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CONGO BIOFUEL

1ST AGRI HUB – INDUSTRIAL START-UP

PROJECT QUALITY PLAN

EX-DE 06 01/04/2023 Issue for FINAL G. Fayad E. Hawash RO. Habib N.Capretti
EX-DE 05 30/03/2023 Issue for APPROVAL G. Fayad E. Hawash RO. Habib N.Capretti
EX-DE 04 15/02/2023 Issue for APPROVAL G. Fayad E. Hawash RO. Habib N.Capretti
EX-DE 03 05/01/2023 Issue for APPROVAL G. Fayad E. Hawash RO. Habib N.Capretti
EX-DE 02 13/12/2022 Issue for FINAL G. Fayad E. Hawash RO. Habib N.Capretti
EX-DE 01 29/11/2022 Issue for APPROVAL G. Fayad E. Hawash RO. Habib N.Capretti
EX-DE 00 21/11/2022 Issue for Comments G. Fayad E. Hawash RO. Habib N.Capretti
Validity Revision
Status Number Contractor Contractor Contractor Company
Date Description
Prepared Checked Approved Approved
Revision Index
Company logo and business name Project name Company Document ID
CONGO BIOFUEL
30A100DBQB23010
ENI Congo SA
Contract N.
Contractor logo and business name Contractor Document ID

CTR CONSTRUCTION
30A100DBQB23010
Job N.
Facility and Sub Facility Name Scale Sheet of Sheets

1st Agri Hub - Industrial Start-Up - General NA 1 / 77

Document Title Supersedes N.

PROJECT QUALITY PLAN Superseded by N.


Plant Area Plant Unit
NA NA
File Name: 708011486.docx

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TABLE OF CONTENTS

1.0 INTRODUCTION................................................................................................................................................ 3
1.1 SCOPE................................................................................................................................................................. 3
1.2 DEFINITION.......................................................................................................................................................... 4
2.0 REFERENCES................................................................................................................................................... 5
3.0 QUALITY POLICY & QUALITY OBJECTIVES.................................................................................................. 6
3.1 QUALITY POLICY................................................................................................................................................. 6
3.2 QUALITY OBJECTIVES.......................................................................................................................................... 7
4.0 QUALITY POLICY OF CTR FOR CPY.............................................................................................................. 7
5.0 QUALITY PURPOSE OF CTR FOR CPY.......................................................................................................... 7
6.0 CONTROL OF PROJECT QUALITY PLAN....................................................................................................... 8
6.1 EXPLANATION...................................................................................................................................................... 8
6.2 CONTROL OF PROJECT QUALITY PLAN................................................................................................................ 8
6.3 IMPLEMENTATION OF QUALITY PLAN................................................................................................................... 8
7.0 QUALITY MANAGEMENT SYSTEM................................................................................................................. 9
7.1 GENERAL REQUIREMENT..................................................................................................................................... 9
7.2 OVERALL REQUIREMENT..................................................................................................................................... 9
7.3 DOCUMENT CONTROL........................................................................................................................................ 11
7.4 CONTROL OF RECORD....................................................................................................................................... 13
7.5 MANAGEMENT RESPONSIBILITY & COMMITMENTS.............................................................................................. 14
7.6 DESIGN & ENGINEERING.................................................................................................................................... 18
7.7 PROCUREMENT QUALITY PLAN & PROCEDURE.................................................................................................. 21
7.8 CONSTRUCTION QUALITY PLAN & PROCEDURE................................................................................................. 31
7.9 CONTROL OF MONITORING AND MEASURING DEVICES.......................................................................................39
7.10 QUALITY TRAINING PROGRAM, MEASUREMENT, ANALYSIS & IMPROVEMENT...................................................39
7.11 INSPECTION AND TESTING................................................................................................................................ 47
7.12 PUNCH LIST PROCEDURE........................................................................................................................................ 50
7.13 FINAL QUALITY DOSSIER INDEX PROCEDURE............................................................................................................... 56
APPENDIX I............................................................................................................................................................... 56
APPENDIX II.............................................................................................................................................................. 57
APPENDIX III............................................................................................................................................................. 58
APPENDIX IV............................................................................................................................................................ 59
8.0 ANNEXES........................................................................................................................................................ 60
8.1 EQUIPMENT CALIBRATION LIST (QCF_004)...................................................................................................... 61
8.2 PUNCH LIST FORM – (PL _00).......................................................................................................................... 62
8.3 NON-CONFORMANCE REPORT – (QCF_NCR_001)..........................................................................................63
8.4 INTERNAL AUDIT PLAN SCHEDULE..................................................................................................................... 64
8.5 TECHNICAL QUERY FORM (TQ_01)................................................................................................................... 65
8.6 REQUEST FOR INSPECTION FORM (RFI_01)...................................................................................................... 66
8.7 MATERIAL ACCEPTANCE REQUEST (MAR)........................................................................................................ 67
8.8 QUALITY MANAGEMENT SYSTEM – RESPONSIBILITY MATRIX.............................................................................68
8.9 QUALITY TRAINING PLAN SCHEDULE................................................................................................................. 71
8.10 PROJECT QA ACTIVITY FLOW CHART.............................................................................................................. 72
8.11 PROJECT SITE QC ACTIVITY FLOW CHART..................................................................................................... 73
9.0 LIST OF FORMS.............................................................................................................................................. 74
9.1 LIST OF PROJECT QUALITY CONTROL PLANS.................................................................................................................. 74
9.2 LIST OF PROJECT QUALITY FORMS.............................................................................................................................. 74
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1.0 INTRODUCTION

In December 2020 , ENI agreed to discuss circular economy and sustainable agricultural initiatives to develop

biofuels and bio-feedstock industry in Congo Republic, supporting the Country to reach its decarbonization targets

through 2030.

During 2022, CPY and Congo Republic Government will jointly conduct studies to assess the feasibility and

economic attractiveness of projects in the areas of agricultural development, used cooking oil, bioethanol and bio-

refining with the purpose of leveraging agricultural waste and vegetable oil as a feedstock for bio-refineries. More

specifically CPY and Congo Republic Government has agreed on developing fast track activities for agricultural

development activities, reaching production of bio feedstock by 2023.

The agricultural development project focuses on the development of sustainable oil crops cultivations in Congo

Republic such as cover crops (brassica carinata, camelina sativa), castor seeds, croton trees in agro-forestry

systems and other agro-industrial co-products.

The agricultural project includes the construction and the management of agricultural hubs (AGRI HUBS) to extract

oils from oilseeds to be used as feedstock for biofuel production. The AGRI HUBS will be developed by ENI Congo

S.A.; the first AGRI HUB will be completed within 2023.

1.1 Scope

The project quality plan describes the requirements of quality management system and the activities stipulated. It

provides the basic document used for the quality management system, and supplies the information that is identical

with the quality management system.

The Plan is applicable for the Project Management, Engineering, Construction, Installation, and Commissioning of

the Bio-Fuel Industrial Startup AgriHub Project.

Scope of Work for the EPCIC (Engineering, Procurement, Construction, Installation and Commissioning)

CONTRACT for the AGRI HUB PLANT. The activities to be conducted are the following:

 Civil /Structural /Architecture

 Electrical

 I&C

 Mechanical

 Process

 Safety
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 Balance of plant

CTR Scope of WORK includes:

a) Management, Project Control and Administration

b) Detailed Engineering Design

c) Procurement, Supply and Transportation

d) Plant Construction, erection and installation including site erection of procured equipment and facilities for

construction

e) Pre-commissioning & Commissioning

f) Start up and Performance Tests

g) General Services, including Construction Camp, facilities, utilities and services for SITE and Camp

1.2 Definition

PROJECT BioFuel Industrial Startup Agri Hub


COMPANY (CPY) ENI CONGO
PMC Project Management Consultant
CONTRACTOR (CTR) ZEROCK CONSTRUCTION
QUALITY Compliance with the specification and requirement of the CONTRACT

INSPECTION Activity where the characteristics of item(s) or service(s) are subject to examination,
and/or measurement, and/or testing to determine compliance with the specification
QUALITY CONTROL Activity where the characteristics of item(s) or service(s) are subject to inspection and
(QC) correction to ensure compliance with the specification. QC includes inspection
QUALITY Activity where a proactive, planned and systematic program is used to ensure the
ASSURANCE (QA) item(s) or service(s) are in compliance with the specification.
QUALITY Activity that provides for managing the integration of QA with cost and schedule to
MANAGEMENT ensure the item(s) or service(s) are reliable and safe.
QUALITY AUDIT Activity that provides management with a method to monitor performance of QA
Documents that are prepared and utilized for the purpose of verifying and recording
QUALITY RECORDS compliance of any operation directly related to the product quality. The record may be
in the form of hard copy or electronic media
HSE Health, Safety, Environment
PQP Project Quality Plan
QMS Quality Management System
ITP Inspection Test Plan

WBS Work Breakdown Structure

MDR Master Document Register

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TDR Technical Document Register


LLI Long Lead Item
FOB Free/Freight on Board
RFQ Request for Quotation
CAD Computer-Aided Design
ISO International Standardization Organization
WPS Welding Procedure Specification
WPQR Welding Procedure Qualification Record
NDE Non-Destructive Examination
TPI Third Party Inspection
NCR Non-Conformance Report
PO Purchase Order
MR Material Requisition
FOC Fiber Optical Cable
EPCIC Engineering, Procurement, Construction, Installation and Commissioning
NDT Non-Destructive Testing
OEM Original Equipment Manufacturer
ITB Invitation to Bid Document
RCU Root Causes Analysis
CAR Corrective Action Request
MMD Monitoring Measuring Devices

2.0 REFERENCES

2.1 ISO 9001: 2015 Quality Management System – Requirements

2.1 ISO 10005: 2018 Quality Management – Guidelines for Quality Plans

2.1 ISO 9000: 2005 QMS – Fundamentals and Vocabulary

2.1 Doc. N° SGI-QUAL-014 ENI Quality Management Specification

2.1 ISO 10006 QMS - Guidelines for quality management in projects

2.1 ISO 19011 Guideline for Auditing Management Systems.

2.1 ISO 31000 Risk Management.

2.1 ZCNL-QAQC-QCM-210121 Contractor Quality Manual

2.1 30A100GPG00200 Material Management Procedure

2.1 30A100GPG00190 KPI Data Typology Definition

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3.0 QUALITY POLICY & QUALITY OBJECTIVES

3.1 Quality Policy

To ensure the satisfaction of our Clients, ZEROCK must achieve and maintain the highest levels of quality in all
areas of its activity.
Therefore, we commit to:
• Always follow all of the requirements of our customers while taking into account the acquired experiences.
• Develop, maintain and continuously improve on a quality management system based on the idea of ISO
9001 and other standards/codes, this will not only improve the quality of operations but also bring about
reduction in overall costs of rendering services and products.
• Involve all our staff in the development process so that everyone is aware of the importance of its activities
and how it contributes to the achievement of the Company.
• We strive to establish a good name through our dedication in delivering quality workmanship and integrity
of our services. Our concern for development move us to implement solutions that greatly promote
customer satisfaction.

Our company implements these commitments, in line with the quality of the group policy, through the following
activities:
• Satisfaction of our customers,
• Continuous control of business processes by monitoring indicators and targets communicated,
• Staff training in System Quality Management,
• Analysis, at the annual management review, of the results and the definition of an action plan to improve
our system of quality management.

The Engagement of all employees to these commitments and their implementation is a key element of our
success and strengthen our strategic positioning in the field of construction.

Maroun Kassouf

Managing Director

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3.2 Quality Objectives

The Project Quality Objectives are:

(a) Quality Management Objectives:


1. Strictly observe the rules and regulations of the project quality management system, enhance leadership,
participate in by all employees, use method of management of system and process to exercise scientific
management on project quality work, complete the project to the satisfaction of CPY, perform audit,
continually improve the quality of the project.
2. Prepare quality management documents covering the entire project, enhance internal audit, fill in and
maintain process record, promote effective implementation of quality system, pass the audit performed by
CTR.

(b) Project/Product Quality Objective:


1. Design Input Review Rate 100%;
2. Purchased Material Inspection Rate 100%;
3. Welding Repair Rate less than 2%;
4. One-time Put into Operation Successful Rate 100%.

The quality policy and quality objectives embody the quality goal and direction, and are important part of project
general policy and objectives. It constitutes a framework for quality review and continual improvement.

All employees shall study them conscientiously and observe them strictly.

4.0 QUALITY POLICY OF CTR FOR CPY

“Insisting on adopting the advanced applicable technique and scientific management CTR will supply the

satisfactory products and services to CPY and carry out, maintain and improve continued the quality management

system.”

The policy is adapted to the purpose of CTR, and is an important integrated part of business policy of CTR.

The policy shows that CTR will meet the requirements of CPY the products and the continual improvement.

The policy provides a range used for establishing and reviewing the quality objective of CTR.

The leaders at all levels shall communicate the quality policy to all management departments, professional offices,

teams and branches in order to enable the staff of CTR to understand correctly the policy and insist on putting into

effect.

The reviews of the quality policy shall be carried out continuously by CTR, to ensure the continual compatibility,

sufficiency and effectiveness; the policy shall be revised to be adapted to the change of environment of CPY, if

necessary.

5.0 QUALITY PURPOSE OF CTR FOR CPY

Ensure the finished products are 100% qualified, set up the consciousness of providing product with high quality,

and devote major efforts to developing the activity of creating the excellence products.
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Achievement rate of contract execution is 100%.

Do the good job during the construction and do the good improvement work after the project put into operation.

Carry out comprehensive project management, and make great efforts to keep the project management to be

connected with the orbit of international universal management model.

Carry out comprehensive quality management and insist on the continual improvement of the quality management

system.

All staff shall recognize and implement seriously the quality objective, establish the correspondent quality objective

with the departments related to the quality together, to enable more detailed and to be measurable, and to permit to

be identical with the quality policy, in order to ensure the implementation of the quality objective.

6.0 CONTROL OF PROJECT QUALITY PLAN

6.1 Explanation

This Project Quality plan defines and stipulates the project quality objectives, project organization and

responsibilities, resources management, process controls, project quality requirements, measurement and

analysis. The project quality plan outlines and ensures that the quality of work is up to company standards and

specifications.

6.2 Control of Project Quality Plan

The Quality Assurance/ Quality Control Department (QA/QC department) shall be responsible for the preparation of

this quality plan. The Project Manager (PM) shall be responsible for review of this project quality plan.

Other departments concerned of CTR shall jointly review it. The Project Quality plan will not come into effect until

authorized personnel of CTR approve it.

The project quality plan shall be reviewed by the project management team representatives and approved by the

project manager, then issued to CPY for approval.

6.3 Implementation of Quality Plan

The Project Manager shall organize all the departments of the Project and Subcontractors to implement and

maintain this project quality plan. All the construction departments and/or Subcontractors shall follow it strictly. The

QA/QC department shall supervise and inspect the implementation of this project quality plan with other

departments concerned. The QA/QC department is responsible for the implementation of this project quality plan.
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7.0 QUALITY MANAGEMENT SYSTEM

7.1 General Requirement

CTR top management has established quality management system and, QA/QC Department has developed this

project quality plan in accordance to ISO 9001-2015 standards and taking into consideration CPY quality system

specifications and project documents. All staff of the project shall implement and maintain the quality management

system and continually improve its effectiveness. The project quality documents will exercise control on processes

based on the following requirements.

a) Identify the processes needed for the quality management system.

b) Determine the sequence and interaction of these processes.

c) Determine methods and criteria needed to ensure that both the operation and control of these

processes are effective.

d) Ensure the availability of resources and information necessary to support the operation and

monitoring of these processes.

e) Monitor, measure and analyze these processes.

f) Perform actions necessary to achieve planned results and continual improvement of these

processes. Subcontractors shall abide and establish their own quality management system and prepare quality

plan accordingly based on the requirement of the project quality plan and their scope of work to be carried out.

