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PCT 201084

This document outlines the Quality Control Procedures (QCP 5.8) for suppliers to the Eaton-Euclid Facility, detailing the quality assurance requirements for raw materials, parts, and services. It specifies the necessary quality systems, supplier qualification processes, and the rights of access for audits, as well as the requirements for special process suppliers and vendor quality requirements. Additionally, it emphasizes the importance of maintaining certifications and adhering to change notification protocols to ensure compliance and product reliability.

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Khaled Omar
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0% found this document useful (0 votes)
23 views12 pages

PCT 201084

This document outlines the Quality Control Procedures (QCP 5.8) for suppliers to the Eaton-Euclid Facility, detailing the quality assurance requirements for raw materials, parts, and services. It specifies the necessary quality systems, supplier qualification processes, and the rights of access for audits, as well as the requirements for special process suppliers and vendor quality requirements. Additionally, it emphasizes the importance of maintaining certifications and adhering to change notification protocols to ensure compliance and product reliability.

Uploaded by

Khaled Omar
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
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Page 1 of 12

Quality Control Procedures QCP. 5.8

QUALITY REQUIREMENTS FOR THE SUPPLIER BASE

1.0 PURPOSE

The purpose of this procedure is to define Quality Assurance requirements for suppliers of Eaton-Euclid Facility.

2.0 SCOPE

The procedure applies to suppliers of raw materials, parts and services, whether foreign or domestic. The
procedure also applies to second-tier or sub-suppliers that produce materials or provide processes critical to end
item life and reliability.

In case of conflict between the Purchase Order, Drawings and Specifications and this document, the supplier must
contact the purchasing agent for clarification.

3.0 APPLICABLE DOCUMENTS

QCP 2.4 Visual Acuity Requirements for Visual Inspection


QCP 5.1 Selection of Qualified Suppliers
QCP 5.4 Source Inspection
QCP 5.5 Certified Supplier Program
QCP 5.7 Vendor Survey and Audit Procedure
QCP 5.8.2 Supplier Packaging Specification
QCP 5.8.3 Counterfeit Parts Protection Plan
QCP 15.1 Acceptance Sampling Inspection
QCP 15.1.1 Sampling Inspection (Pratt & Whitney)
QCP 21.0 Software Quality Assurance Program
SOP 13-10-010.0-00-022 Eaton Supplier Gage Policy
SOP 52-08-0000-00-038 General Workmanship Standards for Castings
SOP 52-08-0000-00-044 Visual Acceptance Standard for Pumping Gear Teeth, Journals, Faces, Splines and
Reliefs
SOP 52-08-0000-00-058 Visual Acceptance Standards for Shafts
SOP 52-08-0000-00-059 Visual Acceptance Standards for Gear Pump Housings, Impeller covers, Volutes
and Plates
SOP 52-08-0000-00-060 Visual Acceptance for Bearings
SOP 52-08-0000-00-083 Visual Acceptance for Carbon Seals
SOP 52-10-005.0-00-001 Sample Casting Approval
SOP 52-10-005.1-00-001 Supplier Rating System
SOP 52-10-007.0-00-004 First Article Inspection Requirements (Eaton Purchased Parts)
SOP 52-10-005.8-00-001 Requirements for Suppliers for Prevention of F,O,D to Flight Hardware
SOP 52-10-011.1-00-001 Nonconforming Material – At Suppliers
Supplier Request for Material Review Board Action
ENG 01-1024 Supplier Request for Design Change Procedure
ANSI/NCSL-Z540 Calibration Laboratories & Measuring and Test Equipment
PDL Parts Data List (PDL)
TAP-LI-66 Requirements for Suppliers for Parts and Assemblies

Date of Issue: 03/06/1987 Revision: Rev AT 09/30/2021 (Changes denoted by )


Prepared by: Approved by:
“Signature on File” K. Greenlief “Signature on File” M. Mulroy

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Quality Control Procedures QCP. 5.8

TAP-LI-67 Requirements for Suppliers for Parts and Assemblies - Specific Production
Shipments
TAP-LI-71 Requirements for Sellers of Raw Materials
VQR Vendor Quality Requirement (VQR)
FC 9274 Supplier Request for Design Change Form
FC 9332 Quality Escapes Personnel List
AS 9103 Variation Management of Key Characteristics
AS 9120 Quality Management Systems – Aerospace Requirements for Distributors
Eaton Global Supplier Excellence Manual

4.0 QUALITY ELEMENTS

4.1 Quality Systems

Requirements shall be in effect for those suppliers who directly supply material, service, and special processes -
regardless of tier. (e.g., first / second tier, etc,)

 Distributors – Distributors shall have a quality system that conforms to AS 9120.

