Operator GMP (Cell Therapy Products) 80-100%
Operator GMP (Cell Therapy Products) 80-100%
Operator GMP (Cell Therapy Products) 80-100%
Operator GMP (Cell Therapy Products) 80-100%
Universität Basel
Pharma, Medizintechnik
Basel
Art der Beschäftigung: Vollzeit
96.000 CHF – 117.000 CHF (von XING geschätzt)Vor OrtZu den Ersten gehörenOperator GMP (Cell Therapy Products) 80-100%
Über diesen Job
Operator GMP (Cell Therapy Products) 80-100%
As a joint venture of the University of Basel and the University Hospitals Basel, the Department of Biomedicine (DBM) brings together basic and clinical scientists to advance the understanding of health and disease.
We are home to more than 67 research groups and over 800 employees across six locations in the heart of Basel. Our collaborative and international environment fosters innovation, excellence, and impactful research.
The Cancer Immunotherapy, led by Prof. Dr. med. Heinz Läubli, is looking for an Operator GMP (Cell Therapy Products) 80–100%.
Join our community and help shape the future of biomedicine.
Your position
- Manufacturing of cell-based (primary human immune cells) medicinal products in a GMP facility
- GMP-compliant documentation, including the accurate completion of production logs, batch records, deviation reports and more
- Validation of new procedures and qualification of new equipment for GMP use
- Material management for GMP manufacturing campaigns
- Performing environmental monitoring of the cleanroom
- Development of assays (viability, potency, identity, purity) for cell-based medicinal products
Your profile
- Experience in cell culture of mammalian cells (preferably primary human immune cells) and standard analytical methods used in immunology and cell culture
- A high degree of reliability, flexibility, a problem-solving attitude, the ability to work independently and excellent teamwork skills
- Completed apprenticeship as a laboratory technician (EFZ) or a university degree in science (biological background)
- Experience in the manufacturing of ATMPs according to GMP regulations
- Motivation to work in a cleanroom environment and knowledge of GMP-compliant documentation
- Excellent knowledge of German and English (written and spoken)
We offer you
- Participation in a broad spectrum of projects and tasks translating research into the manufacture of GMP-compliant medicinal products to be used in Phase I/II clinical trials
- An interesting and challenging position within a dynamic, interdisciplinary team
Application / Contact
The position is initially limited to one year, with the possibility of extension. The application deadline is 1st December 2026.
Please click the button below to apply:
The position is initially limited to one year, with the possibility of extension. The application deadline is 1st December 2026.
Please click the button below to apply:
