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.
Requirements
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.
Numbers & Facts
Location
San Diego, California
Website
genovice.com
Skills
Biologyunmatched
Biotech and Pharmaceuticalunmatched
Documentationunmatched
Drug Manufacturingunmatched
Environmental Sciencesunmatched
GMP (Good Manufacturing Practices)unmatched
Manufacturingunmatched
Organizational Skillsunmatched
Quality Assuranceunmatched
Quality Controlunmatched
Quality Managementunmatched
Support Documentationunmatched
Technical Editingunmatched
Technical Writingunmatched
Writing Skillsunmatched
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