Operations Junior Expert

Arcadis; Oost-Vlaanderen; Hybride; EUR 42 000 - 54 000; Plein temps

Résumé du poste

Arcadis seeks a CAR-T Operations Junior Expert to join our GMP‑compliant manufacturing team. You will perform CAR‑T process steps from culture to cryopreservation in a clean room and adhere to SOPs for quality and traceability.

You will collaborate across departments on shift schedules, contribute to process improvements and maintain GMP documentation and environmental monitoring, while developing your expertise in ATMP technologies.

Qualifications

• Bachelor's degree in sciences, (bio)engineering, biotechnology, pharmacy or related field or equivalent through experience.
• GMP/ATMP environment experience and aseptic techniques are assets but not required; training provided.
• Fluent in Dutch or English with strong oral and written communication skills.

Responsabilités

• Perform CAR-T process activities: accurately perform steps in the CAR-T manufacturing process including cell culture, purification, aseptic processing and cryopreservation.
• Comply with SOPs and batch records to ensure quality and safety of cellular therapies.
• Collaborate with teams to complete production tasks according to a shift schedule.
• Contribute to process optimizations and efficiency improvements.
• Maintain GMP environments with focus on equipment cleanliness and environmental monitoring.
• Complete GMP documentation to ensure compliance and traceability.

Connaissances

Team player

Independent work

Interpersonal skills

Empathy

Flexibility

Problem solving

Multitasking

Willingness to learn

Formation

Bachelor's degree in sciences or related field

Description du poste

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.