Approved PQP Al Nowaiser
Approved PQP Al Nowaiser
Approved PQP Al Nowaiser
COPYRIGHT
No part of this program may be reproduced in any form by print, photocopy, microfilm or any other
means wholly or in part or disclosed to any person outside Alnowaiser for Trading and Contracting
Company without the written permission of the Management Representative/General Manager.
APRIL 2019
Table of Contents
REVISION RECORD
02 11/04/2019 GM
STATEMENT OF POLICY
The management AL-NOWAISER acknowledges the need to perform and maintain the QA/QC
Program and QC Plan for construction , design, procurement, Installation, testing and
commissioning.
The overall responsible for the AL-NOWAISER Quality Program / Quality Plan lies with QA/QC
Manager. The QA/QC team shall be given authority and independence to perform their roles
effectively. Their responsibility is to ensure that all the clients' requirements and AL-NOWAISER's
high quality standards are strictly adhered to and the authority to hold any operation to ensure
compliance with the applicable documents such as industry standards and customer specific
standard requirements for construction , design, procurement, Installation, testing and
commissioning.
The QA/QC Team is independent in performing its duties and responsibilities to perform the
highest standards of implementation of the CONSTRUCTION QA/QC Program and QC Plan to
ensure attainment of customer delight.
All CONSTRUCTION team shall be aware of this Quality Program / Quality Plan, and must adhere
to the requirements and no deviations from the methods set forth herein shall be permitted.
PURPOSE
The objectives of this Quality Program / Quality Plan relative to the Quality Control Process and
Procedures as follows:
• Ensure that the QA/QC activities during site preparation and mobilization stage up to
testing/commissioning and Energize the S/S that all items of work are in compliance with
applicable material standards and customer specified requirements.
• Ensure that during Design & Engineering all performance and material specifications are
applied.
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Quality Control Program & Quality Control Plan
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• Define QA/QC Inspection schedules in accordance with the Project and Test Schedules where
applicable and work instruction.
• Ensure that the items and services, which do not conform to the specified requirements, are
controlled in accordance with the documented procedures.
• Ensure all non-conformance reports, customer complaints and corrective action
requirements are properly addressed and recorded.
• Ensure all the aspect are documented, certified and completed in compliance to the Approved
test Plans and Technical Specification along with all the Approved Projects Scope of Work and
Contract to the satisfaction of the Customer.
• Ensure all QA/QC documents are completed and accomplished for all phases Mobilization,
Engineering, procurement, Construction, Supply Materials, Installation, Testing
Commissioning and Energize the S/S.
• DOCUMENT - Information and its supporting medium paper, magnetic, electronic or optical
computer disc, photograph or a combination thereof.
• DOCUMENTATION REVIEW - Means the examination of the documentation for completeness
and correctness.
• INSPECTOR - Means the person acting as the authorized representatives either by,
Contractor, Customer or Third Party commissioned by any of the contractual parties
conducting the inspection on the Customers behalf.
• NONCONFORMITY - Situations where a requirement was not full field.
• PROCEDURE - Specified way to carry out an activity or a process.
• QUALITY PROCEDURES -The written instructions for implementing various components of
the organization’s total Quality.
• QUALITY RECORDS - A controlled, dated and signed document relating to measurable
activities with respect to the Quality of the design, procurement, construction Installation,
testing and commissioning. Documents cover full details of description, completeness and
accuracy of items and correctness of all requirements as specified for the purpose and usage
in compliance to the Approved Final Design drawings and documents.
• RECORD - Document stating results achieved or providing evidence of activities performed.
• REVIEW - Activity undertaken to determine the suitability, adequacy and effectiveness of the
subject matter to achieve established objectives.
• REWORK - Action of non conforming product to make it conform
1. Project Manager
Project Manager has the overall responsibility for safety and will be the prime contact with AL-
NOWAISER Project Management Team. He shall ensure that the Project Health and Safety Policy
and all specific legal requirements applicable to the Project are complied with at all times.
