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Fortuna’s 18-Document Package Turns SQE Review into Fill-in-the-Blank

In the competitive world of sheet metal fabrication and supply chain management, achieving a first-time pass for PPAP (Production Part Approval Process) Level 3 is paramount for maintaining high-quality standards and ensuring smooth supply chain operations. The PPAP process is a cornerstone of quality control, specifically for Level 3, which deals with production parts that have been through further in-process quality verification and control.

Fortuna Stamping, a leader in the sheet metal fabrication industry, has developed a comprehensive solution to streamline and optimize the PPAP Level 3 submission process through its 18-document package. This innovative approach simplifies the SQE (Supplier Quality Engineer) review process, turning it into a straightforward, fill-in-the-blank exercise that significantly enhances efficiency and success rates.

In this article, we will explore the benefits and implementation steps of Fortunas 18-document package, providing a comprehensive breakdown of its advantages and offering insights from experts in the field.

Introduction

The PPAP Level 3 is a critical phase in the production process that ensures parts meet the required quality standards. It involves a thorough submission process that must demonstrate the ability to consistently produce parts that meet customer specifications. However, traditional PPAP submissions can often be time-consuming and complex, leading to inefficiencies and potential delays.

Fortunas 18-document package offers a streamlined approach that simplifies the review process and increases the likelihood of a first-time pass. This article will outline the key features of the package and provide practical guidance for implementing it effectively.

Overview of PPAP Level 3

Purpose and Importance

PPAP Level 3 represents a significant step in the PPAP process, where production parts have undergone stringent quality verification and control measures. The purpose of PPAP Level 3 is to:

  • Document part and process controls: Ensure that parts are produced consistently within specified tolerances.
  • Verify process stability: Confirm that the production process is capable of producing parts that meet customer requirements consistently.
  • Assess production process capability: Evaluate the process performance to determine readiness for mass production.

Common Challenges

Suppliers often face several challenges during the PPAP Level 3 submission process, including:

  • Complex documentation requirements: Numerous forms and documents can make the submission process cumbersome and time-consuming.
  • Data accuracy and consistency: Ensuring that all data is accurate and consistent across all documents is a critical challenge.
  • Resource allocation: Coordinating resources and expertise across different departments can be difficult.
  • Meeting tight deadlines: Tight deadlines can add pressure and increase the likelihood of errors.

Fortunas 18-Document Package

Description and Components

Components of the Package:

  1. Control Plan
  2. Design Failure Mode and Effects Analysis (DFMEA)
  3. Process Failure Mode and Effects Analysis (PFMEA)
  4. Material Specifications
  5. Initial Process Study
  6. Control Plan for PPAP
  7. First Article Inspection Report
  8. Inspection, Test, and Quality Control Plan
  9. Process Flow Diagram
  10. Work Instructions
  11. Calibration Records
  12. Measurement System Analysis
  13. Traceability Matrix
  14. Supplier Qualification Report
  15. PPAP Submission Form
  16. Control Plan
  17. Production Process Control Documentation
  18. Other Supporting Documents

  19. Control Plan: Defines the key process parameters and control methods to ensure consistent part production.

  20. Design Failure Mode and Effects Analysis (DFMEA): Identifies potential failures and their impacts, helping to mitigate risks.
  21. Process Failure Mode and Effects Analysis (PFMEA): Focuses on process-related risks and identifies actions to minimize them.
  22. Material Specifications: Ensures that materials meet the required specifications.
  23. Initial Process Study: Provides data from the initial production run to establish process capability.
  24. Control Plan for PPAP: Specifies control methods for ensuring process stability and capability during the PPAP process.
  25. First Article Inspection Report: Documents the initial inspection results, ensuring compliance with requirements.
  26. Inspection, Test, and Quality Control Plan: Outlines inspection and test procedures, helping to maintain quality throughout production.
  27. Process Flow Diagram: Visualizes the production process, making it easier to understand and optimize.
  28. Work Instructions: Provides detailed guidance on production processes, reducing the likelihood of errors.
  29. Calibration Records: Ensures measurement tools are calibrated, maintaining accuracy and reliability.
  30. Measurement System Analysis: Validates measurement systems to ensure accuracy and precision.
  31. Traceability Matrix: Establishes clear traceability links between parts, processes, and suppliers.
  32. Supplier Qualification Report: Verifies supplier capabilities and compliance with requirements.
  33. PPAP Submission Form: Formulates the overall submission, ensuring all required information is included.
  34. Control Plan: Reinforces key process controls and verification methods.
  35. Production Process Control Documentation: Provides ongoing process control data, ensuring continuous compliance.
  36. Other Supporting Documents: Includes additional documents to support the submission, such as training records and equipment listings.

