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1 день назад

Senior Manufacturing Systems Engineer: Automation PLC

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
Senior Manufacturing Systems Engineer: Automation PLC (Biotech Manufacturing): Building and maintaining PLC, SCADA, HMI, and DeltaV automation systems for a GMP drug substance manufacturing plant with an accent on system integration, validation, and lifecycle management. Focus on leading standalone system implementation and start-up, troubleshooting complex control systems, and developing reliable automation solutions for new manufacturing technologies.

Location: Holly Springs, North Carolina, United States; onsite role with 24 x 7 onsite/on-call operational support

Company

hirify.global is a biotechnology company developing and manufacturing medicines across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Provide technical leadership to automation engineers supporting GMP drug substance plant operations.
  • Develop and maintain PLC automation solutions using Allen Bradley, Siemens, and other platforms integrated with Emerson DeltaV.
  • Develop and maintain SCADA, Trailblazer reporting, equipment PLCs, interface hardware, and HMI systems.
  • Lead standalone system implementation, start-up, control panel and HMI design, troubleshooting, root cause analysis, and incident investigations.
  • Translate process requirements into automated solutions and support capital projects, new product introductions, and new technology deployments.
  • Support computerized systems validation, data integrity assessments, preventive and corrective maintenance, and continuous improvement initiatives.

Requirements

  • High school diploma/GED with 10 years of engineering experience, associate degree with 8 years, bachelor’s degree with 4 years, master’s degree with 2 years, or a doctorate.
  • Experience with PLC design, controls engineering, troubleshooting, programming, installation, and lifecycle management of standalone control and instrumentation systems.
  • Experience with Rockwell industrial automation hardware and system integration using OPC, Foundation Fieldbus, Profibus, or DeviceNet.
  • Knowledge of GMP, GAMP, GxP, 21 CFR Part 11, ASTM 2500, S88, S95, and validation documentation in regulated manufacturing environments.
  • Experience with capital project lifecycle management, process control strategies, technical documentation, and project execution.
  • Strong leadership, mentoring, technical writing, communication, and presentation skills.

Nice to have

  • Degree in electrical engineering, computer science, chemical engineering, or biotech engineering.
  • Experience with biopharmaceutical production facilities and utility systems such as autoclaves, parts washers, clean steam generators, WFI systems, filter integrity testers, and wastewater treatment.
  • Experience delivering improvements in safety, reliability, productivity, cycle time, and plant utility consumption.

Culture & Benefits

  • Collaborative, innovative, science-based work environment.
  • Work on a new drug substance manufacturing facility using disposable technologies, stainless steel equipment, and Industry 4.0 capabilities.
  • Opportunity to contribute to sustainability initiatives targeting reduced carbon emissions and waste.
  • Competitive benefits and comprehensive total rewards aligned with local industry standards.
  • Inclusive workplace with reasonable accommodation available during hiring and employment.

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