Senior Associate Scientist, LNP Process Development

Bristol Myers Squibb

Cambridge (MA)

On-site

USD 111,000 - 134,000

Full time

3 days ago
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Benefits offered by this job

Flexible Time Off
11 paid holidays

Job summary

Bristol Myers Squibb in Cambridge, MA is seeking a Senior Associate Scientist for the LNP Process Development team. The role focuses on developing, characterizing, and implementing robust preclinical and clinical manufacturing processes for lipid nanoparticles, spanning early development to clinical manufacturing support.

The successful candidate will plan and execute lab studies, contribute to protocols, reports, and regulatory documentation under senior guidance, with opportunities for growth

Qualifications

  • Degree in Bio/Chemical Engineering, Bio/Chemistry, or related field.
  • BS with 6+ years’ experience or MS with 4–6 years’ experience or PhD with 0–2 years’ experience.
  • Experience with nanoprecipitation, filtration, and innovative separation processes.
  • Strong DoE and multivariate data analysis fundamentals.
  • Experience with process analytics and biophysical characterization (DLS, ribogreen, HPLC).
  • Knowledge of cGMP, ICH, and QbD in clinical manufacturing.

Responsibilities

  • Execute lab experiments for LNP process development and scale-up.
  • Design experiments for optimization and characterization using QbD and DoE.
  • Prepare protocols and reports for early- to late-stage development.
  • Perform routine analytical testing for LNP characterization.
  • Collaborate with R&D, analytics, and manufacturing to advance pipeline.

Skills

DoE principles
Multivariate data analysis
Statistical methods
Laboratory data interpretation
LNP process development

Education

BS in Bio/Chemical Engineering or related
MS in related field
PhD in related field

Tools

DLS
HPLC
RiboGreen
TFF/UF-DF

Job description

Bristol Myers Squibb in Cambridge, MA is seeking a Senior Associate Scientist for the LNP Process Development team. The role focuses on developing, characterizing, and implementing robust preclinical and clinical manufacturing processes for lipid nanoparticles, spanning early development to clinical manufacturing support.

The successful candidate will plan and execute lab studies, contribute to protocols, reports, and regulatory documentation under senior guidance, with opportunities for growth

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