ML20126H490
| ML20126H490 | |
| Person / Time | |
|---|---|
| Site: | FitzPatrick  |
| Issue date: | 06/30/1988 |
| From: | Holbrook W WYLE LABORATORIES |
| To: | |
| Shared Package | |
| ML20126H461 | List: |
| References | |
| NUDOCS 9301050225 | |
| Download: ML20126H490 (5) | |
Text
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i QUALITY ASSURANCE PROGRAM MANUAL i
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t QUALITY DIRECTIVES up WYLE LABORATORIES Eastern Test and Eng!neering operations Scientific Services & Systems Group Huntsville, Alabams i
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MANUAL NUMBER:
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i POLICY AND APPROVAL e
4 Wyle Laboratories was established in 1949 as an independent testing laboratory providing services to the aerospace industry. From this very early experience with testing, Wyle has played a leading role in the development of testing techniques and procedures which are now recognized throughout all industry as the standard for test control.
Having been a party to the development of the world's testing standards, and having been in the testing business for over thirty years, management recognises the sound business value of maintaining formal programs to ensure the quality of testing end engineering operations.
Itis the polley of the management of Wyle Laboratories to maintain the highest standards of quality throughout ali its operations in accordance with all applicable recognised standards. The detailed requirements for ensuring the highest standards of quality are contained in this Quality Assurance Program and are applicable to all groups resident at and certain groups managed from the Huntsville Facility. This Quality Assurance Program is designed to ensure compliance with applicable provisions of 10 CFR 21,10 CFR 50/ Appendix B, ANSI Standard N45.2, RDT.F2 2T, MIL-Q-9858A, NHB 5300.4 (1D) & (10), NHB 5300.4 (ID.2), Mlb!-45208A, MILSTD 45662, BS 5882, and other customer. imposed speelfications.
To ensure effective implementation of the Quality Assurance Program, Wyle Laboratories has designated a Quality Assurance Manager who is responsible for maintaining the high quality standards. The Quality Assurance Manager Teports to top management, and his authority, in quality matters is absolute and unquestioned.
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INTRODUCTION The purpose of this Quahty Assurance document is to establish the basic operating policies and specify requirernents for the procedures td be employed by all entitles located at or directed from the Wyle Laboratories llantsville facility to meet the applicable requirements of the latest revisions of 10 CFR 21,10 CFR 50/ Appendix B, ANSI Standard N45.2, RDT-F2 2T, MIL-Q.9858A, NHB 5300,4 (1B) & (1C),
N11B 6300.4 (1D 2), MIL-I-45208A, MIL-STD-45062 BS 5882, and other customer imposed specifications.
The total quality program functions under the direction and guidance of the Quality Assurance Monager. IIe is responsible for maintaining surveillance over the Quality Assurance activities through direct supervision over Quality Assurance personnel in areas requiring surveillance.
Quality Ast,urance influence begins with a review of the basic contract or purchase order to determine
.i the quality needs. Subsequent quality activity is monitored by implementation of detailed inspection checkpoints determined by Quality Assurance. Scheduled quality audits are imposed by the Quality Assurance Manager to evaluate program effectiveness.
The e%ctiveness of the quality program if enhanced by the authority granted the Quality Assurance Manager to suspend any operation, or to reject materials, services, or procedures which do not meet established standards. Quality Assurance operations are not influenced or teduced by considerations -
such as schedules, rework, costs or budgetary responsibilities, or engineering changes, since all deviations from requirements are coordinated with the Quality Assurance Manager who has unimpeded access to top management for the resolution of critical problems.
Through stringent controls adequate quality records of all related operations are documented and -
maintained to serve as evidence of qualitv. Final reports are thoroughly reviewed by Quality Assurance.
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