Resumen: is responsible for maintaining, monitoring, and continuously improving the Quality Management System (QMS), ensuring compliance with applicable ISO standards, internal policies, customer requirements, and manufacturing procedures. Responsabilidades:
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Maintain, monitor, and continuously improve the Quality Management System (QMS) in accordance with ISO 9001 requirements.
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Ensure compliance with internal quality policies, procedures, work instructions, standards, and customer requirements.
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Plan, coordinate, and conduct internal quality audits across manufacturing processes and support functions.
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Support external, certification, surveillance, recertification, and customer audits.
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Identify nonconformities, process deviations, and potential compliance risks.
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Coordinate and follow up on corrective and preventive actions to ensure timely and effective closure.
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Facilitate root cause analysis using methodologies such as 5 Whys, Fishbone Diagram, 8D, and Pareto Analysis.
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Track audit findings and ensure corrective action plans are implemented and verified for effectiveness.
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Manage the document control system, including procedures, work instructions, forms, policies, records, and related QMS documentation.
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Ensure current and approved documentation is available at the appropriate points of use.
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Coordinate document revisions and changes related to manufacturing and quality processes.
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Monitor and report Quality Management System KPIs and performance indicators.
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Prepare QMS performance information and supporting documentation for Management Review meetings.
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Partner with Production, Manufacturing Engineering, Quality, Maintenance, Materials, Supply Chain, and other departments to ensure ISO compliance.
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Provide training and guidance to employees regarding ISO requirements, quality procedures, document control, and QMS expectations.
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Promote and participate in continuous improvement initiatives to reduce risks, process deviations, and recurring nonconformities.
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Support risk assessments related to manufacturing processes, operational changes, and quality systems.
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Maintain objective evidence and quality records required to demonstrate compliance during audits.
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Monitor action plans resulting from audits, quality issues, process deviations, and compliance findings.
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Support process standardization across manufacturing operations.
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Identify opportunities to improve the effectiveness and efficiency of the Quality Management System.
Bachelor's degree in:
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Industrial Engineering
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Manufacturing Engineering
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Quality Engineering
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Mechanical Engineering
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Electromechanical Engineering
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Industrial Management
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Or a related engineering or technical field.
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Minimum 2–3 years of experience in Quality Management Systems within a manufacturing environment.
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Hands-on experience with ISO 9001 requirements and implementation.
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Experience conducting internal audits and supporting external audits.
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Experience managing corrective actions and nonconformities.
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Experience with document control and QMS documentation.
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Experience working with cross-functional manufacturing teams.
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Experience in the metal-mechanical, automotive, refrigeration, electronics, or high-volume manufacturing industry is preferred.
