Iso Coordinator

**Acosta Employment Agency is recruiting for an important company in San**

**Antonio, Tx.**

**ISO COORDINATOR**

**_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 up-to 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 non-conformances.

**_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 non-conforming 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 solutions/corrective actions are implemented.
- Initiate action to prevent the occurrence and recurrence of non-conforming 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 follow-up 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 follow-up
- 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 9001:2015, others as needed
- Provide leadership and assist in corrective action plans
- Experience/Knowledge in Automotive Manufacturing preferred but not required

**_Qualifications_**
- Bachelor's 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 (English/Spanish).

**_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.

Tipo de puesto: Tiempo completo

Salario: A partir de $1.00 al mes

Horario:

- Lunes a viernes