Facilites Engineer

Scorpion Therapeutics; Bloomingdale (IL); On-site; USD 90,000 - 130,000; Full time

Job summary

Scorpion Therapeutics is seeking a Facilities Engineer to support GMP radiopharmaceutical manufacturing, overseeing startup, commissioning, maintenance, and routine operations of facility infrastructure.

You will perform preventative maintenance on HVAC, utilities, and safety systems; manage work requests via CMMS; develop and review change controls and validation protocols; and help investigations for deviations.

Qualifications

• Bachelor's degree in Mechanical, Electrical, or Chemical Engineering must have 5+ years facilities experience in cGMP environments.
• Proficiency in electrical, mechanical, and carpentry tasks.
• Strong communication and documentation skills.
• Ability to work indoors/outdoors with exposure to hazardous materials.
• Valid driver’s license; ability to lift 50 lbs.; willingness to work flexible hours including evenings and weekends.

Responsibilities

• Perform preventative maintenance on HVAC, utilities, and safety systems.
• Troubleshoot equipment issues.
• Manage work requests via CMMS.
• Author change controls and validation protocols.
• Support investigations for deviations.
• Coordinate with external vendors.
• Ensure compliance with FDA, cGMP, and radiation safety standards.

Skills

Facilities maintenance

Preventive maintenance

HVAC systems

Electrical work

Carpentry tasks

CMMS

Documentation

Communication

Education

Bachelor's degree in Mechanical, Electrical, or Chemical Engineering

Tools

CMMS

Job description

Role

Facilities Engineer supporting GMP radiopharmaceutical manufacturing, overseeing startup, commissioning, maintenance, and routine operations of facility infrastructure.

Responsibilities

perform preventative maintenance on HVAC, utilities, and safety systems; troubleshoot equipment issues; manage work requests via CMMS; author change controls and validation protocols; support investigations for deviations; coordinate with external vendors; ensure compliance with FDA, cGMP, and radiation safety standards.

Requirements

Bachelor's in Mechanical, Electrical, or Chemical Engineering with 5+ years facilities experience in cGMP environments; proficiency in electrical, mechanical, and carpentry tasks; strong communication and documentation skills; ability to work indoors/outdoors with exposure to hazardous materials; valid driver’s license; ability to lift 50 lbs.; willingness to work flexible hours including evenings and weekends.

HighValue

GMP radiopharmaceutical manufacturing, utilities, HVAC, safety systems, validation, calibration, troubleshooting, regulated environment compliance, CMMS use, radiation safety, facility startup and routine operations.

WorkSetup

onsite with potential for occasional flexible hours; work in a sterile, hazardous environment with strict safety protocols.