- Participation in the manufacturing process. Work aseptically in a clean room environment with human hematopoietic stem cells and vector technologies (BSL2).
- Execution of all assigned manufacturing activities in accordance with the production plan and the applicable GMP, safety and environmental guidelines.
- Production of GMP documents. Documentation of manufacturing steps, recording of deviations and assistance with the appropriate measures in line with the GMP requirements.
- Execution of studies as part of the process development team. Assistance in cell culture, viral transduction, and performance of analytical methods. Maintenance of up-to-date, accurate and comprehensive documentation records and reports.
- Preparation and maintenance of equipment and environment for use.
- Management of material supply and storage (inspections and documenting of deliveries, stocking, release etc.).
- Participation in all role-relevant training and maintenance of the required training levels.
- Commitment and willingness to continuously improve.
- Bachelor's degree in life sciences or minimum 2 years of work experience in a similar position. Advanced degree with relevant experience will be considered.
- Minimum of 2 years of experience in process development or GMP manufacturing of pharmaceuticals (preferred experience in cell product manufacturing).
- Experience in handling of human derived material in the BLS2 environment, cell culture and molecular biology techniques, automated cell processing systems.
- Familiarity with GMP compliant manufacturing of cell products, materials and equipment qualification is an advantage.
- Knowledge of GMP regulations and guidance relevant to cell and gene therapy manufacturing is an advantage.
- Fluent verbal and written communication in English. Good communication skills in German is an advantage.
- Good knowledge of MS Office
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Production Operator - Zurich, Schweiz - University of Zurich
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Beschreibung
Your responsibilities
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What we offer
You can expect an interesting job to which you can actively contribute to. A diverse and motivated team awaits you with the aim of bringing the therapy into a phase I/II clinical trial. We offer you well-established training in the GMP-regulated environment. The conditions of the contract and the salary are subject to the regulations at the University of Zurich, cantonal regulations and your qualifications.