Example of IATF Process IA checklist

Process :         Management Representative
Name Of Auditors :Date :
Name Of Audittees :Time :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDIT  AUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission. 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Does he know his responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
4.2.3Check on random basis that the document distribution with current revision and issue date are being maintained. 
4.2.3Check whether the Master Files for the Process Approaches and Relevant Document are being maintained. 
4.2.3Check & Verify that the acknowledgement taken from the concerned dept. for the documents mentioned in the document distribution record. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDIT  AUDIT OBSERVATIONS
5.6 /8.2.2Do they have Annual Plan for Internal Quality Audits and Management Review Meeting  & the same plan is being followed or not. 
8.2.2Check the availability of  Department & Month -wise trend graphs made for audit non- conformances for comparison. 
8.2.2Review the action taken by the dept. to close the non-conformance are implemented effectively and also review the verification results. (Verify Non Conformity Report with the help of evidences) 
8.2.2Are they using proper check list for Internal Audit covering all the requirement of ISO/TS- 16949: 2002. 
5.6Check whether all the clauses of ISO/TS are being discussed during management review meeting.( Key Performance Indicators must be reviewed in MRM ) 
5.6Check whether the periodic follow-up being done with the concerned HOD’s for the points raised during management review meeting. (Verify the current status of the Minutes of Management Review Meeting report ) 
5.6.2Check whether the Overall Cost of Quality for the Organization are being calculated. 
5.6.2Check whether the Action Plan is being taken from the concerned dept. for reducing cost of quality. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same is made. i.e.K.P.I. Trends 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDIT  AUDIT OBSERVATIONS
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
5.5.3Check whether the Inter-relation Matrix of the department is displayed at appropriate place and do they aware about the inter- relations with the other department 
4.2.4Check whether the Record Matrix for all the Quality System Documents made and displayed at appropriate place. Also verify that, the documents are located as mentioned in the record matrix. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
6.4Check the condition of 5S. 
          Signature of Auditors                                                                        Signature of Audittees
Process :       Engineering
Name Of Auditors :Date :
Name Of Audittees :Time :
 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Are they aware about Company Quality Policy, Vision & Mission. 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart 
4.2.1Do they have Procedures & Formats of APQP, New Parts Development , Handling ECN, Supplier Selection , Resource Management, Initial Supply Control, in line with TS Standards. ( Verify the effectivness of the procedures ) 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
4.2.3Check whether the distribution records are being maintained whenever new or revised documents issued. 
4.2.3Check whether the List and Distribution records are being maintained for external origin documents. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
4.2.3.1Check whether the engg. Drawings and all relevant documents are being revised in case of ECN received from customer. (i.e. find out any of the engineering change made in process and review the PPAP file revised accordingly and document issue record.) 
7.1Check whether the APQP study are being carried for all the new components parallel with Time Planning Chart. (Find out any component being developed in Tool Room and co-relate the same with APQP stages). 
7.3.6Check whether the PPAP files are being made during Pilot Lot Production of the new components and submitted to customer. (i.e. Find out any component for           which Pilot Lot being manufactured and co- relate the same with PPAP file.) 
7.3.6Check whether the PPAP files for existing components are being made . (Verify any one of the existing part and relevant PPAP documents) 
7.3Check whether APQP & PPAP files consist all the documents as per Check List for APQP & PPAP. 
7.3.6Check whether the Mistake Proofing, Productivity and Cost Saving concept are being considered during tool designing. 
7.3.2.2Check and co-relate the Process Control Sheet with relevant Control Plan. 
7.3.6Check whether the Action Plans are being made on the basis of feedback received from customer for new components. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.3.2Check whether the Bench Marks during APQP are decided on the basis of competitor data or data of similar products. 
7.5.1.5Check whether the Tool Progress Chart are being made & followed in case Tools are fabricated from outside agency. 
7.5.1.1Check whether the Control Plan Compatible with FMEA. 
4.2.3Date of implementation of engineering change is being maintained ( ECN Records ). 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. (Verify the list of documents handed over during transfer of part for production ) 
6.3 / 6.4Do they have List of Infrastructure & Work Environment and actions have been taken where available infrastructure is not good. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement? 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made. i.e. On Time Submission of PPAP. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
5.5.3Check whether the Inter-relation Matrix of the department is displayed at appropriate place and do they aware about the inter- relation with the other department 
4.2.4Check whether the Record Matrix for all the Quality System Documents made and displayed at appropriate place. Also verify that, the documents are located as mentioned in the record matrix. 
