VDart
Software Verification Engineer
VDart, Palo Alto, California, United States, 94306
Title: Software Verification Engineer
Location Palo Alto, CA (Onsite)
Type: Contract
Job Description:Minimum of 5+ years of experience in software testing, preferably in the medical device industry.Experience with testing tools and frameworks (e.g., ClearQuest, Jama).Familiarity with regulatory standards and guidelines for medical devices (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304).Skills and Competencies
Strong understanding of software development and testing methodologies.Excellent analytical and problem-solving skills. Attention to detail and a high level of accuracy.Proficiency in scripting or programming languages (e.g., Python, C#) for test automation.Good communication and teamwork skillsKey Responsibilities
Test Planning and Design
Develop comprehensive test plans, test cases, and test scripts based on software requirements and design specifications.Ensure test plans cover all functional and non-functional requirements, including performance, reliability, and security.Documentation and Reporting
Document test results, including detailed descriptions of defects and steps to reproduce them.Generate and maintain test reports, defect logs, and other documentation required for regulatory compliance.Communicate test outcomes and defect status to development teams and management.Collaboration
Work closely with software developers, and systems engineers, to understand software requirements and functionality.Compliance and Standards Ensure testing activities comply with relevant regulatory standards (e.g., FDA, ISO 13485, IEC 62304).Stay updated with industry best practices and evolving regulatory requirements for medical device software
Education-
Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field .
Location Palo Alto, CA (Onsite)
Type: Contract
Job Description:Minimum of 5+ years of experience in software testing, preferably in the medical device industry.Experience with testing tools and frameworks (e.g., ClearQuest, Jama).Familiarity with regulatory standards and guidelines for medical devices (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304).Skills and Competencies
Strong understanding of software development and testing methodologies.Excellent analytical and problem-solving skills. Attention to detail and a high level of accuracy.Proficiency in scripting or programming languages (e.g., Python, C#) for test automation.Good communication and teamwork skillsKey Responsibilities
Test Planning and Design
Develop comprehensive test plans, test cases, and test scripts based on software requirements and design specifications.Ensure test plans cover all functional and non-functional requirements, including performance, reliability, and security.Documentation and Reporting
Document test results, including detailed descriptions of defects and steps to reproduce them.Generate and maintain test reports, defect logs, and other documentation required for regulatory compliance.Communicate test outcomes and defect status to development teams and management.Collaboration
Work closely with software developers, and systems engineers, to understand software requirements and functionality.Compliance and Standards Ensure testing activities comply with relevant regulatory standards (e.g., FDA, ISO 13485, IEC 62304).Stay updated with industry best practices and evolving regulatory requirements for medical device software
Education-
Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field .