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No: ESCL-QSP-006
Rev. No: 00
Issue Date:12th Nov, 2012
Page 1 of 5
PREVENTIVE ACTION
PROCEDURE
Issue Date
Revision
00
12/11/2012
Identification
First Issue
Prepared by
Management
Representative
(MR)
Reviewed
Approved by
by
Production
Manager
Managing
Director
Change/Amendment No.
Date
Page
Description of Change/Amendment
Rev. No: 00
Issue Date:12th Nov, 2012
Page 3 of 5
1.0
PURPOSE
The purpose of this procedure is to define the methodology for preventive action in
ESCL processes and activities in order to determine action to eliminate the causes of
potential nonconformities and prevent their occurrence.
2.0
SCOPE
This procedure is applicable to all potential nonconformities identified in ESCL
operations and activities.
3.0
REFERENCES
NIS ISO 9001:2008, Quality Management Systems Requirements
NIS ISO 9000:2005, Quality Management Systems Fundamentals and Vocabulary.
ESCL Quality Manual (ESCL-QM-001)
Form 107, Corrective/Preventive Action Request.
Form 109, Corrective/Preventive Action Log.
4.0
4.1
4.2
4.3
4.4
4.5
5.0
5.1
Every Function: Has the duty and responsibility to report any observed potential
nonconformity as it relates to his activities/processes (see Form 107).
5.2
5.3
Process Owner: Responsible for the implementation of action needed to correct the
cause of potential nonconformities in his process.
5.4
5.5
6.0
PROCEDURE
6.1
Potential nonconformities are identified based on data and information from relevant
sources including lessons learned from past experiences and trends (see the
Appendix which shows the flow chart for handling potential nonconformities and
preventive action in ESCL).
6.2
Sources of the data and information mentioned in 6.1 above include but are not limited
to:
reported potential nonconformity by personnel (see Form 107)
review of client needs and expectations including concessions;
output from data analysis (see section 8.4 of ESCL Quality Manual);
evaluation of historical data including audit results;
product and process measurements;
service delivery reports; and
relevant quality management system records;
6.3
Appropriate investigation and/or data analysis is carried out to determine the causes
of the potential nonconformities that are of significant effect in terms of costs,
product/service performance, safety and customer satisfaction.
6.4
The proposed preventive action is evaluated in order to assess the implications and
ensure that on implementation the potential nonconformity will not occur.
6.5
Every process owner ensures that any recommended preventive action as it relates to
his area of work is satisfactorily implemented.
6.6
The department/unit heads and top management closely monitor and review the
effectiveness of the preventive action taken on potential nonconformities related to
their processes and ensure a satisfactory close out.
6.7
Records of the preventive action and the results of preventive action taken as it
relates to a specific process/contract is maintained and serve as an input for
preventive measures in future jobs (see Forms 107 and 109).
7.0
RECORDS
7.1
7.2
APPENDIX
Sources of Data
Preventive Action
Project Processes
Concessions
Audit Results
Process
Measurements
Quality Records
Service Delivery
Records
Client Complaints
Action required?
Determine steps
needed to deal
with potential
nonconformity
appropriate to the
effect of the
potential problem
Implement preventive
action