6.4Check the condition of 5S. 
              Signature of Auditors                                                  Signature of Audittees
Process:      Plant Maintenance
Name Of Auditors :Date :
Name Of Audittees :Time :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission. 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart 
4.2.1Do they have Procedures & Formats defined for executing the work. 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
7.5.1.4Verify & co-relate the Breakdown Maintenance Report & Preventive Maintenance Schedule with History Cards. ( Check for availability of P.M.Plan Vs Actual status) 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
8.2.3Review the History Card, if any problem repeated for any critical machine then proper analysis is being done.( Verify the action plan for Improvement ) 
7.5.1.4What is their system of Predictive Maintenance and are they using proper checklist for the same. 
7.5.1.4On the basis of history card , do they prepare predictive maintenance plan & follow the same. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made. i.e. Key Performance Indicators. 
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
7.5.1.4Are they maintaining Pending Job Register for pending jobs related with maintenance? 
8.5.2.2Review the process and Check that Preventive actions are being implemented where any problem likely to occur and review also Effectiveness & Efficiency parameter for the same.. 
7.6.2.Check whether all the measuring devices are properly calibrated & identified i.e. Pressure Gauges, Welding Machine Instruments, Tachometer or speedometer. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
6.3Do they have List of Infrastructure & Work Environment and actions have been taken where available infrastructure is not good.Check for availability of contingency plan. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement? 
6.4Whether the safety devices are effectively implemented in shop floor. Check the condition of 5S. 
                Signature of Auditors                                               Signature of Audittees
Process :          Stores & Despatch
Name Of Auditors :Date :
Name Of Audittees :Time :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission. 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority  for achieving the departmental objectives? Check the availability of Organisation Chart . 
4.2.1Do they have Procedures & Formats defined for executing the work. 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
8.5.2.2Review the process and Check that Preventive actions are being implemented where any problem likely to occur and review also Effectiveness & Efficiency parameter for the same, are they  are likely to fail from target. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.4.3.2Do they have List of Direct on Line Items and are they updating the same periodically. 
7.4.1Do they have list of Process Consumables and Machine Spares indicating the sources. 
7.5.5Check and co-relate whether the material is being issued on the line as per the requirement  of Bop /raw material given by In-charge Planning. 
7.5.5Check & Physically verify that proper monitoring of KANBAN system is being done as per the norms decided. ( Verify the availability of Inventory Norms ). 
7.5.5Check whether the material lying at Receipt Store indicating the Inspection and Test Status of the goods. 
7.5.5Check & Co-relate that the Weekly Plan for PPC made on the basis of stock statement & Customer requirement. 
7.5.5Are they maintaining the extra freight paid record and are they taking action to avoid the extra freight in future. 
7.5.5Check whether the corrective actions are being taken and recorded in case of Delivery Performance Rating is less that 100%. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.5.5Do they intimate their Out-station Customer (Distance>200 Kms.) Through Advance Shipment notification at the time of dispatch. 
7.5.5Do they have packing instructions for all the finished goods to be dispatched? And also verify that material is being packed as per the Packing Instructions. 
7.4.3.2Check whether the DOL items are being received along with DOL Stickers. 
7.5.5.1Check whether the stock of the material at incoming stages are being maintained as per Inventory Norms. 
7.5.5.1Check what is the criteria or basis for deciding Inventory Norms . 
7.5.5.1Are they calculating the Inventory Turnover Ratio and what is their target. Verify the Trend of inventory turnover ratio. 
7.5.5.1Do they have any action plan for reducing inventory. 
7.4.1Are they maintaining the List of Minimum Spares / Consumables required. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.5.5.1Do they have any disposal system for slow moving or obsolete material lying at store and are they making action plan for disposal. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and  trend graphs for the same made . 
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement. 
6.4Check the condition of 5S. 
            Signature of Auditors                                                 Signature of Audittees
Process :         Purchase
Date :Name Of Auditors :
Time :Name Of Audittees :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission. 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart . 
4.2.1Do they have Procedures & Formats defined for executing the work. (Purchasing, Supplier Selection & evaluation, Supplier Development etc.) 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
7.4.3Check whether the Vendor Capability Assessment is being carried out before selecting the vendor. 
