Senior Associate Scientist, Bioprocess Analytics
$156,000–$156,000 year
On-siteFramingham, Massachusetts, United States
Job Summary
Drive method development and innovation by supporting cutting-edge analytical method platforms including HPLC/UPLC, LC-MS, cIEF, and binding assays. Deliver independent analytical testing supports across various non-GMP platforms to enable R&D biologics development programs. Manage and execute projects with minimal supervision, including planning assignments, interpreting test results, and troubleshooting to ensure on-time delivery. Communicate scientific findings by drafting technical reports, study protocols, and result summaries for cross-functional teams. Leverage digital and AI-powered tools to enhance data analysis workflows and accelerate method development. Foster collaboration by maintaining strong communication with internal colleagues across multiple concurrent projects.
Required Qualifications
- Bachelor's degree in Analytical Chemistry, Biochemistry, Biology, Biotechnology, Bioengineering or a related discipline
- 3–5 years of relevant experience
- Master's degree
- 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
- Location: Framingham, MA
Desired 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
- 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
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