Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
1 Scope………………………………………….... 2
2 Objective…………………………………….…. 2
3 Applicable Documents………………………... 2
4 Definitions and Abbreviations………………… 3
5 Deficiency Classification………....…………… 5
6 Instructions…………………………………..…. 5
7 Responsibilities………………………………… 6
1 Scope
For Non-RVL material (project approval) where RIO was involved to perform
inspection/vendor qualification, an EDR can be issued and RIO investigation shall
focus only on the inspection agency/inspector performance. Completion of the
EDR Closing Form 8.3-F-02-VID is not required.
1.2 The EDR scope extends to include correction/ rectification of deficiencies in case
of direct purchase orders placed by Saudi Aramco. Inspection Department
(ID)/Vendor Inspection Division (VID) role is limited to investigate the
deficiencies with the vendor and close the EDR when the Originator organization
confirms that the correction/rectification is satisfactorily completed.
2 Objective
3 Applicable Documents
Page 2 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
General Supervisor: Operating Facility Supervisor level responsible for the area
where the defective material is observed.
Page 3 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
they are visually inspected (per the applicable Inspection Plan “SA-175 form”) and
released for shipment by the assigned Inspection Office. It is also required that
these materials are procured from approved manufacturing plants. These materials
should be linked to the applicable inspection plan “SA-175 form”.
Category B (IDCAT-B): When materials under this category are procured, it’s a
requirement that the Inspection Office reviews the certificates (as per the applicable
inspection plan “SA-175 form”) and releases the materials for shipment. It is also a
requirement that these materials are procured from approved manufacturing plants.
These materials should be linked to the applicable inspection plan “SA-175 form”.
Category C (IDCAT-C): When materials under this category are procured,
inspection is not required (i.e., no visual inspection and no certificate review).
However, it is required that these materials are procured from an approved
manufacturing plant. These materials should not be linked to any inspection plan
“SA-175 form”.
Category S (IDCAT-S): When materials under this category are procured, it is
required that they are visually inspected or certificates are reviewed (as per the
applicable Inspection plan “SA-175 form”) and the materials are released for
shipment by the assigned Inspection Office. This category is applicable for
inspectable spare parts only. Approval for manufacturing plants supplying these
materials is not necessary (to allow procurement of spare parts to run existing
equipment purchased from a supplier who might be put on hold). These materials
should be linked to the applicable inspection plan “SA-175 form”.
Material: For the purpose of this document, material is defined as the final
product/equipment/service supplied by Company approved vendors.
Non-Inspectable Material: Any material that do not fall under any of the categories
A, B, C, or S defined herein under Inspectable Material.
PQM: Project Quality manager responsible for planning, executing and controlling all
Page 4 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
PQL: Project Quality Leader assigned for small/medium or group of small projects.
5 Deficiency Classification
PQM, PQL or General Supervisor is responsible to classify the deficiencies at the stage
of reporting an EDR as either major or minor. Deficiencies shall be classified as major
if one of the following conditions applies, otherwise, minor classification shall be
assigned:
5.1 Deficiencies that put quality and integrity of the project/facility including its
workers and equipment at risk. That is, the deficiencies that prevent putting a
facility in operation as they represent, if not corrected, an evident danger to
Company property or personnel safety, and those that may impact the safe
commissioning, start up, and operation of the facility.
5.2 Actions that violate the corporate values such as submitting forged items and/or
counterfeit materials.
5.3 Minor EDRs repeated for the same deficiency with the same vendor.
Note: Major EDRs shall be escalated in accordance with SAEP-397 and shall not be
closed until the Vendor Escalation Process is completed.
6 Instructions
Page 5 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
Note: First time originator must complete the online EDR course number 40080017.
6.3 For indirect orders, EDR shall only be issued after an NCR/INCR has been
reported already.
6.4 EDR shall be completely created in SAP-QM to include all required fields listed
in paragraph 7.1.4.3.
6.5 Major EDRs shall be submitted by PQM, PQL or General Supervisor while the
minor ones are acceptable to be submitted on unit supervisor level.
6.6 SAP tasks will be assigned to RIO to kick off investigation with the vendor.
6.7 The EDR investigation may require RSA input if technical feedback is deemed
necessary by RIO.
7 Responsibilities
7.1.1 Make sure an NCR/INCRs has been issued for deficiency correction /
rectification in case of indirect purchase order.
7.1.2 Evaluate the deficiency as per Table 1, Appendix B based on which the
Originator decides whether to issue an EDR or not.
Note: If the deficiency is not listed in Table 1, Appendix B, PQM/PQL/GS and
SAIR, as applicable, need to evaluate whether the vendor caused the
deficiency. If yes, the deficiency should be considered as an EDR
case. Originator is always recommended to discuss the selected
deficiency with EDR Coordinator.
7.1.4.2 The purchase order, and photos of the defects and the defective
material shall be attached in SAP-QM
Page 6 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
7.2.1 Make sure that NCR/INCR has been issued prior to reporting the EDR.
7.2.2 Review the EDR and classify the deficiency as “Major” or “Minor” as
per Section 5.
Page 7 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
7.2.3 Submit major EDRs immediately after the Originator has created it in
SAP-QM. EDRs left with created status (SAP status “CRTD”) for three
(3) business days will be archived and Originator will be required
reinitiate and the EDR once again.
7.3.1 Make sure that the vendor is approved at the stage of issuing the EDR.
7.3.2 Review and acknowledge the EDR via an email to EDR Coordinator.
7.3.3 Provide the needed purchase order information such as inspection lot
number, 9COM, …, etc., to the Originator.
