Total Quality Management (TQM)
Total Quality Management (TQM)
Total Quality Management (TQM)
In each different people, the quality definition is varied and some might say that quality
definition refers to ‘conformance to specification’ and others ‘fitness for use’. As we see it
there is no definite definition of quality. TQM is defined as an integrated effort designed to
improve quality performance at every level. The main concept of TQM is to meet the quality
expectation of customer. TQM is a management style that implies non-stop process of quality
improvement of products, processes and personnel work. This is a bunch of methodologies
that drive company to strategic goals achievement through unceasing quality development. It
is focused on production of goods and services that possess high-quality from viewpoint of
customers. TQM was elaborated on basis of Edward Deming's theory. W. Edwards Demings
defines Total Quality Management as a philosophy which advocates four basic principles:
Quality management is concerned with controlling activities with the aim of ensuring that
products and services are fit for their purpose and meets the specifications. TQM recognizes
that all businesses require "processes" that enable customer requirements to be met. Process
in this case refers to the management of resources and activities to produce the product or
service. TQM focuses on the ways in which these processes can be managed with two main
objectives which is, total customer satisfaction and zero defects. In order to achieve these
objectives, a set of concepts is developed to ensure the objectives met.
Concept Main Ideas
Customer focus Goal is to identify and meet customer needs.
Continuous improvement A philosophy of never-ending improvement.
Employee empowerment Employees are expected to seek out, identify, and correct quality
problems.
Use of quality tools On-going employee training in the use of quality tools.
Product design Products need to be designed to meet customer expectations.
Process management Quality should be built into process; sources of quality problems
should be identified and corrected.
Managing supplier quality Quality concepts must extend to a company’s supplies.
TPM is a method, which involves total participation on all levels and functions in an
organization in order to raise overall effectiveness of equipment used in the production. TPM
could be considered as result of Preventive Maintenance (PM) and TQM combination
because major elements of TPM are employees, processes, and equipment. In manufacturing
industries, TPM is one of the very important factory maintenance methodologies that are used
throughout a product life cycle that try to optimize the effective use of production
installation. TPM seeks to engage all levels and functions in an organization to maximize the
overall effectiveness of production equipment. This method further tunes up existing
processes and equipment by reducing mistakes and accidents. The goal is total elimination of
all losses, idling and minor stoppages, reduced speed, defects and rework, spills and process
upset conditions, and starts up and yield losses. The main goals of TPM are zero equipment
breakdown and zero product defects, which lead to improved utilization of production assets
and plant capacity.
The 8 pillars of TPM to eliminate waste (MUDA):
7. Safety, hygiene, and environment: for achieving zero work-related accidents and for
protecting the environment.
8. Office TPM: for involvement of all parties to TPM since office processes can be improved
in a similar manner as well
Advantages of VSM:
The use of VSM can help to map out the process cycle times, down times, in-process
inventory, material movement, and information flow path. From this information, a new
improved VSM can be developed and implementation of improved VSM can lead to desired
change in manufacturing techniques and programs such as JIT, 5S, Kanban, and
manufacturing cells can be planned to reduced and eliminate waste.
Process Activity Mapping
SMED
In production management, SMED stands for Single Minute Exchange of Die: tool change
(few) minutes. This concept introduces the idea that any change in general machine or
initialization process should take no more than 10 minutes, hence the phrase single minute
(minute express the single digits). Means for tool change time from the manufacture of the
last piece of a series valid until obtaining the correct part of the first series following, not only
the time of change and physical adjustments in the machinery. There are two types of setup:
2. External times: Applies to operations performed (or can be) with the machine running, or
during the production period.
Internal and external setup
In traditional settings, the internal and external setup is mixed. It is a preliminary phase,
where, what could be converted from external setup to internal setup are made. It is necessary
to study in detail the real conditions of the machine. A good approximation is a continuous
analysis of production with a stopwatch. A more efficient way is to use one or more video
cameras whose footage will be analysed in the presence of the same workers.
It is the first stage of the SMED method, and is the most important distinction between
internal and external setup.
The goal is to transform the external internal setups, therefore allowing the running of the
equipment as long as necessary. It is essential here to perform a detailed chronological list of
the operations that are performed during the machine stopped. It is therefore advisable to
monitor operations in at least 10 different batches/ sample. Then be evaluated in detail of the
operations to determine which can be moved and simplified.
3rd Stage: Evaluation of all aspects of the setting operation
The objective of this stage is to further minimize time settings. Though the conversion of
setup can save time by reducing external setup, the settings can be evaluated to further reduce
changeover time. This is done by relating and study the previous case with the new setup to
determine the reduced time achieved of the new setup method compared to the days before
the proposed and validate against them with at least 10 different batches/ sample.