- Review Quality Management System policies & procedures updates and controls
- Maintain administrative document and record retention controls
- Execute operating facilities internal/external audit; readiness, scheduling, payments, and report management
- Develop and manage the QA training program
- Develop expertise with regards to industry policy, regulatory rules and actions as well as industry association rules and actions
- Provide leadership & guidance with regards to impact of proposed or released industry regulatory and/or association rule changes as it affects the Quality Management System
- Exude complex problem solving activities within manufacturing or engineering
- Work with appropriate manufacturing and supplier personnel for facility certification
- Collaborate with other departments to exchange quality information and to promote quality principals
- Participate in meetings and provides training as required
- Bachelor's degree required, technical discipline preferred
- 5 years of Quality Assurance, Manufacturing, or Engineering experience
- Strong interpersonal skills, ethics, and an energetic attitude
- Attention to detail, must be meticulous and consistent
- Strong communication, presentation, and organizational skills
- Experience with MS Office Suite, MS SharePoint
- Ability to conceptualize, analyze, plan and organize projects
- Ability to interpret and evaluate engineering drawings and regulatory codes
- Knowledge of manufacturing processes, product testing, standards and/or regulations
- Willingness to learn about Welding, Coatings, and NDT principles, disciplines, and science
- Six Sigma or Lean skills and tools exposure is a plus
- Travel up to 20% - Must be able to travel to Mexico and Canada
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Quality Compliance Specialist - Dallas, United States - Trinity Industries
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Description
TrinityRail is hiring a Quality Compliance Specialist at our Dallas, TX HQ.
Apply promptly A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.
What you'll do:
What you'll need:
*THIS IS NOT AN IT OR MEDICAL RELATED ROLE*
EOE