As a Quality Control Support Technician at Legend Biotech, you're stepping into a role that’s more than just a job. It is your chance to make an impact on patients’ lives worldwide. Being part of our Quality Operations Team, you will work closely with team leads and QC analysts to clean and disinfect materials, and to ensure a seamless transfer of samples between different production zones and logistics centres. Your dedication supports the timely delivery of our groundbreaking therapies to patients who need them the most.  

What can you expect? 

As a QC Support Technician in CAR-T Manufacturing, you are at the core of our quest for quality. Your role is pivotal in ensuring our cell therapy products meet the rigorous standards required for clinical trials and commercial distribution.  

Your day-to-day responsibilities include, among others:   

• Quality control support: Your hands-on support with daily QC analyses ensures the integrity of our pioneering therapies. 
• Material management: From controlling to disinfecting equipment and managing lab materials and waste, your attention to detail keeps our processes running smoothly. 
• Transfer of samples: You play a crucial role in the safe transport of samples, maintaining the precision required for accurate results. 
• Environmental monitoring: You support the environmental monitoring analyses in grade C and D environments.  
• Documentation of your activities: You document all your disinfection and cleaning tasks in a correct way in logbooks, forms or e-LIMS, the quality control software we use here.  

Working in an aseptic 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: A secondary school degree sets the stage for this role, but it's your quality mindset, precision, and eagerness to learn that matters most to us.  
• 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 and excellent organisational skills. Your ability to work systematically and embrace the rigors of a GMP environment is essential
• Expertise: You have a positive attitude. You communicate clearly and openly, and you are a true team player.   

What do we offer?  

• A meaningful job, close to your home, with a very nice work-life balance. You work 4 days, then you have 4 days off.  
• 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 additional legal vacation days, 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. 

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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. 

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Want to Make a Real Impact? Join Our QA Document Control Specialist Talent Pool!

The Quality Assurance Document Control Specialist role is a position with responsibilities for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will ensure compliance within the document management system, document storage and retention, and document issuance and reconciliation.

What can you expect?

• Responsible for managing the document control systems and processes for the site.
• 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.
• Issuance of batch related documentation in support of GMP manufacturing.
• Reconcile GMP documentation following document lifecycle requirements.
• Creation and issuance of GMP logbooks.
• Responsible for storage and archival of GMP documents and batch related records.
• Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
• Review and approve SOPs, and other documentation.
• Drive continuous improvement.
• Have advanced computer skills to increase department's productivity, as well as broadening technical and scientific knowledge.

Who are we looking for?

Education: 

• You are an undergrad, have a secondary degree or equivalent through experience.

Experience:

• Not required.
• It is preferable that the candidate has experience working in a GMP environment, but this is not a must.

Language:

• Dutch and technical English

Strengths: 

What do we offer you? 

• A meaningful job with an excellent work-life balance. You will work 4 days, followed by 4 days at home.
• 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 of €7/day , group and hospitalization insurance once you start your permanent contract, double vacation pay, and performance bonuses. 

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. 

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Wil je écht impact maken? Sluit je aan bij onze Talent Pool voor QA Document Control Specialist!  

De rol van Quality Assurance Document Control Specialist omvat verantwoordelijkheden ter onderscheiding van het documentbeheerproces binnen een celtherapie-productiefaciliteit voor zowel klinische als commerciële activiteiten in een steriele GMP-omgeving. Je zorgt ervoor dat het documentbeheersysteem, de documentopslag-, bewaring, de uitgifte en reconciliatie van documenten voldoen aan alle compliance vereisten.

Wat mag je verwachten?

• Je beheert de documentcontrolesystemen en -processen voor de site. 
• Je fungeert als Document Control reviewer voor nieuwe en herziene procedures en documenten om naleving van globale en lokale procedures te garanderen. 
• Je ondersteunt gebruikers van het Document Management Systeem bij workflows en gebruik van het elektronische systeem. 
• Je beheert het periodieke reviewproces voor procedures. 
• Je staat in voor de uitgifte van batchgerelateerde documentatie ter ondersteuning van GMP‑productie. 
• Je reconcilieert GMP‑documentatie volgens de vereisten van de document lifecycle. 
• Je maakt en geeft GMP‑logboeken uit. 
• Je bent verantwoordelijk voor opslag en archivering van GMP‑documenten en batchrecords. 
• Je voert taken uit in lijn met veiligheidsbeleid, kwaliteitssystemen en cGMP‑vereisten. 
• Je beoordeelt en keurt SOP’s en andere documentatie goed. 
• Je stimuleert continuous improvement. 
• Je beschikt over geavanceerde computervaardigheden om de productiviteit van het team te verhogen en je technische en wetenschappelijke kennis uit te breiden. 

