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Systems Verification Engineer II

United States, San Jose 48.00 - 52.00 USD / Hour · Job Posted January 11, 2026
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Job Description

Systems Verification Engineer II. This is a contract only position. At Client Biosciences, our purpose is to help all people live healthy lives. We are a world leader bringing innovative tools to research and clinical laboratories in basic research, drug discovery and development, biopharmaceutical production and disease management. We develop technology that enables faster diagnosis and better clinical outcomes. To ensure that our cell analysis products deliver outstanding performance and exceed our customers’ expectations, Client Biosciences is seeking a passionate and capable systems test engineer to contribute to a cross-disciplinary product development team, and to develop method improvements that drive greater efficiency and productivity of the Systems Verification and Validation team. The Systems Verification and Validation Engineer II is a hands-on testing and problem-solving role that will involve conducting experiments using flow cytometry.

Job Responsibility

  • Work closely with systems engineers and the product development team to enable the successful application and integration of hardware, reagents, and software in flow cytometry products
  • Assess the suitability of design architectures and features to meet the needs of the customer
  • Apply engineering, statistics, and scientific theory to measure and quantify performance of cell analysis products
  • Design, plan, and conduct experiments to assess the technical capability, feasibility, and performance of sub-systems and systems
  • Develop and execute formal protocols, analysis and interpretation of results, and communication of results and their impact to the project and the customer through written reports, design reviews, and interactive discussions
  • Identify and pursue opportunities to facilitate more reliable and efficient verification and verification testing, such as automated test fixtures, simulation and analysis capabilities

Requirements

  • Minimum Bachelor’s Degree in an engineering, technology, or science field
  • Minimum of 2 years relevant experience or a combination of equivalent education and experience
  • Minimum of 2 years experience in product development, instrumentation development, medical devices, test engineering, or other relevant industry experience
  • Demonstrated knowledge and application of fundamental engineering concepts
  • Ability to quickly grasp the functionality and interdependencies of complex multidisciplinary systems
  • Apply systematic troubleshooting and debugging skills
  • Strong interpersonal skills
  • Excellent written and oral communication skills
  • Ability to prepare and process biological samples in a wet-lab Biosafety Level 2 Laboratory
  • Ability to apply careful attention to detail
  • Ability to understand the broader impact of design features, testing methods, and test results
  • Ability to critically evaluate proposed study designs
  • Proficient in data extraction, manipulation, and interpretation
  • Experience in statistics, design of experiments, calculating sample sizes and estimating statistical power of study designs
  • Experience using MATLAB, SAS, JMP, R, MiniTab, or LabVIEW for scripting, data analysis, or automation
  • Flow cytometry experience is highly preferred
  • US Citizens Or GC Holders Only

Nice to have

  • Knowledge in systems engineering practices, experience in developing good requirements
  • Experience in product development process and design control
  • Experience working within a regulated medical device industry
  • Knowledge of immunology and/or experience in assay development or application
  • Experience in the cultivation, processing, or handling of cells
  • Experience working in a Biosafety Level 2 Laboratory
  • Knowledge of flow cytometry instrumentation and/or flow cytometry applications
  • Knowledge or experience in FDA submissions
  • Knowledge or experience interpreting CLSI guidelines

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