 Suppliers of material to be incorporated in end items that are sold under the regulatory approval for repaired
hardware (MRO) shall be approved per Eaton Supply Chain Policy SD-004-01.

 Special Process Suppliers – Special Process suppliers shall have a quality system that conforms to AS/EN9100
or accredited to AC7004 (by PRI-Nadcap).

 Calibration Suppliers – Calibration suppliers shall have a quality system that conforms to A2LA, ISO 17025
(Guide 25) or other national certifying body.

 Raw Materials Suppliers – Raw material suppliers shall have a quality system that conforms to relevant
industry quality standards, and airworthiness regulatory requirements, as required.

 Suppliers performing acceptance test for MRO operations shall provide objective evidence for the following:
 EASA Certification  Operations specifications
 FAA Certification  Capabilities List meeting Work Scope

 All other suppliers – All other suppliers shall have a quality system that conforms to AS/EN9100.

Conformity to the above quality standards must have evidenced by either: third party certification or a Euclid-
approved audit to assess any gaps to the AS/EN9100 requirements.

A supplier may be audited at any time for reasons not limited to performance and may be liable for the actual costs
of such audits at Eaton’s option.

4.2 Supplier Qualification and Approval

4.2.1 Suppliers are evaluated and approved in accordance with QCP 5.7 - Vendor Survey and Audit Procedure.

4.2.2 Suppliers must maintain an approved Quality Management System and maintain acceptable levels of performance,
such as Quality (DPPM) and Delivery (On Time Delivery) in order to remain on the Euclid Approved Vendors List
(AVL) - Reference QCP 5.7.

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Quality Control Procedures QCP. 5.8

4.2.3 At Eaton’s option, calibration sources may submit A2LA, ISO 17025, or equivalent accreditation in place of a
requested survey.

4.2.4 Any third-party providing services to audit to the above-mentioned standards must be accredited from a country-
authorized entity such as ANSI-ASQ National Accreditation Board (ANAB).

4.3 Right of Access

4.3.1 The supplier shall provide Eaton, Eaton Customers, and/or a specified third party (customer/ government or
regulatory agency), right of access to the facility and all records related to product ordered by Eaton or Eaton
suppliers and right to perform an audit or inspection at the supplier’s facility.

4.3.2 Such audits or inspections shall not be used as evidence of effective control of quality. The results of such audits
or inspections, does not absolve the supplier of the responsibility to provide acceptable product and does not
preclude any subsequent rejection by Eaton or its customer.

4.4 Sub-Tier Selection/Control Requirement Flow-down to Sub-Tiers Suppliers

4.4.1 Eaton reserves the right to specify or approve sub-suppliers contracted by its suppliers for work performed on
Eaton material. This includes but is not limited to special process, materials testing services, distributors, and other
subcontractors.

4.4.2 Suppliers shall flow down all relevant quality requirements imposed by this manual and other contractual
documents to sub-tier suppliers, including government-regulatory and/or industry requirements.

4.5 Special Process Suppliers

4.5.1 A special process is one that is specialized and/or complex in nature and must be performed by qualified personnel
and/or on qualified equipment. It usually applies where uniform conformance to the requirements cannot be assured
by inspection of the articles alone or requires destructive testing. "Qualified" personnel or equipment are personnel
or equipment that have been certified to meet specific qualification requirements or tests stipulated in applicable
control documents. A special process may include inspection, test or fabrication processes such as:
• Magnetic Particle Inspection (MPI)
• Fluorescent Penetrant Inspection (FPI)
• Ultrasonic Inspection
• Radiographic Inspection
• Leak Testing
• Welding/Brazing
• Soldering
• Heat Treating
• Plating
• Electric Discharge Machining (EDM)

4.5.2 All suppliers (regardless of tier) shall use only the Euclid Facility’s Approved Special Process suppliers, when
required by Purchase Order and/or VQR.

