Certified Internal Quality Auditor - ISO9001:2015 - English

Globally recognized and accredited Online Training and Certification course on Certified Internal Quality Auditor - ISO9001:2015 

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Language: English

Instructors: Aryan Viswakarma

Validity Period: 365 days

$520 50% OFF

$260

Why this course?

Description

Course: Internal Quality Auditor (IQA)

Course Duration: 24 hrs

Applicable Standard: ISO9001:2015 and ISO19011:2018

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) and report on the effective implementation and maintenance of the management system in accordance with the standard.

Prerequisites

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

  1. A 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.
  • Learners need to appear for the final test within 12 months of purchasing the course. Course access will remain till the access period as per the applicability.
  • *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.
  • Learners can clear their doubts arising during the study within 06 months from the date of purchasing the course.
  • 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 ISO9001, ISO14001 Certified, IAO Accredited and GOI registered organization for Consultancy, Training, Project Management and Certification purposes.

  • 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 info@qualityhubindia.com /qhi2017@gmail.com 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, 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 info@qualityhubindia.com /qhi2017@gmail.com

*Prices may change at any time without prior notice.

REQUEST FOR COURSE VALIDITY EXTENSION

  • STEP 1 - Select the validity period for a course extension
  • STEP 2 - Pay and Share screenshot on Mail: qhi2017@gmail.com

    

You can also pay by scanning a QR code. Kindly share screenshot on mail at qhi2017@gmail.com with full details after payment (Name, Email id, Contact No. and Course Name)

Course Curriculum

Intro to Quality HUB India
Welcome and Study Instruction (English)
Quality HUB India "THE BEST Online Learning Platform of 2022" award by Business Connect Magazine
Section 01 : Introduction to Quality Management System
(P1)Why QMS and Benefits ? (English)
(P2) How to implement QMS (English)
(P3) Process and Process Approach (English)
(P4)Difference between ISO9001-2008 and ISO9001 - 2015 (English)
(P5) PDCA Cycle in ISO9001 (English)
(P6)Different Terminologies Old Vs New (English)
(P7) Quality Management Principles Old Vs New (English)
(P8) Development of ISO and Risk Based Thinking (English)
Levels of Documents (English)
Benefits of Implementing QMS ISO13485 (Medical Devices) (English)
Section 02 : Understanding ISO9001:2015 Clauses
QMS -ISO9001 Scope-Clause 1.0 (English)
QMS - ISO9001 Normative References - Clause 2.0 (English)
ISO9001- Context of the Organization- Clause 4.0 (English)
QMS -ISO9001 - Leadership Clause 5.0 (English)
ISO 9001-Clause 5.2 and 5.3 (Policy and Organizational Roles) (English)
QMS - ISO 9001 -Clause 6.0 (Planning)- (English)
QMS - ISO9001 -Clause 7.0 (Support)- (English)
Clause 7.1.5 ISO9001 (English)
Clause 7.1.6 to 7.2 ISO9001 (English)
Clause 7.3 to 7.5 (ISO9001) English
QMS -ISO9001- Clause 8.1-8.2 (Operational Planning)- (English)
QMS- ISO9001- Clause 8.3 -8.4 (Design and Development) (English)
ISO9001- Clause 8.5 -8.7 (Production and Service Provision)- (English)
QMS -ISO9001-Clause 9.0 (Performance Evaluation)- (English)
QMS -ISO9001 -Clause 10 (Improvement)-(English)
Section 03 : Clause 3 (Terms and Definitions)
ISO9001- Clause 3 (Terms and Definitions) - (Part1)
ISO9001- Clause 3 (Terms and Definitions) - (Part2) (English)
Section 04 : Risk Assessment Methods and Case Studies
Risk Assessment- Methods and Criteria (English)
Risk Assessment (Common at Organization Level) (English)
Risk assessment (Case Study)- Production (English)
Section 05 :QMS Support Modules
Quality Management System 'Applicability' or Clause Exclusions (English)
QMS Document Control Matrix (English)
Difference between Repair and Rework (English)
What is a "Turtle Diagram" and How to use it? (English)
Types of Processes: COP, MOP and SOP (English)
Quality Objective Tracker System - English
Difference between 'System' and 'Process' (English)
What is an Audit? Types of System Audits (English)
Important Audit Terms and Definitions (English)
Document VS Record (English)
Contingency Plan
What is Contingency Plan and QMS requirement? (English)
Contingency Plan (Case study) - English
Various aspects pertaining to Management Representative (MR)
(P2) Skill, Exp, Challenges for Management Representative(MR) (English)
(P1) Roles and Responsibilities of an Management Representative(MR) (English)
Management Review Meeting (MRM)
(P1) Management Review Meeting(English)
(P2) Management Review Meeting(English)
Process Audit
What is Process Audit and why it is important? (English)
Process Audit Plan - A sample (English)
Process Audit Check Sheet (Case Study) - (English)
Section 06 : ISO19011:2018 - Guideline for Conducting Audit
ISO19011 - Clause 1 (SCOPE) and 2 (NORMATIVE REFERENCE)-(English)
ISO19011- Clause 3 (Terms and Definitions) - (Part1) - (English)
ISO19011- Clause 3 (Terms and Definitions) - (Part2) (English)
ISO19011- Clause 4 (Principles of Auditing)-(English)
ISO19011- Clause 5 (Managing an Audit Program)-(English)
Internal Audit Schedule-(English)
ISO19011- Clause6(Part1) - Performing an Audit -(English)
ISO19011- Clause 6 (Part2)- Audit Check List -(English)
ISO19011- Clause6(Part1) - Performing an Audit -(English)
ISO19011-Clause 6- Interviewing Technique -(English)
ISO19011-Clause6 -Conducting the audit-(English)
ISO19011- Clause 6.4.2- Third Party Opening Meeting -(English)
ISO19011-Clause 6.4.7-Collecting Information -(English)
ISO19011- Clause 6.4.8 (Generating Audit Findings)-(English)
ISO19011- Clause 6 (Audit Reporting) -(English)
ISO19011- Clause 6 ( NC Reports) -(English)
ISO19011- Clause 6 - Closing of Audit-(English)
ISO19011- Clause 7 (Part1)-(English)
ISO19011- Clause 7 (Control of Audit)-(English)
ISO19011- Clause 7.2.4 (Auditor Competency) -(English)
Skills and Traits of Auditor (English)
Section 07 : NC Report Writing
Content of NC Report (English)
NC Report Writing (Case Study) (Part 1) - English
NC Report Writing (Case Study) (Part 3) - English
NC Report Case Study (17 cases) - English
Third Party NC report writing (Case Study) (Part 1) - (English)
Third Party NC report writing (Case Study) (Part 2) - (English)
Major NC Vs Minor NC VS OFI (English)
Flow of Non Conformity Closure in an Audit (English)
10 Steps for Non Conformity Closure in an Audit (English)
Section 08 : 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_
Internal Quality Auditor - Practice Test
Section A - Multiple Choice Questions
Section B: Descriptive (Short answer type questions)
Section C: Descriptive answer type questions
Section D: NC Report Writing
Section 09: E-Books, Format, Template & Check sheet (QMS , EMS & OHSAS)
ISO_9001_2015 pdf
ISO 9001_ 2015 in Plain English
ISO 9001-2015 Checklist
Process Audit Check Sheet_V0
Doc Control Matrix_QHI.pdf
Recommended Next Courses for Carrier Growth
Confirmation for Final Test
Registration Form

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