Thursday, December 4, 2014

Continuous Improvement Using ProjX, Part 4

Halden Zimmermann's Latest Blog Post

Halden Zimmermann’s latest blog post





Halden Zimmermann: Best Practice Network Team Creation Phase II: Analyze


Create Process Documents Identify Opportunities



  • Begin this phase at the same time as Phase I (i.e, at first benchmarking meeting) and continue with conference calls between meetings; when monthly benchmarking meetings are complete, continue with bi-monthly face-to-face meetings rotated between the member plants with conference calls between meetings.

  • CreateProcessMap


What stages comprise the process?



  • What are the desired outputs of each stage?

  • What inputs to each stage influence the output?

  • Create Cause and Effect Matrix

  • What are our external and internal customers’ requirements (i.e., what are

  • the key attributes of our product)?

  • Rank requirements by importance to customer (including customer in

  • process is desirable)

  • Rank inputs identified on the process map by their effect on customer

  • requirements/key attributes

  • Create Process FMEA (Failure Modes Effect Analysis)

  • Use ranking of inputs in Cause & Effect matrix to determine which stages of process are most critical (e.g., drying)

  • For these stages, what are the failure modes of the process? Failure modes are the opposite of the desired outputs.

  • What are the potential causes of each failure mode?

  • Rank severity, frequency of occurrence and likelihood that the failure mode will not be detected – these three rankings are multiplied to produce a risk priority number (RPNs) for that failure mode. Rankings are achieved by consensus of member plants or averaged across the member plants.

  • Rank failure modes by RPN. High RPN represents significant improvement opportunity.

  • Introduce concept of control plan but do not complete at this time

  • This is the plan to prevent the failure modes from occurring.

  • What are the spec limits?

  • Is the process capable relative to spec limits?

  • What are the measurement systems? Where and when do we measure?

  • What is the variation due to the measurement system itself (gauge R&R study)?


What do we do if we are out of spec/control (reaction plan)?






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