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IMS Internal Auditor (ISO9001:2015 / IATF16949:2016 + ISO14001:2015 + ISO45001:2018)

Globally Accredited Online Training and Certification course on IMS Internal Auditor (ISO9001, ISO 14001 & ISO45001)

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Language: Hindi

Instructors: Aryan Viswakarma

Validity Period: 1095 days

$324 12.35% OFF

$284

Why this course?

Description

Course: Internal Auditor- Integrated Management System

Course Duration: 29 hrs

Applicable Standard: ISO9001:2015 / IATF16949:2016 + ISO14001:2015 + ISO45001:2018

Course Objectives

To provide students with the knowledge and skills required to perform an internal audit of part of the management system based on ISO 9001 (or equivalent) or IATF16949:2016 or ISO14001 or ISO45001 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. Basic knowledge of the concepts of quality management and the relationship between quality management and customer satisfaction
  2. Understand management terms and definitions, used by the ISO 9000 series, ISO14001 & ISO45001 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 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 Mailqhi2017@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

Welcome and Study Instruction
Welcome and Study Instruction (03 min)
QHI ISO9001 & ISO14001 Certification + Candidate Certificate verification on QHI portal
Quality HUB India is now IAO Accredited Institution
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)
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
ISO 9001:2015 & IATF16949:2016 - Context of the Organisation, Leadership and Planning
ISO9001:2015 & IATF16949:2016- Resources, Awareness and Employee Motivation and Empowerment
ISO9001:2015 & IATF16949:2016 (Clause 8)-Operations
ISO9001:2015 & IATF16949:2016 (clause 9 and 10)Performance Evaluation and Improvement
Applicability and Exclusions in ISO9001 & IATF16949
Levels of Documents (Hindi)
Document vs Records (Hindi)
Section 1.1 : Risk Assessment Method, Criteria and Case Study
Context and Risk Assessment (Method & Criteria)
Context and Risk Assessment (Case Studies – Plant & Functional Level)
Section X: 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 1.2: System Support Modules
Awareness on Core Tools (APQP, PPAP, MSA, SPC, FMEA)
Manufacturing Process Audit - Standard Requirement , Auditor Competency, Details with format
Turtle Diagram - Process Mapping Technique
Responsibility, Authority and Competency
COP, MOP and SOP - Types of Process and its importance
Process Audit VS Product Audit
What is Contingency plan
Contingency Plan - Case study
QMS Implementation Plan - Gantt Chart
Section 2: Environment Management System (ISO14001:2015)
EMS-Score and Normative Reference (Clause 1 and 2)
Environment Management System- Terms and Definition (Clause 3.0)
Environment Management System ISO14001:2015 - (Introduction and Clause 4 to 10)
Environment, Health & Safety (EHS) – Risk Assessment Case Study
Introduction to Aspects and Impacts
Aspect-Impact Identification Tools
Aspects-Impact - Case study
Section 3: OHSAS (ISO45001:2018)
BS-ISO45001:2018 Occupational Health & Safety Management System -(Clause 6 and 7)
BS-ISO45001_Part1 (Clause 4 and 5)-Introduction, Understand the org. and Leadership and commitment
BS-ISO45001 (Clause 8,9 and 10)- Operation, Performance evaluation And Non Conformity
OHSAS Scope and Normative Reference
Risk and Uncertainty
What is Work Permit System (PTW) and 7 types of Work permits
Classification (Types) of Fire. US Vs AU Vs IS Standard
Types of Fire Extinguishers
Section 4: Modules on Auditing Guideline (ISO19011)
Internal System Audit- Module 1 – Terms and Definitions & Principles of auditing
Internal System Audit - Module 2 (Performing an Audit)
Internal System Audit - Module 3- Conducting the audit activities
Internal System Audit - Module 4- Audit Reporting & NC Writing
Internal System Audit - Module 5- Competency of a Good Auditor
Auditing Guideline Standard ISO19011-2018- Changes
Major VS Minor Non Conformance (NC) - Explained with examples
Flow of Non Conformity Closure (Hindi)
10 Steps of Non Conformity Closure (Hindi)
Audit Incidents and NC Writing (Very Important)
QMS NC Writing -Internal Audit
QMS NC Writing -Internal Audit - 2nd
QMS NC Writing - Third Party
EMS NC Report Writing
ISO45001 - NC Writing
Clause Identification Exercise for Students:
QMS Clause Exercise (Download and identify clause reference to ISO9001 & IATF16949)
EMS Clause Exercise (Identify Clause reference to ISO14001:2015)
Section 5: Others Modules for Study
Internal System Audit Process – Process & formats explained with example
Management Review Meeting (MRM) – Process, formats explained with example -V1
Different NC Terms and its definitions
Management Representative(MR) - Roles, Responsibilities etc
Direct Link Modules
Difference between Rework and Repair (new)
Verification Vs Validation (Hindi) .
'Audit Planning' & 'Tips for the Auditor' – Video from ‘QHI’
‘System’ VS ‘Process’ – Differences explained with example
Quality Management System (ISO9001:2015/ IATF16949:2016) - Practice Test
Factory Act - Practice Test
E - Books (QMS , EMS & OHSAS)
ISO_9001_2015 pdf
IATF 16949-2016 pdf
ISO 9001-2015 Checklist
Process Audit Check Sheet_V0
ISO_14001_2015 reference standard
ISO 45001-2018 reference standard
Context_Issues and Risk Assessment Criteria (EHS)
Sample EHS POLICY
Human Injury Categories
Master List of Records-EHS
Master List of Documents- EHS
IMS Audit Check Sheet
The Factories Act 1948 (reference document)
Recommended Next Courses for Carrier Growth
Confirmation for Final Test
Registration Form

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