Control Plan Checklist

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Label Value Notes
Created by checklistguro.com
Process Definition & Documentation (STEP)
Process Name (TEXT)
Process Description (including flow) (TEXT)
Process Location(s) (TEXT)
Process Step Number(s) (NUMBER)
Equipment/Machines Used (TEXT)
Process Flow Diagram (PFD) (UPLOAD)
Raw Materials Used (and suppliers) (TEXT)
Critical Process Parameters (CPP) (STEP)
Temperature (during process X) (NUMBER)
Pressure (during process Y) (NUMBER)
Cycle Time (seconds) (NUMBER)
Material Type (SELECTION options: Material A, Material B, Material C)
Feed Rate (units/minute) (NUMBER)
Equipment Status (SELECTION options: Operating, Idle, Maintenance)
Justification for CPP Selection (TEXT)
Control Methods & Procedures (STEP)
Inspection Frequency for CPP X (SELECTION options: Continuous, Hourly, Shiftly, Daily, Weekly)
Maximum Allowable Variation for CPP Y (NUMBER)
Detailed Procedure for Measuring CPP Z (TEXT)
Equipment Used for CPP Measurement (e.g. Caliper, Gauge) (SELECTION options: Caliper, Micrometer, Gauge, Other (Specify))
Methods for CPP Control (SELECTION options: Statistical Process Control (SPC), Automated Adjustment, Operator Adjustment, Preventative Maintenance)
Date of Last Calibration for Measurement Equipment (DATE)
Time of CPP Measurement (DATE)
Measurement System Analysis (MSA) (STEP)
Repeatability (r) Value (NUMBER)
Reproducibility (R) Value (NUMBER)
Equipment Variation (Ev) Value (NUMBER)
Operator Variation (Ov) Value (NUMBER)
Gauge Repeatability and Reproducibility (GR&R) % (NUMBER)
MSA Study Type Performed (e.g., PPAP, Gage R&R) (SELECTION options: PPAP, Gage R&R, Attribute Gage R&R, Variable Gage R&R, Length Study, Other)
Summary of MSA Study Findings and Conclusions (TEXT)
MSA Study Result (Overall Assessment) (SELECTION options: Acceptable, Needs Improvement, Unacceptable)
MSA Study Completion Date (DATE)
Process Capability & Performance (STEP)
Process Cp (Current Process Capability) (NUMBER)
Process Cpk (Current Process Capability Index) (NUMBER)
Target Cp (Desired Process Capability) (NUMBER)
Target Cpk (Desired Process Capability Index) (NUMBER)
Date of Capability Study (DATE)
Summary of Capability Study Results and Analysis (TEXT)
Description of any actions taken to improve process capability. (TEXT)
Number of Samples Used in Capability Study (NUMBER)
Is the process currently capable? (Based on target Cpk) (SELECTION options: Yes, No, Needs Further Investigation)
Control Plan Implementation & Training (STEP)
Number of personnel trained on the Control Plan (NUMBER)
Date of most recent Control Plan training (DATE)
Summary of Control Plan training content (key topics covered) (TEXT)
Training Method Used (e.g., Classroom, Online, On-the-Job) (SELECTION options: Classroom, Online, On-the-Job, Other)
Departments Receiving Control Plan Training (SELECTION options: Production, Quality, Maintenance, Engineering, Other)
Verification Method for Training Effectiveness (e.g., Quiz, Observation) (SELECTION options: Quiz, Observation, Practical Demonstration, Other)
Notes on any deviations from the planned training schedule or content. (TEXT)
Control Plan Review & Updates (STEP)
Last Control Plan Review Date (DATE)
Frequency of Control Plan Review (in months) (NUMBER)
Summary of Review Findings & Changes (TEXT)
Areas Reviewed During Update (Select all that apply) (SELECTION options: Process Parameters, Measurement Systems, Reaction Plans, Training Procedures, Equipment, Materials, Supplier Performance)
Rationale for Changes Made (if applicable) (TEXT)
Impact of Changes on Process Capability (e.g., Sigma Level - if applicable) (NUMBER)
Approval Status of Updated Control Plan (SELECTION options: Approved, Rejected, Pending Approval)
Reviewer Signature (SIGNATURE)
Reaction Plan (Corrective Action) (STEP)
Severity Level of Deviation (SELECTION options: Minor, Moderate, Major, Critical)
Detailed Description of Deviation (TEXT)
Root Cause Analysis Documentation (TEXT)
Corrective Action Proposed (TEXT)
Date Corrective Action Implemented (DATE)
Effectiveness Verification Method (TEXT)
Effectiveness Verification Result (e.g., % improvement) (NUMBER)
Verification Result (SELECTION options: Meets Requirements, Does Not Meet Requirements, Requires Further Action)
Additional Comments/Notes (TEXT)
Signature of Person Implementing Correction (SIGNATURE)
Record Keeping & Traceability (STEP)
Date of Record Creation (DATE)
Lot/Batch Number (NUMBER)
Operator Notes/Comments (any deviations from standard) (TEXT)
Quantity Produced (NUMBER)
Record Status (e.g., Complete, Pending Review, Approved) (SELECTION options: Complete, Pending Review, Approved, Rejected)
Attach Supporting Documentation (e.g., Calibration Certificates, Inspection Reports) (UPLOAD)
Method of Traceability (e.g., Serial Numbers, Barcodes, Batch Codes) (SELECTION options: Serial Numbers, Barcodes, Batch Codes, Unique Identifiers, Other)
Description of Traceability Method and its Scope (TEXT)

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