Who we are

About Stripe

Stripe is a financial infrastructure platform for businesses. Millions of companies - from the world’s largest enterprises to the most ambitious startups - use Stripe to accept payments, grow their revenue, and accelerate new business opportunities. Our mission is to increase the GDP of the internet, and we have a staggering amount of work ahead. That means you have an unprecedented opportunity to put the global economy within everyone's reach while doing the most important work of your career.

About the team

To avoid the worst effects of climate change, most climate models agree the world will need to remove 5-10 billion tons of carbon dioxide from the atmosphere per year by 2050, in addition to dramatically reducing emissions. The Climate team’s goal is to get carbon removal on its best possible trajectory to increase the likelihood that the world builds the carbon removal capacity needed to reach these climate goals.

In 2021 we launched Stripe Climate enabling merchants to direct a fraction of their revenue to help scale emerging carbon removal technologies in just a few clicks. In 2022 we launched Frontier, an advance market commitment to buy $1B+ of permanent carbon removal by 2030. Still, carbon removal is in its early innings–to reach the volume of carbon removal the world needs, demand will have to be driven by governments. In 2023, we hired our first policy lead and in 2025 we funded 8 Stripe Climate Fellows to seed ambitious policy ideas. In 2026, we are ramping up our focus on accelerating demand for carbon removal through policy around the world.

What you’ll do

Responsibilities

 As Stripe's senior EU Market Development Lead, this person will set the vision for growing long-term carbon removal demand in the region and partner closely with NGOs and policymakers to help those policies materialize. 

You’ll be responsible for:

• EU Market Demand (~40%): Dramatically growing the global market for CDR using a wide breadth of demand-side policy levers, including compliance market integration, tax credits, subsidies, and direct procurement. You will partner with the EU NGO ecosystem and oversee Stripe’s policy partners across the EU to both accelerate carbon removal’s eligibility within existing policies as well as generate new ideas (more here).  
• EU Offtake Demand (~40%): Securing a believable trajectory to long-term government demand for Frontier’s offtake portfolio (more here). You will lead location-specific advocacy efforts to help accelerate development and unlock demand for Frontier’s most promising carbon removal projects.
• Global Demand (~20%): Leading new initiatives to unlock global demand. You will work closely with Stripe’s Policy Lead and Frontier’s scientific diligence team to vet market opportunities and grow voluntary and policy support in new regions (the Middle East, Australia, etc.). 

This role requires someone with exceptional policy & regulatory intuition, a track record of getting big things done fast, excellent judgment to make the ‘right’ recommendations, and the fearlessness and humility to help drive progress in a quickly-changing field. 

Who you are

We're looking for someone who meets the minimum requirements to be considered for the role. If you meet these requirements, you are encouraged to apply. The preferred qualifications are a bonus, not a requirement.

Minimum requirements

• BA or BS degree
• 7-10+ years of relevant experience in policy, government, or regulatory affairs
• A track record of generating and implementing ambitious policy initiatives
• Extensive history of engaging with government officials, policymakers, and bureaucrats
• Off-the-charts stakeholder management intuition 
• Excellent oral and written communication skills - especially adept at translating technical jargon into layman’s terms and summarizing complex concepts in a succinct manner

Preferred qualifications 

• Has a strong existing network of policymakers and NGOs in Europe
• Has a deep understanding of policies surrounding climate and carbon markets and the landscape of carbon removal technologies 
• Has worked at the intersection of climate tech and policy
• Is an exceptionally fast learner. Enjoys (and has experience) quickly ramping on new policy and technical topics
• Is uniquely good at getting to the crux of an issue, and can quickly sort the signal from the noise
• Is low ego, and has a proven track record for working well across teams and with external partners

You must be based in Europe, preferably Brussels, or the UK.

We are looking for a passionate CAR-T Operations Expert to join our team in Ghent. Ready to make a difference in patients' lives and lead innovative CAR-T cell therapy projects? Let us hear from you. We'd love to meet you!   

What Can You Expect?

As a CAR-T Operations Expert, you will be a specialist in specific parts of the CAR-T production process. Here's what you'll do: 

• Perform and oversee CAR-T process activities: You will participate in and oversee specific parts of the CAR-T manufacturing process such as component preparation, CAR-T processing, filling and finishing, and cryopreservation.
• Compliance and documentation: You ensure that all activities comply with cGMP and GDP standards. You will develop and maintain GMP documents to ensure compliance and traceability.
• Operational support: You manage daily production planning and support production surveys. You will create and review operational procedures, including work instructions, master batch records and forms.
• Collaborate and continuously improve: You will work with various teams to streamline and optimize processes. You will also participate in Lean & Operational Excellence projects. 
• Training: You will train and coach junior colleagues. 
• Technology and Systems: You will support the testing and implementation of various software for production output systems such as eLiMS, MES and SAP. 

Who Are We Looking For?

Education:  

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

Experience: 

• You have at least 3 years of operational experience within a cGMP or ATMP environment and with aseptic techniques in clean rooms, preferably in the biotech or pharmaceutical industry. Previous experience in manufacturing, quality or engineering is required.  

Languages:  

• You are fluent in Dutch or English, with strong oral and written communication skills.  

Strengths: 

• You are a true team player with strong relational, analytical and problem-solving skills. You are detail-oriented and strive for excellence. You are also motivated and enthusiastic, but it is your "can-do" mentality that typifies you the most.   

Expertise: 

• You have a thorough knowledge of cGMP regulations and cell culture techniques.
• You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook.
• Experience with cGMP systems such as PASx, eLIMs, Siemens and SAP are a nice plus.     

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

We zijn op zoek naar een gepassioneerde CAR-T Operations Expert om ons team in Gent te versterken. Klaar om een verschil te maken in het leven van patiënten en om innovatieve CAR-T-celtherapieprojecten te leiden? Laat van je horen. We maken graag kennis met je!

Wat kan je verwachten?

Als Ops Expert ben je een specialist in specifieke onderdelen van het CAR-T-productieproces. Dit is wat je zult doen:

• Uitvoeren en toezien op CAR-T-procesactiviteiten: Je neemt deel aan en superviseert specifieke onderdelen van het CAR-T-productieproces, zoals componentvoorbereiding, CAR-T-verwerking, afvulling en afwerking, en cryopreservatie.
• Naleving en documentatie: Je zorgt ervoor dat alle activiteiten voldoen aan cGMP- en GDP-normen. Je ontwikkelt en onderhoudt GMP-documenten om naleving en traceerbaarheid te garanderen.
• Operationele ondersteuning: Je beheert de dagelijkse productieplanning en ondersteunt productievergaderingen. Je stelt operationele procedures op en beoordeelt deze, waaronder werkinstructies, master batch records en formulieren.
• Samenwerken en continu verbeteren: Je werkt samen met verschillende teams om processen te stroomlijnen en te optimaliseren. Je neemt ook deel aan Lean- & Operational Excellence-projecten.
• Training: Je traint en coacht junior collega’s.
• Technologie en systemen: Je ondersteunt het testen en implementeren van diverse software voor productie-outputsystemen zoals eLiMS, MES en SAP.

Wie zoeken we?

Opleiding: 

• Je hebt minimum een bachelor diploma in wetenschappen, (bio)-ingenieurswetenschappen, biotechnologie, farmacie of een gerelateerd studiegebied, of je bent gelijkwaardig door ervaring.

Ervaring:

• Je hebt minstens 3 jaar operationele ervaring binnen een cGMP- of ATMP-omgeving en met aseptische technieken in cleanrooms, bij voorkeur in de biotech- of farmaceutische sector. Eerdere ervaring in productie, kwaliteit of engineering is vereist.

Talen:  

• Je bent vloeiend in het Nederlands of Engels, met sterke mondelinge en schriftelijke communicatievaardigheden.

Strengths:

• Je bent een echte teamspeler met sterke relationele, analytische en probleemoplossende vaardigheden. Je bent detailgericht en streeft naar uitmuntendheid. Je bent daarnaast gemotiveerd en enthousiast, maar het is vooral je “can-do” mentaliteit die je typeert.

Expertise: 

• Je hebt een grondige kennis van cGMP-regelgeving en celkweektechnieken.
• Je kunt vlot werken met Microsoft Office-tools zoals Word, Excel, PowerPoint en 
  

Wat bieden wij jou?

• Een betekenisvolle job die rechtstreeks bijdraagt aan het welzijn van patiënten.
• Een uitstekende work-life balance. Je werkt 4 dagen en geniet daarna van 4 dagen vrijaf.
• Een ondersteunende en innovatieve werkomgeving. We hechten veel waarde aan leren en persoonlijke ontwikkeling.
• De kans om samen te werken met mensen van over de hele wereld.
• Een contract van onbepaalde duur en een aantrekkelijk salarispakket, aangevuld met tal van extralegale voordelen, zoals extra wettelijke
• vakantiedagen, maaltijdcheques, groeps- en hospitalisatieverzekering, dubbel vakantiegeld en een eindejaars- en prestatiebonus.
• Veel leuke en informele evenementen.

Over Legend Biotech

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zich toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën voor de behandeling van chronische en levensbedreigende ziekten, zoals kanker.

Het bedrijf werd opgericht in 2014 en heeft zijn hoofdkantoor in Somerset, New Jersey. Legend Biotech telt inmiddels meer dan 2.400 medewerkers verspreid over zes wereldwijde productiesites. Twee van deze sites bevinden zich in Gent: Obelisc (Technology Park Zwijnaarde) en Tech Lane (Eilandje Zwijnaarde).

In Gent richt Legend Biotech zich op de productie van geavanceerde CAR-T-celtherapieën voor de behandeling van multipel myeloom, in nauwe samenwerking met Johnson & Johnson.

Ben je klaar om het voortouw te nemen in een van de meest innovatieve sectoren in de biotechnologie? 
Als CAR-T production supervisor bij Legend Biotech leid je een gemotiveerd team van operators in een cleanroom faciliteit, waar je zorgt voor een vlotte werking en een hoge kwaliteitsstandaard van begin tot eind. Je helpt ervoor te zorgen dat de dagelijkse activiteiten soepel, veilig en volgens de GMP-normen verlopen. Je begeleidt je team met alle verantwoordelijkheden die daarbij horen: het faciliteren van de groei van je team, het inspireren van hen in hun dagelijkse taken en het handhaven van kwaliteitsniveaus, en het oplossen van problemen zodra er uitdagingen ontstaan.