7.3.4 Provide the Originator with all procurement NCR/INCRs for the
defective equipment during manufacturing, as applicable.
7.3.5 Upon completion of any EDR, SAIR will use the EDR Closing Form
contents to prepare and log a lesson learned in VID Lesson Learned
ShareK website.
7.4.1 Make sure all necessary information and documents for the defective
material are completed and in line paragraph 7.1.4. If not, EDR
Coordinator will reject the EDR immediately, report the reason of
rejection to PQM/PQL/ General Supervisor, and document the rejection
in SAP-QM.
7.4.3 Approve and assign the EDR tasks on SAP-QM to the Responsible
Inspection Office EDR Coordinator to start the investigation. If the
deficiency involves more than one vendor located at different RIO areas,
the tasks will be assigned to the RIO responsible for the final release of
the material.
7.4.4 If RIO investigation reveals that the deficiency was not caused by the
vendor such as transportation, site preservation, etc. EDR Coordinator
will reject the EDR and will make sure that all supporting documents are
attached to SAP-QM.
7.4.5 Prepare a monthly EDR status report and submit it to RIO Supervisors and
copy to QAU Supervisor and VID Superintendent.
7.4.6 Complete the EDR on SAP-QM after RIO completes the EDR Closing
Page 8 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
Form 8.3-F-02-VID.
7.4.7 Share the completed EDR Closing Form 8.3-F-02-VID with the
Originator.
7.5.2 Review the monthly EDR status report and take actions accordingly to
ensure appropriate management of EDRs and ensure the EDR tasks are
completed within eight (8) weeks of the initial task assignment date or
within an agreed-upon date with a documented valid justification.
7.5.3 Review vendors’ corrective actions, may initiate vendor evaluation and
decide based on that whether the vendor approval status should be
changed in line with the Vendor Performance Escalation process.
7.5.4 Review and approve the EDR Closing Form 8.3-F-02-VID and provide
feedback to the vendor accordingly.
7.6.1 Represent RIO as the focal contact to communicate with the RIO
inspector and EDR Coordinator.
7.6.2 Receive tasks from EDR Coordinator and assign them to the RIO
Inspector.
7.6.3 Should assign or make sure that RIO Inspector assigns ETC to the EDRs
into SAP within five (5) working days of receiving the tasks from EDR
Coordinator.
7.6.4 Should ensure that the EDR status update is documented into SAP-QM
on bi-weekly basis.
7.6.5 Follow up with RIO inspector to ensure that the EDR tasks are
completed within eight (8) weeks of the initial task assignment date or
within an agreed-upon date with a valid justification. The justification
needs to be approved by RIO Supervisor and communicated to EDR
Coordinator in order to change the EDR completion date on SAP-QM.
Page 9 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
7.6.6 Make sure that the signed EDR Closing Form 8.3-F-02-VID is attached
and notify EDR Coordinator to close the EDR accordingly.
7.7.1 Review the tasks assigned by RIO EDR Coordinator and should assign
an ETC within five (5) working days.
7.7.3 Review the deficiency against the purchase order requirements and
contact EDR Coordinators, vendor, etc., as necessary to understand the
nature of the deficiency. RIO Inspector may need to conduct a physical
inspection on the defective material in case the material is returned to the
vendor’s shop floor for further investigation.
7.7.5 When the root causes and corrective actions require technical expertise,
RIO Inspector or RIO EDR Coordinator will create a CRM request to
seek RSA feedback based on which the vendor shall revise the root
causes/corrective action, as applicable, and attach the CRM with the
singed EDR Closing Form 8.3-F-02-VID in SAP-QM.
7.7.6 If the investigation reveals that the deficiency is not caused by the
vendor, EDR Coordinator will reject the EDR or archive it if the
deficiency is found caused by transportation.
Page 10 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
7.7.9 RIO Inspector shall not complete the EDR Closing Form 8.3-F-02-VID
until the accepted corrective actions plan is duly implemented or the
escalation process is completed, as applicable. Once the form is
completed, RIO Inspector/RIO EDR Coordinator shall immediately
complete the tasks of the EDR notification in SAP-QM, attach the form,
and notify both RIO EDR Coordinator and EDR Coordinator.
Revision Summary
10 December 2015 Major revision as a result of a comprehensive six sigma study targeting reduction of number
defective material received at Saudi Aramco projects. The study revealed that improvement
is required in the EDR reporting phase where plenty of EDRs were rejected, investigation
phase where several EDRs found with incomprehensive/incomplete investigations, and in the
closing phase where EDRs were closed without acceptable and documented root cause
analysis and corrective actions.
Page 11 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
Deficiency Observed
Issue NCR/INCR
No
Do not issue EDR EDR Case Origniator
Yes
Archive EDR
Assign Tasks to RIO
Yes
RSA Input
Yes
Initiate CRM Request
Required
No
RIO
No
Verify satisfactory
plan/ Evaluate Vendor/Escalate
implementation** Issue**
Yes
Page 12 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
Page 13 of 14
Document Responsibility: Project Quality Standards Committee SAEP-380
Issue Date: 10 December 2015
Next Planned Update: 10 December 2018 Equipment Deficiency Report
Project BI/JO Project Name/Facility Name RIO Inspector/Engineer Login ID Tel. No.
Description of Deficiency
Root Cause
CRM# :
Corrective Action
Correction/Disposition:
Preventive Measures:
S ignatory
Role Name Signature Date
RIO Supervisor
VID Superintendent*
Page 14 of 14