Your new company

Our client, in Belgium, is a global biotechnology company dedicated to treating and curing life-threatening diseases. They develop cell therapies across a diverse range of technology platforms, including autologous and allogenic chimeric antigen receptor T–cell and NK cell – based immunotherapy. They are committed to improving the lives of patients worldwide at multiple sites and their goal is to reimagine healthcare and to deliver transformative treatments in the fields of oncology and cell therapy.

Your new role

• Coordination of daily production activities: You will coordinate essential parts of the CAR-T production process and manage the operational teams in your clean room.
• Quality and compliance:
  You will manage all quality aspects of production activities in your clean room and ensure strict compliance with cGMP standards.
• Collaboration:
  You will work closely with various teams and departments to integrate new technologies and processes.
• Operational excellence:
  You will optimise production processes and contribute to initiatives to increase efficiency, reduce costs and improve quality.
• Safety and environment:
  You will oversee the implementation of safety and environmental health procedures.
  
  

What you'll need to succeed

• At least 2 years working in a cGMP or ATMP environment, preferably in the biotech or pharmaceutical industry. You have substantial experience with grade C aseptic GMP manufacturing. You have a proven track record of leading teams or managing projects.
• At least a bachelor’s degree or Masters in sciences, (bio) engineering, biotechnology, pharmacy or another related field of study.
• You are a true team player who also enjoys working independently. You are good at prioritising, problem-solving and multitasking. You know how to keep a cool head, even under very stressful circumstances.
• You are fluent in Microsoft Office applications such as Outlook, Excel, Word and PowerPoint.
• You are fluent in Dutch or English, with strong oral and written communication skills.
• You have a thorough knowledge of cGMP regulations and clean room operations.
• You are flexible, problem-solving and can multitask well, and you have a strong desire to learn and grow.
  
  

What you'll get in return

Our client in Belgium is offering contracts directly so you will sign your contract with them. After successful interview rounds and offer acceptance, you will get a meaningful job that contributes directly to the well-being of patients with an excellent work-life balance. You’ll be part of a supportive and innovative working environment that encourages learning personal development. Alongside that, you will get the chance to work in a multinational setting with an open – ended contract and an attractive salary package (4000 to 4700 brutto per month excl. shift allowance). You will be working in a shift schedule, working 4 days on with 4 days off, no night shifts are expected of you in this role. Other secondary benefits include additional statutory vacations, meal vouchers, group and hospitalisation insurance, an end-of-year bonus and performance bonus.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.