Wat kan je verwachten?

Als CAR-T production supervisor ben je de drijvende kracht achter onze operaties. Dit zijn jouw verantwoordelijkheden:

• Leiden & inspireren: operationele teams aansturen en belangrijke stappen in het CAR-T productieproces overzien.
• Kwaliteitsgarantie: je beheert alle aspecten van de kwaliteit en zorgt voor strikte naleving van de cGMP-normen.
• Samenwerken en oplossen: jij bent het aanspreekpunt wanneer uitdagingen opkomen in productie en werkt nauw samen met andere afdelingen om oplossingen te vinden.
• Organiseren: je beheert en bekijkt kritieke documentatie zoals procedures, werkinstructies, logboeken en overdrachtsformulieren. Je houdt ook toezicht op de vrijgave en beoordeling van batchrecords voor kwaliteitscontrole.
• Talent trainen en ontwikkelen: als manager zorg je ervoor dat je team de vaardigheden en kennis heeft om uit te blinken.
• Operationele uitmuntendheid stimuleren: projecten lanceren om de efficiëntie te verhogen, kosten te besparen en de kwaliteit te verbeteren. Inspireer elke dag voortdurende verbetering.

Wie zoeken we?

Opleiding

• Je hebt een bachelor- of masterdiploma in wetenschappen, bio-ingenieurswetenschappen, farmacie of een gerelateerd vakgebied, of bent gelijkwaardig door ervaring.

Ervaring

Je hebt:

• Ervaring in het leiden van een team in een gereguleerde omgeving,
• Of minstens 3 jaar ervaring in een GMP- of ATMP-omgeving (bij voorkeur in de biotech- of farmaceutische industrie) en ambitie voor de nieuwe uitdaging van het leiden van een team.

Expertise

• Je hebt kennis van cGMP-regelgeving en cleanroomoperaties.
• Je werkt vlot met Microsoft Office-tools zoals Word, Excel, PowerPoint en Outlook.
• Bekendheid met Manufacturing Execution Systems (MES) en Electronic Batch Record (EBR)-systemen is een plus.

Talen

• Je spreekt en schrijft vloeiend Engels.

Skills

• Uitstekende communicatie- en organisatorische vaardigheden.
• Empathische people manager met sterke leiderschapskwaliteiten.
• Positieve, flexibel en inspirerend onder snel veranderende omstandigheden.
• Probleemoplossend, sterk in prioriteiten stellen en multitasking.
• Oog voor detail en procedures.

Wat bieden wij?

• Een betekenisvolle job die rechtstreeks bijdraagt aan het welzijn van patiënten.
• Een uitstekende work-life balance. Je werkt 4 dagen en geniet daarna 4 dagen vrij.
• Een ondersteunende en innovatieve werkomgeving waarin leren en persoonlijke ontwikkeling worden aangemoedigd.
• De kans om samen te werken met mensen van over de hele wereld.
• Een contract van onbepaalde duur en een aantrekkelijk salarispakket, aangevuld met tal van extralegale voordelen zoals extra wettelijke vakantiedagen, maaltijdcheques, groeps- en hospitalisatieverzekering, dubbel vakantiegeld, een eindejaarspremie en een prestatiebonus.
• Tal van leuke en informele evenementen.

Over Legend Biotech

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zich toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën voor de behandeling van chronische en levensbedreigende ziekten, zoals kanker.

Het bedrijf werd opgericht in 2014 en heeft zijn hoofdkantoor in Somerset, New Jersey. Legend Biotech telt inmiddels meer dan 2.400 medewerkers verspreid over zes wereldwijde productiesites. Twee van deze sites bevinden zich in Gent: Obelisc (Technology Park Zwijnaarde) en Tech Lane (Eilandje Zwijnaarde).

In Gent richt Legend Biotech zich op de productie van geavanceerde CAR-T-celtherapieën voor de behandeling van multipel myeloom, in nauwe samenwerking met Johnson & Johnson.

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

Ben jij gepassioneerd door het creëren van betekenisvolle medewerkerservaringen via slimme, eerlijke en toekomstbestendige beloningssystemen? Als Compensation & Benefits Specialist bij Legend Biotech maak je deel uit van een samenwerkend team dat ervoor zorgt dat onze mensen zich gewaardeerd voelen—door competitieve verloning, doordachte voordelen en duidelijke communicatie. Je combineert operationele verantwoordelijkheid met analytische inzichten en helpt mee om total rewards-strategieën vorm te geven die zowel onze medewerkers als ons bedrijf ondersteunen.

Wat kan je verwachten?

Je maakt deel uit van een dynamisch en collaboratief HR-team waarin jouw bijdrage ervoor zorgt dat onze compensatie- en benefitsprocessen vlot verlopen. In deze ondersteunende rol help je bij het beheren van benefitprogramma’s, het waarborgen van datanauwkeurigheid en het coördineren met payroll en HR-systemen.

Je werkt nauw samen met de Compensation & Benefits Lead en cross-functionele teams, waarbij je hands-on ervaring opdoet in compensatie- en benefitsprocessen. Dit is een uitstekende kans om je expertise uit te bouwen, bij te dragen aan procesverbeteringen en initiatieven te ondersteunen die ons helpen competitief te blijven in het aantrekken en behouden van talent.

Dit ga je doen:

• Beheer de administratie van extralegale voordelen zoals groepsverzekering, hospitalisatieverzekering, mobiliteitsoplossingen, enz.
• Assisteer bij het uitvoeren van salarisbenchmarks en marktvergelijkingen.
• Ondersteun de ontwikkeling en uitvoering van compensatiestrategieën en budgetsimulaties.
• Beheer diverse benefitprogramma’s zoals het fietsleaseprogramma, warrants, flex income plan, mobiliteitsbudget, … en fungeer als eerste aanspreekpunt voor alle operationele vragen.
• Assisteer bij de jaarlijkse salarisreview en het bonus- & meritproces.
• Volg wijzigingen in sociale wetgeving op en vertaal deze naar HR-praktijken rond compensatie & benefits.
• Werk samen met payroll om een correcte salarisverwerking te garanderen.
• Neem deel aan diverse projecten rond prestatiegerichte beloning, functieclassificatie, …
• Rapporteer aan de Compensation & Benefits Lead en werk nauw samen met de Head of Payroll, Compensation & Benefits EU en het payrollteam.

Wie zoeken we?

Opleiding

• Bachelor- of masterdiploma in HR, Economie of gelijkwaardig door ervaring.

Ervaring

• Minimaal 5 jaar ervaring in Compensation & Benefits of Payroll.

Talen

• Vloeiend Nederlands en Engels.

Expertise

• Bekendheid met HR-systemen zoals Protime, eBlox en Workday is een plus.
• Grondige kennis van Belgische C&B-praktijken en wettelijke kaders.

Skills

• Analytische mindset met sterke aandacht voor detail.
• Uitstekende kennis van Excel en vaardigheid in data-analyse.
• Duidelijke en zelfverzekerde communicator—in staat om complexe onderwerpen eenvoudig uit te leggen.
• Discreet, betrouwbaar en servicegericht.
• Samenwerkende en proactieve teamspeler.

Wat bieden wij jou?

• Een betekenisvolle rol in een groeiend biotechbedrijf waar jouw werk echt impact heeft.
• Een vast contract met een competitief salaris en een breed pakket aan extralegale voordelen.
• Kansen om te leren, te groeien en bij te dragen aan innovatieve HR-praktijken.
• Een diverse en internationale werkomgeving.
• Tal van leuke en informele teammomenten.

Over Legend Biotech

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zich toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën voor de behandeling van chronische en levensbedreigende ziekten, zoals kanker.

Het bedrijf werd opgericht in 2014 en heeft zijn hoofdkantoor in Somerset, New Jersey. Legend Biotech telt inmiddels meer dan 2.400 medewerkers verspreid over zes wereldwijde productiesites. Twee van deze sites bevinden zich in Gent: Obelisc (Technology Park Zwijnaarde) en Tech Lane (Eilandje Zwijnaarde).

In Gent richt Legend Biotech zich op de productie van geavanceerde CAR-T-celtherapieën voor de behandeling van multipel myeloom, in nauwe samenwerking met Johnson & Johnson.

Are you passionate about creating meaningful employee experiences through smart, fair, and future-proof reward systems? As a Compensation & Benefits Specialist at Legend Biotech, you’ll be part of a collaborative team that ensures our people feel valued—through competitive compensation, thoughtful benefits, and clear communication. You’ll combine operational ownership with analytical insight, helping us shape total rewards strategies that support both our employees and our business.

What can you expect?

You’ll be part of a dynamic and collaborative HR team where your contributions help keeping our compensation and benefits operations running smoothly. In this supporting role, you’ll assist in managing benefit programs, maintaining data accuracy, and ensuring timely coordination with payroll and HR systems.

You’ll work closely with the Compensations & Benefits Lead and cross-functional teams, gaining hands-on experience in compensation and benefits processes. This is a great opportunity to build your expertise, contribute to process improvements, and support initiatives that help us stay competitive in attracting and retaining talent.

Here is what you will do:

• Manage the administration of fringe benefits such as group insurance, hospitalization insurance, mobility solutions, etc.
• Assist in conducting salary benchmarks and market comparisons.
• Support the development and execution of compensation strategies and budget simulations.
• Support various benefits programs such as the bike lease program, warrants, flex income plan, mobility budget,... and become the first point of contact regarding all operational questions.
• Assist in the yearly salary review and bonus & merit process.
• Monitor changes in social legislation and translate them into HR practices related to compensation & benefits.
• Collaborate with payroll to ensure accurate salary processing.
• Participate in various projects related to performance-based rewards, job classification, ...
• Report to the Compensation & Benefits Lead and collaborate closely with the Head of Payroll, Compensation & Benefits EU and the payroll team.

Who are we looking for?

Education

• Bachelor’s or Master’s degree in HR, Economics, or equivalent through experience.

