Operations Technician - Pharma

Our client, based in Zwijnaarde, is a global biotechnology company that brings innovative cell therapy to Ghent.

The team makes a daily difference in the lives of many patients suffering from cancer and other life-threatening diseases.

The company is currently in a phase of strong growth and is looking for motivated and dedicated team members.

Are you ready to make a difference? As an Operations Technician at our client, you will be at the forefront of revolutionizing cell therapy processes. Your role will involve conducting operations, including cell culture, purification, aseptic processing, fill & finish, and cryopreservation, while ensuring compliance with safety policies, quality systems, and cGMP requirements.

Key Responsibilities:

Cleanroom Manufacturing: Operate daily in a Grade A/B/C/D cleanroom environment, maintaining equipment and facility cleanliness.

Aseptic Processing: Manufacture clinical and commercial-grade ATMPs through aseptic manual processes, including cell isolation, selection, activation, transduction, culture, fill and finish, and cryopreservation.

Quality Control: Perform in-process control testing on batch samples, ensuring high standards of cell counting and viability.

Equipment Maintenance: Keep equipment running smoothly by following instructions, troubleshooting issues, and coordinating repairs.

Process Optimization: Contribute to process optimization, introduce new products, procedures, and equipment in GMP areas.

Documentation: Support writing and revising SOPs and other production-related documents, manage raw materials, consumables, and waste.

Continuous Improvement: Participate in QMS-related tasks, including Change Control Requests, deviations, and CAPA.

• As an Operations Technician, you have obtained a master's degree in Science, Bio-Engineering, BioTechnology, Pharmacy, or related field, or equivalent experience.


• Knowledge of GMP regulations & EMEA- guidance is preferred but not mandatory.


• Strong interpersonal skills with a focus on teamwork.


• Clear verbal and written communication skills with attention to detail.


• Familiarity with cGMP regulations and ATMP (Advanced Therapy Medicinal Products) guidance for cell-based product manufacturing.


• Strong problem-solving abilities with a positive attitude.


• Self-motivated with a desire to learn and teach others.


• Proficiency in Microsoft Office applications.


• Experience with cGMP systems like PASx, eLIMs, Siemens, and SAP is preferred.