Software Development Quality Engineer Ii

Abbott

Sylmar, CA, United States
Base: $81,500.00 – $141,300.00; bonus/equity: not ...
Onsite
2-5 years software testing experience
Firmware and embedded systems knowledge
Fda gmp and iso 13485 compliance
Abbott is seeking a Software Development Quality Engineer II for their Sylmar, CA location. The role focuses on quality engineering for software used in medical devices, emphasizing collaboration, testing methodologies, and adherence to regulatory standards

Job Summary

  • This role is responsible for ensuring software reliability and supporting the design of new products in firmware and communication software within a global healthcare leader.
  • The position requires executing Design Verification and Validation activities while maintaining strict adherence to FDA regulations and ISO 13485 standards.
  • Employees benefit from an international career growth path, free medical coverage options, high employer retirement contributions, and tuition reimbursement programs.

Matching Summary

Match Score: 85

Abbott is seeking a Software Development Quality Engineer II for their Sylmar, CA location. The role focuses on quality engineering for software used in medical devices, emphasizing collaboration, testing methodologies, and adherence to regulatory standards.

Salary

Base: $81,500.00 – $141,300.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement plan, tuition reimbursement

Skills & Requirements

Must-have

  • 2-5 years software testing experience
  • Firmware and embedded systems knowledge
  • FDA GMP and ISO 13485 compliance
  • Manual and automated test execution
  • Design Verification and Validation (V&V)
  • C/C++ or Python programming skills

Nice-to-have

  • Prior medical device industry experience
  • ASQ CSQE certification preferred
  • Agile/Scrum methodology background
  • Cross-functional collaboration skills
  • Experience with static analysis tools

Key Requirements

  • Bachelor's degree in Engineering or Technical Field
  • Minimum 2-5 years combined software development and testing experience
  • Detailed knowledge of FDA, GMP, IEEE 1012, and ISO 13485
  • Proficiency in C, C++, C#, Python, or Java
  • Experience with Git, Jira, or similar defect tracking tools

Work Rights

Not specified

Tailored Resume

Cover Letter