Capa Engineer Ii

Abbott

Des Plaines, Illinois, United States
Base: $61,300.00 – $122,700.00; bonus/equity: not ...
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Bachelor's degree in engineering or life science
2 years engineering or technical operational experience
Knowledge of fda quality system regulations 21 cfr part 820
** Abbott is seeking a CAPA Engineer II for its Molecular Diagnostics division in Des Plaines, Illinois. The role involves managing the CAPA process, ensuring compliance with quality standards, and collaborating with cross-functional teams to enhance operational efficiency. **

Job Summary

  • This role is responsible for facilitating and executing the CAPA process within Abbott's Molecular Diagnostics Business Unit.
  • The position requires leading cross-functional teams using methodologies like Six Sigma to resolve quality-related issues effectively.
  • Employees gain access to comprehensive benefits including free medical coverage options, a high employer retirement contribution, and tuition reimbursement programs.

Matching Summary

Match Score: 75

** Abbott is seeking a CAPA Engineer II for its Molecular Diagnostics division in Des Plaines, Illinois. The role involves managing the CAPA process, ensuring compliance with quality standards, and collaborating with cross-functional teams to enhance operational efficiency. **

Salary

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

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Life Science
  • 2 years engineering or technical operational experience
  • Knowledge of FDA Quality System Regulations 21 CFR Part 820
  • Experience with GMP and ISO 13485:2016 standards
  • Proven CAPA and quality assurance project management skills

Nice-to-have

  • Master's degree in related field
  • Six Sigma root cause analysis training
  • Prior medical device industry experience
  • Cross-division business unit model experience
  • Ability to travel approximately 10% internationally

Key Requirements

  • Bachelor's Degree in Engineering, Healthcare, or Life Science
  • 2 years of relevant engineering or technical experience
  • Detailed knowledge of FDA regulations and ISO 13485
  • Strong communication and leadership capabilities

Work Rights

Not specified

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