QA Documentation Specialist — GMP Records & Archiving

PCI Pharma Services in San Diego is seeking a QA Documentation Associate I to coordinate review and approval of GMP documents within an electronic document management system. You will work with document authors and reviewers to ensure timely processing of changes.
Minimum 0–2 years of documentation experience is required; a High School Diploma is required with Associates degree preferred. Proficiency in Microsoft Office and data entry is essential.

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