ISO 9001:2015
AUDIT CHECK-SHEET FOR QUALITY DEPARTMENT
Note: All procedures and formats are made for easy of work and for ISO documentation should have format numbers/procedure number/document number with revision.
Annual instrument calibration plan.
· All instruments should be calibrated within given time of calibration due date.
· Annual calibration plan is nothing but a planning of calibration of all instruments and gauges.
· The planning should in such a way that the instruments periodically go to the calibration in such a way that during calibration of some instruments alternate instrument should available in company to avoid work disturbance.
Instrument history card.
· It is the document in which past calibration history is record.
· In this card instrument name with its uncertainty and error should be record.
· Surveyor can check this error increment during its history.
Identification tag for Rejection, Hold & accepted material.
· For identification of material at inward, in-process and final stage should be tag out by Hold, Accepted and Rejected.
· Tags should contain specific information of part number, numbers of quantity, reason for holding and rejecting, concern person sign etc.
In process inspection report.
· There are various processes are carried out in shop that we are inspected but many peoples does not record those inspections.
· There should be each stage of inspection should be recorded in the form of report as soon as inspection is over.
· In In-process inspection may include cutout marking, fit-up, welding, non-destructive test, pneumatic test, blasting & painting, final dimension etc.
Final inspection report.
· Before dispatch of the finish goods there should be checklist for final inspection.
· In this report may include paint finish, visual, any damages, working reports, mounting gauges calibration etc.
· It may include overall system dimension report as per GA (general arrangement drawing) drawing.
Inward material inspection report.
· All inward material which is require for project is thoroughly checked and checked parameters should be recorded in the inward inspection reports.
· You can make a different formats for different category of material but the main format number should be same.
· All material acceptance standard should be predefined.
Rejection area for in-process rejection.
· Rejection area should be allotted for rejected material at inward and in-process.
· This avoids the mixing of non-conforming material into accepted material.
Quality objective.
· Quality objective should be predefined.
· Main goal of quality department should be clear.
· In Quality objective may occurs ‘On time calibration’, ‘only ok material go on assembly’, NCR closing within 7 days etc. this type of objective is define for quality department.
· As per all objective should maintain all documentation.
Inward material inspection planned vs actual.
· This term is only for inward inspector.
· Inward inspector make his inspection plan for the next day as per purchase order receiving date.
· And store a data in the form of excel sheet for actual received material.
· On comparison of both make a bar chart for that to know the efficiency of work.
Supplier evaluation.
· Make all supplier list with their receiving material.
· Make a format containing all data regarding supplier evaluation.
· It may contain all product list of supplier scope, his turnover, list of employees, ISO version, calibration and all other information related to our products.
Risk analysis.
· Risk is the probable accident or non-conformance in the product.
· Is the risk are predefined then all possible risk effects may decrease by implementing some new methods.
· Risk are related to work, safety, driving, overhead crane, painting, smog etc.
· All defined risk should have mitigation plan that is a plan to reduce the defined risk.
Continuous improvement project (CIP).
· It is small departmental projects that make some improvement in ongoing process, work, product etc.
· CIP project may have subject in risk analysis, welding improvement, supplier improvement, some profile checking machine to reduce time of inspection etc.
SWOT analysis.
· It is different for each person in the department.
· S-Strength
· W-Weakness
· O-Opportunities
· T- Threats
· You can make only one documents for a department by adding all persons above characteristics.
Periodically audit at supplier end.
· Make a proper audit data sheet for supplier regarding our product.
· And you can decide the frequency of audit.
· But the audit should be within 3 months or within 6 months.
· All audit data should be recorded.
Departmental organization chart.
· Departmental organization chart shows the designation of all employees work under each department.
· It also shows that which person is doing work under his supervisor.
· All person qualification should be mention in departmental organization chart.
Comments
Post a Comment