Computer System Validation Consultant - Katalyst CRO : Job Details

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• Perform lifecycle computer-related systems validation in the biological manufacturing (GMP) industries with a minimum of six (6) years of experience.
• Support client sites with computer-related systems validation activities.
• Work in a GMP environment, developing lifecycle documentation, executing protocols, and leading projects for computerized systems such as laboratory, computer, and LIMS systems.
• Identify gaps in lifecycle documentation and lead efforts to address them.
• Support the CSV team in achieving its goals and objectives.

• Bachelor's degree in Computer Science preferred, or an equivalent combination of education and experience.
• Experience with computerized systems (e.g., Laboratory, LIMS, etc.) and ERP systems (SAP, QMS (Veeva Vault), LIMS (MODO), PV Works).

• Seniority level: Mid-Senior level
• Employment type: Contract
• Job function: Quality Assurance
• Industries: Pharmaceutical Manufacturing

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