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Senior Associate Scientist, Bioprocess Analytics

Job in Framingham, Middlesex County, Massachusetts, 01704, USA
Listing for: BioSpace
Full Time position
Listed on 2026-08-22
Job specializations:
  • Research/Development
    Research Scientist, Biotech Research, Biotechnology
Salary/Wage Range or Industry Benchmark: 110000 - 140000 USD Yearly USD 110000.00 140000.00 YEAR
Job Description & How to Apply Below

Senior Associate Scientist, Bioprocess Analytics

Location:

Framingham, MA

About The Job

Sanofi is committed to being a world-class biologics research organization, striving to bring next generation, transformative therapies to patients. Our Bio Analytics US team, as part of Global CMC Development organization, plays a critical role in advancing Sanofi's R&D pipelines from early discovery through late-stage development.

We are seeking a talented and highly motivated Senior Associate Scientist with expertise in Analytical Chemistry/Biochemistry to join the Bio Process Analytics group in Framingham, MA. In this role, you will be a key contributor to a multidisciplinary team, driving analytical method development, optimization and routine testing to support R&D programs to meet project goals within established timelines.

This position offers meaningful growth opportunities from expanding technical expertise and assuming increasing project leadership responsibilities, to charting a pathway toward senior scientific or leadership roles within Bio Process Analytics and the broader Bio Analytics organization.

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.

Main Responsibilities
  • As a Senior Associate Scientist, you will be a highly productive contributor to the Bio Process Analytics team. Primary responsibilities include:
  • 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.
Basic Qualifications
  • Bachelors degree in Analytical Chemistry, Biochemistry, Biology, Biotechnology, Bioengineering or a related discipline with 35 years of relevant experience, or masters degree with 13 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, Mass Lynx, or Open Lab.
  • Demonstrated ability to independently manage multiple concurrent projects across varied analytical testing platforms.
Preferred Qualifications
  • 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.
Soft Skills
  • 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.
Why choose us?
  • Bring…
Position Requirements
10+ Years work experience
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