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24 часа назад

Process Maintenance Technician (Oligonucleotide Manufacturing)

30 - 47$
Формат работы
onsite
Тип работы
fulltime
Грейд
middle
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
Process Maintenance Technician (Oligonucleotide Manufacturing): Maintaining, troubleshooting, and repairing GMP process equipment for oligonucleotide manufacturing at an expanding biopharma production site with an accent on mechanical, fluid handling, pneumatic, thermal control, and low-voltage systems. Focus on equipment installation, commissioning, qualification, preventive maintenance, and accurate documentation in a regulated manufacturing environment.

Location: US-CO-Frederick; onsite manufacturing and utility areas

Salary: $30.69–$47.96 per hour, plus eligibility for bonus, stock, and benefits.

Company

hirify.global supports biopharma companies and is expanding a Frederick, Colorado manufacturing site for oligonucleotide DNA/RNA therapeutics.

What you will do

  • Perform planned and unplanned maintenance on GMP manufacturing equipment.
  • Troubleshoot and repair mechanical, fluid handling, pneumatic, and thermal control systems, including pumps, valves, regulators, agitators, and piping.
  • Support equipment installation, commissioning, and qualification during the site expansion.
  • Perform preventive maintenance and low-voltage electrical and controls troubleshooting.
  • Document maintenance activities in a computerized maintenance management system and follow GMP procedures and SOPs.
  • Communicate repair status and equipment conditions with engineers, operators, and maintenance colleagues.

Requirements

  • Associate degree, trade school certification, or equivalent hands-on experience.
  • At least 3 years of maintenance technician experience in a manufacturing environment.
  • Strong mechanical troubleshooting and repair skills in process or industrial systems.
  • Experience in GMP, FDA-regulated, or similar regulated environments, with knowledge of good documentation practices.
  • Ability to interpret P&IDs, equipment manuals, and maintenance documentation.
  • Knowledge of lockout/tagout and controlled work permit safety practices; ability to stand, climb, reach, bend, and lift up to 50 lbs with assistance.

Nice to have

  • Experience in pharmaceutical, life sciences, or other highly regulated industries.
  • Exposure to automated process equipment and industrial control systems.
  • Experience with CMMS tools such as Blue Mountain RAM, Maximo, or SAP.
  • Fabrication, welding, or basic machining experience.

Culture & Benefits

  • Full-time weekday schedule initially, with a day shift.
  • The schedule may transition to a fixed off-shift or include on-call, weekend, and occasional off-hours support as production expands; advance notice and compensation apply.
  • Work takes place in a fast-paced, highly regulated manufacturing environment with exposure to chemicals, moving equipment, and industrial systems.
  • Benefits include bonus and stock eligibility.
  • Occasional travel may be required.

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