Vaccine Formulation Scientist, Early-Stage Research

RiseMe

Cambridge (MA)

On-site

USD 90,000 - 150,000

Full time

4 days ago
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Job summary

The Scientist, Early Formulation at GSK in Cambridge, MA, will design, test, and optimize vaccine formulations across modalities for preclinical studies. The role emphasizes bench-scale formulation, stability testing, and data-driven decisions to guide antigen design and lead selection.

You will work in a hands-on lab, document studies, and collaborate with multi-disciplinary teams to advance portfolio decisions while adhering to EHS and quality standards.

Qualifications

  • BS, MS or PhD in pharmaceutical sciences or related field.
  • Laboratory experience with formulation studies and stability design.
  • Experience with analytical techniques (HPLC, particle sizing, pH, viscosity).
  • Experience documenting studies in notebooks and reports.
  • Strong ownership and cross-functional collaboration skills.
  • Good verbal and written communication.

Responsibilities

  • Design, prepare and test vaccine formulations at bench scale.
  • Screen and compare vaccine modalities for in vitro/in vivo evaluations.
  • Operate high-throughput formulation processes and apply DTO workflows.
  • Characterize physicochemical properties and critical quality attributes.
  • Design stability studies and interpret data for project teams.
  • Maintain accurate lab records and present data clearly.

Skills

Biotechnology
Cell Biology
Cross-Functional Teamwork
Science Documentation

Education

Bachelor's degree in pharmaceutical sciences
Master's degree in pharmaceutical sciences
PhD in pharmaceutical sciences

Tools

HPLC
Particle sizing
pH measurement
Viscosity measurement
DSF
Single-particle measurements

Job description

The Scientist, Early Formulation at GSK in Cambridge, MA, will design, test, and optimize vaccine formulations across modalities for preclinical studies. The role emphasizes bench-scale formulation, stability testing, and data-driven decisions to guide antigen design and lead selection.

You will work in a hands-on lab, document studies, and collaborate with multi-disciplinary teams to advance portfolio decisions while adhering to EHS and quality standards.

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