GMP Cell Therapy Technician – Immunology Manufacturing

University Hospital Basel; Basel; In loco; CHF 65.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Relocation support

25 vacation days + flexible days

Career development

Childcare options

Descrizione del lavoro

University Hospital Basel is seeking a skilled professional to manufacture cell-based medicinal products in a GMP facility and ensure GMP‑compliant documentation. You will validate new procedures and equipment, manage materials for GMP campaigns, and monitor the cleanroom environment.

Candidates should have cell culture experience, strong reliability, and an ability to work independently in a collaborative, interdisciplinary team, with fluency in German and English.

Competenze

• Experience in cell culture of mammalian cells, preferably primary human immune cells.
• Reliability, flexibility, problem solving, ability to work independently and strong teamwork.
• Completed apprenticeship as a laboratory technician (EFZ) or university degree in science (biological background).
• Experience manufacturing ATMPs per GMP regulations and knowledge of GMP-compliant documentation.
• Excellent knowledge of German and English (written and spoken).

Mansioni

• Manufacture of cell-based medicinal products in a GMP facility.
• GMP-compliant documentation including production logs, batch records, deviation reports, etc.
• Validation of new procedures and qualification of new equipment for GMP use.
• Material management for GMP manufacturing campaigns.
• Perform environmental monitoring of the cleanroom.
• Development of assays for viability, potency, identity, and purity of cell-based medicinal products.

Conoscenze

Cell culture experience

GMP experience

Independent work

Teamwork

Problem solving

Formazione

Laboratory technician EFZ apprenticeship or biology degree

Strumenti

GMP documentation

Descrizione del lavoro

University Hospital Basel is seeking a skilled professional to manufacture cell-based medicinal products in a GMP facility and ensure GMP‑compliant documentation. You will validate new procedures and equipment, manage materials for GMP campaigns, and monitor the cleanroom environment.

Candidates should have cell culture experience, strong reliability, and an ability to work independently in a collaborative, interdisciplinary team, with fluency in German and English.