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In order to obtain an accurate picture of the dependability of a potential supplier, the vast majority of importers choose to conduct audits at the physical location of the supplier. It is possible that you are conducting an audit of:
Excellence
Processes & systems
With the assistance of these audits, you will have a better understanding of how capable your potential supplier is of meeting your expectations and how trustworthy you can consider them to be if you choose to do business with them. If you choose to do business with them, you will also have a better understanding of how trustworthy they are.
The question that needs to be asked is whether or not you are one hundred percent confident that the supplier will be able to do a good job and that they can be trusted with both your orders and your money. If you are not, then the question needs to be asked. The question that needs to be asked is whether or not you are one hundred percent confident that the supplier will be able to do a good job if you do not get an in-depth understanding of the capabilities, systems, adherence to the law, and safeguards that the supplier possesses.
In this piece, I'd like to compare and contrast what are known as traditional quality inspection services management system audits based on ISO 9001 with what I refer to as process-specific audits. Traditional 3D Laser Scanning Services management system audits are based on the quality inspection services management standard ISO 9001. To begin, I'll be contrasting and comparing what are known as traditional quality management system audits based on ISO 9001 with other types of quality management system audits.
[color= rgb(49, 133, 155)]1. Tests to Determine the Overall Level of Quality[/color]
In order to simplify the process of producing the checklist, we gave it a broad scope and made it flexible enough to be applied to any kind of procedure.
In this episode of the podcast, we discuss inspections companies assurance inspections in great depth. We cover a wide range of topics, some of which are listed below:
The following components of a quality control management system are going to be scrutinized by the auditor to determine whether or not they are in place:
Are the necessary checks that need to be performed on the inputs being performed?
Is there an adequate amount of management to ensure that the process continues to run smoothly?
Are the outputs subjected to an adequate level of checking and validation before being made public?
To what degree does the gauge's calibration, in addition to the calibration of the other checking instruments, guarantee accuracy?
Etc.(I had previously compiled a list of the most common checkpoints, and you can find that list here; it can also be found here.)Using this method, it is possible to find manufacturers who are disorganized and lacking in organizational skills.
As a consequence of this, there is a substantial amount of value to be obtained by inquiring about these matters.
Why is it that this particular kind of audit is practically always considered to be the standard?
The following justifications come to mind:
A sensible action to take is to recruit quality auditors who are able to inspect any facet of a manufacturing facility's operations and then train those auditors. These quality auditors are highly knowledgeable in a broad range of subject matters. That is the recommendation made to the people who have hired the third-party agencies as a service by each and every one of those agencies.
The fact that every single one of the checkpoints is, in one way or another, derived from the ISO 9001 standard gives the impression that there is absolutely no subjectivity involved in the process at all.
Drawbacks
Quality auditors, for the most part, have only a surface-level understanding of the manufacturing processes they are tasked with examining. This is true of the vast majority of quality inspection auditing jobs. Because they concentrate the vast majority of their auditing efforts on the areas surrounding and connecting the processes, it is highly likely that a substantial number of problems will go unnoticed.
Ingenious factories are able to script a visit and use it to their advantage in order to gain an advantage when working with a lax auditor. This is done in order to gain an advantage. If the customer so desires, this type of service has the potential to swiftly transform into a document check in a meeting room rather than an inquisitive tour of the factory.
The findings, in many instances, lead to solutions that are geared toward increasing the size of the supplier inspection services department. Case in point: Case in point:The addition of additional controllers at each and every stage of production, as well as additional engineers to prepare procedures, etc., is one of these potential solutions. There are also other potential solutions. And because of this, there is a problem that needs to be fixed. Because the owners and managers of Chinese factories are notoriously price-conscious, they almost never accept suggestions of this kind. This is a direct consequence of the fact that Chinese factories are notoriously cheap.
[color= rgb(49, 133, 155)]2. Inspections and Detailed Analyses of the Working Procedures[/color]
In order for the auditor to be able to provide this kind of service, they need to have hands-on experience with the process that is being questioned, and they need to work off of a checklist that outlines the primary risks that need to be evaluated. In addition, the auditor needs to work off of a checklist that outlines the primary risks that need to be evaluated.
It is helpful in catching factories that are not well organized because it also includes checkpoints related to the Social Compliance Audit system. On the other hand, it enables the auditor to catch the following as well:
There is a problem with factories that do not know what they are doing (for example, having jigs that allow operators to place a part in the wrong position or having a so-called engineer who does not know the melting temperature of the polymers that are most commonly used in manufacturing), and this is a problem for the manufacturing industry as a whole.
It is in everyone's best interest to steer clear of manufacturing facilities that routinely engage in activities that are detrimental to the third party audit company of the products they produce (for example, making use of recycled material for plastic injection molding or skipping steps while setting up). It is in everyone's best interest to steer clear of manufacturing facilities that routinely engage in activities that are detrimental to the cmm inspection services of the products they produce.
Problems are more likely to occur in manufacturing facilities that do not pay sufficient attention to the long-term stability and reliability of their production processes (for example, by having maintenance programs that are not suitable for their needs or by operating their machines at speeds that are inappropriately high for their needs). This can lead to an increase in the likelihood that problems will occur in the facility.