Title Page
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Location
RECEIVING AND STORAGE
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Is incoming materials and loading equipment stored in accordance with their release status (FIFO) to prevent it from being damaged or mixed?
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Is transport and storage conditions for materials that could be damaged by temperature, humidity, vibration etc. and effect the quality of the final product defined and and can evidence be provided?
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Is "suspect"/quarantined products securely stored to prevent unauthorized access?
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Is there a receiving stamp and a FIFO on the material, is FIFO and batch traceability ensured when the materials are further processed?
IDENTIFICATION AND LABELLING.
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Is every pallet bin labeled, and does the label match the part inside the bin?
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Does the bin label (Route Card) include all of the processes that the part goes through, and are the current and previous processes scratched out on the label?
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Is the bin labeled with the in process label (wash card, final stage card, progression card or ok to use card)?
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Are all of the bins in the WIP area labeled, and does the label include the NPO number or the quantity of parts inside the bin?
WIP AREAS
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Are Storage Locations/Containers clean and orderly (5s Standards in place and maintained)?
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Is Shelf Life determined and monitored (specified maximum, minimum and interim storage times)?
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Is the storage and processing of parts protected from environmental and climatic influences or contamination?
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In the bin, all the packed products, and not protruding higher than the bin height?
MANAGEMENT REVIEW BOARD
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Is the data on the MRB updated daily?
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Is the scraped and suspect parts labelled and laid out on the table neatly?
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Is the data and information updated (score cards, 8Ds and customer complains, Is it in line with the actual database on the quality drive?
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Is the process accountability board updated?
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Are all the tickets issued have relevant escalation on them?
CONTROL OF NON-CONFORMANCE
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Are Customer Requirements complied with (production material, components, ) ?
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Does every workstation have a suspect and scrap bin?
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Is the three scrap rule (PI 90/91) being utilized for non-conforming parts?
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Do employees know the product and are they aware of the consequences of faulty workmanship for the supply of parts and the quality of the final product (SOP/WI59/Training matrixes?
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Are all non-conforming components listed on the scrap sheet (QUA-F-028), as well as the total quantity of non-conforming parts?
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Are all the parts separated accordingly in a bin (part name, number and label), is there rework labelling on the bin with parts required to be reworked?
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Are all the components that need to be reworked segregated into the quarantine area?
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Is the quarantine register up to date?
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Is all scrap removed from the area at the end of every production run or shift?
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Is conditions governing rework specified and secured within the process (e.g. part identification, re-checking/inspection etc.)?
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Is a rework list that includes all parts that need to be modified and that also shows which parts are really being reworked available?
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Are the individuals performing the rework aware of the approved (signed off) rework instructions?
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FIRST-OFF, LAST OFF VERIFICATION
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Is the first off done and accepted (QUA-F-007 First Off Submissions sheet), there's an availability of the approved first-off on the first-off tray?
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In the case of the First-Off not being accepted or approved, are relevant leaders aware of the escalation?
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Are all the First-Off parts on the tray relevant to the part being currently ran?
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Are all the first-off dates (current day date) accurate and updated?
START-UP VERIFICATION
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Is the Approval Process followed prior to starting/re-starting production?
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Is the start-up verification sheet filled in?
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Before the commencement of the production run on that press, have all the detected errors been corrected?
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Are all necessary sheets—such as the press total check sheet and quality focused checks—present, as well as the necessary data and signatories?
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Are there reaction to out of specification conditions?
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Are the poke-yokes verified and signed off?
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Is the poke-yoke register updated?
MASTER SAMPLE ROOM
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Is the room clean and neat, all the samples are in their correct place?
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Are all the aisles divided up per customer? Are all the parts that have been hung labeled?
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When a part is moved out of the room, is the master movement sample log sheet being filled out?
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If not, how do they keep track of where and who took the sample out of the room?
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Do all of the parts that are available in the sample room appear in the master sample part register?
GAUGE ROOM
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Is the space orderly and clean, and are the aisles all divided according to customers?
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Are all the gauges and checking fixture present? Records must be available and status displayed on the checking fixture or gauge.
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Are all gauges and checking fixtures calibrated?
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Are all the checking fixtures and gauges in good condition?
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Do all the parts on the measuring device and checking fixture match those in the control plan's gauge instruction illustration?
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Does the gauge have a serial number?
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Are the gauges clean and the writing on them is visible?
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Does the personnel use the checking fixture or gauge properly?
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There's no damage on all gauges ang checking fixtures?
FINISHED GOODS STORE
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Is the products/components protected from damage by suitable storage and packing?
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Is internal and customer-specific packing instructions known and implemented?
FINAL SHIPPING AREA
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Are all the parts on the bin corresponding with labelling (part number, quantity, customer) on the bin?
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Does the bin have labels with both the internal part number and the customer part number?
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Is the awareness of all the current Quality Alerts(QA) and Special labelling?
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Are the parts ready to be shipped quality approved (Quality Stamp)?
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Does the quantity of parts ready to be shipped align with the invoice?
ADHERENCE TO PROCEDURE.
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Are Work Instructions for production personnel & Control Plans for Quality personnel available at the work station?
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Are Test Methods, Test Frequencies & Approval Criteria defined and followed?
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Is process parameters that influence product characteristics/quality fully stated?<br>
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Is the control limits in the process control charts defined, identifiable and plausible?
5'S SAFETY &ENVIRONMENT
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Is there signage indicating which PPE is required or required for the area? Is everyone wearing the necessary PPE?
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Is the workstation kept clean? No unnecessary material or dirt?
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Are cleaning cycles for storage areas, work-sations and containers defined and monitored?
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Does the workplace material flow process ensure the safe handling of parts and or other materials?