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