Professional Documents
Culture Documents
UNRESTRICTED
April 2000
Keywords:
BS EN ISO 9000
Organisational Structure
Quality Manual
Quality System
Quality Policy
Quality Assurance
Quality Control
Quality Management
Quality Plan
Quality Control Plan
Quality Audit
Process Control
Procedures
This document is the property of Petroleum Development Oman, LLC. Neither the whole nor any
part of this document may be disclosed to others or reproduced, stored in a retrieval system, or
transmitted in any form by any means (electronic, mechanical, reprographic recording or otherwise)
without prior written consent of the owner.
Signed :............................................................
UER (OTT/1)
CFDH Materials and Corrosion
The following table lists the four most recent revisions to this document. Details of all revisions prior
to these are held on file by the issuing department.
Version No.
Version 1.0
April 2000
Date
24/04/2000
Author
OTT/151
Checked
OTT/15
Scope / Remarks
Revision and re-formatting of
(September 1995 issue).
ERD 84-02
SP-1171
Version 1.0
Specification for Quality Assurance of Design, Construction and Engineering Works
Contents
1. Introduction............................................................................................................................1
1.1 Purpose..............................................................................................................................1
1.2 Changes to the Specification.............................................................................................1
1.3 Specification Owner's Responsibility................................................................................1
1.4 Effective period..................................................................................................................1
1.5 Review and Improvement..................................................................................................1
2. Specification Requirements..................................................................................................2
2.1 Scope..................................................................................................................................2
2.2 Quality System...................................................................................................................2
2.3 Documents to be Submitted...............................................................................................4
2.3.1 Quality System.......................................................................................................4
2.3.2 Quality Manual......................................................................................................5
2.3.3 Contract Quality Plan (CQP).................................................................................6
2.4 Quality Management during the Contract......................................................................12
2.5 Documentation................................................................................................................12
2.6 Quality Assurance, Inspection (Quality Control) and Verification Personnel................12
2.7 Qualifications and Duties of The Suppliers Quality Assurance, Inspection (Quality Control)
and Verification Personnel..............................................................................................14
2.7.1 Corporate Quality Assurance Manager...............................................................14
2.7.2 Quality Assurance Engineer................................................................................15
2.7.3 Quality Control Inspector - Multi-Discipline (Welding, Painting, NDE)..........16
2.7.4 QC Inspectors - Civil and Structural...................................................................16
2.7.5 Q C Inspectors - Instrumentation........................................................................17
2.8 Quality Assurance Auditing............................................................................................17
2.9 Purchasing.......................................................................................................................18
2.10 Inspection, Measuring and Test Equipment..............................................................18
2.11 Third Party Certification...........................................................................................19
2.12 Pressure Vessels.........................................................................................................20
2.12.1 Vessels Manufactured Outside Oman..................................................................20
2.12.2 Vessels Manufactured in Oman..........................................................................21
2.13 Static Equipment.......................................................................................................21
2.14 Quality System Certification:....................................................................................22
Appendix A - Glossary of Definitions, Terms and Abbreviations.........................................23
Appendix B References.........................................................................................................25
Appendix C - Contract Quality Plan and Contract Quality Plan Guidelines....................26
User Comment Form................................................................................................................36
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April 2000
1.
Introduction
1.1
Purpose
This specification revises and replaces ERD 84 -02, 1995, Quality Assurance Engineering
Reference Document, issued in September 1995. The purpose of this Specification is to
specify the Company's minimum requirements for Quality Assurance in all Contracts and
Purchase Orders with their nominated Suppliers (Consultants, Contractors and Vendors).
This specification is intended to set Company Quality Assurance Standards during design,
procurement and construction phase of facilities
1.2
1.3
1.4
Effective period
The requirements of this specification shall remain in force indefinitely unless superseded
by an authorised revision.
1.5
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2.
Specification Requirements
2.1
Scope
This specification presents the Company's minimum requirements for Quality Assurance in
all Contracts and Purchase Orders with their nominated Suppliers (Consultants,
Contractors and Vendors). The requirements are based on the use of the BS EN ISO 9000
Series of Quality Management and Quality Assurance Standards.
