Quality Systems Coordinator - Ciudad Juarez, México - Ergomotion

Descripción

Under general guidance, will ensure maintenance of Keeson's Quality Management System (QMS) standards and processes in North America to ensure products meet defined standards and requirements.

• Maintain all relevant systems, procedures, standards & requirements as defined/outlined in the Keeson Quality Management System (QMS).
• Interface with appropriate departments and customers to ensure products are produced to the required standards.
• Maintain strong relationships with internal and external stakeholders to ensure optimal performance of QMS related objectives.
• Respond rapidly to questions from factory employees, Ergomotion and Keeson teams, customers, and management to meet production Quality Goals and customer needs; provide technical expertise as required.
• Work collaboratively with key stakeholders to facilitate delivery and compliance with Keeson's Quality Management System.
• Undertake internal and process audits of the QMS as directed.
• Pursue thorough investigation of root cause to Ensure corrective actions & preventative measure are sufficient for addressing nonconformities.
• Verify closure of nonconformities via confirmation of corrective action/preventative measure effectiveness through data collection.
• Organize and compile quality data to achieve clear, consistent, efficient processing and reporting of Quality Statistics.
• Liaise between customers, Ergomotion and Keeson teams regarding Quality Issues, Product Performance, requirements & standards.
• Maintain the Quality Assurance process to support continuous quality improvement as necessary through audit reviews & reporting procedures.
• Maintain quality data in an orderly, systematic, and usable form to allow for accurate, and retrievable information in a timely manner.
• Provide input into the corrective action process that includes collecting, monitoring, organizing, resolving, and providing timely feedback on quality issues.
• Maintain formalized RCCA (Root Cause Corrective Action) reporting for North America.

• Associate degree in related field plus 2 years quality systems experience, or equivalent, preferably in a highvolume manufacturing environment.

• Availability to work extended hours including occasional nights, weekends, and holidays.
• Willingness to travel up to 20% of time (domestic & international).

• Fluent English (required)
• Fluent Spanish (required)