Quality Engineer Ii

AbbVie

Sylmar, California, United States
Base: $81,500.00 – $141,300.00; bonus/equity: not ...
Quality engineering methodologies
Process control systems implementation
Capa systems leadership
Abbott is a global healthcare leader that helps people live more fully at all stages of life with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines

Job Summary

  • Abbott is a global healthcare leader that helps people live more fully at all stages of life with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines.
  • The Quality Engineer II will lead quality engineering efforts to support product development and manufacturing, ensuring compliance with regulatory standards and driving continuous improvement.
  • Abbott offers training, career development, competitive compensation, health and well-being programs, paid time off, and a 401(k) retirement plan with company match.

Matching Summary

Abbott is a global healthcare leader that helps people live more fully at all stages of life with a portfolio spanning diagnostics, medical devices, nutritionals, and branded generic medicines.

Salary

Base: $81,500.00 – $141,300.00; Bonus/Equity: Not specified; Benefits: Training, career development, health care, paid time off, 401(k) with match

Skills & Requirements

Must-have

  • Quality engineering methodologies
  • Process control systems implementation
  • CAPA systems leadership
  • FDA, GMP, ISO 13485 compliance
  • Statistical/data analysis skills
  • Product and process improvement
  • Cross-departmental project leadership

Nice-to-have

  • Medical device experience
  • Six Sigma and Lean Manufacturing
  • Strong verbal and written communication
  • Ability to work in matrixed environment
  • Multitasking and prioritization skills
  • Team and individual contributor
  • Advanced computer skills

Key Requirements

  • BS degree in Engineering or Technical Field
  • 2-5 years engineering experience
  • Knowledge of FDA, GMP, ISO 13485, ISO 14971
  • Project management and leadership skills
  • ASQ CQE or other certifications preferred
  • Experience with Six Sigma and Lean Manufacturing
  • Prior medical device experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter