Job Description
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, etc.
Supporting identifying Gaps in Lifecycle documentation and leading efforts to correct the Gaps.
Support the CSV team to ensure they are achieving all identified goals and objectives.
Requirements: Minimum of Six (6) years performing lifecycle computer-related systems validation in the biological manufacturing (GMP) industries.
Computer Science bachelor's degree: preferred.
The equivalent combination of education/experience may be accepted in lieu of degree.
Experience with computerized systems (e.g., Laboratory, LIMS, etc.).
Experience with ERP systems (SAP, QMS (Veeva Vault), LIMS (MODO), PV Works). Katalyst Healthcares and Life Sciences
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