Project Engineer
Contract W2
Contract Independent
Contract Corp To Corp
No Travel Required
Hybrid
Depends on Experience


DCode Talent
Fitment
Dice Job Match Score™
⏳ Almost there, hang tight...
Job Details
Skills
- HVAC
- WFI
- GMP
- CQV
- Pharma
Summary
100% on-site work required in Newark, DE; applicants must be local.
Job Summary:
- Lead end-to-end capital projects for pharmaceutical utilities and facility systems (e.g., HVAC, clean utilities, WFI, clean steam) ensuring project scope, schedule, and budget compliance.
- Manage multiple engineering projects, including facility upgrades, infrastructure improvements, packaging, and inspection system installations.
- Provide technical leadership and ensure compliance with GMP regulations, CQV (Commissioning, Qualification, Validation), and validation requirements for facility and utility projects.
- Develop, monitor, and control capital budgets, forecasts, and financial performance across various projects.
- Oversee construction activities, including contractor management, bid evaluation, field coordination, and ensuring safety compliance.
- Ensure strict adherence to project governance, design reviews, change control processes, and documentation of validation activities (IQ/OQ/PQ).
- Collaborate with internal teams (Facilities, Manufacturing, Quality, Validation, and EHS) to ensure site readiness and operational reliability.
- Manage relationships with external vendors, contractors, and engineering firms to guarantee quality, safety, and timely completion of projects.
- Require a Bachelor’s degree in Engineering and 7–10+ years of relevant experience in pharmaceutical/biotech facilities project management.
- Advanced skills in project scheduling (Microsoft Project or similar), budgeting, cost control, and a deep understanding of GMP, pharmaceutical utilities, and equipment qualification.
- Lead end-to-end capital projects for pharmaceutical utilities and facility systems (e.g., HVAC, clean utilities, WFI, clean steam) ensuring project scope, schedule, and budget compliance.
- Manage multiple engineering projects, including facility upgrades, infrastructure improvements, packaging, and inspection system installations.
- Provide technical leadership and ensure compliance with GMP regulations, CQV (Commissioning, Qualification, Validation), and validation requirements for facility and utility projects.
- Develop, monitor, and control capital budgets, forecasts, and financial performance across various projects.
- Oversee construction activities, including contractor management, bid evaluation, field coordination, and ensuring safety compliance.
- Ensure strict adherence to project governance, design reviews, change control processes, and documentation of validation activities (IQ/OQ/PQ).
- Collaborate with internal teams (Facilities, Manufacturing, Quality, Validation, and EHS) to ensure site readiness and operational reliability.
- Manage relationships with external vendors, contractors, and engineering firms to guarantee quality, safety, and timely completion of projects.
- Require a Bachelor’s degree in Engineering and 7–10+ years of relevant experience in pharmaceutical/biotech facilities project management.
- Advanced skills in project scheduling (Microsoft Project or similar), budgeting, cost control, and a deep understanding of GMP, pharmaceutical utilities, and equipment qualification.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
- Dice Id: 91166691
- Position Id: 496-43174-
- Posted 8 days ago
Company Info
About DCode Talent
At Dcode Talent, we specialize in IT staffing and consulting services, connecting skilled professionals with top companies. Our expertise spans across multiple industries, ensuring that businesses find the right talent and IT professionals achieve their career goals.
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