Назад
Company hidden
5 дней назад

OEM Engineer (PLC/SCADA)

75 000 - 80 000
Формат работы
hybrid
Тип работы
fulltime
Английский
b2
Страна
Netherlands
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

Мэтч & Сопровод

Для мэтча с этой вакансией нужен Plus

Описание вакансии

Текст:
/

TL;DR

OEM Engineer (PLC/SCADA): Define and document user requirements for OEM PLC/SCADA systems in a regulated pharma manufacturing environment with an accent on engineering design, commissioning, and qualification of automation systems. Focus on implementing Siemens WinCC SCADA and TIA Portal solutions, partnering with site teams, and ensuring compliant, secure implementations aligned with standards.

Hybrid • Boxmeer (Netherlands)

75 000 - 80 000 EUR per year

Company

IT consultancy firm helping startups and corporations create and deliver innovative software solutions (AI, ML, BI, Web, Automation) for industries including Pharma, Telecom, Energy, and Automotive.

What you will do

  • Define and document user requirements for OEM PLC/SCADA systems.
  • Review and approve design and technical documentation for automation systems.
  • Partner with local site project teams to scope and implement changes on OEM PLC/SCADA systems.
  • Engineer, commission, and qualify Siemens WinCC SCADA and TIA Portal solutions.
  • Follow SDLC procedures for system changes, including requirements updates, RTM, change control, implementation, and testing.
  • Educate and support local teams on automation standards, technology selection, and validation processes.
  • Collaborate with Digital and IT departments for compliant implementations.

Requirements

  • Experience in PLC application engineering.
  • Strong hands-on experience with Siemens WinCC SCADA and TIA Portal.
  • Proven experience in engineering design, commissioning, and qualification of PLC/SCADA systems.
  • Solid background in business analysis for small to mid-sized projects.
  • Experience with SDLC, change management, and validation processes.
  • Strong communication skills and ability to work closely with site teams and stakeholders.

Nice to have

  • Knowledge of GxP-regulated pharmaceutical environments.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →