作業を録画するだけでSkillを作れるMicrosoft Skill Recorderを製造業の品質判定業務で使えるか試してみた

$commit="<40文字のリリースコミットハッシュ>"; $env:SKILL_RECORDER_COMMIT=$commit; irm "https://raw.githubusercontent.com/microsoft/skill-recorder/$commit/install.ps1" | iex

---
name: transcribe-inspection-results
description: "Fill inspection record forms with test measurements from raw inspection reports, verify values against acceptance criteria, and determine pass/fail status for product batches."
allowed-tools:
  - Read
  - Write
  - Glob
---

## When to use

Use this skill to transcribe test measurements from a raw inspection report into a formal inspection record form. This applies when you have completed field inspections and need to:
- Transfer test data (adhesion, holding force, microbial counts, appearance) into an official record
- Cross-reference each value against product-specific acceptance criteria
- Determine and document the batch's overall pass/fail status

The skill is most useful when dealing with pharmaceutical or medical device batches where regulatory compliance requires documented verification of measurements against defined ranges.

## Procedure

**1. Open the raw inspection results document**

Read 20260731_検査結果.docx to identify all test measurements recorded during the inspection. Extract:
- Adhesion test values (e.g., force in N/10mm)
- Holding force test results (e.g., duration and stability observations)
- Microbial test data (e.g., bacterial count in CFU/g, pathogen presence)
- Appearance inspection findings

**2. Locate the blank inspection record form**

Use Glob to find 検査記録表 20260811.docx in the 検査記録 directory. If the template is not found by its literal name, search the 検査記録 directory for the most recent record form matching the current inspection date. Open the form in your document editor.

**3. Open the acceptance criteria reference**

Read 製品別_検査項目判定基準一覧.xlsx to view the product-specific test ranges and thresholds. This spreadsheet defines the acceptable minimum and maximum values for each test parameter and identifies which results are pass (合格), fail (不合格), or conditional.

**4. Copy product identification data**

From 20260731_検査結果.docx, extract:
- Product name and category
- Inspection lot number (e.g., LOT20260729-03)
- Inspection date
- Process stage (e.g., manufacturing stage)

Enter these into the corresponding header and metadata fields of the inspection record form.

**5. Transcribe physical test measurements**

Copy each physical property measurement from 20260731_検査結果.docx into the appropriate row of the inspection form:
- Adhesion test value
- Holding force test result and observations
- Any other mechanical or physical property tests

**6. Transcribe microbial test results**

Copy the microbial analysis data from 20260731_検査結果.docx into the microbiological test section of the form:
- Bacterial count (生菌数)
- Pathogen presence results (特定病原菌)
- Any other sterility or microbial findings

**7. Record appearance and quality observations**

Enter appearance inspection findings and supplementary quality notes into the form's notes section:
- Surface defects or coating observations (e.g., streaks, discoloration)
- Batch-specific quality concerns or recommendations
- Any notes from the inspection team

**8. Verify each measurement against criteria**

For each transcribed test value, cross-reference 製品別_検査項目判定基準一覧.xlsx to confirm the value falls within the acceptable range. Note:
- Values clearly within range → pass
- Values at or beyond the boundary → flag for review
- Values with conditional acceptance rules → apply the condition

Document any exceptions or boundary cases in the form's review notes.

**9. Determine overall pass/fail status**

Based on your criteria verification in step 8, make the final determination:
- If all test values pass their ranges → record as passing (合格)
- If any test value fails its range → record as failing (不合格)
- If results are acceptable with documented exceptions → record as conditional approval and note the exception

Document the decision in the form's final status field, with a brief justification if conditional approval is used.

**10. Finalize and save the inspection record**

Review the completed form to ensure:
- All required fields are filled
- All values are accurate and match the raw results
- The pass/fail determination is clearly visible

Save the form with a clear filename that includes the batch identifier (e.g., the lot number). Ensure the file is stored in 検査記録 for future reference and archival.

## Input and edge cases

- **Missing or unclear raw results**: If 20260731_検査結果.docx lacks a specific measurement, mark that field as "not reported" in the form and note it in the review section.
- **No matching record form template**: If 検査記録表 20260811.docx is not found, create a new record form using a standard template or blank document with the required section headings.
- **Criteria ambiguity**: If 製品別_検査項目判定基準一覧.xlsx does not list the product or test parameter, document the assumed acceptance range and escalate to quality assurance for confirmation.
- **Conditional acceptance**: If test results are borderline, document the condition clearly in the notes so future reviewers understand the approval rationale.