Experience

• Minimum 5 years of experience in Compensation & Benefits or Payroll.

Languages

• Fluent in Dutch and English.

Expertise

• Familiarity with HR systems like Protime, eBlox, and Workday is a plus.
• Solid understanding of Belgian C&B practices and legal frameworks.

Strengths

• Analytical mindset with strong attention to detail.
• Proficient in Excel with an ability to manage and analyze data
• Clear and confident communicator—able to simplify complex topics.
• Discreet, reliable, and service-oriented.
• Collaborative and proactive team player.

What do we offer you?

• A meaningful role in a growing biotech company where your work has real impact.
• A permanent contract with a competitive salary and a wide range of fringe benefits.
• Opportunities to learn, grow, and contribute to innovative HR practices.
• A diverse and international work environment.
• Plenty of fun and informal team moments.

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. 

This position is responsible for providing operational excellence and project management support to our two cell therapy manufacturing plants in Belgium. 

You will play a key role in strengthening the continuous improvement culture, building Lean and 6Sigma skills within the organization and lead complex, cross functional optimization initiatives.  

You combine project management; strong stakeholder management and communication skills with training and coaching skills to drive effective communication, coordination and collaboration.

What can you expect?

Here’s what you’ll do:

• Co-own the Operational Excellence program for the site, focusing on building a strong continuous improvement culture and developing Lean & 6sigma capabilities across the organization. 
• Provide training, coaching and development of Lean and 6sigma capabilities, including:
  • Support the selection of green belt trainees and projects, help organize GB training in collaboration with our J&J partners, coaching and and review of Green Belt projects to support certification
  • Deliver basic statistics training and support teams with questions related to DMAIC, data analysis and structured problem-solving
  • Optimize and maintain templates and tools
• Educate, coach and lead OpEx deployment leads in operational departments  
• Lead complex Lean and Six Sigma improvement projects requiring Black Belt–level expertise, supporting strategic objectives of the organization, such as:
  • Cost optimization
  • Lead time reduction 
  • Deviation reduction
  • Scheduling and shift regime optimization 
  • Cleanroom efficiency improvements
• Serve as a subject-matter expert for advanced statistics and data analysis questions 
• Use Lean and Six Sigma methodologies, including 5S, standard work, visual management, Kanban, Pareto analysis and others, to structure and improve initiatives. 
• Build and maintain strong working relationships with peers across the organization 

Who are we looking for?

Education

• Minimum bachelor degree
• Black Belt certification

Experience

• Minimum 5 years of experience in Industrial Operations environment, of which 3 years of experience in Pharma 
• Experience in lean process optimization tools: black belt certified
• Experience in 6sigma problem solving methodology and tools: green belt certified 
• Knowledge and experience in human factors are a plus 

Languages

• Fluent in English  
• Good knowledge of Dutch is a plus

Strengths

• Collaborative team player with strong interpersonal skills  
• Excellent communication skills and stakeholder management  
• Able to engage, motivate and lead matrix teams across various levels  
• You have a strong analytical mindset with the ability to translate data into insights 
• Strong coaching and training skills  
• Skilled at instilling and reinforcing organizational culture 

Expertise

• End-to-end project management skills  
• Strategic thinking and vision creation
• Proficient in data analysis  
• Leading-cross functional and matrix teams initiatives
• Effective use of escalation paths to drive impact  
• Independently initiating, building and managing projects from zero 

What do we offer you? 

• A meaningful job with impact on the organization. 
• 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.

In deze functie ben je verantwoordelijk voor het bieden van operationele excellentie- en projectmanagementondersteuning aan onze twee cell therapy productiesites in België.

Je speelt een sleutelrol in het versterken van de continuous improvement-cultuur binnen de organisatie, het opbouwen van Lean- en Six Sigma-vaardigheden en het leiden van complexe, cross-functionele optimalisatie-initiatieven.

Je combineert projectmanagementvaardigheden, sterk stakeholdermanagement en communicatieve vaardigheden met training- en coachingcompetenties om effectieve communicatie, coördinatie en samenwerking te stimuleren.

Wat mag je verwachten?

Dit is wat je gaat doen

• Mede-eigenaarschap opnemen van het Operational Excellence-programma voor de site, met focus op het uitbouwen van een sterke continuous improvement-cultuur en het ontwikkelen van Lean & Six Sigma-capabilities binnen de organisatie.
• Training, coaching en ontwikkeling van Lean- en Six Sigma-competenties, waaronder:

  • Ondersteunen bij de selectie van Green Belt-trainees en projecten
  • Organiseren van Green Belt-trainingen in samenwerking met onze J&J-partners
  • Coaching en review van Green Belt-projecten ter ondersteuning van certificatie
  • Geven van basisstatistiektraining en ondersteuning van teams bij vragen rond DMAIC, data-analyse en gestructureerde probleemoplossing
• Optimaliseren en onderhouden van templates en tools
• Opleiden, coachen en aansturen van OpEx deployment leads binnen operationele afdelingen
• Leiden van complexe Lean- en Six Sigma-verbeterprojecten die Black Belt-expertise vereisen, ter ondersteuning van strategische doelstellingen van de organisatie, zoals:

  • Kostenoptimalisatie
  • Verkorting van doorlooptijden
  • Reductie van deviatie’s
  • Optimalisatie van planning en shiftregimes
  • Efficiëntieverbeteringen in cleanrooms
• Optreden als subject-matter expert voor geavanceerde statistiek- en data-analysevraagstukken
• Toepassen van Lean- en Six Sigma-methodologieën zoals 5S, standard work, visual management, Kanban, Pareto-analyse en andere om initiatieven te structureren en verbeteren
• Opbouwen en onderhouden van sterke werkrelaties met peers binnen de organisatie

Naar wie zijn we op zoek?

Opleiding

• Minimaal een bachelor diploma
• Black Belt-certificering

Ervaring

• Minstens 5 jaar ervaring binnen een industriële operations-omgeving
• Minstens 3 jaar ervaring binnen de farmaceutische sector
• Ervaring met Lean procesoptimalisatietools: Black Belt-gecertificeerd
• Ervaring met Six Sigma probleemoplossingsmethodologieën en -tools: Green Belt-gecertificeerd
• Kennis en ervaring met human factors is een plus

Talen

• Vloeiend Engels
• Goede kennis van het Nederlands is een plus

Skills

• Samenwerkingsgerichte teamplayer met sterke interpersoonlijke vaardigheden
• Uitstekende communicatievaardigheden en sterk stakeholdermanagement
• In staat om matrixteams op verschillende niveaus te engageren, motiveren en aan te sturen
• Sterke analytische mindset met het vermogen om data te vertalen naar inzichten
• Sterke coaching- en trainingsvaardigheden
• Bekwaam in het uitdragen en versterken van organisatiecultuur

Expertise

• End-to-end projectmanagementvaardigheden
• Strategisch denkvermogen en visieontwikkeling
• Vaardig in data-analyse
• Leiden van cross-functionele en matrixteaminitiatieven
• Effectief gebruik van escalatiepaden om impact te realiseren
• Zelfstandig initiëren, opbouwen en managen van projecten vanaf nul

 Wat wij jou bieden?

• Een betekenisvolle job met een goede work-lifebalance.
• 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.

Our Operations Team in Ghent is looking for a passionate CAR-T Operations Junior Expert. Do you want a meaningful job? Here you contribute to the fight against cancer every day!

What Can You Expect?

The role of a CAR-T Operations Junior Expert is exciting and challenging. Here's what you'll do: 

• Perform CAR-T process activities: You will accurately perform various steps in the CAR-T manufacturing process. From cell culture and purification to aseptic processing and cryopreservation, you will ensure the highest quality and safety standards in the clean room. 
• Compliance with quality standards: You will closely follow Standard Operating Procedures (SOPs) and batch records to ensure the quality and safety of our cellular therapies. 
• Collaboration: You will work closely with various teams and departments to complete production tasks according to a shift schedule. 
• Innovate and improve: You will contribute to process optimizations and efficiency improvements. 
• Environmental monitoring: You will maintain GMP production areas, focusing on equipment cleanliness and environmental monitoring.
• GMP documentation: You will complete all necessary GMP documents to ensure compliance and traceability.

Who Are We Looking For? 

Education

• You have at least a bachelor's degree in sciences, (bio)engineering, biotechnology, pharmacy or another related field of study or you are equivalent through experience. 

Experience

• Practical experience within a cGMP or ATMP environment and with aseptic techniques in clean rooms is certainly an asset but not a must. In any case, we offer you the necessary training so that you can get started smoothly in your new role.    
• Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, and Outlook) is required. 

Languages

• You are fluent in Dutch or English, with strong oral and written communication skills. 

Strengths

• You are a true team player but also enjoy working independently. You have strong interpersonal skills and a healthy dose of empathy. You are flexible, problem-solving and can multitask well. You have a strong desire to learn and grow. 
• You bring a hands-on mindset paired with a strong focus on quality and detail.

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.  

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

Ons Operations Team in Gent is op zoek naar een gepassioneerde CAR-T Operations Junior Expert. Wil jij een betekenisvolle job? Hier draag je elke dag bij aan de strijd tegen kanker!

Wat kan je verwachten?

De rol van CAR-T Operations Junior Expert is boeiend en uitdagend. Dit ga je doen:

• Uitvoeren van CAR-T procesactiviteiten: Je voert nauwkeurig verschillende stappen uit in het CAR-T productieproces. Van celcultuur en zuivering tot aseptische verwerking en cryopreservatie: je zorgt voor de hoogste kwaliteits- en veiligheidsnormen in de cleanroom.
• Naleving van kwaliteitsnormen: Je volgt strikt de Standard Operating Procedures (SOP’s) en batchrecords om de kwaliteit en veiligheid van onze celtherapieën te waarborgen.
• Samenwerking: Je werkt nauw samen met verschillende teams en afdelingen om productietaken volgens een shiftschema uit te voeren.
• Innoveren en verbeteren: Je draagt bij aan procesoptimalisaties en efficiëntieverbeteringen.
• Omgevingsmonitoring: Je onderhoudt GMP-productiegebieden met focus op reinheid van apparatuur en omgevingsmonitoring.
• GMP-documentatie: Je vult alle noodzakelijke GMP-documenten in om compliance en traceerbaarheid te garanderen.