7.3.6Are they receiving all the applicable PPAP documents from the supplier during new sample submission? (Verify the List of PPAP Documents ) 
7.4.1Do they have List of Approved Vendors for Job Work Material, BOP,. Raw Material Process Consumables and Machine Spares. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
7.4.1.2Are the entire supplier certified to ISO-9000 or they have plan to get certification and also verify the progress being done by supplier for getting ISO-9000  certification. 
7.4.1.2Check whether the System Audit of ISO-9002 supplier are being carried out as per ISO/TS- 16949:2002 Check Sheet. ( Verify the Supplier Audit Check sheet ) 
7.4.3.2Do they have any documented criteria for declaring any item as Dol or Non-DOL. Also verify that that criteria is being followed. 
7.4.3.2Do they have DOL items Audit Plan for verifying the Quality Status of the lots of the DOL items. 
7.4.1.2Check whether the Follow-up audit is being carried out after target dates for verification of the corrective actions against supplier audit. 
7.4.3.2Are they considering the Extra Freight and Line Stoppage factors during calculation of Vendor Performance  Rating. 
7.4.3.2Do they receive Corrective Action Report in case Vendor Delivery Rating observed less than100%. 
7.4.3.2Do they receive Corrective Action Report in case of Quality Problems (QPCR). 
7.4.3.2Check whether the Purchase Order indicating the 100% On-time delivery requirement and Inspection Criteria. (Packing instructions & mode of transports / special requirements) 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
7.4.1Check whether they are dispatching vendor delivery schedule letters on time. 
7.4.1Check whether the Schedule vs. Supply statement are being made and 
7.4.3.2Are they maintaining the extra freight paid record which is paid due to vendor mistake and are they taking action to avoid the extra freight in future. 
7.4.3.2Do they have List of DOL Items and are they updating the same periodically. 
7.4.1Do they have list of Process Consumables and Machine Spares indicating the sources. 
7.4.1Check whether the amendment in BOP/RM requirement given by In-charge- Planning is incorporated in the Vendor Schedules. 
7.4.1Are they maintaining the Pending Purchase Order File for follow-up with vendors. 
5.1.1Do they monitor & make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
7.4.1.3Check the criteria of Vendor selection in line with Procedures. Verify at random the evaluation  sheet of any of the running vendor. 
7.4.2Do they inform the Vendor Rating to concerned vendors for improvement 
7.4.3.2Do they have any action plan for Vendor Upgradation. 
6.4Check the condition of 5S. 
            Signature of Auditors                                                                          Signature of Audittees
Process :     PPC
Name Of Auditors :Date :
Name Of Audittees :Time :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDIT  AUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission . 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart . 
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives  and are they following the same or not. 
7.5.1.6Check & Co-relate that the Weekly Schedule for Production Dept. is being made on the basis of Inventory Status and Dispatch Schedule received from Dispatch Section. 
7.5.1.6Do they prepare the Weekly Production Plan for each section and send to the respective  section In- charge. 
7.5.1.6Do they submit the weekly Raw Material /BOP requirement to Purchase Deptt. 
7.5.1.6Check whether they revise the production plan and send to the concerned  section incharge ,in case of amendment in schedule received from Mktg. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDIT  AUDIT OBSERVATIONS
7.5.1.6Do they make Shop-wise Monthly trend graph (Actual Production Vs Production Planned.) 
6.4.4Check whether the Shop-wise OEE trend Graphs are being made and action are being  taken where OEE observed less. 
7.5.16Are they getting Countermeasure Report from concerned section in case of production failure. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
6.3 / 6.4Do they have List of Infrastructure & Work Environment and actions have been taken where available infrastructure is not good. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement. 
8.4.1Do they monitor their Key Performance Indicator & Analyse for Failures. Do they take preventive measures to eliminate such  failures. 
7.2.2.2 &Do they Maintain : 
7.2.3a) Master List of Products – Customer & Model
Wise.
b) List Of Machines & equipments with capacity.
c) Partwise No. of Tools & respective machine
capacity requirement.
d) Annual & Monthly Delivery Requiremets –
Customerwise.
e) Cycle time for all the operations.
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDIT  AUDIT OBSERVATIONS
6.3.2Do they know the contingency plan to meet Customer’s Requirements 
6.4Check the condition of 5S. 
          Signature of Auditors                                                 Signature of Audittees
Process:  PRODUCTION
Name Of Auditors :Date :
Name Of Audittees :Time :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission . 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart . 
