Ready to support life-saving therapies while keeping our systems running smoothly?
Join our Technical Operations team in Ghent and become a key player in the CAR-T Asset Management group. If you thrive in a structured environment, love organizing and documenting, and want to contribute to cutting-edge cell therapy production, then this is your opportunity to make a meaningful impact.
What can you expect?
As a C&Q Support Technician, you'll be the backbone of our computerized GMP systems, ensuring everything runs like clockwork. Here's what you'll do:
* Day-to-day equipment administrator activities: Manage day-to-day equipment administrator activities in cleanrooms, including user access management, audit trail extraction, file deletion, backups, and document this in line with Good Documentation Practices.
* Data Management: Export run data to centralized locations upon request and maintain oversight of user access requests and segregation of duties.
* Archiving: Support both paper and digital archiving of executed Commissioning & Qualification (C&Q) documentation and track oversight.
* Documentation Support: Collect prerequisite documentation for C&Q and periodic review activities to ensure smooth execution.
Who are we looking for?
Education
* You hold a graduate or bachelor's degree in Science, Engineering, Bioengineering, or a related technical discipline. (preferred but not required)
Experience
* You have at least 1 year of experience in a regulated environment (preferred but not required).
Languages
* You communicate clearly English, written and spoken.
Strengths
* You're highly organized, detail-oriented, and have a "right-first-time" mindset.
* You can work independently, prioritize tasks, and adapt flexibly to ensure business continuity.
Expertise
* You're proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).
* You understand the importance of procedures and documentation in a GMP environment.
What do we offer you?
* A meaningful and impactful career in the rapidly evolving field of cell therapy manufacturing.
* A supportive and innovative work environment. We value and encourage learning and personal development.
* The opportunity to work with people from all over the world.
* A contract of indefinite duration and an attractive salary package complemented by many fringe benefits, such as additional statutory vacations, meal vouchers, group and hospitalization insurance, double vacation pay, an end-of-year and performance bonus.
* Many fun and informal events.
About Legend Biotech
Legend Biotech is a global biotechnology company dedicated to developing, manufacturing, and commercializing innovative and life-saving cell therapies for the treatment of chronic and life-threatening diseases, such as cancer.
The company was founded in 2014 and is headquartered in Somerset, New Jersey. Legend Biotech now employs over 2,400 people across six global manufacturing sites. Two of these sites are in Ghent: Obelisc (Technology Park Zwijnaarde) and Tech Lane (Eilandje Zwijnaarde).
In Ghent, Legend Biotech focuses on the production of advanced CAR-T cell therapies for the treatment of multiple myeloma, in close collaboration with Johnson & Johnson.
Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
Legend Biotech maintains a drug-free workplace.