The important thing to remember when gathering evidence is that the more evidence the better - that is, the more evidence you gather to demonstrate your skills, the more confident an assessor can be that you have learned the skills not just at one point in time, but are continuing to apply and develop those skills (as opposed to just learning for the test!). Furthermore, one piece of evidence that you collect will not usualy demonstrate all the required criteria for a unit of competency, whereas multiple overlapping pieces of evidence will usually do the trick!
From the Wiki University
What evidence can you provide to prove your understanding of each of the following citeria?
Establish the scope of the QA system
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Define the enterprise needs and expectations in product quality Completed |
Evidence:
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Detail existing systems and requirements for incorporation into the QA system Completed |
Evidence:
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Define the scope of the CCP-based quality system to encompass production system and product requirements Completed |
Evidence:
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Design the system to prevent and control identified hazards Completed |
Evidence:
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Conduct hazard analysis and assessment
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Assess every step in the production process for potential food safety hazards Completed |
Evidence:
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Establish CCPs to identify where each significant hazard can be prevented or controlled Completed |
Evidence:
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Assign a measurable or recognisable standard for each CCP to define the critical limits Completed |
Evidence:
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Validate the critical limits technically and scientifically Completed |
Evidence:
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Ensure all documents, work procedures and processes required for the system are developed, available and in use
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Describe all products and processes covered by the QA system in a standardised format defining product characteristics relevant to food safety Completed |
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Review work instructions and standard operating procedures (SOPs) for accuracy, relevance and sufficiency to prevent hazards Completed |
Evidence:
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Implement documented procedures for monitoring CCPs Completed |
Evidence:
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Implement documented procedures to ensure any CCPs that are outside critical limits are brought back within limits, and affected product is suitably handled Completed |
Evidence:
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Implement documented procedures to ensure the QA system is regularly verified and audited as working effectively Completed |
Evidence:
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Maintain the availability and data storage of all records and documents for the system Completed |
Evidence:
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Respond to non-conforming product or processes
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Identify procedures for taking corrective action Completed |
Evidence:
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Implement corrective and preventative measures to prevent recurrence Completed |
Evidence:
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Develop or revise procedures to support control measures Completed |
Evidence:
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Identify processes or conditions that could result in a breach of procedures, and take corrective action Completed |
Evidence:
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Introduce process changes and control so that quality assurance requirements are accomplished Completed |
Evidence:
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Review product sampling and test results
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Identify product sampling procedures Completed |
Evidence:
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Identify post-collection procedures according to SOPs Completed |
Evidence:
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Review test results and ensure quality assurance requirements are accomplished Completed |
Evidence:
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Audit, verify and validate the system
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Revise, verify and validate safety plans to reassess hazards, CCPs, critical limits, testing methods and all related procedures of the QA system to ensure they are appropriate to the enterprise requirements Completed |
Evidence:
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Follow up and act on internal or external audit findings Completed |
Evidence:
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Investigate and act on reported quality hazards and non-conformances Completed |
Evidence:
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Review the CCP-based QA system to take account of any process changes or product specifications Completed |
Evidence:
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