About this opportunity
Katalyst CRO lists this Senior Validation Engineer - GMP Compliance Lead opportunity in charleston, South Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Katalyst CRO is seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. You will plan, execute, review, and approve validation documentation for equipment, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations.
Responsibilities include leading DQ/IQ/OQ/PQ, authoring validation plans and reports, and mentoring junior staff.
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Worksite address
charleston, SC, 29408, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.