Role OverviewWe 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 ResponsibilitiesConduct process calculations for utility systems (pumps, water treatment, HVAC) to improve energy efficiencyDesign and evaluate pipe diameter modifications, airflow systems, and clean/black utility networksPerform feasibility studies for CO2 reduction initiatives in pharmaceutical facilitiesCollaborate with cross-functional teams (maintenance, validation, EHS) to implement upgradesEnsure all modifications comply with GMP and pharmaceutical regulatory requirementsDocument engineering changes and support commissioning/qualification activitiesTechnical Focus AreasBlack 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 QualificationsBachelor’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 QualificationsExperience 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.