Cell Therapy Process Development Scientist
University of Basel
Basel, Switzerland
Your position
The successful candidate will play a pivotal role in translational activities related to the development of cell therapies in compliance with good manufacturing practice (GMP) standards.
Key responsibilities include:
- Implementation and validation of GMP manufacturing protocols and quality control (QC) measures;
- Design and execution of laboratory tasks including cell culture, QC assays, and material preparation;
- Data management and protocol documentation according to GMP requirements;
- Integration of new equipment/technologies and operations into GMP;
- Collaboration with cross-functional teams to troubleshoot and optimize production processes;
- Support the preparation of data and documentation for regulatory submissions.
Your profile
We are looking for a candidate with:
- A university degree in Biomedical sciences or related Life sciences field;
- Strong technical expertise in laboratory techniques including cell culture, QC assays, and material preparation;
- Extensive experience in designing, interpreting, and documenting screening, optimization, and validation experiments;
- Passion for translational research, with the ability to independently navigate challenges and contribute innovative solutions;
- Strong collaboration skills to work effectively with internal and external partners;
- An entrepreneurial mindset;
- Excellent spoken and written English communication skills.
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