What can you expect?   

To support the operational readiness, start-up, and long-term success of our Facility Start-up, we are looking for Ops (Jr/Sr) Expert who are excited to help build a new manufacturing capability from the ground up. In this role, you will be part of the Operational Core Team and contribute to facility readiness, technology transfer activities and the successful transition towards commercial manufacturing operations. As the facility start-up progresses towards clinical and commercial readiness, you will contribute to the creation and improvement of work instructions, SOPs, and practical workflows for personnel, materials, waste, and logistics management across the manufacturing areas.

Here's what you'll do:  

• You will support the startup and operational readiness of our manufacturing and GMP facility. This includes helping establish process flows, supporting cleanroom readiness, implementing 5S principles, and optimizing the storage of equipment and materials. You will work closely with cross-functional teams to build efficient operational processes from the ground up. 

• You will actively contribute to process optimization, automation initiatives, and operational excellence projects. By observing floor operations and collaborating with stakeholders across the organization, you will help identify opportunities to improve efficiency, workflow design, and manufacturing readiness. 
• You will work closely with Manufacturing, MSAT, Quality, Engineering, Site Strategy & Excellence, Warehouse, Facility, IT, and other departments to ensure smooth operations and successful execution of manufacturing activities. 

Who are we looking for? 

Education  

• Technical bachelor’s degree, Master’s degree, or equivalent education/experience in Science, Biotechnology, Biomedical Sciences, or a related field, potentially with prior experience of hands-on operations in a cGMP or ATMP environment within the biotech or biopharma industry. 

Experience  

• Experience with isolators, media preparation, cleanrooms, or aseptic manufacturing. 

• Experience working with cGMP systems such as PAS-X, eLIMS, MES, and SAP is preferred. 

Languages  

• Professional proficiency in English, both verbal and written. 
• Proficiency in Dutch is a nice to have 

Strengths  

• You are a true team player but also enjoy working independently. 

What do we offer you?  

• A meaningful job where you will be making the difference by implementing a new phase in Legends' history. During the project phase (foreseen till +/- mid 2028), you will work 40h/week from Monday till Friday in a flex regime. As soon as the project phase ends, you will work in the existing shift regime, meaning 4 days of work and 4 days off (average working time 35 hours). Please be prepared to work across various shifts in the range starting from 6AM and ending by 2AM. 

• Many fun and informal events.