Training course
Overview
Quality Control is
a comprehensive professional training course designed for quality control officers,
quality inspectors, quality engineers, production supervisors, laboratory
personnel, manufacturing professionals, construction and engineering teams,
operations managers, technical specialists, and professionals responsible for
monitoring, verifying, and improving the quality of products, services,
processes, materials, and technical work. The course develops the practical
knowledge and skills required to establish effective quality control systems,
perform inspections and testing, identify defects and nonconformities, analyse
quality data, implement corrective actions, and maintain consistent product and
process performance. Participants learn how to translate quality requirements
into measurable controls and practical inspection activities throughout the
operational lifecycle.
The course integrates established
quality control principles with internationally recognised standards and
frameworks, particularly ISO 9001 Quality Management Systems, ISO 19011
Guidelines for Auditing Management Systems, ISO 10005 Quality Plans, ISO 10012
Measurement Management Systems, and relevant principles of statistical process
control, quality assurance, risk-based thinking, and continuous improvement.
Practical tools include inspection and test plans, quality checklists, sampling
plans, control charts, Pareto analysis, histograms, process maps, check sheets,
defect registers, nonconformity reports, corrective action logs, calibration
records, supplier quality assessments, quality dashboards, acceptance criteria,
and statistical quality-control techniques.
Effective quality control requires
systematic monitoring of materials, processes, equipment, workmanship, outputs,
documentation, and measurement systems. Quality professionals must be able to
detect deviations early, distinguish isolated defects from systemic problems,
assess the significance of nonconformities, investigate root causes, and
implement effective corrective measures. This course addresses practical
quality challenges such as defective materials, process variation,
equipment-related quality problems, inconsistent workmanship, inspection
failures, inaccurate measurements, supplier defects, documentation gaps,
customer complaints, rework, scrap, and recurring nonconformities. Real-world
scenarios enable participants to practise making quality decisions using
evidence, specifications, standards, inspection results, and quality
performance data.
Through practical inspection
exercises, quality-data analysis, control-chart activities, sampling exercises,
root cause investigations, nonconformity simulations, corrective-action
workshops, supplier-quality case studies, audit preparation activities, and an
integrated quality-control capstone, participants develop immediately
applicable quality-management capabilities. The programme progresses from
quality-control fundamentals through inspection planning, measurement systems,
statistical process control, sampling, process capability, nonconformity
management, root cause analysis, supplier quality, risk-based controls, auditing,
digital quality tools, and advanced continuous improvement. Participants gain
practical methods for reducing defects, controlling process variation,
improving compliance, strengthening product and process reliability, and
building a culture of consistent quality performance.
Course
Duration
5 Days (40 Hours)
Target
Participants
This course is suitable for:
• Quality control officers, inspectors, and technicians
• Quality assurance and quality management professionals
• Quality engineers and manufacturing quality engineers
• Production and operations supervisors
• Manufacturing and industrial operations professionals
• Construction and civil engineering quality personnel
• Mechanical, electrical, instrumentation, and technical inspection
professionals
• Laboratory and testing personnel
• Maintenance and reliability professionals involved in quality control
• Procurement and supplier quality professionals
• Project managers and project quality coordinators
• Health, safety, environment, and compliance professionals with quality
responsibilities
• Process improvement and operational excellence professionals
• Technical managers and supervisors responsible for quality performance
• Professionals responsible for inspection, testing, measurement, verification,
and nonconformity management
• Professionals preparing to assume responsibilities in quality control and
quality management
Course
Objectives
By the end of the training,
participants will be able to:
• Explain the principles, purpose, scope, and organisational importance of
quality control
• Distinguish quality control, quality assurance, quality management,
inspection, testing, and continuous improvement
• Apply ISO 9001 principles and risk-based thinking to operational
quality-control activities
• Develop practical quality-control plans, inspection and test plans,
checklists, acceptance criteria, and control points
• Identify quality requirements from specifications, drawings, procedures,
contracts, standards, regulations, and customer expectations
• Plan and conduct effective inspections, tests, sampling activities,
verification, and acceptance processes
• Apply statistical process control techniques to monitor process variation and
detect abnormal conditions
• Use control charts, histograms, Pareto analysis, check sheets, process maps,
and other quality tools effectively
• Understand measurement-system principles, calibration, traceability,
accuracy, precision, and measurement uncertainty
• Apply appropriate sampling concepts and acceptance-sampling techniques to
quality-control decisions
• Analyse process capability and distinguish common-cause from special-cause
variation
• Identify, document, classify, and control defects, deviations, and
nonconformities
• Conduct structured root cause analysis using Five Whys, Fishbone Diagrams,
Pareto Analysis, and related techniques
• Develop effective corrective and preventive actions and verify their
effectiveness
• Control rework, scrap, concessions, deviations, and product or process
