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QC Technician – Raw Material Services (m/f)
View: 170
Update day: 26-11-2025
Category: Quality Assurance / Quality Control
Industry: Biotechnology Pharmaceuticals Biotechnology Research Pharmaceutical Manufacturing
Position: Entry level
Job type: Full-time
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Job content
Description de l’emploiQCTechnician –Raw Material Services (m/f)
Position Summary
Based in Gosselies, the mission of Catalent Cell and Gene Therapy is to deliver optimized process industrialization capacities to cell therapy organizations and speed up the arrival of their therapies onto the market. From technology selection to business modelling, through GMP manufacturing, process development, quality services, Catalent’s teams are fully committed to helping their clients fulfill their objective of providing sustainable and affordable therapies to their patients.
To lead its increasing number of development and manufacturing projects, Catalent Cell and Gene Therapy is looking for a highly motivated QC Technician – Raw material Services.
The Role
The QC Technician – Raw material Services main role is to perform all administrative and laboratory activities inside the RM Services platform.
The responsibilities can be adapted and may cover the following topics: Raw Material Release, Sampling Management, outsourcing testing, Materiel qualification plan support,...)
Support the start of our commercial facility with a GMP quality grade and in an efficient way.
The RM Technician – RM Services reports to the QC Supervisor.
In order to fulfill his / her role, he / she:
- Performs his/her duties and document his/her work according to Catalent’s current procedures and GMP rules.
- Performs QC tasks in due time according to the planning and in compliance with effective instructions and procedures .
- Request the picking of the incoming material reference samples and assure their storage in the appropriate conditions.
- Performs the QC sampling of the raw materials
- Participates to RM routine testing (visual inspection, ID testing …).
- Prepares and follows the samples for analytical subcontracting. (outsourcing activity)
- Reference and retention QC samples management.
- Performs release of Raw Material
- Warns immediately the Supervisor or Manager in case of unusual event / result / OOS.
- Double checks filled forms or data generated from analytical subcontracting activities.
- Initiates or reviews DEV, OOS, CHC linked to RM Services platforms and leads necessary investigation. Implement CAPA.
- Draft Purchage order for analytical subcontracting testing.
- Drafts QC documents
- Follows the needed training on due time.
- Maintains open, effective, constructive and positive communication with all other QC members and with other departments.
- Participates actively to the weekly QC meeting.
- Works to keep department KPI in green.
- Takes part to internal and/or external audits, if necessary
- Bachelor’s degree in biology, biomedical sciences, biochemistry, clinical chemistry, biochemistry or equivalent
- Experience in cell therapy or quality control of cells from human tissue origin is an asset.
- 2 years of experience in cGMP environment and/or quality control
- Experience in cGMP environment and/or quality control is a plus.
- Organization skills, multitasking, flexibility and autonomous.
- Teamwork
- Results oriented; problem solving.
- Quality minded, rigorous and pro-active.
- Fluent in French
- English at least A2 level
- Computer skills: Microsoft Office, Compliance Wire, TrackWise are a plus.
- Delivers Results.
- Leads with Integrity and Respect.
- Demonstrates Business Acumen.
- Fosters Collaboration and Teamwork.
- Champions Change.
- Engages and Inspires.
- Coaches and Develops.
- Full-time position (40h/week).
- An indeterminate contract.
- The opportunity to take part in a growing dynamic Biotech company.
- A human-sized working environment with a convivial atmosphere.
Catalent s’engage à assurer la santé et la sécurité de ses employés, ses visiteurs, des clients et patients qu’elle sert. En raison de la pandémie mondiale, nous avons modifié bon nombre de nos processus de recrutement et d’intégration afin de préserver la sécurité de chacun. Les équipes des ressources humaines communiqueront tous les processus et procédures de sécurité nécessaires à chaque étape
Catalent. Plus de produits. De meilleurs traitements. Fournis de manière fiable. ™
Visitez www.catalent.com/careers pour explorer les opportunités de carrière.
Catalent est un employeur favorisant l’égalité des chances et l’action pour l’équité . Tous les candidats qualifiés seront considérés pour un emploi sans distinction de race, de couleur, de religion, de sexe, d’origine nationale, d’incapacité, de statut de vétéran protégé, d’orientation sexuelle ou d’identité de genre. Si vous avez besoin d’une aide raisonna ble pour une partie du processus de candidature ou d’embauche en raison d’un handicap, vous pouvez soumettre votre demande en envoyant un courrier électronique confirmant votre demande d ’adaptation et en indiquant le numéro du poste, le titre et l’emplacement à l’adresse DisabilityAccommodations @ catalent. com. Cette option est réservée aux personnes nécessitant une adaptation en raison d’un handicap. Les informations reçues seront traitées par un employé américain de Catalent, puis acheminées vers un recruteur local qui fournira une assistance pour assurer la prise en compte appropriée du processus de candidature ou d’embauche.
Avis aux représentants des agences et des entreprises de recherche: Catalent Pharma Solutions (Catalent) n’accepte pas les CV non sollicités d’agences et / ou de sociétés de recherche pour cette offre d’emploi. Les curriculum vitae soumis à un employé de Catalent par une agence tierce et / ou une entreprise de recherche sans accord de recherche écrit valide et signé, deviendront la propriété exclusive de Catalent. Aucun frais ne sera payé si un candidat est embauché pour ce poste à la suite d’une recommandation non sollicitée d’une agence ou d’une entreprise de recherche. Merci.
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Deadline: 10-01-2026
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