7.2 Overall Requirement

CTR is committed to develop, document, implement, maintain and continuously improve the Quality Management

System.

a) The quality management system covers the detailed process required by the contract document, for managing

the quality of engineering, procurement, construction, installation and commissioning and warranty of project.

b) In order to guarantee the above-mentioned process and the operation and control of the external contract

process the quality management system is set up to ensure the implementation of Quality Assurance and Quality
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Control and supply all the relevant quality assurance requirements to its Subcontractors & suppliers etc. involved in

the project for compliance.

c) The necessary resource and information shall be provided to ensure the operation of process and the

effectiveness of the supervision.

d) With the aid of analyzing the information which come from the supervising and measuring process the

corrective and preventive measures shall be taken for the continual improvement of these processes, to realize the

quality policy and quality objective of CTR.

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7.3 Document Control

CTR set up and carry out strict control of quality records and documents required by the quality management

system, in order to ensure that the holders of the documents can make good use and prevent the misuse of the

invalid or scrap documents.

7.3.1 Administration department shall be responsible for the control of quality system document,

technical documents, correspondence and the documents from out-side, for example, regulatory and

statutory documents. It shall also direct, monitor and inspect the document control of other departments.

7.3.1.1 Each department shall appoint a person as document controller who is responsible for receiving,

dispatching, registering, numbering and filing the document within scope of work of his own department.

7.3.1.2 The numbering system of project quality system document shall observe the requirements of the CPY

project document control procedure.

7.3.2 Control of quality management system documents.

Scope of quality management system documents:

 Controlled quality system documents issued by CTR.

 Project quality plan, project quality control procedures, inspection test procedures and management

instruction.

 Contract documents, procurement documents, correspondence and records.

7.3.3 Control of technical documents.

Scope of the technical document

a) Drawing,

b) Project Execution Plan,

c) Construction plan,

d) Construction instruction,

e) Standards and specifications,

f) Inspection and test procedures for different disciplines,

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g) Pre-commissioning and commissioning plan,

h) Design change order,

i) Work interface record.

7.3.3.1 Distribution of construction drawings:

a) According to contract requirement and project internal procedure, engineering drawings shall be made

available to Administration Department and logged by Administration Department.

b) A distribution matrix shall be prepared by document controller. After the matrix is approved by Deputy Project

Director the drawings can be distributed and the recipient shall sign his name on Distribution log.

c) The document controller in each department shall be responsible for control and distribution of the drawings

received. After completion of the project, drawings shall be returned to administration department for hand-over or

destroy except the drawings must be kept for future use.

7.3.3.2 The Administration department shall register and file project specification and standards. The obsolete

specifications may be kept by document controller for the purpose of knowledge preservation, but they

must be marked with the stamp “For Reference Only”.

7.3.3.3 The technical documents prepared by each department shall be jointly reviewed by related departments

and distributed by administration department after approval by Deputy project director (DPD) in-charge.

7.3.3.4 The control of as- built technical documents and data shall observe requirement of the project contract

and as-built drawing of detail design procedure manual.

7.3.4 Correspondence.

7.3.4.1 A letter is prepared when the giving or issuing of approvals, certificates, consents, determinations, notices

and request, which shall be type-written, printed or electronically made and signed by project

management or the authorized representative. The letter number is assigned by administration

department.

7.3.4.2 A transmittal is used to convey technical documents and drawings. All transmittal shall be numbered and

prepared by using approved transmittal coversheet. The transmittal number is assigned by administration

department. For the numbering system of letter and transmittal, see the project document and control

procedure and relevant internal management stipulations prepared by administration department.

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7.3.4.3 Each department shall prepare their own list of quality system documents and list of technical documents.

Documents shall be distributed by use of distribution record of documents.

7.3.4.4 Changes to documents and data shall be reviewed and approved by the same department that performs

the original review and approval. The invalid and/or obsolete document shall be promptly removed from all

points of issue or use, or otherwise assured against unintended use.

7.3.4.5 Other content not mentioned here shall observe the project document and data control procedure and

relevant internal management stipulations prepared by administration department.

7.4 Control of Record

CTR shall set up and carry out the record control, as well as the controls of mark, storage, protection, index and

preservation period, and provide evidences in which the product has satisfied the requirement and the quality

management system has been operated effectively.

7.4.1 QA/QC department is a responsible department of controlling QA/QC records. It shall be in charge of quality

records including but not limited to records of quality management review, quality audit, corrective and

preventive actions, non-conformance report (NCR), site inspection and test and so on. It shall monitor and

audit quality records prepared and controlled by each department.

7.4.2 Each department shall be responsible for development, control and management of quality records required

by responsible processes of QMS process function distribution chart. Each department shall also prepare

the numbering system of the records. “Records List” used in each department shall be established and

maintained by each department. Records shall be legible, readily, identifiable and retrievable.

7.4.3 Except the records and formats that shall be handed over to CPY or placed in CTR archive, Project records

shall be retained till the end of commissioning.

Quality system implementation records shall be retained till the completion of the project.

7.4.4 The records that need to be handed over or filed shall follow the contract and CTR regulation and rules.

7.4.5 The detailed requirements of control of record shall refer to quality.

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7.5 Management Responsibility & Commitments

CTR consists of leadership planning layer, function department management layer and execution layer.

7.5.1 Project Quality Management Organization & Information Flow Chart

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7.5.2 Management Commitment

The authorities and responsibilities of Project Manager and Main Department Managers, especially their duties to

the QAQC activities in the Project, are described as below:

7.5.2.1Project Manager

Project Manager makes commitment to: observing CTR’ President’s commitment, focusing on quality, executing

the contract strictly, satisfying CPY contract requirement, developing and implementing the quality management

system, exercising effective control on various processes that impact project quality and various processes

developed from the project, providing to CPY the satisfactory project.

The following activities shall be done to keep the commitment:

 Communicating to all employees in the project the requirements and importance of CPY’s and local

regulations, statutes and laws.

 Establishing the project quality objectives. The status of implementation and fulfillment of project objectives

shall be considered as the basis of evaluating the effectiveness of project quality management system.

 Providing the necessary resource for implementation, establishment and improvement of quality management

system.

 Analyzing the quality at regular interval, evaluating the suitability, effectiveness and adequacy of the quality

system.

 Administration Department Secretary Group shall perform practical works to assist project management in

taking on commitment.

7.5.2.2QA/QC Manager

Under the leadership of the project top management of CTR, the QA/QC Manager shall exercise quality

management on their quality processes listed at PROJECT’s QUALITY DELIVERABLES Documents.

Based on project requirements and if necessary, subcontractors shall provide their own QC inspectors, whose

qualification shall be identified and approved by CPY and the work be supervised by CTR.

 QA/QC Manager shall be reporting to and receiving Project direction from the Project Manager.

Communicating the QA/QC events with the Deputy Project Manager. In case of quality related concerns which

cannot be resolved by the Deputy Project Manager (DPM), the QA/QC Manager can communicate with the
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Project Manager, The Vice President and the President of CTR.

 The QAQC Manager is responsible for the development and maintenance of Project Quality Plan for assuring

that the project activities are performed and accomplished in accordance with the Project Quality Plan and

approved procedures.

 QA/QC Manager specific responsibilities include, but not limited to:

 Strictly observe the rules and regulations of the project quality management system, enhance leadership,

participate in by all employees, use method of management of system and process to exercise scientific

management on project quality work, complete the project to the satisfaction of CPY, perform audit,

continually improve the quality of the project.

 Prepare quality management documents covering all the project, enhance internal audit, fill-in and maintain

process record, promote effective implementation of quality system, pass the audit performed by CTR.

 QA/QC Manager shall be responsible for development of project quality objectives and resolve the objectives

into each department. Each department heads and Subcontractor shall establish its own quality objectives.

QA/QC Manager will check and review the status of implementation.

 QA/QC Manager shall be responsible for Quality management system planning and continual improvement is

an important part of planning quality management system.

 The integrity of the quality management system is maintained where changes to the quality management

system are planned and implemented.

 QA/QC Manager shall be responsible to oversee all aspects of quality for works managed, designed, and

constructed by CTR and its assigned Subcontractors.

7.5.2.3Procurement Manager

Reporting to and receiving operational guidance from the Project Manager. The Procurement Manager is

responsible for all procurement activities and Quality Activities related for the Project and take direct responsibility

for Project procurement performance.

Procurement Manager specific responsibilities include, but not limited to:

 Functional and operational direction and coordination of the Project Management Organization.

 Interfacing with Project Management Organization for the development, implementation, and control of

procurement policies and procedures.


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 Procurement of equipment, materials, and services; vendor evaluation and shop inspection.

 The Procurement Manager is also responsible for material receiving and warehousing at each site and

maintains a full control of materials issued for construction.

7.5.2.4Construction Manager

Reporting to and receiving technical and administrative direction from the Project Manager. The Construction

Manager is responsible for all construction activities and Quality Activities related for the Project.

Construction Manager specific responsibilities include, but not limited to:

 Construction direction.

 Material control during construction.

 Design document constructability review/input.

 Implementation of construction plan and procedures.

7.5.2.5Control Manager

Reporting to and receiving Project direction from the Project Manager. The Control Manager is also responsible for

the overall monitoring of the Project's performance against the approved budget and schedule.

Control Manager specific responsibilities include, but not limited to:

 Administration and maintenance of the Project schedule.

 Cost control, accounting, trending and estimating services and progress reporting.

7.5.2.6HSE Manager

Reporting to and receiving the direction from Deputy Project Manager for project related issue but directly refer to

the HSE department for the implementation of the safety criteria with the project.

The HSE Manager is responsible for the safety, environment protection and health of the Project and also for safety

of construction personnel and equipment on site which will be protected and prevented with the applicable safe

facilities and makes the overall construction in safe and sound condition.

7.5.2.7Document Control Manager

Reporting to and receiving Project direction from the Deputy Project Manager. The Document Control Manager is

responsible for the reception, classifying, numbering, issuance, callback of quality documents, and, takes part in

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reviewing of as-built documents, organizes translation and typing of notices, records and documents of quality

conference.

7.5.2.8Site Quality Manager

Quality Site manager is assigned for site follow up on each activity of quality management. He Reports to and

receiving Project direction from the QA/QC Manager. He shall be responsible for overall quality control activities of

construction and related activities.

Instructing and training the Inspectors from construction teams with their task, the quality site manager is fully

responsible for implementing the Project Quality Plan at site.

7.5.2.9Quality Inspectors - II

Report to Site Quality Manager. The Inspector’s responsibilities are included as below:

 Receive Instructions from Site Quality Manager and feedback quality information timely.

 Strictly execute & follow inspection plans and procedures.

 Conduct quality control and quality inspection according to regulation and requirement.

 Fill and keep records of site inspection, tracking and urging reclamation of quality deficiency.

 Feedback quality information at site to Quality Site Manager should be in time.

Through various meetings, reports, documents internal publications and computer compiler network, the horizontal

and vertical connection between various different layers and function of CTR will be kept to link up the information

in relation to the QMS to ensure the effectiveness of the process of QMS.

7.6 Design & Engineering

Engineering department is responsible for engineering control and part of engineering work, it shall conduct

supervision on all engineering and design work.

7.6.1 Design & Engineering Planning:

Under the guidance of Engineering Manager, Engineering department shall carefully study the Main Contract,

especially about the technical part, identify the customer’s requirement and ensure that engineering shall satisfy the

requirement and achieve the expected objectives.

During the design and development planning, the engineering department shall determine:

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 The design and development stages, for example, intermediate design and final design, basic design and

detailed design.

 The review, verification and validation that are appropriate to each design and development stage. The

records of the review, verification and validation shall be maintained.

The responsibilities and authorities for design and development.

 The Engineering Manager shall manage the interfaces between different groups involved in design and

development to ensure effective communication and clear assignment of responsibility.

 If there are some changes to the requirement of engineering, the planning output shall be updated, as

appropriate, as the design and development progresses.

7.6.2 Design & Engineering Inputs.

Engineering department shall identify and document the design and development inputs. These inputs of the

project include:

 Contract document: there are a lot of basic technical requirement, data and drawings in the documents. It

describes the project facilities, operation and control philosophy, scope of work, technical specifications of

different disciplines and survey data.

 Functional and performance requirements of the project. They specify the quality of design documents.

Designers shall pay attention to the suitability, safety, economy, construction easiness of the design

document.

 Applicable statutory and regulatory requirement of local authorities and international associations.

 Environment protection, forestation and other potential social requirement.

 The inputs shall be reviewed for adequacy. Requirements shall be complete, unambiguous and not in conflict

with each other.

7.6.3 Design & Engineering Output.

Design & Development outputs shall:

 Meet the input requirements for design and development.

 Provide ER (Engineering Requisition)document used for purchasing, drawings, operation and maintenance

manual.

 Contain or reference project acceptance criteria.


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 Specify the characteristics of the project that are essential for its safe and proper use.

 The type of output may be documents, specifications, drawings and data sheets.

 The outputs of design and development shall be approved by engineering department manager, project

director and customer (if required) prior to release.

7.6.4 Design & Engineering Review.

 The purpose of the review is to ensure the suitability of stage and final design results to the internal and

external resources, the adequacy of conformity with general design inputs, and the effectiveness of achieving

established effects.

 Engineering department shall determine the review requirements and perform review for the design at

appropriate design stages.

 The type of review may be meeting review, expert review, review at different levels, trade review.

 Participants in such review shall include representatives of function concerned with the design and

development stages being reviewed.

 Records of the results of the reviews and any necessary actions shall be maintained.

7.6.5 Design & Engineering Verification.

 Verification shall be performed in accordance with planned arrangement to ensure that the design and

development outputs have met the design and development input requirement.

 Design verification may take activities such as:

a) Perform alternative calculations.

b) Comparing the new design with a similar proven design, if available.

c) Undertaking test and demonstration.

d) Especially when new structure, new material and new technology are adopted in the project, verification

activities shall be determined in design planning and must be conducted.

e) Records of the results of the verification and necessary actions shall be maintained.

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7.6.6 Design & Engineering Validation.

 The validation shall be performed to ensure that the resulting project is capable of meeting the requirements

for the specified application or intended use.

 Wherever practicable, validation shall be completed prior to the delivery or implementation of the project.

 Records of the results of validation and any other necessary actions shall be maintained.

7.6.7 Control of Design & Engineering Changes.

 Lead Engineer is responsible for collection of all design change requests and raises formal “Design Change

Request (DCR)” for modification to all approved or issued engineering documents.

 DCR shall be registered and distributed to the engineers concerned for their review of the impact on the work.

 Engineering manager shall authorize the DCR and seek the approval from customer, then forward a copy of

the DCR to responsible engineer to modify the design.

 The design changes cannot be implemented prior to review, verification, validation and approval.

 Records of the results of the review of changes and any necessary actions shall be maintained.

7.7 Procurement Quality Plan & Procedure

The purpose of control over the purchasing process is to ensure that the purchasing product conforms to specified

purchase requirement.

7.7.1 Vendor Evaluation Procedure:

7.7.1.1 Request for Evaluation

 The Project Procurement Manager, on identifying the need for procurement of Goods and/or Services,

reviews the Company approved vendors list to select suitable vendors or suppliers to tender.

 If after Confirming that the selected vendors and/or suppliers are not on the approved vendor list, the Project

Procurement Manager submits a formal request to the Quality Manager to evaluate and assess the suitability

of the candidate vendors for approval.

 On receipt of request for evaluation of candidate vendors, the Quality Manager shall assign a QA Engineer to

perform the vendor evaluation activities.

 QA Engineers, under the control of their Quality Manager, then obtain the necessary information and data

from the vendors

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 All the documents submitted by the vendors shall be reviewed for approval.