2. QA/QC MANAGER
• The QA/QC manager reports directly to the senior management.
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Quality Control Program & Quality Control Plan
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9. Procurement Manager
• The Procurement Manager will be reporting directly to Project Manager.
• This Procurement department will be describes the procedures and responsibilities for the
purchasing of all material and equipment supplied by AL-NOWAISER. The main objective is
to ensure that purchased products conform to specific technical requirements of the contract
Document. In addition it will ensure that material delivery lead times will be taken into
account so as to ensure that all material is available to start as per the project plan so as to
meet the final delivery date to the customer.
• He shall be responsible for the preparation of all relevant documentation and design drawings
technical discussions with customers for clarification of scope of work and specifications
.technical assistance for the preparation of pre-qualification documents
• He shall discuss necessary requirements of resources like tools, materials and manpower with
the Construction Manager.
• Clarification on client or end user queries with respect to scope of work and specifications.
To ensure that all Punch list / snag closed as per customer requirement QC team must follow FRM-011
form and make sure that all points closed.
Document Control
We attached in Annexure#1 with this QC plane AL-NOWAISER Document Control procedure which we
follow to ensure that all activities are documented clearly and any person can reach the required
document easily.
• Final set of design documents and drawings shall be prepared and will be stamped “AS- BUILT”. A
copy of these drawings/documents is to accompany the Materials/Equipment unless otherwise
specified by the Customer.
1. PURPOSE
To ensure that purchased services conform to specified requirements, evaluation of Subcontractors &
Suppliers & Third Party shall assess the following:
1. Their ability to meet Subcontractor & Suppliers & Third Party requirements with respect to
Schedule, Quality and Safety.
2. The extent of control to be exercised by over Subcontractor & Suppliers & Third Party together
with the extent of verification required at Subcontractors’ premises.
2. SCOPE
The Program covers all such services for permanent and temporary works for the Project, which directly
affect the quality of works.
3. RESPONSIBILITIES
The personnel involved in this Program are:
4. PROCEDURES
1. Subcontractor & Suppliers & Third Party are selected from a list of ‘Approved Suppliers,’ which is
updated regularly and when necessary.
2. The selection of Subcontractor & Suppliers & Third Party is based on the following criteria, which are
applied where necessary and according to importance:
a. Safety program
b. Safety record
c. Requirements of the client
d. Approval of the client
e. Passing the Safety Audit
f. Previous experience
g. Internal requirements and specifications
h. Status with respect to ISO 9001 and ISO 45001 certificates
i. Reputation
j. Quality and properties of offered services
k. Payment and delivery conditions
l. Qualification and training of the Subcontractor & Suppliers & Third Party personnel
3. Whenever possible, at least two approved Subcontractor & Suppliers & Third Party are addressed for
each Purchase Order.
4. The status of Subcontractor & Suppliers & Third Party is regularly reviewed and kept up-to-date.
5. The performance of Subcontractor & Suppliers & Third Party is evaluated by the General Manager.
6. The performance of Subcontractor & Suppliers & Third Party are reviewed in the Safety Management
Review Meeting.
7. Project Manager will monitor Subcontractor & Suppliers & Third Party safety performance on the
working site by:
a. Monitoring the usage of the safety gears
b. Monitoring the safety behavior of the subcontractor & Suppliers & Third Party.
c. Monitoring the safety meeting attendance sheet & safety record.
5. RECORD KEEPING
The documentation/forms to be maintained for this Program are:
SUPPLIERS ACTIVITIES
(General Manager)
Approved Supplier
Supplier List Source out Approved Supplier
evaluation Report
Is Supplier in list? PUR-FRM-003
PUR-FRM-002
Y
Inquiry Send Inquiry (At least 3 Supplier) if any
PUR-FRM-004
If Quotation is
approved?
