Job Description

SUMMARY: 

As a Senior Verification and Validation Engineer (V&V) , you will be responsible for ensuring Accuray products are safe, effective, reliable, and ready for customer use through deep technical understanding, risk-based testing, system integration, and verification and validation activities. Product Test Engineering partners with Systems Engineering, Software Engineering, Hardware Engineering, Service, Manufacturing, Regulatory, and Project Leadership teams throughout the development lifecycle to identify risks early, influence product quality, establish production-equivalent test environments, execute testing, investigate anomalies, and support successful product releases.  

Successful candidates are highly adaptable problem solvers who enjoy learning complex systems, troubleshooting difficult technical issues, collaborating across disciplines, and driving high-quality outcomes in a regulated medical device environment.  

REPORTING TO/DEPARTMENT: 

Reports to the Sr Manager, Product Test Engineering

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Requirements and Risk Analysis: Review and understand user, system, and design requirements to develop effective verification and validation strategies and identify project risks early.  

• Project Participation and Technical Leadership: Support project planning, estimation, and execution activities. Partner with engineering teams throughout development to improve quality, testability, and release readiness.  

• Test Strategy and Test Case Development: Design, document, and maintain verification, validation, integration, workflow, regression, and functional test cases aligned to project requirements and intended use.  

• Test Execution: Execute testing activities across software, hardware, networking, workflow, and integrated system environments while producing objective evidence suitable for design history file deliverables.  

• Anomaly Investigation and Troubleshooting: Identify, document, reproduce, investigate, and track anomalies. Work with cross-functional teams to support root-cause analysis and issue resolution.  

• Test Environment Ownership: Configure, maintain, and improve production-equivalent test environments including computers, networks, databases, medical device hardware, software installations, and supporting infrastructure.  

• System Integration: Develop a broad understanding of system interactions across Accuray products and subsystems to support integration, regression analysis, and release activities.  

• Quality Advocacy: Advocate for release-quality design outputs, testability, serviceability, usability, and overall product quality throughout the development lifecycle.  

• Collaboration: Work closely with engineers, project managers, service personnel, manufacturing, regulatory, and other Product Test Engineering team members to facilitate successful project execution.  

• Continuous Improvement: Contribute to process improvements, test suite modernization, cross-training initiatives, and organizational knowledge sharing.  

REQUIRED QUALIFICATIONS:

Required:

• Bachelor's degree in Engineering, Computer Science, Physical Sciences, or a related technical field, or an equivalent combination of education and experience.  
• 3–5 years of experience in testing, verification, validation, systems engineering, product development, or a closely related technical discipline.  
• Strong troubleshooting and problem-solving skills with the ability to diagnose complex hardware, software, networking, and system-level issues.  
• Ability to quickly learn new technologies, products, and workflows while balancing multiple priorities.  
• Excellent written and verbal communication skills and the ability to collaborate effectively across cross-functional teams.  
• Ability to work independently while maintaining accountability for deliverables and project commitments.  
• Experience creating technical documentation, executing formal test activities, and communicating technical findings.  

Preferred or Desired:

• Experience within an FDA-regulated medical device environment or other regulated industry.  

• Experience testing complex integrated systems that include software, hardware, networking, and workflow components.  

• Experience with requirements management, defect tracking, and test management tools.  

• Experience establishing and maintaining test environments and laboratory infrastructure.  

• Knowledge of verification, validation, integration, regression, and risk-based testing methodologies.  

• Experience supporting product releases, system integration activities, and cross-functional project teams.  

• Experience authoring technical documentation and objective evidence for regulated development activities.  

WORKING CONDITIONS

• Indoor Environment: The position takes place indoors, providing a comfortable and climate-controlled workspace.
• Physical Demands: This role may involve standing or walking for extended periods of time, requires manual dexterity and the ability to handle delicate, high-value equipment. Ability to lift and carry equipment or materials required.
• Work Schedule: Standard working hours are Monday through Friday; however, evening, weekend or other work outside normal business hours and overtime may be required.
• Computer Usage: Proficiency with computers, including software applications and communication tools, is essential for tasks and collaboration.
• Personal Protective Equipment: Must wear appropriate personal protective equipment (PPE) and ahere to safety protocols and cleanliness standards.

To qualify for this position, candidates must be able to furnish proof that they are authorized to work in the country they are applying on a permanent basis without sponsorship.