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. Xxxxx 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. Xxxxx 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, Xxxxx shall incorporate the foregoing into a Control Plan which will be mutually agreed upon and approved by Medtronic. Xxxxx 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 Xxxxx with a copy to Medtronic. On an ongoing basis, Xxxxx will monitor production and complete inspection of each Lot/batch per the Control Plan to ensure conformance. Xxxxx 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. 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).
CONTROL PLAN. As a part of its agreement with the Government, the service provider is required to develop, implement, and maintain a Quality Control Plan (QCP) that describes the methods it will use to review its performance to ensure it conforms to the performance requirements. (See Attachment 1 for a summary list of performance requirements.) Such reviews are performed by the service provider in order to validate its operations, and assure the Government that the services meet the performance standards. The service provider’s QCP should include monitoring methods that ensure and demonstrate its compliance with the performance standards. This includes inspection methods and schedules that are consistent with the regular reviews conducted by DRO. The reports and other results generated by the service provider’s QCP activities should be provided to the COTR as requested. The frequency and type of the service provider’s reviews should be consistent with what is necessary in order to ensure compliance with the performance standards, but no less frequent than what is described in the Government’s monitoring instrument/worksheets (See Attachment 3). The contractor/service provider is encouraged not to limit its inspection to only the processes outlined in the Government’s standard; however, certain key documents must be produced by the provider to assure the Government that the services meet the performance standards. Some of the documentation that must be generated and made available to the COTR for inspection is listed below. The list is intended as illustrative and is not all-inclusive. The service provider must develop and implement a program that addresses the specific requirement of each standard and the means it will use to document compliance. Written policies and procedures to implement and assess operational requirements of the standard Documentation and record keeping ensuring ongoing operational compliance with the standards (e.g.; inventories, logbooks, register of receipts, reports, etc.) Staff training records Contract discrepancy reports (CDRs) Investigative reports Medical records Education curricula (in accordance with state education criteria and standards) and child development records Records of legal and counseling services (with consideration of attorney-client confidentiality) Records of investigative actions taken Equipment inspections System tests and evaluation
CONTROL PLAN. The supplier undertakes to maintain a production control plan. The yearly requalification must be included.
CONTROL PLAN. In this section the Supplier shall provide a Control Plan describing sequences of the work, milestones, key points, reviews and a WBS along with a corresponding detailed schedule. It shall include at least the following:
