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Scientist Synthetic Biology/Gene Therapy (m/f/d)
View: 171
Update day: 24-10-2024
Category: R & D IT - Software
Industry: Human Resources Services
Position: Mid-Senior level
Job type: Full-time
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Job content
The PositionAre you ready for your next challenge?Our vision is to create novel and highly differentiated medicines. To this end, we discover and develop novel therapeutic antibodies and next generation biologics, such as bispecific antibodies, fusion proteins or AAV vectors for gene therapy. Our ambition is to deliver such novel molecules to patients with game changing clinical benefit.We are looking for a Scientist in Synthetic Biology/Gene Therapy (m/f/d) with a keen interest in the fields of rAAV gene therapies. You will join the department of Cell Technologies, which belongs to a unit called Large Molecule Research within Roche Pharma Research and Early Development (pRED).This position therefore offers the opportunity to interact with numerous functions within Roche also at different sites to deliver novel medicines to patients.Your Team In a NutshellYou will be part of ambitious matrix teams, which drive different rAAV gene therapy projects of the Synthetic Biology program in Targeted Modalities (TMo). These teams involve Roche colleagues with different expertise and level (e.g. students, lab technicians, scientists and project managers). Each voice is valued and we highly appreciate contribution of different perspectives that often leads to innovative solutions for our challenging projects.The Job In a NutshellYour work focuses on development and application of synthetic biology tools for cell engineering and rAAV vector engineering. You have a strong background in ML-guided barcoded library generation & screening to run design-build-test-learn cycles for engineering & optimization of genetic elements.The Main Tasks Of This Position- DESIGN: You will design rAAV gene libraries using computational tools based on your deep understanding of how to connect genetic/RNA/protein elements to create synthetic systems that are functional in mammalian cells.
- BUILD: You will apply cutting-edge genome editing and other cell engineering technologies to generate tailor-made cell lines for assays, production and screening.
- TEST: You will use existing and establish new functional readouts, e.g. FACS, reporter cell systems, microfluidic systems and NGS, to select for desired cell populations and isolate desired DNA sequences.
- LEARN: You will use state-of-the-art data analysis software but also apply self-written scripts (e.g. R / Python or others) to analyze and consolidate large data sets that support informed or ML-guided decision-making for the next design cycle.
- A strong background in cutting-edge technologies for generation & screening of barcoded libraries is necessary for this position. Ideally in the context of rAAV gene therapies
- A University degree in biotechnology, synthetic biology or similar area including PhD helps you to fulfill those tasks
- Ideally, you have already applied your programming skills to analyze large data sets or have used machine learning approaches to tackle biological questions
- Expertise in molecular biology (e.g. plasmid design, gene switches, RNA engineering, library design & transformation, DNA sequencing) and cell engineering (transfection, CRISPRa/i, gene tagging) is required. Experience in the following techniques and readouts are desired: FACS analysis, microfluidic devices, cell culture automation and NGS
- We can trust in your project management skills
- Fluent English language skills are natural to you
- Strong IT and data analysis skills as well
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Deadline: 08-12-2024
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