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9 дней назад

Process Engineer III - Inspection (Relocation Assistance)

80 000 - 121 250$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
US
Релокация
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Process Engineer III - Inspection (Relocation Assistance) (Automated Inspection/GMP): Leading the reliability, validation, and inspection readiness of automated vision and inspection equipment in a GMP-regulated biomanufacturing environment with an accent on equipment performance, compliance, and throughput. Focus on optimizing detection capability, reducing false rejects and downtime, troubleshooting complex mechanical, electrical, controls, and vision issues, and driving lifecycle improvements.

Location: USA - OH - West Chester; relocation assistance offered

Salary: $80,000–$121,250 per year

Company

hirify.global is a technology-focused biomanufacturing company developing sustainable, end-to-end manufacturing solutions for medicines.

What you will do

  • Own the reliability strategy for automated inspection systems, including vision systems, cameras, sensors, and reject mechanisms.
  • Analyze equipment performance, reject-rate data, and trends to identify failure modes and implement corrective and preventive actions.
  • Lead troubleshooting for mechanical, electrical, controls, and vision-related issues while providing technical guidance to engineering, maintenance, and operations teams.
  • Maintain validated and inspection-ready systems and author or approve URS, FAT/SAT, commissioning, and IQ/OQ/PQ documentation.
  • Lead investigations into deviations, non-conformances, and customer complaints, and support change control and regulatory inspections.
  • Drive improvements in false rejects, detection capability, downtime, OEE, obsolescence management, and inspection processes using data analysis, Lean, and Six Sigma.

Requirements

  • Significant experience supporting automated inspection or vision systems in a GMP-regulated manufacturing environment.
  • Experience with equipment validation, including IQ/OQ/PQ, and lifecycle management.
  • Experience leading technical investigations, root cause analysis, and change control processes.
  • Strong understanding of equipment reliability principles, including MTBF, MTTR, FMEA, and risk management.
  • Bachelor’s degree in Mechanical, Electrical, Controls, Biomedical, or related engineering discipline is preferred.
  • Visa or work authorization sponsorship is not available.

Nice to have

  • Experience with camera-based inspection platforms and PLC/controls troubleshooting.
  • Experience supporting regulatory inspections, CMMS systems, and reliability analytics.
  • Project management experience in capital or long-term reliability initiatives.
  • Lean Manufacturing or Six Sigma certification.

Culture & Benefits

  • Full-time employment with an annual cash bonus program.
  • 401(k) plan with a company match.
  • Medical, dental, and vision healthcare benefits.
  • Paid vacation, holidays, and other leaves of absence.
  • Tuition reimbursement, family-building benefits, life and disability insurance, and caregiving support.

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