Supply Chain Project Specialist

Legend Biotech; Oost-Vlaanderen; Sur place; EUR 65 000 - 90 000; Plein temps

Avantages offerts par ce poste

Meal vouchers

Company laptop

Smartphone

Insurance

End-of-year bonus

Performance bonus

Bicycle lease

Résumé du poste

Legend Biotech is seeking a Supply Chain Project Specialist in Ghent to own quality investigations and GMP documentation within a fast-paced warehouse setting. You will drive root-cause analysis, CAPAs, and robust documentation for compliant operations.

You will collaborate with cross-functional teams globally and locally to implement warehouse process improvements, ensuring sustained quality and regulatory alignment in a regulated biotech environment.

Qualifications

• Quality investigations related to warehouse operations and deviations.
• GMP-compliant documentation and SOP/WI writing.
• Cross-functional collaboration and process improvement.

Responsabilités

• Own quality investigations for warehouse operations, define timelines and CAPAs.
• Contribute to GMP documentation and SOPs to ensure audit readiness.
• Collaborate with global and local teams to implement process changes.

Connaissances

Quality investigations

GMP documentation

Stakeholder management

Project management

Lean methodologies

Formation

Bachelor's degree Life Sciences/Supply Chain

Outils

ERP/WMS

Description du poste

To support our Supply Chain organization in Ghent, we are looking for aSupply Chain Project Specialistwhois passionate about quality,complianceand process improvement in an operational warehouse setting.

What can you expect?

As a Supply Chain Project Specialist, you will take ownership of quality and documentation activities within a fast-paced operational environment. You will play a key role in conducting quality investigations andwritingGMP documentation related to our warehouse operations. You will work closely withdifferent global and localteamswithin and outside the Supply Chain organizationto ensure that deviations are investigated thoroughly, procedures are written accurately, and processes are continuously strengthened in line with GMP expectations.

You are responsible for;

• Quality Investigations: You take ownership of quality investigations related to warehouse operations, including both batch-related and non-batch related deviations. When a deviation occurs, you investigate what happened, built a clear timeline, assess the potential impact and define the right corrective and preventive actions. You perform a root cause analysis and work closely with the involved process to understand the situation,identifytherisksand ensure that corrective actions are implementedcorrectlyand on time. You ensure that investigations are documented in a clear,accurateand compliant way.
• GMP Documentation:Youcontribute tothe audit readiness of warehouse operations by ensuring thatstandard operatingproceduresand work instructionsare complete,accurateandinspection ready. You helpidentifyimprovement opportunities andgaps in current processes or documentation and contribute to sustainablecontinuousimprovements. You understand the importance of GMP compliance and Good Documentation Practices and act within the necessary accuracy and sense of responsibility.
• Stakeholder Management & Collaboration:You collaborate closely with local and global cross-functional teams such as Warehouse Operations, Supply Chain, Quality Assurance,etc.onthe implementation of warehouse process changes.You gather input, challenge where needed and ensure strong alignment before changes are implemented. You know how to ask the right questions, understand processriskand build trust with stakeholders.

Whoare welookingfor?

Education

• A minimum of a bachelor's degree in Life Sciences, Supply Chain, Logistics or a related field.

Experience

• A minimum of three years of experiencein supply chain, manufacturing, quality and compliance, technicalwriting,..ina highly regulated environment.
• Experience in a GMP-regulated pharmaceutical or biotech environment is a strong asset.
• Experience with writing standard operation procedures and work instructions is a strong asset.

Expertise

• Supply Chain & Logistics: you have a comprehensive understanding of supply chain management principles including warehouse,logistics, inventorymanagementandreplenishmentstrategies.
• Regulatory Compliance & Quality Standards:you have in-dept knowledge of Good Manufacturing Practices and Good Documentation Practices.
• ERP & Warehouse Management Systems: you are familiar with Enterprise Resource Planning systems and Warehouse Management Systems toenableinventory tracing, procurement, andlogisticsoperations.
• Project Management:You have a first experience in project management, applying lean methodologies and tools (white or yellow belt level).

Languages

• Fluent knowledge of Dutch and English (written and spoken) is required.

Strengths

• You are an analytical and critical thinker with a problem-solving mindset.
• You have strong technical writing skills andare able totranslate complex processes into clear,preciseandGMP-compliant documentation.
• You are highly organized and capable of prioritizing and multitasking. You enjoy working independently in a dynamic and fast-growing environment.
• Youare able tobuild trust with different stakeholders and work constructively withinternal and externalteams that may have different priorities.
• You are comfortable in using digital and AI-assisted tools to improve efficiency and data analysis.

Whatdo we offeryou?

• A meaningful job with an excellent work-life balance. This position falls into our standard Monday to Friday daytime schedule (40h/week) depending on operational needs.
• 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 permanent contract of indefinite duration and an attractive salary package complemented by a wide range of fringe benefits, including additional statutory holidays, meal vouchers, company laptop, smartphone and subscription, net allowance, group and hospitalization insurance, double holiday pay, end-of-year bonus, performance bonus and the possibility to participate in our bicycle lease plan.
• 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 ParkZwijnaarde) and Tech Lane (EilandjeZwijnaarde).

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.

Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

Legend Biotech maintains a drug-free workplace.

You can find more information about how we collect, use, and protect your personal data for recruitment purposes, including your rights under applicable data protection laws, in our Candidate Privacy Notice here: en/candidate-privacy-notice (Dutch: nl/candidate-privacy-notice).