Sr. Quality Engineer

Abbott

Saint Paul, Minnesota, United States
Base: $78,000.00 – $156,000.00; bonus/equity: not ...
Onsite
Fda gmp iso 13485 compliance knowledge
Six sigma and lean manufacturing methodologies
Risk analysis and capa investigation leadership
Abbott is seeking a Senior Quality Engineer for its Vascular Division in Saint Paul, Minnesota. This fully onsite role requires substantial experience in quality engineering within the medical device sector, focusing on process improvement, compliance, and leadership

Job Summary

  • The Senior Quality Engineer will lead the investigation and resolution of product nonconformances while implementing effective process control systems.
  • Abbott offers comprehensive benefits including free medical coverage, high employer retirement contributions, and tuition reimbursement programs.
  • This fully onsite role in Saint Paul, Minnesota supports the manufacturing of life-changing vascular medical devices used by thousands globally.

Matching Summary

Match Score: 85

Abbott is seeking a Senior Quality Engineer for its Vascular Division in Saint Paul, Minnesota. This fully onsite role requires substantial experience in quality engineering within the medical device sector, focusing on process improvement, compliance, and leadership.

Salary

Base: $78,000.00 – $156,000.00; Bonus/Equity: Not specified; Benefits: Free medical coverage, retirement plan, tuition reimbursement

Skills & Requirements

Must-have

  • FDA GMP ISO 13485 compliance knowledge
  • Six Sigma and Lean Manufacturing methodologies
  • Risk analysis and CAPA investigation leadership
  • Critical To Quality parameter monitoring
  • Medical device Class II & III experience

Nice-to-have

  • Multi-departmental project team leadership
  • Strong statistical data analysis skills
  • Advanced technical report writing abilities
  • Collaborative communication with vendors
  • Certified Quality Engineer accreditation

Key Requirements

  • Bachelor's Degree in Engineering or Technical Field
  • Minimum 6 years of related work experience
  • Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971

Work Rights

Not specified

Tailored Resume

Cover Letter