
Staff Verification Engineer (Andover, MA)
- Andover, MA
- Permanent
- Full-time
- Medical device industry, where one of the following is applied: Food & Drug Administration (FDA), Good Manufacturing Practice, FDA 21 Code Federal Regulation (CFR) Part 820, or
- Test revision control management solution experience such as: Jama, Cockpit, Azure DevOps or Helix/TestTrack.
- Identify, troubleshoot, and validate fixes for hardware or software failures.
- Drive or support requirements creation and review for systems design inputs and sub-system requirements.
- Test Development involving test planning, authoring, executing, and reporting.
- Python Test Development.
- MATLAB or LabVIEW test development or data analysis.
- Visual Studio Development or Test Automation.
- Software Code Analysis and unit test tools (LDRA, SonarQube, VectorCast, Ceedling, or similar).
- Requirement and Test Management tools (Helix, DevOps, DOORS, or similar).
- Bugs tracking tools (JIRA, Bugzilla, or similar).
- Digital circuits, microprocessor hardware, and software (work experience or graduate-level educational course work acceptable).
- Test experience with at least one of the interface communications buses: CAN (Controller Area Network), RS232 (Recommended 232), USB (Universal Serial Bus), I2C (Inter-integrated
- Failure Mode & Effects Analysis for medical device systems and sub-components.
- EMC Test Plan and Test Setup Development.