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Aerospace Monitoring Measurement Procedure

Monitoring-Measurement Procedure AS9100 | AQP1180

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AS9100 Quality Procedures Manual $ 499.00
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easily editable in ms wordAerospace Monitoring Measurement Procedure AS9100

The Monitoring-Measurement Procedure AS9100 establishes methods the company uses to monitor and measure conformance with requirements. The aerospace procedure applies to all company products and process, including raw materials, parts, and subassemblies used to manufacture aircraft products. (7 pages, 1621 words)

Monitoring Measurement AS9100 Responsibilities

Department Managers are responsible for producing and using process monitoring and measuring data to continuously improve The Company’s Quality Management System.

The Quality Assurance Manager is responsible for the accuracy of all process monitoring and measuring devices.

Monitoring Measurement AS9100 Definitions

Critical Product Parameter – Product measurement that materially affects the conformance of the material, component, or product to requirements.

Critical or Key characteristic – Feature of a material, part, or process, variation of which will significantly influence a product’s fit, performance, service life, or manufacturability.  Key characteristics essential to meeting product goals are identified so that Company resources can be focused on them.  Key characteristics are often identified by the customer but can also be identified by the Company, subcontractors, or suppliers.

First article inspection (FAI) – where a representative item from the first production run of a new part or assembly is used to verify that the production processes, production documentation, and tooling can produce parts or assemblies that meet requirements.

Monitoring and Measuring Equipment – Devices used to collect data and measure, gauge, test, inspect, or otherwise examine items to determine their compliance with specifications.

Other Product Parameter – Product measurement that does not affect conformance with requirements, but which may relate to the state of the process system.

Sampling inspection – Statistical inspection using one or more samples; in acceptance sampling inspection, a decision to accept or not accept an inspection lot is based on a sampling plan.

Special Cause of Variability – External action on a process (or a process failure) that causes unpredictable variations from a normal distribution. Special causes of variability are indicated when a process is out of control or when non-normal distributions of data (as defined by Quality Assurance) are observed.

Validation – Confirmation, by providing objective evidence, that requirements for a specific intended use or application have been fulfilled; assuring that equipment, processes, software, and/or systems operate as intended so products consistently meet specifications. Among the processes that typically require validation are:

  1. Mechanical and electrical assembly;
  2. Chemical/biological processing; and
  3. Automated inspection, sterilization, packaging, and/or storage.

Monitoring Measurement Procedure AS9100 ActivitiesAerospace Monitoring Measurement Procedure

  • Aerospace Product Monitoring and Measuring-General
  • AS9100 Quality Inspection Documentation
  • AS9100 First Article Inspection (FAI)
  • Reporting Monitoring Measurement Data
  • Process Nonconformity
  • Review of Process Monitoring Measurement

References

  1. AS9100:2016 Rev D, “Quality Management Systems – Requirements for Aviation, Space, and Defense Organizations”, SAE International, Sept., 2016.
  2. AS9102:2014 Rev B, “Aerospace First Article Inspection Requirements”, SAE International, Oct., 2014.
  3. Engineering Statistics Handbook, National Institute of Standards and Technology Information Technology Laboratory (NIST ITL) – http://www.itl.nist.gov/div898/handbook/pmc/pmc.htm.  Pay special attention to chapter 6, “Process or Product Monitoring and Control”.  Section 6.2 explains acceptance testing and sampling plans.
  4. Quality Procedures
  • AQP1030 Control of Nonconforming Outputs
  • AQP1040 Nonconformity and Corrective Action
  • AQP1060 Management Review
  • AQP1100 Design Development
  • AQP1170 Monitoring Measuring Resources Control
  • AQP1200 Data Analysis Continual Improvement

Monitoring-Measurement AS9100 Forms

  • Validation records (and record requirements)
  • Process data logs
  • Control charts
  • Process monitoring reports

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