Software Development Engineer In Test Ii - Medical Devices

Job Description
Responsibilities:
Design, implement, and deliver reliable, high quality, robust automation software and/or software tools targeted for testing complex medical instruments to meet regulatory standards
Create, maintain and review testing project documents including tool development plans and software tool validation plans
Drive software tool requirements with other members of the software quality engineering team as appropriate
Participate in the investigation and resolution of software defects.
Utilize software engineering best practices (e.G., unit testing, integration testing, static analysis, code reviews)
Work cooperatively within the software quality and software group to deliver projects on-time and on budget.
Description:
Develop software test suites, implement automated test cases with a focus on functionality, performance, code coverage and regression testing;
report software problems, verify fixes and review user documentation.
Test software products for stability, usability, precision, accuracy, and reliability. Formulate and maintain test strategies;
creating test plans andtest cases for regression and functional testing of software products.
Develop a understanding of the companies’ Quality Management Systems (QMS) policies and regulations, and apply them appropriately to all aspects of your assignments.
You will be required to participate in testing software products for stability, usability, precision, accuracy, and reliability. Create test cases for regression and functional testing of software tools.
Work directly with project team members, including software engineers, during key points along the software development process. Use the principals of the software development life cycle throughout the entire SQE process.
Participate in product meetings throughout the development process to assist with the delivery of a quality software product.
Use project planning and monitoring methods to confirm timely project completion.
Report problems via the defect tracking system to analyze, research, and track software defects through their resolution. Verify code fixes and sign off on resolutions.
Analyze test results and prepare SQE summary reports.
Ensure adherence to regulatory standards, including FDA guidelines, and IEC 62304, and KMC Quality Procedures throughout the software development lifecycle.