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
7.5.1.6Are they following Monthly / Weekly Production Plan and correlate the same with daily loading plan for critical machine. 
8.2.3Check whether all the relevant Process Sheets/Work Instructions are displayed on the machine for all the components while in operation. Are they properly controlled & Legible. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.3.2.2Review the fitment/critical function of the products being manufactured and check the fitment/critical dimensions are highlighted in process sheet as Ma/Cr. 
7.5.2Check whether Process Qualification of all the components have been made and co-relate the Parameter finalized with the parameter monitored on machine and mentioned in process sheet. 
8.2.3.1Check and Co-relate the Process Sheets with Relevant control Plan for the dimensions. 
6.3.2Do they have Contingency Plan for the Critical eventualities (I.e. Critical Machines, Tools ,Machines, Tools, Jig& fixtures) and do they made any action plan whenever there is non availability of source for the same. 
4.2.3Check whether the Uncontrolled copy of the Work Instruction/Procedures or photocopy of the control stamped W.I./Procedures are being used. 
7.5.2Check whether the machine parameters of special processes are being monitored and recorded. ( PPM ,FEED,Pressure, Shut Height etc.) 
7.5.1.6Check whether the Daily Production Records are being maintained. 
8.3.2Review the Rework & Rejection status of the shop and verify that re-inspection of the reworked pieces & proper disposal of scrapped parts. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
8.1.2Are they conducting SPC (Attribute/Variable) for Cr/Ma Characteristics and action plans are being followed where Cp/Cpk value found less than 1.33. 
6.4.2Check whether the 5-S & Safety Instructions are displayed at the appropriate places and being effectively implemented. 
8.3.4Review the Inspection records , if production is carried out under any deviation then, under deviation note approved from Head-QA. (Verify Deviation Notes ). 
7.5.3.1Check whether the Inspection & test Status of the Products In-process is being maintained as per the Prescribed Procedure. 
8.2.3.1Do they have identified & displayed any reaction plan for taking action immediately on the Process Non-conformances. 
7.5.3.1Check whether the Product Identification and Traceability is being maintained. Verify the identification of Master samples & Limit samples . 
7.5.2Check & Co-relate the Process parameters mentioned in process Sheets with the parameters finalized in Process Qualification Records. 
8.3.2Check whether Rework Are has been identified & Rework Instructions Displayed at appropriate place. 
8.5.2.Check whether the daily non-conformances register is being maintained & co-relate the same with the rejection lying at shop floor. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
8.5.2Are they making summary of the non-conformances observed on daily basis and are they taking corrective action for the same. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . i.e. Rejection, Rework, Plan Vs Produced etc. 
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
8.5Are they maintaining the Before and After Status for the Projects where Mistake Proofing done.(This may be recorded in the format of Kaizen Projects) 
8.2.3Check whether the machine -wise OEE trend Graphs made and analysis done where OEE found Less. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
7.5.2Check whether the Operators are adequately qualified for operation . ( Verify the Skill Matrix ). 
8.5.2.2Review the process and Check that Preventive actions are being implemented where any problem likely to occur and review also Effectiveness & Efficiency parameter for the same, are likely to fail from target. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.5.5Check whether the Packing Instructions displayed if On-line packing is being done. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement. 
8.2.4Do they carry out the inspection of the first of Pieces processed at the time of setting. (FOP -First of Production Approval). 
8.2.4Check whether the Recording of the FOP and Patrol inspection is being carried out. 
7.5.1.3How do they inform the Maintenance department regarding Die Repair ? Do they verify & record the inspection results whenever there is loading of Die after maintainence or repair ? 
8.2.4Do they have the Inspection Reports for the Product found non-conforming during Patrol Inspection being carried out. 
8.2.4Check whether the Final Inspection is being carried out for the components, which are directly submitted to the dispatch section after completion of the process.(Final Inspection of the Components arenot being done by the QA Dept.) 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
8.2.4Do they have Final Inspection Standards or customer Specified Standard for the components being processed. 
6.2.2.2Do they have identified Training needs for their operator’s Skill Upgradation.? Is there any annual Training plan / Schedule ? 
              Signature of Auditors                                                Signature of Audittees
Process :     HR
Name Of Auditors :Date :
Name Of Audittees :Time :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission . 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart . 
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives  and are they following the same or not. 
6.2.2Check whether the Training Programmes are being held as per the Monthly/Annually Schedule. 
