Senior Associate Scientist Purification Process Development

Job Title:

Senior Associate Associate - Purification Process Development

Location:

Waltham, MA

The Genomic Medicine Unit (GMU) in Sanofi is responsible for the design and optimization of viral vector manufacturing processes and platforms. This organization encompasses vector and cell line engineering, upstream and downstream process development, analytics, and clinical manufacturing support.

The GMU purification process development group is responsible for the development of AAV and non-viral vector processes and for supporting viral vector purification from next-generation production platforms to enable high-dose gene therapy programs. The Senior Research Associate (SRA) – Downstream Process Development role requires leadership both inside and outside the laboratory and will rely on industry expertise and the exploration of novel technologies in order to build robust and efficient purification processes consistent with patient safety standards.

We are looking for a candidate with experience in AAV and/or non-viral purification development, scale-up and manufacturing, and technology transfer.

Join the engine of Sanofi’s mission - where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions.

We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

• Support to develop, design and conduct viral vector purification experiments and evaluate new technologies to increase product yield and process understanding
• Develop, maintain and demonstrate advanced knowledge of principals and techniques in column chromatography and other areas of downstream purification
• Maintain industry knowledge and awareness of new and relevant technologies, and be willing to publish findings and to speak both internally and externally as industry leaders
• Lead / support development of study design, optimization of purification process conditions, media screening and perform troubleshooting experiments and communicate findings with appropriate working groups
• Perform data analyses, contribute to technical reports and internal/external presentations
• Support scale-up activities to implement a manufacturing process based on applied DSP knowledge
• Communicate effectively with internal and external teams, e.g. CDMOs for tech transfer activities
• Contribute to manuscript and patent writing for external publications and patent applications, respectively
• Self-motivated and display sound technical judgement
• Build a culture of support and collaboration among colleagues

• Bachelor's OR Master's degree in:
  Chemical Engineering, Biological/Life Sciences, or a related field

• Bachelor's holders: 2+ years of experience in laboratory or related settings
• Master's holders: 6+ months of experience in laboratory or related settings
• Academic or research experience will be considered.
• Knowledge of purification technologies and operations such as:
  Depth filtration, AKTA, automated protein purification chromatography, tangential flow filtration, UF/DF, virus clearance and inactivation or filtration unit operations at various scales.
• Understanding of chromatography principles and separation methods
• Technical report writing skills
• Ability to learn and perform viral vector analyses using new tools and techniques
• Good laboratory practices (GLP), including detailed lab notebook documentation