Quality Engineer I

Abbott

Plymouth, Minnesota, United States
Base: $50,700.00 – $101,300.00; bonus/equity: not ...
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Bachelor's degree in engineering or technical field
0-2 years of engineering experience
Knowledge of fda regulations and gmp
** Abbott is seeking a Quality Engineer I for its Electrophysiology division in Plymouth, Minnesota. The role involves ensuring compliance with quality systems for new and modified products while supporting cross-functional teams and enhancing product quality. **

Job Summary

  • This position supports the Electrophysiology division by assuring new or modified products conform to requirements and establishing compliance with the quality system.
  • The role involves leading process control systems, implementing CAPA mechanisms, and conducting experiments for process optimization to meet internal and external requirements.
  • Abbott offers comprehensive benefits including free medical coverage options, a high employer contribution retirement plan, tuition reimbursement, and education benefits.

Matching Summary

Match Score: 75

** Abbott is seeking a Quality Engineer I for its Electrophysiology division in Plymouth, Minnesota. The role involves ensuring compliance with quality systems for new and modified products while supporting cross-functional teams and enhancing product quality. **

Salary

Base: $50,700.00 – $101,300.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Bachelor's degree in engineering or technical field
  • 0-2 years of engineering experience
  • Knowledge of FDA regulations and GMP
  • Experience with CAPA systems and risk analysis
  • Ability to work in matrixed cross-functional teams

Nice-to-have

  • Prior medical device industry experience
  • Six Sigma and Lean Manufacturing methodologies
  • ISO 13485 and ISO 14971 standards knowledge
  • Post market surveillance experience
  • Clean room environment work capability

Key Requirements

  • Bachelor's degree in engineering or Technical Field
  • 0-2 years Engineering experience
  • Compliance with FDA regulations and GMP
  • Strong verbal and written communication skills

Work Rights

Not specified

Tailored Resume

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