Quality Management Systems Manager

Integra Mission CriticalHouston, TX
Onsite

About The Position

The Quality Management Systems Manager is responsible for leading the design, governance, administration, and continuous improvement of Integra’s Quality Management System (QMS) across corporate, engineering, manufacturing, integration, commissioning, and field services operations. This role serves as the operational owner of the QMS, ensuring that processes, procedures, records, roles, responsibilities, metrics, audits, corrective actions, and management review activities are clearly defined, consistently executed, and aligned with ISO 9001 principles, customer requirements, regulatory expectations, and Integra’s business objectives. Working closely with Operational Excellence, Manufacturing Quality, Engineering Quality, Supplier Quality, and field operations, the Quality Management Systems Manager strengthens process discipline, audit readiness, document control, performance visibility, and continual improvement across a multi-site, mission-critical environment.

Requirements

  • Minimum of 10 to 12 years of progressive experience in quality management systems, quality assurance, internal auditing, document control, corrective action management, process governance, or QMS administration within manufacturing, engineering, construction, mission-critical, industrial, energy, or complex equipment environments.
  • At least 3 to 5 years of experience leading QMS programs, audit programs, process improvement initiatives, people, or cross-functional quality system activities.
  • Bachelor’s degree in engineering, quality management, industrial technology, construction management, business, or a related technical field preferred; equivalent experience may be considered.
  • ISO 9001 Lead Auditor certification strongly preferred; ASQ, Six Sigma, Lean, Certified Manager of Quality/Organizational Excellence, or related quality credentials are a plus.
  • Demonstrated experience maintaining, improving, or scaling a QMS; managing internal audit programs; supporting external audits; facilitating management review; and driving corrective action closure across multiple functions or sites.
  • Strong working knowledge of ISO 9001 principles, process ownership, risk-based thinking, management review, internal auditing, root cause analysis, CAPA, document control, records management, training compliance, and QMS performance metrics.
  • Excellent written and verbal communication skills, strong attention to detail, practical problem-solving ability, and confidence working with leaders, auditors, customers, process owners, and cross-functional teams.
  • Ability to travel domestically and internationally as required to support audits, site assessments, QMS deployment, and quality system improvement activities (10-20%).

Nice To Haves

  • ISO 9001 Lead Auditor certification strongly preferred
  • ASQ, Six Sigma, Lean, Certified Manager of Quality/Organizational Excellence, or related quality credentials are a plus.

Responsibilities

  • Own the administration, governance, and ongoing improvement of the Quality Management System, including process architecture, controlled documentation, records, procedures, standards, workflows, and system health monitoring.
  • Ensure QMS processes are clearly defined, assigned, communicated, and integrated into core business processes across corporate, manufacturing, integration, commissioning, engineering, supplier quality, and field teams.
  • Maintain alignment between the QMS, ISO 9001 principles, customer requirements, regulatory expectations, internal policies, and Integra’s enterprise quality operating model.
  • Partner with process owners to document, standardize, and improve key business processes using risk-based thinking, measurable controls, and clear ownership of QMS requirements.
  • Maintain quality frameworks, document control practices, records management, and data integrity controls that support standardized execution, traceability, compliance, and audit readiness.
  • Own and manage the QMS internal audit program, including annual audit planning, audit criteria, schedules, execution, reporting, finding closure, and effectiveness verification.
  • Serve as the primary company liaison for external quality system audits, registrar audits, customer audits, and applicable third-party quality organizations.
  • Coordinate audit preparation activities, ensuring objective evidence, records, process owners, audit responses, and corrective actions are complete, accurate, and available on schedule.
  • Lead management review planning and execution by consolidating QMS performance, audit results, corrective action status, customer feedback, process performance, risks, opportunities, resource needs, and improvement actions into an executive-ready summary.
  • Track decisions and actions from management review to ensure leadership commitments, resource needs, and improvement priorities are assigned, followed up, and closed effectively.
  • Strengthen corrective and preventive action processes, ensuring NCRs, audit findings, customer concerns, process gaps, and repeat issues are addressed through disciplined root cause analysis, containment, corrective action, and effectiveness checks.
  • Define, track, and report QMS performance metrics such as audit completion, finding closure, corrective action aging, repeat findings, document control performance, training compliance, customer feedback, and overall QMS effectiveness.
  • Analyze QMS data and quality trends to identify systemic gaps, process risks, recurring nonconformities, and improvement opportunities across functions and sites.
  • Partner with Operational Excellence, Continuous Improvement, and process owners to implement preventive controls, standardized work, and sustainable improvements that strengthen QMS maturity.
  • Stay current on ISO standard revisions, QMS best practices, audit expectations, lean/Six Sigma methods, and industry quality requirements that may affect Integra’s quality system and certification readiness.
  • Support process owners by clarifying QMS responsibilities, documentation expectations, audit evidence requirements, process controls, and improvement actions.
  • Develop and deliver QMS awareness, documentation, audit readiness, corrective action, and process compliance training for employees, leaders, and functional quality teams.
  • Support customer pre-qualification, sales, and project pursuit activities by coordinating accurate quality system responses, surveys, certifications, and controlled quality documentation.
  • Facilitate clear communication between quality specialists, operational leaders, engineering, manufacturing, commissioning, field teams, and executive management on QMS expectations, quality system performance, and improvement priorities.
  • Supervise, coach, and develop QMS coordination, audit support, documentation, and administrative personnel to ensure workload clarity, accountability, and timely completion of quality system activities.

Benefits

  • Competitive pay with incentive opportunities that recognize your results and contributions.
  • Medical, dental, and vision coverage that supports you and your family’s total well-being.
  • Life and disability insurance programs that provide protection when it matters most.
  • A variety of voluntary benefits so you can personalize coverage to fit your needs.
  • Generous paid time off to relax, travel, and maintain a healthy work-life balance.
  • Education assistance and tuition support to help you build skills and advance your career.
  • Retirement and savings programs that help you achieve long-term financial confidence.
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