Title Page

  • Document No.

  • Site

  • Conducted on

  • Prepared by

  • Location
  • Personnel

3 - Control Procedures.

3.0 - Control Procedure.

  • 3.1 - Does the document comply with the statements contained in section 3.1?

  • 3.2.1 - Are all Standards, Codes of Practice and other technical data being suitably controlled by the technical manager?

  • 3.2.1.1 - Are relevant copies of items controlled and available on Sharepoint?

  • 3.2.2 - Are the copies in the technical library the most current version?

  • 3.2.3 - Have all publication been reviewed, at least annually, and a verification signature been made in the appropriate column of the standards register?

  • 3.2.4 - Are all superseded copies of the Standards and/or references either destroyed or marked 'Superseded'?

  • 3.2.5 - Has the Technical Manager ensured that only current versions of Standards etc. are in circulation and issued on a controlled basis?

  • 3.3.1 - Has all incoming correspondence been opened and distributed promptly for action or information as appropriate?

  • 3.3.2 - Have all documents issued been reviewed for adequacy and approved by signature prior to issue?

  • 3.3.3 - Have all documents been distributed to locations that require them, and old documents been withdrawn?

  • 3.3.4 - Have newly issued documents been entered on the document register, are identifiable, and controlled by the technical manager?

  • 3.3.5 - Does the Technical Manager have the master copy and maintain, each of the controlled documents?

4 - Production.

Section 4 relates to items covered under separate operational procedures and covered by separate audits.

5 - Inspection & Testing.

  • 5.1 - Can the Technical Manager demonstrate that there is a schedule of minimum test frequencies, and the frequencies are being adhered too?

  • 5.2.1 - Can the technical Manager demonstrate that continuous observation and inspection is being undertaken by the Plant Operatives?

  • 5.2.2 - Are all instances of non-conformity being reported to the quarry manager for remedial action?

  • 5.3 - Can the technical Manager demonstrate that the materials produced are being tested in line with sections 1 & 2 of section 5.3 in the Factory Production Manual?

  • 5.3.3 - Can the Technical Manager provide any Non- Conformance Reports, and the corresponding test results?

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  • 5.3.4 - Can the Technical Manager provide evidence of repeat testing, and where non-conformance is confirmed, the remedial action taken?

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  • 5.5 - Can the Technical Manager provide evidence of a Material Test Certificate, with the accompanying Grading Summary Report from an authorised source?

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  • 5.6 - Can the Technical Manager provide evidence, for materials that require it, a recent CE certificate, and that materials are conforming to the required standard?

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  • 5.7 - Can the Technical Manager provide evidence of traceability throughout the testing process, evidenced by a unique number allocated to the sample?

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  • 5.8 - Can the Technical Manager provide evidence that non-conforming products are being reported for reworking and/or disposal?

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5.9 & 5.10. Refer to Calibration - Laboratory Equipment and Calibration - Reference Equipment. Neither sections apply to the scope of this audit as we use the services of an external UKAS Lab.

6 - Records

  • 6.1 - Is the technical Manager aware of his responsibilities relating to the maintenance of records?

  • 6.2 - Can the Technical Manager demonstrate the following records;

  • CE Certificates.

  • Sampling & Testing records.

  • Non-conformance reports.

  • Corrective action reports.

  • Sub-contract services, testing reports and records (UKAS).

  • 6.3 - Can the Technical Manager demonstrate the retention of records, dating back 6 years?

7 - Control of Non-conforming product.

  • 7.1 - Can the Technical Manager demonstrate the recording of products in the register?

  • 7.2 - Can the Technical Manager demonstrate the investigation of a non- conformance?

  • 7.3 - Can the Technical Manager demonstrate the corrective action taken in the event of a non-conformance, and its entry in the Corrective Action Register?

8 - Handling & Storage of product.

  • 8.1 - Are products stored in dedicated areas?

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  • 8.2 - Are materials stored is such a way that cross contamination is prevented?

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  • 8.3 - Are the storage areas well maintained?

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  • 8.4 - If material becomes cross contaminated, is there a dedicated area set aside to quarantine the material until it can be reprocessed or disposed of?

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9 - Delivery of product.

  • 9.1 Are all parts of section 9 of the manual being adhered to?

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10- Training.

  • 10.1 - Are all personnel appropriately trained for the duties they are carrying out?

  • 10.2 - Can the Technical Manager retrieve the training records of personnel engaged in the activities?

11 - Completion.

  • Auditors Name

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  • Technical Managers Name.

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  • Date & Time of completion.

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