R&D Test Engineer

• Support hardware testing activities to develop and commercialize complex instrumentation in the medication safety space
• Support engineering studies and Design Verification activities for the Intelliport products including disposable sensors and several reusable electro-mechanical devices
• Contribute to the improvement of testing methods, measurement system development & analysis of test methods, the improvement of fixtures, data processing and analysis
• Ensure that our products meet our customer’s expectations and regulatory requirements.

• Experience testing medical device product for Design Verification
• Knowledge on testing hardware by following test protocols
• Post-educational experience in Medical Device Design
• Design for Six Sigma, Design for Manufacturability and Reliability training / experience
• Graduate degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering or Applied Physics
• CAD modeling such as Solidworks or ProE
• Excellent written & verbal communication skills
• Self-directed with the ability to learn and adapt quickly to new technologies and trends
• Strong organization and coordination skills
• Ability to work independently after appropriate direction
• Careful, deliberate, disciplined, meticulous, and well organized in performing laboratory tests and recording results
• Ability to read and follow Standard Operation Procedures, Good laboratories Practices, Good Documentation Practices knowledge
• Bachelor’s degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering, Applied Physics or similar
• Proficient in reading and understanding assembly drawings, manufacturing and test instructions, and service manuals.

Knowledge of disciplined product development processes, regulatory, quality requirements and design controls, such as 21 CFR 820.30