Job Description:

Design, troubleshoot, optimize, and maintain utility systems (HVAC, chilled water, steam, compressed air, process gases, etc.) for pharmaceutical manufacturing facilities.

Develop and review P&IDs, equipment specifications, and engineering calculations to ensure system reliability, energy efficiency, and regulatory compliance.

Provide technical support during capital project design, installation, commissioning, and qualification phases.

Conduct root-cause analysis on utility/facilities issues and implement preventive maintenance or upgrade solutions.

Collaborate with maintenance, operations, and project teams to minimize downtime and support 24/7 manufacturing operations.

Ensure all work complies with cGMP, FDA/EMA guidelines, and internal engineering standards.

Qualifications:

2–7 years in facilities/utility engineering

GMP experience in Pharma Background

AutoCAD experience