As a Production Supervisor, you are responsible for the daily production process of personalized cell therapy, both for clinical and commercial purposes. You will lead various units within the CAR-T production process and ensure safe and compliant production activities in accordance with cGMP requirements, all while coordinating and overseeing operations from your dedicated office workspace, maintaining a clear overview of the production floor and ensuring smooth cross-team collaboration.

Your tasks will include:

- Lead and supervise operational units within the production process, including component preparation, production support, CAR-T processing, filling & finishing, and cryopreservation.
- Serve as the first point of contact for production issues and collaborate closely with Manufacturing Operations, QC IPC, Quality, Facilities & Engineering, MS&T;/Manufacturing Excellence, Training, Planning, and Supply Chain.
- Act as a domain expert for Quality and Operations in cGMP areas and play a central role during GMP inspections and external audits.
- Manage all quality-related aspects of production, including documentation (procedures, work instructions, logs, transfer forms), batch record review and release, and adherence to cGMP standards.
- Coordinate quality system activities such as Change Controls, Deviations/Events, and CAPA.
- Ensure proper training for all team members and promote a culture of continuous learning.
- Drive operational excellence by initiating improvements that enhance efficiency, reduce costs, and improve quality.

Who we are looking for:

- Bachelor’s or Master’s degree in Science, Bio-Engineering, Pharmacy,



or a related field, or equivalent through experience.
- Minimum 3 years of experience in a production environment, preferably in biotech or biopharma.
- Experience in management, for example as a production lead, supervisor, coordinator, or similar leadership role.
- Solid knowledge of cGMP regulations, cleanroom operations, and familiarity with Microsoft Office; experience with MES/EBR systems is a plus.
- Strong communication, organizational, and leadership skills with an empathetic and people-oriented management style.
- Positive, adaptable, and capable of prioritizing, multitasking, and solving problems effectively, with a strong attention to detail.
- Fluent in English (additional languages are a plus).

What we offer you:

- A meaningful job that directly contributes to the well-being of patients.
- Work in a supportive, innovative, and diverse team, where learning, personal development, and loyalty are encouraged.
- Collaborate with colleagues from around the world in an environment that values team spirit.
- Celebrate legendary moments with treats, fun gadgets, and enjoyable events.
- Attractive salary package including shift premiums, meal vouchers, eco vouchers, group and hospitalization insurance, double vacation pay, and end-of-year and performance bonuses.
- You will work in a system with a 4-day work, 4-day off schedule, ensuring a good balance between work and personal life.
- You will combine +/- 2 shifts and should be open for the night shift.

If this role feels like the challenge you’ve been looking for, we’d love to connect with you! Apply now!

📌 Production supervisor (España)
🏢 Start People Belgium
📍 España