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Production Supervisor - Biotechnology - EN - GMP & Clean Room M/V/X

Référence 5768073 | Créé le 25 février 2026

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  • Temps de travail : Temps plein
  • Type de contrat : Durée indéterminée
  • Famille de métiers : Etudes, recherche et développement / Recherche fondamentale et appliquée

Description de la fonction

  • Leading team of up to 10 pax within Production environment - GMP - Clean Room
  • Supervisor - state of the art Biotech Production - constant improvement

Our client is a global market leader within bio pharmaceutical field specialising in the discovery, development, manufacturing, and commercialisation of cell therapies.

In order to sustain their constant growth, they are actively looking for a Production Supervisor - Biotech - Micro Biology.


Leadership and supervision: You will manage operational teams and supervise various operational units within the production process. Quality and compliance: You manage all aspects of quality and ensure strict compliance with cGMP standards. As a domain expert for Quality and Operations, you play a central role in GMP inspections. Collaboration: You are the first point of contact for production problems and work closely with other departments to find solutions. Documentation management: You will manage and review critical documentation within the production areas, such as procedures, work instructions, logs and transfer forms. Batch record supervision: You oversee the release and review of batch records for quality control. Training: As a manager, you make sure that everyone on your team gets the training they need to perform at their best. Operational excellence: You initiate projects that increase efficiency, reduce costs and improve quality. You encourage and inspire your team to continuously improve.

Profil

Education You have a bachelor's or master's degree in science, bio-engineering, pharmacy or a related field of study or you are equivalent through experience. Experience You have at least 3 years of experience in a GMP or ATMP environment, preferably in the biotech or pharmaceutical industry. Experience with aseptic GMP production is nice to have. Expertise You have a knowledge of cGMP regulations and clean room operations. You can work fluently with Microsoft Office tools such as Word, Excel, PowerPoint and Outlook. Familiarity with Manufacturing Execution Systems (MES) and Electronic Batch Record (EBR) systems is a plus. Languages You speak and write fluent English. Strengths You have excellent communication and organisational skills. You are an empathetic people manager with strong leadership skills. You have a positive attitude and adapt easily to rapidly changing circumstances. You inspire others to do the same. You are good at problem solving, prioritising and multitasking. You have an eye for detail and procedures.

Compétences linguistiques

  • Néérlandais (atout)

    • Comprendre : Expérimenté - (C1)
    • Écrire : Expérimenté - (C1)
    • Lire : Expérimenté - (C1)
    • Parler : Expérimenté - (C1)

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Comment postuler ?

Nom de l'employeur
MICHAEL PAGE INTERNATIONAL (BELGIUM)
Personne de contact
Belgium Stepstone
Mode de présentation
postuler via le site Web
Website
Site de l’employeur