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Senior Associate Scientist, GMU CMC Drug Product Development

Waltham, Massachusetts Permanent Posté le   Jun. 11, 2025 Expire le   Jul. 25, 2025 Salary Range   USD 73,500.00 - 106,166.66
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Job Title: Senior Associate Scientist, GMU CMC Drug Product Development

Location: Waltham, MA

About the Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate Progress. Join our Genomic Medicine Drug Product Development Team as a Senior Associate Scientist and you’ll have the opportunity to work on different facets of drug product formulation and process development for modalities such as Lipid Nanoparticles (LNPs), Adeno-Associated Virus (AAV) and Protein Therapeutics.

We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities

  • Execution of formulation, process development, analytical characterization and stability studies in multidisciplinary teams

  • Work with internal and external partners to efficiently and comprehensively address formulation, stability and compatibility aspects using established assays, across a variety of technological platforms and disciplines.

  • Planning, prioritization and initiation of concurrent experimental procedures for multiple programs to ensure their timely completion is essential

  • Maintain a strong work ethic and good documentation practices including electronic laboratory notebook maintenance and writing of technical reports and SOPs

  • Analyze, compile and present results to internal and cross functional teams comprised of members from multiple groups and stakeholders.

About You

Basic Qualifications

  • Master’s degree in chemical engineering, biochemistry, pharmaceutical science, or a related discipline or a Bachelor’ degree with a minimum of 2 years of experience

  • The ability to collaborate effectively with peers across a spectrum of disciplines is required.

  • Ability to multi-task and learn new skills and possess flexibility and adaptability that is needed in a fast-paced team environment

Advanced (or Preferred) Qualifications

  • Lab experience on nanoparticle research, such as LNPs and AAVs

  • Experience in gene therapy, particularly formulation and process development of lipid nanoparticles and viral capsids-based drug product is a significant plus

  • Advance knowledge and experience in using biophysical techniques and analytical tools is an added benefit

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 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.

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.

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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.

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