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Senior Validation Lead – cGMP & IQ/OQ/PQ Expert
Job in
Cincinnati, Wayne County, Illinois, USA
Listed on 2026-01-01
Listing for:
Salas O'Brien
Full Time
position Listed on 2026-01-01
Job specializations:
-
Engineering
Regulatory Compliance Specialist
Job Description & How to Apply Below
A full-service engineering firm is seeking a Lead Validation Specialist. This role involves conducting cGMP audits, managing validation efforts, and interfacing with clients and contractors to develop protocols that comply with FDA regulations. The ideal candidate will have a Bachelor's degree with 5-7 years of experience in an FDA-regulated environment, demonstrating strong project management and communication skills. Full-time position with opportunities for career advancement in a fast-paced industry.
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Position Requirements
10+ Years
work experience
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