Contract Duration: 12 months (with potential extension)Working Model: Onsite Discipline: Engineering / Project Delivery Role Overview An experienced Senior Project Engineer is required to support the delivery of capital and improvement projects within a GMP-regulated pharmaceutical manufacturing site.
The role sits within a global engineering framework and is responsible for managing projects from concept through commissioning and qualification, ensuring delivery to scope, schedule, cost, quality, and EHS standards.
This is a hands-on project delivery role, requiring strong cross-functional coordination and technical problem-solving capability in a live manufacturing environment.
Project Delivery & Leadership Lead engineering projects end-to-end, ensuring delivery on time, within budget, and aligned to business objectives Scope new engineering projects and support capital approval processes Coordinate commissioning, qualification, and handover activities Lead and participate in cross-functional project teams Manage interfaces with internal departments and external suppliers Engineering & Technical Support Troubleshoot process and equipment issues impacting manufacturing Review existing systems (process, E&I, structural, safety, and documentation)Support constructability, maintainability, and operability assessments Coordinate P&IDs, technical documentation, and engineering deliverables Project Controls Project cost estimating, forecasting, tracking, and reporting Project scheduling, progress reporting, and risk management Resource planning and coordination Conduct retrospective project reviews and lessons learned Compliance & Quality Ensure compliance with c GMP, EHS, and site engineering standards Support deviation investigations and corrective actions Ensure documentation is completed in line with GDP requirements Support validation, MSAT, operations, facilities, and quality teams Stakeholder Engagement Provide regular updates to management and stakeholders Facilitate effective communication across project teams Support training related to new or modified equipment/processes Qualifications & Experience Third-level qualification in Engineering or Science Minimum 3 years' experience in a pharmaceutical or regulated manufacturing environment Proven experience delivering engineering projects in a GMP setting Experience with Lean, Six Sigma, or structured problem-solving methodologies Experience working within large, multinational engineering teams Strong working knowledge of MS Word, Excel, and Outlook Strong teamwork and collaboration skills Customer- and results-focused mindset High attention to detail and strong technical aptitude Effective problem-solving and decision-making ability Adaptable, proactive, and self-motivated
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