QA Document Control Specialist I/II/III

QA Document Control Specialist I/II/III Legend Biotech is a global biotechnology company dedicated to treating life‑threatening diseases. Headquartered in Somerset, New Jersey, we develop advanced cell therapies across multiple technology platforms. Role Overview The QA Document Control Specialist is an exempt level position responsible for supporting the document management process within a cell therapy manufacturing facility. In a sterile GMP environment, the position ensures compliance with the document management system, document storage and retention, and document issuance and reconciliation. Key Responsibilities Serve as a Document Control reviewer for new and revised procedures and documents to ensure compliance with global and site procedures. Support Document Management system users with workflow handling and electronic system usage. Manage the periodic review process for procedures. Issue batch‑related documentation in support of GMP manufacturing. Reconcile GMP documentation following document lifecycle requirements. Create and issue GMP logbooks. Manage storage and archival of GMP documents and batch‑related records. Perform tasks in a manner consistent with safety policies, quality systems and cGMP requirements. Review and approve SOPs and other documentation. Drive continuous improvement. Apply advanced computer skills to increase department productivity and broaden technical knowledge. Collaborate with quality counterparts in Manufacturing Operations, Engineering, Validation, Quality Control, Operations Technical Support, Supply Chain and Planning. Requirements Minimum of a Bachelor’s degree in Science, Information Science or a related technical discipline. Minimum of 2 years relevant work experience, preferably in an aseptic manufacturing facility, quality assurance, manufacturing compliance, clinical quality, or cell therapy. Knowledge of GxP quality systems and relevant regulations (e.g., 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 (TruVault/Veeva) preferred. Strong written and verbal communication skills and analytical/problem‑solving abilities. Flexible, highly motivated, strong organization skills, and ability to multi‑task with attention to detail. Base Pay $70,671 – $92,757 USD Benefits Legend Biotech offers a best‑in‑class benefits package that includes medical, dental, vision, 401(k) with company match, equity and stock options, paid parental leave, paid time off (15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, 3 floating holidays), flexible spending and health savings accounts, life and AD&D insurance, disability coverage, legal assistance, supplemental plans, commuter benefits, family planning resources, and well‑being initiatives. EEO Statement Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. We ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, age, disability, national origin, marital status, genetic information, citizenship status, veteran status, or any other characteristic protected by applicable law. Employment is at‑will and may be terminated at any time with or without cause. Legend may adjust base salary or other discretionary compensation at any time based on individual performance, team, or market conditions. Legend maintains a drug‑free workplace. #J-18808-Ljbffr