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Scientist
| Company | Sanofi |
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| Location | Framingham, MA, USA |
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| Salary | $84000 – $121333.33 |
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| Type | Full-Time |
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| Degrees | Bachelor’s, Master’s |
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| Experience Level | Mid Level |
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Requirements
- Earned Master’s degree in Biotechnology, or related field, with a minimum of 1+ years of relevant experience; OR Bachelor’s degree in Biotechnology, or related field, with a minimum of 3+ years of relevant experience.
- Downstream processes at the small to an intermediate scale of cGMP biologics production.
- Experience with chromatography and/or TFF including, UD/DF, micro filtration, nano filtration, and filtration.
- Experience authoring and executing protocols, as well as interpreting data, and report generation.
- Experience operating and troubleshooting process equipment.
Responsibilities
- Work with a global group of engineers and scientists to develop robust and scalable downstream processes for monoclonal antibodies, bispecific antibodies, Fc-, Fab-, fusion proteins, enzymes, and other recombinant proteins to support GMP manufacture.
- Work on MSAT development and pilot-scale projects, including regular team meetings and updates for data management, investigations, technical report writing, and regulatory filings.
- Ability to overcome challenges, with creative and innovative solutions.
- Support the Develop and implement new cutting-edge technologies, for DSP sciences for life cycle management projects.
- Support technology transfer including projects for internal and external partners.
- Support DOE studies to establish proven and acceptable ranges (PAR) for process characterization.
Preferred Qualifications
- Process scaling and/or technology transfer experience is preferred.
- Virus clearance studies exposure is helpful.
- Experience working with automated chromatography platforms (e.g., GE Healthcare AKTA) would be ideal.
