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 systemsClean Utilities : WFI, purified water, clean steamEnergy Optimization : CO₂ reduction strategies, thermal efficiency improvementsPharma Standards : GMP, ISPE guidelines, risk assessments (FMEA)Required Qualifications
Bachelor’s / Master’s in Chemical / Process / Mechanical Engineering3–5 years of process engineering experience in GMP pharmaceutical environmentsProficiency in :Process design calculations (pipe sizing, airflow, pump systems)Utility system optimization (energy / CO₂ reduction focus)GMP documentation and change controlFluent in English, Dutch is an additional bonusWillingness to work on-site 2–4 days / weekPreferred Qualifications
Experience with pharmaceutical cleanroom environmentsKnowledge of CFD modeling or process simulation toolsFamiliarity with ISO 50001 energy management standardsIf you are interested, please attach an updated CV and I'll try to be in touch as soon as possible.