Naar wie zijn we op zoek?

Opleiding 

• Je bent een bachelorstudent, hebt een secundair diploma of beschikt over gelijkwaardige ervaring. 

Ervaring 

• Niet vereist. 

• Ervaring in een GMP-omgeving is een plus, geen must. 

Talen 

• Nederlands en technisch Engels. 

Sterktes 

• Sterke schriftelijke en mondelinge communicatieskills 
• Sterke analytische vaardigheden, probleemoplossend vermogen en vaardigheden in conflicbemiddeling 
• Zeer goed georganiseerd, detailgericht en in staat om meerdere taken tegelijk te beheren. 
• Vermogen om prioriteiten aan te passen en deadlines te halen in een snel veranderende omgeving. 
• Flexibel en gemotiveerd, inclusief flexibibiliteit in werkroosters. 
• Sterke interpersoonlijke vaardigheden en vlot communiceren op alle niveaus binnen de organisatie. 
• Vermogen om zelfstandig te werken met een hoge mate van verantwoordelijkheid. 

Expertise 

• Kennis van GxP-kwalieitsystemen, inclusief relevante regelgeving en richtlijnen (zoals 21 CFR, ICH Q10, EU GDP/GMP, Part 11 / Annex 11, PIC/S, MHRA). 
• Operationele ervaring met elektronische kwaliteitsystemen. 
• Ervaring met Document Management Systems (bv. TruVault, Veeva). 
• Goede kennis van Microsoft Office (Outlook, Excel, Word, PowerPoint). 

 Wat wij jou bieden? 

• Een betekenisvolle job met een uitstekende work-lifebalance. Je werkt 4 dagen. Daarna geniet je van 4 dagen vrij. 
• Een ondersteunende en innovatieve werkomgeving. Wij waarderen en moedigen leren en persoonlijke ontwikkeling aan.  
• De kans om samen te werken met mensen van over de hele wereld. 
• Een contract van onbepaalde duur en een aantrekkelijk salarispakket aangevuld met heel wat extralegale voordelen, zoals extra wettelijke vakantiedagen, maaltijdcheques, groeps- en hospitalisatieverzekering, dubbel vakantiegeld, een eindejaars- en prestatiebonus. 
• Veel leuke en informele evenementen.  

Over Legend Biotech 

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zicht toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën, waaronder behandelingen voor hardnekkige ziekten zoals kanker.  

Sinds onze oprichting in 2014 in Somerset, New Jersey, zijn we uitgegroeid tot een bedrijf met meer dan 2400 medewerkers in zes productie-eenheden wereldwijd.  

In Gent richten we ons op de productie van onze geavanceerde CAR-T-therapie voor de behandeling van multipel myeloom, in samenwerking met Johnson & Johnson.  

As Quality Control Manager Techlane, you will balance ramp‑up activities with routine QC operations, while continuously improving efficiency, developing your team, and strengthening laboratory performance. You will combine scientific expertise with people leadership to ensure robust, compliant, and future-ready QC operations in a highly regulated cGMP environment. This role offers the opportunity to make a tangible impact on product quality, patient safety, and the continued growth of our organization, while driving continuous improvement initiatives and mindset.

What can you expect?

Here’s what you’ll do:

• Lead, coach, and develop QC laboratory associates, including hiring and performance management
• Ensure appropriate training in cGMP, safety, and technical competencies
• Oversee QC testing activities
• Review and approve laboratory data, test methods, and procedures
• Lead and support laboratory investigations (events, deviations, invalid assays)
• Ensure maintenance, calibration, and qualification of laboratory equipment
• Drive test method verification, qualification, validation, and transfer activities
• Act as a subject matter expert in troubleshooting complex laboratory issues
• Collaborate closely with Quality Assurance, Manufacturing, Engineering, MSAT, and Maintenance
• Manage departmental resources, budgets, and staffing plans
• Contribute to global QC laboratory strategies aligned with compliance and business objectives
• Drive continuous improvement and lead improvement projects.

Who are we looking for?

Education

• Bachelor’s degree (minimum) in a scientific or technical field, such as Life Sciences, Chemistry, Biochemistry, Biotechnology, Microbiology, Pharmaceutical Sciences, or a related discipline.

Experience

• 8-10 years of relevant experience in a regulated pharmaceutical, biotech, or cell therapy environment
• 5+ years of proven people leadership experience
• Experience in aseptic manufacturing is strongly preferred
• Hands-on experience with quality systems and regulatory requirements
• Familiarity with Eudralex, ICH and 21 CFR.

Languages

• Fluent in Dutch and English

Strengths

• Strong leadership and people management skills
• Excellent interpersonal, written, and verbal communication abilities
• Highly organized, proactive, and solution-oriented
• Able to manage multiple priorities in a fast-paced environment
• Comfortable making critical decisions with limited information

Expertise

• EU/FDA guidance for cell-based products and cGMP regulations
• Chemical, biochemical, and microbiological concepts
• Aseptic processing in ISO 5 cleanrooms and biosafety cabinets
• Process excellence tools and continuous improvement methodologies

What do we offer you? 

• A meaningful job with a good work-life balance.
• 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, a company car, 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.

Wat mag je verwachten?

• Leidinggeven aan, coachen en ontwikkelen van QC‑laboratoriummedewerkers, inclusief aanwerving en prestatiemanagement
• Zorgen voor gepaste training in cGMP, veiligheid en technische competenties
• Toezicht houden op QC‑testactiviteiten
• Reviewen en goedkeuren van laboratoriumdata, testmethoden en proceduresL
• Leiden en ondersteunen van laboratoriumonderzoeken (events, afwijkingen, ongeldige analyses)
• Zorgen voor onderhoud, kalibratie en kwalificatie van laboratoriumapparatuur
• Aansturen van verificatie, kwalificatie, validatie en overdracht van testmethoden
• Optreden als subject matter expert bij het oplossen van complexe laboratoriumproblemen
• Nauw samenwerken met Quality Assurance, Manufacturing, Engineering, MSAT en Maintenance
• Beheren van afdelingsmiddelen, budgetten en personeelsplanning
• Bijdragen aan globale QC‑laboratoriumstrategieën in lijn met compliance‑ en bedrijfsdoelstellingen
• Aansturen van continuous improvement‑initiatieven en verbeterprojecten

Naar wie zijn we op zoek?

Opleiding 

• Minimaal een Bacheloropleiding in een wetenschappelijke of technische richting, zoals Levenswetenschappen, Chemie, Biochemie, Biotechnologie, Microbiologie, Farmaceutische Wetenschappen of een aanverwante discipline.

Ervaring 

Talen 

• Vlot in Nederlands en Engels

Sterktes 

Expertise 

 Wat wij jou bieden?

• Een betekenisvolle job met een goede work‑life balance
• Een ondersteunende en innovatieve werkomgeving waarin leren en persoonlijke ontwikkeling worden aangemoedigd
• De kans om samen te werken met collega’s van over de hele wereld
• Een contract van onbepaalde duur en een aantrekkelijk loonpakket, aangevuld met tal van extralegale voordelen zoals extra wettelijke vakantiedagen, een bedrijfswagen, maaltijdcheques, groeps‑ en hospitalisatieverzekering, dubbel vakantiegeld en een eindejaars‑ en prestatiebonus
• Heel wat leuke en informele activiteiten

Over Legend Biotech 

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zicht toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën, waaronder behandelingen voor hardnekkige ziekten zoals kanker.  

Sinds onze oprichting in 2014 in Somerset, New Jersey, zijn we uitgegroeid tot een bedrijf met meer dan 2400 medewerkers in zes productie-eenheden wereldwijd.  

In Gent richten we ons op de productie van onze geavanceerde CAR-T-therapie voor de behandeling van multipel myeloom, in samenwerking met Johnson & Johnson.  

Do you have an eye for detail and want to become the go-to person for sample logistics and documentation? As we continue to expand our operations in Ghent, we are looking for a QC Sample Coordinator for our Techlane facility. 

What can you expect?

As a QC Sample Coordinator, you are responsible for sample management. You play a key role in ensuring that all samples are managed, documented, stored, and shipped correctly and compliantly. You are responsible for;  

Sample logistics & coordination 

• Preparing documents and coordinate internal and external sample shipments, including ad-hoc transports, together with the QC Support Technicians.
• Aligning inventories with ELIMS and logbooks.
• Performing period inspections and retain consolidations.
• Partnering closely with the Operations team, Logistic centre, etc.to ensure smooth sample coordination.

Documentation 

• Preparing and reviewing sample documentation.
• Initiating and support non-conformance sample investigations and manage CAPA records related to sample management.

Troubleshooting and process improvements 

• Being the point of contact in case of deviations (ex. Label issues) and coordinating with internal and external stakeholders to resolve issues. 
• Driving improvements in procedures and work instructions. 

Who are we looking for?

Education

• You obtained a Bachelor's degree or equivalent relevant experience.

Experience  

• You have hands-on experience in a GMP environment, preferably in quality control. 

Languages  

• You are fluent in English and/or Dutch. 

Strengths  

• You have a hands-on mentality.
• You have strong communication skills that foster collaboration and sets clear expectations with different stakeholders.
• You have strong coordination skills and are able to keep an overview.
• You are able to stay calm, focussed and motivated under tight deadlines. 

What do we offer you? 

• A meaningful job with an excellent work-life balance. You will work in our shift system; working 4 days - enjoying 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.

As a QC Supervisor you are responsible for a team of QC Analysts and QC Support Technicians, providing feedback, assistance with troubleshooting and deviations whilst ensuring a clear working schedule. You build up trust amongst the colleagues and other teams.

What can you expect?

• Direct Lead: You are the direct lead for the team. (+- 20 people). You provide them with clear objectives, feedback, goals and assist them in achieving these.
• Connector: When needed, you ensure alignment within the team or other departments such as Operations or Maintenance & Engineering.
• Decision Maker: You’re able to independently make decisions when needed. When issues come up, you’re able to connect with the right people to make informed choices.
• Planner: In case of planning disruptions such as unplanned absence, you adjust schedules and task allocation to ensure ongoing quality control activities.

Who are we looking for?

Education 

• Minimum of a Bachelor Degree in a related field.

Experience

• A minimum of 3 years of experience within the Pharmaceutical or BioTech industry, preferably within Quality Control.
• A first experience in a leading role is a very strong advantage.

Languages

• English at a fluent level is a must have for this role. Dutch is a nice to have.

Strengths

• Strong communication skills and interpersonal skills.
• The ability and willingness to support and coach others.

What do we offer you? 

• A meaningful job with an excellent work-life balance. You will work 4 days, followed by 4 days off.
• A supportive and innovative work environment. We value and encourage learning and personal development.
• The opportunity to work with people from different departments & regions.
• 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.

Als QC Supervisor ben je verantwoordelijk voor een team van QC‑analisten en QC Support Technicians. Je geeft feedback, ondersteunt bij troubleshooting en afwijkingen, en zorgt voor een duidelijke werkplanning. Je bouwt vertrouwen op binnen het team en met andere afdelingen. 

Wat mag je verwachten?

Direct leidinggevend 

Je bent de rechtstreekse leidinggevende van het team (ongeveer 20 personen). Je geeft duidelijke doelstellingen, feedback en richting, en ondersteunt hen bij het behalen van hun doelen. 

Verbinder 

Wanneer nodig zorg je voor afstemming binnen het team of tussen andere afdelingen zoals Operations of Maintenance & Engineering. 

Beslisser 

Je kan zelfstandig beslissingen nemen wanneer dat nodig is. Bij problemen weet je de juiste stakeholders te betrekken om onderbouwde keuzes te maken. 

Planner 

Bij verstoringen in de planning, zoals onverwachte afwezigheden, pas je schema’s en taakverdelingen aan om de continuïteit van de kwaliteitscontroleactiviteiten te garanderen. 

Naar wie zijn we op zoek?

Opleiding  

• Minimaal een bachelor in een relevant vakgebied. 

Ervaring 

• Ten minste 3 jaar ervaring in de farmaceutische of biotechsector, bij voorkeur binnen Quality Control. 

• Een eerste leidinggevende ervaring is een sterk pluspunt. 

Talen 

• Vloeiend Engels is een must. 

• Nederlands is een nice-to-have. 

Sterktes 

• Sterke communicatie- en interpersoonlijke vaardigheden. 

• Bereidheid en vermogen om anderen te ondersteunen en coachen. 

 Wat wij jou bieden? 

Een betekenisvolle job met een uitstekende work-lifebalance. Je werkt 4 dagen. Daarna geniet je van 4 dagen vrij. 

