Factory Audits & Quality Inspections During & Post COVID-19: On-site Supplier Audits + Remote Participations by International Buyers (Ⅱ) (Continued from the last issue)
Understand the history and current status of the supplier's QMS ● If the supplier is a manufacturer in the automotive supply chain, it must obtain the third party certification of IATF16949:2016 for its QMS. The real purpose for the supplier to be certified to IATF16949 is to ensure the QMS can provide continuous improvement, emphasize defect prevention, and reduce deviation and waste in the automotive supply chain. It also avoids multi-party certifications, providing a general QMS for the automotive industry. And it checks whether the customer specific QMS requirements are effectively implemented. If the supplier cannot be certified to ITAF16949:2016, it will also mean that the supplier will lose its supplier qualification. Therefore, for the suppliers who have passed the third-party certification, obtained the ITAF16949:2016 QMS certification and met the requirements of ITAF16949:2016 QMS standard, a second-party audit can still be conducted at an appropriate time or waived; For those who have the certification only but fail to implement or just partially implement the IATF16949:2016 standard in the operations, a second-party audit should be carried out.
● For suppliers who have not passed the third party ISO9001:2015 QMS certification, a second-party audit of the supplier should be conducted using the ISO9001:2015 standard.
● For suppliers who have passed the ISO9001:2015 QMS audit but not the third-party IATF16949:2016 QMS certification, a second-party supplier audit should be conducted according to the IATF16949:2016 standard.
● For suppliers not in the automotive supply chain, they are required to meet the standard of ISO9001:2015.
Evaluate the suppliers' potential internal and external risks The greater the changes of the suppliers’ internal and external environment, the higher the potential risks. In this case, we should increase the frequency of audit to ensure that the risk can be effectively controlled.
Assess the suppliers' performance evaluation results The audit frequency could be determined based on the performance evaluation of suppliers. For suppliers with poor performance, the audit frequency should be increased. For suppliers with good performance evaluations, the audit can be waived or carried out according to the annual audit plan.
Evaluate the importance of the suppliers’ product and process control For suppliers producing very important products and with higher requirements for product realization process control, the audit frequency should be increased, especially for the products with higher safety requirements on vehicles.
▌Determine the audit details
Audit plan The audit plan is the result of planning the specific audit activities according to the customer's requirements, which should usually be documented; The details of the audit plan are related to the scope and complexity of the audit. The contents usually include audit purpose, audit criteria, audit scope, audit team members and audit activity arrangement.
The audit plan is usually prepared by the audit team leader and submitted to the customer for approval before the audit can be implemented.
Types of audit
The audit types mainly include: QMS audit, manufacturing process audit and product audit. The QMS is a required and systematic quality management model established within the organization, which is based on the organization’s strategic decision. Combining resources and processes, it is a systematic management based on process management methodology, where key parts of the QMS based on the characteristics of the company are integrated, generally covering processes of management activities, resource provision, product realization, measurement, analysis and improvement activities. This system covers the entire process of planning, implementation, monitoring, correction and improvement for the determination of customer requirements, design and development, production, inspection, sales, and pre-delivery. The QMS is generally documented and becomes the requirements of the organization's internal quality management.
For suppliers with third-party certified management system certificate and basically meets the requirements of IATF16949:2016 standard, we can also undertake second-party system audit. (To be continued) |