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Job description
PharmaLogic Holdings Corp. seeks a Director of 211 Manufacturing Quality & Regulatory Affairs to provide enterprise quality governance for US facilities and client programs under 21 CFR Parts 210 and 211. You will lead the QMS, regulatory compliance, inspection readiness, and continuous improvement across sites.
Ideal candidates have 10+ years in pharma/biotech manufacturing, 5+ years in quality leadership, and proven success with FDA inspections in CDMO or regulated settings.
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Who can apply
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