Teva Manufacturing & Quality Systems Specialist 

Chile, Santiago Metropolitan Region, Santiago 

193892457

• Serve as an IT liaison and business process expert in the areas of supply chain, operations, inventory management, lab systems and quality. Analyzing the business needs, validating solutions with the client, and working with local and regional IT to support the critical aspects of the business.
• Maintain focus on process analysis and re-engineering with an understanding of technical problems and solutions and the relationship to the business and technical environment.
• Collaborate with customers, staff, regional IT colleagues, and other stakeholders to support existing processes and technologies in the supply chain, operations and quality areas. Identify customer requirements; assess impacts to the delivery and development of applications and other IT functions. This may involve some or all lab systems, engineering systems, or both, depending on the site(s) supported and other resources supporting the site(s).
• Administer and support all laboratory computer systems – LIMS (Labware), CDS (Empower), standard-alone computerized instruments and other applications identified by laboratory management. Support interfaces to these systems and troubleshoot as required.
• Develop and support appropriate administration and master data maintenance processes and procedures to ensure efficient day-to-day laboratory system operation.
  Develop, maintain and deliver appropriate training modules for laboratory systems. Act as a key site expert of laboratory processes to provide appropriate knowledge to laboratory system implementations.
• Support the implementation and ongoing use of MES, serialization, and OEE systems. Knowledge of ERP systems such as SAP is required to understand the key interfaces for MES and Batches / Dispensing systems.
• Administer local systems as necessary. Work to a local / global support model for day-to-day administration; not compromising the data integrity of these systems.
• Maintain the integrity of global and local systems and ensuring backup up solutions are in place by the global or local ITMUs using standardized solutions.
  Consider all regulatory compliance requirements for system implementation and maintenance including GMP, computer systems validation, SOX, security and risk. Assist in the generation and execution of validation deliverables.
• Ensure appropriate service levels are developed and monitored for support of global and local systems working with the global team, external partners and providers of software. Ensure support partners perform

• Careers IT related or engineerings
• 4+ years of experience in pharmaceutical or related manufacturing industry and Supply Chain, Operations, Quality, Enterprise Asset Management, and Costing functions is a plus.
• English is a plus
• Experience in systems related to the pharma industry

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