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DescripciónDescription
Manufacturing support for all required validation procedures for manufacturing equipment. Supports product and processes (verification and standard), lines capacity, lines balancing, new line introduction, layout, process improvements, optimizations of manufacturing efficiency. Will develop documentation (protocols, reports, procedures, etc.), execute validation protocols, feasibility studies, metrology. Perform capacity analysis, line balancing & capacity study. Establish and monitor engineering standards. Actively participate in the activities of continuous improvement of manufacturing processes. Support quality system, CAPA, NCRs, customer complaints. Promote cost reduction activities.
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Requisitos Requirements
BS Engineering with five (5) years or more of experience in similar position for pharmaceutical or medical devices manufacturing. Previous experience managing validations, CAPA, equipment integrations, Root cause investigations. Required experience in equipment and process support for a regulated industry. Excellent computer skills. CAD experience and development of 3D models, preferred. Fully bilingual. (Professional Services Contract -6 months) 212753
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