7.7.1.2 Evaluation Methods

Upon receipt of a request, the Quality Manager shall determine evaluation method(s) to be applied
among following alternatives and the QA Engineer nominated by Quality Manager shall initiate the
actions necessary for vendor evaluation.
 Through Vendor’s performance history

 Through Vendor’s current quality system

 Through Vendor's facility assessment

7.7.1.3 Performance History

 The QA Engineer shall evaluate the vendor’s performance history of providing GOODS which conform to the

specification of M/R.

 Evaluation will be made on the basis of the CONTRACTOR’s records on the subject vendor’s previous

supplying performance, quality of GOODS, quality of services, and so on.

 QA Engineer shall obtain relevant information from the Project Procurement Manager or the related corporate

discipline.

 The Project Procurement Manager shall obtain the sales references from the vendors, and each vendor shall

ensure that his sales references should be true.

 The vendor’s performance history shall cover recent 5 years from the date of evaluation. If the vendor has no

performance experience of recent 5 years or if he is a new market-comer, the Project Procurement Manager

shall obtain from the vendor assessable information such as that of supplying similar item or service, current

capability of supplying GOODS, physical condition of the current manufacturing facility / equipment or

management attitude toward quality.

7.7.1.4 Quality System

 The QA Engineer shall make an objective evaluation of the vendor’s current quality system through

documented qualitative and quantitative information. This evaluation shall include reviewing the vendor’s

Quality Management System, Manual, and Procedures, as appropriate.

 The QA Engineer shall make out the Vendor Evaluation Report which shall be approved by the Quality

Manager.

7.7.1.5 Facility Assessment

 The Quality Manager has responsibility of determining the facility-assessed vendor taking into consideration of
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criticality of GOODS.

 The Quality Manager shall assign a Lead Auditor as an assessment team leader and, if needed, Auditors as

assessment team members. The assessment team shall carry out the Facility Assessment in accordance

with the “Audit Procedure”.

 The Lead Auditor shall prepare the Vendor Evaluation Report. The Vendor Evaluation Report shall, as a

minimum, include assessment scope, assessment team, persons interviewed, summary of assessment

results including vendor quality system manual revision number and date, evaluation of the quality system/

facilities/personnel and comments, if any, and the Lead Auditor's recommendation.

 The comments shall be categorized as follows:

 Major findings: Findings which require much time and efforts for corrective action.

 Minor findings: Findings which can be corrected easily and promptly.

 The Vendor Evaluation Report shall be forwarded to the Quality Manager for his review and approval.

7.7.1.6 Vendor Approval

 The Quality Manager has authority to approve the vendors on the basis of vendor evaluation. For minor

findings recorded during a vendor assessment, the Quality Manager may approve that vendor by obtaining

the vendor's written agreement for adequate corrective action within a due date. In case of major findings, the

vendor shall not be approved.

 The Quality Manager shall notify the vendor in writing, the following:

 CONTRACTOR acceptance of the vendor's quality system

 Identified lapses and inadequacies for corrective action.

 Any proposal by CONTRACTOR to use a vendor who is not on the Company Approved Vendors List shall be

referred to Company for guidance on the level and participation of Company in audit and assessment

activities. Project approval to use vendors, after any audit and assessment will come from Company.

7.7.1.7 Company Approval

 The Vendor Evaluation Report shall be submitted to Company for approval.

7.7.1.8 Company Approved Vendor List

 GOODS shall be procured from the only vendors who are listed on the COMPANY Approved Vendor List and

who are additionally approved by Company.

 Once the additional vendors are approved by Company through the procedure described above, the approval
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notice shall be handled in the same manner as a Company document.

 The Project Procurement Manager shall update and maintain the COMPANY Approved Vendor List whenever

additional vendors are approved by COMPANY.

7.7.1.9 Document Maintenance

 The Quality Manager will be responsible for maintenance of all documents related to vendor evaluation.

7.7.2 Purchasing Process:

7.7.2.1 The project shall establish the criteria for selection, evaluation and re-evaluation of suppliers. It shall

evaluate and select suppliers based on their ability to supply product in accordance with the project

requirement.

7.7.2.2 Procurement department, engineering department, construction department and contract department are

all responsible departments of the purchase process.

7.7.2.3 Procurement department shall develop procurement manual to define the criteria of selection, evaluation

and re-evaluation of suppliers.

a) Evaluation of supplier about qualification, certification, history, reputation, financial status.


b) Product quality status and experience of suppliers.
c) Supplier’s quality management system and its assurance ability.
d) Degree of customer ‘s satisfaction.
e) Service and support ability after delivery by supplier.
f) Establish a short name-list for qualified suppliers.

7.7.2.4 Engineering department, together with relevant departments, shall evaluate the qualification, certification,

experience and quality assurance ability of design Subcontractor for selection of qualified design

Subcontractor.

7.7.2.5 Construction department, together with other relevant departments, shall be responsible for development of

ITB document (Invitation Bidding Document) for construction Subcontractor, in which criteria of evaluation

and selection shall be defined.

Its work at this stage shall include but be not limited to the following:

a) Evaluating the qualification, certification, experience, quality assurance ability, etc.

b) Evaluating competence of management staff and skilled workers.

c) Evaluating the equipment ability.

d) Forming a short name- list of construction Subcontractor.


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7.7.2.6 Contract department shall prepare terms and conditions of the ITB document according to the main

contract, law and other related regulatory and statutory requirements and monitor the observation of the

above.

7.7.2.7 Records of the results of monitoring and any necessary actions taken shall be maintained.

7.7.3 Purchasing Information:

7.7.3.1 Procurement department shall define the goods requirement about specification, quality, acceptance,

delivery, price and quantity in the Purchasing order.

7.7.3.2 Engineering department shall prepare design sub-contract document, in which design requirements and

design scope shall be defined.

7.7.3.3 Construction department, together with relevant departments, shall prepare the documents about project

subcontract and labor service subcontract. In these documents, construction department shall provide the

following information:

a) Work-scope, characteristics of subcontract project.

b) Requirement of work period, quality and safety of subcontract project.

c) Requirement of product and service supplied.

d) Requirement of acceptance and delivery of the subcontract project.

e) Requirement of equipment and personnel supplied by supplier.

f) Requirement of work processes and quality management system of supplier.

7.7.3.4 Contract department shall prepare legal content of the subcontract.

7.7.3.5 The adequacy of specified purchase requirement shall be confirmed and approved prior to communication

to the supplier.

7.7.3.6 The content of the purchase order includes the vendor's quotation number, quotation date, the RFQ

package that was issued to solicit the bid, the equipment specification number and drawing numbers

issued with the RFQ, all inspection notices, hold points for witness and notification requirements, and all

vendor documentation and data required. The equipment specification refers to all codes, standards, and

stamps to which the CONTRACTOR. must adhere.

7.7.3.7 Procurement and project teams should review and approve purchasing documents for accuracy to the

specifications prior to their release. To eliminate any delays caused by the vendor not having a hard copy

of the Purchase Order in his possession, a Purchase Order Authorization Letter can be faxed to the
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vendor, which allows him to process the order without any delays. An acknowledgement copy of the

purchase order is also issued to the successful CONTRACTOR. to sign and return, acknowledging their

agreement with pricing, description, delivery, and the commercial terms of the sale.

7.7.4 Purchased Product & Services Verification:

CTR or authorized Third Party Representative may verify at the source or upon receipt that the purchased products

and service conform to requirements. Verification by CPY or a Third-Party Representative does not reduce CTR's

responsibility.

a) QC Department shall be responsible for quality control in the all processes of procurement. It shall prepare

product inspection and test plan/ procedure, which shall be approved by customer, and conduct the verification of

purchased product.

b) The QC group shall review the procurement documents and ensure the suitability, adequacy and effectiveness

of these documents.

c) The QC group shall conduct inspection and test for delivered material and equipment.

d) If necessary, the QC group can perform verification at the supplier’s premises and make verification

arrangements and method of product release in the purchasing information before verification.

e) Engineering department shall verify the achievements of design Subcontractor at different design stages.

f) Construction department shall verify that the construction progress and quality of subcontracted work meet the

requirements of Subcontract.

g) All the records of the verification shall be maintained.

7.7.4.1 Source Inspection

CTR shall inspects the work of OEM vendors, suppliers, sub-vendors, and manufacturers as necessary to obtain

equipment and materials conforming to project specifications.

CTR shall develop source inspection and surveillance program including quality surveillance schedule to ensure

quality of procurement.

7.7.4.2 Inspection & Test Plans

CTR’ s Vendors shall prepare and use the Inspection and Test Plans which give detailed instructions for the

inspectors. These Inspection & Test Plans are approved by CTR and CPY representatives prior to any inspection

activity being performed.

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Procurement inspection for designated items begins with the award of the purchase order and concludes when the

inspector has duly released the equipment from the vendor's shop after successful completion of all inspections.

7.7.4.3 Inspection Coordination & Responsibilities

The Procurement Inspection Supervisor coordinates inspection activities. After receiving the assignment from the

Procurement Inspection Supervisor, the source inspector reviews the order and conducts a pre-inspection meeting,

followed by an initial inspection visit.

Progressive inspection visits will be conducted to perform the required equipment inspection as outlined in the

Inspection and Test Plans. The Source Inspector maintains the field file and reports the results to the responsible

office. The Procurement Inspection Supervisor also coordinates source inspection activities with CPY designated

Inspection personnel. The third-party inspector selection and approval shall be endorsed by CPY.

7.7.4.4 Criticality Rating of Equipment & Materials

CTR will perform, as a minimum, equipment inspection according to required inspection levels. CTR may deviate

from these recommendations upon approval from CPY according to project and work requirements.

CTR will perform the inspection and test work to different vendor according to the Risk Number (RN) (1-18), and

finalize the Rating Classification (CR) (I , II , III or IV) of equipment and material, finalize the frequency of

inspection according to RN and CR.

7.7.4.5 Work Process Control

CTR identifies and plans the production and, where applicable, installation processes which directly affect quality

and ensures that these processes are carried out under controlled conditions.

These include:

a) Documenting work instructions defining production and installation, where the absence of such instructions

would adversely affect quality.

b) Monitoring and control of suitable process and product characteristics during production and installation.

c) Approval of processes and equipment.

d) Stipulated criteria for workmanship in written standards or representative samples of same.

7.7.4.6 Special Processes

When results of certain processes cannot be fully verified by subsequent inspection and testing of the product

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(e.g., heat treating, NDE, cleaning, etc.) Processing deficiencies may become apparent only after the product is in

use. Then continuous monitoring and/or compliance with documented procedures is required to ensure that the

specified requirements are met.

7.7.4.7 Receiving Inspection & Testing

CTR ensures that incoming items are not used or processed until they are inspected and conformance to

requirements is verified according to the quality plan or documented procedures.

7.7.4.8 In-Process Inspection & Testing

CTR inspects, test and identifies the work as required and uses process monitoring and control methods to

conform to requirements.

CTR holds the work until the required inspection and testing are complete or necessary reports have been

received and verified.

7.7.4.9 Final Inspection & Testing

No work will be released or delivered to CPY until all inspection and testing of the activities specified in the Quality

Plan has been satisfactorily completed and the associated data and documentation are available and properly

authorized.

7.7.4.10 Inspection & Test Records

CTR will maintain records which give evidence that the work has passed inspection and/or testing with defined

acceptance criteria.

7.7.4.11 Non-Conformance Control

CTR procedures ensure that nonconforming products are not used or installed.

Control provides:

a) Identification, documentation, evaluation, segregation (when practical).

b) Disposition of nonconforming work.

c) Notification to the functions concerned.

The Quality Plan defines responsibility for review and authority for the disposition of nonconforming work. Where

required by the contract, the proposed repair of nonconforming work is reported to CPY representative. Repaired

and repeated work will be re-inspected using the same inspection method that discovered the defect in accordance

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with documented procedures.

7.7.4.12 Corrective Action

CTR takes the following action to correct nonconforming work:

a) Establishes, documents, and maintains procedures for investigating the cause.

b) Takes corrective action needed to prevent recurrence.

c) Detects and eliminates the root cause(s) by analyzing all processes, work operations, deviations, quality

records, service reports and complaints.

d) Initiates preventive action, commensurate with the risks encountered, to deal with problems.

e) Verifies that corrective action is taken and that it is effective.

f) Implements and records change in procedures resulting from corrective action, if any.

7.7.4.13 MATERIAL CONTROL

(1) General

2) Material control refers to the various measures adopted to reduce the amount of loss of materials at the time of

receiving, storing and issuing the designated materials.

3) Material control in practice is exercised through periodical records and reports relating to purchase, receipt,

inspection, storage and issuing direct and indirect materials. Proper control over material can contribute

substantially to the efficiency of a job activities.

(2) Objectives

 To enable uninterrupted progress of work.

 To ensure requisite quality of materials.

 To minimize wastage.

 To provide information and traceability.

7.7.4.14 Handling, Storage, Packing & Delivery

Handling, storage, packaging, preservation, and delivery of material is on a per project basis appropriate to satisfy

the requirements of the quality system and contract specifications. Major equipment and materials are handled

according to procedure in a manner that prevents the loss of product value.

Equipment and material are stored according to procedure in a manner to prevent the loss of value, preventing

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damage or deterioration. Equipment/material easily affected by adverse conditions such as moisture, radiation and

windstorm will be stored in an appropriate secured warehouse.

Any special storage preparations or ongoing maintenance will be performed upon receipt of such material (i.e.,

electric motor bumped and kept dry with lights, desiccant installed in crates or boxes as required, etc.) and

throughout storage as required.

Packing or crating of equipment/material will be performed by reputable packager and may be witnessed by an

experienced CTR representative or employee if required. Each crate/package will be marked as is required by

customs for exit of the country of origin and for entrance to the country of end use (Republic of Congo).

Each crate will also be marked with numbers (e.g., crate 1 of 24) to alert the receiver as to how many crates should

be received. An itemized report is created which lists the contents of each crate-by-crate number, vendor, cost,

and date shipped. This report is provided to the receiver to assist with receipt of material. Like items are crated

together to ensure ease of receipt of material, as well as the ability to track the material during shipment.

Shipments of equipment/material may include a CTR representative at the receiving end (foreign port) to witness

the loading of the material onto local trucks, clearing local customs, and to the destination to ensure proper receipt

of material. The freight forwarder will also be present to ensure that there are not time delays due to paperwork or

language difficulties when clearing customs.

7.7.4.15 Quality Records

CTR maintains procedures for identifying, collecting, indexing, accessing, and storage of quality records such as

material test records, pressure test certificates, compliance certificates, FAT inspection etc which shall be available

by CTR.

Quality records are maintained to demonstrate conformance to specified requirements and the effective operation

of the quality system. Pertinent vendor quality records are included. Each project contract specifies the disposition

and/or the retention time required for the various documents.

The requirement for maintaining these records to demonstrate achievement of the required quality and the

effective operation of the quality system become part of the job completion as witnessed and accepted by CPY. All

quality records are turned over to CPY as part of the Project Records Books as required by the Contract.

7.7.4.16 Internal Quality Audits

CTR Quality Assurance department performs internal quality audits which include CTR and its Subcontractor
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activities.

All audits are planned and scheduled. However, unscheduled audits may also be performed in the situations

where there may be serious quality problems for the activities performed by CTR or the Subcontractors.

All audits are performed by the qualified and certified auditors. Audit results will be documented and provided to

the audited organization.

7.7.4.17 Training & Qualifications

CTR maintains procedures for identifying the training needs and provides for training of all personnel performing

activities affecting quality. Personnel performing specific assigned tasks are qualified on the basis of appropriate

education, training and/or experience, as required. Appropriate records of training are maintained.

7.8 Construction Quality Plan & Procedure

7.8.1 Levels of Quality Surveillance


Levels of quality surveillance will be generated to suit the project requirements and will be specified in the Quality

Plan.