Wie zoeken we?

Opleiding

• Je hebt minimum een bachelordiploma in wetenschappen, (bio)ingenieurswetenschappen, biotechnologie, farmacie of een ander gerelateerd vakgebied, of bent gelijkwaardig door ervaring.

Ervaring

• Praktische ervaring binnen een cGMP- of ATMP-omgeving en met aseptische technieken in cleanrooms is zeker een plus, maar geen must. In elk geval bieden we jou de nodige training zodat je vlot aan de slag kan in je nieuwe rol.

Talen

• Je spreekt vloeiend Nederlands of Engels en beschikt over sterke mondelinge en schriftelijke communicatieskills.

Skills

• Je bent een echte teamspeler, maar werkt ook graag zelfstandig. 
• Sterke interpersoonlijke vaardigheden en een gezonde dosis empathie.
• Flexibiliteit, probleemoplossendheid en je kan goed multitasken.
• Leergierig en wil graag groeien.

Wat bieden wij?

• Een betekenisvolle job die rechtstreeks bijdraagt aan het welzijn van patiënten
• Een uitstekende work-life balance. Je werkt 4 dagen en geniet daarna 4 dagen vrij.
• Een ondersteunende en innovatieve werkomgeving waarin leren en persoonlijke ontwikkeling worden aangemoedigd.
• De kans om samen te werken met mensen van over de hele wereld.
• Een contract van onbepaalde duur en een aantrekkelijk salarispakket, aangevuld met tal van extralegale voordelen zoals extra wettelijke vakantiedagen, maaltijdcheques, groeps- en hospitalisatieverzekering, dubbel vakantiegeld, een eindejaarspremie en een prestatiebonus.
• Tal van leuke en informele evenementen.

Over Legend Biotech

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zich toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën voor de behandeling van chronische en levensbedreigende ziekten, zoals kanker.

Het bedrijf werd opgericht in 2014 en heeft zijn hoofdkantoor in Somerset, New Jersey. Legend Biotech telt inmiddels meer dan 2.400 medewerkers verspreid over zes wereldwijde productiesites. Twee van deze sites bevinden zich in Gent: Obelisc (Technology Park Zwijnaarde) en Tech Lane (Eilandje Zwijnaarde).

In Gent richt Legend Biotech zich op de productie van geavanceerde CAR-T-celtherapieën voor de behandeling van multipel myeloom, in nauwe samenwerking met Johnson & Johnson.

Our Operations Team in Ghent is looking for skilled individuals to join our mission of transforming medicine.

This is more than just a job—it’s an opportunity to advance your career in a dynamic, purpose-driven environment. Whether you have a secondary education with hands-on experience or are a recent graduate with a bachelor’s degree in life sciences or related fields—and especially if you’ve worked in cleanrooms, pharmaceutical manufacturing, or chemical processing—we’d love to hear from you.

We are looking for dedicated process operators to join our team at a leading biotechnology company.

What can you expect?

Your journey begins with extensive training, where we immerse you in the world of aseptic (germ-free) and GMP (Good Manufacturing Practice) operations, including the crucial procedures you need to master.

Afterward, you will join our dynamic and driven Operations team, which works together every day to fulfill our mission. Alongside your fellow operators and team leaders, you will perform aseptic and manual production processes according to strict, proven procedures.

• Daily aseptic and manual production processes
• Working in a cleanroom lab environment
• Executing production steps in controlled environments (grade A/B/C/D) such as spiking, media changes, cell culture, and freezing therapeutic products.
• Managing equipment: inspections and maintenance
• Thorough cleaning and disinfection of materials
• Supporting transitions between production zones
• Ensuring patients receive high-quality therapies on time

Who are we looking for? 

Education

• You have a Graduates or Bachelor's degree in pharmaceutical or biotechnological sciences or a related field of study.
• Or you have relevant experience, we believe that your mindset, passion, sense of accuracy and commitment to quality are more important than the education you took.

Experience

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

Languages

• You are fluent in English.
• Fluent knowledge of Dutch is a plus.

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.
• You have excellent organizational skills, with a penchant for structure and order.
• You can work accurately and diligently, with a keen eye for detail.
•  You are an effective communicator and a true team player. 
• You thrive in fast-paced environments and are eager to learn.

What do we offer?  

• A meaningful job with an excellent work-life balance. You will work 4 days. After that you will enjoy 4 days off.  
• Be prepared to work across various shifts, including: 6:00-16:00, 7:00-17:00, 8:00-18:00, 10:00-20:00, 12:00-22:00, 14:00-00:00, 15:00-01:00 and 16:00-02:00
• 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. 

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. 

#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. 

Wil jij een sleutelrol spelen in een snelgroeiende biotechomgeving waar kwaliteit, innovatie en patiëntimpact centraal staan? Als Payroll Manager bij Legend Biotech zorg je voor een vlekkeloze, tijdige en volledig compliant payroll voor België en Ierland. Je combineert operationele excellentie met optimalisatie, en leidt een team dat elke dag het verschil maakt voor onze medewerkers.

Wat kan je verwachten?

• Volledige ownership nemen over de payroll voor België en Ierland en ervoor zorgen dat elke loonrun vlekkeloos, correct en compliant verloopt — maand na maand.
• Alle payroll inputs, controles en berekeningen valideren en waken over datakwaliteit binnen HRIS, payroll en Time & Attendance (T&A).
• Sociale wetgeving en wijzigingen moeiteloos vertalen naar duidelijke payrollprocessen en heldere interne richtlijnen.
• Sterke samenwerkingen uitbouwen met externe payroll en T&A partners en een efficiënte, kwalitatieve en transparante dienstverlening garanderen.
• Fungeren als go-to expert voor complexe payrollcases, root-cause analyses uitvoeren en zorgen voor duurzame oplossingen.
• Rust en betrouwbaarheid brengen in een complexe shift- en T&A-omgeving en ervoor zorgen dat medewerkers correct vergoed worden voor wat ze doen.
• Structurele issues rond shiftcomplexiteit monitoren en processen en controles proactief verbeteren.
• Continu vooruitkijken en processen, systemen en controles optimaliseren om payroll schaalbaar, future proof en minder afhankelijk van manuele acties te maken.
• Als people leader een payrollteam (circa. 4 direct reports) coachen, motiveren en laten groeien, met een sterke focus op kwaliteit, ownership en samenwerking.
• Als strategische partner samenwerken met HR, Finance en de business en adviseren over de payrollimpact van veranderingen en projecten.

Wie zoeken we?

Opleiding

• Master in HR, Finance, Business of gelijkwaardige ervaring.

Ervaring

• Minstens 10 jaar ervaring in Belgische payroll in een middelgrote tot grote organisatie.
• Sterke ervaring met shift‑populaties en complexe T&A‑omgevingen.
• Leidinggevende of coördinerende ervaring binnen payrollteams.

Talen

• Vloeiend in Nederlands en Engels.

Skills

• Diepgaande kennis van payrollprocessen, controles en rapportering.
• Goede kennis van sociale wetgeving (België vereist, Ierland is een plus).
• Ervaring met payrollsystemen, HRIS, T&A en Excel. Protime, eBlox en Workday zijn een grote troef.
• Sterk analytisch vermogen, nauwkeurig, oplossingsgericht en hands‑on.
• Uitstekende communicatieve vaardigheden en stakeholder management.
• Integriteit, discretie en een pragmatische manier van uitleggen van complexe topics.

Expertise

• Procesoptimalisatie, standaardisatie en (semi‑)automatisatie.
• System ownership van payroll, payroll interfaces en T&A.

Wat bieden wij jou?

• Een zinvolle rol in een groeiend biotechbedrijf waar jouw werk echt impact heeft.
• Een ondersteunende, innovatieve werkomgeving met veel aandacht voor leren en ontwikkeling.
• De kans om samen te werken met collega’s van over de hele wereld.
• Een contract van onbepaalde duur met een aantrekkelijk salarispakket en ruime extralegale voordelen (bedrijfswagen met laadkaart, maaltijdcheques, hospitalisatie‑ en groepsverzekering, eindejaars- en performance bonus, …).
• Veel leuke en informele team‑ en bedrijfsactiviteiten.

Over Legend Biotech

Legend Biotech is een wereldwijd biotechnologiebedrijf dat innovatieve en levensreddende celtherapieën ontwikkelt, produceert en commercialiseert. Sinds onze oprichting in 2014 in Somerset, New Jersey, groeiden we uit tot meer dan 2.400 medewerkers verspreid over zes wereldwijde productiesites.
In Gent focussen we ons op de productie van geavanceerde CAR‑T‑therapieën voor de behandeling van multipel myeloom, in nauwe samenwerking met Johnson & Johnson.

Do you want to play a key role in a fast-growing biotech environment where quality, innovation and patient impact are central? As a Payroll Manager at Legend Biotech, you ensure a flawless, timely and fully compliant payroll for Belgium and Ireland. You combine operational excellence with continuous optimization and lead a team that makes a difference for our employees every day.

What can you expect?

• Taking full ownership of the payroll for Belgium and Ireland and ensuring that every payroll run proceeds flawlessly, correctly and compliantly — month after month.
• Validating all payroll inputs, checks and calculations and safeguarding data quality within HRIS, payroll and Time & Attendance (T&A).
• Translating social legislation and changes effortlessly into clear payroll processes and clear internal guidelines.
• Building strong collaborations with external payroll and T&A partners and guaranteeing an efficient, qualitative and transparent service provision.
• Acting as the go-to expert for complex payroll cases, performing root-cause analyses and ensuring sustainable solutions.
• Bringing calm and reliability to a complex shift and T&A environment and ensuring that employees are correctly compensated for what they do.
• Monitoring structural issues around shift complexity and proactively improving processes and controls.
• Continuously looking ahead and optimizing processes, systems and controls to make payroll scalable, future proof and less dependent on manual actions.
• Coaching, motivating and growing a payroll team (circa 4 direct reports) as a people leader, with a strong focus on quality, ownership and collaboration.
• Working as a strategic partner with HR, Finance and the business and advising on the payroll impact of changes and projects.

