We are seeking a dedicated Software Test Engineer to join our dynamic team. In this role, you will analyze and review product specifications to ensure testability, develop and document test protocols for both manual and automated test cases, and collaborate closely with developers to verify intended functionality and identify any deviations. Your responsibilities will also include executing formal verification test runs on configuration-controlled systems, interpreting test results, and documenting encountered defects. This role requires effective coordination with fellow testers and developers to streamline testing efforts and resolve issues promptly. Key Responsibilities: Analyze and review product specifications to ensure testability. Develop and document test protocols for manual and automated test cases. Perform test case dry runs and collaborate with developers to clarify intended functionality. Execute formal verification test runs on configuration-controlled systems. Interpret test results and document encountered defects. Collaborate closely with other testers and developers to coordinate testing efforts and resolve issues. Perform other duties as assigned. Minimum Requirements: Bachelor’s degree or its foreign equivalent in Software Engineering, Computer Science, or a related field, plus 8 years of experience as a software engineer, test engineer, or in a related occupation. 5 years of experience in software testing. 2 years of experience testing FDA Class II or Class III medical device software. 2 years of experience testing PET imaging systems and PET emission sources. 2 years of experience working with diagnostic images. 2 years of experience working with Linux (Ubuntu) or equivalent Unix variant. 2 years of experience writing and executing automated test scripts. 2 years of experience with requirements-based testing. 2 years of experience using ALM tools for managing requirements, test, and issue tracking (e.g., HP/ALM, Helix, Rational, etc.). 2 years of experience writing technical documentation for medical device design history files compliant with FDA 21 CFR Part 820. Note: This position offers remote and telecommuting flexibility, with a requirement for in-office presence at least 3 days per week.

Employment Type: Full-Time

Salary: $168000.00 Per Year

Education Level: No formal educational credential