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Systems Verification Engineer II
Ref No.: 18-11194
Location: San Jose, California
Position Type:Non-IT
Start Date / End Date: 08/13/2018 to 08/12/2019
Our client, a leading fortune company is looking for Systems Verification Engineer II. This is for an initial duration 12 months contract position in San Jose, CA.


The Systems Verification Engineer II will work closely with systems engineers and the product development team to enable the successful application and integration of hardware, reagents, and software in client flow cytometry products, with emphasis on assessing the suitability of design architectures and features to meet the needs of the customer. He/She applies engineering, statistics, and scientific theory to measure and quantify performance of client cell analysis products. 

Required Skills:
  • For this position Flow cytometry experience is highly preferred but the other qualifications are a plus as well. 
  • Requires a minimum of a Bachelor’s Degree in an engineering, technology, or science field with a minimum of 2 years relevant experience or a combination of equivalent education and experience. 
  • Typically requires a 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, to include lasers, optics, fluidics, electro-mechanical devices, software, algorithms, biological samples, and biochemistry. 
  • Apply systematic troubleshooting and debugging skills, practice in “systems thinking” problem solving approaches 
  • Ability to prepare and process biological samples in a wet-lab Biosafety Level 2 Laboratory 
  • Ability to understand the broader impact of design features, testing methods, and test results to the user, customer, regulator, and to the marketability of the product. 
  • Proficient in data extraction, manipulation, and interpretation 
  • (Preferred) 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 
  • 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
Qualified candidates please respond with updated word doc resume to Krishna Ramanuja at . Thanks!