AUDITOR DE CALIDAD
At a glance
Mid-level Audit & Controls role at Dana. Escobedo.
Pay not stated Audit & Controls salary
financeroles summary, based on the employer's posting.
What you'll do
- Check production stages against product specifications and procedures to confirm internal and customer requirements are met
- Review quality-system documents for compliance with ISO standards and customer-specific requirements
- Track shift defects and reports from other teams, recording them and following up on process corrections
- Compare inspected materials with production-line requirements before approving them to continue through operations
- Identify and separate nonconforming products, issue NCMRs, and arrange their transfer to quarantine
What you bring
- You can assess production work against product standards, procedures, and customer requirements
- You can verify quality-system documentation against ISO 14001, ISO 45001, ISO/IATF-16949:2016, and customer-specific rules
- You can monitor CEP statistical results and use them to flag process instability or low capability
Who this fits
This role suits someone focused on production-quality checks, document compliance, defect follow-up, and nonconforming-product control. The position is based in Escobedo, Mexico.
From the employer
Job Purpose
Audit and ensure compliance with product standards and specifications in any of the phases of the processes in the production areas, according to the established procedures, to ensure that they meet internal and customer requirements. Ensure that the documents found within the quality management system comply with the requirements of ISO 14001, ISO 45001, ISO/IATF-16949:2016 and specific customer requirements.
Job Duties and Responsibilities
Keep track of the faults found during your shift and those that were reported by other areas, through the registration of SIP, FTQ, and other records as the case may be, and have the attention and correction of the process.
Approve the materials in the production lines, comparing what is required against what is inspected, in order to continue the operation process.
Register, segregate, identify and dispose of the non-compliant product, issuing an NCMR, so that it can be physically transferred to the quarantine area.
Perform random monitoring of the statistical results defined in the CEP, for decision-making of problems of instability and low ability.
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