QA Document Control Specialist

Job Description

Legend Biotech is seeking a Quality Assurance Document Control Specialist to monitor the integrity of documents within a GMP-controlled environment. The specialist will manage the document lifecycle, ensuring quality and compliance in the production of cell therapy products.Role responsibilities include:

• Managing document control systems
• Reviewing procedures and documents for compliance
• Providing support for the Document Management System
• Overseeing the issuance of batch-related documentation
• Handling the reconciliation and archiving of GMP documentation

The ideal candidate will have:

• A secondary school or bachelor's degree
• Proficiency in Dutch and/or English
• Strong organizational and multitasking skills
• Familiarity with Microsoft Office applications

Legend Biotech offers:

• An indefinite contract
• An attractive salary
• Additional legal vacation days, meal vouchers, group and hospitalization insurance
• Annual double vacation pay, end of year bonus, and a performance bonus
• Opportunity to volunteer for numerous projects and charities