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Document Management Associate

Job in San Diego, San Diego County, California, 92189, USA
Listing for: BioPhase
Seasonal/Temporary position
Listed on 2026-01-14
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 28 - 30 USD Hourly USD 28.00 30.00 HOUR
Job Description & How to Apply Below

Base pay range: $28.00/hr - $30.00/hr

Senior Clinical Recruiter at Bio Phase Solutions | Life Sciences

Location: San Diego, CA (Fully Onsite)

Pay Rate: $28-30/hr

Employment Type: Temp-to-Hire

About the Role

Bio Phase 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 Responsibilities
  • Manage and maintain controlled documents and records in accordance with GMP and quality standards
  • Support document storage, revision control, access permissions, and archival processes
  • Assist with issuing batch records and controlling label stock
  • Support internal and external audits by providing requested documentation
  • Collaborate with cross‑functional teams across Quality, Manufacturing, and Operations
  • Assist with SOP drafting, revisions, and training support as needed
  • Ensure document integrity, compliance, and confidentiality at all times
Qualifications
  • Bachelor’s degree in Biology or a related field (or equivalent experience)
  • 1–2+ years of experience in a GMP Quality or Manufacturing environment
  • Familiarity with GMPs and regulated documentation practices
  • Experience drafting, revising, or managing controlled documents preferred
  • Strong attention to detail and organizational skills
  • Comfortable working both independently and in a team‑based environment
  • Fully onsite in San Diego
  • Office‑based role with extended computer use
  • May require lifting up to 20 lbs occasionally
Seniority level

Associate

Employment type

Contract

Job function

Research

Industries

Biotechnology Research and Pharmaceutical Manufacturing

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Position Requirements
10+ Years work experience
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