4.5.3 Any Supplier may request that a sub-tier supplier be added to the Euclid Eaton facility’s Special Process List
(SPL) through the appropriate Euclid Supply Chain contact, however, such sources may not be used prior to
receipt of documented Eaton Quality approval per QCP 5.7. Actual costs associated with the approval process for
a new sub-supplier, such as an on-site audit, may be assessed to the requestor.

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Quality Control Procedures QCP. 5.8

4.5.4 Eaton Aerospace acknowledges NADCAP (National Aerospace and Defense Contractors Accreditation Program)
special process accreditation program administered by the Performance Review Institute (PRI). For the processes
listed below, all special process suppliers must be Nadcap accredited and approved by Eaton Euclid, unless
specifically exempted by contract terms exhibiting an Eaton Supplier Quality approval.

4.5.5 Result and scope of special process approvals are listed in the Eaton Euclid’s SPL. The SPL is maintained and
available on the Euclid Facility’s website.

4.5.6 Detailed requirements pertaining to controls for special processes may appear in government or industry
specifications that are called out in the contract or on product definition documents.

4.6 Source Inspection

4.6.1 Source Inspection shall be in accordance with QCP 5.4. Eaton shall have the right to visit a supplier's facility to
inspect products, witness inspections or tests and evaluate the Supplier’s Quality Management system. Visits may
also extend to supplier sub-tier suppliers.

4.6.2 The supplier's gauges and measuring and testing devices shall be made available to Eaton Source Inspectors for use
at the supplier's facility for determining product conformance to contract requirements.

4.6.3 The supplier shall keep records of inspection data. The data shall include (at a minimum) the following
information: part number, name, purchase order, lot number (if applicable), drawing revision, AQL, lot size,
sample size, characteristics inspected, inspector's acceptance stamp, serial numbers, and number of pieces accepted
and rejected. The characteristics to be inspected shall either be listed individually or in distinct groupings.

The supplier must complete required inspection and document the results prior to the arrival of the source
inspector.

4.6.4 The supplier shall include with the parts shipment and certification package the Source Inspection Tag and Source
Inspection Plan provided by the Eaton Source Inspector.

4.6.5 Final acceptance of the supplier’s product shall be made at Eaton and acceptance by Eaton Source Inspectors does
not relieve the supplier of the responsibility for the acceptability of contracted items.

4.6.6 The supplier shall notify Eaton Purchasing at least four working days prior to the need for source inspection.
Source inspection will be performed in accordance with QCP 5.4.

4.7 Vendor Quality Requirements - (VQR)

4.7.1 When quality requirements are extensive, Vendor Quality Requirements (VQR) document will be called out as part
of the Purchase Order.

4.7.2 The Engineering documents (drawing part number, specification number) called out on the VQR are part of the
contract as stated therein. Other documents referenced in the VQR (e.g. Laboratory Instructions, Government
Specifications, Eaton Quality Control Procedures (QCP’s), etc.) which require supplier certification will be listed
with appropriate revision and/or amendment number on the Parts Data List (PDL), or will be listed on the
purchase order itself. Any document revision levels listed on the purchase order will supersede the PDL levels.

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Quality Control Procedures QCP. 5.8

4.7.3 All specifications listed on the VQR requiring supplier certification become part of the contract and must be
certified to by the supplier upon submittal of parts or special processes to Eaton for acceptance. Approved
radiographic technique and layout reports are also part of the contract requirements. If the supplier does not have
access to the specified documents, the supplier must request a copy of the documents from Eaton Purchasing.

