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обновлено 21 час назад

FLS Automation Engineer (Pharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
c1
Страна
Ireland
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
FLS Automation Engineer (Pharmaceutical Manufacturing) (DeltaV/Siemens S7): Supporting automation systems at a pharmaceutical manufacturing facility in Carlow with an accent on troubleshooting, field testing, equipment checks, and cGMP compliance. Focus on diagnosing complex automation issues, maintaining OEM and DeltaV systems, and reviewing SDLC documentation in a regulated environment.

Location: Onsite in Carlow, Ireland

Company

hirify.global is an employee-owned international project delivery firm serving the pharmaceutical, food, medtech, and mission-critical sectors.

What you will do

  • Provide automation support for DeltaV, Siemens S7 PLC, and OEM automation systems.
  • Perform field testing for network connectivity, instrumentation devices, and software functionality.
  • Diagnose automation issues and coordinate resolutions with vendors.
  • Complete system backups and scheduled checks on OEM and DeltaV equipment.
  • Download and update recipes for OEM and DeltaV systems.
  • Review functional specifications, design specifications, and code reviews during investigations.

Requirements

  • At least 3 years of experience in a similar automation engineering role.
  • At least 1 year of pharmaceutical industry experience.
  • Essential experience with Siemens S7 PLCs and/or DeltaV; experience with Historian systems is relevant.
  • Experience troubleshooting OEM and DeltaV systems, with familiarity with networking and IT.
  • Relevant Computer Science or Engineering degree, or equivalent qualification.
  • Fluent English required, both written and verbal.

Culture & Benefits

  • Permanent onsite position supporting a regulated pharmaceutical manufacturing facility.
  • Work within an employee-owned international project delivery firm.
  • Follow global policies, regulatory requirements, and current good manufacturing practice standards.

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