6.2.2Check whether the Induction Trainings are being Provided to New Entrant and Records are being maintained. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
6.2.2Check whether the Monthly Schedule consist On The Job Training requirements. 
6.2.2Are they getting feedback from the participants after completion of training programme. 
6.2.2Check whether the Training Effectiveness assessment frequency  is defined & being carried out as per plan. 
6.2.2In case Skill Improvement is not found during Effectiveness Assessment , Verify the Action Plan made for improvement in future. 
6.2.2.4Check whether the Job Description Manual Updated whenever new designation  introduced in the organization. 
6.2.2Check Competency Norms and Matrix for all the Critical Stages in the Departments  have been made. 
6.2.2Are they identifying the training needs before imparting trainings. 
6.2.2Check whether Attendance Records for the Training Programmes are being maintained. 
6.2.2Do they have Plan Vs Actual Trend Graphs for the Training Programmes. 
6.2.2.4Check whether the suggestions are being received. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
6.2.2.4Check whether the assessment of the valid suggestions are being carried out properly by section in charge(s). 
6.2.2.4Do they have any Evaluation criteria for deciding Prize for the  valid suggestions  received. 
6.2.2.4Do they have decided the schedule for Empowerment Assessment of the Employees and the same is being followed. 
6.2.2.4Check whether the Action Plan made where discrepancies found during empowerment assessment. 
6.2.2.4Do they have Monthly Trend Graphs for No. of Suggestions  Received. and no. of suggestions implemented. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend   graphs for the same made . i.e. Training Scheduled Vs Actual, No. of Suggestions Received Vs No. of Valid Suggestions,  Down Time due to Manpower, Employee Turnover Ratio, Skill Enhanced Trend Through Training etc. 
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness  and Efficiency target and are they following the same. 
5.5.3Review the Communication Matrix of the department, is there any communication  missing which is provided by the department and check is it displayed at appropriate place. 
6.3.2Do you have contingency plan for Resource related eventualities. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
6.3 / 6.4Do they have List of Infrastructure & Work Environment and actions have been taken where available infrastructure is not good. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements. 
6.4Check the condition of 5S. 
              Signature of Auditors                                                  Signature of Audittees
Process :    Unit Head
Date :Name Of Auditors :
Time :Name Of Audittees :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Does he aware about Company Quality Policy, Vision & Mission 
5.5Check whether the company objectives (Business Plan) are identified on the basis of Quality Policy. 
5.5Does he knows his responsibilities & authorities for achieving the departmental objectives. Check the availability of organisation chart. 
4.2.1Does he have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
5.5Check whether he has made any road map or action plan to achieve the company objectives . 
5.4.1Check whether the monitoring of Business Parameters are being done. 
5.1.1Does he have trend graph for the objectives defined in Business Plan. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.1.1Check and review the Monitoring of individual departmental performance is being done as per plan. ( MRM Report ) 
8.5Check whether the Review of Kaizen Projects are being done . Check whether the Continuous Improvement Projects are being identified on the basis of Business Parameters. 
6.4Check the condition of 5S. 
              Signature of Auditors                                                 Signature of Audittees
Process:      Tool Management
Date :Name Of Auditors :
Time :Name Of Audittees :
 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission . 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives? Check the availability of Organisation Chart . 
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
7.5.1.5Do they have  Master list of Tooling  and are they updating the same whenever new tool received . 
7.5.1.5Check & verify physically that, Breakdown reports are being received for the tools lying at Tool Maintenance dept. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.5.1.5Are they up-dating the Tool Breakdown History in Tool Histoy card. 
7.5.1.5Do they have any Preventive maintenance schedule for Press Tools and verify that the schedule is being followed. 
7.5.1.5Are they getting comments of the Shift Supervisor after repairing and trial of the tool. 
7.5.4.1Check whether the Identification of Customer Supplied Product Tools are being done properly for ownership. 
7.5.1.5Check whether Tool Status cum Rectification Reports are being maintained during loading and unloading of the tool for recovery. 
