Certified Internal Quality Auditor - ISO9001:2015 and IATF16949:2016

Globally recognised and accredited Online Training and Certification course on Internal Quality Auditor - ISO9001:2015 and/or IATF16949:2016

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Language: Hindi

Instructors: Aryan Viswakarma

Validity Period: 365 days

$580 50% OFF


Why this course?


Course: Internal Quality Auditor (IQA)

Course Duration: 25 hrs

Applicable Standard: ISO9001:2015 or IATF16949:2016

Course Objectives

To provide students with the knowledge and skills required to perform an internal audit of part of a quality management system based on ISO 9001 (or equivalent) or IATF16949:2016 and report on the effective implementation and maintenance of the management system in accordance with the standard.


It is recommended that all students have the following prior knowledge:

  1. Basic knowledge of the concepts of quality management and the relationship between quality management and customer satisfaction
  2. Understand quality management terms and definitions, used by the ISO 9000 series of standards
  3. At least 1 year of industry experience

Who Should Attend?

This course is ideal for those who are responsible for internal management system audits including department managers, supervisors, quality representatives, engineers, and administrative staff who have a focus on business improvement, performance, and profitability.

Certification Exam

  • Each certification candidate is required to pass a written examination that consists of multiple choice and/or descriptive questions measuring comprehension of the Body of Knowledge.
  • The exam will be conducted online.
  • It is only offered in English.
  • The exam Should be taken within a year of the date of registration of the course.
  • *Taking an exam after one year will incur a fee*
  • After the certificate is issued, you must wait 30 days to get a hard copy of the certificate.
  • For Sample Certificate Click Here

Pass Criteria:  > 60% marks

For candidates clearing the exam successfully certificate shall be issued by Quality HUB India, which is a registered organization with GOI for training and certification courses.

  • Note: One extra opportunity will be given to unsuccessful candidates free of charge.

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PS: Please contact us at +91-8094078781 or drop a mail at [email protected] /[email protected] if you notice any unlawful activity taking place in the name of Quality Hub India.

Format, Pdf, E-books, Templates availability:

All supporting format, Pdf, E-books, and Templates as per the course requirement and within the scope, has been uploaded in the portal in the course section and downloadable.

No additional documents, formats, templates, etc shall be provided by QHI.

Policy on Cancellation and Refunds

  • The course to which you have subscribed cannot be replaced with another course.
  • It is not possible to cancel a course once it has been purchased.
  • There are no refunds for fees.
  • Courses are not transferrable.
  • Course Extension is possible. (How to seek a course extension, details are listed below)

For Technical Support-

Contact us at +91-8094078781 / 8824314500 or drop a mail at [email protected] /[email protected]

*Prices may change at any time without prior notice.


  • STEP 1 - Select the validity period for a course extension.
  • STEP 1 - Pay and Share screenshot on Mail: [email protected]


You can also pay by scanning a QR code. Kindly share screenshot on mail at [email protected] with full details after payment (Name, Email id, Contact No. and Course Name)

