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Globally recognised and accredited Online Training and Certification course on Internal Quality Auditor - ISO9001:2015 and/or IATF16949:2016
5.0 (563 ratings)
Language: Hindi
Instructors: Aryan Viswakarma
Validity Period: 365 days
Why this course?
Course: Internal Quality Auditor (IQA)
Course Duration: 24 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.
Prerequisites
It is recommended that all students have the following prior knowledge:
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
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.
Copying, Selling, or Harming videos-
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
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
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)
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 | |||
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 | |||
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Confirmation for Final Test | |||
Registration Form |
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