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1. PURPOSE
1.1 To provide the instructions for the establishment and implementation of control
requirements of processes and process equipment for periodic type control
activities in relation with the proper functioning of the process.
2. DEFINITIONS
2.2 Equipment: All apparatuses used to process engines and/or components. This
shall include materials and environmental conditions.
2.4 Special Processes: Those processes which modify or change the inherent
physical, chemical or metallurgical properties of an item, or non conventional
methods which remove or deposit material on the item during or after
fabrication which can not be fully evaluated by nondestructive means, or
those used to maintain process control such as nondestructive testing
3. GENERAL
3.2 PCPs will be developed when specific instructions are required to perform
inspection/test of parts, assemblies and or special processes (including
chemical, metallurgical lab) for all processes that affect quality.
5.1.1 Prepare and revise PCPs for control of special process and PCPs not related to
special process.
5.1.4 Provided proper judgment with respect to the needs standard or special
tooling.
5.1.6 Hand over the entire original PCP documents to ERTD area for keeping as
master documents.
5.1.7 Revise PCPs as required to provide planning consistent with the latest
technical documents requirement and specifications.
5.1.8 Issue and update index of all PCPs every 6 (six) months.
Note : Change that does not affect performance of operation, such as
planning, time or typographical error does not require Approval.
5.1.10 PCP will be numbered consecutively to avoid duplication and data collection
activities.
5.2.1 Prepare and revise PCPs for control of NDT processes following instruction on
Exhibit 1 and 2.
5.2.3 PCP will be numbered consecutively to avoid duplication and data collection
activities.
5.2.5 Provide proper judgment with respect to needs of standard or special tooling.
5.2.6 Issue and update index of all PCPs every 6 (six) months.
Note : Change that does affect performance of operation such as planning,
time or typographical errors do not require Approval.
5.2.8 Hand over the entire original PCP documents to ERTD area for keeping as
master documents.
5.3.1 Review and approve all PCP’s not related to Special Processes issued by Special
Process Engineering.
5.3.4 Recommend changes to PCP’s based on result from Quality Control Inspection
and/or process review studies.
5.4.1 Review and approve all PCPs related to the special processes (QE17-022).
5.4.4 Recommend changes to PCP’s based on result from Quality Control Inspection
and/or process review studies.
EXHIBIT 1
SUBJECT: ........(3)....................................................
FORM No QE01-1
CONTROLLED COPY DO NOT DUPLICATE PAGE 1 OF.....
Block Description
No
1 INT. PRODUCED DOC. NAME:
Write the type of document. Example: PMP, PCP, EEO, etc,.
2 NUMBER:
Write the sequence number of each type of internally produced document.
3 SUBJECT:
Write the title of each internally produced document.
4 ISSUE NUMBER:
Letter used in sequence any time the Internally Produced document is reissued. If
original issue add “A”.
5 REVISION NUMBER:
Number used in sequence any time a revision is issued. If initial issue enter “0”.
6 REV. DESCRIPTION:
Brief explanation of the revision being issued. If initial issue, enter "NEW”
7 DATE:
Date of Issue / Revision will be applied after final approval This will be the issued
date listed in the index.
8 SUPERSEDES:
Any paragraph which is no longer necessary because of this revision. If none, enter
“NONE”. Enter page No, paragraph, revision number and date. Only the page with
the revision will be replaced together with the issue / revision sheet . Not all the
document. The other pages will indicate the previous revision numbers. When
previous issue is superseded, enter previous issue letter, document number and
title and date of previous issue.
9 ISSUED BY:`
The name and signature of the originator as per this PCP.
10 APPROVED BY:
The name and signature of the person approving the document as per this PCP
NOTE: Only the single page (current form QE01-1) containing the latest revision
need to be distributed with a revision. Previous revision history will be on file
by the quality systems. The page (current form QE01-1) with the latest
revision will be numbered always as the page 1.
NOTE: THE PAGE FOOTER WILL HAVE THE STATEMENT “CONTROLLED COPY DO
NOT DUPLICATE” AND THE PAGE NUMBER
EXHIBIT 2
Requirement
FORM No QE17-1
CONTROLLED COPY DO NOT DUPLICATE PAGE 2 OF ....
APPENDIX 1
Balancing BL
Assembly AS
Chemical Cleaning CC
Disassembly DA
Eddy Current Inspection ET
Electroplating EP
Flow Test FT
Heat Treatment HT
Inspection (Visual/Dimensional) IV
Magnetic Particle Inspection MT
Mechanical Cleaning MC
Paint Shop PS
Penetrant Inspection PT
Pressure Check PC
Prep to Ship PH
Shipping and Receiving SR
Shot Peening SP
Thermal Spray TS
Test TE
Ultrasonic Inspection UT
Weld Shop WS
Radiographic Inspection RT
Example :