Job Title: Validation Engineer Location: Indianapolis / Bloomington, IN (100% Onsite) Duration: Long term Contract Interview Mode: Onsite (Local candidates preferred) Overview We are seeking a Validation Engineer with strong experience in Computer Systems Validation (CSV), equipment qualification, and GMP-regulated environments. The ideal candidate will support validation activities, documentation migration, and equipment qualification to ensure compliance with regulatory standards. Key Responsibilities Lead migration of legacy validation documents into the Kneat digital platform, ensuring accuracy and compliance Perform equipment qualification for lab instruments (pH meters, thermal mixers, peristaltic pumps, nutating mixers, etc.) Execute temperature mapping studies, including work with Ellab systems or similar equipment Support Computer Systems Validation (CSV) activities and documentation Assist Process Engineering teams to ensure project timelines and milestones are met Ensure all validation activities comply with GMP and regulatory requirements Maintain clear, accurate, and compliant documentation Required Qualifications Bachelor s degree in Engineering, Science, or related field 6+ years of experience in Computer Systems Validation (CSV) 4+ years of experience in pharmaceutical manufacturing environment Hands-on experience with equipment qualification and validation Strong knowledge of CSV principles and regulatory compliance Experience working in onsite, fast-paced environments #J-18808-Ljbffr
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