Utility Building; CUB Engineer; Contractor - Boise
Listed on 2026-02-09
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Engineering
Electrical Engineering, Quality Engineering, Operations Engineer, Process Engineer
Job Summary
Our client is looking for a CUB Engineer to oversee the operation, monitoring, maintenance, and optimization of Central Utility Building systems that support GMP pharmaceutical manufacturing and laboratory operations. This role ensures the reliable and compliant delivery of critical utilities including clean steam, WFI, chilled water, hot water, compressed air, process gases, HVAC, and electrical systems. The CUB Engineer plays a key role in maintaining operational continuity, regulatory compliance, and patient safety.
Responsibilities- Operate, monitor, and maintain pharmaceutical utility systems including boilers, clean steam generators, chillers, cooling towers, WFI and purified water systems, compressed air, vacuum, HVAC, and electrical infrastructure
- Ensure uninterrupted delivery of utilities to GMP manufacturing suites, clean rooms, and laboratory environment
- Monitor system performance using Client, SCADA, or EMS platforms and respond to alarms, deviations, and system upsets
- Perform routine inspections, preventive maintenance, and troubleshooting of utility equipment
- Support commissioning, qualification, and requalification activities for new or modified utility systems
- Maintain accurate documentation, logbooks, SOPs, and maintenance records in accordance with GMP requirements
- Support deviation investigations, root cause analysis, and CAPA implementation
- Coordinate with Facilities, Maintenance, Engineering, Quality, and external vendors
- Support shutdowns, maintenance outages, and capital improvement projects
- Identify opportunities to improve system reliability, compliance, and energy efficiency
- Ensure compliance with FDA, OSHA, EPA, and site safety requirements
- Bachelor's degree in Engineering (Mechanical, Electrical, Chemical, or related discipline) or equivalent facilities experience
- Experience supporting utility systems in a GMP regulated pharmaceutical or biotech manufacturing environment
- Working knowledge of pharmaceutical utilities such as WFI, clean steam, compressed air, chilled water, and HVAC
- Ability to read and interpret P&IDs, electrical one-line diagrams, and mechanical drawings
- Familiarity with GMP documentation practices and change control processes
- Strong troubleshooting, communication, and cross-functional collaboration skills
- Ability to support off hours, on call, or shift based operations
- Experience supporting aseptic manufacturing or cleanroom environments
- Knowledge of USP, FDA, and EMA requirements related to pharmaceutical utilities
- Experience supporting regulatory inspections and audits
- Exposure to commissioning, qualification, or validation activities
- Experience working in 24/7 manufacturing environments
- May require rotating shifts, nights, weekends, or on call coverage
- Work performed in mechanical rooms, utility spaces, and GMP manufacturing areas
- Use of required personal protective equipment and adherence to site safety policies
Shift: M-F - 1st shift and OT eligible
Current location: Lebanon, IN (some travel may be required)
Position Type: Long-term contractor (3+ months) with future opportunities across the U.S. for excellent performers
Pay: Hourly pay is commensurate with experience/negotiable
Benefits: Eligible for benefits after 90 days including medical, dental, vision, and 401(k)
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