Supplier Quality Engineer I

Abbott

Sylmar, California, United States
Base: $72,100.00 – $114,700.00; bonus/equity: not ...
Onsite
Bachelor's degree in engineering or technical field
2 years work-related experience
Medical device or pharmaceutical quality assurance
Abbott is seeking a Supplier Quality Engineer I for its Sylmar, California location. The role involves maintaining supplier quality standards, conducting audits, and ensuring compliance with regulatory requirements in the medical device sector

Job Summary

  • This onsite role at Abbott's Sylmar, CA location focuses on maintaining the Division Approved Supplier List and assessing new suppliers through audits.
  • The position requires evaluating exception reports for nonconforming materials and ensuring root cause investigations are completed per FDA regulations.
  • Employees benefit from a comprehensive package including free medical coverage options, high employer retirement contributions, and tuition reimbursement programs.

Matching Summary

Match Score: 85

Abbott is seeking a Supplier Quality Engineer I for its Sylmar, California location. The role involves maintaining supplier quality standards, conducting audits, and ensuring compliance with regulatory requirements in the medical device sector.

Salary

Base: $72,100.00 – $114,700.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement savings plan, tuition reimbursement

Skills & Requirements

Must-have

  • Bachelor's degree in Engineering or Technical Field
  • 2 years work-related experience
  • Medical device or pharmaceutical quality assurance
  • FDA QSR and ISO 13485 knowledge
  • ISO 14971 risk management expertise

Nice-to-have

  • Masters Degree preferred
  • ASQ CQE certification preferred
  • Strong communication and interpersonal skills
  • Collaborative team player
  • Experience with Agile Manufacturer's Tab

Key Requirements

  • Bachelor's Degree in Engineering or Technical Field
  • 2 years' work-related experience
  • Quality Assurance experience in medical device/pharma
  • Working knowledge of FDA QSR, ISO, MDD, IVDD
  • Detailed knowledge of FDA, GMP, ISO 13485, ISO 14971

Work Rights

Not specified

Tailored Resume

Cover Letter