Course Curriculum

Welcome and Study Instruction
Intro to Quality HUB India
Course Instructions & Study Guidelines(Hindi)
QHI Certification, Accreditation, Affiliation, Membership & Collaboration (Hindi)
Mr. Aryan Viswakarma (Founder CEO QHI & NAPL) Introduction (Hindi)
QHI Awards and Recognitions (Hindi)
Quality HUB India "THE BEST Online Learning Platform of 2022" award by Business Connect Magazine
Section 1: QMS (ISO9001:2015 & IATF 16949:2016)
ISO 9001:2015 & IATF16949:2016- Introduction, Difference in clauses ISO9001 2008 vs 2015, 7QM Principles & Risk based Thinking
QMS- (C1)- QMS Requirements & Scope of ISO9001
QMS - Clause 2 (Normative Reference) - 07 min
Clause 3 (Terms and Definitions) - (Part1 - 3.1 to 3.4)Terms Related to Person or People, Organisation, Activity and Process
Clause 3 (Terms and Definitions) - Part 2 Terms related to system, Requirement and Result
Clause 3 (Terms and Definitions) _Part 3 Terms related to data, Information, document and Audit
Terms & Definitions - IATF16949 - Part1- Aftermarket, Accessory Challenge Part, Pertaining to Design and Laboratory
Terms and Definitions - IATF16949 - Part 2- Multidisciplinary Approach, Production Shutdown, Trade off curves
Documented Information Control System and Document Control Matrix (32 min)
Applicability and Exclusions in ISO9001 & IATF16949- (17 min)
What is Contingency plan - (18 min)
Contingency Plan - Case study - (15 min)
QMS Implementation Plan - Gantt Chart (19 min)
Levels of Documents (Hindi)
Clause 4,5,6 & 7
ISO 9001:2015 & IATF16949:2016 - Context of the Organisation, Leadership and Planning
ISO9001:2015 & IATF16949:2016- Resources, Awareness and Employee Motivation and Empowerment
Clause 8 Operation
Clause 8 Operation(P1) - Operations, Operational Planning and Control and Requirement for Product and Services
Clause 8 Operation(P2) -Organisation manufacturing Feasibility and Product Design
Clause 8 Operation(P3) -Manufacturing Process design input and Product Approval Process
Clause 8 Operation(P4) -Design and Development Outputs and Type and extent of control - Supplemental
Clause 8 Operation(P5) - Statutory and Regulatory Requirements and Second-Party Audits
Clause 8 Operation(P6)-Supplier Development and Standardized work- Operator Instructions and visual standards
Clause 8 Operation(P7)- Verification of job setups and Identification and Traceability
Clause 8 Operation(P8)- Property Belonging to customer or external Providers
Clause 8 Operation(P9)- Release of Product and Services
Clause 8 Operation(P10)- Control of Non Confirming Outputs
Clause 9 and 10
ISO9001:2015 & IATF16949:2016 Performance Evaluation and Improvement
Section 5: System Support Modules
Awareness on Core Tools (APQP, PPAP, MSA, SPC, FMEA) - (81 min)
Manufacturing Process Audit - Standard Requirement , Auditor Competency, Details with format (39 min)
Different NC Terms and its definitions (Hindi)
Process Audit VS Product Audit - 14 min
Management Review Meeting (MRM) – Process, formats explained with example - (22 min) -V1
Management Representative - Roles, Responsibilities etc (34 min)
Turtle Diagram - Process Mapping Technique
COP, MOP and SOP - Types of Process and its importance
Responsibility, Authority and Competency
Document vs Records (Hindi)
Section 2: Context and Risk Assessment
Context and Risk Assessment (Method & Criteria)
Context and Risk Assessment (Case Studies – Plant & Functional Level)
Section 3 : Internal Audit (ISO19011)
Internal System Audit- Module 1 – Terms and Definitions & Principles of auditing - (48 min)
Internal System Audit - Module 2 (Performing an Audit) - (30 min)
Internal System Audit - Module 3- Conducting the audit activities - (50 min)
Internal System Audit - Module 4- Audit Reporting & NC Writing - (43 min)
Internal System Audit - Module 5- Competency of a Good Auditor - (38 min)
Auditing Guideline Standard ISO19011-2018- Changes (24 min)
Major VS Minor Non Conformance (NC) - Explained with examples (22 min)
Flow of Non Conformity Closure (Hindi)
10 Steps of Non Conformity Closure (Hindi)
Section 4: QMS Audit Incidents and NC Writing (Very Important)
QMS NC Writing -Internal Audit
QMS NC Writing -Internal Audit - 2nd
Internal System Audit Process – Process & formats explained with example
QMS NC Writing - Third Party
Section 6: Clause Identification Exercise for Students:
QMS Clause Exercise (Download and identify clause reference to ISO9001 & IATF16949)
Answers to Practice Questions on QMS Clauses _ISO9001 & IATF16949_
Section 7: Direct Link Modules
ISO 9001:2015 (Latest Quality Management System)
IATF 16949 :2016 (Automotive Quality Management System) –Part 1
IATF 16949:2016 (Automotive Quality Management System) –Part 2
Rework Vs Repair (new) - 14 min
Verification Vs Validation (Hindi) .
'Audit Planning' & 'Tips for the Auditor' – Video from ‘QHI’
‘System’ VS ‘Process’ – Differences explained with example
Policy, Process and Procedure – Difference Explained
What an Audit is and Types of Audit? (Hindi). ऑडिट क्या है और कितने तरह के होते है (हिंदी में सीखे)|
'Audit Planning' & 'Tips for the Auditor' – Video from ‘QHI’
4 Phases of an Audit – How to plan audit effectively
Practice Test (IQA)
Section A - Multiple Choice Questions
Section B: Descriptive answer type questions
Section C: Descriptive answer type questions
Section D: NC Report Writing
NC Report -Clause Answers
Section 8: E-Books, Format, Template & Check sheet (QMS , EMS & OHSAS)
ISO_9001_2015 pdf
IATF 16949-2016 pdf
ISO 9001_ 2015 in Plain English
ISO 9001-2015 Checklist
Mandatory Doc & Records_IATF
Process Audit Check Sheet_V0
Doc Control Matrix_QHI.pdf
Frequently Asked Questions & Answers on IATF 16949
IQA Audit Checksheet (IATF)
Process Audit Check Sheet_V0
Recommended Next Courses for Career Growth:
Confirmation for Final Test
Registration Form

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