Document Management Associate

Document Management Associate (Temp-to-Hire)BioPhase is seeking a Document Management Associate to support quality and compliance activities within a GMP-regulated environment. This is a fully onsite, temp-to-hire opportunity based in San Diego, ideal for someone with hands-on experience managing controlled documents and supporting audits.Key ResponsibilitiesManage and maintain controlled documents and records in accordance with GMP and quality standardsSupport document storage, revision control, access permissions, and archival processesAssist with issuing batch records and controlling label stockSupport internal and external audits by providing requested documentationCollaborate with cross-functional teams across Quality, Manufacturing, and OperationsAssist with SOP drafting, revisions, and training support as neededEnsure document integrity, compliance, and confidentiality at all timesQualificationsBachelor's degree in Biology or a related field (or equivalent experience)1-2+ years of experience in a GMP Quality or Manufacturing environmentFamiliarity with GMPs and regulated documentation practicesExperience drafting, revising, or managing controlled documents preferredStrong attention to detail and organizational skillsComfortable working both independently and in a team-based environmentWork EnvironmentFully onsite in San DiegoOffice-based role with extended computer useMay require lifting up to 20 lbs occasionally