What are the responsibilities and job description for the Quality Person In Plant position at Legend Biotech?
As a Quality Person in Plant, you will become part of our vibrant Operations Team, dedicated to excellence, innovation, and continuous improvement. Are you ready to embrace challenges and grow beyond your dreams? Then join us and become a Legend in your own right. Here your passion and commitment to quality will pave the way for life-saving therapies, making an impact on patients' lives around the globe.
What can you expect?
Responsibilities
In our GMP-controlled environment, your expertise ensures the highest quality of cell therapy products. Your tasks and responsibilities include, but are not limited to:
We are looking for people who thrive in a GMP-regulated environment, and who are passionate about quality.
Legend Biotech is a global biotechnology company developing, manufacturing, and commercializing innovative and life-saving cell therapies in the fight against diseases that are considered intractable and incurable, including cancer.
Since our establishment in 2014 in Somerset, New Jersey, we have grown into a company of more than 1,800 employees spread across six manufacturing units worldwide. Two of these are in Ghent: Obelisc (Technologie Park, Zwijnaarde) and Tech Lane (Eilandje Zwijnaarde)
In Ghent, Legend Biotech focuses on producing its advanced CAR-T therapy for the treatment of multiple myeloma, a common but difficult-to-treat blood cancer, and on bringing this live-saving therapy to patients in Europe and far beyond.
Creating hope and new opportunities for patients and contributing to a future where all cancers are curable is what everyone drives here at Legend Biotech, regardless of their role or function.
Apply now and join us in our mission to transform the world of oncology and medicine, one patient at a time.
What can you expect?
Responsibilities
In our GMP-controlled environment, your expertise ensures the highest quality of cell therapy products. Your tasks and responsibilities include, but are not limited to:
- Quality Oversight and Compliance: You are a guardian of quality within our plant overseeing adherence to all high-quality standards across our manufacturing process. You regularly perform quality checks and audits on processes, documentation, and manipulations, ensuring compliance and excellence at every step.
- Process Documentation and Operational Support: You are responsible for real-time review of process documentation, supporting unit operations, and, when necessary, release activities ensuring accuracy and compliance. You work hand in hand with site personnel, offering guidance and collaborating to resolve manufacturing challenges efficiently and effectively.
- Continuous Improvement and Safety: You proactively work to minimize deviations and non-conformances by embedding a culture of continuous improvement and strict adherence to compliance standards. You actively contribute to the investigation and resolution of manufacturing deviations, CAPAs, change controls, and complaints, ensuring lessons learned are applied and improvements are made.
- Regulation and Inspection Readiness: You play a critical role in preparing for and supporting regulatory inspections and audits, always maintaining a state of inspection readiness. You perform internal housekeeping audits to continuously uphold and enhance our standards.
- Maintain Safety and GMP Compliance: You execute all tasks in alignment with safety policies, quality systems, and GMP requirements, ensuring a safe and compliant working environment.
We are looking for people who thrive in a GMP-regulated environment, and who are passionate about quality.
- Education: You have a bachelor's, master’s or PhD degree in science, information science or another related technical discipline.
- Experience: We offer extensive, in-house training after which you can start working smoothly in your new role.
- Languages: You are proficient in Dutch and English, with strong written and oral communication skills.
- Strengths and expertise: You are decisive, highly organized, detail-oriented, and a true team player. In addition, you also possess rock-solid interpersonal and analytical skills.
- A meaningful job, with a 4-days on and 4-days off regime, which can create opportunities for a nice work-life balance.
- At Legend Biotech, you find more than a career. We offer you a path to growth, learning and personal development in an innovative environment, surrounded by colleagues you can really count on.
- Enjoy the opportunity to work with people from all over the globe. We are fully committed to diversity and inclusion and value every voice.
- The opportunity to volunteer for numerous projects and charities, allowing you to develop new skills.
- An indefinite contract and an attractive salary complemented by a comprehensive package of fringe benefits such as meal vouchers, group and hospitalization insurance. And as icing on the cake, you'll also receive annually double vacation pay, an end of year bonus and a performance bonus.
- A lot of fun and informal events.
Legend Biotech is a global biotechnology company developing, manufacturing, and commercializing innovative and life-saving cell therapies in the fight against diseases that are considered intractable and incurable, including cancer.
Since our establishment in 2014 in Somerset, New Jersey, we have grown into a company of more than 1,800 employees spread across six manufacturing units worldwide. Two of these are in Ghent: Obelisc (Technologie Park, Zwijnaarde) and Tech Lane (Eilandje Zwijnaarde)
In Ghent, Legend Biotech focuses on producing its advanced CAR-T therapy for the treatment of multiple myeloma, a common but difficult-to-treat blood cancer, and on bringing this live-saving therapy to patients in Europe and far beyond.
Creating hope and new opportunities for patients and contributing to a future where all cancers are curable is what everyone drives here at Legend Biotech, regardless of their role or function.
Apply now and join us in our mission to transform the world of oncology and medicine, one patient at a time.