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Leads complex cross-functional sustaining engineering and product lifecycle projects for commercially released medical devices. Manages scope, schedules, resources, risks, dependencies, design changes, supplier qualification, manufacturing transfers, cost reductions, quality improvements, and supply continuity initiatives. Coordinates Engineering, Quality, Regulatory, Manufacturing, Operations, Supply Chain, and Product Management stakeholders. Ensures execution complies with quality systems, Design Controls, change control procedures, and regulatory standards while providing executive reporting and driving resolution of competing priorities.

Designs and maintains scalable automated test frameworks for distributed microservices, hybrid cloud environments, physical and embedded devices, and protocol integrations. Develops simulators, reusable libraries, CI/CD test automation, reporting, and hardware-in-the-loop solutions. Performs system, integration, regression, performance, reliability, and verification testing while maintaining traceability. Collaborates with software, hardware, systems, and quality teams, contributes to test strategy, improves product observability, reviews code, and mentors engineers.

Supports accounting and financial reporting through journal entries, account reconciliations, accruals, close activities, variance analysis, audit support, and financial reporting. Investigates discrepancies, maintains internal controls and SOX compliance, collaborates with cross-functional teams, and assists with process improvements and special projects.

Leads Masimo’s US Field Implementations organization, overseeing clinical specialists, automation engineers, project delivery, hospital technology deployments, and implementation partners. Owns end-to-end execution from contract signing through go-live, including KPIs, quality, cost, resource planning, and time to revenue. Aligns implementation activities with Sales, manages third-party surge capacity, and applies Danaher Business System practices to improve operational performance. Develops distributed teams, manages budgets and talent, and ensures compliance across regulated healthcare environments.

Develops and maintains scalable automated test frameworks for distributed systems, devices, microservices, and hybrid cloud environments. Builds reusable test libraries, hardware-in-the-loop simulators, protocol integrations, and automated testing for system, integration, regression, performance, and reliability validation. Integrates testing into CI/CD pipelines, analyzes results, maintains test environments, produces verification records, and collaborates with software, hardware, systems, test, and quality engineering teams to improve product testability and compliance.

Develops, validates, optimizes, and continuously improves manufacturing processes, equipment, tooling, and fixtures for medical devices. Supports new product introduction, scale-up, production readiness, process capability, quality, and manufacturability. Investigates process issues through root cause analysis, implements corrective actions, applies statistical controls, and identifies yield, cycle-time, scrap, and cost improvements. Creates manufacturing documentation and collaborates with Manufacturing, Quality, Regulatory, Supply Chain, and design teams. This is a full-time onsite role in Irvine, California, with up to 20% travel.

Supports the development, validation, optimization, and continuous improvement of manufacturing processes and equipment for medical products. Responsibilities include new product introduction, process scale-up, equipment qualification, manufacturing documentation, statistical process control, root cause analysis, corrective actions, automation, and cost reduction. The role collaborates with Manufacturing, Quality, Regulatory, Supply Chain, and engineering teams while independently managing moderately complex assignments in a regulated manufacturing environment.

Leads the design, development, validation, and optimization of biomedical signal-processing algorithms for noninvasive medical monitoring technologies. Applies statistical analysis, numerical modeling, optimization, and software development to clinical and engineering datasets. Supports embedded implementation, regulatory requirements, design controls, and commercialization. Collaborates with hardware, software, systems, clinical, quality, regulatory, and product teams while providing technical leadership, mentoring junior engineers, and contributing to innovation, documentation, and intellectual property.

Develop hospital and private healthcare accounts, drive sales of patient monitoring technologies, manage the full sales cycle, conduct product demonstrations and clinical evaluations, provide customer training, support implementations, and build relationships with clinicians and decision-makers. The role also includes account planning, forecasting, clinical research support, event representation, competitor monitoring, and regular territory travel.

The Sr Business Systems Analyst will support Oracle E-Business Suite projects for Finance, working with users to identify requirements, implement solutions, and improve processes.