7.5.1.5Do they receive the Tool Breakdown report from concerned Shift Incharge or observation from std room during validation for repairing the jig/fixtures 
7.5.1.5Are they up-dating the Tool Breakdown History Card after trial of the repaired tool 
7.5.1.5Check and Co-relate the Tool History Record and Tool Breakdown Reports. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
7.5.1.5Whether the product is inspected after tool repair & recorded in Inspection Sheet. Verify the records. Does any procedue exists for the same. ( Verify QA / Prod. Approval after repair) 
5.1.1Check whether the Effectiveness Indicators are identified by the department and  trend graphs for the same made . i.e. B.D. Hrs Trend Graph 
5.1.1Do they have done analysis and make any action plan for achieving their Effectiveness and Efficiency target and are they following the same. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement. 
8.5.2.2Review the process and Check that Preventive actions are being implemented where any problem or customer complaint likely to occur and review also Effectiveness & Efficiency parameter for the same, are they  are likely to fail from target. 
7.5.2Check whether the Operators are adequately qualified for Tool Repair . ( Verify the Skill Matrix ) 
6.4Whether the safety devices are effectively implemented in shop floor. Check the condition of 5S. 
      Signature of Auditors                                             Signature of Audittees
Process :         Quality Assurance
Date :Name Of Auditors :
Time :Name Of Audittees :
 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission. 
5.5Check whether the departmental objectives are identified on the basis of Quality Policy. 
5.5Do they know their responsibility & authority for achieving the departmental objectives. Verify the Organisation  Chart. 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives and are they following the same or not. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
8.5Do they have identified the continuous improvement projects to achieve the departmental objectives and improvements in Audit Results, Conformity to Product Requirement. 
6.4Whether the safety devices are effectively implemented in shop floor. Check the condition of 5S. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Receiving Inspection
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
7.4.3Do they have any list of Inspection Quality Standards for all the items. (BOP, Raw Material, Job Work Items) and are they updating the same whenever new item added ? Whether DOL items are identified & approved supplier list maintained ? 
7.4.3.1Check whether the verification of the each lot of Non- DOL Items is being done and recorded. (BOP, Raw Material, Job Work Items). 
7.4.3.2Do they receive the Dimensional Report with each lot of the DOL/Non DOL from the vendors. 
7.4.3.2Check & verify that, material test report of the material is being received from the vendors with every lot. Are they verifying the major characteristics (e.g. Hardness , Penetrations etc.) 
7.4.3.2Have they maintained a list of Inhouse inspection & test instruments for carrying out Inspection & testing activities. 
7.4.3.2Do they have any plan for Third part inspection/test of Incoming parts & whether the frequency have been defined.
8.2.4Check whether the Quality of the Product being monitored in case of any BOP/Raw material issued due to urgent production requirement. 
7.1.2Do they refer Zero Defect Sampling Plan for selecting the sample size during inspection. If no, Which sampling method they follow & is it effectively implemented. 
7.4.3Do they get Under Deviation Note approved from Head- QA whenever there is urgent requirement and part is not conforming the requirements. (Verify Deviation Records) 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.5.1.1Do they raise & receive Quality Problem   Countermeasure Report from the vendors in case of   non- conformances observed in Non-DOL / DOL Items ( NCs from Internal/Inhouse Customers & from the External Customers ). 
8.5.2 , 8.5.3Do they verify the effectiveness of Corrective & Preventive actions furnished by vendors in case of NCs. How they Close the QPCR. 
8.4, 8.5Are they carrying out Supplier Quality Rating. What are the criteria for Rating. How do they Inform the same to the vendors. Is there any vendor upgradation plan for improvement in their quality. 
7.4.3.2Do they examine and give their remarks on the test report received from vendor for DOL  items. 
7.4.3.2Do they have any DOL item Audit Plan for verification of the Quality Status of the DOL items periodically and are they following the same plan. 
7.4.3.2What is the criteria for declaring any item as a DOL Item and are they conducting Audit of the items to be declared for DOL Supplies. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1Do they record the COPQ due to BOP items ? 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Product Audit
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
8.2.2.3Check whether they have made any schedule for product audit and that is being followed. 
8.2.2.3Do they have audit check list for all product being manufactured  considering  customer  specific requirement,drawings,packing & product data & audit is being done as per check list ? 
8.2.2.3Do the have a list of qualified auditors & and audit is being done by qualified auditors ? 
8.2.2.3Check whether corrective & preventive action is being taken for any non-conformity observed & effectiveness of action taken is also being measured. 
5.1.1 , 8.4Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Final Inspection
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
8.2.4Do they have Component Wise Matrix Chart indicating the responsibilities for final inspection of the finished goods being manufactured in the different shops. 
