cGMP Consulting is seeking a motivated and detail-oriented individual to manage electronic batch records through the PAS-X system, including template design, compliance oversight, and change control for manufacturing documentation. This mid-level role offers leadership and responsibility in a dynamic, GMP-compliant manufacturing environment. The ideal candidate will excel in leading cross-functional collaboration, troubleshooting, change management, and EBR release activities while demonstrating independence. This candidate should have a strong understanding of current Good Manufacturing Practices (cGMP) and FDA regulations and guidelines, including 21 CFR Part 11. This is a Contract to Hire position located in Melrose Park, IL.
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Job Type
Full-time
Career Level
Mid Level