Quality & Process Improvement Coordinator

Q--lab-Corporatio; Westlake (OH); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Profitability bonus

Company retirement plan

Benefits package

Generous PTO

Westlake HQ

Job summary

Q-Lab Corporation in Westlake, Ohio is seeking a Quality Coordinator to own nonconforming material, CAPA, inspections, and quality reporting. You will collaborate with Engineering, Manufacturing, Purchasing, and Warehouse to drive data-driven improvements in product quality.

The role emphasizes cross-functional coordination, root cause investigations, and continuous process improvement, with an emphasis on timely corrective actions and quality documentation.

Qualifications

• Experience with quality systems and nonconforming material processes.
• Familiarity with supplier quality and CAPA.
• Experience in manufacturing quality environments.
• Ability to read drawings and inspection standards.
• Data-driven problem solving and reporting.

Responsibilities

• Own nonconforming material lifecycle and disposition.
• Coordinate cross-functional quality activities.
• Prioritize investigations by risk and production needs.
• Prepare weekly and monthly quality reports.
• Coordinate CAPA and corrective actions.
• Develop and improve inspection procedures and quality docs.
• Lead quality dashboards and trend analysis.
• Supervise inspectors and provide coaching.

Skills

Quality problem-solving

Cross-functional collaboration

Data analysis

Inspection methods knowledge

Project management

Education

Associate's degree or equivalent in quality/manufacturing/engineering

Bachelor's degree in related field

Tools

Microsoft Excel

Job description

Q-Lab Corporation in Westlake, Ohio is seeking a Quality Coordinator to own nonconforming material, CAPA, inspections, and quality reporting. You will collaborate with Engineering, Manufacturing, Purchasing, and Warehouse to drive data-driven improvements in product quality.

The role emphasizes cross-functional coordination, root cause investigations, and continuous process improvement, with an emphasis on timely corrective actions and quality documentation.