CAR-T Operations Technical Lead Clean Room
Ghent, East Flanders, Belgium
Company Information
Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK) cell-based immunotherapy.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Role Overview
Our Operations Team in Ghent is on the lookout for a passionate CAR-T Operations Technical Lead in the Clean Room. Ready to make an impact? Then apply now and join a team dedicated to pushing the boundaries of personalized medicine!
What Can You Expect?
As a CAR-T Operations Technical Lead in the Clean Room, you will make an immediate difference in the lives of patients. Here's what you'll do:
* Coordination of daily production activities: You will coordinate essential parts of the CAR-T production process and manage the operational teams in your clean room.
* Quality and compliance: You will manage all quality aspects of production activities in your clean room and ensure strict compliance with cGMP standards.
* Collaboration: You will work closely with various teams and departments to integrate new technologies and processes.
* Operational excellence: You will optimize production processes and contribute to initiatives to increase efficiency, reduce costs and improve quality.
* Safety and environment: You will oversee the implementation of safety and environmental health procedures.
Who Are We Looking For?
Education:
* You have a bachelor's or master's degree in science, bioengineering, pharmacy or a related field of study or you are equivalent through experience.
Experience:
* You have at least 2 years of experience in a cGMP or ATMP environment, preferably in the biotech or pharmaceutical industry. You have substantial experience with grade C aseptic GMP manufacturing. You have a proven track record of leading teams or managing projects.
Languages:
* You are fluent in Dutch or English, with strong oral and written communication skills.
Strengths:
* You are a true team player who also enjoys working independently. You are good at prioritizing, problem solving and multitasking. You know how to keep a cool head, even under very stressful circumstances.
* You have an eye for detail and procedures. You have a positive attitude.
Expertise:
* You have a thorough knowledge of cGMP regulations and clean room operations.
* You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
What Do We Offer?
* A meaningful job that contributes directly to the well-being of patients.
* An excellent work-life balance. You work 4 days. Then you enjoy 4 days off.
* 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.
* An open-ended contract 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.
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