Associate Scientist

Sanofi • Framingham, MA

8d

About The Position

The Technical Pilot Plant Downstream Purification (TPP-DSP) group purifies proteins in intermediate to large scale batches to support early to late-stage development projects. Collateral duties are generating data to enable robust technology transfers to clinical and commercial manufacturing facilities and evaluating new purification technologies. The TPP-DSP group is part of the Bioprocess Engineering department and of the larger Sanofi Global CMC Development organization. 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. About Sanofi: 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.

Requirements

• Bachelor's degree in chemical engineering, biochemistry or related discipline.
• Associate degree in scientific discipline with minimum two years of relevant experience, mainly in protein purification activities such as chromatography, tangential flow filtration and viral filtration.
• Must be able to work in a team setting.

Nice To Haves

• Laboratory experience, in either an academic or industrial setting.
• Experience purifying proteins at gram level.
• Ability to program Unicorn controlled skids.
• Excellent communication skills.
• Ability to work within a team.
• An understanding of scientific principles underlying and/or experience with purification technologies and operations.
• Excellent organization, and written and oral presentation skills
• High level of scientific curiosity.

Responsibilities

• Execute electronic batch records.
• Prepare single-use assemblies, buffers and solutions used in the manufacturing process.
• Perform routine equipment calibration and qualifications.
• Operate downstream purification equipment such as chromatography and tangential flow filtration skids.
• Routinely move heavy barrels and equipment.
• Maintain adequate levels of supplies.
• Assist in creating standard operating procedures and batch records and their continuous improvement.
• Schedule and coordinate PM and calibration activities to ensure equipment readiness.
• Participate in implementing new technologies such as integrated and continuous processing, and inline buffer conditioning.

Benefits

• 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 it’s 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees