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Genovice

San Diego / Global

QA Documentation Specialist

Job Description

QA Documentation SpecialistLocation: San Diego, CA Type: Full Time Industry: Pharmaceutical ManufacturingPosition Overview: Our client is seeking a QA Documentation Specialist to support the development, revision, and review of GMP manufacturing documentation. The ideal candidate will have pharmaceutical or life-sciences experience and a strong understanding of how to create and assemble clear, compliant batch records.Key Responsibilities:Create, revise, format, and review master batch records and related manufacturing documents.Work with Quality, Manufacturing, and technical subject-matter experts to collect required information.Ensure documents comply with GMP, good documentation practices, and site procedures.Manage document revisions, approvals, and version control.Identify documentation gaps and support corrections.Qualifications:Experience developing or reviewing batch records in a pharmaceutical, biotech, or life-sciences environment.Working knowledge of GMP and good documentation practices.Strong technical writing, editing, formatting, and organizational skills.Experience with document-control or electronic quality-management systems is preferred.
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