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Quality Management Systems Specialist

Job in Boulder, Boulder County, Colorado, 80301, USA
Listing for: Sarpi Thinktech
Full Time position
Listed on 2026-06-03
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, QA Specialist / Manager
  • Engineering
    Quality Engineering, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Quality Management Systems Specialist

Veolia Group is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia Group designs and implements innovative solutions for decarbonization, depollution, and resource regeneration, supporting communities and industries in their ecological transformation. Within this framework, Veolia's Water Technology Business brings together a dedicated team of experienced professionals committed to tackling the world's most complex challenges related to water scarcity, quality, productivity, and energy.

Together, we pursue a shared mission to create a more sustainable future.

Job Description

Position Summary

Our Analytical Solutions product line business has an exciting opportunity available for a Quality Management System (QMS) Specialist. The QMS Specialist will be responsible for managing all aspects of site-wide ISO compliance efforts including, facilitating external and internal audits of the quality management system and product regulatory compliance. A key interface with operations, engineering, manufacturing, supply chain, logistics, customers, vendors, and third-party compliance partners to ensure quality management systems requirements are met.

The person in this role must have the ability to develop training materials to continually improve an ISO certified site. Evaluate risk to the organization and its customers by auditing product quality plans, product design and development records, and other QMS related documented information. Coordinates site-wide customer and third-party compliance audits. Make recommendations for corrective actions and risk reducing measures, based on trends in audit findings.

Key Responsibilities:

  • Lead the development, implementation, and improvement of Company s QMS to maintain compliance to ISO requirements (ISO 9001, ISO 17025, and ISO 17034)
  • Author, review or revise QMS relevant controlled documents
  • Support QMS alignment with other company programs and management system
  • Coordinate QMS internal and external audits
  • Administrator for QMS related business systems such as QMS document control, QMS record controls, and QMS learning management
  • Develop and facilitate QMS training plans
  • Manage the QMS Corrective Actions process and confirm effectiveness
  • Develop, implement, maintain and improve quality assurance systems, including tools, policies, training and processes
  • Assist problem solving team and participate in continuous improvement initiatives
  • Manage quality data for accuracy and report generation
  • Ensures processes for products and services conform to established company, customer, and regulatory requirements
  • Supports product compliance regulations (RoHS, REACH, Conflict Minerals, etc.) and documents compliance for customer inquiries
  • Reviews, analyzes and reports on quality discrepancies related to processes
  • Improves training and auditing along with following up with process owners for lean, focused improvements while leveraging the Plan-Do-Check-Act (PDCA) cycle
  • Comply with all company policies including inclusion and diversity, quality, and environmental, health, and safety.
Qualifications

The ideal candidate will have excellent quality compliance skills and experience to be part of a high performing quality team to ensure regulatory compliance in an exciting, fast-paced business. This role will help develop and lead compliance to international quality standards, lead change throughout the business, partner cross-functionally to innovate new ideas, and implement best-in-class quality programs.

Knowledge, Skills, and Abilities:

  • Quality Assurance and/or Lean Six Sigma Certification
  • Certified lead auditor ISO 9001:2015 and working experience as an ISO internal auditor
  • Project planning and organization
  • Working experience of developing QMS documents, procedures, and working instructions
  • Experience in problem solving methodologies such as PDCA (Plan Do Check Act), root cause corrective action (RCA and CAPA), etc.
  • Knowledge and application of quality concepts such as Lean Manufacturing, 5s, Six Sigma, ISO 9001:2015, ISO 17025:2017, ISO…
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