0048V6269 Facilities Project Engineer Consultant

0048V6269 Facilities Project Engineer Consultant
Please contact Amanda Mazza, amanda@tworivercp.comFacilities Project Manager Job Responsibilities:

• Lead full lifecycle capital projects with a focus on pharmaceutical utilities and facilities systems (HVAC, clean utilities, WFI, clean steam), ensuring delivery on scope, schedule, and budget
• Manage concurrent engineering projects including facility upgrades, infrastructure improvements, packaging, and inspection systems
• Provide technical leadership for GMP-regulated facility and utility projects, ensuring compliance with CQV and validation requirements
• Develop and control capital budgets and forecasts, track spend, and manage financial performance across projects
• Oversee construction activities and contractor execution (preferred), including bid evaluation, field coordination, and safety compliance
• Ensure adherence to project governance, design reviews, change control, and validation documentation (IQ/OQ/PQ)
• Collaborate cross-functionally with Facilities, Manufacturing, Quality, Validation, and EHS to support site readiness and operational reliability
• Manage external vendors, contractors, and engineering firms to ensure quality, safety, and timely project delivery

Job Requirements:

• Bachelor’s degree in Engineering required; strong project scheduling, budgeting, and leadership skills expected
• 7–10+ years of experience in pharmaceutical/biotech environments with a focus on utilities, facilities, and capital projects
• Advanced proficiency with Microsoft Project or similar tools for complex project scheduling
• Strong experience in capital budgeting, forecasting, and cost control, particularly for facility and construction projects
• Strong knowledge of GMP requirements and equipment qualification
• Deep understanding of pharmaceutical utility systems (HVAC, clean rooms, WFI, clean steam, process gases, building management systems)
• Experience with facility design, equipment layout, and infrastructure integration
• Knowledge of GMP requirements, equipment qualification (IQ/OQ/PQ), and validation lifecycle
• 100% on-site presence required (Newark, DE)

LOCATION
Newark, DE

EMPLOYMENT
C2C or W2

 

Powered by JazzHR

pZEyzyvedW