Carestream
Carestream
Carestream izstrādā attēlveidošanas risinājumus, ko izmanto tādās veselības aprūpes jomās kā pediatrija, sporta medicīna un veterinārmedicīna, kā arī nesagraujošās pārbaudes tehnoloģijas drošībai kritiski svarīgām nozarēm, tostarp aviācijai un cauruļvadu pārvaldībai. Uzņēmums apvieno veselības aprūpes attēlveidošanas, ražošanas un tehnisko kompetenci, īpašu uzmanību pievēršot inovācijām un izcilai darbības kvalitātei. Tā karjeras profils atspoguļo lielu starptautisku organizāciju, kurā darbinieki palīdz izstrādāt produktus un pakalpojumus, kas atbalsta klīnisko lēmumu pieņemšanu un rūpniecisko drošību.

Senior NDT Quality Engineer

Lead quality engineering across Carestream Health’s NDT manufacturing operations, overseeing quality systems and process controls. Drive audits, investigations, corrective actions, validation, and product quality improvements.

Apraksts

  • Serve as the quality subject matter expert for NDT manufacturing operations.
  • Provide hands-on quality engineering support and lead quality activities across electromechanical assembly, testing, inspection, packaging, and service.
  • Ensure products and processes meet approved specifications and quality requirements.
  • Initiate, conduct, lead, or facilitate investigations into manufacturing defects, nonconforming materials, supplier issues, service failures, and customer complaints.
  • Apply structured root-cause analysis, risk assessment, and corrective and preventive action methods.
  • Monitor and analyze supplier quality, product performance, and CAPA data.
  • Apply statistical methods and key metrics to identify trends, reduce defects, and improve process capability and product quality.
  • Develop and maintain control and inspection plans, sampling methods, acceptance criteria, quality procedures, work instructions, investigation reports, and other controlled quality records.
  • 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 improve product quality and operational performance.

Prasības

  • Bachelor’s degree in a STEM field, such as mechanical, electrical, industrial, manufacturing, or biomedical engineering, or a related discipline.
  • At least seven years of quality engineering experience.
  • Working knowledge of ISO 9001.
  • Experience applying quality-system, documentation, risk-management, and regulatory requirements in manufacturing.
  • Experience investigating product and process nonconformities.
  • Experience leading structured root-cause analysis.
  • Experience implementing lasting 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.
  • Supplier qualification, supplier audits, supplier corrective actions, statistical-analysis software, ERP systems, or electronic quality-management systems experience is desired.
  • Experience in diagnostic equipment, radiographic imaging, or another regulated manufacturing setting is desired.
  • Experience supporting electromechanical assembly, system-level testing, troubleshooting, returned-product analysis, installation, or service 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 or Black Belt, or ISO 13485 or ISO 9001 audit certification or training is preferred.

Priekšrocības

  • Home office arrangements for positions eligible for remote work.
  • Reasonable accommodations for individuals with disabilities.

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