QC Methods Engineer

PPG Industries (UK) Limited; Shildon; On-site; GBP 50,000 - 70,000; Full time

Job summary

PPG Industries – Shildon is seeking a QC Methods Engineer to oversee quality control procedures, keep audit-ready documentation, and support key QC systems (ETQ, QPulse, LIMS).

The role emphasizes data analysis, SPC, root cause investigations, CAPA implementation, and cross-functional collaboration with QA, Operations and Engineering to drive process improvements and regulatory compliance.

Qualifications

• Over 5 years in a Quality Control environment.
• Knowledge of ISO 9001, AS9100 or equivalent quality standards.
• Over 5 years in a highly regulated environment (Pharma/Food/labs).
• Experience using data analysis to inform improvements with test methods.
• Structured background using Root Cause Analysis & CAPA.

Responsibilities

• Manage QC procedures, SOPs, and metrics within ETQ.
• Support QC systems including ETQ, QPulse, LIMS and related tools.
• Maintain quality records, certificates and inspection reports audit-ready.
• Lead Change (MOC) process.
• Analyze quality data to identify trends and improvement opportunities.
• Perform SPC analysis and provide performance reporting.
• Lead root cause investigations using 5 Why, Ishikawa, 8D, and PDCA.
• Implement and track CAPA for sustained improvements.
• Lead equipment qualification activities and calibration programs.
• Monitor calibration and servicing performance metrics.
• Provide technical guidance on QC processes.
• Plan, conduct and support internal audits of quality systems and labs.
• Support customer, regulatory, and certification audits.
• Track audit findings and closure of corrective actions.
• Manage QC training administration and competency records.
• Collaborate with QA, Operations and Engineering on non-conformances and validations.

Skills

Quality control

Data analysis

Root cause analysis

CAPA

Audit readiness

Tools

ETQ

QPulse

LIMS

Mainti4

Gemba

Job description

QC Methods Engineer

PPG Industries – Shildon

Key Responsibilities

Quality Systems & Compliance

• Manage QC procedures, SOPs, and associated metrics within the electronic Quality Management System (ETQ).
• Support important QC systems including ETQ, QPulse, LIMS, sample management, Mainti4, and Gemba.
• Maintain quality records, certificates, inspection reports, and associated documentation accurately and keep them audit‑ready.
• Manage Change (MOC) process.

Continuous Improvement & Data Analysis

• Analyse quality and laboratory performance data to identify trends, process variation, and improvement opportunities.
• Perform Statistical Process Control (SPC) analysis and provide meaningful performance reporting.
• Lead root cause investigations using structured problem‑solving methodologies such as 5 Why, Ishikawa, 8D, and PDCA.
• Implement and track corrective and preventive actions (CAPA) to ensure sustainable improvements.

Equipment & Laboratory Support

• Lead equipment qualification activities and support calibration and maintenance programmes.
• Monitor calibration and servicing performance metrics to ensure compliance and operational readiness.
• Provide technical guidance on QC processes and best practices.

Audit & Quality Assurance

• Plan, conduct, and support internal audits covering quality systems, documentation, safety, and laboratory compliance.
• Support customer, regulatory, and certification audits.
• Track audit findings and ensure implementation and closure of corrective actions.

Training & Cross-Functional Collaboration

• Manage QC training administration, competency records, and training metrics.
• Promote QC personnel in quality systems and problem‑solving techniques.
• Collaborate with QA, Operations, and Engineering teams on non‑conformances, process improvements, new product introductions, and validation activities.
• Act as an important contributor to departmental and site continuous improvement projects.

Qualifications

• Experience working within a Quality Control environment for over 5 years.
• Knowledge of ISO 9001, AS9100, or equivalent quality management standards.
• Over 5 years experience working in a highly regulated environment (Pharma/Food/labs).
• Experience using data analysis to inform improvements with test methods.
• Structured background using Root Cause Analysis & CAPA.

A PPG oferece igualdade de oportunidades a todos os candidatos e colaboradores. Todos os candidatos qualificados receberão consideração para emprego sem distinção de sexo, gravidez, raça, cor, credo, religião, origem nacional, idade, deficiência, estado civil, condição de veterano, orientação sexual, identidade ou expressão de gênero.

Se você precisar de algum ajuste devido a uma deficiência, por favor envie um e‑mail para [e-mail].