Sr Engineer Process Engineering Implant

GlobalFoundriesNew York, NY
Onsite

About The Position

Develop and modify process formulations, methods and controls to meet quality standards. Create, analyze and review technical charts. Establish SOP (Standard operating process) and FMEA (Failure mode and effects analysis) for related process. Review product development requirements for compatibility with processing methods to determine costs and schedules. Integrate equipment and material capabilities to meet process module and technology specifications. Design, execute, and analyze experiments to develop advanced Frontend-of-line (FEOL), Middle-of-line (MOL) Implant processes to meet technology (e.g. performance, yield, and reliability) and manufacturing (e.g. process stability, cost of ownership) targets. Support the cross functions team and Quality organization to ensure technology meets qualification and reliability requirements. Drive CIP (Continuous improvement plans) to improve process performance indices. Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements. Work and collaborate other projects and/or assignments as needed.

Requirements

  • Bachelor’s degree in Chemical Engineering, a related field, or a foreign equivalent
  • 2 years of progressively responsible post-baccalaureate experience in job offered or any engineering related job titles.
  • Applicant must possess at least 2 years of experience in (1) SPC tools to monitor and control the quality of manufacturing processes; (2) FMEA line yield improvements; (3) Design of Experiments & JMP; (4) Tool matching and performance improvements; (5) Frontend-of-line (FEOL), Middle-of-line (MOL) Implant processes to meet technology (e.g. performance, yield, and reliability); (6) aligning product development requirements for compatibility with processing methods; (7) semiconductor process engineering; and (8) implant equipment operation and troubleshooting.

Responsibilities

  • Develop and modify process formulations, methods and controls to meet quality standards.
  • Create, analyze and review technical charts.
  • Develop and modify process formulations, methods and controls to meet quality standards.
  • Establish SOP (Standard operating process) and FMEA (Failure mode and effects analysis) for related process.
  • Review product development requirements for compatibility with processing methods to determine costs and schedules.
  • Integrate equipment and material capabilities to meet process module and technology specifications.
  • Design, execute, and analyze experiments to develop advanced Frontend-of-line (FEOL), Middle-of-line (MOL) Implant processes to meet technology (e.g. performance, yield, and reliability) and manufacturing (e.g. process stability, cost of ownership) targets.
  • Support the cross functions team and Quality organization to ensure technology meets qualification and reliability requirements.
  • Drive CIP (Continuous improvement plans) to improve process performance indices.
  • Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements.
  • Work and collaborate other projects and/or assignments as needed.
  • Perform all activities in a safe and responsible manner and support all Environmental, Health, Safety & Security requirements, and programs.
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