The body of this specification is the Quality Assurance Specification and forms part of the
Contract or Purchase Order. Terms and abbreviations used are defined in Appendix A and
referenced standards are listed in Appendix B.
Appendix C, Contract Quality Plan and Quality Control Plan Guidelines, offers Suppliers
(Consultants, Contractors and Vendors) guidelines on the contents and development of a
Contract Quality Plan and Quality Control Plan, that will meet the requirements of this
specification.
2.2
Quality System
The Supplier (Consultant, Contractor, Manufacturer and Vendor) shall implement and use a
Quality System that complies with the appropriate Standard from the ISO 9000 Series,
(latest edition), as listed below, and the requirements of this specification.
BS EN ISO 9001:
Quality Systems - Model for quality assurance in design
development, production, installation and servicing.
or
BS EN ISO 9002 :
Quality Systems - Model for quality assurance in production,
installation and servicing.
The Standard shall be selected to cover all work activities (consultancy, project
management, procurement, construction, and provision of goods, products or services),
associated with the Contract or Purchase Order.
Where the Contract includes design work, ISO 9001 shall be used. Where the Contract is
purely for production, construction, installation, commissioning and hand over, then ISO
9002 shall be used.
If any part of the Contract is Sub-Contracted, the Supplier shall comply with Clause 4.6.2
in ISO 9001/9002, which requires the Sub-Contractor to maintain an appropriate Quality
System. The Sub-Contractor shall implement a Quality System that meets the requirements
of ISO 9001 or ISO 9002, as appropriate for the sub-contracted work. The Supplier shall
remain ultimately responsible for the quality of the Sub-Contractor's work.
The term Process Control in ISO 9000, shall be considered to embrace all work activities
from Tendering and Contract Award to Completion of the Contract. Activities such as;
Contract Management, Cost Control, Planning and Scheduling, Progress Measurement,
Reporting, 'As Built' Documentation etc. shall have properly documented Procedures or
Work Instructions.
Suppliers in selected Work Categories may be required to attain Third Party Registration
of their Quality System. The registration shall be from an Accredited Certifying Body (for
example, BSI, BV, DNV, Lloyds etc.), who are themselves accredited by a National
Accreditation Authority to assess Quality Systems. Work Categories required to attain
registration will be informed by the Work Category Custodian (see clause 2.14).
Where Suppliers are not required to attain Third Party Registration, they shall demonstrate
that they have a Quality System that complies with ISO 9001 or 9002, as appropriate for
the contract or purchase order scope. Consideration should be given to attaining Third
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2.3
Documents to be Submitted
With Tender
2.3.1
Quality System
2.3.1.1
2.3.1.2
If the Suppliers Quality System is not certified to ISO 9001 or 9002, the
Supplier shall submit evidence, that an acceptable Quality System,
complying with either ISO 9001 or ISO 9002, as appropriate, is in operation.
This requirement can be fulfilled by submitting any of the following:
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2.3.2
Quality Manual
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With Tender
2.3.3
The Contract Quality Plan shall be approved by the Company, (QA & QC section) prior
to work commencing. This plan shall be an updated revision of the Tender issue plan.
The CQP shall include and address all the relevant and applicable elements of ISO 9001
or 9002 as appropriate.
1.
2.
Index.
Revision Status.
Distribution List.
3.
2.3.3.2
General
1.
2.
3.
1.
2.
3.
4.
5.
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Index.
Revision Status, together with the Control Mechanism of the CQP and a
Distribution List. The Company distribution shall be as the Contract documents,
with a minimum of:
- Company Representative.
- Head of Quality Assurance Services, OTT/15
- Company Site Representative.
- In-charge Interior QA & QC Services - OTT/151
Details of the Suppliers Procedures for preparing, reviewing, revising and reissuing the Contract Quality Plan during the Contract shall be stated in the CQP.
Details of how the Corporate Quality System documentation shall be applied and
implemented on the Contract. The CQP shall include contract specific quality
system structure.
Detailed Scope of Work of the Contract, together with a detailed description of the
Quality related aspects of the Contract. Inclusion of copy of sheets from Contract
shall not be acceptable.
Identify all work activities and sub-activities, including those performed by SubContractors, to be controlled by the CQP.
Detailed methodology how quality system and work performed by Sub-Contractor
shall be monitored and controlled by the Supplier.
