Production Supervisor

Il y a 3 jours

OostVlaanderen, Oost-Vlaanderen, Belgique Start People Belgium Temps plein 65 000 € - 90 000 € Contrat

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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, flexible, 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.

Production Supervisor

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