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Quality Engineer

Sriven Systems Inc.

Illinois, United States · Sözleşme

Başvuran ilk kişi siz olun

Deneyim
5+ yıl
Maaş
Açılışlar
1
Yayınlandı
2 saat önce
Çalışma modu
Ofiste
Sürdürmek
Başvuru yapılması gerekmektedir.

İş tanımı

Job Overview

Seeking an experienced Quality Engineer to lead quality enhancement and project management efforts in a manufacturing setting. This role involves managing multiple cross-departmental projects from conception to production, ensuring products meet regulatory standards, quality benchmarks, and delivery timelines.

Key Responsibilities

  • Oversee quality engineering projects with comprehensive control over scope, schedule, budget, and risk factors.
  • Guide collaborative teams that include Engineering, Manufacturing, Quality Assurance, Supply Chain, and Suppliers.
  • Support stages including New Product Introduction, process transitions, launch activities, and readiness for manufacturing.
  • Plan and carry out validation procedures such as IQ/OQ/PQ, along with APQP, PPAP, FMEA, control plans, and process qualifications.
  • Perform in-depth root cause evaluations employing 8D, Fishbone diagrams, and 5 Whys techniques to solve quality problems and implement corrective actions.
  • Implement continuous improvement leveraging Lean principles, Six Sigma methodologies, and statistical tools.
  • Manage Engineering Change Orders and maintain robust change control and documentation.
  • Coordinate supplier quality audits, inspections, and oversee corrective measures as needed.
  • Monitor key performance indicators and deliver concise status updates and presentations to leadership teams.
  • Maintain compliance with industry regulations such as ISO 9001, ISO 13485, AS9100, IATF 16949, and FDA/cGMP as relevant.

Required Qualifications and Skills

  • Proficiency in project management tools including MS Project, Smartsheet, and Primavera.
  • Deep knowledge of quality engineering practices in manufacturing environments.
  • Experience with CAPA processes, NCR documentation, and root cause analysis (8D, 5 Whys).
  • Competence in APQP, PPAP, DFMEA/PFMEA, and development of control plans.
  • Expertise in IQ/OQ/PQ validation and verification procedures.
  • Strong background in Lean Manufacturing techniques and Six Sigma practices.
  • Applied skills in GD&T, Statistical Process Control, and statistical software such as Minitab.
  • Experience managing supplier quality, conducting audits, and overseeing corrective actions.
  • Effective cross-functional leadership and superior communication abilities.

Industries Served

  • Medical Devices
  • Automotive
  • Aerospace
  • Industrial Manufacturing
  • Pharmaceutical Manufacturing
  • Consumer Products

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