END
QUALITY INSPECTIONS
• REQUESTS FOR INSPECTION (RFI)
The QA/QC Engineer shall ensure that all activities covered in the scope of work are in
accordance with the specifications, standards and contractual requirements by
performing preliminary inspection before being released for inspection by the customer.
Upon completion of the inspection a Request for Inspection shall be sent to the Customer.
This will be done with a minimum time of one week or based on customer mandated time
duration to the scheduled inspection and witnessing.
• QA/QC INSPECTION LOG BOOK
The QA/QC Engineer will record in a Log Book, all the comments and observations for the
deficiencies found in the project. The purpose of the logbook is to record the quality
control activities of QA/QC Engineer during the staging stages for all projects.
Whenever such deficiencies, violations and non-conformances are found, actions done to
facilitate the corrective actions shall also be recorded. All deficiencies found by the QA/QC
Engineer shall be recorded in the Non Conformance Report. The logbook shall serve as
basis for the NCR. Project Staging Team shall be responsible to rectify any QA/QC
Engineer observed deficiencies or any non conformance work.
QA/QC Engineer shall ensure that all unsatisfactory observations on a pre-requisite stage
are cleared before any activity proceeds to the succeeding stage.
• INSPECTION AND WORK STATUS
AL-NOWAISER shall establish an Inspection and Test Plan for the project to ensure that
the required inspection and tests are performed based on schedule throughout the staging
process.
This will also ensure that the required resources are available to meet the work schedule
and that the status of the inspection and test work is known throughout the project. This
will also ensure conformity of the materials/equipment, based on the approved Base
Design/Detailed Design submitted, meet all the requirements and ensure that the
investigation, reporting and documentations are executed consistently along with the test
certificates of equipment from the manufacturers.
• QUALITY PROCEDURES: AND QUALITY RECORDS
- Mobilization Inspection Procedure
- Engineering process
- Civil Work Instruction process
- Procurement Instruction process
- Subcontractor Process
- Work Instruction for Installation stage
- Work Instruction for Testing and Commissioning stage.
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Quality Control Program & Quality Control Plan
Revision 02 Issue Date: 11/Apr/2019
• DEFINITION
Non-Conformance is defined as something that is not adhering or complying with the standards or
specifications.
• QUALITY RECORD and QUALITY PROCEDURE
Quality Inspection Report (QIR/NCR)
Control of Noncompliance
• INITIATING A NON-CONFORMANCE
Any Non Conformance can either be initiated by the QA/QC ENGINEER or the designated
QA/QC ENGINEER of the Customer, during the QA/QC inspection activities.
• RESPONSIBILITY
Quality Control Engineer identifies and reports Non-Conforming items and imposes corrective
action. He is responsible for conducting all the required inspections, tests and examinations.
• CONTROL OF NON-CONFORMING ITEMS
The non-conformities identified by the QA/QC ENGINEER will initiate an immediate
investigation and the corresponding report shall be forwarded to the Technical Services Lead
Engineer for corrective action with a copy sent to the Manager of the Energy Automation
Division.
• NON-CONFORMANCE REPORTING (NCR)
For any non conformance detected during the procurement phase. NCR shall be prepared by the
QA/QC ENGINEER and directly addressed to the Vendor. A copy of this NCR shall be forwarded to
the procurement Officer and production Engineer giving a complete description of the non-
conformance observed and suggested remedial actions to be implemented.
• CORRECTION OF NON-CONFORMING ITEMs
The method of correcting a non-conformance shall be proposed by the QA/QC ENGINEER and it
is the responsibility of the Lead Engineer Customer Support Services to approve and execute the
corrective action. The correction shall be any of the following:
- Re-work. The process by which a non-conforming item is changed to make it conform to
specifications by further work, e.g. re-machining, re-welding, re-assembling, replacement
of parts, other means.
- Repair. This is the process of restoring non-conforming characteristics to a condition
acceptable to the Customer so that it conforms to the original requirements or the
• All non-conformance reports (NCR) shall be documented and maintained in an NCR/QIR Close-
out of all NCR's from design, procurement, manufacturing/fabrication, assembling, Shipping,
Storage, construction Installation, testing and commissioning shall therefore be traceable.