7.8.2 Inspector Qualifications

For civil, structural, piping, mechanical, electrical, instrument and FOC disciplines, CTR describes what type of

personnel in the organization will perform in-process and final inspections.

All inspectors covering assignments for critical welded fabrications will be certified by The American Welding

Society, The American Petroleum Institute, or similar international institutions approved by CTR and CPY.

All inspectors witnessing or evaluating non-destructive testing will be certified to SNT-TC-1A, Level II.

As with engineering and procurement, CPY will review and approve Construction staffing where necessary.

7.8.3 Control of Production & Services Provision.

7.8.3.1 Control department shall prepare overall progress schedule according to the requirement of the contract

and construction characteristics. It shall prepare the procedures for progress controlling and monitoring.

These procedures and documents shall be based on level-4 schedule, which shall be duly filled by

authorized field engineers, verified by construction department, and then put into the databank of the

progress monitoring system.

7.8.3.2 Construction department shall prepare “Construction Procedure” or “Work Instruction” for these

key/special processes. These documents shall be reviewed by related department and submitted to CPY
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representative for approval.

7.8.3.3 Construction department shall check and inspect the material and equipment provided by Sub-

contractor/Vendor for their conformity of quality requirements. It shall also check and review the

qualification of the personnel who engages in the key/ special process.

7.8.3.4 For the covered work, construction department shall fill in “Covered Work Record” and invite CPY’s

representative, QC inspector to the jobsite to jointly inspect the covered work. If acceptable, countersign

“Covered Work Record”, then cover the work. The covered work record shall be maintained.

7.8.3.5 Based on workload, work schedule and work characteristics, construction department shall develop a

“Construction Equipment Plan” and “Work Force Balance Plan” and implement by itself or urge

Subcontractor to implement these plans.

Construction department or Subcontractor shall also provide or use sufficient monitoring and measuring

devices whose precision and accuracy shall meet the requirement of specification, standards and codes.

7.8.3.6 QA/QC department shall develop quality control plan for key/special processes and conduct inspection

and surveillance for these processes.

QA/QC department shall check the calibration status of monitoring and measuring devices to make sure that their

precision, accuracy and validity meet the project requirement.

7.8.3.7 Construction department shall prepare “Construction Record” and QA/QC department shall fill in the “QC

inspection and test records”. One process cannot be passed to next process until the required inspection

and tests have been completed or necessary reports have been received and verified.

7.8.3.8 The project cannot be delivered until final inspection and test have been done and associated data and

documentation are handed over and approved.

7.8.3.9 If non-conforming product is found out, it shall be reviewed in accordance with documented procedure. It

may be:

a) Reworked to meet the specified requirements.

b) Accepted with or without repair by concession.

c) Re-graded for alternative applications.

d) Rejected or scrapped.

For the detail, see Control of Nonconforming Product

7.8.4 Validation of Process for Production & Service Provision.

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7.8.4.1 Some processes for production and service provision shall be validated because the resulting output

cannot be verified by subsequent monitoring or measurement, or their deficiencies become apparent only

after the product is in use or the service has been delivered.

7.8.4.2 Construction department shall identify the special processes, prepare “Construction Procedure” or “Work

Instruction”, define criteria of review and approval, and provide suitable equipment and qualified personnel

for performance of these processes.

7.8.4.3 Process review, equipment status, personnel qualification etc., shall be recorded and

maintained.

7.8.4.4 If there are some changes to important material /product parameter, the process shall be

revalidated.

7.8.5 Identification & Traceability.

7.8.5.1 In order to preclude the product or its status from confusion or misuse during the product realization and

achieve the purpose of traceability of product or service, a suitable means shall be taken to identify the

product, product status and the unique identification of the product where traceability is a requirement.

7.8.5.2 Procurement, construction and QA/QC department are all responsible departments of the process.

7.8.5.3 Procurement department shall maintain the original identification No. on purchased material and

equipment. When marking by itself is necessary, the type and content shall conform to the requirement of

documentation and product.

7.8.5.4 The records of identification shall be registered in a list.

7.8.5.5 Construction department shall check the identification No. before withdrawing material from warehouse.

7.8.5.6 Construction department shall mark the sub-projects and construction processes, for example, pipeline

No., weld No., welder No.

7.8.5.7 Construction Record may be an identification of installation work.

7.8.5.8 QA/QC department shall be responsible for identification of product status, for example, the status of

inspection and test (Hold for inspection, acceptance, reject, valid, invalid…).

7.8.5.9 Where traceability is a requirement, all the responsible departments shall take the responsibilities to

control and record the unique identification of the product.

For example, when material shall be separated or covered, the worker or warehouse keeper shall transfer the

identification marking. Construction engineer shall monitor and document the marking transfer to assure the

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traceability of the material. QC inspector shall supervise the process of identification transfer.

7.8.6 Customer Property:

This Project is an EPC (Engineering, Procurement, Construction) project. When any of CPY’s property is

transferred to CTR. CTR shall exercise care with them, protect the existing property of CPY and restore to original

profile after installation. Construction department shall record the status of the customer property and report

happenings to customer or related department.

7.8.7 Preservation of Product.

7.8.7.1 Preservation shall be controlled in accordance with an approved Preservation Procedure.

Preservation records shall be maintained by Procurement and Construction team till final handover to CPY.

7.8.7.2 Procurement department shall set up warehouse and material yard for storage of material and equipment.

The type and size of warehouse or yard shall meet the quality and quantity requirements of material. The

method of control over the material or equipment shall observe the normal practice and Vendor’s

recommendation. Care shall be taken for identification, handling, package and storage.

7.8.7.3 Construction department shall be responsible for product preservation during construction. Safety

measures shall be taken to protect the products from damage, loss and deterioration.

7.8.8 Non-Conformity Management Procedure

7.8.8.1 Identification & Segregation Of Non-Conforming Product

After identifying the non-confirming items, it shall be tagged with label or wrapping an identification tape

around. Segregate them in order to prevent them from being used, inform the Discipline Supervisor and fill

out the NC Report.

Each non-conforming product shall be segregated or isolated in a location set aside for this purpose

where practicable.

7.8.8.2 Handling Of Non-Conforming Product

The non-conforming product is handled in one of the following ways.

• By taking action to eliminate the non-conformity.

• By accepting product under concession by relevant authority from CTR in consultation and by raising
Technical Query / Deviation Request to CPY.

• By re-grading the product to preclude its original intended use.

• By scrapping the non-conforming product & replacing with new product.

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• Repaired or Re-worked Product shall be re-inspected in accordance with the original Quality Control
Plan or with approved documented procedures by which it was inspected initially.

• Non-Conformances observed during construction activities at site locations shall be recorded for all
actions taken up to close out of the NCR and the records shall be maintained.

7.8.8.3 Initiation Of Non-Conformance Report

• Originator of NCR shall record the non-conformance in section 1 of the NCR and Corrective Action
Request form QCF_NCR_001 on what it is and what it should be basis, and by describing the relationship
to the applicable standard, specification or code.

• Investigate the non-conformance and record the root cause thereof in conjunction with Project
QA/QC Manager or the person nominated by him at work site as applicable.

• The action party, to whom the NCR has been issued, shall review the same and sign at part-1 to
signify his acceptance of the non-conformity

7.8.8.4 Proposed Action

The discipline supervisor or head of department shall propose the disposition of the non-conforming product
in conjunction with Project QA/QC Manager or the person nominated by him by filling part “2” of the NCR and
Corrective Action Request form QCF_NCR_001 from one of the remedial actions indicated, adding
explanatory notes if necessary, and then signs it.

The Project QA/QC Manager or his assigned field expert engineer shall consult CPY technical team
authorities for critical decision making where applicable.

The disposition action shall be one of the following:

• Repair/re-work or take remedial action to correct the product so as to be acceptable to the specified
requirements.
• Accept as “Fit For Purpose”
• Re-grade product to preclude its original intended use or for its alternate use.
• Scrap or return the product for replacement.

7.8.8.5 Repair Re-Work Or Remedial Action

The Head of Department or Action Party shall propose the method of repair or re-work in conjunction with
Project QA/QC Manager or the person nominated by him. He shall seek technical advice where required for
a suitable repair or re-work or remedial actions method from appropriate field expert Engineer.

The Head of Department shall also propose a reasonable time frame for completion of remedial action. He
shall then complete part 2 of the NCR and return the NCR to Project QA/QC Manager or the person
nominated by him for assessment.

7.8.8.6 Accept as “fit for purpose”

The Site Superintendent or Head Of Department or Action Party evaluates the non-conformed product to be
of minor nature and considers that repair or re-work is not necessary, then he shall justify it in conjunction
with Project QA/QC Manager or the person nominated by him to accept as it is, stating that the non-

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conformed product is still fit for the purpose. “Fit for Purpose” decision requires CPY approval. However,
appropriate corrective action shall be taken to prevent recurrence of the same.

When a decision is made “Accept as is” in order to use the non-conforming product, an engineering
justification shall be arranged stating that the product is “Fit For Purpose” through CTR project group and a
written approval for the said concession shall be sought from CPY.

7.8.8.7 Re-Grade For Alternate Use

The Head of Department evaluates in conjunction with Project QA/QC Manager or the person nominated by
him, that the rejected product cannot be repaired and used for the intended purpose. In order to use the non-
conforming product, it may be determined to alter & re-grade it to use for another purpose precluding its
original intended use.

A written approval for the above said “Re-grade for alternate use” shall be sought from CPY representatives
through a documented correspondence justifying the reasons why the product cannot be repaired and why it
is necessary to use for the alternate purpose.

7.8.8.8 Scrap And Replace

The Head Of Department evaluates in conjunction with the Project QA/QC Manager or the person nominated
by him, that the rejected product can neither be repaired and used for the intended purpose nor can be used
for alternate purposes. In this circumstance, it may be determined to remove and scrap the non-conforming
product from the site. However, the product shall be suitably replaced in an appropriate time frame.

CPY shall be informed through documented correspondence, in case it is recommended to scrap and
replace the non-conforming product.

7.8.8.9 Corrective Action

While proposing actions and approving to handle the non-conforming products, the appropriate corrective
actions also shall be specified where applicable by the Head Of Department or Action Party in conjunction
with Project QA/QC Manager or the person nominated by him:

• Immediate corrective action shall be taken to correct the product so that it shall be acceptable to the
specified requirements.

• Appropriate corrective actions shall be taken in order to avoid the recurrence of the nonconformity.

7.8.8.10 Assessment Of Proposed Action

The Project QA/QC Manager or the person nominated by him seeks advice from field experts depending on
the nature of technical problems involved for critical resolution of the NCR.

However, QA/QC Senior Inspector can be authorized to make assessment of proposed corrective actions at
work site and sign in part two of NCR box.

7.8.8.11 Completion Of Agreed Action

The Head of Department or Action Party shall ensure timely execution of the agreed corrective actions
specified on the NCR and complete part 3 of the form. Where repair / re-work or remedial action is proposed,
it shall be carried out following the original procedure and closely monitored by the QA/QC Inspectors.

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If COMPANY Specification calls for a repair procedure, then the repair or re-work shall be executed using
repair procedure.

7.8.8.12 Follow Up And Close Out Of NCR

The QC Coordinator / QA/QC Inspector shall follow up all agreed corrective actions and re-inspect the
product and shall ensure that it has been corrected to the specified requirements where applicable and that
the approved disposition has been implemented. He shall then complete and sign part 4 of NCR at the re-
inspection box.

The Project QA/QC Manager shall review the NCR and close out the NCR if the resolution of NCR is
correctly carried out as per this procedure.

7.8.8.13 NCR Issued by CPY

The Project QA/QC Manager shall review all NCRs from CPY, investigate and resolve the issues to close-out
NCRs.

7.8.8.14 Non-Conformance At Suppliers Premises

Non-conformance identified through surveillance inspection / external audits at the Suppliers/Vendors


premises shall be recorded & controlled by issuing Corrective Action Request. The CAR shall be followed up
for its close out and resolved in a reasonable time frame.

The suppliers/vendors shall also review, investigate & resolve any non-conforming product using their own
internal quality management system where possible and reasonably practicable.

7.8.8.15 Non-Conformance Register

The Document controller shall maintain a NCR master register. He / she shall record all unique reference
numbers for all NCRs received from all work locations showing the current status, actions taken and close
out status.

Separate register will be maintained by the Document Controller showing similar details of NCRs from CPY
and CARs raised as a result of findings at the supplier’s premises.

A copy of master register for NCRs will be forwarded to CPY as and when required.

7.8.8.16 Review Of Corrective Actions

The Head of Department in conjunction with the Project QA/QC Manager or the person nominated by him
shall investigate the cause of the non-conformity and decide on the corrective/preventive actions to be taken.
Any investigation results / reports / records made in case of major non-conformity, shall be attached to the
NCR. The cause of non-conformity and proposed corrective / preventive actions, with the target completion
date shall be documented in the NCR and Corrective Action Request form QCF_NCR_001.

The QA/QC Supervisor/ Senior Inspector shall forward the copy of the NCR to the Project QA/QC Manager
when part two of the NCR/CAR (Proposed Disposition) is completed. Later shall review and propose
alternate corrective actions at the event that the action proposed are not adequate to prevent future
recurrence.

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In the case of a Major NCR raised either by CTR or CPY or external third party, the Project QA/QC Manager
shall monitor the implementation of corrective actions by the relevant line department and close out the NCR
upon satisfactory implementation of the corrective actions.

7.8.8.17 Quality Control Data Package

The original NCR raised shall be compiled in the relevant Quality Control Data Package as applicable. A
copy of the closed-out NCR shall be kept at file.

7.8.8.18 NCR and Corrective Action Request form

QA/QC DEPARTMENT
Non-Conformance Report and Corrective
Doc
Action Request QCF_NCR_001
No.

Rev
0
No.

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7.9 Control of Monitoring and Measuring Devices

7.9.1 Based on project characteristics, progress and workload, Construction department shall prepare

“Monitoring and Measuring Devices (MMD) Requisition Plan” in which the number, type, category shall be

defined.

7.9.2 Construction department shall get these devices calibrated at specific intervals or prior to use against

measurement standards traceable to international and national measurement standards.

7.9.3 Procurement department shall provide the devices (buy or rent) used in the course of procurement and

protect the devices from damage and deterioration during handling and storage. For the monitoring and

measuring devices provided by supplier or used at jobsite by supplier, construction department shall

review the list of MMD and check the records of calibration status prior to use.

7.9.4 QA/QC department shall check and keep track of the calibration status of these devices.

7.9.5 When the devices are found to be out of calibration, the validity of the previous measuring results shall be

assessed and recorded. Construction and QA/QC departments shall take appropriate actions for the

devices and any product affected.

7.9.6 Records of the results of calibration and verification shall be maintained.

7.9.7 When used in the monitoring and measurement of specified requirements, the ability of computer

software to satisfy the intended application shall be confirmed. This shall be undertaken prior to initial use

and reconfirmed as necessary.

7.10 Quality Training Program, Measurement, Analysis & Improvement

7.10.1 Quality Training Program

7.10.1.1 CTR policy is to employ project personnel who have previous demonstrated experience in working with

the standards and codes applicable to the project. Project personnel shall be qualified for their function.

Additional specific operator training will be provided if required.

7.10.1.2 Training needs shall be the subject of discussion at management review meetings.

7.10.1.3 All personnel in the project who may have an effect on project quality and who will stay on the project for

more than two months shall have a quality induction. Records showing this induction shall be maintained.

7.10.1.4 The QA/QC Manager shall ensure that managers, site senior staff and quality related personnel are

familiarized with:

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 The essentials of the ISO 9000 series of standards.


 The project quality system as set out by this project quality plan.
 The quality management procedure applicable to each manager’s work and duties
 Implementation of detailed procedures such as QCP’s, ITP’s.

