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Designs, develops, tests, and maintains embedded software for medical monitoring products using C and C++. Responsibilities include microcontroller and hardware-interface development, bare-metal and RTOS applications, software architecture, debugging, performance optimization, documentation, risk analysis, code reviews, and regulated-product traceability. The role collaborates with multidisciplinary teams and mentors junior engineers. Preferred work includes embedded CI/CD pipelines, medical-device software, early-stage hardware prototyping, and Python-based testing or automation tools.

Develop and maintain full-stack cloud services integrating with medical products. Design enterprise microservices and distributed systems, implement APIs and AWS services, conduct code reviews, develop software, and support testing, deployment, and monitoring. Collaborate across the full product lifecycle while following regulatory, architectural, Agile, DevOps, and CI/CD practices.

Leads full-stack development of cloud services integrating with medical products. Designs, codes, reviews, tests, deploys, and supports enterprise-scale software using AWS, microservices, APIs, databases, containers, and modern development frameworks. Evaluates cloud technologies, defines system requirements, documents solutions for regulatory and business needs, applies Agile practices, and coordinates work across product development stages.

Lead application and product security for mobile apps, Software as a Medical Device, APIs, and cloud-connected healthcare software. Responsibilities include threat modeling, architecture reviews, security risk assessments, vulnerability remediation, security testing analysis, regulatory documentation, incident response support, and secure development process improvement. The role partners with engineering, quality, regulatory, and clinical teams to embed risk-based security throughout the product lifecycle.

Provides technical leadership for architecture, design, development, debugging, integration, and lifecycle management of embedded software for implantable and external neuromodulation products. Leads technical decisions, evaluates RTOS, hardware, security, and communication approaches, mentors distributed teams, resolves complex system issues, ensures IEC 62304 and IEC 60601-1 compliance, and advances Agile, DevOps, continuous integration, and automated testing practices.

Leads and develops a mechanical engineering team delivering medical and electromechanical products from concept through design transfer, production, and post-market improvement. Directs new product development and sustaining engineering, provides technical leadership, ensures compliance with design controls and quality systems, and manages investigations, corrective actions, resources, suppliers, and cross-functional collaboration in a regulated global environment.

Manage and resolve pricing, invoicing, and delivery disputes; prepare settlement documentation; produce KPI and compliance reports; improve dispute processes; liaise with national and regional contacts.

Analyzes global service and repair processes, system issues, and master data to identify root causes and implement sustainable improvements. Supports issue resolution, data governance, system enhancements, UAT, business requirements documentation, process documentation, and continuous improvement initiatives. Partners with IT, operations, supply chain, finance, and master data teams to improve efficiency, data quality, consistency, and service performance.

Leads mechanical design, analysis, documentation, and sustaining engineering for medical devices. Owns product development projects from concept through release, conducts design reviews, creates drawings, supports change management and risk assessments, and ensures compliance with quality, regulatory, manufacturing, and design-control requirements. Provides technical leadership, mentoring, and cross-functional collaboration across global engineering teams.

Support medical device product design, development, optimization, sustaining engineering, and release activities. Create component and assembly drawings using ASME guidelines, apply GD&T and tolerance stack-up analysis, and ensure designs meet safety, reliability, and manufacturability requirements. Collaborate with global cross-functional teams, vendors, manufacturers, clinicians, and other stakeholders while following design controls, PLM processes, and applicable medical device standards.