Details of how Quality Planning shall be undertaken and controlled.
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With Tender
2.3.3.3
1.
1.
2.
3.
2.3.3.4
Organisational Structure
1.
2.
3.
1.
Version 1.0
2.
3.
4.
5.
6.
Detailed list of the Contract and other documents whose requirements are to be
met, together with their revision status.
Indicate the location where these documents are available, the Procedures for
controlling and revising them and the person responsible.
Include a Distribution Matrix for all documents.
A final Contract specific Organisation Chart, highlighting Quality Assurance,
Quality Control, and Inspection and Verification personnel. Confirm mobilisation
dates for all staff down to Foreman level.
Provide a Corporate Organisation Chart identifying by Name and Job Title all
personnel who will interface with the Contract personnel, Sub-Contractors,
Vendors or the Company. Define roles, responsibilities and reporting relationships
of all personnel identified in the Contract specific organisation with interface with
Corporate personnel.
Where duties other than Quality Assurance and Inspection are to be carried out by
Quality Assurance / Inspection personnel, details of other duties shall be submitted,
together with the times to be spent on each activity.
Details of any Sub-Contractors Quality Assurance / Inspection personnel,
indicating how the Supplier will monitor and control the Sub-Contractors Quality
System.
Details of the training schedule for all persons to be employed on the Contract
(include all training, not just Quality training). Include all personnel requiring
formal certification for the Contract, for example, Welders.
Submit CVs of QA and QC personnel together with copies of qualifications
including training, for review and approval by Company QA / QC section.
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2.3.3.5
2.3.6.6.
3.
4.
1.
2.
3.
4.
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List of all Corporate Quality System Procedures, Work Procedures and Contract
Specific Procedures, Work Instructions, Checklists and Standard Forms, with
current Revision Status and Issue Date, that shall be used on the Contract without
revision. Documentation requiring revision to meet Contract requirements, shall be
listed indicating dates when shall be issued and the person(s) responsible for
revision and implementation. The listing shall follow the normal workflow.
Indicate dates when Contract specific Procedures and Work Instructions shall be
issued and the person(s) responsible for developing, reviewing and implementing
them.
The Supplier shall provide the Company on request, all-Corporate Quality System
Procedures, Work Procedures, Work Instructions, Checklists and Standard Forms
applicable and required for the Contract. They shall be issued as Controlled
Copies to the Company within 2 weeks of Contract award or whenever demanded
by Company. This may be in the form of a separate Contract Procedures Manual or
separate volume of the Contract Quality Plan.
Copies of Contract Specific Procedures, Work Instructions, Checklists and Standard
Forms shall be issued to the Company within 4 weeks of Contract award (or at
least 2 weeks before the work activity commences, for Contracts of less than 6
weeks duration.
List of procedures and work instructions that shall be used on the Contract by SubContractor(s) for assigned work activities, including those to be developed or
revised by dates.
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With Tender
2.3.3.7
2.
3.
4.
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2.
List of QCP, with current Revision Status and Issue Date, to be used on the
Contract. Indicate dates when Contract specific QCP will be issued and the
person(s) responsible for developing, reviewing and implementing them. All QCPs
shall be approved by the Company prior to work commencing. Above include
QCP(s) from Sub-Contractor(s).
Controlled Copies of all Corporate and Contract Specific QCPs, including those
from Sub-Contractor, to be used on the Contract shall be included in the CQP.
- The Quality Control Plans shall include:
- List of Activities and Sub-Activities requiring Quality Control and or stage
inspection.
- Controlling Document (Suppliers Procedure / Work Instruction, Contract
Specification, Specifications (SP), Procedures (PR), ERD, DEP, International
Code or Standard).
- Specified Acceptance / Rejection Criteria and Actual Value(s). When it is
practically not possible to indicate or accommodate Actual Value(s) in QCP, then
cross reference to source providing such information shall be shown in QCP(s)
(for example, Clause Reference, Table in SP, PR, ERD, DEP, Code or Standard
etc.).
- Suppliers Verification Personnel responsible for the Quality Control activity.
- Verifying Document / Quality Control Record, where test results are recorded
and endorsed by the Suppliers Verification Personnel.
