An Equipment Engineer is required to support a regulated biopharmaceutical manufacturing facility, with primary responsibility for syringe filling and single-use formulation equipment. The role focuses on equipment implementation, start-up, and ensuring systems are fully compliant, reliable, and ready for routine manufacturing operations.Key ResponsibilitiesSupport installation, start-up, validation, and routine operation of new process equipment.Assist with equipment project delivery, including calibration, testing, spares, and handover to operations.Ensure systems meet site, safety, and regulatory requirements.Develop maintenance strategies and initial preventive maintenance programs.Work cross-functionally with engineering, manufacturing, quality, automation, IT, and EHSS teams.Support vendor coordination and supplier management.Contribute to troubleshooting and resolution of technical issues.RequirementsEngineering degree with 5+ years’ experience in regulated manufacturing.Strong knowledge of GMP and quality systems.Experience with new equipment introduction and technology transfer.Background in formulation and/or fill-finish operations preferred.Strong technical documentation and communication skills.Organised, proactive, and comfortable working in fast-paced project environments.
#J-18808-Ljbffr