7.10.1.5 CTR has established and maintains a training process to:

 Identify competency needs for personnel who perform tasks affecting quality.
 Provide training to address these needs.
 Assess the effectiveness of the training provided.
 Ensure that personnel are aware of the relevance and importance of their activities and how
they contribute to the achievement of the quality objectives
 Maintain records of education, experience, training, and qualifications per the control of
documented information procedure
 The manpower required for execution of the project shall be adequate to suffice the task and
in line with the requirement of CPY.

7.10.1.6 Training Program:

CTR regards employees as its greatest asset. To this end, the company maintains an established employee
qualification/training program. All personnel are classified on the basis of appropriate education, training, skills, or
experience. Records of all training activities are kept in each employee’s file at the regional or corporate office
whichever is applicable.

7.10.1.7 Training Requirements Review

 The responsibility for identifying employee-training requirements lies with each department
manager.
The purpose for the review is to identify competency needs for all personnel performing
activities affecting quality.
 Job requirements, internal audit reports, and corrective action activities determine employee-
training needs. In addition, an annual review and midyear review is conducted with each
employee, at which time the employee’s training needs, as well as the effectiveness of the
previous training is discussed.
 Each employee is made aware of the relevance and importance of their activities and how
they contribute to the achievement of the quality objectives.

7.10.1.8 Formal and Informal Training

 All employees receive an “on-the-job” training by the responsible area supervisor. After a
30-day trial period, all new/transferred employees are evaluated against the position
requirements and if performance is found to be satisfactory, qualification for the applicable
position is awarded.
 New employees receive indoctrination into the quality system from the Quality Manager.
 Designated employees may receive formal off-site/on-site training/seminars in various job-
related disciplines/topics, as determined by the responsible supervisor/manager.

7.10.1.9 Induction & Training for Sub-Contractors

 CTR quality team arranges the training program for the key personnel of the sub-contractor
to induce the awareness about quality till the bottom line.
 The quality manager is responsible for the conduction of the training program.
 There are various training modules developed for this kind of trainings.

7.10.1.10 Training and Qualification of Inspectors

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 CTR ensures that the inspectors are having the required qualification to ensure the
effectiveness of quality objective.
 The competency of the personnel to perform inspections is developed by one of the following
methods:
 Providing personnel with working knowledge of appropriate contract details, documents, codes, practices
followed & standards.
 Training or orientation in general and specialised methods of planning and performing inspections.
 On the Job training under direct supervision of experienced qualified inspector.
 The QA/QC manager regularly evaluates the inspectors for proficiency and skill development

7.10.2 Monitoring & Measurement

7.10.2.1 Customer satisfaction

1) Scope of Application

CTR shall monitor information and the perception of CPY’s satisfaction. The methods for obtaining

information on such perception may include letters and correspondences, CPY’s complaints, claim

analysis, direct communication, compliments, electronic communication systems, comments during

meetings, etc.

2) Responsibility and Authority

The Project Manager shall be responsible for:

 Deciding the primer monitoring methods considering the above information sources, and

implementing effective survey and analysis.

The Quality Manager shall be responsible for:

 Following up internal issues that may affect CPY’s satisfaction.

 Obtaining feedback from the assigned auditor over customer’s satisfaction. Such information shall be

collected during the quality audits.

3) Development

The investigation and analysis of Customer’s satisfaction shall consider the following:

 The quality of the service supplied, and Customer’s satisfaction over the final product.

 The level of cooperation and reliability with regards to Customer’s expectations.

 Major aspects from the Customer’s point of view.


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 Customer’s satisfaction / dissatisfaction may be subjective and perceived in several ways, and if

necessary, it may be described in the Interface / Coordination Procedure.

 CPY’s satisfaction shall be measured in accordance with the performance rating included in the Key

Performance Indicator Procedure, which shall be developed and issued to CPY for its approval. This

procedure shall include a list of all performance indicators for the Engineering, Procurement and

Construction stages and the weight value for each indicator (or index) giving as a result the

performance rating of the Project.

7.10.2.2 Contract department is responsible for monitoring and measurement of CPY satisfaction, working out CPY

satisfaction index in order to carry out effective monitoring and measurement. Every half year, contract

department shall collect, analyze and evaluate project monthly reports, fill in “Statistic Form of Customer

Satisfaction” and report to CTR.

7.10.2.3 Contract department is responsible for analysis and evaluation of information collected from

implementation, amendment and change of the contract and routine communication with customer, the

result shall be the input of continual improvement. Other departments (including engineering department,

procurement department, construction department, control department and QA/QC department) shall

establish effective approach to communication with customer in order to obtain, monitor, collect the

information as to whether CTR has met CPY requirements.

7.10.2.4 Main source of customer information:

a) Feedback from CPY to product or service

b) Customer requirement, service information and contract information;

c) Change of market requirement;

d) Information related to rivals;

e) Survey to customer;

f) Complaint of customer.

g) Information from monitoring and measurement.

7.10.2.5 CPY visitation shall be conducted by the form of technical review meeting and weekly progress review

meeting. It shall inspect and check construction progress, quality, service and other items to ensure

conformity to contract requirements. Visitation can be implemented by the method of visitation meetings.

The minutes of the meeting shall be signed by CPY and CTR representatives.
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7.10.2.6 Other aspects about CPY satisfaction shall observe CTR Procedure “Monitoring and Measurement of

Customer Satisfaction”.

7.10.3 Internal Audit

7.10.3.1 QA/QC department is responsible for internal audit, preparing “Quality Assurance Audit Plan”, helping the

audited departments to correct the nonconformity and verifying the corrective actions. The audit

document shall be maintained. For the QA work flow, see the attachment IV “Project QA Activity Flow

Chart”.

7.10.3.2 QA/QC department shall prepare internal audit plan at the beginning of each year and get the approval of

project leader in charge. The plan shall define the requirement of the audit criteria, scope, frequency,

methods, audit implementation, audit report, corrective/preventive action, verification and documentation.

7.10.3.3 Internal audit should be conducted once a year. For a department, the audit interval shall be less than 12

months. For each internal audit, all the procedures and sites involved in the quality management system

shall be covered. Regular internal audit may involve the whole quality system or parts of it. Random

internal audit can be conducted at any time when special condition occurs (e.g., there is a great change

to the function).

7.10.3.4 QA/QC department shall select and appoint qualified auditors to conduct audits. Auditors shall not audit

activities related to their own work to ensure the objectivity and impartiality of the audit process.

7.10.3.5 Auditors shall objectively describe the nonconformity, communicate with the audited department who shall

analyze the causes of nonconformity and bring forward correction methods and finish correction within

limited time.

7.10.3.6 The lead auditor shall prepare audit report which can be used as input to evaluate project quality

management system and continual improvement. The audit results shall be handed over to the

departments having been audited.

7.10.3.7 For the internal audit control, refer to the procedure “Internal Audit Control Procedure”.

7.10.3.8 Monitoring and measurement of processes

QA/QC department is responsible for monitoring and measurement of the processes. It shall develop QC plan and

procedures, which define the processes of quality management system and the methods to monitor and

measure them.

7.10.3.9 The main methods to monitor and measure processes are process audit, process review, routine process

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supervision and inspection, data analysis and so on. These methods shall demonstrate the ability of the

processes to achieve planned result.

7.10.3.10 Construction department shall conduct related monitoring and measurement of the

construction processes according to relevant procedures.

7.10.3.11 Monitoring and measurement shall be taken for:

a) Special processes;

b) Processes controlled with parameters;

c) Processes needed for approval;

d) Related releases.

7.10.3.12 Corrective actions shall be taken to the nonconformity discovered in monitoring and

measurement of processes. The collected data and information shall be analyzed. If necessary, preventive actions

shall be taken.

7.10.3.13 Monitoring and measurement of product

7.10.3.14 QA/QC department is responsible for the monitoring and measurement of in-process and

final products, preparing “Process control procedure” and “Control procedure of in-process and final

inspection and test”, determining the appropriate stages to monitor and measure the products.

7.10.3.15 QA/QC Department shall prepare QC Plan in which “H”, “W”, “C” points (Hold point, Witness

point, Certification point) shall be inserted. When works reach these points, Construction department shall

issue IN (Inspection Notification) attached with checklist and relating documents to QA/QC inspectors to

engage in joint inspection. For the QC work flow, see the attachment V “Project Site QC Activity Flow

Chart”.

7.10.3.16 Procurement department is also the responsible department of this process, it shall monitor

and measure the purchased products, prepare inspection and test procedure for purchased products,

determine the appropriate stages of monitoring and measurement, verification method, acceptance criteria

and suggestions for nonconformity. The monitoring and measurement of the purchased products shall

observe the procedure “Quality Control Procedure” prepared by procurement department.

7.10.3.17 All functional departments shall maintain records of monitoring and measurement. Evidence

of conformity with the acceptance criteria shall be maintained. The persons authorizing release of product

shall be determined.

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7.10.3.18 Product release and service delivery shall not proceed until the planned arrangements have

been satisfactorily completed, unless otherwise approved by a relevant authority (where applicable, by the

customer). For emergency release, see the procedure of inspection and test for delivered material.

7.10.3.19 Supervision and control shall be taken on the material purchased by CTR or supplied by

suppliers, and irregular supervision or tour inspection shall be taken on construction processes. The

results shall be recorded and maintained.

7.10.4 Analysis of Data

7.10.4.1 QA/QC department is responsible for collection, filing and statistical analysis of data.

7.10.4.2 The collected data shall include:

a) Customer “CPY” satisfaction (suggestion, complaint).

b) Data related to quality system implementation: information of monitoring and measurement of process, the

ability of product realization, the results of quality analysis meeting, internal audit conclusion, output of top

management review in office of CTR.

c) Data related to product: quality records, non-conforming information of product.

7.10.4.3 The project shall demonstrate suitability and effectiveness of the quality management system and

evaluate the opportunities of improvement through data analysis. This mainly includes:

a) The present status and trend of customer satisfaction. Analyzing the main customer complaints and improving

quality management system.

b) Conformity to quality management system. Analyzing problems according to data statistic, analyzing the

processes in which the problems lie and then improve them.

c) The present status and trend of change to processes and products. Analyzing if potential problems exist,

determining the necessity to take preventive action.

7.10.4.3.1Suppliers. Analyzing suppliers’ products, production processes and quality management system,

determining the necessity to enforce the control on them

7.10.5 Improvement

7.10.5.1 Continual improvement

7.10.5.1.1 The project shall continually improve the effectiveness of the quality management

system through implementation of the quality policy, quality objectives, audit results, data analysis,

corrective and preventive actions and management review.


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7.10.5.1.2 QA/QC department is responsible for continual improvement of quality management

system.

7.10.5.1.3 The project shall plan for improvement when:

a) Any information indicating unsatisfied result arise;

b) Rational suggestions from employees are accepted;

c) The customer requirements cannot be met properly;

d) Wide scope or not only one department is involved in corrective or preventive actions.

7.10.5.1.4 Processes and methods of continual improvement

a) Seek the opportunities and ways of improvement by monitoring and measurement of quality management

system, product, and customer satisfaction, and by means of internal/external audit, control of nonconformance

and data analysis.

b) Realize improvements through preparation and implementation of corrective and preventive actions, this is the

main and effective method to continually improve quality management system.

c) Determine new improvement target by the output of management review from head office of CTR.

7.10.5.1.5 QA/QC department shall collect, analyze information to prepare the project quality information sheet

and report to CTR Head Office at the end of each month.

7.10.5.2 Corrective action

7.10.5.2.1 QA/QC department is responsible for monitoring, inspection, check, following-up

and verification of corrective action, preparing Quality Control Plan for “Corrective and preventive action control

procedure”. The relevant functional departments are responsible for implementation of corrective action in their own

departments.

7.10.5.2.2 The following requirements shall be defined in the corrective action procedure.

a) Reviewing nonconformities (including CPY complaints);

b) Analyzing and determining the causes of nonconformities;

c) Evaluating the need for action to ensure that nonconformities do not recur;

d) Determining and implementing action needed;

e) Records of the results of action taken;

f) Reviewing corrective action taken.

7.10.5.2.3 All departments concerned of the project shall actively take corrective actions,

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eliminate the causes of nonconformity to prevent recurrence. If the nonconformity is caused by CTR or

any of its Subcontractors, they shall take corrective actions and implement them separately, the

responsible department of the project shall verify the implementation results.

7.10.5.2.4 The information of corrective action shall be the input of management review in

head office.

7.10.5.3 Preventive action

7.10.5.3.1 QA/QC is responsible for monitoring, inspection, check and following-up and

verification of preventive action. Relevant functional departments are responsible for implementation of

preventive action in their own departments.

7.10.5.3.2 The following requirements shall be defined in the preventive action procedure.

a) Determining the potential nonconformities and their causes;

b) Evaluating the need for action to prevent occurrence of nonconformities;

c) Determining and implementing action needed;

d) Records of the results of action taken;

e) Review of preventive action taken.

7.10.5.3.3 Different types of quality analysis meeting shall be held for solution of the problems

about product quality and quality system. For example, weekly meeting between CTR and CPY, project

internal weekly meeting, technical meeting, etc. These meetings shall analyze the status of product quality

and quality system implementation and determine the preventive actions.

7.10.5.3.4 All departments of the project shall actively take actions to prevent nonconformity

occurrence by collecting and analyzing information and eliminating the causes of nonconformities.

d) The information of preventive action shall be the input of management review.

7.11 Inspection and Testing

7.11.1 Inspection And Test Plans

7.11.1.1 Work shall be inspected in accordance with each relevant Inspection & Test Plan.

7.11.1.2 Inspection personnel shall be assigned based on their previous experiences for similar

projects and qualification requirements.

7.11.1.3 The ITP shall set out in matrix form the sequence of inspection steps, (process description),

specific quality control requirements, notification requirements for COMPANY inspections (RFI), responsibilities,
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applicable procedures, acceptance criteria, verifying documents, review, witness and hold points. QCP’s shall be

produced in addition to ITP’s if complexity or specific inspection instructions so demand.

7.11.1.4 ITP’s and QCP’s shall be prepared and submitted to COMPANY one month before work is

planned to start.

7.11.1.5 Verifying documents shall be completed as work proceeds and shall not be left until the end

of the job. The ITP is to be used as a plan only and acceptance signatures shall be obtained on the inspection /

NDE report /RFI forms. Signing off and submission to COMPANY (if required) shall follow as soon as possible after

the work is completed.

7.11.1.6 All incoming material and equipment shall be inspected for damage and conformance to

requirements. Should incoming material not have the required Material Release, inspection shall be conducted to

confirm compliance with applicable codes and standards, prior to being released or used as a part of the work. All

incoming products and materials are subject to receiving inspection.

INPROCESS INSPECTION AND TESTING

7.11.1.7 The in-process quality control and inspection activities are performed to verify the

requirements set forth in the inspection and test plans, QCPs and function test procedures are strictly complied to

ensure the satisfactory performance of the work. Test results shall be evaluated for compliance with the specified

requirements, where if these results are within specified acceptance criteria, they shall be accepted.

FINAL INSPECTION AND TESTING

7.11.1.8 The process of final inspection and testing of products and materials shall be addressed in

the project ITP’s and QCP’s as well COMPANY requirements, as applicable.

INSPECTION AND TEST RECORDS

7.11.1.9 Work, inspection and test records such as weld reports, heat treatment charts, etc., shall be

collated and indexed in preparation for inclusion in the final handover documents.

7.11.1.10 Records shall provide sufficient information and be subject to review by COMPANY at any

stage.

CONTROL OF INSPECTION, MEASURING AND TEST EQUIPMENT

7.11.1.11 All inspection, measuring and test equipment used on the project shall be controlled and
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calibrated in accordance with specified project procedure, which identifies calibrated instruments and their re-

calibration cycle.

