Title Page

  • Audit Title

  • Client / Site

  • Conducted on

  • Location

Quality Management System

  • Does the supplier operate a quality management system that is formally certified to the relevant ISO or an equivalent industry standard, by an accredited body?<br> <br>

  • Does the QMS contain a Quality Policy, Quality Manual and procedures for control of documents & records, internal audits, control of nonconforming product, corrective actions and preventive actions?<br> <br>

  • Have the core documents of the QMS been reviewed within the last 12 months? <br>

Sales

  • Are customer purchase orders reviewed including as a minimum, adherence to delivery dates, materials, part numbers and any drawings provided and where provided; are JF Nuclear Ltd material purchasing specifications adhered to ?<br> <br>

  • Is there a contract review process in place, where Order Number, Drawing Number, Revision, Quantity, Delivery, Certification and Inspection Criteria are identified?<br> <br>

  • How are revision changes to drawings and products communicated to production to ensure they are working to revised requirements?<br> <br><br>

Purchasing

  • Are documented purchase orders issued to suppliers, containing information on product requirements, materials and any applicable acceptance criteria?<br><br>

  • Is there a documented approved supplier list? <br>

  • Is there a grading system to the approved suppliers ?<br> <br>

  • Are suppliers evaluated prior to being approved and is this evaluation conducted on a periodic basis, with records maintained?<br> <br>

Training

  • Are documented training records in place for all employees ? <br><br><br>

  • Are employee training needs analysed and reviewed periodically? <br>

Production Planning

  • Is production capacity information maintained and evaluated against required and future production needs? <br>

  • Are manufacturing resource planning (MRP) tools or software in place, that visibly show work in progress, work pending and work that is late for completion?<br> <br>

Production Process

  • Are production programmes on machinery and plant, or any pre-calibration routines verified prior to running production?<br><br>

  • Are routing cards or similar used to identify key production stages to production operatives? <br>

  • Are production process procedures available to operators? <br>

Goods-in Inspection

  • Explain how items and raw materials are inspected prior to being booked in?<br> <br>

  • How are goods receiving non conformities dealt with is there a dedicated quarantine area? <br>

  • Are goods received referenced to the PO

  • How are raw materials segregated, ferrous / non ferrous

  • How is material certification controlled

Engineering

  • How are drawings released into manufacture

  • How are old revisions or superseded drawings removed from circulation<br> <br>

  • If there is a query on the drawing, how is the question answered / resolved

Inspection & Test

  • Are all critical inspection and testing stages documented and available ?<br> <br>

  • How do you ensure final inspection and testing requirements are met as specified by the client ?<br> <br>

  • Are all critical dimensions documented stating the actual results achieved?<br><br>

  • Is inspection and testing conducted with equipment capable of measuring to the specified tolerances? <br>

  • Are you aware of any client requirements regarding the tolerance range of measuring equipment (Re: RR SABRe)

  • Is all measuring and inspection equipment uniquely identified and calibrated on a periodic basis?<br> <br>

  • Do you have any reference measuring equipment e.g. Master Slip gauges

Non conformances and Corrective and Preventive Actions

  • How are non-conformances investigated and recorded ?<br> <br>

  • Is there a process for correcting product non-conformances through rework or concession ?<br> <br>

  • How is a non conforming product controlled

Monitoring and Analysis

  • Are internal KPI's set ?<br> <br>

  • Is there an internal audit schedule in place ?<br> <br>

  • Does senior management review the QMS at planned intervals?<br> <br>

  • How are changes to the QMS controlled

Material / Product Storage

  • Are components and/or materials stored so as to be traceable to the original purchase order and/or manufacturer's batch/lot number?<br> <br>

  • Is there material traceability from the goods inward inspection of the raw material, through production and manufacture to the certification supplied with delivery to the customer?<br> <br><br>

Dispatch & Documentation

  • Are all products dispatched with reference to the Purchase Order?<br> <br>

  • Are copies of inspection and/or testing records available for dispatch to the customer if requested? <br>

Maintenance

  • Are preventive maintenance plans documented and records maintained? <br>

  • Is there a program for capability improvement

Health & Safety

  • Is Health & Safety adhered to

  • Is PPE freely available at the point of use, how is this recorder the

  • Is all lifting equipment controlled in line with LOLER

  • Is there a requirement for any specialist medicals, and how are these recorded

  • Do you record eye test results for inspection staff

Environmental

  • How are issues with environment dealt with

  • Is there an active waste segregation process in places

  • Is the air quality monitored

  • Do you record the levels of noise in the workplace

Supplier Feedback

  • Is there any feedback from the supplier

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