Overview
The project Engineer will support the delivery of capital and process improvement projects within a regulated pharmaceutical manufacturing environment. The role involves managing projects from concept through to commissioning and handover, ensuring they are completed safely, on time, and within budget.
Duties
Manage end-to-end equipment projects
Develop and execute project plans, budgets, and schedules
Coordinate with operations, quality, validation, and external vendors
Oversee design, installation, commissioning, and qualification (IQ/OQ/PQ)
Ensure compliance with GMP, safety, and regulatory standards
Ensuring that all HSE aspects are considered through all phases of the project, including design, construction, commissioning through to handover to Operations
Monitor cost, timelines, risks, and performance
Lead contractors and construction activities on site
Drive continuous improvement and equipment reliability initiatives
Prepare and deliver project reports and documentation
Support change control and deviation investigations
Communicate with internal teams
Requirements
Degree in Engineering (Mechanical, Chemical, Electrical, or Process)
3+years’ experience in pharma/biopharma manufacturing
Experience working in a GMP-regulated environment
Proven delivery of capital projects or equipment upgrades
Strong knowledge of project lifecycle
Cost control and scheduling experience
Engineering standards and compliance
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