4.8 Notification of Changes at Suppliers

4.8.1 All changes to product, process at suppliers must be submitted to the Eaton Euclid buyer in writing using the
supplier change request form on the supplier portal. The change(s) shall not be implemented until approved in
writing by Eaton. Changes requiring approval, at a minimum, are listed below:

Type of change Examples


Product Design  A change to the engineering drawing of the product or sub-assemblies; including
dimensional, material, or specification changes
Manufacturing  A change in the manufacturing process or method that may have an impact to
Process/ the form, fit, or function of the product, including:
Inspection  New or modified tooling, dies, and mold patterns, or reintroduction of inactive
Sequence tools, dies, and mold patterns
 Upgrade or rearrangement of existing tooling or equipment
 Process change related to components of production products internally or
externally
 Changes to a casting process per SOP 52-10-005.0-00-001 Sample Casting
Approval
 Change in testing or validation method
Material /  New source of the raw material
Material Source
Sub-Supplier  Change of Tier-1 Supplier manufacturing location
Source  Change of Sub-Tier Supplier or change of existing Sub-Tier Supplier’s
manufacturing location
Special Process  Changes to heat treat, plating, welding, painting, or other process changes that
cannot be verified without destructive testing

Eaton may elect to require formal FAIR submission and approval, testing validation or other Product Realization
process. Suppliers shall not ship products to Eaton prior to approval.

Failure to contact Eaton and obtain written approval prior to implementing changes and shipment of product shall
result in:
 Issuance of a DMR.
 Supplier compensating Eaton for all associated collateral costs and expenses.
 Possible New Business Hold.

4.8.2 Product design changes for source-controlled components will be processed by Eaton Engineering in accordance
with specification 01-1024 – Supplier Request for Design Change Procedure.

4.8.2.1 Supplier’s authorization to proceed with the revision is an approved release of the Supplier Request for Design
Change Form (FC 9274). This approval copy will be forwarded to supplier from the Purchasing Agent.

4.8.2.2 Suppliers shall maintain history approval records of these change requests.

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Quality Control Procedures QCP. 5.8

4.9 Certifications

4.9.1 Suppliers shall submit certifications with the shipment as indicated on the Purchase Order and VQR.
Certifications are to include the Government or Military Specifications (MS) plus latest revision and/or
amendments that the parts were processed to. Instructions for preparing the certifications are contained in the
following:

Document No. Description


TAP-LI-66 Requirements for Suppliers for Parts and Assemblies
TAP-LI-67 Requirements for Suppliers for Parts and Assemblies, Specific Production Shipments
TAP-LI-71 Requirements for Sellers of Raw Material

4.9.2 Suppliers shall require sub-tier suppliers of material, processes and/or operations to submit similar certifications
as objective evidence of compliance to requirements. These records shall either accompany delivered items to
Eaton or be kept on file in accordance with contract requirements.

4.10 Supplier Rating System

4.10.1 Each supplier supplying materials and products to Eaton is rated on Quality Performance (DPPM) and On Time
Delivery (OTD) on a monthly basis. The numerical rating is calculated from a weighted composite of the
supplier's delivery and quality performance.

4.10.2 The supplier ratings are published on a quarterly basis. The individual supplier's rating is considered when new
orders for like products are placed by Eaton Purchasing. See QCP 5.1 - Selection of Qualified Suppliers.

4.10.3 When any component of a supplier's performance is determined to be unsatisfactory, Eaton shall communicate
its concern to the supplier by telephone, letter, Corrective Action Request or a visit to that supplier for discussion
or audit. If a supplier's performance thereafter continues to remain unsatisfactory, the supplier’s status on the
Approved Vendor List may be downgraded from an approved level to a conditionally approved or unapproved
level.

4.11 Government Source Inspection

4.11.1 When government source inspection is indicated on the Purchase Order, the supplier shall, upon completion of the
parts, notify the government representative who normally services that plant that Government Source Inspection
is required. Confirmation of the requirements for Government Source Inspection will be forwarded in the form of
a letter of delegation from the Government Quality Assurance Representative at Eaton to the Government Quality
Assurance Representative at the supplier location. If there is no representative available, the supplier shall notify
the nearest Army, Navy, Air Force or Defense Supply Agency Inspection Office. The supplier shall notify Eaton
Purchasing, in the event none can be located.

4.12 Documentation

4.12.1 Quality procedures and work instructions that define requirements necessary for effective operation of the Quality
Program is “Quality Documentation”. The supplier is required to have detailed procedures describing the
Inspection System for the control of receiving, in-process and final inspection as well as assembly and test if
applicable. The supplier is also required to have detailed inspection instructions describing inspections and tests
that are carried out in the above areas to verify that supplier supplied Eaton parts and/or operations meet
requirements.

