Principal Scientist

BioSpace; Waltham (MA); On-site; USD 140,000 - 200,000; Full time

Job summary

Sanofi is seeking a Principal Scientist in Waltham, MA to join the Genomic Medicine Cell Therapy Process Development Group. You will lead scale-up activities from bench to pilot scales (200L-2000L) and guide process development for robust, scalable cell culture bioprocesses.

The role emphasizes hands-on lab work, cross-functional collaboration with downstream teams, and presenting findings to senior leaders.

Qualifications

• Masters degree in Chemical Engineering or related with 6+ years in large-scale bioreactors.
• Strong background in cell culture bioreactor operations and scale-up technologies.
• Experience in biotech/pharmaceutical industry within a cell culture role and an excellent understanding of operational excellence.
• Experience with perfusion process operations at various scales.
• Understanding of engineering principles related to cell culture process is required.

Responsibilities

• Lead scale-up activities from bench scale to pilot scale (200L-2000L).
• Collaborate with process development scientists to translate laboratory findings into scalable, robust manufacturing processes.
• Review and approve JSAs written by equipment owners and provide feedback.
• Train employees to adopt best practice for safety, efficiency and operational success.
• Build robust internal interfaces with the CMC community and promote adoption of best practices.
• Demonstrate expertise in upstream process operations at all scales.
• Lead root cause analysis (RCA) investigations for process deviations, equipment failures at pilot scale.
• Present findings and/or results to senior management, external stakeholders, and industry leaders at national/international conferences.

Skills

Bioreactor operations

Scale-up technologies

Perfusion processes

Process automation

Cross-functional collaboration

Education

Masters in Chemical Engineering

PhD in related field

Tools

None

Job description

About The Job

The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best-in-class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors and cell therapy products. Sanofi is looking for an experienced cell culture development professional with experience in cell therapy process development to join the Genomic Medicine Cell Therapy Process Development Group located in Waltham, MA in the role of Senior Scientist. The Genomic Medicine Cell Therapy Development group within Sanofi operates with the mission to develop robust, scalable, and innovative cell culture processes for Sanofis genomic medicine pipeline. This position is a senior individual contributor embedded within the Upstream Scale-Up Laboratory, responsible for execution of cell culture bioprocesses at pilot and manufacturing scales (200L2000L). This role serves as a technical cornerstone of the scale-up team, driving process understanding, operational excellence, and cross-functional alignment with downstream Scale-Up Laboratory team and manufacturing organizations. While this position carries no direct people management responsibilities, the incumbent is expected to demonstrate strong technical leadership guiding peers, influencing process strategy, and serving as a subject matter expert (SME) in upstream bioprocessing. The role operates at the intersection of process science, engineering rigor, and operational execution, requiring both hands-on laboratory proficiency and the strategic mindset to translate bench-scale learnings into robust, scalable processes. Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In R&D, youll drive breakthroughs that could turn the impossible into possible for millions.

Job title

Principal Scientist

• Location: Waltham, MA

Main Responsibilities

• Lead scale-up activities from bench scale to pilot scale (200L2000L), applying engineering principles (mixing, mass transfer, shear stress, dissolved oxygen control) to ensure process comparability at large scale.
• Collaborate with process development scientists to translate laboratory findings into scalable, robust manufacturing processes.
• Review and approve JSAs written by equipment owners and provide feedback.
• Train employees to adopt best practice for safety, efficiency and operational success.
• Build robust internal interfaces with the CMC community and promote the adoption of best practices.
• Demonstrate expertise in upstream process operations at all scales.
• Lead root cause analysis (RCA) investigations for process deviations, equipment failures at pilot scale.
• Present findings and/or results to senior management, external stakeholders, and industry leaders at national/international conferences.

About You

• Masters degree in Chemical Engineering, or related discipline with a minimum of 6 years of relevant experience to large-scale bioreactors, or a Ph.D degree with a minimum of 4 years of industry experience related to large-scale bioreactors.
• Strong background in cell culture bioreactor operations and scale-up technologies.
• Experience in the biotech/pharmaceutical industry within a cell culture role and an excellent understanding of the operational excellence.
• Experience with perfusion process operations at various scales.
• Understanding of engineering principles related to cell culture process is required.
• Ability to lead matrix teams for operations and lab management.

Preferred Qualifications

• Experience managing cross-functional team and initiatives.
• Experience in cell culture process development for AAV manufacturing.
• Expertise in mammalian cell culture and related aspects such as cell metabolism/media optimization, engineering fundamentals on cell culture scale-up/down, cell biology/physiology.
• Process automation experience.

Why Choose Us

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether its through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks gender-neutral parental leave.
• Be part of a pioneering biopharma company that engages patients early in drug development and uses their insights to design studies that reflect real-world needs.
• Help improve the lives of millions of people globally by making drug development quicker and more effective.
• Work at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.