Industrial Control Panel Manufacturing: The Process of Quality
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Many articles list what to look for in a quality industrial control panel, but few mention how that quality is ensured for every control panel when 1,000 identical panels are being manufactured. Ensuring quality in orders of ten to twenty panels is vastly different from orders of 500 or more. In industrial control panel manufacturing, maintaining consistent quality across large orders requires a process of quality in 5 key areas:
These 5 areas should be part of an established Quality Management System, or QMS. This article describes what to look for in each area to assess an industrial control panel manufacturer’s process of quality.
Quality Doesn’t “Just Happen” in Control Panel Manufacturing
For customers assessing control panel manufacturers, all suppliers may seem similar. They are all control panel experts who build panels every day - so quality just happens, right?
Although it may seem that way, manufacturing large orders of 1,000 or more industrial control panels is very different from building orders of ten to twenty custom panels. For small custom orders, control panel shops can rely on veteran employees who review every detail of each panel to ensure quality. However, for orders of more than 30 panels, this type of review is no longer feasible.
Ensuring quality in orders of 10 to 20 panels is vastly different from orders of 500 or more. In industrial control panel manufacturing, maintaining consistent quality across large orders requires a well-established process of quality.
So, if the experts can’t review every panel in large orders, how can quality be ensured for each panel? Achieving a process of quality for control panel manufacturing requires the development of a Quality Management System.
A Quality Management System Specifies the Entire Process
According to the American Society for Quality, a Quality Management System is
"a formalized system that documents processes, procedures, and responsibilities for achieving quality policies and objectives. A QMS helps coordinate and direct an organization’s activities to meet customer and regulatory requirements and improve its effectiveness and efficiency on a continuous basis."
For a QMS to be effective, the manufacturer must develop written procedures and store them in an accessible location. In addition, manufacturers must complete regular internal audits to assess the effectiveness of each procedure. Records of each audit must be maintained.
For failures in any area of an audit, the responsible department must generate a Corrective Action Report describing the actions required to fix the problem. Employees in that department must complete the Corrective Actions and update the original procedure, or create a new procedure. The manufacturer must then test the new procedure to ensure it resolves the problem.
The Process of Quality for Control Panel Manufacturing: 5 Key Areas
To ensure consistent quality across large and highly variable orders, as part of their QMS suppliers must have a well-established internal process of quality in risk management, document control, change management, internal audits, and nonconformance handling.
These areas are especially important since many control panel manufacturers are smaller than the companies that outsource to them. To meet the manufacturing quality standards of large companies, control panel manufacturers must have documented and continuously improved processes in the form of a QMS. All employees must consistently follow the system.
Risk Management
In industrial control panel manufacturing, risk mitigation strategies become even more important as the volume of customer panels increases. The following sections describe five areas in which manufacturers can reduce risk in the control panel manufacturing process.
Risk mitigation is crucial when manufacturing industrial control panels in volume. Therefore, manufacturers should have multiple risk management strategies in place as part of their Quality Management System.
Consider the following when assessing a supplier’s level of risk management:
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Document Control
Since a Quality Management System requires written documents and records, how should manufacturers create, organize, and manage these documents?
The supplier should have a clear, written procedure guiding the creation, organization, and storage of documents. The procedure should make it easy for all employees to find the information they need by facilitating consistent document numbering and storage as well as a consistent way of organizing information.
The following questions can help you assess a supplier’s Document Control system:
Change Management
To manage and track customer requests to change a control panel order, it is important that the panel manufacturer has a controlled and scalable process to manage changes while still ensuring quality.
The supplier’s process becomes even more important if a customer needs to change an order that is already in process.
Since situations may arise that require changes to in-process orders, it is important to evaluate potential suppliers in this area. In-process changes may be beyond the scope of the manufacturing contract in place, so a supplier may not be obligated to make changes.
Therefore, it is important to understand the supplier’s customer service culture. Suppliers with a strong focus on customer service are more likely to go above and beyond to truly help a customer find a solution even in situations that are outside the scope of the contract.
Evaluate the following to assess a supplier's process and customer service focus:
Internal Audits
Maintaining a process of quality in industrial control panel manufacturing requires a commitment to continuous improvement. Conducting regular internal audits is an important part of this commitment.
Consider the following questions to help you evaluate a supplier’s level of commitment:
Nonconformance Handling
Nonconformances for control panel manufacturers are typically defined as any failure to meet customer specifications or documented internal processes.
Corrective Action Reports are investigations carried out internally to determine the source of a nonconformance.
Corrective Actions are reactions to a nonconformance, dictated by a corrective action report, and intended to fix the root cause and/or modify a process or processes so that the cause is monitored to prevent a reoccurrence. ?
The questions below can help you evaluate a supplier’s commitment to addressing nonconformances:
Panel Manufacturing Quality Process: Conclusion
To ensure quality and consistency in the manufacturing of large volumes of industrial control panels, manufacturers must develop a quality process that the company regularly audits and improves. The presence of this process is a key area that differentiates control panel manufacturers from panel shops.
Consider assessing potential manufacturing partners based on their process of quality in risk management, document control, change management, internal audits, and nonconformance handling. Decide whether suppliers fit your outsourcing needs based on their assessment score.