Facilites Engineer

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.