Position Overview
We are seeking a Test Engineer responsible for the preparation, execution, and reporting of Verification and Validation (V&V) testing for MRPC products. The role involves supporting both sustaining engineering activities and new product development projects.
Key Responsibilities
1. Verification & Validation Preparation
- Collaborate with cross-functional engineering teams to ensure system requirements are testable.
- Assist in identifying and coordinating internal and external testing capabilities.
- Develop test plans and test protocols to guide verification and validation activities.
- Support the design and creation of test fixtures and test setups.
- Ensure all test equipment is calibrated, prepared, and available for scheduled testing activities.
2. Test Execution
- Perform testing activities according to approved test protocols and project schedules.
- Execute verification and validation tests in line with the project test plan.
- Conduct real-time evaluation of test results and provide updates to project management.
- Document observations and findings during testing activities.
3. Test Reporting
- Capture test data and results and document key observations in formal reports.
- Prepare and maintain test documentation in accordance with project requirements.
- Coordinate with cross-functional teams to review and release final documentation.
Education & Experience
- Bachelor’s degree in Engineering, Technology, or a related technical discipline, or equivalent hands-on experience in testing engineering.
- 4+ years of experience in verification and validation or product testing.
Required Skills
- Strong communication and organizational skills.
- Experience in verification and validation testing within product development environments.
- Ability to collaborate with engineering teams to interpret requirements and define testing strategies.
- Adaptability to work in a fast-paced and evolving product development environment.
Preferred Skills
- Experience with medical device testing under IEC/ISO 60601-1 standards.
- Knowledge of patient monitoring systems, functions, and parameters.
- Understanding of MR-Safe, MR-Conditional, and MR-Unsafe labeling requirements.
- Experience with automated testing processes to improve test efficiency.
- Knowledge of test setup design and fixture development.
- Ability to disassemble and reassemble products to create production-equivalent test devices.
- Experience with test scheduling, scoping, and coordination to support project management planning.