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Topics
Aerospace Industry Quality perspective
CAA Roles, Responsibilities and Regulatory requirements
Principles of Military aerospace requirements and regulations
Overview government space organization roles, responsibilities, and regulations
Overview airworthiness and aviation safety requirement
First Article Inspection
Design, Development, Verification and Validation
Aerospace Material Traceability Requirements
Describe aerospace material/parts status accountability systems
Aerospace subContractor Approval and Control requirements
Variation management of Key Characteristics
FlowDown of AQMS & Quality Requirements
Foreign Object Damage/Debris (FOD) Prevention Program requirements
Use of Customer Supplied Products
Calibration Controls and Positive Recall System
Acceptance Authority Media
Nonconforming Material Management, system requirements and operation
Sampling Inspection/Statistical Process Control requirements and limitations.
Requirements and Limitations
Aerospace Special Processes
Configuration Management/Requirements Control
Manufacturing Techniques
Control of production and service provision
Tool Control
Describe the product qualification process
Describe/explain source approval process.
Maintenance Regulations (e.g., European Aviation Safety Agency [EASA]/Federal Aviation Regulations [FAR] 145/14
Return to Service Processes
Overview of Flight Test process
Identify and verify an effective functional check flight process Prior to Flight
Weight and Balance
Wing Walking
Aircraft Marshalling Techniques.
how each of the learning objectives relates to the 9110 audit process
Standard
AS9100 & AS9101
2 CAA requirements
15 Calibration controls and positive recall system for monitoring and measuring devices.
History of the standard, reasons for introduction, relation with airworthiness requirements., Describe the purpose of a qu
and its role in helping an organization operate with increased effectiveness, consistency, and customer satisfaction. Explain
the ISO 9000 series of standards and how they relate to the applicable AQMS standard. Describe the continuing process o
standards and ISO 19011, the impact that these developments may have on the audit process, and the need for auditors to
the eight Quality Management Principles and how they relate to the AQMS.
Difference between customer quality requirements and airworthiness requirements. Major content of EASA Part 21 and
requirements, Design Organization Approval (DOA), Production Organization Approval (POA), and Manufacturing Organ
approvals; type certification, supplier control principles, certifying staff, accountable manager, and use of EA
Use of Allied Quality Assurance Publication (AQAP), status, military as customers, relation to contractual req
Government space organization roles, responsibilities, and standards
Purpose of FAI, structure and use of 9102, and supporting forms
See CAA requirements, difference and relation between safety and quality; responsibility of supplier and customer; an
subcontractor.
The management model for design, design and change control, difference between verification and validation; type cer
design data.
Upwards and downwards traceability, lot control, serialized items, marking, records for traceability, and traceabilit
Accounting for all parts during manufacturing (e.g., split batches).
Responsibility for quality, supplier auditing, Approved Supplier List, function of incoming and source ins
Principles of statistical control, attributive and contributive measuring, Cp and Cpk, 6 Sigma, method(s) and approach to re
to establish key characteristics.
Subtier control, role of the contract, and purchasing data.
Definition of FOD, FOD prevention, FOD inspections/detections, and FOD audits.
Responsibility for quality of customer supplied product and use of customer approved sources.
Description of 'positive' recall, administration, use of stickers, release after calibration, sub contracting of calibration, and
calibration'
Use of stamps, stamp control, marking, and electronic sign off
Responsibilities, identification, quarantine rules, Material Review Board, dispositions, release of nonconforming pro