Supplier Terms and Conditions
GENERAL: Novium Quality System is based on the requirements of AS9100
Rev D requirements. As a Supplier (Seller) to Novium (Buyer), the Seller
agrees to meet the following stipulations for AS9100 requirements for
the purchase order or subcontract, hereafter referred to as the “Order”.
Definitions: For the purpose of this document, the terms and definitions
given in AS9100 Rev D shall apply.
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1. Final Approval - Buyer reserves the right of final approval of
product, procedures, processes, and equipment.
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2. Approved Quality Management System (QMS) - Buyer reserves the right
to review and approve Seller Quality Management System for Seller’s
use in supplying supplies or services to the Buyer. Maintenance
organizations shall be required to have any required QMS approvals and
other approvals, certificates, ratings, licenses, and permits required
by applicable statutory and regulatory requirements.
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3. Configuration Control - The Seller shall maintain the proper
identification and revision status of specifications, drawings,
process requirements, inspection/verification instructions and other
relevant technical data used in the performance of requirements of
this Order. The Seller shall use technical data at the contractually
specified revision or at the latest revision in effect at the time of
contract award, if not specified.
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4. Certified Personnel & Certifying Staff - The Seller shall ensure
that all personnel are properly qualified to perform the work required
to support the Order, including having the proper certification to
perform special processes, tasks and maintenance required by the
purchase requirement. The Buyer reserves the right to review all
documentation supporting qualification of Seller or Seller’s subtier
personnel and Certifying Staff.
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5. Buyer Approvals - Buyer reserves the right to approve or specify
any designs, tests, inspection plans, verifications, use of
statistical techniques for product acceptance, and any applicable
critical items, including key characteristics.
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6. Test Requirements - Buyer reserves the right to designate
requirements for test specimens for design approval, inspection and
verification, investigation or auditing.
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7. Records Retention - The Seller is required to retain all records
related to this Order, including objective evidence of the quality of
any items supplied (manufacturing, assembly, inspection,
physical/chemical test reports, test and special process records and
material certification records) for a period of seven (7) years after
the final payment. Records shall be made available to Buyer upon
request and at no additional charge.
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8. Calibration - All Sellers providing calibration services shall be
required to be compliant to ANSI Z540 (or equivalent). All calibration
certificates shall identify standards used and shall be traceable to
NIST (National Institute of Standards Technology).
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9. Approved Processors - Where required on the Order, Seller shall
utilize only Buyer/Customer approved special process sources.
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10. Nonconforming Product/Material – The Seller shall maintain a
documented procedure for control of nonconforming product. The Seller
shall notify the Buyer in the event of nonconforming product/material
to include post-delivery. Only the Buyer’s authorized Quality and
Project Managers may disposition acceptance or rejection of the
Seller’s Nonconforming product/material, as coordinated thru the
Buyer’s Contract Representative.
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11. Changes Notification Requirement - The Seller shall notify the
Buyer of any changes to a product’s design, development, processes,
manufacturers/suppliers, manufacturing location, and/or quality
management system approval status. Seller shall obtain written
approval from the Buyer’s Contract Representative (all as coordinated
with and authorized by the Buyer’s Technical Representative) before
delivering product affected by any such changes.
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12. Right of Entry/Access - Buyer, its customers and regulatory
authorities reserve the right of access to all supplier facilities, at
any level of the supply chain, performing work on the Order and to all
applicable records. The Seller is required to provide support in the
form of labor, materials, information, tools and equipment necessary
to execute verification and survey activities.
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13. Flow Down Requirement - The Seller shall flow down all
applicable Buyer, Customer, U.S. Government (hereafter referred to
as Customer), Regulatory and/or AS9100/AS9110 requirements to
sub-tier suppliers (including requirements in the purchasing
documents and key characteristics where required). However, Buyer
does not allow Seller to subcontract any product or process to a
sub-tier supplier without prior expressed written consent of the
Buyer, through the Buyer’s Contract Representative.
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14. Verification of Purchased Product - The Seller is responsible
for conformity of all products purchased from suppliers/processors,
including from sources defined by the Buyer or Buyer’s Customer.
Unless specifically authorized by the Buyer, Seller is not
authorized to release purchased product for use until completion of
all required verification activities. If approved by Buyer, Sellers
documented procedures must include provisions for identification and
records to allow recall and replacement if it is subsequently found
that the product does not meet requirements.
