Facilities Engineer — GMP Utilities & Maintenance

Perspective Therapeutics, Inc.; Chicago (IL); On-site; USD 90,000 - 120,000; Full time

Job summary

Perspective Therapeutics, Inc. is building a new radiopharmaceutical manufacturing site in Chicago and seeks a Facilities Engineer to support startup, commissioning, qualification, and ongoing operation of facility infrastructure.

The role collaborates with Engineering, Validation, QA, Operations, and external vendors to implement preventive maintenance, calibration programs, and robust documentation in line with FDA/cGMP. Strong problem-solving and safety focus are essential.

Qualifications

• Bachelor’s degree in engineering (Mechanical, Electrical or Chemical) with related facilities experience.
• 5–8 years of facilities maintenance experience in a cGMP facility or equivalent.
• Experience with GMP documentation practices and maintenance records.
• Basic electrical troubleshooting and repair skills.
• Knowledge of carpentry repair and painting is a plus.

Responsibilities

• Perform preventive maintenance on HVAC, BAS/BMS, cleanroom systems, boilers, chillers, and other facility infrastructure.
• Troubleshoot equipment performance and calibration issues and support commissioning/qualification activities.
• Manage CMMS work requests with accurate logs, materials, and labor hours.
• Draft change controls, validation protocols, and technical documents per GMP requirements.
• Support root-cause investigations for facility-related deviations.

Skills

Communication

GMP knowledge

Electrical troubleshooting

Mechanical troubleshooting

Tools handling

Education

Bachelor's degree in Mechanical/Electrical/Chemical Engineering

Tools

CMMS

Hand tools

Electrical testing

Job description

Perspective Therapeutics, Inc. is building a new radiopharmaceutical manufacturing site in Chicago and seeks a Facilities Engineer to support startup, commissioning, qualification, and ongoing operation of facility infrastructure.

The role collaborates with Engineering, Validation, QA, Operations, and external vendors to implement preventive maintenance, calibration programs, and robust documentation in line with FDA/cGMP. Strong problem-solving and safety focus are essential.