Auditors hold classes monthly; welcome to inquire.

Course Background

IATF 16949:2016 was released on October 1, 2016. The main changes in this version are influenced by the new ISO 9001:2015 edition, and revisions were made to the previous version in line with specific customer requirements.

Regarding the new standard: The first edition of IATF 16949:2016 will replace the third edition of ISO/TS 16949. The goal of developing this new edition of the standard is to further develop and refine the quality management system in the automotive industry, achieving continuous improvement, emphasizing defect prevention, and reducing variability and waste in the supply chain.

This course aligns with the ISO9001:2015 revised structure, explains the elements and standards of IATF16949:2016, and clarifies the latest recognized interpretations with SI. It meets the requirements of certification audits and customer audits. The training will emphasize the specific management requirements and methods in the automotive industry: process approach requirements, management of customer-specific requirements, management of product-specific characteristics, traceability requirements, and the new structure consistent with ISO9001:2015, risk management requirements, management of safety-related requirements, management of embedded software products, temporary change control, NTF (No Fault Found) management requirements, supplier management and development requirements, etc. This facilitates learners in understanding the new edition requirements internally to address external audits from second and third parties.

Target Audience:

Automotive industry department heads, department managers, and in-department administrators; automotive parts manufacturers; companies that have adopted or are planning to implement the old version of TS16949; automotive industry supplier quality engineering (SQE) departments; automotive industry quality engineers; automotive manufacturing system advancement personnel; and individuals seeking to enhance their company's quality management.

Course Outline:
This course combines the requirements of the company's new version transition process, explains the elements and standards of IATF 16949:2016, and systematically elaborates on how to respond to and meet the new version requirements. Through the training, participants gain an understanding of standard requirements and practices, preparing them to undertake revision work within the company or for individuals who have completed the transition but require further improvement. It also equips them with knowledge to handle external audits from second and third-party auditors.

[Part 1]
1. Your Definition of Standard
2. IATF 16949 Overview
3. Understanding and Application of Process Methods and Risk-Based Thinking Models
[Part Two] Standard Layout
Standard Sections 4-5-6 Description
1) Framework and logical relationship
2) How to Plan a Comprehensive Quality Management System
3) Writing the Quality Manual and Precautions
4) Scope of Quality System to Be Clarified
5) Identification and Evaluation Management Process for CSR
6) Planning of Responsibilities and Authority with Cautionary Notes
7) How to Develop a Business Plan (Policy and Goal Management)
8) How to Plan Management Processes to Comply with IATF 16949 Regulations
9) Product Safety Management Process, integrated with Special Characteristic Management
10) New Edition on How to Implement Emergency Plans
Section 7 Standards Description
1) Resource Management Framework Description
2) Human Resources Management Requirements Description
3) Position Requirements & Configuration
4) Employee Training and Competency Management
5) Auditor (Internal and Second-Party) Management Requirements
6) Employee Awareness and Motivation Management
7) Equipment Management Process Description
8) Equipment feasibility planning and manufacturing exploration
9) TPM Overview
10) The differences between preventive maintenance, periodic inspections, and predictive maintenance
11) Explanation of OEE and equipment maintenance-related indicators
12) Industrial Mold Management Requirements Explanation
13) Requirements for Inspection and Measurement Equipment Management
14) How to Meet the New MSA Requirements
15) Description of Internal and External Laboratory Management Requirements
16) Environmental Safety Overview
17) Establishment of a Knowledge Management System
18) Experience/Lesson Learned Management Guidance
19) Requirements for Document and Record Management
20) Explanation of the Retention Period for the New Edition Records
Section 8: Product Realization
Product Implementation Framework Description (combined with APQP framework)
2) How to Conduct a New Product Feasibility Evaluation (in conjunction with the APQP Phase I)
3) Contract Order Review Requirements
4) New Edition on Product Process Design Requirements (Expanding on the Second and Third Phases of APQP)
5) How to Conduct Product Process Confirmation (Incorporating APQP Phase 4, and PPAP Implementation)
6) Description of Change Management Process (Product Process Change, Temporary Change, 4M Change)
7) Supplier Management Process Outline
8) How to Select Suppliers
9) How to Conduct Supplier Risk Assessment
10) Supplier System Development Requirements
11) Key Components of Supplier Performance Monitoring
12) Supplier Second Party Audit Precautions and Standard Requirements
13) Methods and Process for Supplier Development
14) Framework for Product and Service Provision
15) Process Control Description
16) Job Preparation Verification & Shutdown Verification
17) Identification and Traceability Requirements Explanation
18) Traceability Plan Requirements
19) Product Protection Requirements Explanation
20) Service Description (including warranty, after-sales failure analysis, and NTF requirements)
21) Product Release Control Instructions
22) Material Product Control and Regulatory Compliance Statement
Chapter 9-10 Description
1) Explanation of Three Monitoring Methods in the System
2) Key Requirements for Customer Satisfaction Analysis
3) Production Process Monitoring (SPC) Description
4) Requirements for KPI Monitoring
5) Internal Audit Requirements Explanation
6) Management Review Understanding
7) Improvement Description
Part 3: Exam
Exam

Companies with over 10 staff can arrange on-site training, with systematic explanations provided.

Registration Methods: [Through InteractBar, WeChat, phone, QQ online, or by directly visiting our company, etc.]

Companies with over 10 employees can arrange on-site training, with the system being explained in detail.

Training Fee: RMB 1,980 per person

(Including training, teaching materials, resources, exams, certificates, Chinese cuisine, registration, etc.)

Certification Assessment
Certification of Internal Auditor issued to those who pass the examination