Supply Chain Project Specialist

Welcome to the Latest Job Vacancies Site 2025 and at this time we would like to inform you of the Latest Job Vacancies from the Legend Biotech with the position of Supply Chain Project Specialist which was opened this.

If this job matches your qualifications, please send your application directly through our latest Job site. Indeed, every job is not easy to apply because it must meet several qualifications and requirements that we must meet in accordance with the standard criteria of the Company who are looking for potential candidates to work. Good job information Supply Chain Project Specialist below matches your qualifications.

Position OverviewAre you ready to play a pivotal role in revolutionizing healthcare? At Legend Biotech, our mission is straightforward but bold: to cure life-threatening diseases through groundbreaking cell therapies. As a Supply Chain Project Specialist, you support the seamless transition of our pioneering cell therapies from demand to delivery.What can you expect?The role of a Supply Chain Project Specialist is very challenging and diverse. The role focusses on project management and deviation investigation. Besides that you're involved in compliance, quality control, stakeholder management, and continuous improvement within the supply chain of our CAR-T operations.Here's a snapshot of your core responsibilities:

• Project management, alignment, and reporting: You lead and support warehouse and supply chain projects using project management principles and Lean Six Sigma methodologies. This involves preparing a business case, project planning, execution according to timelines, resource management, aligning with business requirements and GXP standards and reporting outcomes to stakeholders.
• Quality and compliance: You lead quality investigations, ensure timely closure of deviations, and maintain compliance with GXP, quality, training, EHS, and security requirements. This also includes managing CAPAs (Corrective and Preventive Actions) and ensuring their effectiveness.
• Audit and documentation: You participate in internal audits, identify and document improvements and gaps in GMP procedures. You lead efforts to update Standard Operating Procedures (SOPs) and Work Instructions (WIs) in compliance with legal, safety, and quality standards.

Who are we looking for?For this role we have some requirements in mind but more important than the list below is your drive, enthusiasm, and the collaborative spirit you will bring to our team.Education:

• You have a master’s degree in science, supply chain, logistics or a related field of study or equivalent work experience.

Experience:

• You have at least 5 years of experience in supply chain or quality, preferably in the pharmaceutical industry.

Languages:

• You are fluent in English, and preferably you are proficient in Dutch too, with strong written and oral communication skills.

Strengths:

• You are highly organized and capable of prioritizing and multitasking. You enjoy working independently in a dynamic and fast-growing work environment.
• You have very strong communication and interpersonal skills. You excel in building strong partnerships with both internal and external stakeholders, at all levels of the organization and across various disciplines.
• You are an analytical and critical thinker with a problem-solving mindset.
• Your unwavering commitment to continuous improvement, safety, and compliance acts as a catalyst for change for everyone you work with.

Expertise:

• Supply chain and logistics: you have a comprehensive understanding of supply chain management principles, including warehousing, logistics, inventory management, planning and scheduling.
• Regulatory compliance and quality standards: you have in-depth knowledge of Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).
• Project Management: You have a proven track record in project management, and lean methodologies and tools. Certifications in project management and Lean Six Sigma are a plus.

What do we offer?

• A meaningful job that directly contributes to the well-being of patients around the globe.
• A supportive and innovative work environment, where learning and personal development are encouraged and valued.
• The opportunity to work with people from all over the globe. We are fully committed to diversity and inclusion, and we value every voice.
• An indefinite contract and an attractive salary complemented by a nice package of fringe benefits such as additional legal vacation days, meal vouchers, group and hospitalization insurance, annually double vacation pay, an end of year bonus and a performance bonus, reflecting our appreciation for your dedication and hard work.
• A lot of fun and informal events.

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.

How to Submit an Application:

After reading and knowing the criteria and minimum requirements for qualifications that have been explained from the Supply Chain Project Specialist job info - Legend Biotech Ghent, Flemish Region above, thus jobseekers who feel they have not met the requirements including education, age, etc. and really feel interested in the latest job vacancies Supply Chain Project Specialist job info - Legend Biotech Ghent, Flemish Region in 2025-05-14 above, should as soon as possible complete and compile a job application file such as a job application letter, CV or curriculum vitae, FC diploma and transcripts and other supplements as described above, in order to register and take part in the admission selection for new employees in the company referred to, sent via form this bottom.