- Hold, Witness, Surveillance, Monitoring and Review points by the Supplier,
Third Party or Company, shall be identified. Appropriate legends for 'Hold',
'Witness', 'Review', 'Surveillance' and 'Monitoring' shall be used in the QCP(s).
- Sub-Contractor(s) QCP(s) and quality document(s) shall be reviewed and
endorsed by Contractor, before submitting for Company approval.
- When TPI is a Contract requirement, the QCP(s) and Quality document(s) shall
also be reviewed and endorsed by the nominated TPI Agency.
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With Tender
2.3.3.8
Quality Records
1.
None.
2.
3.
4.
Include details of all Quality Records and their formats and Test Packs to be used on
the Contract, either by the Supplier and or Sub-Contractors. Where new
documentation is required, denote who is responsible for developing and approving
the documentation and the date when it will be completed.
The Verifying Document / Quality Record shall show the specified value and the
measured value. Where it is reasonably difficult to show specified value, adequate
details of reference standard/code/ERD/SP/DEP shall be provided for specified
value.
Verifying Documents that shall be issued to the Company as Quality Records shall
be identified and given a reference number.
Include a Distribution Matrix for all Quality Records, which shall include
the following as a minimum:
- Records to be reviewed by the Company during the Contract.
- Records requiring Approval / Hold & Witness by the Company.
- Records to be handed to the Company.
- Records to be kept for use by the Supplier only.
- Define the content and format of Test Packs, per discipline, and shall be agreed
with the Company Representative in advance. Records of Company approval
shall be maintained by the Supplier.
2.3.3.9
Audit Schedule
1.
1.
2.
2.
3.
4.
5.
6.
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Include a detailed Audit Schedule for the Contract. The schedule shall identify the
Internal Audits the Supplier will conduct on the Quality System throughout the
Contract.
The schedule shall also include details of External Audits the Supplier will carry
out on Sub-Contractors and Vendors.
A Compliance Audit shall be carried out at least once per month on all work
activities that have recently commenced.
External and internal audits shall be carried out by trained, qualified and
experienced auditors. Auditors shall possess IRCA, UK or equivalent auditing
qualification. (Note: Also see clause 2.8 of this SP).
Supplier shall provide a copy of their internal and external audit notification to
Company QA / QC section at least five working days in advance of the planned
audit date. Company reserves the right to join the audit as an observer.
Supplier shall provide Company QA / QC section copies of all internal and external
audit reports along with audit check list used during audits.
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With Tender
2.3.3.10
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2.4
The following Quality matters shall be reported in the Contract Weekly / Fortnightly / Monthly
Report:
Summary of Contract Quality Plan development and Procedure development and approvals.
Summary of Internal and External Audits carried out, reported against the Audit Schedule.
Listing of Corrective Actions for each Audit, the current status and the planned dates for follow
up and closeout.
Details of any investigations into non-conformance and action to prevent recurrence of any
Quality System failures.
Summary of Tests and Inspections carried out on site and off site and on Sub-Contractors.
During Weekly / Fortnightly / Monthly meeting with Company, the Supplier shall furnish details on
the following items:
Number of Customer Complaints raised during the preceding period and the cumulative total,
action taken to address complaints and close out.
Quality issue raised by Company QA / QC, details of action taken to address the issues and close
out.
Number and nature of variance raised, cumulative numbers, approval status, implementation and
documentation of the variance.
Supplier internal NCRs raised, corrective and preventive action and close out.
Welder performance and repair rates based on radiography.
Status of deployment of QA and QC resources and their Company approval status.
Supplier shall ensure that the site Quality Management System is reviewed at least once in a quarter
2.5
Documentation
Documentation related to the Quality System shall be available at the location where work is being
carried out.
The Supplier shall maintain the latest revision of the relevant Contract Documents, Drawings, all
Contract Technical Specifications (SPs, PRs, ERDs, DEPs, HSE Manual), Standards (BS, DIN,
ASME, etc.), Procedures and Work Instructions, at the location where work is being carried out.
A Document Control procedure shall control the issue, distribution, change, review and withdrawal of
all documentation.
2.6
The Supplier shall nominate. a Senior Manager (Management Representative), who shall have
defined responsibility for the Corporate Quality System, in accordance with Clause 4.1.2.3 of ISO
9001/2.
