AUDITOR DE CALIDAD

Dana; Coahuila; On-site; MXN 240,000 - 360,000; Full time

Job summary

Financeroles is seeking a quality auditor to ensure production processes meet internal and customer requirements. You will audit against ISO standards, verify documentation within the quality management system, and drive corrective actions as needed.

The role involves tracking faults, approving materials on the line, segregating non-conforming items, and conducting statistical monitoring to support stability improvements.

Qualifications

• Must be able to audit production processes and ensure compliance with internal ISO standards.
• Experience documenting quality management activities as part of ISO/IATF-16949:2016 or ISO 14001/45001 is preferred.
• Ability to review procedures and verify conformance to customer requirements.

Responsibilities

• Audit and ensure compliance with product standards in production areas.
• Track faults and correct the process using SIP, FTQ, and related records.
• Approve materials on production lines by comparing requirements with inspections.
• Register, segregate, and dispose of non-compliant product using NCMR, and quarantine as needed.
• Perform random monitoring of CEP-defined statistical results to support problem solving.

Job description

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.