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7 дней назад

Manufacturing System Engineer (DeltaV)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Singapore
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
Manufacturing System Engineer (DeltaV) (manufacturing automation): Supporting and optimizing DeltaV-based manufacturing automation systems in a Singapore biotech manufacturing facility with an accent on system reliability, GMP compliance, and lifecycle management. Focus on troubleshooting batch automation, implementing and qualifying changes, and delivering projects from design through commissioning and handover.

Location: Singapore Manufacturing – Tuas

Company

hirify.global is a biotech company researching, manufacturing, and delivering medicines across oncology, inflammation, general medicine, and rare disease.

What you will do

  • Provide day-to-day technical support for manufacturing automation systems, including troubleshooting, monitoring, incident investigation, and change implementation.
  • Assess, test, deploy, and document automation changes in accordance with SOPs and GMP requirements.
  • Support small-to-medium automation projects from design and risk assessment through commissioning, qualification, startup, and handover.
  • Investigate recurring issues, prepare technical reports, implement technical solutions and CAPA actions, and drive continuous improvement.
  • Support audits and inspections while coordinating with Manufacturing, Quality, Maintenance, Process Engineering, IT/OT, EHSS, and external providers.
  • Provide technical guidance to junior engineers and contractors.

Requirements

  • Degree or equivalent experience in Engineering, Information Systems, Computer Science, or Life Sciences.
  • Experience with manufacturing automation, preferably in biotechnology or pharmaceutical manufacturing.
  • Experience with Emerson DeltaV DCS, DeltaV Batch configuration, ISA-88 principles, and advanced automation troubleshooting.
  • Knowledge of OPC, Foundation Fieldbus, Profibus, pharmaceutical or biotech processes, and EHSS requirements.
  • Experience applying GMP through change controls, deviations, risk assessments, CAPA actions, data-integrity practices, and inspection-ready documentation.
  • Experience delivering automation project work packages and coordinating technical activities in a GMP manufacturing environment.

Culture & Benefits

  • Collaborative, innovative, and science-based working environment.
  • Competitive benefits and comprehensive total rewards aligned with local industry standards.
  • Company-paid medical check expenses required for the role.
  • Inclusive workplace with reasonable accommodation available during recruitment and employment.

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