Specialist, QA Document Control
Oxford BiomedicaDurham, North Carolina, United States
Posted April 8, 2026
Full Time
About the Company
OXB is a quality and innovation-led viral vector CDMO with a mission to enable its clients to deliver life-changing therapies to patients around the world.
Job Description
OXB is seeking a Specialist, QA Document Control to join its Quality team in Durham, NC. The role will cover all aspects of a GMP document lifecycle and day-to-day documentation support for business operations.
Requirements
- Bachelorās degree or higher in Data/Information Management or related field
- Minimum of 3 years of GMP document control or GMP data management experience
- Hands-on experience with creation of GMP documents (e.g. procedures, forms, BRs, etc.)
- Comprehensive knowledge of GMP regulations for document and records management
- Prior experience with electronic document management system (Veeva)
Benefits
- Competitive total reward packages
- Wellbeing programs that support your mental and physical health
- Career development opportunities to help you grow and thrive
- Supportive, inclusive, and collaborative culture
- State-of-the-art labs and manufacturing facilities
