Use this Advanced Product Quality Planning (APQP) Checklist to easily determine the system level project plans utilized, capture photo evidence of the APQP process, document the product and process design, development and validation, schedule inspections and assign actions to cross-functional team members and validate the APQP with digital signatures.
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APQP Checklist (Product Design and Development)
Use this APQP checklist is a step-by-step guide for the product design and development phase of the advanced product quality planning process. Confirm Design FMEA, prototype control plans, engineering specifications, manufacturing process sequence, and process descriptions using this APQP checklist. Take photos of engineering drawings, prototype builds, and other proof of findings for proper documentation of the APQP.
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APQP Checklist (Process Design and Development)
Use this APQP checklist to ensure the performance of Process FMEA, key process characteristics, pre-launch control plans, process capability estimates, operator process instructions, packaging and shipping design, and supplier process sign-offs. Gather the electronic signatures of APQP personnel to authenticate all deliverables.
Downloads: 221Get - Templateby SafetyCulture
APQP Documents Checklist
Use this APQP Documents Checklist to complete all advanced product quality planning requirements. Start by reviewing the voice of the customer, lessons-learned database, and quality policy. Define the project goals by establishing priorities, design, quality and reliability goals, and management support. Finally, carry out all product and process design, development, and validation procedures and apply feedback, assessments and corrective actions for continuous improvement.
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FMEA Template
An FMEA template aims to identify potential problems in a process, product or design and prevent their adverse effects on customers. Monitor the implementation and effectiveness of corrective actions with the use of this template. Enable your team to easily describe the process function, identify the mechanism of failure and determine the RPN. Create and complete corrective actions and validate the FMEA with digital signatures.
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