Quality Management System (QMS). The Contractor shall implement and maintain a QMS to ensure that product integrity meets the Contract requirements. The Contractor's QMS must be clearly defined, and employees providing quality functions must have adequate responsibility, authority, and freedom to identify and evaluate problems and to initiate, recommend, or provide corrective action. The Contractor’s QMS shall be IAW industry standards for the primary functional areas in which they are performing to include but not limited to design, development, production, configuration management, supply chain management, installation, and services. Specific TOs may require the Contractor to hold and maintain particular quality standards at TO award. These standards could include but are not limited to a quality management system which meets the quality requirements as defined in FAR 46.202-4(a), International Organization of Standards (ISO 9001:2008), or Quality Management System – Requirements for Aviation, Space and Defense Organizations (AS9100D) for all work performed at the Contractor’s facilities and onboard NAVAIR and/or NAWCAD facilities, as applicable per TO. The Government reserves the right to require the Contractor to present its certificate of compliance at any time. In addition, TOs may require the manufacturing and quality management systems use ANSI/J-STD-001, Requirements for Soldered Electrical and Electronic Assemblies; IPC-A-610, Acceptability of Electronic Assemblies; and IPC-R-700, Suggested Guidelines for Modification, Rework and Repair of Printed Boards and Assemblies as the required guidelines for producing electrical and electronic assemblies.
Quality Management System (QMS). All Client implementations are managed via an approved set of Standard Operating Procedures (SOPs) which are part of Syneos Health’s Quality Management System (QMS) under the Head of Quality Assurance. Key processes such as project governance, document control, CRM implementation and training are required for assigned operations personnel. Other SOPs such as Change Control, security and access control, asset provisioning, and CRM end-user training are additional required training for implementation teams, which are also delivered and tracked within Syneos Health’s Learning Management System (LMS).
Quality Management System (QMS). The Offeror shall maintain, operate and continually improve a QMS acceptable to the Government in accordance with ISO 9001:2015 or equivalent (Reference Section E, FAR 52.246-11). Quality and reliability shall be continually monitored by the Government to include Statistical Process Control (SPC) and other quality management metrics that depict the effectiveness of the QMS and the achievement of critical process control at both the Offeror’s and major suppliers’ locations. Major suppliers are those who provide components and textile or hardware materials within the Technical Data Package (TDP). Examples include cloth and hardware suppliers, and any Sub Offeror used for an assembly or subassembly. The Government reserves the right to conduct audits of the Offeror’s QMS during all phases of the contract. The Offeror shall be responsible for correcting any deficiencies found during Government auditing or testing in all affected Offeror product. The Offeror shall maintain a calibration system in accordance with ANSI/ISO/ASQ Q10012-2003 or equivalent to ensure that all test, inspection, measurement, and diagnostic equipment to include all accessories and ancillary equipment are properly calibrated and identified by appropriate labeling.
Quality Management System (QMS). The Seller must maintain a documented quality system to address at a minimum: Contract Review, Control of Counterfeit/Fraudulent Material, Receiving and Final Inspection, Calibration of measuring and monitoring equipment (except distributors), Control of nonconforming product, and Corrective Action. Seller’s Quality Management System must ensure all personnel training include awareness of their contribution to product or service conformity, product safety, and the importance of ethical behavior. The status of the external provider’s third-party certification to ISO9001 and/or AS9100 is verified periodically by Resonant Sciences, to ensure continued reliability and performance as an external provider.
Quality Management System (QMS). Must read and understand expectation in QMS, specifically the specification of Ministry of Transportation Contract and the method manual expectations. Must actively participate in the QMS process including ensuring quality accomplishments and accurate work reporting.
Quality Management System (QMS). E.14.1 The contractor shall maintain a QMS International Organization for Standardization (ISO) 9001:2015 or equivalent system including the minimum elements described in E.14.1.1. The contractor shall develop a quality manual that details how each element of the QMS is met, maintained, reviewed and updated as per ISO 9001:2015 or better. The contractor developed manuals and procedures shall be maintained in an electronic database easily accessible by DCMA within the prime contractor's facility. The contractor's compliance with the 100% Final Inspection of the end item per Section E.4 is accomplished by in-process inspections of identified FIR characteristics combined with the final completed trailer inspections.
Quality Management System (QMS). 1.7.1 The Contractor shall have a QMS that follows the requirements of FAR 52.246-11 contained in this contract. The Contractor shall establish, document, implement and maintain a QMS and continually improve its effectiveness IAW the requirements of ISO 9001:2015, or the latest equivalent. All requirements of the contract apply to Subcontractors and Suppliers. The Contractor shall monitor, assess, and audit quality and reliability of the QMS at all Subcontractor and Supplier facilities.
Quality Management System (QMS) documentation. The supplier shall establish and maintain a clearly documented quality system that provides a means of ensuring that products conform to specified requirements, which may include the use of statistical techniques for product acceptance and related instructions for acceptance by Jet Aviation. This system shall control the issue and development of drawings, specifications, procedures. etc. Provision shall be made for the control of obsolete copies and their subsequent archiving and disposal. All records pertaining to quality shall be stored and maintained in a legible form for a minimum of 10 years. Specific projects and/or regulatory bodies may require longer retention periods and this will be notified in advance to the supplier. Jet Aviation has the right to control and monitor your performance, methods, processes and equipment.
