Quality & Process Improvement Coordinator

Simpson Strong-Tie; Stockton (CA); On-site; USD 64,000 - 102,000; Full time

Benefits offered by this job

Quarterly bonuses/commission

Comprehensive benefits

Job summary

Simpson Strong-Tie in Stockton, CA is seeking a Quality Coordinator to drive quality improvements across manufacturing and lab environments. You will implement best practices, reduce defects, and support rapid improvement events and root cause analysis.

You will manage document control, QA records, and QA system updates while interpreting quality policies to ensure ISO compliance and branch objectives. The role requires data analysis skills and strong attention to detail.

Qualifications

• BS in Business, Management, Engineering or related field.
• ISO 9001 Certified/Trained Auditor preferred.
• 3 years’ experience as a Quality Assistant or similar role in a fast-paced manufacturing and/or lab environment required.
• Familiarity with Lean Manufacturing preferred.
• Data Analysis. Ability to interpret technical instructions with multiple variables.
• Attention to Detail and ability to meet deadlines.
• Self-Management and accountability for quality results.
• Prioritization and ability to manage multiple projects.

Responsibilities

• Identify gaps and audit department processes to drive efficiency and quality improvements.
• Use data trends to set priorities and plan quality action projects.
• Lead root-cause analysis of recurring issues and report metrics.
• Support document control, quality records, and QA system updates.
• Interpret quality policies to ensure ISO compliance and maintain QA programs.
• Complete special projects assigned by QA Manager and Branch Manager.

Skills

Data analysis

Attention to detail

Self-management

Prioritization

Interpersonal skills

Lean Manufacturing

3 years QA experience

ISO 9001

Education

BS in Business, Management, Engineering or related field

Job description

Simpson Strong-Tie in Stockton, CA is seeking a Quality Coordinator to drive quality improvements across manufacturing and lab environments. You will implement best practices, reduce defects, and support rapid improvement events and root cause analysis.

You will manage document control, QA records, and QA system updates while interpreting quality policies to ensure ISO compliance and branch objectives. The role requires data analysis skills and strong attention to detail.