DescriptionSystems Verification Engineer (510 Years Experience)
Role Overview:
We are seeking an experienced Systems Verification Engineer with 510 years of handson experience in electromechanical systems development and verification. The ideal candidate will contribute to sustaining engineering efforts ensuring the delivery of robust highquality products through rigorous design verification and validation practices.
Key Responsibilities:
- Create comprehensive design documentation including concept diagrams specifications requirements test plans and V&V (Verification & Validation) reports.
- Perform systemlevel verification and testing for both new and existing electromechanical products.
- Ensure complete traceability between requirements and test cases.
- Develop and execute test protocols to support design verification and validation efforts.
- Oversee the assembly and testing of prototypes collaborating with internal teams and managing external vendors as needed.
- Conduct handson testing and troubleshooting of systemlevel technical issues.
- Design benchtop experiments test fixtures and regression testing to validate functionality safety and performance.
Required Qualifications:
- Bachelors degree in Electrical Engineering Computer Engineering Systems Engineering Biotechnology or a related field.
- Minimum 5 years of experience in system design and verification of electromechanical devices.
- Direct experience with complex electronic systems preferably in regulated environments such as medical devices.
- Strong systems engineering background including requirements development decomposition traceability and verification.
- Proven experience with hardware verification planning and reporting.
- Handson experience in prototype development testing and issue resolution.
- Familiarity with change control processes.
- Excellent organizational and multitasking skills with the ability to manage diverse responsibilities in a fastpaced environment.
Preferred Qualifications:
- Understanding of the complete product development lifecycle.
- Experience with hardware and embedded software integration and verification.
- Proficiency in scripting and data analysis using Python MATLAB or similar tools.
- Knowledge of 3D CAD tools such as Creo SolidWorks or Fusion 360.
- Experience with lowfidelity prototyping methods (e.g. 3D printing PCB design and rework).
- Background in the medical device industry and knowledge of relevant standards such as ISO 13485 and FDA QMS.
- Effective team player comfortable in crossfunctional crosscultural and agile teams.