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Carestream

Senior NDT Quality Engineer

Carestream

. Serve as the Quality Subject Matter Expert for NDT manufacturing operations .

Posted 10/10/2026full-timeRochester • New York • United StatesSenior💰 $103,600 - $138,100 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in quality engineering within NDT manufacturing operations, focusing on root-cause analysis, process validation, and supplier quality management. Proficient in developing quality documentation and implementing corrective actions to ensure compliance with industry standards.

Highest-signal resume keywords
Quality Engineering ExperienceRoot-Cause AnalysisISO 9001 KnowledgeStatistical Process ControlSupplier Quality Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Quality System DocumentationProcess ValidationStatistical AnalysisManufacturing Data AnalysisInspection Plans DevelopmentCorrective and Preventive ActionsRisk ManagementChange Control ActivitiesElectromechanical Assembly SupportTroubleshooting
Soft Skills
Analytical SkillsProject ManagementWritten CommunicationVerbal Communication
Tools & Technologies
Statistical-Analysis SoftwareEnterprise Resource Planning SystemsElectronic Quality-Management Systems
Certifications & Qualifications
ASQ Certified Quality EngineerLean Six Sigma Green BeltLean Six Sigma Black BeltISO 13485 CertificationISO 9001 Audit Certification
Industry Keywords
NDT ManufacturingElectromechanical AssemblyRegulated Manufacturing EnvironmentSupplier AuditsManufacturing DefectsNonconforming MaterialCustomer ComplaintsCAPA DataQuality ProceduresAcceptance Criteria

Tech Stack

Tools & technologies
Assembly

About the role

Key responsibilities & impact
  • Serve as the Quality Subject Matter Expert for NDT manufacturing operations
  • Provide hands-on quality engineering support and lead quality activities for electromechanical assembly, testing, inspection, packaging, and service operations
  • Ensure products and processes meet approved specifications and quality requirements
  • Initiate, conduct, lead, or facilitate investigations of manufacturing defects, nonconforming material, supplier issues, service failures, and customer complaints
  • Use structured root-cause analysis, risk assessment, and corrective and preventive action methods
  • Monitor and analyze supplier quality, product performance, and CAPA data
  • Use statistical methods and key metrics to identify trends, reduce defects, and improve process capability and product quality
  • Develop and maintain control plans, inspection plans, sampling methods, acceptance criteria, quality procedures, work instructions, investigation reports, and other controlled quality documentation
  • Plan, review, and execute qualification, manufacturing validation, measurement-system, and change-control activities
  • Conduct internal, external, customer, and regulatory audits
  • Partner with Manufacturing, Supply Chain, and Engineering to drive product quality and operational excellence

Requirements

What you’ll need
  • Bachelor’s degree in any STEM field, including mechanical, electrical, industrial, manufacturing, biomedical, or a related engineering discipline
  • Minimum 7 years of quality engineering experience
  • Working knowledge of ISO 9001
  • Experience applying quality-system, documentation, risk-management, and regulatory requirements within a manufacturing environment
  • Experience investigating product and process nonconformities
  • Experience leading structured root-cause analysis
  • Experience implementing sustainable corrective and preventive actions
  • Experience analyzing manufacturing data
  • Experience developing process controls, inspection plans, acceptance criteria, validation documentation, or other manufacturing quality records
  • Strong analytical, project-management, written, and verbal communication skills
  • Experience with supplier qualification, supplier audits, supplier corrective actions, statistical-analysis software, enterprise resource planning systems, or electronic quality-management systems is desired
  • Experience in diagnostic-equipment, radiographic-imaging, or another regulated manufacturing environment is desired
  • Experience supporting electromechanical assembly, system-level testing, troubleshooting, returned-product analysis, installation, or service operations is desired
  • Experience with process validation, equipment qualification, test-method validation, measurement-system analysis, statistical process control, process capability analysis, or design of experiments is desired
  • ASQ Certified Quality Engineer, Lean Six Sigma Green Belt or Black Belt, or ISO 13485 or ISO 9001 audit certification or training is preferred

Benefits

Comp & perks
  • Home office settings for remote eligible positions
  • Reasonable accommodations for individuals with disabilities