ISO CORDINADOR
Descripción de la oferta de empleo
ISO COORDINATOR
Note The candidate must be Authorized to work in the United States the company can help with the process.
Job Summary
The ISO Quality Management System Coordinator is responsible to prepare, support, and conduct internal and third party quality audits. Work with external representatives, department and company leaders to develop schedules, review documents and procedures, gather and evaluate information related to quality assurance and summarize and report findings. Maintain an upto date working knowledge of quality systems, methods, and processes in order to conduct audits or advise and consult with internal and external customers. Control adherence to QMS document review periods and health, maintenance and control of QMS document system. Other duties include maintaining company quality systems, contributing to improvement projects, and supporting customers and internal activities to resolve nonconformances.
Responsibilities
Planning
Plan Audit Objectives and Schedule.
Assist with the development and maintenance of Internal Audit Schedule.
Gather information from production, service, development and supporting activities.
Analyze quality systems and previous audit information from multiple sources.
Lead Auditor assist with audit team selection and audit plan preparation.
Represent the audit team with management of the audited areas and with third party auditors.
Conduct Quality Audits
Perform planned and periodic internal quality system assessment.
Gather relevant information from personnel about the approach, deployment, and results of processes and systems.
Identify nonconforming conditions requiring corrective actions, strengths, and opportunities for improvement.
Analyze findings and create summary presentation.
Facilitate closing meeting to review and interpret results with management.
Compile and issue a formal report detailing results.
Follow up on audits to ensure that solutionscorrective actions are implemented.
Initiate action to prevent the occurrence and recurrence of nonconforming conditions.
Assist with determination of corrective actions and continuous improvement.
Support External Audits ISO Registrar, Customer
Respond to auditor requests.
Coordinate audit schedule and logistics.
Prepare audit participants and areas.
Participate or conduct tour.
Coordinate post audit followup and corrective actions.
Support Improvement of the Quality Management System
Maintain and improve the quality management system through assessment and sharing best practices
Support improvement of the quality assessment process
Participate in quality improvement projects
Provide access to standards and documentation
Assist, develop and maintain Quality management systems and internal procedures and systems
Update QMS to meet current system requirements
Provide Customer Support
Communicate assessment findings with stakeholders to ensure intentions and conclusions are fully understood
Consult with company or department representatives regarding quality requirements
Assist in the development and implementation of a Quality Management System for assigned sites, departments, or areas.
Knowledge and Skills Required
Ability to coordinate efficiently to plan, execute audits and followup
Working knowledge of QMS document systems and control practices
Excellent problem solving, presentation, and communication skills
Ability to work independently or in teams
Preferably with knowledge of ISO 90012015, others as needed
Provide leadership and assist in corrective action plans
ExperienceKnowledge in Automotive Manufacturing preferred but not required
Qualifications
Bachelors Degree in Engineering or other technical field required. An equivalent combination of education and experience may be considered.
Certification, such as Lead Assessor course in ISO 9001, Quality Auditor, Six Sigma, or Quality
Improvement Associate preferred Proven experience with use of quality tools FMEA, SPC, 8D, others.
3 to 5 years of work experience in QMS Audits or experience in managing and maintaining quality management system in manufacturing environment.
Fully Bilingual EnglishSpanish.
Physical Demands
Work on office and manufacturing environment
Able to lift at least 30 lbs.
Standing, sitting, walking, reaching with hands and arms.
Standing, sitting, walking, stooping, kneeling, crouching, use of hands to inspect parts, tools or controls.
Occasionally lift and or move product tools, etc.
Working Conditions
Day shift position
Occasional travel to sister companies
Flexible hours to validate and ensure proper implementation of process changes
Fast pace manufacturing environment.
Exposure with Injection molding, paint and assembly process. Tier 1 preferred.
Bolsa de trabajo México ofrecemos puesto de ISO Cordinador para el sector de Investigacion y Calidad en la empresa Acosta Employment de Juárez. Salario acorde a tu experiencia y al salario medio del sector. Actualiza ahora tu currículum vitae y postúlate a este empleo. Tipo de empleo Tiempo Completo.
Detalles de la oferta
- Acosta Employment
- En todo México
- Sin especificar - Sin especificar
- 26/10/2024
- 24/01/2025
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