Who are we looking for?

Education

• Master’s degree in HR, Finance, Business or equivalent experience.

Experience

• Minimum 10 years of Belgian payroll experience in a medium to large company.
• Strong experience with shift‑based populations and complex T&A environments
• Prior team leadership or coordination experience within payroll teams.

Languages

• Fluent in Dutch and English.

Strengths

• Strong knowledge of payroll processes, controls, and reporting.
• Solid understanding of Belgian social legislation (Belgian legislation required, Irish legislation is a plus).
• Experience with Sox audit compliancy is a plus.
• Strong analytical ability, accurate, solution-oriented and hands-on.
• Excellent communication skills and stakeholder management.
• Integrity, discretion and a pragmatic way of explaining complex topics.

Expertise

• Process optimisation, standardisation and (semi‑)automation.
• System ownership of payroll, payroll interfaces and T&A.

What do we offer you?

• A meaningful role in a growing biotech company where your work has a real impact.
• A supportive and innovative work environment that values learning and personal development.
• The opportunity to work with colleagues from all over the world.
• A permanent contract with an attractive salary package and many fringe benefits (company car with charging card, meal vouchers, group & hospitalization insurance, year‑end and performance bonus).
• Many fun and informal team and company activities.

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.

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. 

#LI-AG1

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.  

Are you ready to make a real impact on patients’ lives as a QC Analyst? With the growth of our Quality Operations Team in Ghent, we are looking for new colleagues with a passion for quality who want to help shape the future of cell therapy. If you’re eager to become a quality expert and join a team of experts, you’re in the right place with us!

What Can You Expect? 

As a QC analyst, you will play a critical role in ensuring the highest quality of life-saving cell therapy products. Here's what you'll do: 

• Advanced QC Testing: You will perform QC testing for CAR-T products in IPC laboratories and ensure compliance with all procedures, standards and GMP regulations.
• Environmental monitoring: You verify clean room classification by taking samples of (non-) viable particles and microorganisms.
• Collaboration: You will work closely with the Quality and Operations departments to bring analytical testing from the test bench to production. 
• Documentation and data management: You will review and approve QC data, maintain process integrity through accurate documentation, and manage test results in our eLIMS software. 
• Process Optimization: You will create and review QC documents, SOPs and work instructions and also contribute to process optimizations. 

Who Are We Looking For? 

Education 

• You have a bachelor's degree in lab technologies or other related field, or equivalent experience. 

Experience

• Practical experience in an aseptic production facility within QC or QA is a plus but certainly not a must. We offer you the necessary training to get you started in your new role.   

Languages  

• You have strong written and oral communication skills in both Dutch and technical English. 

Strengths

• You are curious about everything related to quality and you learn quickly.
• You have a sharp eye for detail and work with great accuracy.
• You continue to deliver high-quality work, even under time pressure. 

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.  

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

Klaar om als QC-analist écht impact te maken op het leven van patiënten? Door de groei van ons Quality Operations Team in Gent zijn wij op zoek naar nieuwe collega’s met een passie voor kwaliteit die willen meebouwen aan de toekomst van celtherapie. Wil je groeien binnen een fantastisch team van experten? Dan zit je bij ons helemaal goed!

Wat kan je verwachten?

Als QC-analist speel je een cruciale rol in het waarborgen van de hoogste kwaliteit van levensreddende celtherapieproducten. Dit zijn jouw verantwoordelijkheden:

• Geavanceerde QC-testen: Je voert QC-testen uit voor CAR-T-producten in IPC-laboratoria en zorgt voor naleving van alle procedures, standaarden en GMP-regelgeving.
• Omgevingsmonitoring: Je controleert de cleanroomclassificatie door het nemen van monsters van (niet-)levensvatbare deeltjes en micro-organismen.
• Samenwerking: Je werkt nauw samen met de afdelingen Quality en Operations om analytische testen van de werkbank naar productie te brengen.
• Documentatie en databeheer: Je beoordeelt en keurt QC-data goed, bewaakt procesintegriteit via nauwkeurige documentatie en beheert testresultaten in onze eLIMS-software.
• Procesoptimalisatie: Je stelt QC-documenten, SOP’s en werkinstructies op en draagt bij aan procesoptimalisaties.

Wie zoeken we?

Opleiding

• Je hebt een bachelordiploma in laboratoriumtechnologie of een gerelateerd vakgebied, of je hebt door relevante ervaring een gelijkwaardig niveau opgebouwd.

Ervaring

• Praktische ervaring in een aseptische productieomgeving binnen QC of QA is een pluspunt, maar zeker geen vereiste. We bieden je de nodige training om je nieuwe rol succesvol te starten.

Talen

• Je beschikt over sterke schriftelijke en mondelinge communicatievaardigheden in zowel Nederlands als technisch Engels.

Skills

• Je bent nieuwsgierig naar alles wat te maken heeft met kwaliteit en leert snel.
• Je hebt oog voor detail en gaat nauwkeurig aan de slag.
• Je blijft onder tijdsdruk kwalitatief werk leveren.

Wat bieden wij jou?

• Een zinvolle job met een uitstekende work-life balance: je werkt 4 dagen en geniet daarna 4 dagen vrij.
• Een ondersteunende en innovatieve werkomgeving waarin leren en persoonlijke ontwikkeling worden aangemoedigd.
• De kans om samen te werken met mensen van over de hele wereld.
• Een contract van onbepaalde duur en een aantrekkelijk salarispakket aangevuld met tal van extralegale voordelen, zoals extra wettelijke vakantiedagen, maaltijdcheques, groeps- en hospitalisatieverzekering, dubbel vakantiegeld, een eindejaarspremie en een prestatiebonus.
• Veel leuke en informele evenementen.

Over Legend Biotech

Legend Biotech is een wereldwijd biotechnologiebedrijf dat zich toelegt op het ontwikkelen, produceren en commercialiseren van innovatieve en levensreddende celtherapieën voor de behandeling van chronische en levensbedreigende ziekten, zoals kanker.

Het bedrijf werd opgericht in 2014 en heeft zijn hoofdkantoor in Somerset, New Jersey. Legend Biotech telt inmiddels meer dan 2.400 medewerkers verspreid over zes wereldwijde productiesites. Twee van deze sites bevinden zich in Gent: Obelisc (Technology Park Zwijnaarde) en Tech Lane (Eilandje Zwijnaarde).

In Gent richt Legend Biotech zich op de productie van geavanceerde CAR-T-celtherapieën voor de behandeling van multipel myeloom, in nauwe 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

Wil je écht impact maken? Sluit je aan bij onze QC Support Technican Talent Pool!

Ben je op zoek naar een job waarin je een echte, tastbare impact kan maken? Heb je oog voor detail, netheid en kwaliteit? Dan hebben wij de perfecte kans voor jou! Sluit je aan bij ons dynamische Quality Operations Team in Gent als QC Support Technician. In deze rol ben je een essentieel onderdeel van onze missie om onze levensreddende celtherapieën veilig en tijdig bij de patiënten te krijgen die ze het hardst nodig hebben. Stap in een job die écht het verschil maakt! 

Wat mag je verwachten?

Je werkt nauw samen met teamleaders en QC‑analisten om materialen te reinigen en te desinfecteren en zorgt voor een vlotte overdracht van stalen tussen verschillende productie‑ en logistieke zones. Dit is wat je zal doen: 

• Ondersteunen van kwaliteitscontrole: Je dagelijkse, praktische ondersteuning bij QC‑analyses helpt mee de kwaliteit van onze celtherapieproducten te garanderen. 
• Beheer van materialen: Van het controleren en desinfecteren van apparatuur tot het beheren van labomaterialen en afval — jouw precisie houdt onze processen draaiende. 
• Overbrengen van stalen: Je speelt een cruciale rol bij het veilig transporteren van stalen tussen productie‑ en logistieke zones. 
• Ondersteunen van omgevingsanalyses: Je ondersteunt omgevingsanalyses in grade C- en D‑ruimtes. 
• Documenteren van activiteiten: Je registreert al je reinigings- en desinfectietaken nauwkeurig in logboeken, formulieren of via ons eLIMS‑systeem. 
• Aseptische omstandigheden handhaven: Je werkt in een steriele omgeving en volgens een shiftsysteem (geen nachten, wel weekends). 

Naar wie zijn we op zoek? 

Opleiding 

• Een middelbaar schooldiploma is mooi meegenomen, maar belangrijker zijn jouw motivatie, nauwkeurigheid en leergierigheid. 

Ervaring 

• Ervaring in een operationele omgeving is een plus, maar geen vereiste. 

Talen 

• Je spreekt vlot Nederlands en/of Engels en communiceert helder, open en positief. 

Sterktes 

• Je bent detailgericht en hebt een sterke focus op kwaliteit en compliance. 
• Je werkt systematisch en gestructureerd en volgt strikt GMP-richtlijnen. 
• Je bent een teamplayer die ook zelfstandig goed functioneert. 
• Je beschikt over sterke organisatorische vaardigheden. 

Expertise 

• Je bent vlot met Microsoft Office (Word, Excel, PowerPoint, Outlook). 
• Via interne trainingen krijg je een grondige opleiding in GMP-vereisten en kwaliteitsstandaarden. 

 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.

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.

Leid waar het echt telt.

Bij Legend Biotech draait leiderschap in de eerste plaats om mensen.
Om vertrouwen. Groei. Verantwoordelijkheid. En impact die je echt kunt voelen. 
Bij onze CAR-T productielocaties Obelisc en Tech Lane in Gent zoeken we ervaren supervisors die energie halen uit het coachen van mensen, het leiden van teams en het helpen van anderen om hun beste zelf te worden.

We nemen supervisors aan voor CAR-T Productie, Kwaliteitscontrole (QC) en Onderhoud. Drie verschillende domeinen, één gemeenschappelijk doel: helpen zorgen dat levensreddende therapieën patiënten veilig, betrouwbaar en op tijd bereiken. Dit is een leiderschapsrol waarbij jouw manier van werken mensen, teams en resultaten vormgeeft.