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Quality Control Procedures QCP. 5.8

4.12.2 Sampling Inspection

The supplier may perform 100% inspection of each characteristic or may use sampling inspection to an approved
sampling plan. All sampling plans used shall have a protection level equal to or more stringent than the AQL
values shown in QCP 15.1 or QCP 15.1.1. These plans are a modification of MIL-STD-105 and emphasize the
fact that the plan will never accept a lot when a sample reveals a nonconformance. In all instances, the accept
value shall be 0 and the reject value shall be 1. Eaton QCP 15.1 - Acceptance Sampling Inspection may be used
for supplier inspection as an approved plan.

4.12.3 Visual Standards

Each part will be visually inspected. The visual acceptance criteria of the following SOPs apply to the related
product as noted:

SOP 52-08-0000-00-038 General Workmanship Standards for Castings


SOP 52-08-0000-00-044 Visual Acceptance Standard for Pumping Gear Teeth, Journals, Faces, Splines and
Reliefs
SOP 52-08-0000-00-058 Visual Acceptance Standards for Shafts
SOP 52-08-0000-00-059 Visual Acceptance Standards for Gear Pump Housings, Impeller covers, Volutes
and Plates
SOP 52-08-0000-00-060 Visual Acceptance for Bearings
SOP 52-08-0000-00-083 Visual Acceptance for Carbon Seals

4.12.4 Inspection Data

When required by the Vendor Quality Requirement (VQR) the Supplier shall provide a copy of the final
inspection/test report, signed by the Quality Control Manager or his designated representative providing actual
data to comply with the purchase agreement.

4.12.5 Advanced Product Quality Planning (APQP)

Suppliers shall implement a process conforming to AS9103 (Variation Management of Key Characteristics).
Suppliers shall use recommended risk management process tools (i.e., PFMEA, control plans, process flow
diagrams, etc.).

Specific APQP requirements will be identified by the project team and will be determined by risk assessment.
Consideration will be given to complexity and critically of components and to customer mandated requirements.

4.13 Records

Records as used herein are defined as Quality data which are obtained and recorded as an essential element for the
effective operation of the Quality program. Records are objective evidence that the product meets the
conformance requirements.

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Quality Control Procedures QCP. 5.8

The supplier shall maintain adequate records of inspection and tests performed under his responsibility. These
records shall be kept readily accessible and shall include documents such as:

• Material Verification and Acceptance Records


• Receiving Records
• Personnel Eye Examination Records (per QCP 2.4 – Visual Acuity)
• Inspection Reports
• Laboratory Reports and Nondestructive Test Reports
• Raw Material Certifications
• Certifications of Special Process Equipment and Personnel
• Discrepancy Control and Disposition Records, Inspection Stamp Assignment Records
• Gaging Equipment Verification and Calibration Maintenance Records
• Engineering Design Records for Supplier Designs (records to be kept for life of engine type certificate plus
two years)

All records, unless otherwise specified, shall be retained for a period of 15 years. All records shall be made
available to Eaton on request.

4.13.1 All records for the Adour program, including manufacturing records, shall be retained for a minimum of 40 years.

4.14 Corrective Action

When unsatisfactory supplier quality is detected during Source Inspection or at Eaton and Supplier Quality
concludes that formal corrective action is necessary, Eaton Supplier Quality will issue a DMR via the Eaton
Wisper System.

In the event a supplier is assigned a DMR, at a minimum, the supplier is to address:


• Product in transit from the supplier
• Product in queue for delivery to Eaton
• Suspect product delivered to Eaton

Containment response time is not to exceed 48 hours, two business days or as directed by Supplier Quality
personnel.

The supplier shall communicate corrective actions and containment activity with the applicable Eaton purchasing
agent and with the Supplier Quality Representative that issued the DMR.

4.15 Measuring and Test Equipment

The supplier shall have a system for the control of Measurement and Test Equipment that complies with the
requirements of ANSI/NCSL-Z540, Calibration Laboratories & Measuring and Test Equipment.

Control of measurement and test equipment applies to any equipment used to verify a quality requirement of the
product. Calibrating service may be internal to the supplier’s facility or purchased by the supplier from an
approved external source.

The supplier shall notify Eaton purchasing in the event that measuring & test equipment is found significantly out-
of-tolerance. The supplier must provide traceability to product in the event that measuring & test equipment is
found to be out of calibration between periodic calibrations.

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Quality Control Procedures QCP. 5.8

The Eaton Supplier Quality Engineer shall evaluate any impact to product quality. Traceability to the product must
be controlled by the supplier.

Equipment that must be controlled includes:

 Linear Measurement Equipment


 Test Equipment (Electrical/Functional)
 Process Control Instrumentation
 Personally owned gauges
 Tooling used as a media of Inspection

Eaton consigned measuring & test equipment shall be calibrated in accordance with Eaton Supplier Gauge
Policy-SOP 13-10-010.0-00-022.

4.16 Indication of Inspection Status

The supplier shall be able to identify the inspection status of materials and parts. Identification may be
accomplished by use of tags, routing sheets, stamps or other control devices. If stamps are used, they shall be
distinctly different from the government inspectors’ stamps. Stamps shall be controlled so that they are traceable
to the person performing the inspection and not available for use by unauthorized personnel.

4.17 Nonconforming Material

The supplier shall establish a system for identifying all material that does not meet contractual requirements. The
system shall include methods for segregating or controlling this material to prevent inadvertent use or shipment,
identifying and correcting conditions which caused the non-conforming material.

The supplier shall not ship any nonconforming product to Eaton without written authorization from Eaton
Purchasing.

Eaton realizes that some nonconforming material may be salvageable and for that reason has established a system
(reference SOP 52-10-11.1-00-001 - Supplier Request for Material Review Board Action (MRBA). The supplier
may request the forms and procedure used to initiate this action from Eaton Purchasing.

A supplier may rework nonconforming product using a planned manufacturing process that completely restores
all nonconforming characteristics to the requirements of the contract, specifications, drawing or other approved
product description. Notification to Eaton regarding rework is not required.

All rework shall be documented, and all affected characteristic(s) must be re-inspected to the contracted
requirement.

 NOTE: Parts reworked after source inspection MUST be re-inspected to the contracted source inspection
requirement.

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4.18 Quality Escapes

A Quality Escape is any product known to be defective that has been shipped to Eaton. The supplier shall contact
the Quality Representative listed on form FC 9332 – Quality Escapes Personnel Contact List immediately when a
Quality Escape is discovered. Details of the nonconformance and shipping information must be provided.

Contact will be in the form of a telephone call to personally speak to one of the listed persons in the order shown.
If for some reason that person cannot be contacted by telephone, the next person on the list shall be contacted.
Leaving only an e-mail or voice-mail message is not permitted. Form FC 9332 is available on Eaton’s web site –
http://www.eaton.com/Eaton/ProductsServices/ProductsbyName/Argo-Tech/Argo-
TechEngineSupplierQualityDocuments/index.htm

4.19 Receiving Inspection

Materials shipped to Euclid may be subject to Receiving Inspection. The supplier will provide inspection data,
certifications. etc. as required by the Purchase Order and/or VQR. Inspection at Euclid is intended to supplement
the supplier quality control. Rejected product at Eaton may be returned to the supplier for screening, replacement,
credit or rework.
A copy of the Eaton rejection paperwork must be returned to Eaton with reworked material. Non-conforming
product detected at Receiving Inspection will be reflected in the supplier quality rating.

4.20 Packaging and Shipping

The supplier shall maintain proper control of packaging and shipping operations to assure that items are:

• Shipped in correct quantities and accompanied by the proper paperwork.

• Properly preserved and packaged to protect items from corrosion, contamination and damage in transit.
• Minimum packaging requirements are defined in QCP 5.8.2 - Supplier Packaging Specification.

One copy of the following data shall be included with each shipment of the product when specified in the Vendor
Quality Requirement (VQR).

Inspection Data X-Ray Films Casting Tensile Specimens


Test Data Certifications

NOTE: Casting Tensile Specimens shall be contained in an envelope and shall accompany the paperwork and/or
radiographic film.

4.21 Supplier Visual Acuity Requirements for Visual Inspection

Suppliers are required to establish and maintain a visual acuity program in accordance with QCP 2.4 - Visual
Acuity Requirements for Visual Inspection.

