QC Methods Engineer

PPG; Shildon; On-site; GBP 45,000 - 60,000; Full time

Job summary

PPG Industries in Shildon, UK, is seeking a QC Methods Engineer to drive quality control processes, compliance, and continuous improvement across QC, QA, Process, S&T and Operations. You will be the SME for QC management systems, training programmes, calibration, and root cause investigations.

You will report to the QC Manager and collaborate on audits, CAPA, and data-driven improvements to meet site quality goals and regulatory requirements.

Qualifications

• Over 5 years of experience in a QC environment.
• Knowledge of ISO 9001, AS9100 or equivalent standards.
• Experience in highly regulated environments (Pharma/Food/labs).
• Experience using data analysis to inform improvements.
• Structured problem-solving with 5 Why, Ishikawa, 8D, PDCA.

Responsibilities

• Manage QC procedures, SOPs, and metrics within ETQ.
• Support QC systems including ETQ, QPulse, LIMS, Mainti4 and Gemba.
• Maintain quality records, inspection reports, and audit-ready docs.
• Lead change management (MOC) and CAPA processes.
• Lead equipment qualification and calibration monitoring.
• Plan and conduct internal and external audits.
• Train QC staff and collaborate across QA, Operations and Eng.

Skills

Data analysis

Statistical Process Control

Root cause analysis

CAPA management

Quality systems knowledge

Education

QA/Regulatory knowledge

Tools

ETQ

QPulse

LIMS

Mainti4

Job description

PPG Industries
Shildon

The QC Methods Engineer is responsible for the administration, compliance, and continuous improvement of Quality Control processes to help operate the QC Department. You will be the subject matter expert for QC management systems, QC training programme, equipment qualification, calibration management, and root cause investigations.

Working with QC, QA, Process, S&T, and Operations teams, the QC Methods Engineer ensures compliance with quality standards. The QC Methods Engineer also drives data-driven improvements and supports departmental and site-wide quality goals.

You will report to the QC Manager.

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 the Change (MOC) process.

Continuous Improvement & Data Analysis

• Analyze 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.

Benefits

PPG pay ranges and benefits can vary by location which allows us to compensate employees competitively in different geographic markets. PPG considers several factors in making compensation decisions including, but not limited to, skill sets, experience and training, qualifications and education, licensure and certifications, and other organizational needs. Other incentives may apply.

Our employee benefits programs are designed to support the health and well-being of our employees. Any insurance coverage and benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents. Benefits will be discussed with you by your recruiter during the hiring process.

Equal Opportunity & Disability Accommodation

PPG provides equal opportunity to all candidates and employees. We offer an opportunity to grow and develop your career in an environment that provides a fulfilling workplace for employees, creates an environment for continuous learning, and embraces the ideas and diversity of others. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, color, creed, religion, national origin, age, disability status, marital status, veteran status or sexual orientation, gender identity or expression.

If you need an adjustment due to a disability, please email [e-mail].

You can learn more by visiting https://careers.ppg.com/us/en/candidate-resources.