V&V Engineer - Medical Devices (Surgical Robotics)

Quality Ai; Santa Clara (CA); Hybrid; USD 90,000 - 100,000; Full time

Benefits offered by this job

Bonuses via client and employee refer-

QualityAI Tech academy training

Global career opportunities

Diversity and inclusion

Job summary

QualityAI in Santa Clara, CA seeks a V&V Engineer to lead validation activities for medical devices. The role focuses on writing test procedures, executing plans, and ensuring quality across the software development lifecycle.

3 days onsite in Santa Clara, collaboration with software teams, and ownership of test infrastructure are key aspects. The ideal candidate brings 5+ years in software development, agile experience, and a strong background in medical device verification and validation, with

Qualifications

• Bachelor's degree in software or related engineering field.
• 5+ years in all phases of software development life cycle.
• Experience with design controls in regulated environments, ISO 13485 and 21 CFR 820 is a plus.

Responsibilities

• Write test procedures, test reports, and test plans; execute tests and log defects.
• Collaborate with software teams to devise effective test strategies.
• Review test plans, protocols, and scripts; ensure thorough validation for medical devices.
• Work with cross-functional groups to improve test infrastructure and data analysis.

Skills

Manual/Functional experience

Agile methodologies

Product owner

Jira

Test planning

Communication skills

Education

Bachelor’s in Software or Electrical/Electronics Engineering

Tools

Software branching

Version control

Job description

QualityAI in Santa Clara, CA seeks a V&V Engineer to lead validation activities for medical devices. The role focuses on writing test procedures, executing plans, and ensuring quality across the software development lifecycle.

3 days onsite in Santa Clara, collaboration with software teams, and ownership of test infrastructure are key aspects. The ideal candidate brings 5+ years in software development, agile experience, and a strong background in medical device verification and validation, with