Sop-Nc-01 - Management of NC, Capa
Sop-Nc-01 - Management of NC, Capa
Sop-Nc-01 - Management of NC, Capa
DOC. NO
SOP-NC-01
REV. DATE
02/02/2015
REV. NO.
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REVISION HISTORY
Rev. No
DCN No.
Page No.
Eff. Date
N/A
ALL
02/02/2015
Name
Position
Description of Changes
NEW ISSUANCE
REF. NEW ISSUE DOCUMENT APPROVAL FORM NO.
001
Originated By
Reviewed By
Approved By
BANUN
BANUN
WITHORN ARPANUVAT
Management Representative
Management Representative
General Manager
Signature
Date
Note: The details of changes shall be documented in the DOCUMENT CHANGE NOTICE (DCN).
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Process / Step
Procedure
1.0
Records
PURPOSE
1.1
1.2
1.3
1.4
2.0 SCOPE
2.1
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2.2
2.3
Records
3.0 REFERENCES
3.1 ISO 9001 : 2008 Clause 8.3 (Control of Non-Conforming
Product)
3.2 ISO 9001 : 2008 Clause 8.5 (Improvement)
3.3 ISO 9001 : 2008 Clause 8.2 (Monitoring & Measurement)
3.4 MJE-QM (Company Quality Manual)
4.0 APPENDICES
Nil
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Process / Step
Procedure
7.0
Records
PROCEDURES
7.1
Responsibility
a) HOD / Management Representative/ General
Manager are responsible to ensure effective
implementation of this procedure.
b) However the authority to point out NC materials is
given to all personnel. They may point out the NC to
the departmental Manager/ Head concerned who
then initiated disposition and handling.
c) The Management Representative shall be
responsible to facilitate the continual improvement
of the quality management system through the use
of quality policy, quality objectives, audit results,
analysis of data, corrective & preventive
action & management review
7.2
ii)
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Process / Step
Procedure
c)
Internal Audit
Upon detect any non-conformance during internal
audit process which did not meet audit scope and
criteria(e.g. ISO 9001:2008), internal auditor shall
report non-conformance with objective evidence in
accordance to Internal Audit Procedure. The
correction, corrective action and preventive action
response shall be recorded in the Corrective Action
Request submitted by the auditor to the auditee.
Records
Corrective
Action Request
d) Customer Compliant
Upon received customer complaint, either in verbal
and written format, respective engineer shall carry out
appropriate action accordance with item 3.4.
7.3
Management of Non-conformance
Nonconformance
Record
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Records
7.5
Preventive Action
a) All departmental head shall pro-active to study,
analyzed and determine any potential nonconformance which can cause quality nonconformity in related to their departmental
function.
b) Determination of potential non-conformance may
base on:
Previous process performance or historical
(quality) data
Similar or other industries practice or
experience
Repeating non-conformance
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Process / Step
Procedure
Records
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Process / Step
Procedure
7.6
Records
7.7
Customer
Complaint Log
Sheet
NCR
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Process / Step
Procedure
Records
Continual
Improvement
Action Plan
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Process / Step
Procedure
b) All problems detected shall be recorded in PCAR
and to be submitted to the concerned department for
root cause determination and action taken.
Records
PCAR