Control of Calibrated Equipment Procedure [ISO 9001:2015]

Corresponds to the requirements of ISO 9001:2015 and ISO Provides detailed description of the distribution of responsibilities and actions to address risks and opportunities, which will facilitate the implementation of the procedure in QMS and Processes. Template details: 17 pages PDF preview More info. ISO 9001 is the world’s most popular management system standard. Benefits. ISO 9001:2015 clause by clause. Top tips from our clients. Your ISO 9001 journey. BSI Training Academy. BSI Business Improvement Software Contents Updated in 2015 to make sure it reflects the needs of modern-day business, ISO 9001 is.

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The purpose of this procedure is to define your organization’s responsibilities and activities in order to ensure that all inspection and test equipment used for product, service and process verification is controlled and calibrated against nationally traceable standards at specified intervals and that such devices are available to ensure continuity of measurement capability.

Internal Audit Checklist [OHSAS 18001:2007]

Ez grabber for windows 10. The Occupational Health and Safety Assessment Series OHSAS 18001:2007 audit checklist will help ensure your audits address the necessary requirements. It stands as a reference point before, during and after the audit process and if developed for a specific audit and used correctly will provide the following benefits:

Ensures the audit is conducted systematically
Promotes audit planning
Ensures a consistent audit approach
Actively supports your organization’s audit process (OHSAS 18001:2007, Clause 4.5)
Provides a repository for notes collected during the audit
Ensures uniformity in the performance of different auditors
Provides reference to objective evidence

This OHSAS 18001:2007 audit checklist comprises tables of the certifiable (‘shall’) requirements, from OHSAS 18001:2007, each required is phrased as a question. This audit checklist may be used for element compliance audits and for process audits.

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Gap Analysis Checklist [OHSAS 18001:2007]

The Occupational Health and Safety Assessment Series gap analysis checklist highlights the requirements contained in OHSAS 18001:2007.

After completing the Gap Analysis you will have a list of activities and processes that comply and ones that do not comply (GAPs).

Armed with this knowledge, it allows you to establish accurate budgets, time-lines and expectations which are proportional to the state of your current management system when directly compared to the requirements of the standards.

Work Instruction Template

Work instructions are low-level documents showing operational detail. They are optional.

Work instructions might describe how to operate machinery, how to mix chemicals for a certain process, how to process a purchase order, or anything else that you feel is important enough to document and share.

Many companies avoid over-burdening their quality manual by allowing lower-level documents, such as procedures and work instructions to contain the operational detail. Then, simple reference is made to the procedures and work instructions from within the quality manual itself.

Product Realization & Planning Process

The purpose of this process is to define the activities required to ensure that product realization and planning encompasses the determination of product and process quality objectives, development of required processes, documentation and records. https://gfrenew.amebaownd.com/posts/15917991.

Product quality objectives are defined in drawings and specifications, contracts, standards, samples, workmanship standards, and applicable legal and regulatory requirements.

Product realization planning includes the following:
• Definition and evaluation of production/service processes
• Development of suitable and capable processes
• Identification of special processes and consideration of associated risks and consequences
• Development and implementation of appropriate process control measures
• Development of instructions (where applicable) and training for process personnel
• Identification of the records required to demonstrate product/process quality

Product realization plans are generated collectively by the Production/Service, Engineering and Quality Functions. The plans are defined in associated production/service documents (e.g. process flowcharts, production/service work orders, process control plans, operator/installation instructions, process validation reports, etc.).

Calibration Process

The purpose of this process is to ensure that all inspection and test equipment used for product and process verification is calibrated against nationally traceable standards at specified intervals and that such devices are available to ensure continuity of measurement capability.
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Customer Satisfaction Process

This document describes the methods for measuring, monitoring and interpreting customer satisfaction to determine if you are meeting customer requirements.

A customer satisfaction survey form is sent to the customer with each product or at the completion of service
If a customer does not respond within four weeks, a follow-up telephone call is made and a verbal survey is conducted
The results customer satisfaction data will be used to determine conclusions on the quality of product
Customer satisfaction data is analyzed by the Quality Management Representative to determine trends
The findings are reported to management quarterly and presented at management review meetings

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Customer Complaints & Feedback Process

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The purpose of this process is to monitor, measuring and take appropriate corrective action from customer complaints and feedback.