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15. Delegated Inspection Authority - When appropriate, the Buyer may
delegate the inspection authority to the Seller, if the Seller has
capability and approval to conduct such inspections. The Buyer will
define the inspection requirements (including approved monitoring
and measurement equipment/methods) in the Order and the Buyer will
maintain a record of approval granted to Seller to carry out such
inspections. The Seller shall maintain a record of the delegation
approval and present it with the product at delivery. Delegation of
any inspection authority does not absolve the Seller of performing
all appropriate inspections prior to shipment, or of its
responsibility to provide conforming product, nor will it preclude
subsequent rejection by the Buyer.
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16. Source Inspection/Verification - The Buyer also may perform
inspection activities at the point of origin (Seller’s or its
sub-tier’s facilities) to ensure that purchased product meets
purchase requirements prior to shipment/delivery to the Buyer. When
the Buyer intends to perform verification at the point of origin,
the Buyer will define the intended verification arrangements and the
method of product release in the solicitation and in the Order. The
Seller shall provide support to include, but not limited to labor,
materials, tools and equipment necessary to perform the needed
verification activities and shall provide access to the Buyer to all
facilities where work is performed for the Order. The Seller is
responsible for conformity of all products purchased from
suppliers/processors, including from sources defined by the Buyer or
Buyer’s Customer. Verification and/or acceptance by the Buyer shall
not be utilized by the Seller as evidence of effective control of
quality by the Seller and shall not absolve the Seller of the
responsibility to provide conforming product, nor will it preclude
subsequent rejection by the Buyer.
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17. Customer/Government Source Inspection/Verification – The Buyer’s
Customer/Government (also referred to as “Customer”) may perform
inspection activities at the point of origin (Seller’s or its
sub-tier’s facilities) to ensure that purchased product meets
purchase requirements prior to shipment/delivery to the
Buyer/Customer. When the Buyer’s Customer intends to perform
verification at the point of origin, the Buyer will define the
intended verification arrangements and the method of product release
in the solicitation and in the Order. The Seller shall provide
support to include, but not limited to labor, materials, tools and
equipment necessary to perform the needed verification activities
and shall provide access to the Buyer and Buyer’s Customer to all
facilities where work is performed for the Order. The Seller is
responsible for conformity of all products purchased from
suppliers/processors, including from sources defined by the Buyer or
Buyer’s Customer. Verification and/or acceptance by the Buyer’s
Customer shall not be utilized by Buyer or Seller as evidence of
effective control of quality by the Seller and shall not absolve the
Buyer or the Seller of the responsibility to provide conforming
product, nor shall it preclude subsequent rejection by the Buyer or
Buyer’s Customer.
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18. Counterfeit and Suspected Unapproved Parts - To prevent the
purchase of counterfeit or suspect/unapproved products and to ensure
product identification and traceability (and for other reasons), the
Buyer implements controls that include the requirement of material
verification and traceability to include, but not limited to
Material Certificates, Certificates of Conformity, special tests and
inspections and/or other supporting documentation from the Seller as
is appropriate, as specified in the Order. The Seller agrees to use
commercially reasonable practices to prevent counterfeit work from
being delivered to the Buyer. The Seller shall only purchase new and
authentic materials to be used in products to be delivered to the
Buyer directly from the Original Component Manufacturer (OCM) or
Original Equipment Manufacturer (OEM). Product shall not be acquired
from distributors or brokers unless approved in advance in writing
by the Buyer through the Buyer’s Contract Representative.
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19. Corrective Action Request - Where product or process
non-conformances are identified by the Buyer or its Customer, a
Corrective Action Request (CAR) may be issued to the Seller. The
Seller agrees to take appropriate and timely action to respond to
the CAR with an acceptable corrective action plan, subject to Buyer
approval, and to implement the required corrective actions. When the
Seller does not provide a timely and/or effective corrective action
plan, the Buyer will take appropriate measures such as, but not
limited to, termination for default, withholding payment, removing
Supplier from the Buyer’s Approval Supplier List, and/or legal
action, as appropriate and solely at the Buyer’s discretion.
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20. Supplier Approval – The Seller is responsible for maintaining a
Supplier Register with documentation to support their selection of
subcontractors based on their ability to supply product that fulfill
the Buyer’s Order, including, but not limited to, evidence of
customer-approved processor status. The Seller is responsible for
assuring their subcontractors holds the required approvals and
certificates to provide the purchased product and for applying the
appropriate level of control over the subcontractor’s performance to
assure compliance with the Order. However, the Buyer does not permit
the Seller to subcontract any portion of the Order without prior
written approval from the Buyer’s Contract Representative.
