Join to apply for the Computer System Validation Consultant role at Katalyst CRO . Continue with Google 4 months ago Be among the first 25 applicants. Responsibilities: 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. Qualifications: 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). Additional Details: Seniority level: Mid-Senior level Employment type: Contract Job function: Quality Assurance Industries: Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Katalyst CRO by 2x. Get notified about new Validation Consultant jobs in St Joseph, MO . We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr Katalyst CRO
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