Top Tech Jobs & Startup Jobs

Lead quality, compliance, and product security governance for a healthcare design system. Own QMS documentation, Design History File strategy, traceability, audit readiness, release governance, secure development practices, threat modeling, vulnerability remediation, security evidence, SBOMs, penetration testing, and compliance metrics. Partner cross-functionally with Product, UX, Engineering, Architecture, Quality, Regulatory, and Security teams while driving process improvement and automation.

Leads systems engineering for mobile X-ray products, including requirements definition, architecture, trade studies, design verification and validation, risk management, defect management, regulatory compliance, and quality deliverables. Partners with customers, clinical experts, marketing, software, product, field, and subsystem teams to define digital and clinical application roadmaps. Supports post-production complaint analysis, risk assessments, continuous improvement, and design control milestones.

Develop and optimize tomographic image reconstruction software in C++ for medical imaging scanners. Responsibilities include algorithm implementation in parallel CPU/GPU environments, software architecture, subsystem interfaces, performance optimization, documentation, unit testing, verification and validation support, technical investigations, code reviews, and configuration management.

Develop and maintain application and systems software for ultrasound products. Implement features from design specifications, test and debug software, resolve defects and performance issues, support system integration, and collaborate with senior engineers and global teams. The role also involves following quality and regulatory processes, completing compliance training, and contributing to continuous improvement. New graduates may apply.

Coordinates customer and loaner ultrasound systems through the depot repair process. Responsibilities include reviewing purchase orders, maintaining CRM records, preparing customer communications and return labels, tracking loaners, monitoring inquiries, checking in systems, and ensuring repair queue readiness. The role requires strong organization, communication, customer service, and computer skills, with logistics, asset recovery, medical equipment, CRM, and asset management experience preferred.

Leads architecture, design, implementation, verification, and lifecycle support for mixed-signal hardware used in MR imaging systems. Designs processor- and FPGA-based circuit boards, performs schematic capture, board bring-up, debugging, simulation, laboratory characterization, and system integration. Reviews signal and power integrity, EMC, reliability, and manufacturability. Develops reusable standards, evaluates technologies, influences platform roadmaps, and mentors engineers across multidisciplinary programs.

Leads strategic enterprise relationships with major healthcare customers, developing multi-year account strategies, engaging C-suite stakeholders, coordinating cross-functional GE HealthCare teams, shaping complex enterprise opportunities, and driving funnel health, win rates, pricing discipline, issue resolution, and customer outcomes across equipment, service, and digital portfolios.

Manages sales within a defined territory and named accounts, maintaining customer relationships and serving as the interface between customers and GE. Executes standard sales activities, expands territory and product knowledge, explains technical information, coordinates with internal teams, and resolves commercial issues within established procedures. The role requires communication, planning, marketing, program execution, and judgment within a defined framework.

Analyzes, develops, validates, and improves manufacturing processes for medical ultrasound transducers. Conducts experiments, equipment qualifications, process validations, capability analyses, and troubleshooting. Collaborates with R&D, production, and quality teams; documents procedures and training materials; supports lean manufacturing and continuous improvement; and ensures FDA, safety, and environmental compliance.

Create, update, review, and release technical documentation for medical devices, including user manuals, instructions for use, and product data sheets. Collaborate with project managers, R&D, marketing, regulatory affairs, and subject-matter experts. Coordinate translation and localization, maintain documentation templates and standards, provide status updates, and improve documentation quality and efficiency while following regulatory and quality procedures.