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3 дня назад

Operational Technology Engineer (OT/SCADA)

103 200 - 161 250$
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
Operational Technology Engineer (OT/SCADA) (GMP manufacturing): Optimizing server and network architecture, cybersecurity, and data integrity for automated oligonucleotide manufacturing systems with an accent on SCADA, PLC, BAS, data historians, and regulatory compliance. Focus on integrating manufacturing equipment with Active Directory, supporting resilient OT infrastructure, assessing vulnerabilities, and leading validation and change-control activities.

Location: Frederick, Colorado, United States

Salary: $103,200–$161,250 per year, plus eligibility for bonus, stock, and benefits.

Company

hirify.global develops technology and supports scientific and manufacturing operations, including GMP-regulated oligonucleotide production.

What you will do

  • Act as the interface between Automation Engineering and Information Technology for operational technology priorities.
  • Manage and optimize OT server, network, cybersecurity, and data integrity practices for automated manufacturing systems.
  • Support SCADA, BAS, PLC, data historian, MES, ESXi edge computing, and process control infrastructure.
  • Integrate manufacturing equipment with Active Directory and support archiving, disaster recovery, and business continuity strategies.
  • Troubleshoot OT and IT issues, coordinate equipment outages, and direct third-party vendors when required.
  • Lead functional testing, change controls, validation activities, and technical reviews for OT changes.

Requirements

  • Bachelor’s or master’s degree, or equivalent experience.
  • 4+ years of experience in automated manufacturing; GMP manufacturing experience is preferred.
  • Strong knowledge of operational technology systems, including SCADA and PLCs.
  • Experience with BAS, data historians, MES, and process control systems in a GMP manufacturing environment.
  • Knowledge of FDA GMP, data integrity, cybersecurity, vulnerability assessment, and risk mitigation practices.
  • Experience with business analysis and requirements-gathering techniques.

Nice to have

  • Previous GMP manufacturing experience.

Culture & Benefits

  • Full-time day-shift schedule with no defined end date.
  • Occasional travel is required.
  • Eligibility for bonus, stock, and benefits.
  • Work supports regulated manufacturing, cybersecurity, resilience, and continuous improvement.

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