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About
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 xcfaprz investigations
- Communicate with internal teams
- Degree in Engineering (Mechanical, Chemical, Electrical, or Process)
- 3+yearsβ experience in pharma/biopharma manufacturing
- Experience working in a GMP-regulated environment
- Proven delivery of capital projects or equipment upgrades
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Languages
- English
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