Job Description:
Summary:
Interested in working with a leading Biopharmaceutical company? We are looking for a Document Control Associate who has GMP experience and working knowledge of EDMS to assist the Quality Assurance management.
Location: Los Angeles, CA
Key Responsibilities:
- Managing documents and record workflows using Veeva EDMS.
- Recording, indexing, scanning, and uploading documents into EDMS.
- Supporting Quality Management Systems with deviations, CAPAs, change controls, audits, etc.
- Subject to long periods of sitting/standing; work is all onsite in an office environment.
Requirements:
- Working knowledge of FDA regulations and GMPs.
- Experience with EDMS desired.
- Knowledge of GDPs.
- Knowledge of SharePoint desired.
- Education: Bachelor's Degree (Scientific Discipline preferred).
- Experience: 3+ years of experience in Quality Assurance, Document Control, Records Management, or Manufacturing in a biotech/pharmaceutical company.
