QuidelOrtho
Staff Software Engineer
Rol remoto de Staff Software Engineer con fit claro de ubicación del candidato.
Publicado18 jun 2026
Países elegibles1 país aceptado
Señal de senioritySenior
Modelo de trabajoRemoto
Ubicaciones aceptadas para candidatos
Estados Unidos
Resumen del rol
Staff Software Engineer
Requisitos y responsabilidades
Contenido del rol extraído en secciones para revisar más rápido.
The Responsibilities
- Lead the design of software components and subsystems in alignment with system requirements and architecture
- Lead and influence computing and software architecture decisions across projects and cross-functional teams
- Develop and review code to implement new functionality, enhance existing capabilities, and uphold software quality standards
- Provide level-of-effort estimates, technical input, and risk identification to support planning and delivery commitments
- Gather and document software requirements and specifications
- Implement unit test to meet coverage goals
- Fix defects found during implementation process or reported by the software test team
- Lead complex system integration, debugging, and root-cause analysis across hardware, firmware, and software boundaries
- Drive software process definition and continuous improvement initiatives to improve quality, efficiency, and compliance
- Support and help coordinate release readiness activities, including technical review, defect resolution, and cross-functional alignment
- Perform other work-related duties as assigned.
Required:
- Bachelor’s degree or equivalent in Software Engineering or Computer Science or related field
- 10 years of related experience as a software engineer designing and supporting development of complex embedded systems
- Expert-level programming skills in C/C++
- Repository experience such as Git or SVN
- Experience developing in Linux-based environments
- Experience working on a development team using Agile processes
- Strong knowledge of object-oriented design principles and software design patterns
- Experience developing software for low-power systems across multiple processor architectures (e.g., x86, ARM)
- Experience debugging embedded code
- Able to take complex designs from concept to implementation with minimal supervision
- Experience estimating, planning, and sequencing software development work
- Experience eliciting, documenting, and reviewing software requirements and use cases
- Demonstrates commitment to the development, implementation, and effectiveness of the QuidelOrtho Quality Management System in accordance with ISO, FDA, and other applicable regulatory requirements
- Ability to travel 5% or less, domestically, if working remotely.
Preferred:
- 5 years of experience with software development for medical devices or another regulated industry
- Familiarity with regulated software development standards and practices (for example, IEC 62304, ISO 13485, and software design controls)
- Experience with Qt and QML
- Experience with CI/CD
- Experience with secure software development practices, dependency management, and product cybersecurity considerations
- Experience with Yocto
- Experience using AI-assisted software development tools to improve engineering productivity and code quality
- Experience using different inter-processor and application level communication technologies (I2C, SPI, CANBus, UART, RS485, USB, TCP/IP)
- Experience with VB6 and C#
Internal Partners:
- Systems and Hardware Engineering – system requirements and architectural alignment
- Verification & Validation – verification strategy, execution, and evidence
- Design Quality & Regulatory Affairs – compliance with FDA, ISO 13485, IEC 62304, and internal procedures
- Clinical, Operations, Manufacturing – downstream readiness and operational impact
- Business Unit – customer requirements and feature design
External Partners:
- Third-party software development partners
- Tooling, cybersecurity, and cloud service vendors
- External auditors and regulatory bodies, as applicable
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