QMS Coordinator

Lear Corporation•Grand Prairie, TX

17h•Onsite

About The Position

As a member of the Quality team, the QMS Coordinator will be responsible for the application, sustaining, improving, and auditing of Lear Grand Prairie’s internal quality operating system, ISO 9001: IATF 16949 standard, and customer identified Quality System requirements.

Requirements

Bachelor's degree from an accredited institution
3 years in Quality with manufacturing experience
Strong communication and coordination skills
Experience in Management Systems
Internal Audit qualification in the relevant management systems (i.e., ISO 9001 / IATF 16949)
Expert in problem solving and analytical skills using 8D methodology
Demonstrated ability to motivate people.

Nice To Haves

Expert in Customer Specific requirements
Competent in quality tools, and process/production control methods such as: Problem Solving PFMEA PPAP Capability/Statistics
External audit qualification in relevant quality systems
Proficient with Microsoft Office applications (Word, Excel, PowerPoint, etc.)
Experience with APiS Control Document software or equivalent

Responsibilities

Primary Lead QMS auditor and as required, leads gap assessment activities on applicable procedures to ensure compliance with system requirements.
Primary owner of ISO 9001/IATF 16949 compliance and sustaining conformity for the Lear Grand Prairie plant
Confirm the completion of internal and external management systems audits in accordance with formal audit plans and the effectiveness of identified corrective actions.
Responsible for the organization and participation in external audits conducted by the defined Registrar/Certification Body
Includes the review, follow up, and closure confirmation of corrective actions associated with documented observations or non-conformances.
Provide support and coaching to the plant’s Process Owners, ensuring that all procedures adhere to the standard format requirements.
Coordinate Layered Process Audits (LPA) including generating formal audit plan/schedule and confirmation of completion and follow up on the effectiveness of implemented corrective actions.
Enter weekly/monthly QRS (Quality Report System) information (pieces shipped, IPPM) to LQTS database.
Enter corrective actions from Major Non-Conformance resulting from ISO 9001/IATF 16949 audits to LQTS database.
Internal tracking log (Corrective Action Tracker w/Internal Audit schedule)
Participate in monthly MOS meetings & annual/semi-annual Management Review meetings, contributing to decisions that improve the effectiveness of the plant operating and quality management systems.
Update quality MOS charts for monthly meetings, record and distribute minutes.
Enter monthly MOS key measurable information into MOS-Data Entry database.
Update First Site information center of key measurable MOS charts.