8.2.4Do they have concession records for the material dispatched under deviation after getting approval from customer.(I.e. Co-relate & Verify the same with the Under Deviation Note approved for in-house production of any component.) 
8.2.4Do they have Final Inspection Standards/Customer Specified Standards/ Visual Aids for all the components. 
7.1.2Do they refer Zero Defect Sampling Plan or sampling plan specfd. By customer for selecting the sample size during inspection.(Review the No. of Samples mentioned in Inspection Report) 
8.2.4Check whether the recording of the final inspection is being done. 
8.2.2.3Check whether the Dock Audit of the material lying at dispatch store is being conducted and recording is being done. 
8.2.2.3Do they have relevant checkpoints to be verified during Dock Audit. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
7.5.2Check whether the Inspectors are adequately qualified for Inspection. ( Verify the Skill Matrix ). 
6.2.2.2Do they have identified Training needs for their inspector’s Skill Upgradation.? Is there any annual Training plan / Schedule ? 
7.5.5Do they have packing instructions for all the finished goods to be dispatched? And also verify that material is being packed as per the Packing Instructions. 
7.5.5Check whether the material lying at dispatch store indicating the inspection & test status. 
8.4Are Reaction Plan for Various types of Defects Displayed in concerned shop for containment actions ? 
8.4Do they maintain segregation/rework records ? 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Control Of Non Conforming Products
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
8.3Are the responsibilities and authorities for dealing with non-conforming product defined in the procedure? 
8.3Do the procedure address identification and control of non-conforming products to prevent unintended use or delivery? 
8.3Do the procedure address the ways of disposition of the non-conforming product in form of rework, use-as it is, alternate use? 
8.3Are records & nature of non-conformities maintained? 
8.3Is re-verification carried out for the corrected product? 
8.3Are appropriate actions taken in case of a non- conformity detected after delivery of the product, after analyzing the effects of non-conformity? 
8.3.1What is the criteria of considering suspected products as non-conforming materials (e.g. Lost Test Status, materials tested with instrument out of calibration and obsolete materials )? 
8.3.2Do   work   instructions   for   re-inspection   of   re-work products for the type of defects exist? 
8.3.3How do they inform the Non Conformity to their immediate customer ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
8.3.4Do they maintain Deviation Records ? 
8.4Do they analyse the Non Conformity on Daily & Monthly Basis? 
8.4Do they initiate CAPA for eliminating / Reducing the Non Conformities ? 
8.4Are Reaction Plan for Various types of Defects Displayed in concerned shop for containment actions ? 
8.4Do they maintain segregation/rework records ? 
8.4Do they update / revise the Control Plan / FMEA/PFC/Inspection Standards etc. as a result of CAPA ? 
5.1.1Check whether the Effectiveness Indicators are identified by the department and  trend graphs for the same made . 
5.1.1Do they record the COPQ due to NC items ? 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Callibration
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
7.6.2Do they have Master list of Instruments & gauges & their Locations 
7.6.2Do they maintain callibration schedule for every equipments & gauges. 
7.6.2Do they have a list of Accredited External laboratories for carrying out Callibration. 
7.6.2Do they update the History card of individual instruments 
7.6.2Are all the gauges/instruments are traceable (whether callibrated or not & due dates of callibration etc.) 
7.6.2Check whether the records for the rejected and deviated instruments are being maintained and status is mentioned on the instruments in case being used for inspection. 
7.6.2How do you communicate in case the lot shipped is suspected being made as per rejected gauge/instrument 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Callibration
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
7.6.1Do they have schedule for conducting Measurement System Analysis of all the equipments identified from Control Plans. 
7.6.1Do they have any action Plan, in case of  R & R found Unsatisfactory. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
Lab Management
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
7.6.3.2Do they have a list of Internal Lab scope & External Lab scope. 
7.6.3Check whether the environmental parameters are being monitoring and recorded. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Layout Inspection
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
8.2.4.1Do they have Master list of products. 
8.2.4.1Do they have Layout Inspection Schedule for all regular items processed in the plant (Review the same, is it covering all the items) 
8.2.4.1Check whether the Layout Inspection of the components are being done as per the schedule and recorded. 
8.2.4.1Check & verify that are they taking corrective action whenever any non-conformance observed during Layout Inspection. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
Process Audit
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
8.2.2.3Do they have audit check list for all product being manufactured considering customer specific requirement,drawings,packing & product data & audit is being done as per check list ? 
