Our client's facility is a fast-paced manufacturing environment focused on high-specification production. This location serves as a hub for both Continual Improvement and Capital Projects, ensuring our operations remain at the forefront of industry standards. As we prepare for a series of new projects launching this summer, we are expanding our engineering capabilities to ensure seamless execution and regulatory compliance.As a Project Engineer, you will join an established team & will be the primary driver for end-to-end project execution, bridging the gap between design, validation, and final implementation.ResponsibilitiesEnd-to-End Project Management: Take full ownership of projects from initial drafting and paperwork to final execution.Cross-Functional Collaboration: Partner with Quality, Manufacturing, and Validation teams to ensure project alignment.Validation & Compliance: Prepare all necessary documentation and ensure projects meet strict GMP and Regulatory Control standards.Manufacturing Integration: Coordinate with production schedules to minimize downtime, particularly during the busy summer project window.Technical Drafting: Work directly with drafting and design to move projects from concept to the manufacturing floor.ExperienceWe are seeking a proactive engineer with a strong electrical or electronic foundation and a "can-do" attitude toward complex manufacturing projects.2-3 years of post-graduate experience in a project engineering role.Experience in pharmaceuticals is preferred; FMCG experience will also be considered.Proven experience with validation processes and working within GMP (Good Manufacturing Practice) environments.Understanding of USFDA standards and the ability to conduct Quality Risk Assessments within a manufacturing area.Bachelors of Engineering or similar background. Alternatively a strong technical background will also be considered.To discover more about this opportunity, please apply online or contact Lewis Murray on for a confidential discussion.