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 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.
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.
Practical
- An excellent work-life balance. You work 4 days. Then you enjoy 4 days off.
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