Location: Bengaluru
Company: Fluke Health Solutions
We are seeking an experienced Systems Verification Engineer with 5–10 years of hands-on experience in electromechanical systems development and verification. The ideal candidate will contribute to sustaining engineering efforts, ensuring the delivery of robust, high-quality 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 system-level 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 hands-on testing and troubleshooting of system-level technical issues.
- Design benchtop experiments, test fixtures, and regression testing to validate functionality, safety, and performance.
Required Qualifications
- Bachelor’s 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.
- Hands-on 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 fast-paced 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 low-fidelity 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 cross-functional, cross-cultural, and agile teams.