disposition
• Evaluate supplier quality, incoming materials, subcontracted processes, and
external service performance
• Apply risk-based quality control using process risk assessments, FMEA
principles, control plans, and critical control points
• Support internal audits using ISO 19011 principles and prepare effective
quality evidence and records
• Develop quality KPIs, dashboards, defect trends, cost-of-quality measures,
and performance reports
• Apply digital quality tools, electronic inspection records, data analytics,
and automated quality monitoring
• Implement continuous improvement initiatives using PDCA, Kaizen, Lean, and
data-driven quality methods
• Develop an integrated quality-control strategy through a comprehensive case
study and practical workplace implementation plan
Course
Content
Day
1: Foundations of Quality Control, Standards, Inspection, and Quality Planning
Module 1: Foundations of
Quality Control, Standards, Inspection, and Quality Planning
1. Fundamentals
of Quality Control and Its Role in Organisational Performance
2. Quality
Control, Quality Assurance, Quality Management, Inspection, Testing, and
Verification
3. Quality
Requirements, Specifications, Standards, Drawings, Procedures, and Customer
Expectations
4. ISO
9001 Quality Management Principles and Risk-Based Thinking
5. Quality
Planning, Quality Objectives, Quality Control Plans, and Inspection and Test
Plans
6. Quality
Control Points, Hold Points, Witness Points, Acceptance Criteria, and
Verification Requirements
7. Inspection
Methods, Testing Procedures, Sampling, Documentation, and Evidence Collection
8. Quality
Checklists, Check Sheets, Inspection Records, Defect Registers, and Quality
Documentation
9. Roles,
Responsibilities, Competence, Independence, and Accountability in Quality
Control
10. Case Study:
Developing a Quality Control System for a New Production or Construction
Process
Day
2: Measurement, Statistical Process Control, Sampling, and Process Capability
Module 2: Measurement,
Statistical Process Control, Sampling, and Process Capability
1. Measurement
Systems, Calibration, Traceability, Accuracy, Precision, and Measurement
Reliability
2. ISO
10012 Principles and Effective Measurement Management
3. Measurement
Uncertainty, Gauge Selection, Verification, and Measurement-System Controls
4. Fundamentals
of Statistical Process Control and Process Variation
5. Control
Charts, Control Limits, Specification Limits, and Interpretation of Process
Signals
6. Common-Cause
and Special-Cause Variation and Statistical Process Monitoring
7. Sampling
Methods, Sampling Risk, Acceptance Sampling, and Inspection Levels
8. Process
Capability Concepts, Cp, Cpk, Pp, Ppk, and Capability Interpretation
9. Quality
Data Collection, Histograms, Scatter Diagrams, Trend Analysis, and Data
Visualisation
10. Practical
Exercise: Analysing Quality Data and Developing a Statistical Process Control
Plan
Day
3: Defect Prevention, Nonconformity, Root Cause Analysis, and Corrective Action
Module 3: Defect
Prevention, Nonconformity, Root Cause Analysis, and Corrective Action
1. Defects,
Deviations, Nonconformities, Failures, and Quality Losses
2. Nonconformity
Identification, Classification, Reporting, Containment, and Disposition
3. Nonconformity
Reports, Corrective Action Requests, Deviation Records, and Quality Escalation
4. Root
Cause Analysis Using Five Whys, Fishbone Diagrams, Pareto Analysis, and Fault
Investigation
5. Failure
Mode and Effects Analysis (FMEA) for Quality Risk Identification and Defect
Prevention
6. Corrective
Action, Preventive Action, Action Ownership, Deadlines, and Effectiveness
Verification
7. Rework,
Repair, Scrap, Concession, Waiver, and Product or Process Disposition
8. Customer
Complaints, Quality Incidents, Warranty Issues, and Feedback Analysis
9. Cost
of Quality, Cost of Poor Quality, Rework, Scrap, Waste, and Quality-Related
Losses
10. Case Study:
Investigating a Recurring Defect and Developing an Effective Corrective Action
Programme
Day
4: Supplier Quality, Auditing, Risk-Based Control, and Quality Performance
Module 4: Supplier Quality,
Auditing, Risk-Based Control, and Quality Performance
1. Supplier
Quality Management and Quality Requirements for Purchased Materials and
Services
2. Incoming
Inspection, Supplier Certificates, Material Verification, and Acceptance
Controls
3. Supplier
Performance Monitoring, Supplier Audits, Corrective Actions, and Quality
Improvement
4. Risk-Based
Quality Control and Process Risk Assessment
5. Control
Plans, Critical Quality Characteristics, Critical Control Points, and Process
Controls
6. Internal
Quality Auditing and ISO 19011 Audit Principles
7. Audit
Planning, Evidence Collection, Findings, Nonconformities, and Follow-Up Actions
8. Quality
KPIs, Defect Rates, First-Pass Yield, Rework, Scrap, Customer Complaints, and
Trends
9. Quality
Dashboards, Management Reporting, Quality Reviews, and Escalation Mechanisms
10. Practical
Simulation: Conducting a Quality Inspection, Identifying Nonconformities, and
Preparing an Audit-Based Corrective Action Report
Day
5: Advanced Quality Control, Digital Quality Management, and Continuous
Improvement
Module 5: Advanced Quality
Control, Digital Quality Management, and Continuous Improvement
1. Advanced
Quality Control Strategies for Complex and High-Risk Processes
2. Digital
Quality Management Systems, Electronic Inspection Records, and Automated Data
Capture
3. Quality
Analytics, Automated Monitoring, Predictive Quality, and Data-Driven
Decision-Making
4. Lean
Quality Management, Waste Reduction, Standard Work, and Defect Prevention
5. Continuous
Improvement Using PDCA, Kaizen, Six Sigma Principles, and Structured
Improvement Projects
6. Advanced
Process Capability, Quality Trends, Early-Warning Indicators, and Process
Optimisation
7. Quality
Risk Management, FMEA, Control Strategy, and Preventive Quality Planning
8. Building
a Quality Culture Through Leadership, Employee Involvement, Competence, and
Accountability
9. Integrated
Case Study: Developing an Enterprise Quality Control Improvement Strategy for a
High-Defect Operation
10. Final
Quality Control Simulation, Quality Improvement Plan, Presentation, Feedback,
and Workplace Implementation Strategy


