Project Engineer
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Job Location:
Newark, DE - USA
Monthly Salary:
Not Disclosed
Posted on:
3 hours ago
Vacancies:
1 Vacancy
Job 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 Bachelors 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 Bachelors 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.
