Role Overview
We are seeking a Process Engineer with GMP pharmaceutical experience to optimize utility systems (black/clean) and drive energy-efficient innovations. You will lead feasibility studies, design improvements, and implement solutions to reduce CO2 emissions while ensuring compliance with pharmaceutical standards.
Key Responsibilities
* Conduct process calculations for utility systems (pumps, water treatment, HVAC) to improve energy efficiency
* Design and evaluate pipe diameter modifications, airflow systems, and clean/black utility networks
* Perform feasibility studies for CO2 reduction initiatives in pharmaceutical facilities
* Collaborate with cross-functional teams (maintenance, validation, EHS) to implement upgrades
* Ensure all modifications comply with GMP and pharmaceutical regulatory requirements
* Document engineering changes and support commissioning/qualification activities
Technical Focus Areas
* Black Utilities: HVAC, compressed air, steam systems
* Clean Utilities: WFI, purified water, clean steam
* Energy Optimization: CO2 reduction strategies, thermal efficiency improvements
* Pharma Standards: GMP, ISPE guidelines, risk assessments (FMEA)
Required Qualifications
* Bachelor’s/Master’s in Chemical/Process/Mechanical Engineering
* 3–5 years of process engineering experience in GMP pharmaceutical environments
* Proficiency in:
* Process design calculations (pipe sizing, airflow, pump systems)
* Utility system optimization (energy/CO2 reduction focus)
* GMP documentation and change control
* Fluent in English, Dutch is an additional bonus
* Willingness to work on-site 2–4 days/week
Preferred Qualifications
* Experience with pharmaceutical cleanroom environments
* Knowledge of CFD modeling or process simulation tools
* Familiarity with ISO 50001 energy management standards
If you are interested, please attach an updated CV and I'll try to be in touch as soon as possible.