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Quality Control Procedures QCP. 5.8

4.22 First Article Inspection Requirements for Eaton Purchased Parts

Suppliers of Eaton purchased parts are required to perform First Article Inspection per SOP 52-10-007.0-00-004
(except for casting suppliers). Casting suppliers shall perform First Article Inspection per SOP 52-10-005.0-00-
001. First Article Inspection requirements are flowed down to suppliers via the purchase order.

4.23 Software Quality Assurance Requirements

Suppliers are required to establish and implement a Software Quality Assurance Plan in accordance with QCP
21.0.

4.24 Supplier FOD Prevention Program

Suppliers are required to maintain a system for prevention of Foreign Object Damage (FOD) to flight hardware
meeting the requirements of SOP 52-10-005.8-00-001.

4.25 Counterfeit Parts Protection Plan

Suppliers shall maintain a counterfeit electronic parts protection plan meeting the requirements of QCP 5.8.3.

4.26 Product Conformity, Safety and Ethical Behavior

Suppliers shall communicate to their personnel:


 Their contribution to product or service conformity
 Their contribution to product safety
 The importance of ethical behavior

This communication shall be ongoing, and the supplier’s management shall ensure that personnel understand.

5.0 PARTS DATA LIST (PDL)

The Parts Data List (PDL) referenced on product purchase orders lists Eaton specifications, standards, procedures
and corresponding revision status as of the date of issue. Changes to Quality documents will be reviewed for
content change to determine if a revision to current purchase order PDL’s are warranted. The review activity will
occur during the quality document change and approval process.

It is the responsibility of the supplier to determine and use the current revision of any applicable industrial and/or
government specifications (e.g., ASTM, AMS, MIL, etc).

Copies of current revisions of Eaton specifications (Quality Control Procedures, Engineering, Material and Process
Specifications) are obtained directly from the Eaton website or through your purchasing agent. Eaton supplier
documents are available at:
http://www.eaton.com/Eaton/ProductsServices/ProductsbyName/Argo-Tech/Argo-
TechEngineSupplierQualityDocuments/index.htm.

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6.0 DEMAGNETIZATION OF FERRO MAGNETIC PARTS AND COMPONENTS

All parts and components of assemblies that are manufactured from ferro-magnetic materials and supplied to
Eaton shall be tested for residual magnetism using a magnetic field probe or strength meter. Unless magnetism
requirements are defined on the blueprint or engineering specification, there shall be no residual magnetism with
an absolute value greater than 3 gauss (240 Am-1) anywhere on the part. Inspection data sheets shall show
evidence of this inspection.

7.0 RISK MANAGEMENT AND BUSINESS CONTINUITY GUIDELINES

Eaton expects suppliers to have a comprehensive crisis management approach to deal with potential disruptions.
The approach needs to include plan of action, checklist of activities, communication plans, escalation procedures,
and organization with teams, roles, and responsibilities.

The supplier must provide risk management and business continuity plans and conform to the risk management
and business continuity requirements in the Global Supplier Excellence Manual. Eaton will notify suppliers in
writing when identified as part of a risk situation.

Eaton expects suppliers to plan for the following disruptions:

• Business continuity to deal with event-based risks such as fires, chemical spills, natural disasters, terrorist
threats, medical emergencies, and HR (Example: Strikes)
• Supply Chain continuity to check and prepare the sub tier suppliers to deal with potential disruptions
• Pandemics Preparedness Plan (Example: Avian Flu Pandemic)
• IT Disaster Recovery and IT Security for "Supplier" telecommunications, data, systems and infrastructure
• Eliminate potential disruptions due to Financial and Regulatory Non-Compliance (Example: For US
publicly traded companies – SOX404 or International Financial Reporting Standards (IFRS) in Europe)
• Human Resources guidelines to conducting drug and background checks

Confidentiality Policy (including protection of Eaton Intellectual Property)

Eaton is asking each supplier to develop, deploy and maintain these business continuity planning requirements.
The “Risk Management and Business Continuity – Self Assessment” further explains the criteria for each of the
above continuity requirements.

“Copies Printed from the On-Line System are Considered Uncontrolled”


Rev. AT

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