The Supplier shall assign sufficient Quality Assurance / Inspection (Quality Control) and Verification
Personnel to the Contract to ensure that the Quality Management System, Quality Assurance and
Quality Control are effectively established, implemented and maintained throughout the Contract.
There shall be sufficient personnel to cover all disciplines work and activities, all Sub-Contractor's
work and off site facilities.
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26 - 75
76 150
151 250
> 251
Notes:
The above numbers exclude any personnel employed either by the Supplier or Company from a
Third Party Certification Authority.
Numbers specified in the above Table do not include Corporate QA Personnel.
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2.7
All persons nominated by the Supplier for work within the Quality Assurance, Inspection and
Verification function shall be properly qualified, trained and experienced in the aspects of the work for
which they will be employed. They shall have previously worked on similar Contracts in similar
capacities and shall have formal Quality Assurance / Inspection qualifications.
Supplier's all QA, Inspection (Quality Control) and Verification personnel shall be subject to approval
Company QA / QC section prior to mobilisation on Contract and to site.
Company reserves the right to interview and or submit all QA, Inspection (Quality Control) and
Verification Personnel to an examination to determine their suitability for the work they are required
to carry out and to reject any personnel found unsuitable, at Company's sole discretion.
The duties of the Quality Assurance, Inspection and Verification personnel shall include, but not be
limited to the following activities:
2.7.1
Duties
Notes:
For Design Consultancy contracts, the candidate shall have appropriate technical qualifications on above lines
and possess same number of years of relevant experience as per serial 3 above in the design organisation
involved in oil and gas facility design.
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Qualifications
1 Shall be a Graduate Engineer (B.Sc.Eng. / BE /
B.Tech.) either in Mechanical or Metallurgical or
Welding engineering.
2 Shall be an IRCA, UK Registered Lead Assessor or
equivalent (where equivalent is proposed, Supplier
shall provide evidence of equivalence from
International Accreditation Body (ies)). If the
candidate is in the process of obtaining the registration
with IRCA, UK, then it is mandatory to have an audit
log that is verifiable indicating having performed at
least ten external (2 nd party) Quality SYSTEM audits,
with more than fifteen compliance audits.
3 Shall have minimum of 12 years of, site based,
relevant experience in onshore oil and gas facility
construction, including live installations. He shall
have a minimum of 4 years management experience in
establishment, operation and maintenance of quality
management system in compliance with ISO 9000.
Shall have demonstrable capability of developing
quality system, quality plans, quality control
procedures, inspection plans and contract specific
work procedures.
Duties
Preparation, implementation, monitoring, revision and
updating of the Suppliers Contract Quality Plan.
Development,
preparation,
implementation
and
monitoring of all Contract Specific Procedures and Work
Instructions.
Note 1:
For Design Consultancy contracts, the candidate shall have relevant and appropriate technical qualifications on
above lines and possess same number of years of relevant experience as per serial 3 above in the design
organisation involved in oil and gas facility design.
Note 2:
For Electrical and Civil contracts, the candidate shall have relevant and appropriate technical qualifications on
above lines and possess same number of years of relevant experience as per serial 3 above in oil and gas facility
construction
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and
Version 1.0
2.7.3
Duties
2.7.4
Duties
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Q C Inspectors - Instrumentation
Qualifications
Duties
2.8
The Supplier shall carry out Internal Audits of the Quality System and External Audits of SubContractors throughout the Contract. An Audit Schedule shall be included in the Contract Quality
Plan, which shall be approved by the Company.
The Audit Schedule shall include External Audits carried out by the Supplier on Sub-Contractors.
Compliance Audits shall be carried out at least once per month on all ongoing activities.
For Contracts of less than 4 months duration the Supplier shall include the annual Corporate Audit
Schedule of the Quality System, together with details of supplementary audits planned for the
Contract. Supplementary audits shall include the following as a minimum:
Company Representative,
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The Supplier shall ensure that their Auditors possess following qualifications and experience:
For External Audits - Passed IRCA, UK registered Five days Lead Assessor / Assessor course and
have done minimum 10 external audits (at least 5 as lead auditor).
For Internal Audits - Passed IRCA, UK registered Two days Internal Auditor course and have
done minimum 10 internal audits (at least 5 as lead auditor).
