CONTROL PLAN. Quality Control is the responsibility of the contractor. The Contractor is responsible for the delivery of quality services/supplies. All Offerors will be required to include a Quality Control Plan (QCP) with their proposal at the TO level. The submittal of the Offerors’ QCP will ensure the Offeror has an adequate and standardized procedure in place at contract start to monitor performance. The Offerors’ QCP must be detailed, containing a systematic approach to monitor daily operations of key and essential functions for providing quality service to the Government, i.e. discrepancy identification procedures, corrective action procedures, prevention procedures for occurrence/re-occurrence of discrepancies, trend analysis usage, and customer feedback utilization. Such QCP requirements will increase the likelihood of successful contract performance. After acceptance of the quality control plan the Contractor shall request the contracting officer’s acceptance in writing of any proposed change to his QC system.
CONTROL PLAN. All key process control parameters and key product characteristics shall be documented in product and product line specific Control Plans (including Control Plans of subcontractors),which shall be available to Nokia upon request. Endwave shall update these Control Plans to continuously reflect the current manufacturing situation. The Control Plans shall form one basis for targeting specific continuous quality improvements.
CONTROL PLAN. See Section A for nondisclosure conditions. The Control Plan, if included, is a Class II confidential document belonging to TE Connectivity. A class II document may not be further distributed and is subject to the conditions of the nondisclosure agreement.
CONTROL PLAN. 4.1. - RAW MATERIALS CONTROLS:
CONTROL PLAN. Mxxxx shall collaborate with Medtronic to ensure a thorough understanding and identification of critical process steps, transfer function relationships, acceptable measurement capability and process capability of process input/outputs as to their impact on the critical features. Mxxxx shall collaborate with Medtronic to design an appropriate Control Plan that will ensure the long term stability and capability of the Manufacturing processes. At the time of Qualification, Mxxxx shall incorporate the foregoing into a Control Plan which will be mutually agreed upon and approved by Medtronic. Mxxxx shall provide a measurement system analysis (e.g. gage repeatability and reproducibility, gage to part ratio), for each measurement process utilized in the Control Plan. These analyses and Control Plans will be filed with Mxxxx with a copy to Medtronic. On an ongoing basis, Mxxxx will monitor production and complete inspection of each Lot/batch per the Control Plan to ensure conformance. Mxxxx will include a Certificate of Conformance for each Lot/batch based on conformance to the Control Plan.
CONTROL PLAN. When required by Buyer, the Supplier shall collaborate with Buyer to ensure a thorough understanding and identification of critical process steps, transfer function relationships, acceptable measurement capability and process capability of process input/outputs as to their impact on the CTQ parameters. The Supplier shall collaborate with Buyer to design an appropriate Control Plan. At the time of qualification, Supplier shall incorporate the foregoing into a Control Plan which will be mutually agreed upon and approved by Buyer. Supplier shall provide a measurement system analysis (e.g. gage repeatability and reproducibility, gage to part ratio), for each measurement process utilized in the Control Plan. These analyses and Control Plans will be filed with Supplier with a copy to Buyer. On an ongoing basis, Supplier will monitor production and complete inspection of each lot/batch per the Control Plan to ensure conformance. Supplier will include a Certificate of Conformance for each lot/batch based on conformance to the Control Plan.
CONTROL PLAN. Owner agrees that with the exception of (a) the required additions to the Project set forth in Section 1.9, (b) insubstantial field changes to the location of buildings and infrastructure, and/or (c) and any further plan revisions agreed to in writing by all parties to this Agreement, Owner shall develop the Site exclusively as shown on the Conceptual Layout Plan attached as Exhibit E.
