GMP-Driven Document Control Specialist (On-site)
Codis
Codis is seeking a meticulous Document Control Specialist to join our Quality Assurance team in Brentwood, Missouri. You will maintain controlled quality documents supporting FDA-regulated pharmaceutical manufacturing, ensuring accuracy, organization, and compliance across procedures, records, and audits. Key duties include developing SOPs, coordinating document routing, and maintaining archives, while collaborating with Production, Quality, Purchasing, and R&D. #J-18808-Ljbffr Codis
Vacancy posted 2 days ago
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