Wat kan je verwachten?

Als supervisor leid je waar het echt telt: op de vloer, met je team.

Jouw focus is duidelijk:

• Coaching en people management
  Je leidt een team van operators, analisten of technici.
  Je coacht, ondersteunt en daagt mensen uit om te groeien, verantwoordelijkheden op te nemen en met zelfzekerheid te presteren.
• Structuur en duidelijkheid creëren
  Je brengt rust en focus in een complexe omgeving.
  Je stelt prioriteiten, brengt verwachtingen op één lijn en creëert een veilige ruimte waar mensen kunnen uitblinken.
• Kwaliteit en verantwoordelijkheid
  Je beschermt GMP, veiligheid en compliance via dagelijks leiderschap, niet alleen door papierwerk.
  Je leidt door het goede voorbeeld te geven en bouwt een sterke kwaliteitsmentaliteit op in je team.
• De operatie in beweging houden
  Je houdt toezicht op dagelijkse activiteiten, anticipeert op problemen en handelt wanneer het ertoe doet.
  Je werkt nauw samen met andere teams om problemen op te lossen en processen draaiende te houden.

 Via jouw leiderschap groeien teams, blijven processen op schema en ontvangen patiënten de therapieën waar ze op wachten.

Wie zoeken we?

Opleiding

• Een bachelor- of masterdiploma in een relevant vakgebied, zoals wetenschap, bio-ingenieur of farmacie (voor Productie of QC), of een ingenieurs- of technische discipline (voor Maintenance), of gelijkwaardige ervaring.

Ervaring

• Je hebt ervaring in productie, kwaliteitscontrole of onderhoud binnen een GMP- of ATMP-omgeving in een farmaceutische of biotech omgeving.
• Je brengt ofwel een eerste leiderschapservaring mee of de duidelijke ambitie om door te groeien naar een rol in people management.

Talen

• Je spreekt vloeiend Engels, zowel gesproken als geschreven.
• Kennis van Nederlands is een pluspunt.

Skills

• Je vindt het echt leuk om mensen te leiden en te ontwikkelen
• Je communiceert duidelijk, luistert actief en geeft constructieve feedback
• Je creëert vertrouwen, ownership en motivatie in je team
• Je blijft kalm, gestructureerd en besluitvaardig in een dynamische omgeving

Expertise

• Je brengt een sterke kwaliteit en compliance mentaliteit mee.
• Je bent comfortabel met procedures, documentatie en systemen.
• Je bent hands-on, oplossingsgericht en gedreven door mensen en teamwork.

Wat bieden wij? 

• 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.

Does this feel like your next step?

Als je wilt leiden, sterke teams wilt opbouwen en een echt verschil wilt maken, ontmoeten we je graag. Solliciteer vandaag nog en leid waar het echt telt.

Over Legend Biotech

Met meer dan 2.900 medewerkers wereldwijd is Legend Biotech het grootste zelfstandige celtherapiebedrijf en een pionier in behandelingen die de kankerzorg voorgoed veranderen. We ontwikkelen en commercialiseren de CAR-T celtherapie ciltacabtagene autoleucel (cilta-cel) in samenwerking met Johnson & Johnson. In de EU is cilta-cel goedgekeurd onder de merknaam CARVYKTI® voor de behandeling van volwassen patiënten met hervallen en refractair multipel myeloom die minstens één eerdere behandellijn hebben gekregen.

Legend Biotech is een volledig geïntegreerde, wereldwijde organisatie met productiesites in de Verenigde Staten en Europa. Vanuit onze sites in Gent ondersteunen onze teams de klinische en commerciële bevoorrading van CAR-T therapieën in de volledige EMEA-regio. Zo vertalen we geavanceerde wetenschap elke dag opnieuw naar concrete impact voor patiënten.

Wat ons onderscheidt, is een heldere missie. Bij Legend Biotech Europe weet iedereen waarom hij of zij hier werkt en hoe elke bijdrage, groot of klein, rechtstreeks helpt om levensreddende therapieën te brengen naar patiënten die ze het hardst nodig hebben.

Role

We are looking for an experienced Account Executive to join our commercial Benelux sales team. You will be a key driver in our mission to secure the cloud-enabled digital future, focusing on delighting customers and nurturing trusted partnerships within the Belux commercial market. You will work alongside a global group of professionals to demonstrate the power and agility of cloud transformation to the world.

What you’ll do (Role Expectations)

• Prospect net new opportunities in BeLux commercial market using innovative techniques, tools, and top-tier channel partners including VAR, SI, and SP

• Identify and develop business cases aligned with strategic initiatives, articulating Zscaler’s unique value and differentiation at all levels of customer organizations

• Solve complex customer pain points by effectively positioning Zscaler’s unique value proposition

• Act as a primary sponsor for key partners to co-create joint plans, generate pipeline, and drive opportunities to successful closure

Who You Are (Success Profile)

• You thrive in ambiguity. You're comfortable building the path as you walk it. You thrive in a dynamic environment, seeing ambiguity not as a hindrance, but as the raw material to build something meaningful.

• You act like an owner. Your passion for the mission fuels your bias for action. You operate with integrity because you genuinely care about the outcome. True ownership involves leveraging dynamic range: the ability to navigate seamlessly between high-level strategy and hands-on execution.

• You are a problem-solver. You love running towards the challenges because you are laser-focused on finding the solution, knowing that solving the hard problems delivers the biggest impact.

• You are a high-trust collaborator. You are ambitious for the team, not just yourself. You embrace our challenge culture by giving and receiving ongoing feedback—knowing that candor delivered with clarity and respect is the truest form of teamwork and the fastest way to earn trust.

• You are a learner. You have a true growth mindset and are obsessed with your own development, actively seeking feedback to become a better partner and a stronger teammate. You love what you do and you do it with purpose.

What We’re Looking for (Minimum Qualifications)

• Minimum 5 years of sales experience carrying a revenue quota and selling specifically to the BeLux commercial market

• Fluent Dutch speaking 

• Proven history of a consistent track record in over-achievement and net new logo accomplishments

• Deep experience leveraging channel partnerships to drive business growth

• High degree of discipline to work a sales process from beginning to end and a willingness to be coached

• Demonstrated ability to lead team sales by effectively utilizing internal resources and partners to achieve success

What Will Make You Stand Out (Preferred Qualifications)

• Prior experience selling security, SaaS, or software solutions

• Bachelor’s degree in Business or a related field

#LI-Hybrid #LI-Remote #LI-TR3 

Spektrum supports apex purchasers (NATO, UN, EU, and National Government and Defence) and their Tier 1 supplier ecosystem with a wide range of specialist services. We provide our clients with professional services, specialised aerospace and defence sales, delivery, and operational subject matter expertise. We are looking for personnel to join our team and support key client projects.

Who we are supporting 

The NATO Communication and Information Agency (NCIA) is responsible for providing secure and effective communications and information technology (IT) services to NATO's member countries and its partners. The agency was established in 2012 and is headquartered in Brussels, Belgium.

The NCIA provides a wide range of services, including:

• Cyber Security: The NCIA provides advanced cybersecurity solutions to protect NATO's communication networks and information systems against cyber threats.
• Command and Control Systems: The NCIA develops and maintains the systems used by NATO's military commanders to plan and execute operations.
• Satellite Communications: The NCIA provides satellite communications services to enable secure and reliable communications between NATO forces.
• Electronic Warfare: The NCIA provides electronic warfare services to support NATO's mission to detect, deny, and defeat threats to its communication networks.
• Information Management: The NCIA manages NATO's information technology infrastructure, including its databases, applications, and servers.

Overall, the NCIA plays a critical role in ensuring the security and effectiveness of NATO's communication and information technology capabilities.

The program

Assistance and Advisory Service (AAS)

The NATO Communications and Information Agency (NCI Agency) is NATO’s principal C3 capability deliverer and CIS service provider. It provides, maintains and defends the NATO enterprise-wide information technology infrastructure to enable Allies to consult together under Article IV, and, when required, stand together in the face of attack under Article V.

To provide these critical services, in the modern evolving dynamic environment the NCI Agency needs to build and maintain high performance-engaged workforce. The NCI Agency workforce strategically consists of three major categorise's: NATO International Civilians (NIC)'s, Military (Mil), and Interim Workforce Consultants (IWC)'s. The IWCs are a critical part of the overall NCI Agency workforce and make up approximately 15 percent of the total workforce.

Role ID – CDT-0009

Role Duties and Responsibilities

• Support the lead Project Manager during the final development and pre-launch phase, including coordination with the development team and stakeholders;
• Assist in tracking timelines, deliverables and risks during the run-up to launch;
• Ensure all technical, analytical, and governance elements required for launch are aligned and delivered on time;
• Upon completion of implementation (post-launch), assume full responsibility for day-to-day project management, including scheduling, coordination, documentation, issue tracking, and continuous improvement, including further development activities for the Repository.
• Preparing an onboarding package (login guidance, FAQs, short video tutorials);
• Organising onboarding webinars for first-time users across 32 Allies;
• Coordinating account creation with internal NATO technical services;
• Tracking onboarding progress and reporting outstanding gaps or issues.
• Running regular coordination meetings with internal teams and contractors;
• Maintaining project documentation;
• Monitoring progress and reporting status to senior management;
• Preparing briefing notes, slide decks, speaking points, and demonstration materials related to the Repository;
• Ensuring alignment with related initiatives.
• Liaise regularly with EuRepoC as the primary data provider to coordinate data delivery schedules and ensure alignment with NATO requirements;
• serve as a focal point for coordination with SITCEN which provides technical platform;
• ensure continuous liaison with internal stakeholders (CyOC, CTAB etc.);
• preparing funding documentation for approval, tracking financial execution, liaising with divisional budget officers to secure timely and compliant funding approvals.
• develop proposals for the future evolution of the Repository by identifying functional and analytical gaps, developing proposals for enhancements, preparing an evolution roadmap, and handling engagement with SITCEN, EuRepoC, and other stakeholders on next-generation capabilities and long-term sustainability.
• capture lessons learned during development, testing and launch of the Repository, conduct after-action reviews with stakeholders, and convert findings into actionable recommendations for improving tool functionalities, data quality, and user engagement.
• Support the lead Project Manager during the data processing and analysis stage, including coordination with Allied representatives to facilitate Pledge bilaterals;
• Assist in tracking workflow of Allied analysis and task management through Q1-Q2 2026 and create a structured workflow that leverages the new process delivered by the Data Engineer for the Pledge data portal;
• Ensure all process aspects run smoothly to execute professional bilaterals, including some bilaterals delivered off-site in Allied nations as relevant, until technical, analytical, and governance elements required for launch are aligned and delivered on time;
• Upon completion of implementation (post-launch), assume full responsibility for day-to-day project management, including scheduling, coordination, documentation, issue tracking, and continuous improvement, including further development activities for the Repository.