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21. Purchasing Information – The Seller shall maintain purchasing
records for all procurement actions related to the Buyer’s Order
that includes purchase orders that fully describe the product to be
purchased, including, where appropriate, requirements for: a)
approval of product, procedures, processes, and equipment, b)
qualification of personnel, c) quality management system, d)
identification and revision status of all technical documents, e)
design, test, inspection, verification (including maintenance
process verification), use of statistical techniques for product
acceptance, and related instructions for acceptance, and as
applicable critical items including key characteristics, f) test
specimens for design approval, inspection/verification,
investigation or auditing, g) regarding non-conforming product
notification and disposition approvals, and notification of changes
in product process, suppliers, manufacturing facility locations and
for obtaining approvals thereof, and flow down of requirements to
the sub-tiers, h) records retention, i) right of access, j) specific
authority approval, k) format and content of the delivery
documentation package, and l) conditions under which product
malfunctions, defects and un-airworthy conditions have to be
reported to the Buyer and appropriate concerned Stakeholders.
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22. Production and Service Provisions – The Seller shall control
production and services by planning and carrying out production and
services under controlled conditions, taking into consideration, as
appropriate, processes controls to manage critical items, variable
data as it applies to design, manufacturing and tooling,
identification of in-process inspection/verification points when
conformance cannot be verified at later stages of realization, and
performance of special processes. Controlled conditions shall
include, as applicable: a) information that describes the
characteristics of the product, b) work instructions, c) suitable
equipment such as jigs, fixtures, molds and software programs, d)
monitoring and measuring equipment traceable to NIST, e)
implementation of monitoring and measurement, f) implementation of
product release, delivery, and post-delivery activities, g)
accountability of all product during maintenance such as parts
quantities, split orders and nonconforming product, h) evidence of
completion of all inspection/verification as planned/required, i)
provisions for prevention, detection and removal of foreign objects
(including tools), j) monitoring and controlling utilities and
supplies to the extent they affect conformity to product
requirements (e.g.; water, compressed air, electricity, chemical
products), k) clear workmanship criteria, l) compliance with
standards, quality plans, manufacturers’ recommendations, customer
specifications and or documented procedures, m) maintaining a list
of approved maintenance process capabilities and/or ratings, n)
assuring that maintenance operations does not adversely affect areas
outside the scope of the planned maintenance; and o) utilization of
equipment, tools and materials recommended in the technical data for
the article or as equivalent as approved by the authority.
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23. Maintenance Process Verification – The Seller shall perform
first application of maintenance processes evaluation, verification,
and documentation and if applicable, obtain approval from the Buyer
and/or authority, to verify that new processes (including the
personnel, documentation and tooling, are capable of performing the
maintenance in compliance with established requirements. Personnel
that are authorized approve changes to maintenance processes shall
be identified. The Seller shall control and document changes
affecting processes, maintenance equipment, tools or software
programs and the results of such changes shall be assessed to
confirm that the desired effect has been achieved without adverse
effects to product conformity.
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24. Control of Maintenance Equipment, Tools and Software Programs –
The Seller shall utilize only maintenance equipment, tools and
programs to automate and control/monitor product realization
processes that are defined by the technical data or demonstrated as
equivalent, prior to use. The Seller shall periodically maintain and
inspect the maintenance equipment, tools and programs, and shall
define storage requirements including periodic
preservation/conditions checks.
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25. Post-Delivery Support – The Seller shall have the capability to
provide post-delivery support, as applicable, for a) collection and
analysis of in- service data, b) actions to be taken, including
investigation and reporting, when problems related to the
maintenance performed are detected after delivery, c) control and
updating of technical data d) approval, control and use of repair
schemes, and e) controls required for off-site work.
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26. Validation of Special Processes – The Seller shall validate any
process for production and service provision where the resulting
output cannot be verified by subsequent monitoring or measurement
(Special Processes) to assure compliance with the requirements of
the applicable technical data issued by the design approval holder.
Validation shall demonstrate the ability of these processes to
achieve planned results. The Seller shall establish arrangements for
these processes including, as applicable: a) defined criteria for
review and approval of the processes, b) approval of equipment and
qualifications of personnel, c) use of specific methods and
procedures, d) requirements for records, and e) revalidation.
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27. Monitoring and Measurement of Product – The Seller shall monitor
and measure the characteristics of product, at appropriate stages,
to verify that product requirements have been met. Objective
evidence of conformity of the acceptance criteria shall be
maintained.
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28. Personnel Contribution – The Seller must ensure that their
personnel are aware of their contributions to product conformity and
product safety as well as the importance of ethical behavior.