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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