Quality Control (QC). Tasks performed by the contractor to improve the quality of the organization’s output.
Quality Control (QC). The Contractor shall develop and maintain an effective quality control program to ensure services are performed in accordance with this PWS and task order PWSs. The Contractor shall develop and implement procedures to identify, prevent, and ensure non-recurrence of defective services. The Contractor's quality control program is the means by which he/she ensures that his/her work complies with the requirement of the contract. The
Quality Control (QC). Velovita will replace, within sixty (60) days of purchase any product found to be defec- tive. However, no product(s) should be returned to Velovita prior to the written approval to do so from the Velovita Support Department or email request. In order to assure that replacement product will be issued, strict compliance to the following procedure is re- quired:
1. A written replacement request must be submitted, stating the reason for the request and accompanied by verification of payment and a copy of the Product Order form and packing slip.
2. Upon notification Velovita will instruct the Member where to ship product and will issue an RMA (Return Authorization Number), which must be clearly written on the exterior of the returned package. Upon receipt and verification Velovita will ship out replacement product(s).
Quality Control (QC). Program / Plan
1. Identify all specification tasks;
2. Identify and call out all testing and inspection requirements;
3. Sign off procedure for testing and inspection requirements;
4. Sign off procedure by the COR for item completion; and
5. Government property administration. Contractor shall assign a QC inspector to inspect/test and approve all work prior to notifying the COR and/or Regulatory Bodies (when applicable) for an inspection of work. Minimum notification to the COR shall be 24 hours.
Quality Control (QC). All necessary measures taken by the Contractor to ensure that the quality of an end product or service shall meet contract requirements.
Quality Control (QC). 5.1 No additional testing or modification/deviation from procedures may occur without written approval by the ThermoGenesis Quality Management.
5.2 ImmuneCyte will test ThermoGenesis products using only calibrated and qualified equipment with approved analytical methods.
Quality Control (QC). 29 QC shall consist of members of the production staff and members of the construction quality control staff. 30 The construction quality control staff shall be independent from the production staff and the IQF staff. QC 31 shall be led by the Construction Quality Manager (CQM).
Quality Control (QC). Consultant shall obtain a written plan from the Contractor for quality control (QC) of its work and will monitor the Contractor’s compliance with its QC plan.
Quality Control (QC). The Quality Control (QC) will be subject to specific training and qualification requirements. In addition to the normal duties and qualifications of the Lead Hand position specified herein above, the Quality Control (QC) will be responsible for coaching, directing and auditing of the Deicing & Ramp Specialist during the course of their deicing duties. The Quality Controls will report directly to the Training Supervisor or his designate at the Central Deicing Facility.
Quality Control (QC). As an attachment to this Agreement, the Processor shall provide a written description of the Processor's QC system to the DA. By signing this Agreement, the Processor assures that an effective QC system will be maintained for the duration of this Agreement.
A. The Processor shall transport DF picked up from the DA or the RA; receive, handle, store and deliver end product in a safe and sanitary manner and at the recommended temperature for the specific DF and end product covered by this Agreement.
B. The Processor, with the concurrence of the DA and USDA, may refuse a delivery of DF directly to the Processor’s plant or to his authorized storage agent, which does not meet the federal specifications under which it was purchased and shipped.
C. All end product produced under this Agreement shall be processed according to the health and sanitation standards for plant facilities and food processing established by the locality or state in which the Processor’s plant is located or by the applicable federal standards, whichever are higher.
D. At the option of the DA, samples may be pulled from delivered end product for laboratory testing. The Processor shall pay costs of such tests only if product sample tested fails to meet either Agreement specifications or quality and wholesomeness standards.
E. The Processor shall maintain end product batch identification in the event end product is rejected upon delivery. End product failing to meet Agreement specifications or wholesomeness standards shall be rejected by the DA and the Processor so notified. The Processor shall be given fifteen calendar days from this notice of rejection to negotiate removal of rejected product and replacement of an acceptable end product. If agreement is not reached, the DA or purchasing RA shall have the right to purchase the same or similar product on the open market at the Processor’s expense. If agreement is not reached, the DA is to arrange removal of rejected product. The DA shall proceed to authorize removal and destruction at Processor’s expense.
