Project Engineer

Role Summary:

• 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.

Core Duties and Responsibilities:

• 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

Minimum Qualifications and Experience:

• 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

Please note, we do not require agency assistance with this role.