The Supplier shall maintain a summary log of all Corrective Action Requests raised during Internal
and External Audits. The log shall show:
2.9
Purchasing
The Company reserves the right to inspect products or services purchased by the Supplier from SubContractors (or Vendors). Such inspection shall take place at the source, in the Supplier's premises,
on site or at the Sub-Contractor's premises. Verification or Inspection by the Company is not a
substitute for verification by the Supplier nor absolve the Supplier of its contractual obligations. Hold,
Review and Witness Points shall be identified in the Quality Control Plans for Supplier, Sub-Vendor,
Third Party Inspector / Authorised inspector and Company. Company shall be given at least 10
working days notice to attend such verifications.
The purchase of products and the associated Quality documentation shall be co-ordinated with the
Contract Schedule (programme), to ensure timely delivery. Special attention shall be given to long
lead items.
Generally the Supplier shall only purchase products and services from Company approved sources.
Lists of approved sources (Contractors and Vendors) are available from the Company.
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Bureau Veritas
Germanischer Llyod
The Third Party Certification Authority shall issue the following certification to provide assurance and
evidence that the Works are in conformance with the Contract.
Certificate of Safe Operation (that all plant and equipment is safe for normal operation).
Certificate of Completion (that the Contract can be handed over to the Company for normal
operation).
The Certification shall apply to all design, procurement, on and off site construction, precommissioning, commissioning and hand over activities, included in the Scope of Work of the
Supplier.
The Certification shall also apply to all materials and consumables procured by the Supplier
(Purchased Product ISO 9000) and materials issued free to the Supplier by the Company (Purchaser
Supplied Product ISO 9000). In the later case the Certification shall be limited to ensuring material
certification data is supplied with the material and that the delivered materials as detailed on the
material certification data complies with the requisition and drawings. It shall not include inspection
of Company supplied material outside Oman.
In order to assure conformance to the Contract requirements the following activities shall be
considered as a minimum to be carried out by the Third Party Certification Authority:
Endorse the Suppliers Quality System and Contract Quality Plan to ensure they meet the
requirements of this specification and ISO 9000.
Endorse the Suppliers Procedures and Work Instructions to ensure they meet the specified
requirements.
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Ensure all supporting documentation and Standards, Codes, Specifications are available at the
Work site.
Carry out audits, surveillance, inspection and witnessing sufficient to ensure specified
requirements are met and to enable Certification to be issued.
Ensure proper test & inspection equipment is used, calibrated and certified.
Endorse Quality Records, Commissioning Plans, Operation & Maintenance Manuals and As
Built information.
Report directly to the Company any Non-conformance and Close out the Non-conformance.
Issue Certificate of Compliance, Acceptance, Safe Operation and Completeness, directly to the
Company.
Provide a bond, insurance or guarantee directly to the Company to support the Certification.
Personnel employed by the Third Party Certification Authority shall have qualifications and
experience at least equal to that specified for the Suppliers Quality Assurance Engineer and
Inspection personnel.
Where the Company employs the Third Party Certification Authority, they shall act on behalf of the
Company and shall have the same access to the Suppliers Quality System as the Company.
Oman
Vessels manufactured outside Oman shall be designed and fabricated in accordance with ASME VIII
Division 1 as amended by DEP 31.22.20.31-Gen. or BS 5500 as amended by DEP 31.22.10.32-Gen,
unless specifically stated otherwise in the Specifications. The following shall apply:
Item
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BS 5500
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Inspection &
testing
Certification
Vessel Marking
Note:
Where section numbers are given they relate to the 1999 edition of ASME VIII and 1997 edition of BS 5500 (redesignated PD 5500). If a later edition or addenda exist, the equivalent sections in the latter edition shall take
precedence.
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plan (test & inspection plan), shall include this activity as a hold point for both the third party
certification authority and the company.
The company reserve the right to carry out their own inspection, testing and auditing.
C01
C10
C12
For other Work Categories, the Supplier shall be required to attain Third Party Certification of their
Quality System by an Accredited Certification Body if specified by the Work Category Custodian.
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Supplier
The term Supplier, as used in ISO 9000, shall refer to the Company's
appointed Consultants, Contractors, Manufacturers and Vendors.
