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9 дней назад

Senior Automation Engineer (Biopharmaceutical Manufacturing)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
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
Senior Automation Engineer (Biopharmaceutical Manufacturing): Supporting and integrating PLC, DCS, and MES automation systems for a validated biopharmaceutical manufacturing facility with an accent on systems ownership, validation, and paperless manufacturing. Focus on integrating DCS with MES and historian systems, coordinating technical delivery, and solving complex shop-floor automation challenges.

Location: On Campus, Athlone, Ireland

Company

hirify.global is a mid-sized biotechnology company developing life-changing medicines through a global, inclusive organization.

What you will do

  • Coordinate technical activities for PLC, DCS, and MES contractor operations supporting Athlone initiatives and projects.
  • Own the site PLC/DCS/MES systems, provide operational support, and define sustainable support models.
  • Develop performance indicators and apply deviation, change-control, and validation procedures.
  • Establish quality standards across the automation delivery lifecycle from concept through operation.
  • Provide technical input to OPEX and CAPEX planning, aligning resources with project schedules and budgets.
  • Lead technical forums, influence stakeholders, resolve technical challenges, and advance innovative shop-floor automation solutions.

Requirements

  • B.S. or M.S. degree in Electrical Engineering, Computer Science, Computer Engineering, Chemical Engineering, or Industrial Engineering.
  • Minimum of 15 years of experience as a PLC/DCS/MES Engineer delivering DCS and/or MES requirements.
  • At least 10 years of experience in the biotech or pharmaceutical industry in a manufacturing operational support role.
  • Experience with PI Historian, Thin Manager, and WIN911 systems.
  • Ability to take ownership and collaborate effectively across teams.
  • Strong influencing, knowledge-sharing, process-improvement, project-delivery, communication, and organizational skills.

Nice to have

  • Fluency in German or French.
  • Experience in regulated environments with knowledge of cGMP, OSHA, and EPA requirements.

Culture & Benefits

  • Full-time employment in a well-established biotechnology company.
  • Opportunities for learning, growth, and expanding professional skills.
  • Inclusive culture focused on belonging, diverse perspectives, ethical conduct, and collaboration.
  • Work is performed on campus at the Athlone manufacturing facility.

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