JD
Job Summary
We are seeking a meticulous and detail-oriented Medical Device Software Verification Tester to join our team. The successful candidate will be responsible for verifying software used in our medical devices and ensuring compliance with regulatory standards and internal quality requirements. This role involves designing, implementing, and executing test plans and procedures to identify and document software defects.
Key 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.
Test Execution
• Execute manual and automated tests to identify software application defects.
• Conduct regression testing to ensure existing functionalities remain unaffected by new changes.
• Perform exploratory testing to uncover potential issues not identified by formal test cases.
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.
Qualifications
Education
Bachelor's degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field.
Experience
• 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, Java) for test automation.
Axiom is a global information technology, consulting and outsourcing company and services provider. Our IT solutions empower organizations and individuals throughout the world to maximize value and quality to succeed in today's challenging business environment. As a fast-growing new economy company, we focus our strengths to offer world-class solutions and services through the convergence of technology, innovation, expertise and experience. We provide software consulting, development and IT-enabled services to clients across the globe. We work towards delivering sustained value creation for customers, employees, industries and society at large. Core offerings include data warehousing, middleware development, product development and web-enablement of legacy applications in verticals like telecom, finance, healthcare, manufacturing, energy & utilities, retail & distribution, enablement of legacy Relentless exploration of technology horizons and a Global Delivery Model that is a judicious combination of onsite, offsite and offshore development, offer a complete range of high-ROI business solutions spanning the consulting, technology, operations and process outsourcing value chain.
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