Kelly Services
Computer Systems Validation Specialist
Kelly Services, Wilmington, Delaware, us, 19894
Kelly Services - Computer Systems Validation Specialist - Wilmington, Delaware
Kelly Services is actively recruiting for a Computer Systems Validation Specialist for a Long Term Contract opportunity in Newark, DE.Qualifications:Bachelor’s degree required, preferred in computer science, engineering, or other sciences.Minimum of 2-3 years of experience working with automation and/or computerized system validations.Must have direct experience in validation of computer/automation/software validation (prepare IQ, OQ, PQ protocol, resolve deviations, prepare final summary report) in compliance with FDA 21 CFR Part 11 / 210 / 211.Strong written and oral communication skills.Strong organizational and time management skills.Experience working in a GXP environment.Responsibilities:Support Data Integrity Manager with validation of automated equipment and control systems.Responsible for execution of test scripts, creating, and modifying draft protocols.Responsible for reviewing previously executed CSV activities, identify gaps, including GMP documentation revisions.Support with creating and modifying validation documentation.Write reports which summarize the results of the protocol executions.If you feel you have the knowledge and expertise, apply today to connect with a Kelly professional who will work to enrich your life.
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Kelly Services is actively recruiting for a Computer Systems Validation Specialist for a Long Term Contract opportunity in Newark, DE.Qualifications:Bachelor’s degree required, preferred in computer science, engineering, or other sciences.Minimum of 2-3 years of experience working with automation and/or computerized system validations.Must have direct experience in validation of computer/automation/software validation (prepare IQ, OQ, PQ protocol, resolve deviations, prepare final summary report) in compliance with FDA 21 CFR Part 11 / 210 / 211.Strong written and oral communication skills.Strong organizational and time management skills.Experience working in a GXP environment.Responsibilities:Support Data Integrity Manager with validation of automated equipment and control systems.Responsible for execution of test scripts, creating, and modifying draft protocols.Responsible for reviewing previously executed CSV activities, identify gaps, including GMP documentation revisions.Support with creating and modifying validation documentation.Write reports which summarize the results of the protocol executions.If you feel you have the knowledge and expertise, apply today to connect with a Kelly professional who will work to enrich your life.
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