Are you ready to take the lead in one of the most innovative fields in biotech?
As a CAR-T production supervisor at Legend Biotech, you’ll lead a motivated team of operators in a cleanroom facility, ensuring smooth operations and a high standard of quality from start to finish. You’ll help make sure that daily activities run smoothly, safely, and in line with GMP standards. You’ll be guiding your team with all the responsibilities that come with it: facilitating growth of your team, inspiring them in their daily tasks and maintaining quality levels, and solving problems as challenges arise.

What Can You Expect? 

As CAR-T production supervisor, you’ll be the driving force behind our operations. Your responsibilities will include:

• Leading & inspiring: manage operational teams and oversee key steps in the CAR-T production process.
• Ensuring quality: you manage all aspects of quality and ensure strict compliance with cGMP standards. As a domain expert for Quality and Operations, you play a central role in GMP inspections.
• Collaborating & solving: you'll be the go-to person for production challenges and work closely with other departments to find solutions.
• Keeping us organized: manage and review critical documentation like procedures, work instructions, logs and transfer forms. You'll also oversee the release and review of batch records for quality control. 
• Training & developing talent: as a manager, you'll make sure your team has the skills and knowledge to excel. 
• Driving operational excellence: launch projects to boost efficiency, cut costs, and improve quality. Inspire continuous improvement every day.  

Who Are We Looking For? 

Education

• You have a bachelor's or master's degree in science, bio-engineering, pharmacy or a related field of study or you are equivalent through experience.  

Experience

You have either:

• Experience in people leadership in a regulated environment,
• Or at least 3 years of experience in a GMP or ATMP environment (preferably in the biotech or pharmaceutical industry), and a drive for the new challenge of leading a team.

Expertise

• Comfortable with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
• Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems experience is a plus.
• Knowledge of cGMP regulations and clean room operations is a plus. 

Languages

• You speak and write fluent English.   

Strengths 

• Excellent communication and organizational skills.
• Empathetic leader with strong people management abilities. 
• Positive, adaptable, and inspiring under rapidly changing circumstances. 
• Skilled at problem solving, prioritizing and multitasking.
• Detail-oriented and process-driven.

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.
• 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. 

#LI-AG1

#LI-Onsite

Are you looking for a meaningful job, in which you can really make a difference in patients’ lives? Do you love cleanliness, accuracy, quality and working in a very structured way? Then join our vibrant Operations Team and step into a role where you are not just an employee but a Legend in the making. Sound challenging but no experience yet? Don’t worry, we will teach you how ! Just as we take care of our patients, we take care of our employees. 

What can you expect?  

Here's what you'll do: 

• After an extensive training in aseptic working and Good Manufacturing Practices (GMP), you will join our Operations Team. To clarify for you. Aseptic working refers to a set of practices and procedures applied to ensure sterility in the cleanrooms, where our advanced cell therapies are made. GMP guideliness on the other hand, ensure that our products are produced and controlled according to high quality standards.  

• You, along with your fellow operators and team leads, inspect and maintain the used equipment, clean and disinfect materials meticulously, and ensure a correct transfer between different production zones. You support the daily aseptic and manual production process of our therapy according to strictly defined actions and standard procedures. By doing so you contribute to the timely delivery of high quality and life-saving therapies to our patients.  

• Working in an aspetic environment entails you must also wear sterile clothing. Furthermore, we work in a shift regime, no nights but weekends. 

Who are we looking for? 

We are on the hunt for passionate people ready to make a difference. More important than the list below is your drive and enthusiasm to go for it together.   

Education:

• You have a secundary education diploma or you are equivalent through experience. More important than your degree, is your work ethic and eagerness to learn.  

Experience:

• We offer extensive, in-house training after which you can start working smoothly in your new role.  

Languages:

• You are fluent in Dutch and/or English. 

Strengths:

• You have a strong sense of responsibility. You are fully aware that your tasks are a vital step in our processes to getting our life-saving therapies to our patients in a timely manner. 

Expertise:

• You communicate clearly and openly and you are a true team player.  

What do we offer?

• A meaningful job with an excellent work-life balance. You will work 4 days in shifts, followed by 4 days off. 

• A supportive and innovative work environment that encourages learning and personal development. 

• The opportunity to work with people from all over the world. 

• You start working through interim contracts. After 6 months you'll receive a permanent contract
• An attractive salary package with numerous benefits, including additional statutory vacations, meal vouchers, group and hospitalization insurance, double vacation pay, and performance bonuses. 

• Participation in various 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, including two in Ghent: Obelisc (Technology Park Zwijnaarde) and Tech Lane (Eilandje Zwijnaarde). In Ghent, we focus on the production of advanced CAR-T cell therapies for the treatment of multiple myeloma, in close collaboration with Johnson & Johnson. 

Who we are

DoubleVerify is a leading software analytics firm, publicly traded since April 2021 (NYSE: DV). We are the go-to source for tracking and analyzing digital ads for globally recognized brands and publishers. If you've ever come across an ad online, be it on the Web, Mobile, or CTV device, chances are we measured it.

Serving both advertisers and publishers, DoubleVerify operates on a massive scale, handling over 100B events per day. We verify that all ads are fraud free, appear next to appropriate content, appear to people in the right geography and measure the viewability and user’s engagement throughout the ad’s lifecycle. We also offer tools to empower clients to analyze, visualize and optimize the quality of their ad inventory.

With R&D centers in Belgium, USA, Israel, Finland, and Germany, we are a truly global company. We thrive in a dynamic environment with numerous challenges to solve. If you like to work in a large-scale environment and want to contribute to building products that significantly impact the industry and the web, DoubleVerify is the place for you.

The team and your role

We are looking for a highly motivated individual to join the Publisher Activation team based in Ghent.

The Publisher Activation team is dedicated to creating new integrations and tools that assist our customers, the publishers, in using our measurement technologies. To gather the necessary metrics for our measurement services, we directly integrate with the native browser APIs on the client-side. On the server side, we have multiple components that further process the requests initiated by our client-side scripts.

Our technology stack is built for scale and reliability. We use GitLab for version control and collaboration, with CI/CD and Infrastructure as Code (Terraform) powering our deployment pipeline. Grafana and Prometheus give us real-time visibility into our systems, while Google Cloud Platform and Cloudflare provide our serverless infrastructure. We store our data in BigQuery and rely on tools like Ox, Jest, and Playwright for testing and security. We also make heavy use of AI coding agents like Claude, Copilot, and Cursor to accelerate our development.

As a Junior Software Engineer Intern, you will be involved in the day-to-day activities of our team, including standups, engineering discussions, and code reviews. You will collaborate on our existing projects and also have the opportunity to cover a project from start to end. This is a hands-on position where you will be expected to write code and solve complex problems. You will be able to use agentic AI workflows to speed up your work, and you will also be assigned a mentor who will guide you throughout your internship, providing a rich learning experience. 

Who you are

You…

• are a Master's student in Computer Science or a closely related field. 
• are a problem solver first, not just a coder
• enjoy collaborating and are proactive, but you can also work independently

Extra plus points for:

• Familiarity with: JavaScript/TypeScript, serverless workers, web technologies, automated software testing, browser APIs, code profiling
• Good data analysis skills
• Open Source contributions or public GitHub projects (do share!)

What We Offer

• A dynamic environment that encourages rapid growth
• An 8-week internship during the summer period (Jul, Aug, Sept)
• Mentorship and Learning Opportunities
• A diverse and inclusive company culture
• Fun office perks such as snacks, lunch, etc.
• On-site at our Ghent office at least 3 days/week