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GMP Document Control Specialist

KBI Biopharma, Inc.

KBI Biopharma, Inc. seeks a Document Control Coordinator I/II to manage controlled documentation lifecycle, including issuance, review, approval, and archival in GxP environments. You will support GMP compliance across manufacturing, QA, and regulatory activities for internal stakeholders and clients. Responsibilities include issuing records, maintaining forms and logbooks, processing documents in EDMS, and assisting during audits and inspections. #J-18808-Ljbffr KBI Biopharma, Inc.

Vacancy posted 1 day ago
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