Join to apply for the Computer System Validation Consultant role at Katalyst CRO . Support client site with computer-related systems validation activities. Work in a GMP environment in lifecycle documentation development, protocol execution, and leading project efforts for computerized systems including laboratory, computer, and LIMS systems. Identify gaps in lifecycle documentation and lead efforts to address them. Support the CSV team to ensure they achieve all goals and objectives. Responsibilities Support client site with computer-related systems validation activities. Work in a GMP environment in lifecycle documentation development, protocol execution, and leading project efforts for computerized systems including laboratory, computer, and LIMS systems. Identify gaps in lifecycle documentation and lead efforts to address them. Support the CSV team to ensure they achieve all goals and objectives. Requirements Minimum of six (6) years of experience performing lifecycle computer-related systems validation in the biological manufacturing (GMP) industries. Bachelor's degree in Computer Science preferred. Equivalent education/experience may be accepted. Experience with computerized systems (e.g., Laboratory, LIMS, etc.). Experience with ERP systems such as SAP, QMS (Veeva Vault), LIMS (MODO), PV Works. Seniority level Mid-Senior level Employment type Contract Job function Quality Assurance Industries Pharmaceutical Manufacturing #J-18808-Ljbffr Katalyst HealthCares & Life Sciences
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