Arkansas Staffing
Senior Software Engineer
Arkansas Staffing - Sylmar, California, us, 91392
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Overview
Senior Software Engineer
St. Jude Medical, an Abbott Labs Co. / Sylmar, CA Understand product requirements and use cases, and work on verification applications for Cardiac Rhythm Management (CRM) remote care in the areas including, but not limited to, technical requirements development, identify test strategy, development of test design, test cases, test procedures and scripts, and test execution. Responsible for requirements analysis, development, and testing within Waterfall and Agile Software Development Life Cycle (SDLC) methodologies. Independently develop, debug, and maintain automated test procedures utilizing source code management using tools, including AccuRev, and defect tracking system using tools, including ClearQuest.Work with requirement management system using tools, including IBM DOORs. Participates in and supports the implementation, development, enhancements, and modifications to software test scripts, and procedures. Develop software tests within Windows Operating Systems (OS). Work with and test software deployed in Linux Operating System (OS). Use Visual Studio for software test development with C# programming language. Write automated and manual tests for all levels of testing, including Sanity, Functional, Integration, Regression, and Ad-hoc testing. Working from requirement specifications, writes, updates, or executes test design, test cases, as well as test procedures (automated, semi-automated or manual) and analyzes and reports test results. Apply knowledge of testing clinical workflows and firmware interactions with in-clinic software related to Class III and Class II implantable medical devices such as ICDs, Pacemakers and Heart Monitors. Contributes to and supports writing, updating, developing, and maintaining Hazard/Risk/Cyber Security analysis specifications and cybersecurity testing. Present at design review meetings, documents and resolve issues. Ensures compliance with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, including applied medical device regulation knowledge in areas of verification and validation processes per FDA 21 CFR 820 and ISO 13485. Work with cross-disciplinary engineering teams to drive successful project outcomes. Mentor junior software engineers and contractors. Bachelors or foreign equivalent degree in Software Engineering, Computer Science, Information Systems, or in a related field of study with at least 3 years of professional experience with: (i) using Visual Studio for software test development with C# programming language; (ii) developing software tests within Windows Operating Systems (OS); (iii) working with software deployed in Linux Operating System (OS); (iv) test script source code management using tools, including AccuRev; (v) requirement management system using tools, including IBM DOORs; (vi) defect tracking system using tools, including ClearQuest; (vii) requirements analysis, development, and testing within Waterfall and Agile Software Development Life Cycle (SDLC) methodologies; (viii) applying medical device regulation knowledge in areas of verification and validation processes per FDA 21 CFR 820 and ISO 13485; (ix) applying knowledge of testing clinical workflows and firmware interactions with in-clinic software related to implantable Class III and Class II medical devices such as ICDs, Pacemakers and Heart Monitors; (x) writing automated and manual tests for all levels of testing, including Sanity, Functional, Integration, Regression, and Ad-hoc testing; and (xi) mentoring junior software engineers and contractors. Will accept educational equivalency evaluation prepared by a qualified evaluation service or in accordance with 8 CFR 214.2(h)(4)(iii)(D). Employer will accept any suitable combination of education, training, or experience. An EOE. 40 hrs/wk. $129,667 - $173,300/year.
St. Jude Medical, an Abbott Labs Co. / Sylmar, CA Understand product requirements and use cases, and work on verification applications for Cardiac Rhythm Management (CRM) remote care in the areas including, but not limited to, technical requirements development, identify test strategy, development of test design, test cases, test procedures and scripts, and test execution. Responsible for requirements analysis, development, and testing within Waterfall and Agile Software Development Life Cycle (SDLC) methodologies. Independently develop, debug, and maintain automated test procedures utilizing source code management using tools, including AccuRev, and defect tracking system using tools, including ClearQuest.Work with requirement management system using tools, including IBM DOORs. Participates in and supports the implementation, development, enhancements, and modifications to software test scripts, and procedures. Develop software tests within Windows Operating Systems (OS). Work with and test software deployed in Linux Operating System (OS). Use Visual Studio for software test development with C# programming language. Write automated and manual tests for all levels of testing, including Sanity, Functional, Integration, Regression, and Ad-hoc testing. Working from requirement specifications, writes, updates, or executes test design, test cases, as well as test procedures (automated, semi-automated or manual) and analyzes and reports test results. Apply knowledge of testing clinical workflows and firmware interactions with in-clinic software related to Class III and Class II implantable medical devices such as ICDs, Pacemakers and Heart Monitors. Contributes to and supports writing, updating, developing, and maintaining Hazard/Risk/Cyber Security analysis specifications and cybersecurity testing. Present at design review meetings, documents and resolve issues. Ensures compliance with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, including applied medical device regulation knowledge in areas of verification and validation processes per FDA 21 CFR 820 and ISO 13485. Work with cross-disciplinary engineering teams to drive successful project outcomes. Mentor junior software engineers and contractors. Bachelors or foreign equivalent degree in Software Engineering, Computer Science, Information Systems, or in a related field of study with at least 3 years of professional experience with: (i) using Visual Studio for software test development with C# programming language; (ii) developing software tests within Windows Operating Systems (OS); (iii) working with software deployed in Linux Operating System (OS); (iv) test script source code management using tools, including AccuRev; (v) requirement management system using tools, including IBM DOORs; (vi) defect tracking system using tools, including ClearQuest; (vii) requirements analysis, development, and testing within Waterfall and Agile Software Development Life Cycle (SDLC) methodologies; (viii) applying medical device regulation knowledge in areas of verification and validation processes per FDA 21 CFR 820 and ISO 13485; (ix) applying knowledge of testing clinical workflows and firmware interactions with in-clinic software related to implantable Class III and Class II medical devices such as ICDs, Pacemakers and Heart Monitors; (x) writing automated and manual tests for all levels of testing, including Sanity, Functional, Integration, Regression, and Ad-hoc testing; and (xi) mentoring junior software engineers and contractors. Will accept educational equivalency evaluation prepared by a qualified evaluation service or in accordance with 8 CFR 214.2(h)(4)(iii)(D). Employer will accept any suitable combination of education, training, or experience. An EOE. 40 hrs/wk. $129,667 - $173,300/year.