System Verification engineer

Job Description

Systems Verification Engineer (5-10 Yrs of exp.) Qualifications Create clear product design documentation such as concept diagrams, specifications, requirements, test plans, and V&V reports perform test/verification for NPI or sustaining of innovative electromechanical products Establish and maintain traceability between requirements, and testing Develop test protocols for the purposes of design verification and validation Execute testing and generate associated reports Oversee the building and testing of prototypes, including internal team and external vendor management Performs hands-on system testing and troubleshooting of technical issues Design benchtop tests, fixtures, and regression test plans to prove out concepts, functionality, and safety Required Qualification Bachelors degree in electrical, Computer, Biotechnology, Systems Engineering, or other related field. 5+ years experience in electromechanical device and system design/verification for new product development Direct hands-on systems engineering experience, preferably with medical device electronic systems or other complex electronic hardware. Technical competencies: Experience developing software driven electromechanical devices in a regulated environment. Broad engineering expertise across all engineering disciplines. Direct experience in requirements authoring, decomposition, analysis, traceability, and verification. Direct experience with complex electronics systems/component design. Experience in writing detailed product Verification/qualification plans and reports. Preferred Qualifications Familiarity with all phases of the product development lifecycle. Familiarity with HW / Embedded SW development, integration, and verification Familiarity with scripting and data analysis experience using Python, MATLAB, or equivalent programming languages. Experience working with 3D design tool, Creo , Solid works , Fusion 3Detc. Experience with low fidelity prototyping 3d Printing, PCB design, PCB reworks etc. Experience in the medical device industry, ISO 13845 , FDA quality management system Enjoy working effectively as part of a small, fast-paced, cross-functional, cross-cultural integrated team.