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Quality Management Systems Coordinator

Quality Management Systems Coordinator

General Plastics & CompositesHouston, TX , USA
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Job Details

Description

JOB SUMMARY :

The QMS (Quality Management System) Coordinator is responsible for managing and maintaining the company’s Quality Management System (QMS), including documentation, employee training records, and quality records. This role supports internal audits and may assist with customer-facing documentation, such as DataBooks, as part of cross-training for PTO coverage. In addition to core QMS administration tasks, the QMS Coordinator plays a key role in the digital transformation of the QMS, supporting the implementation of paperless processes and system improvements. The role ensures compliance with ISO 9001 and AS9100 standards, helps streamline documentation and training processes across departments, and collaborates cross-functionally to improve QMS effectiveness and elevate the maturity of the Quality function.

ESSENTIAL DUTIES & RESPONSIBILITIES :

  • QMS Document Control

oManage all QMS documents, including procedures, work instructions, forms, and manuals; ensure revision control and proper approvals.

oSupport other departments in formatting and publishing controlled documents in compliance with company standards.

oEnsure compliance with customer-specific documentation requirements.

  • Training Management
  • oMaintain and update the training matrix or requirements based on role responsibilities.

    oAssign, track, and follow up on training completions for all employees through the QMS or LMS system.

    oCoordinate onboarding training and ensure proper documentation of training records.

    oSupport audit readiness by ensuring training documentation is complete and current.

  • Record Management
  • oCollect, scan, and archive quality records (e.g., inspection records, certifications, work orders).

    oOrganize and maintain electronic and hard copy files in compliance with the company’s record retention policy.

    oRetrieve and prepare quality records as needed for audits or customer requests.

    oAssist the Sales team with documentation requests for customers.

    oAssist in record review to ensure completeness, accuracy and compliance with AS9100 requirements.

  • Internal Audit and Corrective Action Support
  • oAssist in internal process audits and maintaining audit records.

    oSupport internal auditors by managing documentation and tracking / reporting audit trends.

    oEnsure proper storage and organization of audit records.

    oSupport Quality Engineers and team members in filing and organizing evidence related to corrective actions (e.g., photos, training records, updated work instructions).

    oHelp monitor due dates and status of open actions and escalate delays to responsible parties.

  • Customer-Facing Documentation (PTO Coverage Only)
  • oProvide coverage for customer-facing documentation tasks, such as DataBooks, manufacturing record books, and instructions / O&M manuals as part of cross-training during Document Coordinator’s absences.

  • Quality System Support & Improvement
  • oAct as an administrator of QMS software (e.g., QISS) for managing documents and training modules.

    oLead or support initiatives to digitize and automate QMS processes, moving toward a paperless quality system.

    oIdentify and support continuous improvement opportunities related to QMS documentation, records and training management processes.

    oProvide high-level service to both internal and external customers in all quality-related documentation activities.

    oSupport Quality Engineers and Managers in process improvement, data tracking, and risk-based documentation strategies.

  • General Expectations
  • oCross-train with the Document Coordinator for backup coverage as needed.

    oFollow all GP&C safety, quality, and business procedures and maintain a clean and safe working environment.

    oReport all safety incidents, near misses, and injuries immediately.

    oPromote teamwork, communication, and a positive working environment.

    oPerform other duties as assigned by the Quality Manager.

    QUALIFITCATIONS & EXPERIENCE :

  • Bachelor’s degree preferred or equivalent experience in quality, business systems, or related field.
  • 3+ years of experience in document control and QMS administration in a manufacturing environment.
  • Working knowledge of ISO 9001; AS9100 experience preferred.
  • Experience with QMS software implementation, configuration, or digital workflows is a strong plus.
  • Familiarity with paperless systems or digitization initiatives is highly desirable.
  • Strong organizational skills and attention to detail.
  • Strong communication and interpersonal skills, problem-solving ability, and the capacity to manage a heavy and varied workload.
  • Ability to work independently and collaboratively across departments.
  • Basic math skills.
  • Ability to read and write English.
  • Experience with quality principles and documentation requirements.
  • Intermediate proficiency in MS Windows programs; ERP systems, Adobe Acrobat, and Excel proficiency preferred.
  • Ability to learn and adapt to new software tools as required.
  • PHYSICAL REQUIREMENTS & WORK ENVIRONMENT :

  • Mobility throughout the entire plant.
  • Ability to lift a minimum of 30 pounds throughout the shift.
  • Visual and hearing abilities with or without correction.
  • Note : If corrective lenses or glasses are required per employee’s driver’s license, the same will be required when performing duties.
  • Qualifications

    Skills

    Behaviors

    Motivations

    Education

    Experience

    Licenses & Certifications

    Equal Opportunity Employer

    This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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    Quality Coordinator • Houston, TX , USA