Capital Project Engineer

We are seeking an experienced End User Manager to play a critical role in the MA40 facility upgrade project, ensuring the successful integration of laboratory and amenity area enhancements to support a broader site expansion. This role will act as the primary liaison between end users, project teams, and stakeholders, ensuring that the upgraded facility meets operational, research, and workforce needs. 

The ideal candidate will have experience in facility upgrades, stakeholder engagement, laboratory and amenity planning, and project coordination, particularly in pharmaceutical, R&D, or GMP-regulated environments. 

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following…

• Collaborate with the Global Engineering, External engineering partner to ensure timelines, budgets, and objectives are met while prioritizing end-user functionality. 

• Work with architects, engineers, and contractors to ensure that construction and renovation align with intended use and user expectations. 

• Provide oversight on facility modifications, upgrades, and equipment integration, ensuring minimal disruption to site operations. 

• Project Deliverables & Facility Coordination – Review and approve all project deliverables, maintain clear communication with site leadership, and coordinate facility modifications and upgrades to support operational excellence. 

• Safety Leadership & Compliance – Foster a strong safety culture by leading safety discussions, enforcing compliance with policies, and proactively addressing hazards (ZAPS, HAZARD IDs). 

• Project Ownership & Optimization – Oversee change control processes, ensuring they meet regulatory standards, are optimized, and executed according to established schedules. 

• Project Oversight & PMO Alignment – Provide leadership in managing Lab Support projects, ensuring timely updates, adherence to PMO deliverables, and effective execution. 

• Stakeholder & Global Alignment – Build strong relationships with global engineering partners to standardize methodologies, troubleshoot issues, and implement best practices across GSK sites. 

• QC Equipment Lifecycle Management – Ensure proper oversight of QC equipment management, relocation and strategic upgrades. 

• Strategic Scheduling & Risk Mitigation – Work with QC Planners to align timelines for routine tasks and projects while managing team capacity and mitigating delivery risks. 

• Regulatory & Audit Readiness – Serve as an SME in regulatory audits and site investigations, ensuring compliance, interpreting data, resolving issues, and supporting timely resolutions. 

• Quality System & Documentation Oversight – Own and maintain QC documentation, including SOPs, Analytical Methods, Change Controls, and compliance with compendial standards. 

Stakeholder Engagement & Requirements Gathering 

• Serve as the main point of contact for end users, ensuring their needs are fully captured and integrated into the project scope. 

• Work closely with GSK Medicines (Rx) R&D group, GSC laboratory teams, and other facility users to align space utilization with operational goals. 

• Facilitate user workshops, collect feedback, and translate functional requirements into actionable project deliverables. 

Laboratory & Amenity Space Coordination