling. Serve as the inventory ERP subject matter expert, improving workflows, data accuracy, and financial controls across warehouses and contract manufacturers.

Own the medical device complaint lifecycle by triaging and logging complaints in Arena, investigating returned devices, identifying failure modes and root causes, analyzing complaint and return trends with SQL and Python, preparing management reports, following QMS and FDA requirements, improving processes, and closing cases accurately and on time.

Lead development and execution of commercial marketing strategies for medical-device adoption and revenue growth. Manage GTM, launches, integrated channels, KOL engagement, cross-functional alignment, and a high-performing team while tracking KPIs.

Lead hardware and firmware product lifecycle for FDA-regulated medical devices. Define requirements, drive roadmap and launches, ensure Design Controls and HFE compliance, gather user insights, and manage sustaining activities across cross-functional teams.