Software Design Quality Engineer

Abbott

Westford, Massachusetts, United States
Base: $61,300.00 – $122,700.00; bonus/equity: not ...
Onsite
Bachelor's degree in computer science or related field
2-5+ years software design quality experience
Knowledge of iec 62304 and iso 14971 standards
Abbott is seeking a Software Design Quality Engineer for its Vascular division in Westford, Massachusetts. The role involves leading quality engineering deliverables throughout the product lifecycle, with a focus on software design quality and compliance in the medical device sector

Job Summary

  • Abbott is a global healthcare leader seeking a Software Design Quality Engineer to support the Vascular division in Westford, MA.
  • The role involves leading quality engineering deliverables from product concept through commercialization, including risk management and CAPA activities.
  • Employees enjoy benefits such as free medical coverage, high employer retirement contributions, and tuition reimbursement programs.

Matching Summary

Match Score: 85

Abbott is seeking a Software Design Quality Engineer for its Vascular division in Westford, Massachusetts. The role involves leading quality engineering deliverables throughout the product lifecycle, with a focus on software design quality and compliance in the medical device sector.

Salary

Base: $61,300.00 – $122,700.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement plan, tuition reimbursement

Skills & Requirements

Must-have

  • Bachelor's degree in Computer Science or related field
  • 2-5+ years software design quality experience
  • Knowledge of IEC 62304 and ISO 14971 standards
  • Experience with Agile SDLC and risk management
  • Proficiency in Jira and Jama requirements tools

Nice-to-have

  • Master's level degree preferred
  • ASQ CSQE and ISTQB certifications desired
  • Programming experience in C/C++/Java
  • Experience with TestComplete and Coverity tools
  • Clinical or hospital experience desired

Key Requirements

  • Bachelor's degree required
  • 2-5+ years combined experience
  • FDA regulations and GMP knowledge
  • ISO 13485 compliance expertise

Work Rights

Not specified

Tailored Resume

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