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6 дней назад

Maintenance Tech I/II (Cell Therapy)

83 711 - 109 870$
Формат работы
onsite
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
Maintenance Tech I/II (Cell Therapy) (HVAC, Mechanical and Electrical Systems): Maintaining and troubleshooting HVAC, cleanroom, refrigeration, cryogenic, process, electrical, and facility systems supporting cGMP cell therapy manufacturing with an accent on equipment reliability, regulatory compliance, and safe operations. Focus on diagnosing complex mechanical and electrical faults, maintaining validated systems, supporting quality investigations, and ensuring critical utilities operate reliably during production.

Location: Onsite in Raritan, New Jersey, United States; applicants must be authorized to work in the United States. Modified second shift is approximately noon–8:30 p.m., with flexibility for other shifts and on-call support.

Salary: $83,711–$109,870 USD base pay per year, with performance-based bonus and/or equity available for eligible roles.

Company

hirify.global is a global biotechnology company developing cell therapy platforms, including CAR-T, TCR-T, NK, CAR-γδ T, and other therapies for serious diseases.

What you will do

  • Diagnose, troubleshoot, repair, and maintain HVAC, cleanroom HVAC, refrigeration, clean steam, cryogenic storage, process equipment, utilities, and related mechanical systems.
  • Perform preventive, predictive, and reactive maintenance, minor upgrades, installations, and on-site critical utility operations.
  • Repair and troubleshoot instrumentation, electrical devices, circuits, switchgear, controls, motors, PLCs, HMIs, VFDs, and sensors up to 600 volts.
  • Read blueprints, P&IDs, and drawings and document completed work accurately in the CMMS.
  • Support facility projects, asset management, reliability initiatives, maintenance goals, and continuous improvement activities.
  • Support deviations, investigations, out-of-tolerance events, change controls, root-cause analyses, and FMEAs while maintaining compliance with applicable regulations.

Requirements

  • High school diploma with equivalent experience or a B.Sc./M.Sc. in a related biological, biochemical, or bioengineering field.
  • Trade or technical school certification, craft certification, or equivalent military certification; journeyman status in at least one craft is required.
  • At least 8 years of experience in industrial manufacturing or a regulated environment, preferably in cGMP cleanroom manufacturing under aseptic conditions.
  • Experience with CMMS or a similar maintenance management system and proficiency in more than one craft.
  • Working knowledge of HVAC, cleanroom maintenance, electrical theory, mechanical and electromechanical systems, building automation, and environmental monitoring.
  • English proficiency is required, along with authorization to work in the United States.

Nice to have

  • Pharmaceutical or related industry experience.
  • Experience working in controlled cleanroom environments under aseptic conditions.
  • Experience with validated and qualified equipment and associated documentation.

Culture & Benefits

  • Permanent full-time employees receive medical, dental, and vision insurance.
  • Benefits include a 401(k) plan with company match, paid parental leave, paid time off, sick time, floating holidays, and company holidays.
  • Additional benefits include flexible spending and health savings accounts, life and disability insurance, commuter benefits, family planning resources, and well-being programs.
  • Work supports clinical and commercial cell therapy manufacturing in a growing, state-of-the-art facility.

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