Staff Software Test Engineer, Embedded Systems

The Opportunity   QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role QuidelOrtho is seeking a Staff Software Test Engineer, Embedded Systems, to support our R&D Software Engineering team in testing and verifying new capabilities of next-generation diagnostic platforms and developing automated test suites. This includes leading the testing of end-to-end workflows that span instrument functionality, device configuration, cloud connectivity, and system interoperability. You will have the opportunity to own and design automation-ready tests, execute automated test suites, and support the ongoing maintenance and troubleshooting of instrument test automation. In parallel, the team is modernizing our instrument software to support domestic and international growth through modular architecture, enhanced instrument-to-cloud connectivity, improved cybersecurity, and scalable testing practices. This position will be hybrid in San Diego, CA (roughly 1 day-onsite). The Responsibilities Own the technical testing approach for instrument software systems, shaping test strategy, risk-based coverage, and execution across the development lifecycle, while partnering with engineering, quality, and regulatory teams to ensure robust, compliant verification. Author, execute, and verify test plans and test cases to cover documented requirements for instrument software. Design automation-ready test cases, collaborate with engineers implementing test scripts, execute automated tests, and help analyze and troubleshoot automated test frameworks. Lead and work hands-on with internal and third-party development teams, with direct responsibility for testing and ensuring quality for medical instrument software with cloud and connectivity integrations. Collaborate with Project Management as needed to ensure design control and testing documentation are properly managed in an FDA-regulated environment. Provide level-of-effort estimates, technical input, and risk identification to support planning and delivery commitments Perform other work-related duties as assigned Required Skills: Bachelor’s degree in a STEM field or equivalent experience 7+ years of software testing experience Experience with scripting languages such as Python Experience testing embedded software Experience testing in Linux-based environments Experience designing, implementing, and maintaining automated test systems with tools such as Squish, Robot Framework, etc. Planning, writing, and executing test plans and test cases Effective communicator with excellent organizational skills Experience working on a development team using Agile processes Experience estimating, planning, and sequencing software testing work Demonstrates commitment to the development, implementation, and effectiveness of the QuidelOrtho Quality Management System in accordance with ISO, FDA, and other applicable regulatory requirements Preferred Skills: Familiarity with regulated software development standards and practices (for example, IEC 62304, ISO 13485, and software design controls) Experience testing Qt and QML applications with Squish Experience with CI/CD tools for example, GitHub Actions Experience using AI-assisted software testing tools to improve engineering productivity and testing quality Internal Customers: 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 External Customers: Third-party software development partners Tooling, cybersecurity, and cloud service vendors External auditors and regulatory bodies, as applicable How We Work At QuidelOrtho, our culture is shaped by four core behaviors that guide how we collaborate, make decisions, and support each other and those we serve. The ideal candidate will exhibit these behaviors, as we believe they’re essential to how we thrive as a team and achieve meaningful impact: Thrive Together – Collaborate intentionally, grow as a team Make It Happen – Focus on priorities, embrace continuous improvement Commit to Service – Cultivate a service mindset Embrace Inclusion – Be open and authentic, welcome diverse perspectives The Work Environment No strenuous physical activity, though occasional light lifting of files and related materials is required. 30% of time in meetings, working with team, or talking on the phone, 70% of the time at the desk on computer, doing analytical work. Minimal travel required. Travel includes airplane, automobile travel and overnight hotel. Physical Demands No strenuous physical activity required. Occasional light lifting of materials may be needed. Substantial time will be spent in virtual or in-person meetings, engaging with customers, and working on scientific content and documentation. Salary Transparency The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal