What are the responsibilities and job description for the Senior Software Test Engineer - Raleigh, NC (Onsite + In-Person Interview Required) position at Jobs via Dice?
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We are seeking a Senior Software Test Engineer to join our team in Raleigh, NC. The ideal candidate will be responsible for ensuring the quality and compliance of software applications through rigorous manual testing and documentation practices.
Key Responsibilities:
Conduct comprehensive manual testing to validate software functionality, performance, and user experience across various scenarios
Develop, maintain, and execute test protocols and test cases
Prepare detailed test reports, including a complete traceability matrix
Ensure all testing activities comply with Merz SOPs and applicable regulatory standards
Adhere to FDA regulations and IEC 62304 standards for medical device software
Collaborate with cross-functional teams to identify, document, and resolve defects
Perform Additional Duties As Required Based On Business Needs
Required Skills & Qualifications:
Strong experience in manual software testing
Experience with test documentation and reporting
Knowledge of traceability matrix creation and maintenance
Familiarity with FDA regulations and IEC 62304
Excellent analytical and problem-solving skills
Strong communication and documentation abilities
Preferred Qualifications:
Experience in regulated environments (medical devices/pharma)
Prior experience working with SOP-driven organizations
We are seeking a Senior Software Test Engineer to join our team in Raleigh, NC. The ideal candidate will be responsible for ensuring the quality and compliance of software applications through rigorous manual testing and documentation practices.
Key Responsibilities:
Conduct comprehensive manual testing to validate software functionality, performance, and user experience across various scenarios
Develop, maintain, and execute test protocols and test cases
Prepare detailed test reports, including a complete traceability matrix
Ensure all testing activities comply with Merz SOPs and applicable regulatory standards
Adhere to FDA regulations and IEC 62304 standards for medical device software
Collaborate with cross-functional teams to identify, document, and resolve defects
Perform Additional Duties As Required Based On Business Needs
Required Skills & Qualifications:
Strong experience in manual software testing
Experience with test documentation and reporting
Knowledge of traceability matrix creation and maintenance
Familiarity with FDA regulations and IEC 62304
Excellent analytical and problem-solving skills
Strong communication and documentation abilities
Preferred Qualifications:
Experience in regulated environments (medical devices/pharma)
Prior experience working with SOP-driven organizations