Een ondersteunende en innovatieve werkomgeving. Wij waarderen en moedigen leren en persoonlijke ontwikkeling aan.  

De kans om samen te werken met mensen van over de hele wereld. 

Een contract van onbepaalde duur en een aantrekkelijk salarispakket aangevuld met heel wat extralegale voordelen, zoals extra wettelijke vakantiedagen, maaltijdcheques, groeps- en hospitalisatieverzekering, dubbel vakantiegeld, een eindejaars- en prestatiebonus. 

Veel leuke en informele evenementen.  

Over Legend Biotech 

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zicht toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën, waaronder behandelingen voor hardnekkige ziekten zoals kanker.  

Sinds onze oprichting in 2014 in Somerset, New Jersey, zijn we uitgegroeid tot een bedrijf met meer dan 2400 medewerkers in zes productie-eenheden wereldwijd.  

In Gent richten we ons op de productie van onze geavanceerde CAR-T-therapie voor de behandeling van multipel myeloom, in samenwerking met Johnson & Johnson.  

Are you looking to make a tangible impact in your career? Do you have a keen eye for detail, cleanliness, and quality? If so, we have the perfect opportunity for you! Join our vibrant Quality Operations Team in Ghent as a QC Support Technician. In this role, you'll be a vital part of our mission to ensure the safe and timely delivery of our life-saving cell therapies to the patients who need them most. Dive into a job that truly makes a difference! 

What Can You Expect? 

You will work closely with team leaders and QC analysts to clean and disinfect materials and ensure seamless transfer of samples between different production zones and logistics centers. Here's what you will do: 

• Support quality control: Your hands-on and daily support in QC analyses will ensure the quality of our cell therapy products.
• Manage Materials: From checking and disinfecting equipment to managing lab materials and waste, your attention to detail will keep our processes running smoothly.
• Transferring Samples: You play a crucial role in the safe transportation of samples between different production zones and logistics centers. 
• Environmental Monitoring: You will support environmental monitoring analyses in grade C and D environments. 
• Documenting activities: You accurately record all your disinfection and cleaning tasks in logs, forms or our eLIMS software. 
• Maintain aseptic conditions: You will work in a sterile environment and on a shift schedule (no nights, but weekends). 

Who Are We Looking For?

Education

• A high school diploma is nice but for this role your love for quality, accuracy and eagerness to learn are much more important.  

Experience 

• You preferably already have some practical experience in an operational environment, but this is not a must. 

Languages  

• You are fluent in Dutch and/or English. You communicate clearly, openly and positively. 

Strengths

• You are detail-oriented with a strong commitment to quality and compliance. Your ability to work in a systematic and structured manner and follow strict GMP regulations are essential to be successful in this job.
• You are a team player who can also work well independently, with excellent organizational skills.

Expertise

• You are fluent in Microsoft Office applications such as Word, Excel, PowerPoint and Outlook. 
• Through in-house training, we will provide you with a solid understanding of GMP requirements and quality standards that will get you up and running smoothly in your new role.   

What Do We Offer You? 

• A meaningful job with an excellent work-life balance. You will work 4 days. After that you will 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.
• 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 of €7/day , group and hospitalization insurance once you start your permanent contract, double vacation pay, and performance bonuses. 
• 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

Want to Make a Real Impact? Join Our QC Support Technician Talent Pool!

Are you looking to make a tangible impact in your career? Do you have a keen eye for detail, cleanliness, and quality? If so, we have the perfect opportunity for you! Join our vibrant Quality Operations Team in Ghent as a QC Support Technician. In this role, you'll be a vital part of our mission to ensure the safe and timely delivery of our life-saving cell therapies to the patients who need them most. Dive into a job that truly makes a difference! 

What Can You Expect? 

You will work closely with team leaders and QC analysts to clean and disinfect materials and ensure seamless transfer of samples between different production zones and logistics centers. Here's what you will do: 

• Support quality control: Your hands-on and daily support in QC analyses will ensure the quality of our cell therapy products.
• Manage Materials: From checking and disinfecting equipment to managing lab materials and waste, your attention to detail will keep our processes running smoothly.
• Transferring Samples: You play a crucial role in the safe transportation of samples between different production zones and logistics centers. 
• Environmental Monitoring: You will support environmental monitoring analyses in grade C and D environments. 
• Documenting activities: You accurately record all your disinfection and cleaning tasks in logs, forms or our eLIMS software. 
• Maintain aseptic conditions: You will work in a sterile environment and on a shift schedule (no nights, but weekends). 

