On-Site Process & Quality Engineer - Lean Six Sigma

Barr Brands International, Inc.; Memphis (TN); On-site; USD 75,000 - 110,000; Full time

Benefits offered by this job

Six Sigma Certification support

Job summary

Barr Brands International, Inc. is seeking a Process and Quality Engineer to ensure process consistency, efficiency, and quality across manufacturing operations in Memphis. You will lead root-cause analyses, drive continuous improvement initiatives, and ensure compliance with FDA/SQF/ISO standards.

Responsibilities include process optimization, validation activities, SOP development, and cross-functional collaboration with R&D, Maintenance, and Supply Chain to support launches and changes.

Qualifications

• Bachelor’s degree in Mechanical, Chemical, Industrial, or Manufacturing Engineering.
• 5–7 years of manufacturing experience, preferably in a CPG environment.
• Experience implementing Lean, Six Sigma, or continuous improvement projects.
• Experience with QMS and SPC.

Responsibilities

• Analyze and optimize manufacturing processes to improve throughput and quality.
• Lead process validation studies (SPC, DOE, Cp/Cpk).
• Develop SOPs and process control plans.
• Identify cost savings and efficiency opportunities via Lean/Six Sigma.
• Support capital projects including equipment qualification.

Skills

Root cause analysis

Lean Six Sigma

SPC / DOE

Quality systems

Data analysis

Problem solving

Cross-functional collaboration

Training operators

Process mapping

Gage R&R

Education

Bachelor’s degree in Mechanical Engineering

Bachelor’s degree in Chemical Engineering

Bachelor’s degree in Industrial Engineering

Bachelor’s degree in Manufacturing Engineering

Tools

Minitab

Power BI

Excel

ERP/MES systems

DOE

Job description

Barr Brands International, Inc. is seeking a Process and Quality Engineer to ensure process consistency, efficiency, and quality across manufacturing operations in Memphis. You will lead root-cause analyses, drive continuous improvement initiatives, and ensure compliance with FDA/SQF/ISO standards.

Responsibilities include process optimization, validation activities, SOP development, and cross-functional collaboration with R&D, Maintenance, and Supply Chain to support launches and changes.