Verification & Validation Engineer II

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 As we thrive together QuidelOrtho is seeking a Verification and Validation Engineer II to help with formal verification and validation of complex medical devices under the regulations of the FDA. The individual will be part of an engineering team that is responsible for requirements-based test design and execution of test procedures in a BL2 lab environment. The team is highly collaborative and will require regular interactions in formal reviews, test planning activities, and working with software development to reproduce and verify system defects. This position is onsite full-time in Rochester, NY. The Responsibilities Develop Requirements based manual test procedures using HP ALM Quality Center Execute test procedures both in a virtual and lab environment Compile and analyze test results Access requirements for testability and determine best test approach Document and manage system software defects Participate in regular scheduling and team meetings Document and manage Test plans, Tracing and Reports Perform other work-related duties as assigned. The Individual Required: This position is not currently eligible for visa sponsorship. B.S. Degree in Computer Science, Chemistry, Biochemistry, Biology, Engineering, or a related discipline 3-5 years' experience working within a FDA regulated environment supporting software development or quality control Critical thinking, effective communication and strong documentationpractices Ability to travel up to 10% (domestically)Preferred: Agile methodology, Jira, HP ALM Quality Center, Virtual Box, VMware and Unix experience The Key Working RelationshipsInternal Partners: Cross functionally with Software Development, Integration, Project Management and Design QualityExternal Partners: Software Development partners Software Development partners The Work EnvironmentThe work environment characteristics are representative of a manufacturing, laboratory, or warehouse environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues, and samples. Duties will change between lab environment and office. Flexible work hours to meet project deadlines Physical Demands No strenuous physical activity, though occasional light lifting of files and related materials is required. Salary TransparencyThe 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 equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $70,000 to $85,000 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) pla

Created: 2026-05-02