8.2.2.2 /8.5.2/8.5.3Check whether the Process Audits are being carried as per schedule and Corrective Action being taken where non-conformances  observed. 
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
Validation
4.2.1Do they have Procedures / work Instructions & Formats defined for executing the work. Is it effectively implemented ? 
7.6.2Do you have a plan for Validation of Jigs & Fixture / Panel Checkers. 
7.6.2Are the plan being effectively adhered. 
7.6.2Check & verify that, all the parameters are being checked as per drawing / check list during validation and being recorded. 
7.5.2Do you have a plan for process validation & is it effectively adhered. 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
Control of Dawing & ECN
4.2.1Do they have Procedures / work Instructions & Formats defined for executing the work. Is it effectively implemented  ? 
4.2.3.1Do they maintain drawing control register ? 
4.2.3.1Do they maintain ECN register. (Verify any of the ECN being effectively implemented )? 
Handling of Customer Complaints
4.2.1Do they have Procedures / work Instructions & Formats defined for executing the work. Is it effectively implemented  ? 
5.5.3How do they Communicate the Customer Complaints to the concerned department as well as the top management ? 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
7.2.3 ,How do you communicate the CAPA and NC part being 
8.3.3shipped to the customers. Do they have any Time Frame
decided for Customer Complaint Handling (e.g. Time for
Containment action, Corrective action, Preventive action
etc.)
8.5.2 , 8.5.3Do they determine the causes of non-conformity & accordingly initiate CAPA ? 
8.5.2,   8.5.3Do they review the Customer complaint status (e.g. Monthwise, shopwise, modelwise,4M distribution, pareto analysis, Cause & effect Diagram etc. ) 
8.5.2,   8.5.3Is there any criteria for closing the QPCR against Customer Complaints ? 
8.5.2,Do they maintain the record of Segregartion / Repair 
8.5.3done as containment action against customer complaints.
8.5.2.2Do they use error proofing techniques as CAPA? Verify the Records. 
8.5.2.3Do they apply to other similar processes & products the CAPA & Controls implemented to eliminate the cause of non-conformity.                         ( Horizontal deployment ) 
8.5Do they update & record the Non conformity & CAPA details in relevant documents ( e.g. FMEA , Control Plan , Process Flow Diagram , Check sheets, Inspection standards , Visual Aids , Process Control sheets , Product history sheets etc. ) 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT  OBSERVATIONS
5.1.1Check whether the Effectiveness Indicators are identified by the department and trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
            Signature of Auditors                                                                              Signature of Audittees
Process :         Marketing / Business Development
Date :Name Of Auditors :
Time :Name Of Audittees :
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
5.3Do they aware about Company Quality Policy, Vision & Mission. 
4.2.1Do they have Procedures & Formats defined for executing the work. Is it effectively implemented ? 
5.4.1Are   the   Quality   Objectives   deployed   in   the   marketing department?     i.e. Same Objectives as determined along with Quality Policy or Supporting Departmental Objectives. 
5.5Do they know their responsibility & authority  for achieving the departmental objectives. Verify the Organisation Chart. 
5.5Check whether they have made any road map or action plan to achieve the dept. objectives  and are they following the same or not. 
5.5.3Review the Communication Matrix of the department, is there any communication missing which is provided by the department and check is it displayed at appropriate place. 
8.3How customer is informed promptly, when non-conforming products have  been  dispatched to  them?  (If not  covered by QC ) 
CLAUSE NO.ITEMS TO BE AUDITED OR GUIDELINES FOR AUDITAUDIT OBSERVATIONS
8.2.1Is method of measurement of customer satisfaction / perception determined?   i.e. customer feedback, customer audits, customer survey, feedback to obtain product image in the market, handling customer complaints, increased market share, repeat orders, cost effectiveness, enhance met in product properties, product development and innovations, etc. 
8.2.1Verify the Corrective & preventive actions in case the Request For Quotations  ( RFQs) are rejected. 
7.2.2Is the output from the marketing department communicated to the relevant departments? Verify. 
6.2Is  the  competence  defined  for  the  personnel  performing marketing process? 
6.2Are these competence requirements complied with? 
5.1.1Check whether the Effectiveness Indicators are identified by the department and  trend graphs for the same made . 
5.1.1 , 8.4Do they have done analysis and make any action plan for achieving their target and are they following the same ? 
          Signature of Auditors                                                                           Signature of Audittees

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