π Who Should Attend?
- Quality Engineers & Quality Executives
- Management Representatives (MR)
- QA/QC Professionals
- Production & Process Engineers
- Internal Auditors
- Anyone preparing for Quality Manager roles
Module 1 β Fundamentals of Management Systems
- What is IMS (Integrated Management System)
- Overview of ISO 9001, IATF 16949
- Process Approach & Risk-Based Thinking
- PDCA Cycle
- High Level Structure (HLS)
Module 2 β ISO 9001:2015 Requirements
- Context of the Organization (Clause 4)
- Leadership & Commitment (Clause 5)
- Planning & Risk Management (Clause 6)
- Support Processes (HR, Training, Communication, Documentation) β Clause 7
- Operation Control β Clause 8
- Performance Evaluation β Clause 9
- Improvement β Clause 10
Module 3 β IATF 16949:2016 (Automotive QMS)
- IATF Structure & Automotive Approach
- Customer-Specific Requirements (CSR)
- Product Safety & Traceability
- Contingency Planning
- Warranty Management
- Supplier Development & Monitoring
Module 4 β Documentation & MR Responsibilities
- Quality Manual & Policy
- SOPs, Work Instructions, Formats
- Document Control & Record Control
- Role of MR (Management Representative)
- Handling Certification Body Audits
Module 5 β Internal Audit System
- ISO 19011 Guidelines
- Audit Planning & Audit Program
- Process Audit & System Audit
- Audit Checklist Preparation
- Audit Reporting & NCR Writing
- Corrective Action & Effectiveness Check
Module 6 β Risk Management & Opportunities
- Risk Identification Methods
- SWOT & Turtle diagram in QMS
- Risk Register Preparation
- Preventive Action System
Module 7 β KPI & Performance Monitoring
- Setting Quality Objectives
- Department-wise KPIs
- Data Analysis Tools
- Management Review Meeting (MRM) Inputs & Outputs
Module 8 β Nonconformity & Corrective Action
- NCR Handling
- Root Cause Analysis (5 Why, Fishbone)
- CAPA System
- Continual Improvement Methods
Module 9 β Customer Focus & Complaint Handling
- Customer Satisfaction Monitoring
- Complaint Handling System
- 8D Problem Solving
- Cost of Poor Quality (COPQ)
Module 10 β Certification & External Audits
- Stage 1 & Stage 2 Audit Process
- Surveillance & Re-certification Audits
- How to face Auditor Questions
- Common Audit Nonconformities
Module 11 Bonus Practical Sessions
β Live documentation examples
β Audit role-play
β KPI dashboard preparation
β NCR & CAPA case studies
β Core Tools sample formats
π Key Benefits
β Become job-ready for Quality Manager / MR roles
β Understand complete ISO & IATF system implementation
β Gain confidence to face external audits
β Improve problem-solving & risk management skills
β Get practical knowledge, not just theory
π Certification
Participants will receive a Course Completion Certificate after successful training.
π― Quality Manager / MR β Important Interview Questions
πΉ IMS & ISO Basics
- What is an Integrated Management System (IMS)?
- Explain the PDCA cycle with an example from your company.
- What is Risk-Based Thinking in ISO 9001?
- What is the High-Level Structure (HLS)?
- Difference between Quality Assurance and Quality Control?
πΉ ISO 9001:2015 Questions
- What are the main clauses of ISO 9001:2015?
- What is meant by βContext of the Organizationβ?
- How do you identify interested parties?
- What is the role of leadership in ISO 9001?
- What are quality objectives? Give examples.
- What is documented information?
- Difference between document and record?
- How do you control external providers?
- What is operational control?
- What are the inputs and outputs of Management Review Meeting (MRM)?
- What is continual improvement?
- What is the difference between correction and corrective action?
πΉ IATF 16949 Questions
- What is the difference between ISO 9001 and IATF 16949?
- What are Customer Specific Requirements (CSR)?
- Explain product safety requirements in IATF.
- What is contingency planning?
- What is traceability and why is it important?
- What is layered process audit (LPA)?
- What is warranty management?
πΉ Core Tools (Automotive)
- What is APQP and its phases?
- What is PPAP? When is it required?
- What is FMEA? Difference between DFMEA & PFMEA?
- What is Control Plan?
- What is MSA? Types of MSA studies?
- What is SPC? What are control charts?
πΉ MR (Management Representative) Role
- What are the responsibilities of an MR?
- How do you ensure the QMS is maintained?
- How do you report QMS performance to top management?
- How do you prepare for a certification audit?
- How do you handle an auditorβs nonconformity?
πΉ Internal Audit
- What is the purpose of an internal audit?
- Difference between system audit and process audit?
- How do you prepare an audit checklist?
- What is an audit finding?
- Difference between Major and Minor NCR?
- What is audit evidence?
πΉ Risk & Improvement
- How do you identify risks in a process?
- What tools are used for root cause analysis?
- Explain 5 Why analysis with an example.
- What is CAPA?
- What is preventive action in ISO 9001?
πΉ Customer & Problem Solving
- How do you handle a customer complaint?
- What is 8D methodology?
- What is Cost of Poor Quality (COPQ)?
- How do you measure customer satisfaction?
πΉ KPI & Performance Monitoring
- What KPIs are used in the Quality department?
- How do you analyze quality data?
- What is trend analysis?
- How do you present data in MRM?
πΉ Audit Situational Questions
- If an operator is not following SOP, what will you do?
- Auditor found records missing β how will you respond?
- Customer complaint increased suddenly β your action plan?
- Rejection rate increased in production β how will you investigate?
- Supplier quality is poor β how will you control it?