Research Associate Formulation Scientist

January 14, 2026
$38 / hour
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Job Description

Job Summary:

  • Client is seeking a highly motivated formulation scientist to join its Pharmaceutical Research Sciences department in Lexington, Massachusetts.
  • The candidate will be responsible for the formulation and characterization of PEP Product, proteins, small molecules, and bioconjugates.

Duties and Responsibilities:

  • Prepare PEP Product and protein injectable formulations for in vitro and in vivo studies including selection of buffers, excipients, surfactants and conducting the relevant biophysical characterization and stability studies
  • Collaborate with cross-functional teams to ensure the selected dosage form meets the desired biophysical and biochemical profile and contribute to early screening strategies and execution
  • Operate, maintain, and troubleshoot lab instruments such as biophysical and analytical characterization equipment
  • Conduct laboratory work in a safe, efficient manner that ensures a safe working environment for colleagues

Education and Experience:

  • Bachelor’s Degree required.
  • Degree within subject matter expertise (biological, biochemical, or pharmacological sciences) preferred
  • 2+ years’ relevant technical experience required.
  • Experience in preparing injectable formulations for animal studies
  • Experience in managing projects and working collaboratively with cross-functional teams.
  • Experience with spectroscopy, calorimetry, light scattering, and other biophysical methods for PEP Product and protein injectable formulations is a plus.

Knowledge, Skills and Abilities:

  • Highly communicative and able to quickly solve problems as they arise.
  • Strong knowledge and expertise in biophysical characterization and injectable formulation development.
  • Proficient in data analysis and interpretation for drawing conclusions and making recommendations.
  • Excellent scientific communication skills and ability to engage with stakeholders effectively.
  • Strong attention to detail and ability to document experimental work with electronic laboratory notebooks (ELN).
  • General knowledge of cGMP, GLP, and regulatory requirements for pharmaceutical industries a plus.