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manage technical assessments, corrective actions, and equipment improvement initiatives.\nPerforming System Owner assessments and engineering impact assessments related to equipment failures, process deviations, and quality events.\nSupporting technical investigations, identifying equipment failure mechanisms, and developing corrective and preventive actions to reduce recurrence.\nEvaluating the applicability of CAPA and lessons learned to other equipment, systems, and manufacturing areas.\nManaging engineering activities in IBM Maximo, including work order technical review, pre-approval and post-approval activities, maintenance coordination, and follow-up through closure.\nDeveloping and revising preventive maintenance strategies, Job Plans, inspection requirements, and SOPs.\nImplementing engineering controls and completing actions associated with safety incidents and INCA records.\nSupporting equipment troubleshooting, repair coordination, replacement of obsolete equipment, spare parts evaluations, and equipment modernization projects.\nWorking with bio pharmaceutical manufacturing equipment such as centrifuges, autoclaves, process tanks, chromatography and UF/DF systems, homogenizes, filter integrity testers, and associated instrumentation.\nPreparing clear technical reports and assessment rationales, maintaining traceable supporting documentation, and completing actions within established deadlines.\nCoordinating with Manufacturing, Process Engineering, Maintenance, Quality, Automation, Validation, and equipment suppliers.\nManaging multiple concurrent assignments and prioritizing work according to safety, quality, and operational needs..\n Doctorate or Masters + 2 years of Engineering experience orBachelors in Engineering + 4 years of Engineering experience (Chemical, Mechanical or Electrical Engineer)\n\nBilingual (Spanish/English)\n All your information will be kept confidential according to EEO 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