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14 часов назад

Engineer II, Facilities (Biotech)

125 000 - 165 000$
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
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
Engineer II, Facilities (Biotech): Supporting the operation, maintenance, and continuous improvement of GMP facilities, utilities, and infrastructure for cell therapy and viral vector manufacturing with an accent on HVAC, critical utility systems, commissioning, validation, and regulatory compliance. Focus on troubleshooting complex facility systems, managing change controls and CAPAs, and improving asset reliability across engineering projects.

Location: Waltham, Massachusetts, United States

Salary: $125,000–$165,000 per year

Company

hirify.global is a technology-driven biotechnology company developing and manufacturing advanced therapies through integrated technologies, services, and manufacturing expertise.

What you will do

  • Operate, troubleshoot, maintain, and continuously improve GMP facilities, utilities, and infrastructure supporting cell therapy and viral vector manufacturing.
  • Support HVAC, pressurization, airflow, temperature, humidity, water, steam, gas, electrical, vacuum, waste processing, and other critical utility systems.
  • Participate in engineering projects through design, construction, startup, commissioning, validation, SOP development, maintenance planning, and continuous improvement.
  • Lead engineering drawing and piping and instrumentation diagram walkdowns and perform commissioning test protocols for infrastructure and utility systems.
  • Manage asset lifecycle, maintenance, calibration, shutdown planning, utility expansion planning, and CMMS activities.
  • Collaborate with Facilities, Metrology, Capital Projects, Validation, Automation, Quality Control, and Quality Assurance teams.

Requirements

  • Bachelor’s degree in Mechanical, Chemical, Facilities, or Industrial Engineering, or equivalent.
  • 5+ years of experience in a GMP biotech or FDA-regulated environment.
  • Experience troubleshooting equipment and utility issues, performing root cause analysis, managing work orders, and supporting corrective and preventive actions.
  • Knowledge of automated control systems, programmable logic controllers, human-machine interfaces, and human factors.
  • Strong technical writing, interpersonal, verbal communication, organization, independence, and collaboration skills.
  • Experience presenting and defending Facilities Engineering activities during regulatory audits.

Culture & Benefits

  • Work in a highly regulated industrial environment with established safety and quality programs.
  • Support operational excellence, reliability, predictive maintenance, and regulatory compliance.
  • Participate in safety programs addressing risks in laboratory and manufacturing environments.
  • Role requires standing, walking, bending, stretching, climbing step ladders while wearing PPE, and lifting 25–50 lbs.

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