About The Position

The Quality Assurance Systems Engineer supports the maintenance, implementation, and continual improvement of the TAS Quality Management System (QMS). The role partners with process owners and cross-functional teams to strengthen audit readiness, corrective action, risk management, document and change control, quality data analysis, and process improvement. It helps ensure quality processes are documented, implemented, monitored, and improved in accordance with applicable standards, customer and regulatory requirements, and TAS procedures. The role supports quality-system activities across TAS locations and works with Quality, Engineering, Production, Supply Chain, Project Management, and other process owners. It is primarily office-based, with possible visits to manufacturing areas and job sites. Travel between TAS facilities and job sites may be required as business needs require. TAS is a Houston-headquartered company that develops and manufactures packaged modular systems used in data centers, power, and commercial and industrial utility applications. Its five ISO 9001-certified manufacturing facilities are in Houston. TAS is part of Comfort Systems USA, a publicly traded company.

Requirements

  • At least five years of experience in quality assurance, quality systems, manufacturing quality, engineering, or a related field.
  • Experience supporting a Quality Management System in a manufacturing or engineered-to-order environment.
  • Experience with audits, nonconformance investigations, corrective actions, controlled documentation, and process improvement.
  • Experience facilitating root cause analysis and working with cross-functional teams to implement sustainable corrective actions.
  • Strong working knowledge of ISO 9001 quality management system requirements and audit principles.
  • Knowledge of corrective action, root cause analysis, risk management, FMEA/PFMEA, document control, change control, and continual improvement methods.
  • Ability to interpret procedures, specifications, engineering drawings, standards, and customer requirements.
  • Strong technical writing skills, including the ability to create clear, controlled, audit-ready documentation.
  • Ability to organize and facilitate cross-functional meetings, follow up on action items, and drive timely closure.
  • Strong analytical and problem-solving skills, including identifying trends and evaluating corrective-action effectiveness.
  • Ability to manage multiple priorities, projects, and deadlines with limited supervision.
  • Effective written, verbal, presentation, training, and interpersonal communication skills.
  • Proficiency with Microsoft Office applications and quality management or workflow software.
  • Ability to collaborate with Quality, Engineering, Production, Supply Chain, Project Management, and other process owners.
  • Ability to travel between TAS facilities and job sites as business needs require.
  • Commitment to TAS core values: Safety, Integrity, Teamwork, Customer Passion, Growth Oriented, Innovation, and Value Driven.
  • Bachelor's degree in Engineering, Quality, Manufacturing, Industrial Technology, or a related technical discipline from an accredited program, or an equivalent combination of education and relevant experience.

Nice To Haves

  • Experience with Intellect, Power BI, GoCanvas, or similar systems.
  • Working knowledge of manufacturing, fabrication, welding, coating, assembly, inspection, and modular construction processes.
  • Internal Auditor or Lead Auditor training for ISO 9001.
  • ASQ certification such as Certified Quality Engineer (CQE) or Certified Quality Auditor (CQA).
  • Lean Six Sigma Green Belt or higher certification.
  • Experience in modular construction, industrial manufacturing, fabrication, welding, coating, mechanical, or electrical assembly environments.
  • Experience with supplier quality, quality planning, control plans, FMEA/PFMEA, and statistical or trend analysis.
  • Experience supporting certification, customer, regulatory, and third-party audits.
  • Experience managing document control processes.
  • Knowledge of additional standards applicable to TAS operations, such as ISO 14001, ISO 45001, ISO 3834, AISC 207, CSA A277, or ISO 22301.

Responsibilities

  • Support the maintenance, implementation, and continual improvement of the TAS Quality Management System.
  • Coordinate and support internal, customer, certification, regulatory, and supplier audits, including preparation, evidence collection, response development, and follow-up.
  • Track audit findings, NCRs, CARs, and SCARs through containment, root cause, corrective action, effectiveness verification, and closure.
  • Facilitate structured root cause analysis using methods such as 5 Why, Fishbone/Ishikawa, 8D, Pareto analysis, change analysis, or DMAIC.
  • Develop, revise, review, and maintain controlled procedures, work instructions, forms, templates, and records.
  • Administer document and change control to ensure approved revisions are communicated, implemented, and available at points of use.
  • Partner with process owners to evaluate process changes for impacts to quality requirements, risk, documentation, training, resources, and compliance.
  • Support development and maintenance of FMEAs, PFMEAs, risk assessments, control plans, and quality planning tools.
  • Analyze quality data, audit results, nonconformance trends, and recurring issues to identify systemic risks and improvement opportunities.
  • Prepare accurate, audit-ready reports, presentations, dashboards, and management review inputs.
  • Develop and deliver training for new or revised quality processes, procedures, systems, and tools.
  • Promote quality awareness, risk-based thinking, accountability, and consistent application of the QMS across TAS locations.
  • Stay current on standards, codes, customer requirements, and regulations relevant to TAS operations.
  • Support achievement of Quality department objectives and perform other duties assigned by TAS.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service