CONTROL PLAN. See Section A for nondisclosure conditions. The Control Plan, if included, is a Class II confidential document belonging to TE Connectivity. A class II document may not be further distributed and is subject to the conditions of the nondisclosure agreement. Section 8 Measurement System Analysis AAF214, Rev. D, 23-Jun-2017 Not Applicable AAF214, Rev. D, 23-Jun-2017 Section 9 Dimensional Results AAF214, Rev. D, 23-Jun-2017 Organization: Production Part Approval Dimensional Test Results TE Connectivity Brazil Part Name: AMP MCP 2.8K, CONTACT, SWS Inspection Facility TE Connectivity Brazil Cust. Part Number: 1241394-1 Shown on Drawing No.: C-1241437 Engineering Change Level: C16 ITEM DIMENSION / SPECIFICATION SPECIFICATION / LIMITS TEST DATE QTY. TESTED ORGANIZATION MEASUREMENT RESULTS (DATA) OK NOT OK - Construction according: Drawing C-1241437 - - - - According X - Acabamento de construção - - - - According X - Dimensional (mm) Min. Max. Date Nominal - + Part 1 12 1,3 0,2 0,3 1,1 1,6 21-Dec-20 01 1,321 X 13-1 3 0,2 0,2 2,8 3,2 21-Dec-20 01 3,029 X 13-2 3 0,2 0,2 2,8 3,2 21-Dec-20 01 3,022 X 14-1 4,7 0,2 0,2 4,5 4,9 21-Dec-20 01 4,739 X 14-2 4,7 0,2 0,2 4,5 4,9 21-Dec-20 01 4,754 X 15-1 6,3 0,5 0,5 5,8 6,8 21-Dec-20 01 6,367 X 15-1 6,3 0,5 0,5 5,8 6,8 21-Dec-20 01 6,399 X 17 0,32 0,03 0,03 0,29 0,35 21-Dec-20 01 0,322 X 20 19,9 0,5 0,5 19,40 20,40 21-Dec-20 01 19,783 X 22 0,8 0 0,3 0,8 1,1 21-Dec-20 01 0,907 X 23 0,75 0 0,2 0,8 1,0 21-Dec-20 01 0,793 X 42 6,3 0,15 0,05 6,2 6,4 21-Dec-20 01 6,294 X 43 4,2 0,15 0,05 4,1 4,3 21-Dec-20 01 4,131 X 45 4,2 0,2 0,2 4,0 4,4 21-Dec-20 01 4,350 X 47 1,3 0 999 1,3 1000,3 21-Dec-20 01 1,755 X 47 1,3 0 999 1,3 1000,3 21-Dec-20 01 1,699 X 50 1,0 0,15 0,1 0,9 1,1 21-Dec-20 01 0,925 X 51 4,2 0,4 0,3 3,8 4,5 21-Dec-20 01 4,049 X 60 2,5 0,3 0,3 2,2 2,8 21-Dec-20 01 2,596 X 62 1,2 0,2 0,2 1,0 1,4 21-Dec-20 01 1,143 X 70 5,25 0,30 0,30 4,95 5,55 21-Dec-20 01 5,310 X 72 3,30 0,2 0,2 3,1 3,5 21-Dec-20 01 3,212 X 80 3,10 0,1 0 3,0 3,1 21-Dec-20 01 3,044 X 81 0,35 0,1 0,1 0,3 0,5 21-Dec-20 01 0,361 X 85 4,40 0,1 0 4,3 4,4 21-Dec-20 01 4,396 X Page 01 of 01 Pages Signature Title Date Xxxxxx Xxxxxxx xx Xxxxx Quality Engineer June 23, 2021 March PPAP Nº: Rev. 2006 CFG-1003 Section 10 Material, Performance Test Results AAF214, Rev. D, 23-Jun-2017 Production Part Approval Material Test Results Organization: Material Supplier: TE Connectivity Brazil TE Connectivity Brazil Part Name: Cust. Part Number: AMP MCP 2.8K, CONTACT, SWS 1241394-1 Na...
CONTROL PLAN. The supplier defines at his own responsibility the control concept so that the agreed tasks and specifications are fulfilled. Control plan forms the summary of all requirements for quality, its proving and testing criteria established in quality management system of supplier. It represents the termination of all actions of quality planning of the supplier. These control and management plans shall be made for prototype, pre-serial and serial stage. Control plan includes: • management of input materials and parts • management of individual steps of production process, including all control steps • planning of production audits • planning of requalification tests Characteristics signs, recognised by FMEA as relevant for quality and evaluated, shall be shown again in the control and management plan.
CONTROL PLAN. The supplier shall have a Control Plan or equivalent work instructions that define the controls, measurement method, and frequencies used to maintain process control. Variable gages are expected to be used for major, critical, and key characteristics unless agreed to by Snap-on. Measurement Systems Analysis Studies (Xxxx R&R) Gage Repeatability and Reproducibility (Gage R&R) studies are to be completed for all key characteristics where the measurements are made with nonstandard gauges or equipment. Raw data measurements, graphed analysis and results must be included in the submittal. Dimensional Results (Initial Sample Inspection Results-ISIR) The supplier shall provide evidence that dimensional verifications required by the design record (Engineering Print requirements including all notes as specified in the Snap-on top-level drawing) have been completed and results indicate compliance or noncompliance with specified requirements. The supplier is to provide a ballooned drawing with the ISIR for all Level 2 and beyond PPAP, and document all measurements on an agreed number of samples (typically 5). The supplier shall provide same for all unique process streams (e.g. machines /manufacturing locations, molds, dies). Snap-on’s expectation is that all results are compliant. Any discrepancies shall be communicated to Snap-on prior to the submission of the PSW for review and disposition. In addition, process capability must be demonstrated on all special characteristics (see Initial Process Studies (Capability) following).
