Quality Management Systems Specialist
Listed on 2026-06-03
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Quality Assurance - QA/QC
Quality Engineering, QA Specialist / Manager -
Engineering
Quality Engineering, QA Specialist / Manager
Compensation
USD 80,000 - USD 105,000 per year.
Company DescriptionVeolia 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.
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. The role is 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 develop training materials to continually improve an ISO certified site, evaluate risk to the organization and its customers by auditing product quality plans, design and development records, and other QMS related documented information. The specialist coordinates site‑wide customer and third‑party compliance audits, recommends corrective actions and risk‑reducing measures based on trends in audit findings.
- Lead the development, implementation, and improvement of the company’s QMS to maintain compliance with 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 systems.
- 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 its 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.
- Ensure processes for products and services conform to established company, customer, and regulatory requirements.
- Support product compliance regulations (RoHS, REACH, Conflict Minerals, etc.) and document compliance for customer inquiries.
- Review, analyze and report on quality discrepancies related to processes.
- Improve training and auditing while following up with process owners for lean, focused improvements leveraging the Plan‑Do‑Check‑Act (PDCA) cycle.
- Comply with all company policies including inclusion and diversity, quality, and environmental, health, and safety.
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.
- Experience developing QMS documents, procedures, and working instructions.
- Experience with problem‑solving methodologies such as PDCA, 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 17034:2016…
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