 Essential Skills, Experience and Certifications

• Proven project management experience in complex, multi-stakeholder environments.
• Ability to brief senior management clearly and concisely
• Experience developing project documentation, SOPs, roadmaps, or guidance materials.
• Strong organisational skills and attention to detail.
• Ability to work independently and proactively
• Able to translate technical issues into policy-friendly language

 Desirable

• PM certifications (e.g., PRINCE2, PMP, Agile).
• Experience working with NATO structures
• Experience managing digital platforms
• Experience working in cybersecurity/cyber defence related disciplines

 Language Proficiency

• Excellent written and oral English

 Working Location

• Brussels, Belgium

Working Policy

• Onsite

Travel

• Some travel to other NATO sites may be required

Security Clearance

• Valid National or NATO Secret personal security clearance

Spektrum supports apex purchasers (NATO, UN, EU, and National Government and Defence) and their Tier 1 supplier ecosystem with a wide range of specialist services. We provide our clients with professional services, specialised aerospace and defence sales, delivery, and operational subject matter expertise. We are looking for personnel to join our team and support key client projects.

Who we are supporting 

The NATO Communication and Information Agency (NCIA) is responsible for providing secure and effective communications and information technology (IT) services to NATO's member countries and its partners. The agency was established in 2012 and is headquartered in Brussels, Belgium.

The NCIA provides a wide range of services, including:

• Cyber Security: The NCIA provides advanced cybersecurity solutions to protect NATO's communication networks and information systems against cyber threats.
• Command and Control Systems: The NCIA develops and maintains the systems used by NATO's military commanders to plan and execute operations.
• Satellite Communications: The NCIA provides satellite communications services to enable secure and reliable communications between NATO forces.
• Electronic Warfare: The NCIA provides electronic warfare services to support NATO's mission to detect, deny, and defeat threats to its communication networks.
• Information Management: The NCIA manages NATO's information technology infrastructure, including its databases, applications, and servers.

Overall, the NCIA plays a critical role in ensuring the security and effectiveness of NATO's communication and information technology capabilities.

The program

Assistance and Advisory Service (AAS)

The NATO Communications and Information Agency (NCI Agency) is NATO’s principal C3 capability deliverer and CIS service provider. It provides, maintains and defends the NATO enterprise-wide information technology infrastructure to enable Allies to consult together under Article IV, and, when required, stand together in the face of attack under Article V.

To provide these critical services, in the modern evolving dynamic environment the NCI Agency needs to build and maintain high performance-engaged workforce. The NCI Agency workforce strategically consists of three major categorise's: NATO International Civilians (NIC)'s, Military (Mil), and Interim Workforce Consultants (IWC)'s. The IWCs are a critical part of the overall NCI Agency workforce and make up approximately 15 percent of the total workforce.

Role ID – CDT-0007

Role Duties and Responsibilities

• cleaning and structuring Allied-submitted response data and incoming data from a research institution;
• Standardising data formats, categories, and fields in line with the required taxonomy.
• Identifying inconsistencies, gaps, and missing elements in the data and flagging these to the Project Manager (PM);
• Conducting regular data quality checks (accuracy, completeness, timeliness);
• Reviewing data entries and confirming alignment with the NATO Cyber Response taxonomy.
• Ensuring proper data classification and tagging.
• Supporting the PM in preparing feedback to Allies and researchers.
• Working closely with the data engineer to ensure smooth ingestion and integration of data into the platform;
• Supporting testing of data upload tools, visualisation features and filters;
• Helping to document data and refine the Repository’s metadata structure.
• Producing insight reports on Allied response patterns (e.g., most-used measures, speed of response, clustering by threat actor).
• Identifying trends and anomalies in Allied responses over time;
• Preparing data-driven products to support Committee discussions, CDT leadership meeting and strategic messaging;
• Create dashboards and visual analytics.
• Supporting PM in preparing training materials (slides, guides, examples, videos);
• Support in demonstrating data entry and tool navigation during webinar sessions for Allies;
• Providing technical and analytical assistance to first-time users.
• Verify data analysis methods to ensure correct data analysis methods use, support in identifying trends and anomalies in Allied responses over time through a comparative analysis of the previous Pledge cycles (May-June).
• Support the automated creation of dashboards and visual analytics (June-July)

 Essential Skills, Experience and Certifications

• Strong analytical and statistical skills.
• 2+ years working as a data analyst or similar role.
• Experience in data cleaning, transformation, analysis and visualization.
• Proficiency in Python for data processing.
• Ability to prepare visualisations, summaries, and other analytical products for non-technical audiences.
• Very good written and spoken English.
• Strong attention to detail and ability to perform repetitive tasks when needed.
• Ability to work collaboratively within a multi-disciplinary team.

 Desirable Skills, Experience and Certifications

• Experience using ArcGIS software (ArcGIS online, ArcGIS Experience Builder)
• Experience from developing web applications.
• Experience from cyber-security data analysis.
• Experience in preparing education material and providing training to the end-user community.

 Working Location

• Brussels, Belgium

Working Policy

• On-site

Travel

• Some travel to other NATO sites may be required

Security Clearance

• Valid National or NATO Secret personal security clearance

WHO WE ARE 

Zeta Global (NYSE: ZETA) is the AI-Powered Marketing Cloud that leverages advanced artificial intelligence (AI) and trillions of consumer signals to make it easier for marketers to acquire, grow, and retain customers more efficiently. Through the Zeta Marketing Platform (ZMP), our vision is to make sophisticated marketing simple by unifying identity, intelligence, and omnichannel activation into a single platform – powered by one of the industry’s largest proprietary databases and AI. Our enterprise customers across multiple verticals are empowered to personalize experiences with consumers at an individual level across every channel, delivering better results for marketing programs. Zeta was founded in 2007 by David A. Steinberg and John Sculley and is headquartered in New York City with offices around the world. To learn more, go to www.zetaglobal.com.

The Technical Consultant (TC) is a key role within our Global Services organization, responsible for delivering high-quality technical solutions to our clients and partners while ensuring outstanding customer satisfaction.  
This role is based in Belgium and works closely with local and international stakeholders. 
Internally, the TC collaborates on solution design to ensure efficiency, adherence to best practices, and the future-proof use of Zeta’s products. 
The TC owns solution delivery end-to-end, including configuration, quality assurance testing, and technical consultation, working closely with clients and partners to ensure successful UAT and project go-live. 
To be successful in this role, you will be customer-focused, technically adept, and committed to continuous improvement. You will demonstrate strong problem-solving skills, attention to detail, and an autonomous mindset, while remaining flexible and collaborative in a dynamic, project-based environment.

What You'll Do 

• Understand customer business and technical requirements and deliver comprehensive, scalable solutions 

• Lead or contribute to consultative engagements addressing technical and business challenges related to digital marketing initiatives 

• Participate in design workshops and business requirements definition, through to solution sign-off 

• Provide expert input into solution design, identifying delivery impacts and recommending improvements for scalability and long-term support 

• Act as the product expert, understanding capabilities and limitations, and ensuring solutions follow technical best practices 

• Deliver technical consultation, solution configuration, quality assurance testing, and ongoing client/partner support 

• Configure, build, and set up the Zeta platform 

• Interact with both technical and non-technical stakeholders, providing guidance, troubleshooting, and project support 

• Contribute to the creation, management, and presentation of actionable BRDs/SSDs (Blueprints) that align customer business needs with Zeta solutions 

• Work autonomously on smaller or well-defined projects, while collaborating closely with Project Managers, Solution Architects, and other technical experts on larger or more complex engagements 

• Lead internal knowledge-sharing initiatives to support the growth and success of Zeta 

• Identify project risks and issues, proposing alternatives and mitigation strategies 

• Manage multiple concurrent engagements while collaborating with cross-functional team members 

• Deliver new implementations, migrations, and enhancement projects 

• Support Account Executives and Go-To-Market teams by validating solutions and contributing to effort estimations 

• Continuously research emerging technologies, market solutions, and industry trends to stay up to date and bring relevant insights into solution design when needed 

• Be onsite with the client in Brussels up to two days per week to support discovery, delivery, and stakeholder alignment 

• Travel to client or partner sites for onsite discovery and solution presentations as required 

What We’re Looking For 
 

• University degree (Business, Computer Information Systems, or similar degree preferred) or equivalent experience with demonstrated proficiency 

• 3+ years of experience in a technical role 

• Native French speaker with professional proficiency in English; knowledge of Dutch is a strong plus. 

• Based in Belgium and eligible to work in Belgium. 

• Strong presentation and verbal communication skills with technical, non-technical, end-user, and executive audiences 

• Experience developing SQL using RDBMS platforms such as MySQL, Oracle, or MS SQL Server 

• Hands-on experience with HTML, CSS, and JavaScript 

• Familiarity with SOAP and REST APIs, XML/XSL, and integration techniques 

• Ability to collaborate effectively with local and remote teams across multiple time zones 

• Demonstrated ability to work autonomously, take ownership of technical topics, and adapt quickly to different ways of working depending on project size and complexity 

• Experience in the digital marketing and/or loyalty industries is strongly preferred 

BENEFITS & PERKS

-mobile phone subscription, meal vouchers, pension plan 

PEOPLE & CULTURE AT ZETA

Zeta considers applicants for employment without regard to, and does not discriminate on the basis of an individual’s sex, race, color, religion, age, disability, status as a veteran, or national or ethnic origin; nor does Zeta discriminate on the basis of sexual orientation, gender identity or expression.  

