Job Description

SUMMARY Our client is seeking a candidate primarily responsible for executing verification test protocols to qualify new medical device software. The role involves collaboration with cross-functional teams and adherence to established medical device design processes.

ESSENTIAL DUTIES This position supports verification and validation processes during development phases and medical device releases by:

• Conducting manual verification testing of primary software applications and support tools
• Following software quality systems/processes, including bug report generation
• Developing and documenting software verification test reports
• Performing software tool validations
• Assisting with bug reproduction and isolation
• Creating and documenting software requirements
• Identifying and promoting software quality assurance best practices

QUALIFICATIONS

• Fundamental understanding of software systems, testing, and release cycles
• Basic knowledge of FDA and MDR regulations relating to software quality (preferred)
• Strong organizational and communication abilities
• Excellent writing and documentation skills
• Experience troubleshooting various computer issues
• Team-oriented with strong attention to detail
• Proactive approach with thorough task completion
• Ability to thrive in fast-paced environments
• Self-motivated with capability to work independently

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