Auditors begin training sessions 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 edition of ISO 9001:2015, and revisions were made to the previous version based on the customer's specific requirements.
Regarding the new standard: The first edition of IATF16949:2016 will replace the third edition of ISO/TS16949. The goal of developing this new standard is to further develop and improve the quality management system in the automotive industry, to achieve continuous improvement, emphasize defect prevention, and reduce variation and waste in the supply chain.
This course integrates the structure of the new ISO9001:2015 edition, explaining the elements and standards of IATF16949:2016, with the latest recognized interpretations of SI for clarification, meeting certification audit and customer audit requirements. 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 aligned 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 is to help learners understand the new edition requirements internally and prepare for 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 integrates the requirements of the enterprise's new version transition process, explains the elements and standards of IATF 16949:2016, and systematically elaborates on how to address and meet the new version requirements. By attending the training, participants gain an understanding of standard requirements and practices, preparing them to undertake internal revision work or to enhance their operations for those who have already completed the transition but need further improvement. It also equips individuals and companies with the knowledge to handle external audits from second and third parties.
[Part One]
1. Your standard
2. IATF 16949 Overview
3. Understanding and Application of Process Methods and Risk-Based Thinking Patterns
Part Two: Standard Layout
1 Standard 4-5-6 Sections Description
1) Framework and Logical Relationship
2) How to Plan a Comprehensive Quality Management System
3) Writing of 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 Objective Management)
8) How to Plan a Management Process That Meets IATF 16949 Regulations
9) Product Safety Management Process, integrated with Special Characteristics Management
10) New Edition on How to Implement Emergency Plans
Section 7 Standards Description
1) Resource Management Framework Description
2) Human Resource Management Requirements Description
3) Position Requirements and Allocation
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 planning and feasibility for manufacturing
9) TPM Overview
10) The differences between Preventive Maintenance, Periodic Inspection, and Predictive Maintenance
11) Explanation of OEE and equipment maintenance-related indicators
12) Industrial Mold Management Requirements Explanation
13) Requirements for Gaging and Inspection Equipment Management
14) How to Meet the New MSA Requirements
15) Requirements for Internal and External Laboratory Management
16) Overview of Environmental Safety
17) Establishment of a Knowledge Management System
18) Experience and Lessons Learned Management Description
19) Requirements for Document and Record Management
20) Explanation of the Retention Period for the New Version of Records
Chapter 8: Product Realization Section
1) Product Implementation Framework Description (Combined with APQP Framework)
2) How to Conduct a Feasibility Evaluation for New Products (in conjunction with APQP Phase I)
3) Contract Order Review Requirements
4) New Edition on Product Process Design Requirements (expanding on the second and third stages of APQP)
5) How to Conduct Product Process Confirmation (Incorporating APQP Phase 4, and PPAP)
6) Explanation of Change Management Process (Product Process Change, Temporary Change, 4M Change)
7) Supplier Management Process Overview
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) Key Points and Standard Requirements for Second-Party Supplier Audit
13) Methods and Process for Supplier Development
14) Framework for Product and Service Provision Explanation
15) Process Control Description
16) Job Preparation Verification and Shutdown Verification
17) Labeling and Traceability Requirements Explanation
18) Traceability Plan Requirements
19) Product Protection Requirements Description
20) Service Provision 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) Description 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 Description
6) Management Review Understanding
7) Improvement Description
Part Three: Exam
Exam
Over 10 people in the company? We can arrange in-house training with system-specific讲解.
Registration Methods: [Interactive Bar, WeChat, phone, QQ online, or directly visit our company for registration]
Over 10 people in the company can be arranged for on-site training, with a system-based explanation.
Training Fee: RMB 1,980 per person
(Including training, teaching materials, resources, exams, certifications, Chinese cuisine, registration, etc.)
Certification Assessment
Certified Internal Auditor certificate awarded to qualifying exam takers
