Our client, a leading pharma manufacturing company based in Dublin, are hiring a Process Engineer. This role provides technical leadership and support for aseptic drug product manufacturing across contract manufacturing sites in Europe. The position involves supporting new product introductions, lifecycle changes, and commercial operations for a range of sterile injectable and oral solid dose products. The role requires international travel, cross-functional collaboration, and a focus on process troubleshooting, operational improvement, and cGMP compliance.Key ResponsibilitiesServe as a drug product technical expert, supporting aseptic processing, formulation, filling, lyophilisation, inspection, and transportation of vials, syringes, and devices.Collaborate with contract manufacturing SMEs, Global Operations, and Quality teams to identify, troubleshoot, and resolve process and operational issues.Provide process development support, including technology transfer, process characterization, and process validation activities.Review, evaluate, and support deviation investigations and CAPA, providing technical input for continuous improvement.Visit contract manufacturing sites to observe production, build relationships, and implement operational and process improvements.Key Requirements5–8 years' experience in pharmaceutical manufacturing, drug product or drug substance, with strong technical and engineering process knowledge.Hands-on experience with aseptic drug product operations, including sterile filtration, filling, capping, lyophilisation, and equipment/process validation.Proven problem-solving skills, including deviation/CAPA review and investigation.Strong cross-functional communication skills and ability to collaborate with external contract manufacturing partners.Bachelor's degree in Science, Engineering, or relevant discipline; full clean driving licence for travel; cGMP knowledge required.