Senior Associate Scientist - Drug Product Development

Senior Associate Scientist Drug Product Development Location: Cambridge, MA About the Job This position supports the development of oral solid dosage formulations for small molecule drug products. The successful candidate will contribute to the design, development, and optimization of preclinical formulations (conventional and enabling) and clinical solid oral dosage forms (tablet and capsule), from early‑stage development through scale‑up and technology transfer to GMP manufacturing. Working under the guidance of senior team members and in close collaboration with cross‑functional CMC teams, the candidate will apply hands‑on laboratory skills and foundational scientific knowledge to help advance drug candidates into clinical development. 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. 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. Main Responsibilities Support the design and development of oral solid dosage formulations (tablets, capsules, granules) for preclinical and clinical programs. Execute formulation studies including excipient compatibility testing, prototype development, and formulation optimization under guidance. Contribute to the development of conventional and enabling formulations (e.g., amorphous dispersions) to help address bioavailability challenges. Support formulation and process development activities, including granulation (wet and dry), blending, compression/tableting, and encapsulation. Assist in applying DoE methodologies to optimize formulation and process parameters, with guidance from senior scientists. Collaborate within the CMC team as a contributing team member, supporting defined deliverables and milestones. Work with Analytical, Biopharm, Quality, and Regulatory colleagues to support alignment on development strategies. Support Research team interactions to help evaluate molecular attributes relevant to drug delivery and formulation design. Author and review technical reports, batch records, and supporting documentation with guidance from senior staff. Ensure all documentation is accurate, complete, and compliant with requirements. Maintain awareness of current scientific literature relevant to assigned projects. Make decisions that may require extrapolation of technical knowledge; decisions generally impact own work and may impact the work group or project team. Independently plans standard and moderately complex experiments with relevant controls, with limited guidance from supervisor or subject matter experts. Able to plan and manage a set of concurrent experiments. Individual contributor. Understands the responsibilities of being a team member and adheres to appropriate documentation and safety practices. Present internally within the functional group and to other local functions. May present to project or cross‑functional teams as appropriate. Organizes own daily work to meet deadlines. Contributes to team objectives and short‑term operational goals under supervision. About You Basic Qualifications Bachelor’s degree OR Master’s degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biomedical Engineering, Materials Science, Food Science, or a related life science/scientific/engineering discipline. 4+ years (Bachelor's holders) OR 2+ years (Master's holders) of hands‑on experience in product or process development in a pharmaceutical, laboratory or related environment. Experience with oral solid dosage formulation (tablets and/or capsules). Experience running dissolution studies using standard apparatus (USP2, USP4, USP7) and/or Pion equipment. Solubility testing experience. Academic or research experience will be considered but industry experience is required. Preferred Qualifications Experience with enabling formulations such as amorphous solid dispersions, nanosuspensions, or lipid‑based formulations. Excipient compatibility testing and formulation screening experience. Hands‑on experience with tablet presses (rotary and/or single‑station). Experience with granulation equipment (high‑shear, fluid bed, and/or roller compaction). Experience with capsule filling machines and/or coating equipment. Working knowledge of powder characterization techniques. Familiarity with Design of Experiments (DoE) methodologies. Exposure to process scale‑up and technology transfer activities. Experience working with external manufacturing or research partners. Strong problem‑solving skills and scientific curiosity. Effective oral and written communication skills. Ability to work collaboratively in a cross‑functional team environment. Good organizational skills with the ability to manage multiple tasks and projects simultaneously. Why Choose Us 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. 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. Achieve genuine work‑life balance in a supportive R&D environment. high‑quality healthcare prevention and wellness programs at least 14 weeks’ gender‑neutral parental leave 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 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. US and Puerto Rico Residents Only Sanofi Inc. and its U.S. affiliates are Equal Opportunity and affirmative action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, natural or protective hairstyles, 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. North America Applicants Only The salary range for this position is: $75.000,00 - $108.333,33 All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK. We are an R&D driven, AI-powered biopharma company committed to improving people’s lives and creating compelling growth. Our team is guided by one purpose: we chase the miracles of science to improve people’s lives. We want to build a healthier, more resilient world, and turn the impossible into the possible by discovering, developing, and delivering medicines and vaccines for millions of people around the world. Discover more about us visiting or via our movie We are Sanofi Start a career that makes a difference. Reinvention is in our DNA. It’s what drove our evolution from a small French enterprise to one of the world’s leading biopharma companies. Whether it’s using AI to shorten drug‑discovery times or building trust in healthcare, you could be helping our teams make life better for patients, partners, and communities. This is where you grow your career. We open the door for you to explore new opportunities, push your limits, and connect with people who are driven by a shared purpose: we chase the miracles of science to improve people’s lives. #J-18808-Ljbffr Sanofi