An exceptional opportunity has arisen for an Early-Career Engineer to join a premier, global biopharmaceutical facility in Dublin. Supporting state-of-the-art expansion operations, this high-visibility contract role focuses on driving technical training initiatives and advancing digital capabilities across high-speed automated inspection, assembly, and robotic systems.
Key Responsibilities
Review vendor and site technical documentation to design, structure, and deliver practical training programs for Engineering and Maintenance teams across multi-shift operations.
Build a deep technical understanding of cutting-edge automated syringe/vial inspection systems, autoinjector assembly lines, and advanced robotics to effectively translate complex concepts into clear operational guidance.
Drive site-level adoption of real-time equipment data tools and approved AI technologies, empowering technical teams to optimize troubleshooting, condition monitoring, and daily productivity.
Coordinate the rollout of dedicated technician electrical training, design competency assessments, and measure training effectiveness to eliminate technical knowledge gaps.
Establish metrics, track project actions, and present progress reports to engineering leadership, driving continuous improvement based on shift feedback and site performance.
Skills, Attributes & Experience
Degree (BSc / NFQ Level 8 preferred) in Mechanical, Electrical, Automation, Mechatronic, Chemical, or Manufacturing Engineering.
Graduate level up to 2 years of technical experience (industrial placement, internship, or co-op experience strongly considered).
Strong curiosity and foundational knowledge of automated manufacturing equipment, PLCs, machine vision, robotics, or high-speed machinery.
Demonstrated interest in data analytics, digital productivity solutions, and the practical application of AI tools within an engineering context.
Excellent interpersonal and presentation skills with the confidence to lead training sessions, facilitate cross-functional alignment, and partner with multi-level site teams.
Exposure to cGMP, pharmaceutical, or medical device regulated environments is an advantage, though technical drive and adaptability are key.
