INDUSTRIAL AUDIT
Gap between requirement and practice
An industrial audit ensures that a situation aligns with a given framework (specifications, standards, management system, procedures, processes, etc.). It identifies gaps between requirements and actual practices.
Depending on your priorities, we tailor our approach and co-develop the process with you.
Neorys Solutions
MANUFACTURING AUDIT
A technical audit evaluates the efficiency of a supplier’s manufacturing processes.
This industrial audit assesses your supplier’s ability to meet your requirements and priorities.
There are many reasons to conduct a supplier audit, and we adapt our approach to your specific needs.
Typically, a supplier audit focuses on three key aspects:
1- Description of the structure and organization.
2- Evaluation of technical expertise and critical skills.
3- Assessment of production capacity.
At the conclusion of the audit, a corrective action plan is systematically provided.
ORGANIZATIONAL EFFECTIVENESS AUDIT
Organizational performance audits evaluate the effectiveness of management systems (whether or not the sites are certified).
These audits aim to assess the long-term performance of an industrial site rather than providing a snapshot. They can serve various purposes, such as providing a status overview, driving organizational improvement, or preparing for certification.
We conduct these audits using your audit framework, our own, or one co-developed with you, focusing on the following themes:
1-Quality(possible frameworks: ISO 9001, IATF 16949, ISO 22000)
2- Environment (ISO14001)
3- Energy (ISO 50001)
4-Health & Safety (ISO 45001)
TRACEABILITY AUDIT
1- The alignment of the traceability system with the defined priorities.
2- The consistency between system requirements and actual practices.
3- The reliability of collected data.
At the conclusion of the audit, a corrective action plan is systematically provided, along with an evaluation of the effectiveness of these actions once the plan is completed.
Considering your challenges and your objectives, we design your standards with you.
Method
1
PREPARATION
We develop or adapt the audit evaluation framework and collect the relevant elements with regard to the issues addresses
2
REALIZATION
We conduct on-site audits in collaboration with the stakeholders.
3
RESTITUTION
We deliver a conclusive and illustrated audit report, including a corrective action plan and a summary document for decision-makers.
4
FOLLOW UP
We support the implementation and monitoring of the corrective action plan and can assess its effectiveness.
Leverage the synergies of the Qualith group to maximize the benefits of industrial audits by connecting them to other product control stages.
1
Dévelopment product and process
Develop your product designs and industrial processes to control, anticipate, and plan inspections at key stages of production.
2
Industrial site validation and upgrade
Assess and improve the selected industrial site to ensure its suitability for the product in question.
3
Monitoring and control of
production
Inspect and enhance your production from initial runs to finished products before export.