7.11.1.12 Where inspection, measuring and test equipment is found to be out of calibration, the

affected equipments shall be removed from further use immediately, and an evaluation of the previous inspection

and test results made by the concerned equipment, shall be carried out.

7.11.1.13 Contractor shall make sure that the inspection, measuring and test equipment (IM&TE) used

in the performance of their work are calibrated and all the records of calibration shall be provided to COMPANY for

review and approval before using them on site.

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INSPECTION AND TEST STATUS

The inspection and test status of all materials and work within the contract scope shall be known and verifiable at
all times. An up-to-date inspection status report / inspection register shall be maintained, showing when inspections
are scheduled, when inspections were completed and any NCR’s raised.

7.11.2 Field/Site Inspection Coordination Procedure

7.11.2.1 The inspections and tests for control of construction activities shall be conducted to verify the

conformity of products and services to the project requirements, applicable codes and standards for the

construction phase.

7.11.2.2 CTR shall ensure that company and any other nominated third party shall have access to

work site and fabrication shop for the purpose of inspection. The site quality manager and quality control inspectors

shall be responsible preparing and maintaining the inspection procedures and inspection test plans.

7.11.2.3 Inspection and test plans shall address the following:

 Reference Materials such as procedures, codes and standards etc.


 Responsibilities
 Acceptance criteria
 Verifying documents such as certificates, inspection reports, and check lists
 Witness and Hold Points
 Percentage of tests to be done including increased levels when performance requirements are not met or
scope of inspection
 Inspection and tests plan for controls of construction activities including the following:

þ Site preparations, roads and paving, and excavations


þ Civil/Structural/Buildings/underground piping
þ Tanks and Silos Erection
þ Mechanical Equipment
þ Welding/NDE
þ Piping
þ Electrical
þ Instrumentation
þ Blasting/Painting/Insulation
þ Testing Laboratories for soils, concrete, batch plant, mechanical, instrument calibration
þ Any other construction activity within CTR scope of work.

Inspection and testing shall be performed in accordance to the Field quality control procedures as well as the
inspection and test procedure applicable for each item.
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7.11.2.4 The Inspection and testing activities shall be carried out by the Site Quality Manager under

the coordination of the QAQC Manager, who is responsible to

 Perform directly or coordinate the required inspection and test activities


 Collect quality records issued at each phase
 Collect in good manner the ITPs and the relevant quality records, in order to change the final dossier
 Keep all quality records in a proper manner and available to CPY’s inspectors for any review

7.11.2.5 Inspection Personnel

Inspectors for field inspection and test shall be qualified in accordance with the contract requirements.

7.11.2.6 Inspection and Test Report

The result of the inspection shall be recorded in proper forms included in the applicable inspection procedure.
CTR shall submit its test reports to the CPY Representatives as specified by the applicable company standards.
For all other test reports/validation records performed by CTR or its subcontractors, there records shall be
maintained and made available to CPY Representatives for any review.

7.11.2.7 Inspection and Test Status

The inspection and test status shall be kept under control and maintained as identified in the QC Inspection status
report.
The status report shall identify all contractor required inspection and tests for each system when it is scheduled and
when it was completed.
The QC inspection status reports shall be kept current and shall be available for CPY Representatives review at all
times.

7.12 Punch List Procedure

7.12.1 Purpose
This procedure defines a structured approach and the standard requirements for tracking repair
defective items necessary for the completion of systems/sub-systems and for the subsequent
handover of the FACILITY from Construction to Commissioning and to Operations (CPY)

7.12.2 Scope
This procedure describes the standard work process for controlling punch list items where CTR is
responsible for Construction, Pre-commissioning and Commissioning.

Punch listing is to be performed prior to the transfer of responsibilities for a system/subsystem from one
stage to another for the purpose of care, custody and control.

7.12.3 Definition of Punch list


A listing of defects, omissions, damages, or discrepancies that have been observed and recorded during
inspections resulting from joint Company-Contractor system walk downs or as otherwise observed by
either party following completion of scheduled construction or commissioning scheduled inspection and
testing programs.

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7.12.4 Description Of Activities

7.12.4.1 General

Prior to the transfer of responsibilities for a System/Sub-system, a check shall be done by CTR to
verify that the scope of work for the System/Sub-system is completed in accordance with the design,
project specifications, project procedures, and any other contractual requirements. The checks shall
also consist of physical walkthrough and checking of all relevant installations within the identified
System /Sub-system limits.

The checks consist of:

a) An assessment that all tasks have been completed. This is achieved through a review of all
documentation in the System/Sub-system handover package; i.e. check sheets, QA/QC reports,
testing sheets, vendor reports, etc. for accuracy and completeness, and that all inspection and test
requirements have been carried out as specified in the relevant procedures.
b) Review of the “As Built” drawings to verify that they reflect the actual build in the field including a “red
line” mark up of all the changes or modifications.

c) Verification that the System/Sub-system conforms to all project requirements.

7.12.4.2 Punch List Classification

Punch list items shall be classified according to their degree of impact on HSSE, equipment integrity,
and subsequent scheduled activities. The assignment of punch list classification shall be agreed
between CTR Construction, CTR Commissioning and CPY Projects and Operations.

• Category “A” Punch: Must be completed prior to Mechanical completion. It signifies that the
punch list item, defect, missing item, or omission is deemed critical such as those which prevent safe
operation of plant, equipment, system and may jeopardize personnel& or equipment and must be
repaired without which the next activity cannot be undertaken safely. This category shall also include
points that cannot be attended to at a later stage of the project
• Category “B” Punch: Must be completed prior to Handover. It signifies that the punch list item, defect,
missing item, or omission which will not affect the safe progression of the System /Sub-system to the
next stage
• Category “C” Punch: Must be completed prior to PROVISIONAL ACCEPTANCE, or as soon as
practicable thereafter in accordance with a schedule to be agreed with CPY. These punches should
not affect the safe operation of the System /Sub system

7.12.4.3 Punch List Responsibility at Fabrication Shop

All Punch list items identified in the fabrication shop and not completed will be subject to the same
classification stipulated in section 7.14.4.2. However, the Punch list items not executed in shop
prior to site transportation, and thus required to be undertaken post module arrival at site, must be
agreed at site by CTR fabrication team and CPY representatives and the cost of the defect repair
will remain the responsibility of CTR after the transportation of the item from the shop to the site.

7.12.4.4 PUNCH LIST CATEGORIZATION

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• Upon generation of punch items, CTR and CPY will identify the recategorization code of the
generated punch items during Pre-Commissioning and Commissioning phases and update them on
the punch list form.
• When a sub-system is progressed from one stage to the other, the coordinator will automatically
update CPY representatives to reflect the new category of the punch item based on the agreed re-
categorization codes.

7.12.4.5 Punch Listing Phases

Punch list items may be raised, reviewed, and resolved throughout the life of the Project. A formal
inspection and verification assessment shall be carried out on System/Sub-system level at the
following phases of the project:
• Prior to hydrostatic or pneumatic testing of pipe work
• Outstanding FAT Punch items which cannot be closed at factory
• Punch items outstanding from shop
• At Mechanical Completion handover phase prior to issuing the “Sub-System Mechanical
Completion Certificate”
• At Pre-commissioning stage prior to issue “Ready for Commissioning certificate”.
• Commissioning stage prior to issue “Commissioning Completion Certificate”.
• Prior to Handover all required “C” category punch items to be identified.

7.12.4.6 Hydrostatic Or Pneumatic Testing Punch List

1. The primary objective of this punch list is to identify items which will jeopardize the wellbeing
of personnel and the integrity of the pipe work or equipment, if not corrected prior to testing.

2. Second objective is to identify items that if not corrected prior to testing will result in rework
and re-testing.

7.12.4.7 Fat Punch Items

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All the punch items that are originated from factory shall be cleared prior to shipment to the site.
However, some items cannot be closed during factory and these items shall be identified by Quality
Control Team and categorized as A, B or C with the entity responsible for closure. These items must
be closed out at the earliest opportunity.

7.12.4.8 Yard Punch Items

Yard punch items shall be tracked and closed as specified in this document and all referenced
documents. In addition, any punch items that remain open at time of load out, shall be clearly
identified as an attachment to the "Ready for Load Out " certificate and include categorization and
entity responsible for closure.

7.12.4.9 Mechanical Completion Walk Down

When all Construction ‘A’ check sheets have been completed for a sub-system and loaded CTR shall
notify CPY for a joint walk down prior to issuing the “Mechanical Completion Certificate”. Each
discipline representative records discrepancies and non-conformances found during the walk down.
The Punch List items shall be categorised in accordance with section 7.12.4.2 of this document.
The Mechanical Completion Walk down will verify that Mechanical Completion has been sufficiently
progressed so as to move into Pre-Commissioning phase.
All ‘A’ punch list items for Sub-System Mechanical Completion stage of the project shall be cleared
before the “Sub-System Mechanical Completion Certificate” is issued.

7.12.4.10 Ready For Commissioning Walk Down

When all Pre-commissioning B check sheets have been completed for a System/ Sub system, CTR
shall notify CPY for a joint walk down to issuing the “Ready for Commissioning Certificate”.

7.12.4.11 Pre Safety Start-Up Review

A system safety review shall be conducted at Systems’ Commissioning Completion prior to issuing the
“Commissioning Completion Certificate”

When all Commissioning ‘C’ check sheets have been completed for a system, CTR shall notify CPY
for a joint walk down.

7.12.4.12 Post Walk Down Punch List Resolution Process

Punch List coordinator shall arrange a walk down close out meeting within 24 hours to verify the
legitimacy and agree the categorization of punch items after each walk down. Any disputed items
shall be verified and agreed prior to handover the punch list to CPY.

7.12.4.13 Defining Punch Listing Boundaries

All inspections and verifications shall be made against the latest revision IFC, P&IDs, PFDs,
isometric drawings and relevant discipline standards, specifications, and checklists. The boundaries
for verification of the physical works are defined in the system/sub-system identification marked up
drawings which shall be attached to the walk down notification.

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Punch items will be limited to not installed as per IFC drawings, defective items & items that pose a
safety hazard to personnel or may lead to unsafe operation of the plant and shall not include
“preferential engineering” items.

Significant observations regarding the design of the facilities made during walk downs should be
treated as either Non-conformance if not built as per specification with NCRs issued by CPY, or if
additional requirements are identified above the base scope, treated as Contract variations. In either
case, these design observations should not be loaded as punch items as they do not meet the
definition of a punch list item.

7.12.4.14 Punch Listing Notification

Upon readiness of a system/sub-system for a walk down, the turnover coordinator shall issue a
“Request for Inspection” (RFI) to the concerned parties.

When issuing an RFI, CTR shall provide sufficient notice (Five Days) to all concerned parties to
ensure that the required resources are available at the time requested. Minimum requirements for
names of walk down participants must be agreed at the time of RFI issue and the walk down shall be
rescheduled if any required participant is missing. Therefore, it is important that key walk down
personnel be available and where necessary any alternates pre-agreed. The notice shall include all
relevant documentation with the boundaries of the inspection clearly indicated and Punch List for the
subsystem with the current close out status. If deemed necessary and agreed in between CTR &
CPY walk down for a particular system / sub-system may be split up as per discipline.

A “Request for Inspection” log shall be kept in the CTR office and shall be used by all parties.

7.12.4.15 Punch List Recording

During all joint walk downs, a "nominated punch items recorder" shall be named prior to the walk down.
During the walk down and immediately following the walk down, all punch list items from all participants
are to be consolidated on the master punch list. The master punch list will then be reviewed within 24 hrs
jointly with participants to agree punch item categorization. These meetings will be termed "agreement
meetings". Where punch item categorization cannot be agreed, then the punch item in question shall be
elevated to Commissioning/Completions leads and when necessary, Commissioning/Completions
Managers for assignment of category. The escalation process for all punch listing disputes must be
agreed prior to beginning walk down process." In addition, the "Master Punch List" shall be generated by
Contractor and approved by Company for each walk down.

FAT / Yard pending items shall be recorded for further follow up. All punch list generated during the
handover from CTR shall be recorded and included with the RFI.

Subsequently, all deficiencies and non-conformances discovered during walk downs the various
phases shall be recorded.

Rejected Punch items will be returned for submission as change order.

The punch list shall contain the following:

• Sub-system Number
• Punch Listing Phases
• Date of walk down
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• Punch List No.


• Originator Name
• Tag Number
• Material Required (Yes / No)
• Discipline
• Description of the deficiency
• Punch list item Category (A, B and C)
• Signature Blocks for CONTRACTOR and COMPANY representative
• Walk down participants

A Blank Punch List Form is attached.

7.12.4.16 Punch List Review, Monitoring, And Tracking

The Construction and Commissioning engineers shall regularly monitor the progress of outstanding
punch list items clearance and they shall plan/assign the priorities in line with scheduled completion
dates.

During punching it is conceivable that some punch items identified will require Engineering review
and action. The responsible engineer will communicate these punch queries to Engineering
department for mitigation and subsequent corrective implementation at site.

The punch list coordinator will review the status of all punch list items and will closely follow with the
Construction and Commissioning engineers to complete punch list items that would be deemed
critical for releasing completion certificates at the different stages of the project phase.

7.12.4.17 Punch List Clearing And Acceptance

Resolution of punch list items shall be carried out by CTR. Once the Punch list is physically closed
out in field, as per IFC drawings, CTR will sign it off on the original Project Punch List form and
submit it CPY.

CPY shall verify the punch item against IFC drawings and the Accepted Date and the name of
person who has accepted.

The responsibility for clearing punch list items shall rest with CTR Construction unless these punch
list items are agreed to be completed by CTR Commissioning team requested that something within
the Construction work scope be left out to assist with the progression of the Commissioning work
scope; e.g., insulation flange or valve covers left off for a leak test, blind installed in a closed position,
etc.

The responsibility for accepting and signing-off cleared punch list items shall be the responsibility of
CPY for any punch list items generated.

7.12.4.18 Disputed/ Disagreed Punch Items

Disputed punch item will be resolved. They will be resolved at the post walk down meeting between
CTR and CPY. If no agreement can be reached at that level then it will be escalated to Project
Management level for resolution.

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7.12.4.19 Rejected Punch Items

Rejected Punch items are a result of CPY not agreeing with CTR that the quality of the defect repair is
adequate and the defect required further remedial action. If no agreement can be reached that the quality
of the defect repair is adequate then it will be escalated to Project Management level for resolution.

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7.13 Final Quality Dossier Index Procedure

CTR shall prepare a procedure describing how quality documentation and records will be handed over to CPY. The
procedure shall be in compliance with contract requirements and shall enable CTR hand over the QAQC
documentation to CPY. CTR shall propose the procedure for the QAQC dossier which shall include but not limited
to the following:

 Structure of the QAQC Dossier


 List of Documents to be included in the QAQC dossier
 Filing system
 Cover Labels
 File Box type suitable for long preservation
 Volumes Numbering

The following example shows the master index of the QAQC Final Dossier with a brief about the quality
documentation to be submitted in the dossier. A detailed index shall be generated during project execution.

