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Continual_Improvement
Technical Education
Follow
7/18/2024
Continual_Improvement
Category
ЁЯУЪ
Learning
Transcript
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00:00
Continual improvement can be initiated through the use of Quality Policy, Quality Objective,
00:19
Audit Results, Analysis of Data, Corrective and Preventative Actions, and Management Review.
00:26
The requirements cover both the reactive and proactive actions of improvement.
00:34
8.5.1 Continual Improvement
00:38
Continual Improvement draws together various aspects of the QMS.
00:42
Quality Policy, Quality Objectives, Audit Results, Data Analysis, Corrective Actions,
00:50
Preventative Actions, Management Review.
00:53
The ISO 9001 requires continual improvement of the effectiveness of the QMS.
01:02
What drives Continual Improvement?
01:05
Continual Improvement is driven by the objectives set by Top Management.
01:10
As a minimum, Quality Objectives should address 1.
01:14
The improvement of internal efficiency 2.
01:18
Individual customer requirements 3.
01:21
The level of performance that your industry expects
01:25
There is no requirement that the organisation should set objectives for improvement for
01:30
all of its processes at any one time.
01:33
It would be unrealistic to expect an organisation to make progress in all potential improvements
01:39
simultaneously.
01:41
Each improvement will require the commitment of resources which should be prioritised by
01:46
Top Management, especially if investment is required.
01:53
How to identify what needs improving?
01:57
Inputs for improvement opportunities are obtained from
02:01
Customer satisfaction Customer complaints and feedback
02:05
Market research and analysis Inputs from employees, suppliers and other
02:10
interested parties Internal and external audits of the quality
02:15
system Records of product or process non-conformances
02:21
Data from process and product characteristics and their trends
02:28
Opportunities for improvement may also be identified on a special project basis.
02:33
The following are examples of such projects.
02:36
Non-value-added use of floor space Excessive inspection and testing
02:42
Excessive handling and storage Excessive failures and cost to quality
02:48
Machine set-up and change-over times The principles of continual improvement
02:55
The organisation shall establish, document, implement and maintain QMS and continually
03:02
improve its effectiveness in accordance with the requirements of the international standard.
03:08
The organisation shall Identify the processes needed for the quality
03:13
management system and their application throughout the organisation.
03:17
Determine the sequence and interaction of these processes.
03:22
Determine the criteria and methods needed that both the operation and control of these
03:27
processes are effective.
03:30
Ensure the availability of the resources and information necessary to support the operation
03:34
and monitoring of these processes.
03:38
Consider, measure and analyse these processes.
03:43
Implement actions necessary to achieve planned results and continual improvement of these
03:48
processes.
03:51
The organisation shall continually improve the effectiveness of the QMS through the use
03:56
of quality policy, quality objectives, audit results, analysis of data, corrective and
04:02
preventative actions and management review.
04:06
Continual improvement requires management support.
04:09
Top management shall provide evidence of its commitment to the development and implementation
04:13
of the QMS and continually improving its effectiveness.
04:20
Continual improvement of the effectiveness of the QMS must be included in the quality
04:24
policy.
04:26
Also, management review, which must be carried out at planned intervals, must include the
04:32
assessment of opportunities for improvement and the need for changes to the QMS, including
04:38
quality policy and quality objectives.
04:41
As to the requirements of the process, measurement, analysis and improvement, the organisation
04:47
shall plan and implement the monitoring, measurement, analysis and improvement processes needed
04:53
to demonstrate conformity to the product, to ensure conformity of the QMS and to continually
04:59
improve the effectiveness of the QMS.
05:02
This shall include determination of applicable methods, including statistical techniques
05:08
and the extent of their use.
05:13
Management should continually seek to improve the effectiveness and efficiency of the processes
05:17
of the organisation, rather than wait for problems to reveal opportunities for improvement.
05:24
Processes can range from small-step ongoing continual improvements to strategic breakthrough
05:30
improvement projects.
05:32
The organisation should have a process in place to identify and manage improvement activities
05:37
of these processes.
05:41
We have looked at the PDCA cycle and the continual improvement processes should be incorporated
05:46
into it and involve the following steps.
05:52
A process problem should be identified and an area for improvement selected, noting the
05:57
reason for working on it.
06:00
Current situation, the effectiveness and efficiency of the existing process should be evaluated.
06:06
Data to discover what type of problems occur most often should be collected and analysed.
06:13
A specific problem should be selected and an objective for improvement should be set.
06:19
The root causes of the problem should be identified and verified.
06:25
Identification of possible solutions, alternative solutions should be explored.
06:28
The best solution should be selected and implemented, i.e. the one that will eliminate the root
06:33
causes of the problem and prevent the problem from reoccurring.
06:40
Evaluation of effects.
06:41
It should then be confirmed that the problem and the root causes have been eliminated or
06:46
their effects decreased, that the solution has worked and the objective for improvement
06:51
has been met.
06:54
Implementation and standardisation of a new solution.
06:56
The old process should be replaced with the improved process, thereby preventing the problem
07:01
and its root causes from reoccurring.
07:05
Evaluation of the effectiveness and efficiency of the process with the improvement action
07:10
completed.
07:11
The effectiveness and efficiency of the improvement project should be evaluated and consideration
07:16
should be given for using its solutions elsewhere in the organisation.
07:24
So to summarise.
07:26
Continual Improvement.
07:27
This is clearly defined in the ISO 9000 clause 8.5.1, Continual Improvement.
07:34
Normally a continual improvement project is initiated by the top management, particularly
07:39
if there is a cross-functional involvement.
07:41
A project team is usually formalised and supported with resources to carry out the improvement
07:47
project.
07:49
Corrective Action.
07:50
This is clearly specified in the ISO 9001 8.5.2, Corrective Action.
07:57
Whenever non-conformity is encountered in the QMS, the problems be resolved without
08:03
undue delay, according to the corrective action procedure established in the QMS.
08:08
It is a requirement that the corrective action should be effective in eliminating the root
08:12
cause of the non-conformity to prevent it reoccurring.
08:18
Preventative Action.
08:19
This requirement is defined in the ISO 9001 clause 8.5.3, Preventative Action.
08:26
Through the analysis of data on processes, products, suppliers, customer feedback, audit,
08:33
etc., potential non-conformities could be identified and preventative actions taken.
08:40
Preventative actions shall be taken according to the established procedures in the QMS,
08:44
and it is a requirement to review the effectiveness of such actions taken.
Recommended
8:12
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