Job DescriptionThis role is pivotal to the expansion of a technically advanced site that utilizes cutting-edge manufacturing technologies and advanced data platforms to deliver life-changing medicines.As a subject matter expert, you will provide engineering leadership during the design, construction, and startup phases of the facility expansion.ResponsibilitiesProvide bioprocess engineering SME support during facility design, construction, and startupSupport large-molecule upstream and downstream process implementation at commercial scaleContribute to C&Q planning and execution for bioprocess equipment and systemsSupport deviation investigations and root cause analysis related to bioprocess operationsAct as a technical interface between global project teams and site operationsSupport readiness for GMP manufacturing and transition into routine productionEssential RequirementsBachelor's, Master's, or Ph.D. in Process/Chemical Engineering, Bioprocess/Biochemical Engineering, or a related field.7+ years of experience in bioprocess engineering, specifically with large-scale mammalian cell culture.Deep expertise in Upstream and Downstream Large Molecule Manufacturing processes.Experience in design reviews, C&Q (Commissioning & Qualification), SOP development, and Unit Operation Shakedown.Strong grasp of process safety assessments, root cause analysis (RCA), and equipment control strategies.Preferred RequirementsExperience in Tech Transfer of new processes into large-scale facilities.Knowledge of MES EBR requirements and automation optimization.Proven track record in Performance Qualification (PQ) strategy and execution.Ability to work within a diverse cross-functional team (Science, Quality, and Production).Tenacity to identify and implement continuous improvement and cost-saving initiatives.PracticalitiesStart Date: February 1stContract Duration: 12 monthsLocation: Limerick, IrelandInterested?Interviews and offers can move quickly. Send your CV toOluali Titelmanato.-or call today to secure your spot in the process.