Senior Scientist
Sanofi
6 months ago
Remote friendly (Framingham, MA)
United States
Clinical Research and Development
Main Responsibilities
- Develop downstream purification processes in support of early and late-stage drug development programs.
- Support tech transfer of developed processes into the clinical manufacturing team or Industrial Affairs, ensuring safety, environmental, and regulatory compliance.
Responsibilities Include
- Lead development of robust downstream unit operations/processes scalable to pilot, clinical, and commercial manufacturing.
- Evaluate novel purification technologies for manufacturing and process development.
- Develop technical expertise areas; train and guide others.
- Represent the department in cross-functional and/or cross-site interactions.
- Prepare internal technical reports and present/publish technology advancements.
- Stay current with new technologies and published literature (including attending technical forums).
Basic Qualifications
- PhD in Chemical Engineering, Bioengineering, or related fields; or Master’s with at least 4 years relevant experience; or Bachelor’s with at least 6 years relevant experience.
- Ability to work independently in a matrix/collaborative/team-oriented environment.
- Excellent planning, organization, and communication skills.
Preferred Qualifications
- Understanding of scientific principles underlying and/or experience with purification technologies and operations.
- Proficiency in programming languages such as Python, R, Matlab.
- Logical/critical thinking; scientific curiosity and innovation mindset.
Benefits
- Health and wellbeing benefits including high-quality healthcare and prevention/wellness programs.
- At least 14 weeks’ gender-neutral parental leave.
- Develop downstream purification processes in support of early and late-stage drug development programs.
- Support tech transfer of developed processes into the clinical manufacturing team or Industrial Affairs, ensuring safety, environmental, and regulatory compliance.
Responsibilities Include
- Lead development of robust downstream unit operations/processes scalable to pilot, clinical, and commercial manufacturing.
- Evaluate novel purification technologies for manufacturing and process development.
- Develop technical expertise areas; train and guide others.
- Represent the department in cross-functional and/or cross-site interactions.
- Prepare internal technical reports and present/publish technology advancements.
- Stay current with new technologies and published literature (including attending technical forums).
Basic Qualifications
- PhD in Chemical Engineering, Bioengineering, or related fields; or Master’s with at least 4 years relevant experience; or Bachelor’s with at least 6 years relevant experience.
- Ability to work independently in a matrix/collaborative/team-oriented environment.
- Excellent planning, organization, and communication skills.
Preferred Qualifications
- Understanding of scientific principles underlying and/or experience with purification technologies and operations.
- Proficiency in programming languages such as Python, R, Matlab.
- Logical/critical thinking; scientific curiosity and innovation mindset.
Benefits
- Health and wellbeing benefits including high-quality healthcare and prevention/wellness programs.
- At least 14 weeks’ gender-neutral parental leave.