APPENDIX I
MASTER INDEX
(CIVIL)
ITEM DOCUMENT TITLE PAGE NO OF VOLUME
CODE VOL NO
C1.0 QAQC PROGRAM
C1.1 Field Inspection Procedures, work Procedures, QAQC Plan,
ITP, etc..
C1.2 Technical Queries, Non-Conformance Reports, Approval pf
3rd Party and Laboratory
C2.0 MATERIALS AND CALIBRATION CERTIFICATES
C2.1 Mix Design of Concrete and Asphalt
C2.2 Test Certificates of Materials supplied by Contractor
C2.3 Stone Aggregates Analysis Test Reports
C2.4 Soil Analysis Test Reports
C2.5 Paint Data Sheets
C3.0 Inspection and Test Reports
C3.1 Foundation of Tanks
C3.2 Concrete Paving
C3.3 Grading/Filling Sand and Crushed Stone base
C3.4 Foundation Settlement Report

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APPENDIX II
MASTER INDEX
(MECHANICAL)
ITEM DOCUMENT TITLE PAGE NO OF VOLUME
CODE VOL NO
M1.0 QAQC PROGRAM
M1.1 Approved Inspection Test Plan
M1.2 Construction Work Procedures
M1.3 3rd Party NDE Procedure, NDE Technician Certificates
M1.4 Technical Queries, Non conformance Report, Etc..
M2.0 MATERIALS AND CALIBRATION CERTIFICATES
M2.1 Approved Materials supplied by CTR – items used
Mechanical Works
M2.2 Calibration Certificates
M3.0 WELDING AND NDE DOCUMENTS
M3.1 Approved WPS/PQR
M3.2 Qualified Welders
M3.3 Radiographic Test Inspection Report
M3.4 Magnetic Particle Inspection Report
M3.5 Liquid Penetrant Inspection Report
M3.6 Ultrasonic Inspection Report
M4.0 EQUIPMENT & PUMPS
M4.1 Field Test Inspection Check Sheet
M4.2 Elevation and Installation Record
M4.3 Initial and Final Alignment Report
M4.4 Painting and Insulation Reports
M4.5 Lube Oil Flushing Record
M4.6 SAT Report (if any)
M5.0 SILOS/TANKS/COLUMNS/STRUCTURES/STATIONATY
EQUIPMENT
M5.1 Field Test Inspection Check Sheet
M5.2 Elevation and Installation Record
M5.3 Final Visual/Dimensional Report
M5.4 Tank Calibration
M5.5 Hydrotest Reports
M5.6 Painting and Coating Reports
M6.0 HYDROTEST, FLUSHING, TIE-IN PACKAGE, TEST
REPORTS
M6.1 Pressure Test Pack (P&ID, Isometrics, Pipe Support Dwg,
WeldMaps, NDT Reports, Punchlists, Pressure Test Report,
Pressure Gauges and PSVs Calibration Certificates, Flushing
Reports)
M6.2 Tie-in Package (P&ID, Isometrics, Tie-in Location, DPT and
MPI Reports, Fir up Reports, Visual Weld Reports, Valve
Test Reports, RT/UT Reports, Flange Inspection Report)
M7.0 FIRE FIGHTING SYSTEM
M7.1 Room Integrity Test Report
M7.2 Closure and Discharge Test Report
M7.3 Functional Test Report
M8.0 HVAC/EXHAUST SYSTEMS
Air duct smoke/tight Test Report
Refrigerant Piping Leak Test Report
Insulation Test Report
M9.0 LIFTING EQUIPMENT
M9.1 Lifting Equipment Inspection Reports / Certificates
M9.2 Lifting Accessories Inspection Test Reports / Certificates
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M10.0 PAINTING/COATING AND GALVANIZED REPORTS


M10.1 Surface preparation reports
M10.2 Painting Reports
M10.3 Galvanizing Certificates/Reports
M10.4 Holiday Test Reports
M10.5 DFT Gauge / Dial Indicator Calibration Certificate
M11.0 INSULATION REPORTS
M11.1 Equipment Insulation Inspection Reports
M11.2 Insulation Materials certificates / Inspection Report
M12.0 IFC/AS Built Drawings
M13.0 RFI LOG / Request for Inspection
M14.0 Final Release Reports
APPENDIX III
MASTER INDEX
(ELECTRICAL)
ITEM DOCUMENT TITLE PAGE NO OF VOLUME
CODE VOL NO
E1.0 QAQC PROGRAM
E1.1 QC Dossier
E1.2 Field Inspection Procedure
E1.3 Technical Queries, Non-Conformance Reports
E2.0 MATERIALS AND CALIBRATION CERTIFICATES
E2.1 Approved Electrical Materials Supplied by CTR
E2.2 Calibration Certificates
E2.3 Mill test reports & Calibration of electrical equipment
E2.4 Electrical testing Equipment, gauges certificates
E3.0 ELECTRICAL WORKS
C3.1 Electrical Cable Tray Installation checklists, Reference
drawings
C3.2 Electrical Cable Trench Route , installation checklist, cable
megger record and Reference drawing
E4.0 ELECTRICAL WORKS FOR PUMPS AND MOTORS
E4.1 Field inspection checklist for motors
E4.2 Checklists for heaters
E4.3 Checklists for Local Control Switches
E4.4 Electric Motors Datasheets
E4.5 Electrical Inspection Datasheets
E4.6 Cable Megger Records
E4.7 Electrical Equipment Megger Record
E5.0 ELECTRICAL LIGHTING SYSTEM
E5.1 Lighting Panels and Poles
E5.2 Quality Controls Punchlist
E5.3 Inspection checklists for Lighting
E5.4 Above and underground conduit installation
E5.5 Cable Megger Record
E5.6 Illumination Test Record
E5.7 Record Drawings

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APPENDIX IV
MASTER INDEX
(INSTRUMENT)
ITEM DOCUMENT TITLE PAGE NO OF VOLUME
CODE VOL NO
I1.0 QAQC PROGRAM
I1.1 QC Dossier Master index
I1.2 Field Inspection Procedure
I1.3 Technical Queries, Non-Conformance Reports
I1.4 Construction QCP for Instrument works
I2.0 MATERIALS AND CALIBRATION CERTIFICATES
I2.1 Approved Instrument Items and Accessories
I2.2 Approved instrument Cables, supports, trays, tubing
I2.3 Test and Calibration Certificates of instruments
I2.4 Megger Test
I2.5 Digital Multimeter
I2.6 Function Generator
I2.7 Portable Digital Manometer
I2.8 Dead Weight Testing
I2.9 Decade Resistance box
I2.10 Triple Output DC Power Supply
I2.11 Digital Pressure Indicator
I3.0 INSTRUMENTATION AND CONTROL SYSTEMS WORKS
( INSPECTION & TESTING REPORTS)
I3.1 Equipment List and Schedule
I3.2 Material List for sub vendor supplied items
I3.3 Datasheets & Equipment Specifications
I3.4 Site Survey Report
I3.5 Test and calibration of instrument Equipment Record
I3.6 NACE Certificates
I3.7 Cable Megger Test Record
I3.8 Leak Test Report
I3.9 Certificate of Calibration and test Record of instruments
I3.10 Reference Drawings
I3.11 Loop Test Inspection Record
I3.12 Inspection Record prior to Installation
I3.13 Quality Control Punch List
I3.14 Bench Test Record
I3.15 FAT Procedures / Test Reports
I3.16 Equipment test reports
I3.17 Commissioning procedure
I3.18 Commissioning Test sheet

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8.0 ANNEXES

Annex # Doc Name.


8.1 Equipment Calibration List (QCF_004)
8.2 Punch List Form – (PL _00)
8.3 Non-Conformance Report – (QCF_NCR_001)
8.4 Internal Audit Plan Schedule
8.5 Technical Query Form (TQ_01)
8.6 Request for Inspection Form (RFI_01)
8.7 Material Acceptance Request (MAR)
8.8 Quality Management System – Responsibility Matrix
8.9 Quality Training Plan Schedule
8.10 Project QA Activity Flow Chart
8.11 Project Site QC Activity Flow Chart

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8.1 Equipment Calibration List (QCF_004)

CONSTRUCTION CHECK LIST COMPANY IDENTIFICATION CODE


Job-Type-N°
EQUIPMENT CALIBRATION LIST QCF_004
SHEET DOC.CLASS ISSUE
1/1 00
ITP PHASE REF:
REPORT NO.:
_____________________

Calibration Calibration Date of Validity Until ACCEPTANCE


Nº Equipment Type Serial Nº
Agency/ Frequency Calibration YES NO NA

10

11

12

NAME DATE (dd-Mmm-YYYY) SIGNATURE

CONTRACTOR
QCF_004

COMPANY

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8.2 Punch List Form – (PL _00)

ENI BIOFUEL COMPANY IDENTIFICATION CODE


Job-Type-N°
1ST AGRI HUB – INDUSTRIAL START-UP PL_0___
SHEET DOC.CLASS ISSUE
1/1 00
PUNCH LIST FORM ITP PHASE REF:

__________________

UNIT : SYSTEM :

Contractor Client
Drawing : Drawing :

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8.3 Non-Conformance Report – (QCF_NCR_001)


QA/QC DEPARTMENT COMPANY IDENTIFICATION CODE
Job-Type-N°
Non-Conformance Report and QCF_NCR_001
Corrective Action Request SHEET DOC.CLASS ISSUE
1/1 00
ITP PHASE REF:
NCR NO.:
__________________

NON-CONFORMANCE REPORT
CORRECTIVE ACTION REQUEST
AUDIT CUSTOMER COMPLAINT INSPECTION/TEST
NCR/CAR No. Company Audited/Inspection
Date Department:
SUBSYSTEM : Location:
Work Order No.
Ref. Cont Docs/Specs/Stds:
Item Description
MINOR NCR MAJOR NCR
1. NONCONFORMITY DESCRIPTION Discipline
Quality System
Material
Equipment
Welding
Painting
Hydrotest
Fabrication
E&I
Purchasing
Specify if others
____________________
ROOT CAUSE ANALYSIS PREVENTIVE ACTION

NCR RAISED BY ACTION PARTY


Name:
Designation:
Sign:
Date:
2. PROPOSED DISPOSITION
Repair or Rework Accept as Regarde for Alternate Use Scrap & Replace
/ Remedial Action " Fit For Purpose"
Describe recommended immediate actions to correct the product and corrective actions to prevent non-conformities where applicable:

Provided Justifications for actions other than repair or rework Proposed date of Completion

Disposition Proposed by Disposition Assessed by


( Department Head / Discipline Head) (Snr Inspector,QAQC Manager,QAQC Coordinator)
Name:
Designation:
Sign:

Date:
3. EXECUTION OF AGREED CORRECTIVE ACTIONS:
Describe Immediate actions taken to correct the product: State action taken to eliminate or to prevent such non conformace in
the future:

Department/Discipline head Actual Date of Completion:


(Name/Sign/Date)
4. CLOSE OUT OF NCR
Verify that the stated actions have been executed and that such action has resolved this NCR.

Comment if required:

Actions verified by NAME DATE SIGNATURE


QCF_NCR_001

CONTRACTOR

COMPANY

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8.4 Internal Audit Plan Schedule

QUALITY SYSTEM AUDIT SCHEDULE

YEAR 2023

JAN FEB MAR APR MAY JUN JUL AUG SEPT OCT NOV DEC

CIVIL WORKS 50% 50%

PIPING/STRUCTURAL 50% 50%

MECHANICAL & TESTING 50% 50%

ELECTRICAL & 50% 50%


INSTRUMENTATION
PRECOMMISSINIONING 50% 50%

Quality Management System


Documentation requirements
Management commitment
Customer focus
Quality Policy
Planning
Responsibility, authority &
Communication
Management Review
Provision of Resources
Human resources
Infrastructure
Work environment
Planning of product realization
Customer related processes
Design and development
Purchasing & Subcontracting
Production and service provision
Monitoring and measuring devices
Measurement analysis and
improvement
Monitoring and measurement
Control of Nonconforming product
Analysis of Data
Improvement

Note: QA/QC manager will modify the audits schedule in accordance with the revised schedule of the Project

progress when necessary. In accordance with the importance of the work, times of audits could be modified to suit

the conditions of the Project. Additional audits shall be considered in preparation of the schedule. All audit

schedules or changes shall be informed to CPY 7 days before the change takes effect.

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8.5 Technical Query Form (TQ_01)

TECHNICAL QUERY FORM COMPANY IDENTIFICATION CODE


Job-Type-N°
(TQ) TQF_01
SHEET DOC.CLASS ISSUE
1/1 00
ITP PHASE REF:
TQ NO.:
__________________

PROJECT NAME:
UNIT : SYSTEM :
TO : FROM :
SUBSYSTEM : AREA :
TAG Nº : RFI Nº :
Contractor Client
Drawing : Drawing :

TECHNICAL QUERY TITLE :

CRITICALITY: URGENT ROUTINE


CLASSIFICATION : ESSENTIAL NON ESSENTIAL
REQUIREMENT : CLARIFICATION DEVIATION
Signed for and on behalf
QUERY: of CONTRACTOR:

NAME:

DATE:
Signed for and on behalf
COMPANY RESPONSE: of COMPANY:

NAME:

DATE:
ATTACHEMENT: YES NO
......................................................................................................................................................

□ – COMPANY review complete. CONTRACTOR may proceed.

□ – CONTRACTOR may proceed subject to implementation of COMPANY comments.

□ – CONTRACTOR may not proceed. Resubmission required.


Notes: Legible Signature requested
NAME DATE SIGNATURE
CONTRACTOR
TQF_01

COMPANY

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8.6 Request for Inspection Form (RFI_01)


COMPANY IDENTIFICATION CODE
Job-Type-N°
REQUEST FOR INSPECTION FORM
RFI_01
(RFI)
SHEET DOC.CLASS ISSUE
1/1 00
ITP PHASE REF:
RFI NO.:
__________________
DATE:

PROJECT NAME:
UNIT : SYSTEM :
TO : FROM :
SUBSYSTEM : AREA :
Contractor Client
Drawing : Drawing :

REQUEST FOR INSPECTION:


We request your attendance to inspect the following works :
Inspection Time: Location:
Inspection #: First Second Third Other (Please Specify):___________
Type of Inspection: Visual Testing Joint Inspection Hold Point Witness Point
Purpose of the Inspection: Applicable QCP Tick Applicable QCF More Details
o Equipment
o Survey & Setting out
o Earth Works
o Civil & Concrete Works
o Roads & Paving
o Mechanical & Structural
o Piping Works
o Building Works
o Electrical & Instrument Works
o Process Works
Other (Specify):

Particular Details:

ATTACHEMENT: YES NO

ENGINEERS COMMENT: THE WORKS ARE

□ APPROVED AS NOTED

□ APPROVED

□ REJECTED
Notes: Legible Signature requested
NAME DATE SIGNATURE
CONTRACTOR
RFI_01

COMPANY

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8.7 Material Acceptance Request (MAR)

ZEROCK CONSTRUCTION CONGO ENI CONGO


Material Acceptance Request (MAR)
Project :
Client: Ref No. :
Date: Revision:
Contractor : Contract No. :
FROM : Contractor TO : Company

Attachments : Discipline : Approval Required By Date :


Samples Civil

Original Brochures Architectural

Specification Comparison Sheet Mechanical

Others ( state ) Electrical

Other ( state )
Attach all relevant literature marked by "clouding": to identify relevant description, current test certificates, samples as appropriate.

