QA Document Control Specialist
Legend BiotechGhent, East Flanders, Belgium
Posted February 25, 2026
Full Time
About the Company
Legend Biotech is a global biotechnology company that focuses on developing, producing, and commercializing innovative and life-saving cell therapies, including treatments for persistent diseases such as cancer.
Job Description
Join our Talent Pool for QA Document Control Specialist! The role involves managing document control systems and processes for a cell therapy manufacturing facility in a sterile GMP environment. You will ensure compliance with global and local procedures, support users with workflows, and perform tasks in line with safety policy, quality systems, and cGMP requirements.
Requirements
- Bachelor student, secondary diploma, or equivalent experience
- No experience required, but experience in a GMP environment is a plus
- Dutch and technical English language skills
- Knowledge of GxP quality systems, including relevant regulations and guidelines (such as 21 CFR, ICH Q10, EU GDP/GMP, Part 11/Annex 11, PIC/S, MHRA)
- Operational experience with electronic quality systems
- Experience with Document Management Systems (e.g. TruVault, Veeva)
- Good knowledge of Microsoft Office (Outlook, Excel, Word, PowerPoint)
Benefits
- Meaningful job with excellent work-life balance
- Supportive and innovative work environment
- Opportunity to work with people from all over the world
- Contract of indefinite duration
- Competitive salary package
- Additional statutory holiday days
- Meal vouchers
- Group and hospitalization insurance
- Double holiday pay
- Year-end and performance bonus
- Fun and informal events
