Formulations Scientist: Prototype & Dosage Form Dev

Eurofins

New London (CT)

On-site

USD 90,000 - 130,000

Full time

2 days ago
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Benefits offered by this job

Health insurance
401(k) with company match
Paid vacation and holidays
Dental and vision options

Job summary

Eurofins in Groton, CT is seeking a formulation scientist to advance drug product development. The role covers oral, topical, and IV dosage forms for feasibility studies, with emphasis on pre‑formulation and material characterization.

You will work across in‑vitro/in‑vivo models and support protocol creation for clinical study sites. The ideal candidate has hands‑on experience in amorphous dispersions, dissolution testing, and advanced analytical techniques, and can operate independently within

Qualifications

  • Experience with drug formulation and pre-formulation techniques.
  • Understanding of drug candidate properties.
  • Experience with amorphous solid dispersions.
  • Experience with spray dried dispersions or hot melt extrusion.
  • Experience with dissolution testing and Raman/thermal analysis.

Responsibilities

  • Prepare prototype formulations for exploratory studies in in‑vitro and in‑vivo models.
  • Develop oral, topical and intravenous dosage forms for feasibility studies.
  • Measure properties such as solubility, tablet hardness, disintegration, pH.
  • Assess stability and performance of prototype formulations.
  • Develop protocols for preparation of formulations at clinical study sites.

Skills

Drug formulation
Pre-formulation
Amorphous dispersions
Hot melt extrusion
Dissolution testing
Raman analysis
Data analysis

Education

Bachelor's degree in Chemistry

Tools

Raman spectroscopy
Thermal analysis
Dissolution apparatus

Job description

Eurofins in Groton, CT is seeking a formulation scientist to advance drug product development. The role covers oral, topical, and IV dosage forms for feasibility studies, with emphasis on pre‑formulation and material characterization.

You will work across in‑vitro/in‑vivo models and support protocol creation for clinical study sites. The ideal candidate has hands‑on experience in amorphous dispersions, dissolution testing, and advanced analytical techniques, and can operate independently within

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