Role OverviewThis role is responsible for ensuring reliable operation of cleanroom HVAC systems, process utilities (including clean nitrogen and purified water systems), and Environmental Management Systems (EMS) to support GMP-regulated manufacturing. The position works closely with Facilities and Engineering to ensure compliance, stability, and continuous improvement of critical utilities.Key Responsibilities

• Act as SME for cleanroom HVAC, process utilities, and EMS
• Ensure systems operate reliably and in compliance with GMP and regulatory standards
• Monitor system performance through data trending and analysis
• Support preventive maintenance and capacity planning
• Lead troubleshooting, root cause analysis, and CAPA implementation
• Maintain procedures, documentation, and audit readiness
• Manage contractors and supplier performance
• Drive continuous improvement in reliability, efficiency, and sustainability

Profile

• Bachelor’s degree in HVAC, Mechanical, Electrical, Automation, or related Engineering discipline
• 4–6 years’ experience in HVAC/utilities within regulated industries (medical device/pharma preferred)
• Strong knowledge of HVAC standards, cleanroom environments, and GMP/ISO 13485
• Experience with EMS, BMS, and asset management systems
• Strong troubleshooting, analytical, and communication skills
• Fluent in English (Dutch is a plus)

 

Position Benefits

• Competitive annual salary range 
• Exposure to a highly regulated, advanced MedTech manufacturing environment
• Professional development and training opportunities
• Dynamic, collaborative working environment