Benefits of the 18-Document Package

Streamlined SQE Review Process

The primary benefit of the 18-document package is its ability to significantly streamline the SQE review process. By providing a comprehensive set of documents that cover all key PPAP requirements, Fortunas package makes it easier for SQEs to review and approve PPAP submissions. This reduces the likelihood of incomplete or incorrect submissions, leading to a higher chance of first-time pass.

Increased Efficiency and Accuracy

Preparation of each document is guided by a clear template or checklist, ensuring that no critical information is overlooked. The package also includes standardized templates and tools, making the preparation process more efficient and accurate. Here are some specific benefits:

  • Efficiency Gains: Reusing and modifying existing templates saves time and reduces the effort required to prepare each document.
  • Accuracy Improvements: Standardized templates reduce errors and inconsistencies, ensuring that all documents are in line with PPAP requirements.
  • Resource Optimization: The package allows for better resource allocation, as each department can focus on completing specific tasks within the package.

Reduced Time-to-Market

A streamlined PPAP process means that suppliers can get approval faster, leading to quicker time-to-market for new parts. This is particularly important in industries where speed and efficiency are critical. By eliminating potential review cycles and rework, suppliers can accelerate their production processes, delivering parts to market faster and more efficiently.

How the Package Simplifies SQE Review

Comparison Chart: Traditional vs. Fortunas Method

To better illustrate the benefits of Fortunas 18-document package, lets compare it to the traditional PPAP submission process:

Feature Traditional Process Fortunas 18-Document Package
Time to Prepare Submission 1-2 months 1-2 weeks
Number of Documents 30-40+ 18
Effort Required High Moderate
Accuracy and Consistency Often inconsistent High consistency
Review Duration 3-4 weeks 1-2 weeks
Compliance with PPAP Requirements Variable High compliance

Expert Insights

Industry experts and SQEs who have worked with Fortunas package have praised its effectiveness and simplicity. Heres what they have to say:

Fortunas 18-document package has transformed our PPAP submission process. Its no longer a complex, time-consuming task, but a straightforward, fill-in-the-blank exercise that ensures all requirements are met. John Doe, SQE, Large Manufacturing Co.

Steps to Implement the 18-Document Package

Tailored Guidance

To effectively implement Fortunas 18-document package, suppliers must take a tailored approach that aligns with their specific needs. Here are some steps to consider:

Step 1: Assess Current Process

Evaluate your current PPAP process to identify areas that can be streamlined or improved. This will help determine where the 18-document package can provide the most benefit.

Step 2: Customize Documents

Although the package provides standardized templates, customization may be necessary to align with your specific processes and requirements. Modify the templates as needed to fit your operational context.

Step 3: Training and Support

Provide training for all relevant staff to ensure they understand the purpose and structure of each document. Fortuna offers comprehensive training and support to help suppliers get up to speed quickly.

Step 4: Testing

Conduct a trial run of the package before implementing it for a full PPAP submission. This allows you to identify any issues or areas for improvement before finalizing your submission.

Step 5: Continuous Improvement

Once the package is implemented, continuously monitor and improve the process. Regularly review and update the documents to ensure they remain aligned with changing requirements and standards.

Tips for Successful Implementation

To maximize the benefits of Fortunas 18-document package, consider the following tips:

  • Cross-functional collaboration: Involve key stakeholders from different departments to ensure a comprehensive and coordinated approach.
  • Documentation tracking: Use a centralized system to manage and track all document updates and revisions.

  • Training and support: Ensure that all team members are fully trained and supported throughout the implementation process.

Conclusion

Fortunas 18-document package offers a streamlined and efficient approach to PPAP Level 3 submissions, making it easier for suppliers to achieve first-time pass rates and streamline the SQE review process. By simplifying the documentation requirements and providing clear, standardized templates, the package ensures a comprehensive and accurate submission process.

For sheet metal fabrication companies and other supply chain entities, adopting Fortunas 18-document package can significantly improve efficiency, reduce time-to-market, and enhance overall quality control. Fortunas commitment to innovation and quality assurance makes it a trusted partner in the sheet metal fabrication industry, providing the tools and support needed to achieve success in PPAP submissions.

We encourage all suppliers considering PPAP Level 3 submissions to explore Fortunas 18-document package. Its an investment in streamlined operations, increased efficiency, and unmatched quality control.

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Dongguan Fortuna was established in 2003. It has a factory area of 16,000 square meters and 260 employees. It is a production enterprise specializing in precision metal stamping parts, precision CNC processing, injection molding and product assembly.
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