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