Senior Associate Scientist, Bioprocess Analytics

Sanofi•Framingham, MA

7d•$75,000 - $108,333•Onsite

About The Position

Sanofi is seeking a talented and highly motivated Senior Associate Scientist with expertise in Analytical Chemistry/Biochemistry to join the BioProcess Analytics group in Framingham, MA. This role is crucial for advancing Sanofi's R&D pipelines from early discovery through late-stage development. The scientist will be a key contributor to a multidisciplinary team, driving analytical method development, optimization, and routine testing to support R&D programs and meet project goals within established timelines. This position offers significant growth opportunities, including expanding technical expertise, taking on project leadership, and charting a path toward senior scientific or leadership roles within BioProcess Analytics and the broader BioAnalytics organization. The role involves working at the forefront of drug discovery, harnessing cutting-edge AI, data, and digital platforms to push the boundaries of science and make drug development quicker and more effective.

Requirements

Bachelor’s degree in Analytical Chemistry, Biochemistry, Biology, Biotechnology, Bioengineering or a related discipline with 3–5 years of relevant experience, or master’s degree with 1–3 years of relevant experience in research laboratory or biopharma/biotech company (co-ops experience in biopharma/biotech is acceptable)
Hand-on experience with one or more separation science techniques for protein characterization, including UPLC/HPLC, LC/MS, cIEF.
Proficiency with data processing software such as Empower, Chromeleon, MassLynx, or OpenLab.
Demonstrated ability to independently manage multiple concurrent projects across varied analytical testing platforms.
Detail-oriented and well-organized, with strong time management skills and the ability to prioritize effectively in a fast-paced environment.
Ability to communicate complex technical findings clearly and concisely to diverse scientific audiences.
Collaborative team player with a proactive approach to problem-solving and a commitment to scientific rigor.

Nice To Haves

Strong background in LC-MS/MS techniques for protein post-translational modification (PTM) identification and quantitation, glycan analysis and metabolites analysis (amino acids and vitamins), with proficient instrumental operation and troubleshooting skills on Waters or Thermo instrumentation.
Experience in operating automated, high throughput lab instruments (e.g. Agilent Bravo, Hamilton liquid handling systems).
Experience with impurity-based assays including ELISA and qPCR.
Prior experience executing assays in a GLP/GxP-regulated pharmaceutical or biotechnology setting.
Familiarity with iLab Solutions for laboratory data and resource management.

Responsibilities

Drive method development and innovation by supporting the development of cutting-edge analytical method platforms, including HPLC/UPLC, LC-MS, cIEF and binding assays.
Deliver independent analytical testing supports a variety of testing platforms in a non-GMP setting, directly enabling R&D Biologics Development programs.
Manage and execute projects with minimal supervision, including planning work assignments, analyzing and interpreting test results, and conducting troubleshooting to ensure high productivity and on-time delivery.
Communicate scientific finding effectively by drafting technical reports, study protocols, and result summaries, and presenting progress clearly to cross-functional team members.
Leverage digital and AI-powered tools to enhance data analysis workflows and accelerate analytical method development.
Foster cross-functional collaboration by maintaining strong communication with internal colleagues across multiple concurrent projects.