Senior Vnv Engineer

Qualitest Group

Hercules, CA, United States
$100,000 - $110,000 py
On-site
Test methods development/validation
Test execution and analysis
Systems engineering practices
Qualitest Group is seeking a Senior VnV Engineer to join their Hercules, CA team, specializing in the verification and validation of clinical diagnostic products. The ideal candidate will have experience in system testing, knowledge of regulatory standards for medical devices, and strong analytical skills

Job Summary

  • As a Test Engineer within our Global Systems Engineering Organization, you’ll be right at the forefront of Bio-Rad's Clinical Diagnostics R&D Group – heavily involved in System Design Integration/Verification of new clinical diagnostics products across molecular diagnostics, clinical immunology, and immunohematology platforms.
  • You will leverage your knowledge of engineering principles and implement systems engineering practices (requirements, architecture) on new product development projects.
  • We offer a competitive pay, the salary range for the role is $100,000 - $110,000, along with comprehensive benefits including 401k matching and healthcare.

Matching Summary

Match Score: 85

Qualitest Group is seeking a Senior VnV Engineer to join their Hercules, CA team, specializing in the verification and validation of clinical diagnostic products. The ideal candidate will have experience in system testing, knowledge of regulatory standards for medical devices, and strong analytical skills.

Salary

$100,000 - $110,000

Skills & Requirements

Must-have

  • Test methods development/validation
  • Test execution and analysis
  • Systems engineering practices
  • Troubleshooting medical devices
  • Regulatory requirements for medical devices

Nice-to-have

  • Test automation is an advantage
  • Lean mindset
  • Collaborative multidisciplinary team environment

Key Requirements

  • Minimum 2-4 years of experience in system testing
  • Bachelor's or Master's degree in Computer Science or Engineering
  • Knowledge of FDA regulations (21 CFR Part 820), ISO 13485, IEC 62304

Work Rights

Not specified

Tailored Resume

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