Engineering Systems Specialist
Job Summary
Be at the core of high‑impact engineering projects. As an Engineering Systems Specialist, you translate user needs into robust technical specifications, enabling safe, compliant, and future‑ready pharmaceutical installations.
Your Role – Where Engineering Meets Impact
You won’t just document projects, you’ll shape how they are engineered, built, and validated .
* Translate User Requirement Specifications (URS) into clear, structured technical and software specifications that guide project execution
* Define and document PLC and SCADA functional concepts, including system architecture, interfaces, alarms, and data flows
* Develop and maintain core engineering documentation (P&IDs, tag lists, instrument lists, as‑builts) across the full project lifecycle
* Act as the central technical reference for documentation within multidisciplinary engineering teams
* Ensure project documentation is accurate, structured, and audit‑ready, in line with internal quality and GMP standards
* Work closely with project engineers, automation teams, and customers during design reviews and technical meetings
* Support Factory Acceptance Tests (FAT), commissioning, and qualification activities in collaboration with project and validation teams
* Actively contribute to continuous improvement, helping to standardise engineering practices while respecting HSE and ESG principles
What Makes You a Great Fit
* Bachelor’s degree in Engineering or a related technical discipline (or equivalent experience)
* Experience in pharmaceutical, industrial, or regulated engineering environments is a strong advantage
* Experience with industrial automation, PLC/SCADA systems, or pharmaceutical manufacturing environments is a strong asset
* Structured, precise, and comfortable managing multiple projects and interfaces
* Fluent in Dutch and English, with the ability to communicate clearly across technical and non‑technical teams