Contract
The term Contract, as used in ISO 9000, shall refer to the Company's
Contracts and Purchase Orders with Suppliers (Consultants, Contractors,
Manufacturers and Vendors.
Sub-Contractor
The term Sub-Contractor, as used in ISO 9000, refers to any Third Party
or Sub Vendor employed by the Supplier to perform part of the Contract
Third Party Certification The term Third Party Certification refers to services provided by an
independent Third Party Certification Authority, employed by the
Supplier or Company, to assure the Company that work is in accordance
with the Contract and to issue Certificates of Compliance, Completeness,
Safe Operation and Acceptance.
Work Category
The term Work Category, refers to a specific work activity for which the
Company awards Contracts, and maintains a list of qualified Contractors.
The list is maintained by a Work Category Custodian.
The term Quality Control Plan (Inspection and Test Plan), is used to
identify activities that are to be controlled, the controlling specification
and the control mechanisms.
.
shall
should
may
Contractor
The party which carries out all or part of the design, engineering,
procurement, construction, commissioning or management of a project,
or operation or maintenance of a facility.
Manufacturer
User
Abbreviations
Version 1.0
BS
British Standard
CQP
CV
Curriculum Vitae
GU
Guidelines
ISO
ITP
MDI
QA
Quality Assurance.
PQR
PR
Procedure
QC
Quality Control.
QCP
SP
Specification
TPI
WPS
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Appendix B References
In this specification, reference is made to the following publications. Unless specifically designated by
date, the latest edition of each publication shall be used together with any amendments.
DEP 31.22.10.32-Gen
DEP 31.22.20.31-Gen
BS EN ISO 9001
BS EN ISO 9002
BS EN ISO 9004
ISO 10011
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Contract
Contractor
Document Ref.
Revision No.
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1.1
1.2
1.3
Revision Status
Controlled Copy Distribution List
Preparation, Approval, Issue and Revision of the Contract Quality Plan
2.0
2.1
2.2
2.3
2.4
3.0
3.1
3.2
3.3
4.0
Organisational Structure
4.1
4.2
4.3
4.4
4.5
5.0
5.1
6.0
6.1
6.2
6.3
6.4
6.5
6.6
6.7
6.8
Contract Management
Design
Procurement
Civil Engineering
Mechanical Engineering
Electrical Engineering
Instrumentation Engineering
Commissioning, Handover, As Built, Operation & Maintenance Manuals
7.0
7.1
7.2
7.3
7.4
7.5
7.6
7.7
7.8
Contract Management
Design
Procurement
Civil Engineering
Mechanical Engineering
Electrical Engineering
Instrumentation Engineering
Commissioning, Handover, As Built, Operation & Maintenance Manuals
8.0
Quality Records
8.1
8.2
SP-1171
Page 28
April 2000
Audit Schedule
9.1
9.2
9.3
10.0
Other Measures
10.1
To be identified by Supplier
April 2000
Page 29
SP-1171
Version 1.0
Date
1.1.99
1.3.99
Description
Prepared
By
Tender Issue
Project.
Engineer
Contract Issue
Project.
Engineer
Approved
By
Approved by PDO
Quality
Assurance
Manager
Quality
Assurance
Manager
Position
Location
Contract Manager
Head Office
Contractor Representative
Head Office
Head Office
Site
MAF
Site
MAF
Tel. No.
Site
SP-1171
Page 30
April 2000
2.
Corporate
Quality Manual
Contract
Quality Plan
Key
Document
Can be combined
Corporate
&
Contract
specific
Procedures
Provides overview
Assists auditing
Work Instructions
Quality Control Forms &
Checklist
Quality Control Plans
Audit Checklists
April 2000
Page 31
SP-1171
Version 1.0
Title
Rev.
Date
Contract Management
Contract Review
Contract Quality Plan
HSE Plan
Planning & Scheduling
Document Control
Labour, Materials & Plant Resourcing
Interim & Final Payment Certification Contract Reporting to PDO
Training
Quality Auditing
HSE Auditing & Inspection
Technical Queries
Change Orders & Variations
Control of Non-Conforming Product
Corrective Action
Third Party Certification (if required in Scope of Work)
Design
Design control
Drawing control
Design Verification & Technical Reviews
HAZOP/SAFOP
Control of Specifications, ERDs, DEPs, Codes & Standards
Preparation of Requisitions
Materials Tracking & Reporting
Reviewing Vendor Documentation
As Built Information
Operation & Maintenance Manuals
Procurement
Approved Contractors & Vendors List
Requisitions, Purchasing Data & Purchase Orders
Materials Tracking & Expediting
Inspection & Testing (in process & Final)
Control of Customer Supplied Product
Handling, Storage, Packing & Transportation
Goods Inward Inspection
Civil Engineering
Surveying & Setting Out
Earthworks, Trenching, Excavation & Backfilling
Concrete Work
Structural Steelwork
Brickwork & Blockwork
General Building & Architectural Work
Building Services (Plumbing, Electrical, A/C)
Roads & Paving
SP-1171
Page 32
April 2000
Mechanical Engineering
On Plot Piping
Off Plot Piping
Welding
Installation of Static Equipment
Installation of Rotating Equipment
Painting & Coating
Non-Destructive Examination NDE
Electrical Engineering
Protection & Isolation
Installation of Electrical Equipment
Installation of Underground Cables
Installation of Overhead Lines
HV & LV Switch gear
Cathodic Protection
April 2000
Page 33
SP-1171
Version 1.0
Contract Management
- Contract Review
- Contract Quality Plan
- HSE Plan, etc.
Design
- Design Control
- Drawing Control, etc.
Procurement
Approved Contractors & Vendors
Requisitions, etc.
Civil Engineering
Surveying & setting Out
Earthworks, etc.
Mechanical Engineering
Electrical Engineering
Instrumentation Engineering
Commissioning & Handover, etc.
SP-1171
Contract:
Element:
Controlling Document
Identify the documents that
control the activity.
This will be the Suppliers
Procedure, Contract
Specifications, DEP, ERD, BS,
ASME, etc.
Identify the Quality Control
requirements in these
documents.
Identify the Clause reference
that stipulates the
requirements.
Acceptance Criteria.
Frequency of Test.
Identify the actual value of
the specified requirement if
this is a simple measurement.
Alternatively cross reference
to the clause, table, figure,
etc. in the relevant
specification, ERD, DEP, BS,
ASME, etc.
Verification Documents and
Checklists can be used to
show the specified Acceptance
Criteria, if it is not practical to
show details in the QCP. This
enables easy comparison with
measured values.
Contract No.:
Procedure Ref.:
Suppliers
Verification
Personnel
Identify the
Suppliers
personnel
responsible for
verifying the test
results.
Page 34
Verification Document
April 2000
Version 1.0
Activity
Controlling Document
(Suppliers Procedure, Contract
Specification, Standard, ERD,
DEP)
Suppliers
Verification
Personnel
Verification Document.
(Quality Control Form,
Inspection Record etc)
Suppliers Hold,
Witness & Review
H
Company Hold,
Witness & Review
H
QC Eng.
Approved Schedule
Permit to Work
Supplier Procedure
PIPEWORK/3
Mech. Sup.
Approved Permit
Supplier Procedure
PIPEWORK/3
ERD 84-01
Mech. Sup.
Checklist PIPE 01
Supplier Procedure
PIPEWORK/3
ERD 84-01
Mech. Sup.
Checklist PIPE 02
Hydro testing
Supplier Procedure
PIPEWORK/3
ERD 84-01
Mech. Sup.
Checklist PIPE 03
Supplier Procedure
PIPEWORK/3
ERD 84-01
QC Eng.
Checklist PIPE 06
April 2000
Page 35
SP-1171
Version 1.0
Title:
Issue Date:
Page Number:
Heading Number:
Figure Number:
Comments:
Suggestions:
Ref.
Ind.:
Signature:
Date:
Phone:
Date:
CFDH
Ref. Ind.:
Recd.:
CFDH Actions
Recd.
Decision:
Date:
Reject:
Accept, revise at next issue:
Accept, issue temporary amendment
Comments:
Originator
Advised:
SP-1171
Date:
Inits.:
To CFDH:
Inits.:
Document
Control
Section
Advised:
Page 36
Ref.
Ind.:
Date:
Date:
Inits.:
April 2000