• AUDITING OPERATION
- The QA/QC ENGINEER shall establish an audit date and inform all concerned. The audit
team meets with appropriate department directly involved with the subject to be audited
and discuss the constructive purpose of the audit in order to obtain the desired corrective
results.
- The team conducts a tour of the areas to be audited. The relevant personnel are questioned,
observations and sampling is conducted as required.
- The audit team shall identify discrepancies and deficiencies and these will be recorded in
a log.
- A closing meeting between the auditing team and the department involved shall be
conducted and shall discuss audit conclusions and recommendations for corrective actions
which are to be agreed upon and implemented immediately.
• AUDITING REPORT
In preparing the audit reports, the contents shall serve the following objectives:
- To benefit the company and not to criticize any individual but rather provide constructive
guidance on what improvements can be made to meet the quality objectives and ultimate
customer satisfaction.
- The report serves as a notification that the Quality Control Plan is not being effectively
followed or documented which requires management action.
- The report provides evidence that periodic audits of the Quality are carried out.
CONTROL OF DOCUMENTS
PROCEDURE
ISO 9001:2015 & ISO 45001:2018
MR-ISP-001
COPYRIGHT
No part of this procedure may be reproduced in any form by print, photocopy, microfilm or any other
means wholly or in part or disclosed to any person outside Alnowaiser for Trading and Contracting
Company without the written permission of the General Manager.
APRIL 2019
Table of Contents
1.0 OBJECTIVES 3
2.0 SCOPE 3
3.0 RESPONSIBILITIES 3
4.0 PROCEDURE DETAILS 3
4.1 CONTROLLED DOCUMENT 3
4.2 UNCONTROLLED DOCUMENTS 3
4.3 OBSOLETE DOCUMENTS 3
REVISION RECORD
Revision # Date Section Revised Summary of Revision Authorized By
1.0 OBJECTIVES
The objective of this procedure is to ensure effective control of the Integrated Management System
Documents.
2.0 SCOPE
This procedure covers the general correspondence of the company and its application to all required
documents and Records to comply with the requirements of the Integrated Management System.
3.0 RESPONSIBILITIES
General Manager / Management Representative / Respective Department Heads.
INTEGRATED POLICY
LEVEL II- These documents set out the manner in which policies
ISP defined in the Integrated Manual are achieved
WI Work Instructions
Integrated Policy
Integrated Objectives
Management Representative General Manager
Integrated Manual
Integrated Procedures
No
Submit the Technical
documents along with
transmittal letter
Yes
Site Visits
Purchase
Purchase of Items / Requisition
consumables PUR-FRM-001
Mobilization to
Site
Site Preparation /
Discussion with
Client
Start the site development and earth works as per the scope.
1. Performing survey activity
2. Cutting & excavation activity
3. Backfilling & compaction activity
4. Final Grading (Asphalting or Concrete)
Approved
No
Yes
Approved
No
Yes
Approved
No
Yes
Approved
No
Yes
Approved
No
Yes
Approved
No
Yes
Approved
End of Process
No
Submit the Technical
documents along with
transmittal letter
Yes
Site Visits
Purchase
Purchase of Items / Requisition
consumables PUR-FRM-001
Mobilization to
Site
Site Preparation /
Discussion with
Client
Ground Testing Conduct inspection for megger reading and Megger Reading
ground testing for cables
Yes
No
Approved
No
Approved
Yes
Approved
End of Process
No
Submit the Technical
documents along with
transmittal letter
Yes
Site Visits
Purchase
Purchase of Items Requisition
/ consumables PUR-FRM-001
Mobilization
to Site
Site Preparation /
Discussion with
Client
Mechanical Inspection
Submit the mechanical inspection Report
report to the client
No Yes
Approved
Approved
Yes
Approved
End of Process