Who Are We Looking For?

Education

• A high school diploma is nice but for this role your love for quality, accuracy and eagerness to learn are much more important.  

Experience 

• You preferably already have some practical experience in an operational environment but this is not a must. 

Languages  

• You are fluent in Dutch and/or English. You communicate clearly, openly and positively. 

Strengths

• You are detail-oriented with a strong commitment to quality and compliance. Your ability to work in a systematic and structured manner and follow strict GMP regulations are essential to be successful in this job.
• You are a team player who can also work well independently, with excellent organizational skills.

Expertise

• You are fluent in Microsoft Office applications such as Word, Excel, PowerPoint and Outlook. 
• Through in-house training, we will provide you with a solid understanding of GMP requirements and quality standards that will get you up and running smoothly in your new role.   

What Do We Offer You? 

• A meaningful job with an excellent work-life balance. You will work 4 days. After that you will 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.
• 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 of €7/day , group and hospitalization insurance once you start your permanent contract, double vacation pay, and performance bonuses. 
• 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

Lead where it matters most.

At Legend Biotech, leadership is about people first. About trust. Growth. Responsibility. And impact you can truly feel.
At our CAR-T manufacturing sites Obelisc and Tech Lane in Ghent, we are looking for experienced Supervisors who get energy from coaching people, leading teams and helping others grow into their best selves.

We are hiring Supervisors in CAR-T Production, Quality Control (QC) and Maintenance. Three different domains, one shared purpose: helping life-saving therapies reach patients safely, reliably and on time.
This is a leadership role where your way of working shapes people, teams, and outcomes. 

What can you expect?

As a supervisor, you lead where it truly matters: on the floor, with your team. 

Your focus is clear:

• Coaching and people management:
  You lead a team of operators, analysts or technicians. You coach, support and challenge people to grow, take ownership and perform with confidence.
• Creating structure and clarity:
  You bring calm and focus to a complex environment. You set priorities, align expectations and create a safe space where people can excel.
• Quality and responsibility:
  You safeguard GMP, safety and compliance through daily leadership, not paperwork alone. You lead by example and build a strong quality mindset in your team.
• Keeping the operation moving:
  You oversee daily activities, anticipate issues and act when it matters. You work closely with other teams to solve problems and keep processes running. 

Through your leadership, teams grow, processes stay on track and patients receive the therapies they are waiting for. 

Who are we looking for?

Education

• A bachelor's or master's degree in a relevant field, such as science, bioengineering or pharmacy (for Production or QC), or engineering or technical discipline (for Maintenance), or equivalent experience. 

Experience

• You have experience in either Production, Quality Control or Maintenance within a GMP or ATMP environment in pharma or biotech.
• You either bring leadership experience or the clear ambition to grow into a people management role. 

Languages

• You are fluent in English, both spoken and written.
• Knowledge of Dutch is a plus.

Strengths

• You genuinely enjoy leading and developing people.
• You communicate clearly, listen actively and give constructive feedback.
• You create trust, ownership and motivation in your team.
• You stay calm, structured and decisive in a dynamic environment.

Expertise

• You bring a strong quality and compliance mindset.
• You work comfortably with procedures, documentation, and systems.
• You are hands-on, solution-oriented, and driven by people and teamwork. 

What do we offer you?

• A meaningful job with an excellent work-life balance. You will work 4 days. After that you will 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.

Does this feel like your next step?

If you want to lead people, build strong teams, and make a difference where it truly counts, we would love to meet you. Apply today and lead where it matters most. 

About Legend Biotech

With over 2,900 employees worldwide, Legend Biotech is the largest standalone cell therapy company and a pioneer in treatments that are changing cancer care for good. We develop and market the CAR-T cell therapy ciltacabtagene autoleucel (cilta-cel) in partnership with ohnson & Johnson. In the EU, cilta-cel is approved under the brand name CARVYKTI® for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy.

Legend Biotech is a fully integrated global organization with manufacturing sites in the United States and Europe. From our sites in Ghent, Belgium, our teams support the clinical and commercial supply of CAR-T therapies across the EMEA region, translating advanced science into real-world impact for patients.

What sets us apart is clarity of purpose. At Legend Biotech Europe, everyone understands how their role contributes to our mission and how their daily work helps bring life-changing therapies to patients who need them most.

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