We’re committed to building a workplace culture of trust and belonging, so everyone feels invited to bring their whole selves to work. We provide a forum for employees to celebrate, support and advocate for one another. Learn more about our commitment to diversity, equity and inclusion here:  https://zetaglobal.com/blog/a-look-into-zetas-ergs/ 

ZETA IN THE NEWS!

https://zetaglobal.com/press/?cat=press-releases 

#LI-NP1

Spektrum supports apex purchasers (NATO, UN, EU, and National Government and Defence) and their Tier 1 supplier ecosystem with a wide range of specialist services. We provide our clients with professional services, specialised aerospace and defence sales, delivery, and operational subject matter expertise. We are looking for personnel to join our team and support key client projects.

Who we are supporting 

The NATO Communication and Information Agency (NCIA) is responsible for providing secure and effective communications and information technology (IT) services to NATO's member countries and its partners. The agency was established in 2012 and is headquartered in Brussels, Belgium.

The NCIA provides a wide range of services, including:

• Cyber Security: The NCIA provides advanced cybersecurity solutions to protect NATO's communication networks and information systems against cyber threats.
• Command and Control Systems: The NCIA develops and maintains the systems used by NATO's military commanders to plan and execute operations.
• Satellite Communications: The NCIA provides satellite communications services to enable secure and reliable communications between NATO forces.
• Electronic Warfare: The NCIA provides electronic warfare services to support NATO's mission to detect, deny, and defeat threats to its communication networks.
• Information Management: The NCIA manages NATO's information technology infrastructure, including its databases, applications, and servers.

Overall, the NCIA plays a critical role in ensuring the security and effectiveness of NATO's communication and information technology capabilities.

The program

Assistance and Advisory Service (AAS)

The NATO Communications and Information Agency (NCI Agency) is NATO’s principal C3 capability deliverer and CIS service provider. It provides, maintains and defends the NATO enterprise-wide information technology infrastructure to enable Allies to consult together under Article IV, and, when required, stand together in the face of attack under Article V.

To provide these critical services, in the modern evolving dynamic environment the NCI Agency needs to build and maintain high performance-engaged workforce. The NCI Agency workforce strategically consists of three major categorise's: NATO International Civilians (NIC)'s, Military (Mil), and Interim Workforce Consultants (IWC)'s. The IWCs are a critical part of the overall NCI Agency workforce and make up approximately 15 percent of the total workforce.

Role ID – CDT-0008

Role Duties and Responsibilities

• extracting data from input files, transforming data according to the necessary formats and loading data into the Repository platform.
• Ensuring smooth data flow into Pledge data analysis model.
• Maintaining the current data pipelines and developing new data pipelines to incorporate new sources of data.
• Work with the Repository team to understand requirements for analysis and visualization.
• Develop and optimize data models and data views that allow for analysis of all relevant aspects of the data.
• Working with the Pledge team to create an interactive portal/data model to facilitate analysis of Allied returns.
• Support the data analyst in cleaning and standardising data from external sources (Repository and Pledge).
• Identifying inconsistencies, gaps, and missing elements in the data and flagging these to the data analyst and the project manager (PM).
• Investigate potential tools for data processing, data integration and visualization that could be used in a NATO environment.
• Advising the team on technical choices by clearly communicating the options to a non-technical audience.
• Support the data analyst in producing analytical products by creating dashboards and visual analytics.
• Potentially also use large language models to extract insights from unstructured data.
• Document data pipelines, codes and data models.
• Information sharing with the team and onboarding of new team members.

 Essential Skills, Experience and Certifications

• Strong analytical and technical skills.
• 2+ years experience working as a Data Engineer or in a similar role.
• Professional experience in planning and executing the data science lifecycle / data pipelines, including ingestion, pre-processing, quality assurance, analysing, post-processing and visualisation.
• Proficiency in Python for data processing.
• Knowledge of ArcGIS software.
• Very good written and spoken English.
• Proactive and highly detail-oriented.
• Ability to work collaboratively within a multi-disciplinary team and to communicate technical information to non-technical audiences.

 Desirable Skills, Experience and Certifications

• Proficiency in ArcGIS API for Python.
• Professional experience in configuring an ArcGIS Enterprise portal and its applications, such as ArcGIS Experience Builder, ArcGIS Dashboards, ArcGIS Notebooks, Survey123, and Workflow Manager, with preferred basic knowledge of ArcGIS Pro.
• Experience in visualization and building of web applications.
• Knowledge of NATO networks and data engineering/analysis tools available on those networks.
• Ability to work with both structured and unstructured data. Experience from using large language models to analyse text data.
• Experience with cyber-security data analysis.

 Working Location

• Brussels, Belgium

Working Policy

• Onsite

Travel

• Some travel to other NATO sites may be required

Security Clearance

• Valid National or NATO Secret personal security clearance

Spektrum supports apex purchasers (NATO, UN, EU, and National Government and Defence) and their Tier 1 supplier ecosystem with a wide range of specialist services. We provide our clients with professional services, specialised aerospace and defence sales, delivery, and operational subject matter expertise. We are looking for personnel to join our team and support key client projects.

Who we are supporting 

The NATO Communication and Information Agency (NCIA) is responsible for providing secure and effective communications and information technology (IT) services to NATO's member countries and its partners. The agency was established in 2012 and is headquartered in Brussels, Belgium.

The NCIA provides a wide range of services, including:

• Cyber Security: The NCIA provides advanced cybersecurity solutions to protect NATO's communication networks and information systems against cyber threats.
• Command and Control Systems: The NCIA develops and maintains the systems used by NATO's military commanders to plan and execute operations.
• Satellite Communications: The NCIA provides satellite communications services to enable secure and reliable communications between NATO forces.
• Electronic Warfare: The NCIA provides electronic warfare services to support NATO's mission to detect, deny, and defeat threats to its communication networks.
• Information Management: The NCIA manages NATO's information technology infrastructure, including its databases, applications, and servers.

Overall, the NCIA plays a critical role in ensuring the security and effectiveness of NATO's communication and information technology capabilities.

The program

Assistance and Advisory Service (AAS)

The NATO Communications and Information Agency (NCI Agency) is NATO’s principal C3 capability deliverer and CIS service provider. It provides, maintains and defends the NATO enterprise-wide information technology infrastructure to enable Allies to consult together under Article IV, and, when required, stand together in the face of attack under Article V.

To provide these critical services, in the modern evolving dynamic environment the NCI Agency needs to build and maintain high performance-engaged workforce. The NCI Agency workforce strategically consists of three major categorise's: NATO International Civilians (NIC)'s, Military (Mil), and Interim Workforce Consultants (IWC)'s. The IWCs are a critical part of the overall NCI Agency workforce and make up approximately 15 percent of the total workforce.

Role ID – CDT-0006

Role Duties and Responsibilities

• collecting and analysing data on CIS and Cybersecurity projects delivered by NCIA to support advising and (data-driven) decision making by CDT Senior Leadership;
• maintaining a prioritized project list, and contributing expertise during prioritization exercises and monitoring progress;
• actively supporting workshops and coordination meetings as part of the Enterprise Sizing effort;
• developing a database for sizing requirements, and facilitating the completion of new products and processes.
• Close liaison with ACT, capability monitors, program directors, ACO and NCIA to support enterprise coherence and cybersecurity within ICT prioritization and sequencing activities. Prioritization, dependency management, and sequencing are emphasized to optimize the execution of initiatives and ensure strategic alignment and success
• Systematically de-conflict and de-risk initiatives across multiple delivery streams and governance structures, integrating executive portfolio governance into the SEG to guide strategic prioritization, risk tolerance, and resource allocation.
• Supporting the SPG, the plan contributes the Enterprise perspective to Capability Delivery Action Plans at the WG level and serves as the CDT focal point for the WG1/SPG secretariat.
• Support mapping coherence across all Alliance and NATO Enterprise CIS and Cybersecurity CPPs, programs, and projects, developing an operating model for PfM across Enterprise stakeholders to enhance visibility, control, and coordination.
• Perform regular assessments of the NATO Enterprise ICT portfolio, identifying interdependencies, risks, and opportunities for improvement.
• Assess the qualitative data for NATO Enterprise – Enterprise Sizing (as specified in Annex C from SOR/MER 23) and updating the NATO Enterprise List of Entities and Points of Presence.
• Leverage advanced experience and knowledge of MS365 tools to enhance business as usual activities.
• Act as a conduit to drive and support coherence among Enterprise stakeholders in order to facilitate coordination and completion of new products and ways of working.

 Essential Skills, Experience and Certifications

• Over 10 years of experience in project, program, or portfolio management within the ICT industries.
• Proven working experience from multi-cultural, large international organization (e.g. NATO, EU, etc.) – minimum 2 years.
• Experience across different domains and C-suite level stakeholders.
• Extensive team management experience and deep understanding of the digital transformation processes.
• Possessing recognised formal Project Management qualifications, such as PRINCE 2 (Practitioner) / Project Management Professional (PMP).
• Possessing recognised formal Portfolio Management qualifications, such as Management of Portfolios MoP (Practitioner) / Portfolio Management Professional (PfMP).
• Lean and Agile project implementation experience, proved with relevant certifications in Agile methodologies (e.g. CSPO, Agile Coaching ICP-ACC, SAFe Advanced Scrum Master, etc.).
• Organizational Change Management Experience.
• Service Management including ITIL 3 and/or 4.
• Knowledge and experience in state-of-the-art technologies, relevant to the work, i.e. software and development platforms, and familiarity with related international / commercial / industrial products.
• Proficiency in Power BI development, architecture and Azure Fundamentals certification.
• Proven experience in developing and maintaining portfolio dashboards that provide accurate and up-to-date information on project and portfolio status.
• Advanced expertise in the setup, configuration, utilization and administration of MS365 tools.
• Experience in the creation and implementation of Standard Operating Procedures (SOPs) to standardize processes and ensure best practices in project and portfolio management.

 Working Location

• Brussels, Belgium

Working Policy

• Onsite

Travel

• Some travel to other NATO sites may be required

Security Clearance

• Valid National or NATO Cosmic Top Secret personal security clearance