Quality Engineer — Process Excellence & Compliance

Abbott; United States; On-site; USD 61,000 - 123,000; Full time

Benefits offered by this job

Vacation time and personal days

401(k) retirement plan with company-mв

Tuition reimbursement

Health care benefits

On‑site training and career dev

Job summary

Abbott is seeking a Quality Engineer to join our Nutrition division in Sturgis, MI. You will identify and implement robust process controls to support development and ongoing manufacturing, while mentoring teams and driving quality improvements across products such as Similac, PediaSure, and Pedialyte.

The role requires a Bachelor’s or Master’s in a related field with 2–5 years (or 1–3 with a Master’s) of QA/engineering experience, and strong knowledge of FDA/GMP practices.

Qualifications

• Bachelor’s degree in Engineering, Quality Assurance, Manufacturing or related field.
• 2–5 years of relevant experience for Bachelors, or 1–3 years with a Master’s.
• Demonstrated use of quality tools and methodologies.

Responsibilities

• Identify and implement effective process control systems for development and manufacturing of products.
• Lead, coach, and mentor non-exempt and entry level personnel.
• Assist in developing and executing streamlined business systems to identify and resolve quality issues.
• Apply systematic problem‑solving methodologies to resolve quality issues.
• Design and conduct experiments for process optimization and improvement.
• Document experiment plans and results, including protocol writing and reports.
• Lead process control and monitoring of CTQ parameters.

Skills

Quality Assurance

Process Improvement

Six Sigma

Lean Manufacturing

Project Management

Statistical Analysis

FDA GMP Knowledge

Communication

Education

Bachelor’s degree in Engineering/Science

Master’s degree in related field

Job description

Abbott is seeking a Quality Engineer to join our Nutrition division in Sturgis, MI. You will identify and implement robust process controls to support development and ongoing manufacturing, while mentoring teams and driving quality improvements across products such as Similac, PediaSure, and Pedialyte.

The role requires a Bachelor’s or Master’s in a related field with 2–5 years (or 1–3 with a Master’s) of QA/engineering experience, and strong knowledge of FDA/GMP practices.