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Manufacturing Specialist

VirtualVocations
Canton, Ohio, United States
Full-time

A company is looking for a Specialist Manufacturing with extensive GMP experience in drug substance manufacturing.Key ResponsibilitiesOversee and manage NC Class II / III records, CAPA, and change control recordsMonitor site performance metrics and identify improvement opportunitiesCoordinate project activities, including meeting minutes and data analysisQualifications & Requirements5+ years of experience in protein, API, DS, DP, or packaging manufacturing environments5+ years of knowledge in cGMP principles and FDA regulatory guidelinesExperience managing quality records and validation principlesStrong team leadership and facilitation skillsPreferred scientific degree or equivalent practical experience in GMP environments

13 hours ago
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