Facilities Project Engineer || Newark, DE  - onsite

 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.