SUB-SUPPLIER MANAGEMENT Sample Clauses

SUB-SUPPLIER MANAGEMENT. ▇▇▇▇▇ expects its supplier to manage the quality of their suppliers / subcontractors and follow the business ethics. Supplier shall not change their supplier / subcontractor without written approval from ▇▇▇▇▇ after PPAP sign off. Any unfavorable impact (financial or otherwise) resulting from unacceptable quality, deliver, cost or unauthorized change of their suppliers, will be the responsibility of the supplier.

SUB-SUPPLIER MANAGEMENT. 7.5.1 The Supplier must maintain qualifications for subcontractors and the products purchased through them. It is the Suppliers’ responsibility to ensure and control the quality of all components and raw materials that are purchased to manufacture components and parts for ▇▇▇▇▇▇ Scientific. 7.5.2 Suppliers will manage sub-tier Suppliers with controls commensurate with those that ▇▇▇▇▇▇ Scientific applies to direct Suppliers. Suppliers are responsible to ensure that product(s) manufactured utilize only authentic, conforming and specified material requirements as stipulated in the Specifications. Prior to implementing changes, including changes requested by sub-tier Suppliers, Suppliers must notify ▇▇▇▇▇▇ Scientific according to section 7.14.5 of this agreement. 7.5.3 ▇▇▇▇▇▇ Scientific shall be permitted to conduct an audit of the sub-supplier facility. The scope of each audit will be at the sole discretion of ▇▇▇▇▇▇ Scientific. ▇▇▇▇▇▇ Scientific shall notify the supplier of the planned date of the audit. The supplier must notify the sub-supplier of this requirement. Any verification performed by ▇▇▇▇▇▇ Scientific does not relieve the supplier of the responsibility to provide quality products.

SUB-SUPPLIER MANAGEMENT. The quality of procurement scopes must be guaranteed. If services are outsourced to sub-suppliers, the supplier is obliged to transfer the quality assurance specifications made here to the sub-supplier in an appropriate form and to verify compliance with the specifications. This includes the transfer of customer-specific requirements (including end customers), continuous traceability of data and documents as well as other necessary specifications according to the supplier's assessment. Depending on the risk identified, audit measures or other checks must be carried out at upstream suppliers.

SUB-SUPPLIER MANAGEMENT. The requirements of this QAA also apply to the management system that the SUPPLIER sets up with its subcontractors. At the request of STEP-G, the SUPPLIER shall submit product releases from subcontractors and corresponding quality contracts with its subcontractors. The SUPPLIER is responsible for the monitoring and continuous improvement of the subcontractors.

SUB-SUPPLIER MANAGEMENT. SUPPLIER commits himself to pass on ▇▇▇▇▇▇▇▇▇'s quality requirements from this QAA in full to sub-suppliers. These must also be checked by the SUPPLIER in audits at the sub- supplier for introduction and effectiveness. To this end, the SUPPLIER ensures that VDA 6.3 process audits are carried out regularly by certified auditors.

SUB-SUPPLIER MANAGEMENT. 7.5.1 The Supplier must maintain qualifications for subcontractors and the products the quality of all components and raw materials that are purchased to manufacture components and parts for ▇▇▇▇▇▇ Scientific. 7.5.2 Suppliers will manage sub-tier Suppliers with controls commensurate with those that ▇▇▇▇▇▇ Scientific applies to direct Suppliers. Suppliers are responsible to ensure that product(s) manufactured utilize only authentic, conforming, and specified material requirements as stipulated in the Specifications. Prior to implementing changes, including changes requested by sub-tier Suppliers, Suppliers must notify ▇▇▇▇▇▇ Scientific according to section 7.14.5 of this agreement. without ▇▇▇▇▇▇ approval if that component is an approved alternative part or is not specified on the BOM and is equivalent in specification to the original component (i.e., PCB C-type components). 7.5.3 ▇▇▇▇▇▇ Scientific shall be permitted to conduct an audit of the sub-supplier facility. The scope of each audit will be at the sole discretion of ▇▇▇▇▇▇ Scientific. ▇▇▇▇▇▇ Scientific shall notify the supplier of the planned date of the audit. The supplier must notify the sub-supplier of this requirement. Any verification performed by ▇▇▇▇▇▇ Scientific does not relieve the supplier of the responsibility to provide quality products.

SUB-SUPPLIER MANAGEMENT. The quality of procurement scopes must be guaranteed. If services are outsourced to sub-suppliers, the supplier is obliged to transfer the quality assurance specifications made here to the sub-supplier in an appropriate form and to verify compliance with the specifications. This includes the transfer of customer-specific requirements (including end custom- ers), continuous traceability of data and documents as well as other necessary specifications according to the supplier's assessment. Depending on the risk identified, audit measures or other checks must be carried out at upstream suppliers. If the supplier intends to change sub-suppliers, the responsible technical coordinator must be notified in good time to agree the necessary sampling and approval procedures. If the upstream supplier's production facility is located outside EASA countries, it must be ensured that the approval requirements of EASA-Part 21A, Section G, are met.