Material Description : FOR ENGINEER USE ONLY

(A) Proceed
Location / Area : (B) Proceed as Noted
(Resubmit when complied)
Drawing Ref. :

Specification Ref. : Required:

Manufacturer / Supplier : Samples


Company Name : Test Certificate
Country of Origin : Original Brochure
Local Agent : Manufacturer's Guarantee

Delivery : More Information


Production Period :
Total Delivery Time : (C) Do Not Proceed
Expected Date of Delivery on Site :

Time Required at Site: FOR COMPANY'S


REPRESENTATIVE/PROJECT
MANAGER USE ONLY
For Zerock :
NAME : SIGNATURE : DATE : Approved
Approved As Noted

Engineer's Comment : Rejected

NAME : SIGNATURE : DATE :

DISTRIBUTION :
Original : CONTRACTOR

Copies : Company Others: (Please Specify)

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8.8 Quality Management System – Responsibility Matrix

ISO 9001:2000 Standard Clauses / Activity Relevant Procedure Verifying Document/Deliverables Responsible person
4 QUALITY MANAGEMENT SYSTEM
4.1 General requirements Project Quality Plan Documented quality system Project Manager
4.2 Documentation requirements Project Quality Plan Documented quality system QA/QC Manager
4.2.1 General Project Quality Plan Documented quality system QA/QC Manager
4.2.2 Quality Manual Project Quality Plan Project Quality Plan and its Supporting QA/QC Manager
documentation
4.2.3 Control of Documents Project Quality Plan Documents issued by controlled Document Control Engineer
Project Communication and distribution system, distribution records
Document Control
4.2.4 Control of Records, identification, Project Quality Plan All records providing operation of the Document Control Engineer
Storage, protection, retrieval, Project Communication And quality management system
retention and disposition of records Document Control
5 MANAGEMENT RESPONSIBILITY
5.1 Management commitment Project Quality Plan Quality Policy / objectives/records of Project Manager
management review
5.2 Customer focus Project Quality Plan Satisfied customer Project Manager
5.3 Quality policy Project Quality Plan Policy communicated to all levels of Project Manager/QA/QC
project personnel Manager
5.4 PLANNING Project Quality Plan
5.4.1 Quality Objectives Project Quality Plan Documented Quality System Project Manager
5.4.2 QMS Planning Project Quality Plan Documented Quality System QA/QC Manager
5.5.1 Responsibility, authority and Project Quality Plan Organization chart / Job descriptions Project Manager
communication
5.5.2 Management Representative Project Quality Plan Organization Chart QA/QC Manager
5.5.3 Internal Communication Project Quality Plan Project Manager
5.6 Management review Management Review Minutes of meeting / actions Project Manager
QA/QC Manager

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ISO 9001:2000 Standard Clauses / Activity Relevant Procedure Verifying Document/Deliverables Responsible person
6 RESOURCE MANAGER
6.1 Provision of resources Project Quality Plan Refer below Project Manager
6.2 Human resources Project Quality Plan Training/Qualification records, personnel Project Manager
Training & Personnel Qualifications appraisal records
6.3 Infrastructure QMP-PP’s (PMV) Buildings / facilities / IT / Plant Plant (PMV) Manager
6.4 Work environment Project Quality Plan efficiency and effectiveness of people Project Manager
7 PRODUCT REALIZATION
7.1 Planning for product realization All QMP’s Project schedule Controls Manager
7.2 Customer-related processes
7.2.1 Determination of requirements of Contract/Project Specs QCPs & ITPs Project Manager
product
7.2.2 Review of Requirements Project Quality Plan Contract review records MOA Estimation/proposals
depts.
7.2.3 Customer Communication Project Quality Plan Project correspondence/Technical Project Manager
Project Communication And Queries
Document Control
Concession Requests & Technical
Query
7.3 Design and development Not Applicable
7.4 Purchasing
7.4.1 Purchasing Process Project Quality Plan Supplier /Subcontractor records Construction Controls
Supplier Qualification Manager
Subcontracting Procedure
7.4.2 Purchasing Information Project Quality Plan Purchase Order and subcontract data Construction Controls
Supplier Qualification Manager
Subcontracting Procedure

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ISO 9001:2000 Standard Clauses / Activity Relevant Procedure Verifying Document/Deliverables Responsible person
7.4.3 Verification of the purchased products Field Purchasing & Material Approval Inspection reports Material Engineer
Request Procedure
Material Management & Control
7.5.1 Production and service provision Project Quality Plan IFC Drawings/PMV records Construction Controls
Manager/QA/QC Manager
7.5.2 Validation processes for production QCPs WPS/PQR, concrete trial mix design QA/QC Manager
7.5.3 Identification and Traceability Material Certification & Traceability Identification marks and stamps QA/QC Manager
7.5.4 Customer Property Material Management & Control Material inspection and preservation Project Manager
records
7.5.5 Preservation of product Material Management & Control Preservation inspection reports Project Manager
7.6 Control of monitoring and measuring Inspection, Measurement & Testing Calibration records QA/QC Manager
devices Equipment
8 MEASUREMENT, ANALYSIS AND
IMPROVEMENT
8.1 General Quality System Audits Audit reports QA/QC Manager
8.2 Monitoring and measurement Inspection and Test Status Data collection, audit reports, statistical QA/QC Manager
Quality System Audits analysis, inspection testing records
8.3 Control of nonconforming product Control of Non-Conforming products Closed out NCR’s QA/QC Manager
8.4 Analysis of data Corrective & Preventive Action Project Correspondence, QA/QC Meeting QA/QC Manager
records/CCIC Non-Conformities/Letters of
appreciation/CCIC audit reports
8.5 Improvement Project Quality Plan Progressive comparison of data QA/QC Manager
8.5.1 Continual Improvement Project Quality Plan Quality Objectives, audit results corrective QA/QC Manager
Corrective & Preventive Action and preventive action
8.5.2 Corrective Action Corrective & Preventive Action Corrective and preventive action QA/QC Manager

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8.9 Quality Training Plan Schedule

On the Job Training for CTR employees shall be carried out in the following Disciplines and as per schedule below:
 Project Planning & Control
 HSE
 Design / Construction Engineering
 Quality Controls
 Crafts Training
 Equipment Operation

SN Planned Training No. Of Candidates Qualification Estimated


Minimum Duration
(Months)
1 QUALITY CONTROLS 5
Field Density / Plate Load Test 2 B. Sc / B . Eng 3
MPI, DP, UT 2 B. Sc / B . Eng 3
Radiography 1 B. Sc / B . Eng 3
2 PROJECT PLANNING/CONTROL 3
Planning 1 B. Sc 6
Quantity Survey 1 B. Sc 6
Document Control 1 B. Sc 6
3 DESIGN / CONSTRUCTION ENGINEERING 10
Piping 2 B . Eng 6
Instrumentation 2 B . Eng 6
Electrical 2 B . Eng 6
Structural 2 B . Eng 6
Concrete 2 B . Eng 6
4 HSE 5
Safety Induction ALL - 1
First Aid 1 1
Nurse 1 6
Fire Fighting 2 6
Permit to Work 1 6
5 CRAFTS TRAINING 14
Scaffolding 2 - 6
Pipe Fitting 2 - 6
Tube Bending 2 - 6
Rigging 2 - 6
Welding 2 - 6
Iron Bending 2 - 6
Formworks Installation 2 - 6
6 EQUIPMENT OPERATION 3
Forklift 1 - 3
Crane 1 - 3
Batching Plant 1 - 3
TOTAL 40

Training is planned solely for CTR employees involved in the project.

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8.10 Project QA Activity Flow Chart

QA Plan Audit ISO 9001, Contract,


Schedule Project QC Plan and
Procedures

QAQC Department Issue Relevant


Audit Notification Departments
Prepare Checklist

Project Manager

QA Reject
Auditee
Acknowledgement NO

Auditee takes QA Follow


Corrective Preventive. up and Verify
Actions

QA Issue Audit Report


with NCR & CAR YES

QA Accept
QA NO
Yes
Department Finding Exists Observe
Perform Non Conformance
Audit

YES

Satisfactory or only
Suggestions

Audit Report

Filing Audit Report &


NCR Closed Report

This document is property of Eni Congo SA.


It shall neither be shown to Third Parties nor used for purposes other than those for which it has been sent.
Company Document ID Contractor Document ID Sheet of Sheets

30A100DBQB23010 30A100DBQB23010 77 / 81
ENI CONGO SA
Validity Revision
PROJECT QUALITY PLAN Status Number
EX-DE 05

8.11 Project Site QC Activity Flow Chart

Contract Specification, QC Dept Verification and


Engineering QC Dept Surveillance Acceptance
Document, Project
Quality Plan

Site QC Plan, I &TP QC Comments enter Log


QC Procedure Book

CTR Quality Construction Dept.


Department Issue RFI Response Action
at W or H Point

Project Manager
CPY QC Dept receive
RFI
NCR

QC Dept. Reject
Notice to CPY for Joint No
Inspection
NO

YES
QC 2nd
QC Inspection
CTR/CPY
Inspection NO

YES
Engineering
QC Dept. CTR & CPY CTR Quality Dept Issue Department
Accept (Joint Signature) New RFI After Corrective
Action

QC Dept. CPY Reject


Make Note on RFI

QC Dept. File Record

9.0 LIST OF FORMS


This document is property of Eni Congo SA.
It shall neither be shown to Third Parties nor used for purposes other than those for which it has been sent.
Company Document ID Contractor Document ID Sheet of Sheets

30A100DBQB23010 30A100DBQB23010 78 / 81
ENI CONGO SA
Validity Revision
PROJECT QUALITY PLAN Status Number
EX-DE 05

9.1 List of Project Quality Control Plans

SN DOCUMENT CODE DOCUMENT TITLE

1 30A100DBQB23020 Quality Control Plan for Earthworks

2 30A100DBQB23030 Quality Control Plan for Civil and Concrete work

3 30A100DBQB23040 Quality Control Plan for Roads & Paving Works

4 30A100DBQB23050 Quality Control Plan for Mechanical & structural Works

5 30A100DBQB23060 Quality Control Plan for Electrical Works

6 30A100DBQB23150 Quality Control Plan for Instrumentation Works

7 30A100DBQB23070 Quality Control Plan for Piping

8 30A100DBQB23080 Quality Control Plan for Building Works

9.2 List of Project Quality Forms

SN FORM CODE FORM TITLE

1 QCF_001 Excavation

2 QCF_002 Filling & Compaction

3 QCF_003 Geomembrane or Geotextile

4 QCF_004 Equipment Calibration List

5 QCF_005 Topographic Survey

6 QCF_006 Concrete Mix Design Checklist

7 QCF_007 Asphaltic Concrete Checklist

8 QCF_008 Road & Yards Checklist

9 QCF_009 High Strength Bolts Tightening inspection Report

10 QCF_010 Structures Installation Final Inspection Report

11 QCF_011 Inspection Report Of Secondary Steel Structure

12 QCF_012 Columns Foundation / Footing Of Base Plates

13 QCF_013 Structural Steel Release Certificate

14 QCF_014 Weld Fit-Up Inspection Report

15 QCF_015 Weld Visual Inspection Report

16 QCF_016 Material Receiving Inspection REPORT

17 QCF_017 Daily Concrete Pouring Report

18 QCF_018 Pre-Concrete Pouring Inspection Report

This document is property of Eni Congo SA.


It shall neither be shown to Third Parties nor used for purposes other than those for which it has been sent.
Company Document ID Contractor Document ID Sheet of Sheets

30A100DBQB23010 30A100DBQB23010 79 / 81
ENI CONGO SA
Validity Revision
PROJECT QUALITY PLAN Status Number
EX-DE 05

SN FORM CODE FORM TITLE

19 QCF_019 Survey Report

20 QCF_020 Concrete Completion Inspection

21 QCF_021 Welding Consumable Log

22 QCF_022 NDE Request Form

23 QCF_023 Visual and Dimensional Control Inspection Report

24 QCF_028 Field Inspection Of Conduits And Cable Tray Installation

25 QCF_033 Field inspection and testing of lv cable (underground installation)

26 QCF_034 Field inspection of hv cables (underground installation)

27 QCF_035 Checklist for cold shrink stress control hv cable terminations

28 QCF_036 Check list for cable jointing


Field inspection and testing of earthing and lightning protective
29 QCF_037
systems
30 QCF_038 Field inspection and testing of lv cable (above ground installation)

31 QCF_039 Field inspection and testing of hv cables (above ground installation)


Field inspection and testing of earthing and lightning protective
32 QCF_041
systems
33 QCF_043 Field inspection and testing of power tranformers

34 QCF_047 Field inspection of earth and bonding system.

35 QCF_051 Field inspection and testing of switching units (mv/lv switchgear)

36 QCF_052 Survey report road paving

37 QCF_053 Road and pavement inspection record

38 QCF_054 Road completion handover form

39 QCF_060 QCF for factory inspection Mechanical Parts of Machinery

40 QCF_061 QCF for factory inspection Mechanical Parts of Tank/Vessel/Boiler

41 QCF_062 QCF for factory inspection Electrical Parts of Machinery

42 QCF_063 QCF for factory inspection Instrumental parts of machinery

43 QCF_064A DC UPS switchgears and storage batteries – before checks

44 QCF_064B DC UPS switchgears and storage batteries – after checks


DC UPS switchgears and storage batteries - insulation & continuity
45 QCF_065
test
46 QCF_066 Bus ducts installation checklist

47 QCF_067A Report of pneumatic circuit tests

This document is property of Eni Congo SA.


It shall neither be shown to Third Parties nor used for purposes other than those for which it has been sent.
Company Document ID Contractor Document ID Sheet of Sheets

30A100DBQB23010 30A100DBQB23010 80 / 81
ENI CONGO SA
Validity Revision
PROJECT QUALITY PLAN Status Number
EX-DE 05

SN FORM CODE FORM TITLE

48 QCF_067B Pneumatic circuit tests

49 QCF_068 Visual inspection and dimensional checks of primary flow elements

50 QCF_069A Report of process connection test

51 QCF_069B Process connection tests

52 QCF_070A Report of installation inspection of all instruments

53 QCF_070B Installation inspection of all instruments

54 QCF_071A Report of field inspections -test - calibration of special instruments

55 QCF_071B Field inspections -test - calibration of special instruments

56 QCF_072A Report of field inspections -test - calibration of control valves

57 QCF_072B Field inspections -test - calibration of control valves

58 QCF_073A Report of field inspections -test - calibration of psv

59 QCF_073B Field inspections - test - calibration of psv

60 QCF_074B Field inspections - test - calibration of fe -in-line-rupture disk

61 QCF_075A I-o check report of pressure & differential pressure transmitters

62 QCF_075B I-o check of pressure - differential pressure transmitters

63 QCF_076A I-o check report of temperature element (tc-rtd)

64 QCF_076B I-o check of temperature element (tc-rtd)

65 QCF_077A I-o check report of switches

66 QCF_077B I-o check of switches and level switch


I-o check report of miscellaneous instruments (without process
67 QCF_078A
connections)
68 QCF_078B I-o check of miscellaneous instruments (without process connections)
I-o check report of electronic transmitters (without process
69 QCF_079A
connections)
70 QCF_079B I-o check of electronic transmitters (without process connections)

71 QCF_080A I-o check report of detectors (gas, smoke, heat, flame, fire)

72 QCF_081A I-o check report of control valves and on-off actuators

73 QCF_081B I-o check of control valves and on-off actuators

74 QCF_082A Report of functional test - calibration checks of switches

75 QCF_082B Functional tests and calibration checks of switches


Functional tests and calibration checks of temperature gauge & temp.
76 QCF_083A
Element
77 QCF_083B Functional tests and calibration checks of temperature gauge &
This document is property of Eni Congo SA.
It shall neither be shown to Third Parties nor used for purposes other than those for which it has been sent.
Company Document ID Contractor Document ID Sheet of Sheets

30A100DBQB23010 30A100DBQB23010 81 / 81
ENI CONGO SA
Validity Revision
PROJECT QUALITY PLAN Status Number
EX-DE 05

SN FORM CODE FORM TITLE


thermocouples and thermoresistances
78 QCF_084A Functional tests and calibration checks of instruments

79 QCF_084B Functional Tests And Calibration Checks Of Instruments

80 QCF_085 Electrical Connection Tests Of Earthing Network

81 QCF_086A Report Of Electrical Connection Tests Of All Instrument Cables

82 QCF_086B Report Of Electrical Connection Tests Of All Instrument Cables

83 QCF_087A Report Of Electrical Connection Tests Of All Instrument Cables

84 QCF_087B Electrical Connection Tests Of Heat Tracing Cables

85 QCF_088 Piping Installation Checklist

86 MAR Material Approval Request Form

87 SDT Field Soil Density Test Report

88 PLT Plate Compaction Test Report

This list is subject to review as per project requirements.


On review, a new document Issue shall be sent to company for revision & approval.

This document is property of Eni Congo SA.


It shall neither be shown to Third Parties nor used for purposes other than those for which it has been sent.

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